| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87193507-87193788 | Rare:69 | ||||
| chr7:87345443-87345739 | Common:5; Rare:92 | ||||
| chr7:87876122-87876652 | Common:2; Rare:210 | ||||
| chr7:88220022-88220151 | Rare:64 | ||||
| chr7:88306886-88307115 | Rare:49 | ||||
| chr7:90211614-90211944 | Common:4; Rare:101 | ||||
| chr7:90245082-90245243 | Rare:52 | ||||
| chr7:90346462-90346765 | Common:4; Rare:113 | ||||
| chr7:91880668-91880820 | Common:1; Rare:41 | ||||
| chr7:92105563-92105751 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:92134369-92134585 | Rare:71 | ||||
| chr7:92134716-92134890 | Common:3; Rare:53 | ||||
| chr7:92245890-92245979 | Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246105-92246516 | Common:3; Rare:158 | ||||
| chr7:92528397-92528816 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 |