| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:151261210-151261295 | Common:1; Rare:21 | ||||
| chr2:151261306-151261584 | Common:5; Rare:99 | ||||
| chr2:151261657-151262006 | Common:4; Rare:83 | ||||
| chr2:151289048-151290012 | Common:4; Rare:179 | ||||
| chr2:151290127-151290250 | Common:2; Rare:11 | ||||
| chr2:151290428-151290658 | Common:1; Rare:37 | ||||
| chr2:151409785-151410211 | Common:3; Rare:144 | ||||
| chr2:151410299-151410444 | Rare:53 | ||||
| chr2:151410486-151410657 | Common:2; Rare:55 | ||||
| chr2:151828366-151828776 | Common:3; Rare:119 | ||||
| chr2:152098094-152098217 | Common:1; Rare:24 | ||||
| chr2:152098829-152099178 | Rare:128; Clinvar:6; Clinvar (benign):6 | ||||
| chr2:152175376-152175642 | Rare:91 | ||||
| chr2:152175652-152175792 | Common:1; Rare:47 | ||||
| chr2:152175855-152176220 | Common:2; Rare:83 |