| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10973754-10973955 | Common:1; Rare:86 | ||||
| chr7:10974283-10974428 | Rare:48 | ||||
| chr7:12211145-12211395 | Common:3; Rare:113 | ||||
| chr7:12686725-12686915 | Common:2; Rare:59 | ||||
| chr7:12687475-12687645 | Common:5; Rare:39 | ||||
| chr7:13988755-13989155 | Common:3; Rare:125 | ||||
| chr7:13989663-13989859 | Common:1; Rare:53 | ||||
| chr7:13990702-13990816 | Rare:19 | ||||
| chr7:13991286-13991670 | Common:3; Rare:105 | ||||
| chr7:14903135-14903333 | Rare:47 | ||||
| chr7:16420912-16421072 | Common:1; Rare:41; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:16421504-16421614 | Rare:21 | ||||
| chr7:16465796-16465954 | Rare:23 | ||||
| chr7:16645656-16645879 | Rare:74 | ||||
| chr7:16753570-16753800 | Rare:82 |