| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174634541-174634666 | Rare:28 | ||||
| chr2:175168161-175168518 | Common:2; Rare:89 | ||||
| chr2:177216670-177216947 | Rare:87 | ||||
| chr2:177264646-177264874 | Common:2; Rare:73 | ||||
| chr2:177392680-177392778 | Rare:22; Clinvar:1 | ||||
| chr2:178451067-178451304 | Common:5; Rare:71; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:181457236-181457431 | Rare:68 | ||||
| chr2:181458111-181458152 | Rare:14 | ||||
| chr2:182715904-182716407 | Common:3; Rare:162 | ||||
| chr2:182716749-182717037 | Common:1; Rare:64 | ||||
| chr2:182717618-182717692 | Rare:19 | ||||
| chr2:186486055-186486344 | Common:3; Rare:84 | ||||
| chr2:189674449-189674743 | Common:1; Rare:65 | ||||
| chr2:189783939-189784166 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784333-189784518 | Common:2; Rare:63; Clinvar:7; Clinvar (benign):1 |