| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39026214-39026403 | Common:1; Rare:48 | ||||
| chr1:39026735-39026843 | Common:1; Rare:26 | ||||
| chr1:39105231-39105426 | Common:2; Rare:52 | ||||
| chr1:39204535-39204785 | Rare:47 | ||||
| chr1:39268259-39268515 | Rare:41 | ||||
| chr1:39408882-39409186 | Common:4; Rare:111 | ||||
| chr1:39576784-39576983 | Rare:68 | ||||
| chr1:39691380-39691700 | Common:5; Rare:63 | ||||
| chr1:39738726-39739048 | Common:3; Rare:83 | ||||
| chr1:39883441-39883624 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
| chr1:39901810-39902280 | Common:8; Rare:144 | ||||
| chr1:39954983-39955173 | Common:1; Rare:52 | ||||
| chr1:40040401-40040793 | Common:3; Rare:122 | ||||
| chr1:40096636-40097036 | Common:8; Rare:82 | ||||
| chr1:40097160-40097356 | Common:2; Rare:89; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):5 |