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Cell Line Search

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
SCRP2102i	C00492	Human iPS	Coronary artery disease\|Myocardial infarction	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Female	63 Years	Caucasian	No	No
SCRP2106i	KBET2106i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Male	94 Years	Caucasian > European	No	No
SCRP2115i	KBET2115i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Male	94 Years	Caucasian > European	No	No
SCRP2201i	C00496	Human iPS	Coronary artery disease\|Myocardial infarction	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Male	64 Years	Caucasian	No	No
SCRP2208i	KBET2208i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Female	95 Years	Caucasian > European	No	No
SCRP2210i	KBET2210i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Female	95 Years	Caucasian > European	No	No
SCRP2211i	KBET2211i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Female	95 Years	Caucasian > European	No	No
SCRP2305i	KBET2305i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.	Male	86 Years	Caucasian > European	No	No
SCRP2306i	C00498	Human iPS	Coronary artery disease	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Male	82 Years	Caucasian	No	No
SCRP2307i	KBET2307i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.	Male	86 Years	Caucasian > European	No	No

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