| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47906506-47906795 | Common:2; Rare:99 | ||||
| chr2:95828695-95828923 | Rare:35 | ||||
| chr2:113583855-113584110 | Rare:30 | ||||
| chr2:133266858-133267140 | Common:1; Rare:60 | ||||
| chr2:178605210-178605397 | Common:1; Rare:42; Clinvar:5 | ||||
| chr2:188985159-188985258 | Rare:30; Clinvar:4 | ||||
| chr20:19757959-19758258 | Common:4; Rare:108 | ||||
| chr20:36050330-36050644 | Common:1; Rare:108 | ||||
| chr21:16588605-16588745 | Common:1; Rare:40 | ||||
| chr21:26967086-26967366 | Rare:66 | ||||
| chr21:45349849-45350142 | Common:1; Rare:53 | ||||
| chr21:45863320-45863693 | Common:2; Rare:103 | ||||
| chr21:45992071-45992182 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:22298037-22298196 | Common:2; Rare:69 | ||||
| chr22:25447968-25448118 | Common:2; Rare:45 |