| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002221-176002402 | Common:2; Rare:76 | ||||
| chr2:176269349-176269514 | Common:1; Rare:67 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177263449-177263729 | Common:2; Rare:67 | ||||
| chr2:177264637-177264844 | Common:2; Rare:66 | ||||
| chr2:177392659-177392814 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177618708-177619018 | Common:7; Rare:83 | ||||
| chr2:178450724-178450862 | Rare:47 | ||||
| chr2:178451097-178451357 | Common:5; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:178478515-178478680 | Common:1; Rare:55 | ||||
| chr2:180007061-180007421 | Common:1; Rare:85 | ||||
| chr2:180983612-180983987 | Rare:72 | ||||
| chr2:181457265-181457431 | Rare:54 | ||||
| chr2:181891635-181892021 | Common:4; Rare:158 | ||||
| chr2:183078680-183078799 | Rare:23 |