| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100852598-100852786 | Common:2; Rare:48 | ||||
| chr7:100867214-100867418 | Common:1; Rare:61 | ||||
| chr7:101217850-101218192 | Common:3; Rare:106 | ||||
| chr7:102464846-102464993 | Common:1; Rare:64 | ||||
| chr7:106284978-106285107 | Common:1; Rare:42 | ||||
| chr7:107563902-107564006 | Common:2; Rare:60; Clinvar (benign):3 | ||||
| chr7:107744070-107744164 | Rare:32 | ||||
| chr7:112206392-112206712 | Common:1; Rare:104 | ||||
| chr7:123748953-123749258 | Common:2; Rare:114 | ||||
| chr7:135170665-135170911 | Common:3; Rare:88 | ||||
| chr7:155644376-155644703 | Common:2; Rare:108 | ||||
| chr7:157336790-157337061 | Common:2; Rare:123 | ||||
| chr8:6406527-6406664 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:10839826-10840109 | Common:3; Rare:89 | ||||
| chr8:11802422-11802791 | Common:6; Rare:207 |