Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32650426-32650613 | Common:1; Rare:83 | ||||
chr1:32650918-32651325 | Common:2; Rare:151 | ||||
chr1:32651689-32651952 | Rare:68 | ||||
chr1:32753856-32753999 | Common:1; Rare:47 | ||||
chr1:32782352-32782461 | Rare:29; Clinvar:3; Clinvar (benign):2 | ||||
chr1:32786113-32786478 | Common:2; Rare:81; Clinvar:1 | ||||
chr1:32816477-32816775 | Common:1; Rare:59 | ||||
chr1:32816779-32816800 | Common:1; Rare:6 | ||||
chr1:32816840-32817066 | Common:1; Rare:43 | ||||
chr1:32817209-32817838 | Common:1; Rare:165; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32818042-32818094 | Rare:12 | ||||
chr1:32818149-32818489 | Rare:89 | ||||
chr1:33036437-33036562 | Rare:17 | ||||
chr1:33036863-33037121 | Rare:83 | ||||
chr1:33182023-33182222 | Rare:46 |