| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:36389539-36389894 | Common:6; Rare:204 | ||||
| chr7:37920576-37920933 | Common:3; Rare:142 | ||||
| chr7:37921110-37921336 | Common:2; Rare:85 | ||||
| chr7:38178008-38178396 | Common:3; Rare:117 | ||||
| chr7:39566342-39566473 | Common:2; Rare:106 | ||||
| chr7:39623465-39623763 | Rare:178 | ||||
| chr7:39623956-39624380 | Common:8; Rare:182 | ||||
| chr7:39949414-39949883 | Common:13; Rare:329 | ||||
| chr7:39949890-39950384 | Common:2; Rare:231 | ||||
| chr7:40134407-40135096 | Common:1; Rare:375; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:42932132-42932459 | Rare:236 | ||||
| chr7:43729436-43729621 | Common:2; Rare:117 | ||||
| chr7:43758487-43758737 | Common:2; Rare:109 | ||||
| chr7:43869455-43869673 | Rare:124 | ||||
| chr7:43926341-43926488 | Rare:87 |