Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37808180-37808546 | Common:1; Rare:84 | ||||
chr1:38012524-38012826 | Rare:91 | ||||
chr1:38859673-38860028 | Rare:141 | ||||
chr1:39026166-39026399 | Common:1; Rare:58 | ||||
chr1:40257898-40258276 | Common:4; Rare:104; Clinvar:8 | ||||
chr1:40508668-40508807 | Common:4; Rare:39 | ||||
chr1:40692036-40692290 | Common:1; Rare:80 | ||||
chr1:42456219-42456587 | Common:1; Rare:114 | ||||
chr1:42767010-42767306 | Common:4; Rare:94; Clinvar (benign):1 | ||||
chr1:42846391-42846651 | Common:1; Rare:73 | ||||
chr1:42958689-42959020 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):5 | ||||
chr1:43172220-43172352 | Common:1; Rare:66 | ||||
chr1:43358827-43359005 | Rare:45 | ||||
chr1:43367965-43368212 | Rare:67 | ||||
chr1:43389758-43389940 | Common:3; Rare:80 |