| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014016-191014353 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191677823-191678171 | Common:4; Rare:101 | ||||
| chr2:196171336-196171411 | Rare:24 | ||||
| chr2:197401833-197402055 | Common:1; Rare:32; Clinvar (pathogenic):1 | ||||
| chr2:197434975-197435238 | Rare:87 | ||||
| chr2:197453222-197453563 | Rare:118 | ||||
| chr2:197499829-197500144 | Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500221-197500412 | Common:1; Rare:78 | ||||
| chr2:197515829-197516110 | Common:2; Rare:102 | ||||
| chr2:200510058-200510199 | Rare:39 | ||||
| chr2:200857713-200858028 | Rare:81 | ||||
| chr2:200889282-200889456 | Common:2; Rare:67 | ||||
| chr2:200963647-200963897 | Rare:60 | ||||
| chr2:201071586-201071789 | Rare:50 | ||||
| chr2:201116125-201116431 | Rare:57 |