| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40039792-40040240 | Common:5; Rare:147 | ||||
| chr1:40040444-40040858 | Common:6; Rare:250 | ||||
| chr1:40161117-40161416 | Common:1; Rare:108 | ||||
| chr1:40257886-40258286 | Common:8; Rare:214; Clinvar:16; Clinvar (benign):1 | ||||
| chr1:40373510-40373790 | Common:1; Rare:68 | ||||
| chr1:40374160-40374830 | Common:25; Rare:194 | ||||
| chr1:40449740-40450290 | Common:11; Rare:241 | ||||
| chr1:40477136-40477351 | Common:6; Rare:116 | ||||
| chr1:40508626-40508790 | Common:8; Rare:87 | ||||
| chr1:40531290-40531850 | Common:5; Rare:176 | ||||
| chr1:40531850-40532230 | Rare:103 | ||||
| chr1:40665619-40665813 | Common:2; Rare:92 | ||||
| chr1:40691371-40691853 | Common:5; Rare:349 | ||||
| chr1:40691969-40692117 | Common:1; Rare:58 | ||||
| chr1:40692027-40692218 | Common:1; Rare:66 |