| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107563888-107564021 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr7:107580123-107580306 | Common:2; Rare:69 | ||||
| chr7:107744053-107744164 | Rare:37 | ||||
| chr7:108526099-108526427 | Common:5; Rare:106 | ||||
| chr7:108569576-108569958 | Common:1; Rare:140 | ||||
| chr7:112206392-112206751 | Common:1; Rare:129 | ||||
| chr7:112450145-112450465 | Common:6; Rare:88 | ||||
| chr7:114922012-114922185 | Rare:42 | ||||
| chr7:116499509-116499796 | Common:3; Rare:97 | ||||
| chr7:116524547-116524807 | Rare:61 | ||||
| chr7:118184001-118184211 | Common:1; Rare:83 | ||||
| chr7:120988681-120988811 | Rare:30 | ||||
| chr7:122144207-122144460 | Common:1; Rare:55 | ||||
| chr7:123748972-123749241 | Common:2; Rare:98 | ||||
| chr7:127588268-127588483 | Rare:87 |