| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:170770790-170771124 | Common:2; Rare:58 | ||||
| chr2:176105217-176105496 | Common:1; Rare:49 | ||||
| chr2:176117277-176117436 | Rare:66; Clinvar:3 | ||||
| chr2:176637582-176637770 | Common:4; Rare:67 | ||||
| chr2:178413879-178413994 | Rare:35 | ||||
| chr2:188994036-188994330 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:188994530-188994831 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188997162-188997389 | Common:5; Rare:59; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr2:188999468-188999894 | Common:1; Rare:108; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):16 | ||||
| chr2:189003953-189004364 | Rare:119; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):23 | ||||
| chr2:215367885-215368182 | Common:1; Rare:82 | ||||
| chr2:215382214-215382455 | Rare:67 | ||||
| chr2:218402634-218402714 | Rare:25 | ||||
| chr2:222319027-222319307 | Common:1; Rare:54 | ||||
| chr2:231514317-231514550 | Common:5; Rare:93 |