| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101245003-101245144 | Common:1; Rare:62 | ||||
| chr7:101815954-101816047 | Rare:32 | ||||
| chr7:102464846-102465053 | Common:1; Rare:86 | ||||
| chr7:104207915-104208131 | Common:4; Rare:108 | ||||
| chr7:105532079-105532238 | Rare:42 | ||||
| chr7:105876476-105876805 | Common:6; Rare:99 | ||||
| chr7:107563892-107564028 | Common:2; Rare:81; Clinvar (benign):4 | ||||
| chr7:107744053-107744196 | Rare:51 | ||||
| chr7:108569615-108570020 | Common:2; Rare:137 | ||||
| chr7:112206387-112206804 | Common:1; Rare:156 | ||||
| chr7:116499464-116499796 | Common:3; Rare:106 | ||||
| chr7:118183989-118184182 | Rare:72 | ||||
| chr7:122144237-122144422 | Common:1; Rare:38 | ||||
| chr7:123748898-123749241 | Common:3; Rare:124 | ||||
| chr7:127585327-127585427 | Common:1; Rare:26 |