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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
SCRP4203i	KBET4203i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor had a mix of genotypes at the 3 sites.	Male	21 Years	None Reported	No	No
SCRP4301i	C00793	Human iPS	Coronary artery disease	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.	Female	82 Years	Caucasian	No	No
SCRP4305i	KBET4305i	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	29 Years	None Reported	No	No
SCRP4403i	KBET4403i	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	22 Years	None Reported	No	No
SCRP4406i	C00805	Human iPS	Coronary artery disease	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	66 Years	Caucasian	No	No
SCRP4502i	C00808	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.	Female	85 Years	Caucasian	No	No
SCRP4505i	KBET4505i	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	23 Years	None Reported	No	No
SCRP4602i	KBET4602i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Female	23 Years	None Reported	No	No
SCRP4603i	C00815	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	79 Years	Caucasian	No	No
SCRP4703i	C00863	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	78 Years	Caucasian	No	No

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