| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152717829-152717936 | Rare:45 | ||||
| chr2:158968451-158968675 | Rare:69 | ||||
| chr2:159712390-159712571 | Common:2; Rare:76 | ||||
| chr2:171433991-171434225 | Common:1; Rare:63 | ||||
| chr2:171522212-171522520 | Common:3; Rare:75 | ||||
| chr2:174248456-174248744 | Common:1; Rare:87 | ||||
| chr2:174395678-174395749 | Common:1; Rare:22 | ||||
| chr2:177212558-177212794 | Common:2; Rare:103 | ||||
| chr2:177392677-177392840 | Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:186486130-186486354 | Common:3; Rare:77 | ||||
| chr2:189784289-189784506 | Common:3; Rare:70; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190880604-190880846 | Common:4; Rare:74 | ||||
| chr2:191677858-191678140 | Common:4; Rare:78 | ||||
| chr2:197434995-197435205 | Rare:69 | ||||
| chr2:197499820-197500143 | Rare:114; Clinvar:1; Clinvar (benign):1 |