Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882466-179882919 | Rare:220; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179883001-179883153 | Common:3; Rare:59 | ||||
chr1:180502372-180502696 | Common:1; Rare:113 | ||||
chr1:180503185-180503428 | Common:2; Rare:51 | ||||
chr1:180631867-180632135 | Common:5; Rare:97 | ||||
chr1:181088494-181088704 | Rare:67 | ||||
chr1:182391331-182391427 | Rare:21 | ||||
chr1:182604391-182604532 | Rare:28 | ||||
chr1:182789646-182789792 | Common:2; Rare:53 | ||||
chr1:182839206-182839435 | Common:1; Rare:93 | ||||
chr1:182839556-182839742 | Common:2; Rare:85 | ||||
chr1:183472319-183472519 | Common:2; Rare:68 | ||||
chr1:183635660-183636079 | Common:3; Rare:117 | ||||
chr1:183805087-183805232 | Rare:44 | ||||
chr1:184051595-184051799 | Common:3; Rare:82 |