| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171999837-171999975 | Common:1; Rare:57 | ||||
| chr2:172427363-172427758 | Common:9; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172427789-172427967 | Common:1; Rare:58; Clinvar:1 | ||||
| chr2:172556115-172556258 | Rare:42 | ||||
| chr2:173075725-173075979 | Common:1; Rare:73 | ||||
| chr2:173354827-173354908 | Rare:32 | ||||
| chr2:173964107-173964335 | Rare:102 | ||||
| chr2:173965260-173965515 | Common:1; Rare:91 | ||||
| chr2:173965842-173965883 | Rare:13 | ||||
| chr2:174248460-174248751 | Common:1; Rare:89 | ||||
| chr2:174395624-174395876 | Common:2; Rare:82 | ||||
| chr2:174486977-174487416 | Common:2; Rare:111 | ||||
| chr2:176002225-176002398 | Common:2; Rare:71 | ||||
| chr2:176129435-176129721 | Rare:134 | ||||
| chr2:176188538-176188668 | Common:1; Rare:50 |