| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144517324-144517577 | Rare:75; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144517622-144517696 | Rare:26 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144518386-144518532 | Rare:31 | ||||
| chr2:144520136-144520533 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr2:144524431-144524654 | Common:4; Rare:56 | ||||
| chr2:148020681-148021153 | Common:2; Rare:119; Clinvar (benign):2 | ||||
| chr2:148021346-148021509 | Rare:45 | ||||
| chr2:148021544-148021652 | Rare:21 | ||||
| chr2:149587299-149587385 | Rare:21 | ||||
| chr2:149587681-149587827 | Common:1; Rare:41; Clinvar:1 | ||||
| chr2:150485313-150485518 | Common:1; Rare:43 | ||||
| chr2:151289605-151289691 | Common:1; Rare:27 | ||||
| chr2:151289875-151289951 | Rare:12 | ||||
| chr2:151828443-151828793 | Common:2; Rare:97 |