| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:173965281-173965518 | Common:1; Rare:86 | ||||
| chr2:174248460-174248734 | Common:1; Rare:82 | ||||
| chr2:174395618-174395867 | Common:2; Rare:82 | ||||
| chr2:174486964-174487409 | Common:2; Rare:109 | ||||
| chr2:176002221-176002407 | Common:3; Rare:81 | ||||
| chr2:176269386-176269505 | Common:1; Rare:50 | ||||
| chr2:177212416-177212802 | Common:4; Rare:158 | ||||
| chr2:177263422-177263687 | Common:1; Rare:64 | ||||
| chr2:177264558-177264826 | Common:2; Rare:77 | ||||
| chr2:177392651-177393066 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552764-177552829 | Rare:24 | ||||
| chr2:177618708-177619018 | Common:7; Rare:83 | ||||
| chr2:178072708-178072879 | Rare:45 | ||||
| chr2:178450718-178450897 | Rare:64 | ||||
| chr2:178451083-178451424 | Common:6; Rare:102; Clinvar:4; Clinvar (benign):3 |