Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17438042-17438141 | Common:1; Rare:42 | ||||
chr1:17438288-17438922 | Common:9; Rare:233 | ||||
chr1:17439180-17439237 | Rare:12 | ||||
chr1:17439253-17439615 | Common:2; Rare:65 | ||||
chr1:17439628-17440060 | Rare:142 | ||||
chr1:17539656-17539849 | Rare:53 | ||||
chr1:17539853-17540025 | Common:1; Rare:36 | ||||
chr1:18630996-18631218 | Common:1; Rare:55 | ||||
chr1:18631621-18631640 | Rare:7 | ||||
chr1:18902039-18902165 | Common:1; Rare:21 | ||||
chr1:18902457-18902585 | Common:3; Rare:52; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:18902750-18903055 | Common:7; Rare:69 | ||||
chr1:18956602-18957007 | Common:3; Rare:104 | ||||
chr1:19210020-19210592 | Common:1; Rare:169 | ||||
chr1:19210703-19210792 | Rare:20 |