| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196639578-196639824 | Common:2; Rare:57 | ||||
| chr3:196712236-196712344 | Common:2; Rare:35 | ||||
| chr3:196867770-196867946 | Rare:63 | ||||
| chr3:196942375-196942702 | Common:1; Rare:141 | ||||
| chr3:197029800-197029945 | Common:1; Rare:45 | ||||
| chr3:197736807-197737221 | Common:3; Rare:135 | ||||
| chr3:197749292-197749356 | Rare:6 | ||||
| chr3:197749384-197749433 | Common:1; Rare:15 | ||||
| chr3:197749734-197750006 | Common:1; Rare:96 | ||||
| chr3:197750622-197750750 | Common:2; Rare:40 | ||||
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197950779-197950978 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959960-197960264 | Common:1; Rare:109 | ||||
| chr4:337419-337883 | Common:4; Rare:134 | ||||
| chr4:499120-499279 | Common:3; Rare:60 |