| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:172555922-172556107 | Common:1; Rare:72 | ||||
| chr2:173075297-173075496 | Common:1; Rare:32 | ||||
| chr2:173965276-173965508 | Common:1; Rare:81 | ||||
| chr2:174248454-174248725 | Common:1; Rare:82 | ||||
| chr2:174395616-174395812 | Common:2; Rare:62 | ||||
| chr2:174847536-174847724 | Rare:40 | ||||
| chr2:176002178-176002406 | Common:4; Rare:97 | ||||
| chr2:177216739-177216857 | Rare:49 | ||||
| chr2:177263387-177263709 | Common:1; Rare:80 | ||||
| chr2:177264623-177264771 | Common:2; Rare:45 | ||||
| chr2:177392659-177392790 | Common:1; Rare:34; Clinvar:1 | ||||
| chr2:177392929-177393082 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:178451067-178451426 | Common:6; Rare:107; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:182715935-182716480 | Common:3; Rare:179 | ||||
| chr2:182716871-182717070 | Common:1; Rare:35 |