| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131493027-131493107 | Common:1; Rare:25 | ||||
| chr2:134918588-134918873 | Common:1; Rare:117 | ||||
| chr2:135530548-135530821 | Common:1; Rare:58 | ||||
| chr2:135531170-135531514 | Common:1; Rare:72 | ||||
| chr2:135741716-135741978 | Common:1; Rare:100 | ||||
| chr2:135984881-135985207 | Common:1; Rare:76 | ||||
| chr2:135985407-135985720 | Common:4; Rare:131; Clinvar (benign):1 | ||||
| chr2:136118142-136118283 | Rare:40 | ||||
| chr2:138501661-138502015 | Common:2; Rare:127 | ||||
| chr2:142130958-142131171 | Rare:47 | ||||
| chr2:142877556-142877705 | Common:1; Rare:20 | ||||
| chr2:143129014-143129433 | Common:2; Rare:94 | ||||
| chr2:144332446-144332680 | Rare:93 | ||||
| chr2:144513791-144513955 | Rare:44 | ||||
| chr2:144517279-144517796 | Common:7; Rare:146; Clinvar:3; Clinvar (benign):5 |