| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70087294-70087926 | Common:2; Rare:218 | ||||
| chr2:70087934-70088493 | Common:1; Rare:150 | ||||
| chr2:70258014-70258242 | Common:2; Rare:81 | ||||
| chr2:70293621-70293852 | Common:3; Rare:76 | ||||
| chr2:71068038-71068317 | Rare:74 | ||||
| chr2:71068526-71068710 | Rare:84 | ||||
| chr2:71130220-71130667 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453468-71453691 | Common:1; Rare:44 | ||||
| chr2:72887318-72887428 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr2:73071701-73071863 | Common:2; Rare:61 | ||||
| chr2:73233200-73233451 | Common:1; Rare:64 | ||||
| chr2:73385670-73385871 | Common:2; Rare:79; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:73828794-73829024 | Common:1; Rare:52 | ||||
| chr2:73892206-73892476 | Common:2; Rare:55 | ||||
| chr2:73892725-73893108 | Common:3; Rare:67 |