Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31348687-31348932 | Common:1; Rare:52 | ||||
chr1:31669818-31670075 | Common:1; Rare:54 | ||||
chr1:32223819-32224061 | Common:1; Rare:42 | ||||
chr1:32228930-32229154 | Rare:46 | ||||
chr1:32363027-32363348 | Common:2; Rare:62 | ||||
chr1:33159876-33160140 | Common:3; Rare:70 | ||||
chr1:35192220-35192592 | Common:2; Rare:121 | ||||
chr1:36305484-36305706 | Rare:44 | ||||
chr1:39519528-39519708 | Rare:18 | ||||
chr1:39956053-39956148 | Common:1; Rare:13 | ||||
chr1:40388575-40388904 | Rare:70 | ||||
chr1:43439622-43439942 | Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
chr1:43603419-43603694 | Rare:77 | ||||
chr1:43609186-43609454 | Common:1; Rare:69 | ||||
chr1:43609494-43609709 | Common:1; Rare:54 |