| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002225-176002414 | Common:3; Rare:82 | ||||
| chr2:176269383-176269505 | Common:1; Rare:50 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177263475-177263658 | Common:1; Rare:44 | ||||
| chr2:177392651-177392823 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177552761-177552841 | Common:1; Rare:29 | ||||
| chr2:177618699-177619023 | Common:7; Rare:92 | ||||
| chr2:178450731-178450912 | Rare:69 | ||||
| chr2:178451083-178451363 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478515-178478659 | Common:1; Rare:45 | ||||
| chr2:179264502-179264867 | Common:4; Rare:136 | ||||
| chr2:180980281-180980545 | Common:1; Rare:86 | ||||
| chr2:182522351-182522840 | Common:3; Rare:95 | ||||
| chr2:182716228-182716323 | Rare:36 | ||||
| chr2:183078685-183078792 | Rare:19 |