| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88220003-88220103 | Rare:57 | ||||
| chr7:90211633-90211754 | Common:1; Rare:36 | ||||
| chr7:90245083-90245253 | Common:1; Rare:55 | ||||
| chr7:90346564-90346769 | Common:4; Rare:88 | ||||
| chr7:90595875-90596038 | Common:6; Rare:60 | ||||
| chr7:91880646-91880820 | Common:1; Rare:49 | ||||
| chr7:91940831-91941145 | Common:3; Rare:105; Clinvar:6; Clinvar (benign):3 | ||||
| chr7:92134369-92134598 | Rare:74 | ||||
| chr7:92134683-92134898 | Common:4; Rare:63 | ||||
| chr7:92245668-92246537 | Common:6; Rare:265; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92246696-92246945 | Rare:53 | ||||
| chr7:92528326-92528916 | Common:5; Rare:182; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590025-92590142 | Rare:45 | ||||
| chr7:93232169-93232470 | Common:3; Rare:72 | ||||
| chr7:94509791-94510143 | Rare:120 |