| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73005926-73006154 | Rare:13 | ||||
| chr7:74452312-74452629 | Common:1; Rare:57 | ||||
| chr7:74890527-74890836 | Common:2; Rare:104 | ||||
| chr7:74996980-74997277 | Common:1; Rare:54 | ||||
| chr7:75528039-75528310 | Rare:89 | ||||
| chr7:75980265-75980423 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76005788-76005897 | Common:9; Rare:49 | ||||
| chr7:76041211-76041451 | Common:2; Rare:47 | ||||
| chr7:76345015-76345314 | Common:3; Rare:43 | ||||
| chr7:76348209-76348257 | Common:1; Rare:7 | ||||
| chr7:76357658-76357832 | Rare:23 | ||||
| chr7:76423517-76423758 | Common:1; Rare:35 | ||||
| chr7:76582937-76583014 | Rare:14 | ||||
| chr7:77648666-77648877 | Rare:43 | ||||
| chr7:77661361-77661590 | Rare:41 |