Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:141368367-141368585 | Rare:47 | ||||
chr3:141402709-141402990 | Common:2; Rare:76 | ||||
chr3:141431986-141432235 | Common:2; Rare:37 | ||||
chr3:141876014-141876246 | Rare:66 | ||||
chr3:143001472-143001631 | Common:2; Rare:57 | ||||
chr3:146544484-146544945 | Common:5; Rare:113 | ||||
chr3:149377637-149377822 | Common:1; Rare:45 | ||||
chr3:149970365-149970590 | Rare:71 | ||||
chr3:149970812-149971104 | Common:1; Rare:119 | ||||
chr3:149971122-149971347 | Common:4; Rare:104 | ||||
chr3:150408549-150408660 | Rare:38 | ||||
chr3:150603149-150603401 | Common:2; Rare:101 | ||||
chr3:151384744-151385033 | Common:1; Rare:59 | ||||
chr3:152268296-152269092 | Common:3; Rare:247; Clinvar (benign):1 | ||||
chr3:152269101-152269477 | Rare:104 |