| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197453113-197453571 | Rare:152 | ||||
| chr2:197453578-197453655 | Rare:30 | ||||
| chr2:197453858-197454049 | Rare:54 | ||||
| chr2:197499797-197500425 | Common:1; Rare:240; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515927-197516154 | Rare:94 | ||||
| chr2:197676027-197676088 | Rare:13 | ||||
| chr2:199911176-199911399 | Rare:81 | ||||
| chr2:200305758-200306087 | Common:7; Rare:55 | ||||
| chr2:200306400-200306707 | Common:4; Rare:80 | ||||
| chr2:200510017-200510129 | Rare:41 | ||||
| chr2:200609087-200609387 | Rare:74 | ||||
| chr2:200810565-200810610 | Rare:9 | ||||
| chr2:200811362-200811647 | Common:1; Rare:104 | ||||
| chr2:200812279-200812509 | Common:6; Rare:80 | ||||
| chr2:200817337-200817642 | Common:2; Rare:53 |