| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:166126047-166126389 | Common:1; Rare:36 | ||||
| chr2:168211301-168211453 | Common:1; Rare:30 | ||||
| chr2:170743946-170744078 | Rare:23 | ||||
| chr2:170751513-170751718 | Common:1; Rare:32 | ||||
| chr2:170770762-170771137 | Common:3; Rare:69 | ||||
| chr2:172489251-172489490 | Common:1; Rare:50 | ||||
| chr2:175118102-175118360 | Common:1; Rare:60 | ||||
| chr2:177215571-177215935 | Common:1; Rare:75 | ||||
| chr2:177234030-177234474 | Rare:89; Clinvar:2 | ||||
| chr2:177242680-177242846 | Rare:30 | ||||
| chr2:178413629-178413995 | Common:1; Rare:108 | ||||
| chr2:178529185-178529419 | Rare:58; Clinvar:2 | ||||
| chr2:178538706-178539040 | Common:3; Rare:90; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr2:178539206-178539466 | Common:1; Rare:65; Clinvar:7; Clinvar (benign):5 | ||||
| chr2:178554627-178554962 | Rare:92; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):2 |