| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191169533-191169838 | Rare:55 | ||||
| chr2:191173956-191174136 | Common:3; Rare:28 | ||||
| chr2:191178870-191179171 | Common:1; Rare:58 | ||||
| chr2:191247838-191247987 | Common:1; Rare:30 | ||||
| chr2:191305640-191305856 | Common:3; Rare:47 | ||||
| chr2:191354939-191355099 | Common:2; Rare:19 | ||||
| chr2:191355189-191355393 | Common:3; Rare:34 | ||||
| chr2:191356062-191356350 | Common:1; Rare:49 | ||||
| chr2:191363513-191363708 | Common:1; Rare:43 | ||||
| chr2:191366010-191366259 | Common:2; Rare:50 | ||||
| chr2:191370191-191370305 | Rare:27 | ||||
| chr2:191370621-191370817 | Common:1; Rare:26 | ||||
| chr2:191378124-191378482 | Common:2; Rare:72 | ||||
| chr2:191383248-191383413 | Rare:35 | ||||
| chr2:191389439-191389547 | Rare:22 |