| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:189023258-189023295 | Rare:9 | ||||
| chr3:190102737-190102831 | Common:2; Rare:17 | ||||
| chr3:191380687-191380888 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194003623-194003807 | Common:2; Rare:35 | ||||
| chr3:194583925-194584023 | Common:3; Rare:29 | ||||
| chr3:196906382-196906417 | Rare:9 | ||||
| chr3:197613004-197613145 | Common:3; Rare:21 | ||||
| chr4:1961044-1961357 | Rare:71 | ||||
| chr4:6673869-6674099 | Common:11; Rare:109 | ||||
| chr4:6674420-6674661 | Common:1; Rare:98 | ||||
| chr4:8484590-8484659 | Rare:12 | ||||
| chr4:10088293-10088764 | Common:2; Rare:177 | ||||
| chr4:10103645-10103907 | Common:3; Rare:70 | ||||
| chr4:13582703-13582765 | Rare:18 | ||||
| chr4:14173071-14173112 | Common:4; Rare:12 |