| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24360423-24360558 | Common:4; Rare:81 | ||||
| chr2:24360707-24361002 | Common:8; Rare:107 | ||||
| chr2:24793220-24793620 | Rare:157; Clinvar:1 | ||||
| chr2:24971540-24971840 | Common:4; Rare:189 | ||||
| chr2:24971860-24972280 | Common:3; Rare:210 | ||||
| chr2:25041810-25042240 | Common:8; Rare:197 | ||||
| chr2:25251440-25251810 | Common:1; Rare:146 | ||||
| chr2:25252189-25252639 | Rare:161 | ||||
| chr2:25342429-25342595 | Common:1; Rare:35 | ||||
| chr2:25673454-25673714 | Common:1; Rare:96 | ||||
| chr2:25878280-25878787 | Common:10; Rare:247 | ||||
| chr2:25982463-25982787 | Common:1; Rare:81 | ||||
| chr2:26033730-26034251 | Common:8; Rare:377 | ||||
| chr2:26244577-26245012 | Common:4; Rare:313; Clinvar:13; Clinvar (benign):18 | ||||
| chr2:26245040-26245330 | Common:4; Rare:129 |