| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:173075702-173075994 | Common:3; Rare:86 | ||||
| chr2:173354566-173354904 | Common:1; Rare:102 | ||||
| chr2:173965281-173965531 | Common:1; Rare:93 | ||||
| chr2:174248456-174248734 | Common:1; Rare:84 | ||||
| chr2:174395618-174395800 | Common:2; Rare:59 | ||||
| chr2:174486917-174487416 | Common:2; Rare:120 | ||||
| chr2:175168122-175168563 | Common:2; Rare:118 | ||||
| chr2:175181629-175181747 | Common:4; Rare:58 | ||||
| chr2:175181749-175181776 | Rare:4 | ||||
| chr2:176002207-176002431 | Common:4; Rare:91 | ||||
| chr2:176002806-176002936 | Common:1; Rare:18 | ||||
| chr2:176269379-176269520 | Common:1; Rare:55 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177264646-177264776 | Common:2; Rare:42 | ||||
| chr2:177392634-177393059 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 |