| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215311951-215312161 | Common:7; Rare:93 | ||||
| chr2:215435992-215436271 | Common:2; Rare:87 | ||||
| chr2:216013305-216013368 | Rare:20 | ||||
| chr2:216081684-216081979 | Common:1; Rare:90 | ||||
| chr2:216412665-216412781 | Rare:13 | ||||
| chr2:216498715-216498911 | Common:7; Rare:87 | ||||
| chr2:216633291-216633758 | Common:8; Rare:156 | ||||
| chr2:216694580-216694651 | Rare:16 | ||||
| chr2:216694779-216694854 | Rare:16 | ||||
| chr2:218217019-218217287 | Common:2; Rare:87 | ||||
| chr2:218269582-218269759 | Rare:67 | ||||
| chr2:218269966-218270532 | Common:6; Rare:179; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218323004-218323294 | Common:6; Rare:97 | ||||
| chr2:218399731-218400075 | Rare:144 | ||||
| chr2:218568263-218568711 | Common:5; Rare:119 |