| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:136765265-136765545 | Common:7; Rare:85 | ||||
| chr2:138780350-138780530 | Rare:57 | ||||
| chr2:144332449-144332677 | Rare:91 | ||||
| chr2:148020686-148020997 | Common:2; Rare:66 | ||||
| chr2:148875577-148875620 | Rare:18; Clinvar (benign):1 | ||||
| chr2:149330330-149330609 | Common:1; Rare:119 | ||||
| chr2:149587326-149587347 | Rare:5 | ||||
| chr2:149587669-149587882 | Common:1; Rare:62; Clinvar:2 | ||||
| chr2:151409748-151410003 | Common:4; Rare:81 | ||||
| chr2:151828463-151828600 | Common:2; Rare:35 | ||||
| chr2:152175711-152176061 | Common:1; Rare:94 | ||||
| chr2:152335026-152335174 | Common:1; Rare:56 | ||||
| chr2:152717817-152717967 | Rare:60 | ||||
| chr2:152717995-152718285 | Common:1; Rare:93 | ||||
| chr2:152718491-152718659 | Rare:68 |