| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99500244-99500384 | Common:2; Rare:42 | ||||
| chr7:99558532-99558730 | Common:2; Rare:63 | ||||
| chr7:100101352-100101711 | Common:1; Rare:137; Clinvar (benign):1 | ||||
| chr7:100119312-100119748 | Rare:135; Clinvar:1 | ||||
| chr7:100428663-100428793 | Common:3; Rare:45 | ||||
| chr7:100852604-100852749 | Rare:39 | ||||
| chr7:101217849-101218190 | Common:3; Rare:105 | ||||
| chr7:101245040-101245142 | Common:1; Rare:42 | ||||
| chr7:102464846-102465006 | Common:1; Rare:66 | ||||
| chr7:103149302-103149372 | Common:2; Rare:13 | ||||
| chr7:104207959-104208150 | Common:5; Rare:88 | ||||
| chr7:105013597-105013715 | Common:1; Rare:41 | ||||
| chr7:105532067-105532227 | Rare:43 | ||||
| chr7:105876485-105876771 | Common:5; Rare:85 | ||||
| chr7:107563897-107564032 | Common:2; Rare:81; Clinvar (benign):4 |