| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108448529-108448700 | Common:4; Rare:31 | ||||
| chr2:108448950-108449317 | Common:1; Rare:314 | ||||
| chr2:108449320-108450268 | Common:18; Rare:410 | ||||
| chr2:108533861-108534062 | Common:3; Rare:102 | ||||
| chr2:108534065-108534578 | Common:22; Rare:486 | ||||
| chr2:108719293-108719582 | Common:8; Rare:282; Clinvar (benign):4 | ||||
| chr2:108786570-108786868 | Common:13; Rare:253 | ||||
| chr2:109613824-109614470 | Common:18; Rare:627 | ||||
| chr2:110115700-110116070 | Common:9; Rare:211 | ||||
| chr2:110204920-110205112 | Common:2; Rare:142; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:110677974-110678302 | Rare:294 | ||||
| chr2:110732477-110732640 | Rare:56 | ||||
| chr2:110732619-110733101 | Common:5; Rare:170 | ||||
| chr2:111120667-111121078 | Common:10; Rare:377 | ||||
| chr2:111122379-111122785 | Common:9; Rare:394 |