| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177212614-177212817 | Common:1; Rare:86 | ||||
| chr2:177264644-177264797 | Common:2; Rare:50 | ||||
| chr2:177392672-177392834 | Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:182715985-182716480 | Common:3; Rare:173 | ||||
| chr2:189783968-189784123 | Common:3; Rare:57; Clinvar (benign):1 | ||||
| chr2:189784382-189784518 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:190343961-190344077 | Common:1; Rare:26 | ||||
| chr2:197499805-197500416 | Common:1; Rare:234; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:200609092-200609316 | Rare:55 | ||||
| chr2:200889270-200889450 | Common:2; Rare:68 | ||||
| chr2:200963611-200963883 | Common:1; Rare:69 | ||||
| chr2:201071643-201072039 | Rare:82 | ||||
| chr2:201451534-201451749 | Rare:47 | ||||
| chr2:206159370-206159897 | Common:4; Rare:146; Clinvar (benign):1 | ||||
| chr2:206765278-206765633 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):1 |