| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113627088-113627256 | Common:1; Rare:45 | ||||
| chr2:119366804-119367049 | Common:1; Rare:70 | ||||
| chr2:127858107-127858219 | Common:1; Rare:56 | ||||
| chr2:128091064-128091221 | Common:7; Rare:49 | ||||
| chr2:130181553-130181676 | Common:1; Rare:42 | ||||
| chr2:130342127-130342270 | Rare:57 | ||||
| chr2:135531195-135531498 | Common:1; Rare:51 | ||||
| chr2:152717829-152718070 | Rare:94 | ||||
| chr2:159712364-159712554 | Common:2; Rare:77 | ||||
| chr2:177212441-177212793 | Common:4; Rare:145 | ||||
| chr2:177264651-177264854 | Common:2; Rare:65 | ||||
| chr2:186486141-186486344 | Common:3; Rare:64 | ||||
| chr2:188292692-188292844 | Rare:38 | ||||
| chr2:189784305-189784512 | Common:3; Rare:68; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:197499807-197500237 | Rare:159; Clinvar:1; Clinvar (benign):1 |