| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55923456-55923878 | Common:4; Rare:116; Clinvar (benign):8 | ||||
| chr2:61017148-61017295 | Common:3; Rare:37 | ||||
| chr2:61017420-61017767 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144825-61145187 | Common:4; Rare:110 | ||||
| chr2:61177128-61177540 | Common:6; Rare:160 | ||||
| chr2:61178029-61178186 | Common:1; Rare:52 | ||||
| chr2:61178661-61179107 | Common:3; Rare:114 | ||||
| chr2:61184505-61184737 | Common:1; Rare:57 | ||||
| chr2:61185509-61185660 | Common:1; Rare:68 | ||||
| chr2:61185759-61185811 | Rare:15 | ||||
| chr2:61192901-61193047 | Common:1; Rare:37 | ||||
| chr2:61470658-61471014 | Rare:118 | ||||
| chr2:61471145-61471383 | Common:2; Rare:93 | ||||
| chr2:61502020-61502272 | Common:3; Rare:75 | ||||
| chr2:61537572-61537707 | Common:1; Rare:45 |