| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94409974-94410310 | Common:2; Rare:67; Clinvar:5; Clinvar (benign):3 | ||||
| chr7:94410882-94411164 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:94413074-94413208 | Rare:37; Clinvar (pathogenic):1 | ||||
| chr7:94419984-94420295 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94420382-94420648 | Rare:75; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr7:95396925-95397056 | Common:1; Rare:21 | ||||
| chr7:95406143-95406411 | Common:1; Rare:58 | ||||
| chr7:95406985-95407142 | Rare:47 | ||||
| chr7:95414266-95414535 | Common:3; Rare:51 | ||||
| chr7:95424531-95424884 | Common:3; Rare:73 | ||||
| chr7:96321225-96321556 | Common:3; Rare:79 | ||||
| chr7:97972228-97972378 | Common:1; Rare:34 | ||||
| chr7:98213349-98213568 | Common:2; Rare:41 | ||||
| chr7:98214144-98214322 | Common:2; Rare:33 | ||||
| chr7:98284752-98284955 | Common:2; Rare:40 |