| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101217849-101218190 | Common:3; Rare:105 | ||||
| chr7:101244704-101244983 | Common:1; Rare:112 | ||||
| chr7:102464848-102465022 | Rare:70 | ||||
| chr7:103074800-103075226 | Common:7; Rare:169 | ||||
| chr7:105014052-105014261 | Common:3; Rare:86 | ||||
| chr7:105876481-105876835 | Common:6; Rare:104 | ||||
| chr7:106660992-106661286 | Common:2; Rare:74 | ||||
| chr7:107563889-107564047 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):5 | ||||
| chr7:107580147-107580285 | Common:2; Rare:54 | ||||
| chr7:107744089-107744159 | Rare:27 | ||||
| chr7:108569607-108569963 | Common:1; Rare:125 | ||||
| chr7:112206392-112206740 | Common:1; Rare:123 | ||||
| chr7:116499514-116499759 | Common:3; Rare:82 | ||||
| chr7:118183961-118184169 | Common:1; Rare:75 | ||||
| chr7:123748957-123749240 | Common:2; Rare:104 |