| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177213092-177213433 | Rare:145 | ||||
| chr2:177263494-177264006 | Common:4; Rare:132 | ||||
| chr2:177264109-177264468 | Rare:107 | ||||
| chr2:177264613-177264950 | Common:2; Rare:101 | ||||
| chr2:177264956-177265346 | Common:5; Rare:83 | ||||
| chr2:177265469-177265556 | Rare:21 | ||||
| chr2:177392456-177392820 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177552635-177553190 | Common:5; Rare:189 | ||||
| chr2:177618620-177619135 | Common:8; Rare:174 | ||||
| chr2:178112286-178112598 | Common:2; Rare:100 | ||||
| chr2:178112877-178112944 | Common:1; Rare:18 | ||||
| chr2:178194349-178194582 | Common:2; Rare:71 | ||||
| chr2:178450462-178450981 | Common:2; Rare:182; Clinvar:1 | ||||
| chr2:178451078-178451486 | Common:6; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478512-178478740 | Common:1; Rare:73 |