| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392672-177392790 | Rare:30; Clinvar:1 | ||||
| chr2:178451133-178451424 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:182715935-182716386 | Common:3; Rare:148 | ||||
| chr2:187554318-187554529 | Rare:43 | ||||
| chr2:189783979-189784123 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr2:189784369-189784522 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:190343961-190344081 | Common:1; Rare:27 | ||||
| chr2:197453241-197453552 | Rare:102 | ||||
| chr2:197499815-197500416 | Common:1; Rare:233; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:200889112-200889439 | Common:3; Rare:105 | ||||
| chr2:201451453-201451767 | Common:1; Rare:72 | ||||
| chr2:206159389-206159704 | Common:2; Rare:101 | ||||
| chr2:206213358-206213540 | Rare:27 | ||||
| chr2:206765284-206765645 | Common:3; Rare:96; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:207529980-207530102 | Rare:29 |