| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:142130731-142130811 | Common:2; Rare:34 | ||||
| chr2:142130813-142131044 | Rare:64 | ||||
| chr2:143435224-143435531 | Common:3; Rare:49 | ||||
| chr2:144513740-144513954 | Rare:61 | ||||
| chr2:144517279-144517579 | Common:1; Rare:89; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144517745-144518203 | Common:3; Rare:73 | ||||
| chr2:144518357-144518592 | Rare:43 | ||||
| chr2:144519988-144520533 | Common:4; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020686-148021109 | Common:2; Rare:97; Clinvar (benign):2 | ||||
| chr2:148021379-148021531 | Rare:51 | ||||
| chr2:148021571-148021658 | Rare:18 | ||||
| chr2:148875554-148875680 | Common:2; Rare:40; Clinvar (benign):3 | ||||
| chr2:149587299-149587407 | Rare:26 | ||||
| chr2:149587672-149587816 | Common:1; Rare:41; Clinvar:1 | ||||
| chr2:151828310-151828617 | Common:3; Rare:95 |