| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100867194-100867406 | Common:1; Rare:63 | ||||
| chr7:101217850-101218202 | Common:4; Rare:113 | ||||
| chr7:101245015-101245198 | Common:1; Rare:77 | ||||
| chr7:101321733-101321841 | Common:2; Rare:40 | ||||
| chr7:102464848-102464978 | Rare:57 | ||||
| chr7:104207956-104208112 | Common:3; Rare:72 | ||||
| chr7:105014097-105014210 | Common:1; Rare:49 | ||||
| chr7:105532082-105532231 | Rare:39 | ||||
| chr7:105876489-105876818 | Common:6; Rare:95 | ||||
| chr7:106285128-106285455 | Common:5; Rare:112 | ||||
| chr7:107563888-107563996 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr7:107744053-107744156 | Rare:33 | ||||
| chr7:108569584-108569963 | Common:1; Rare:139 | ||||
| chr7:112206392-112206712 | Common:1; Rare:104 | ||||
| chr7:112790350-112790413 | Rare:23 |