| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:98283307-98283651 | Common:3; Rare:72 | ||||
| chr7:98286344-98286496 | Common:4; Rare:33 | ||||
| chr7:100335870-100336156 | Common:1; Rare:93 | ||||
| chr7:100336310-100336329 | Rare:5 | ||||
| chr7:102822444-102822640 | Common:3; Rare:25 | ||||
| chr7:105013036-105013199 | Rare:60 | ||||
| chr7:107951267-107951575 | Common:3; Rare:72; Clinvar (benign):2 | ||||
| chr7:123612044-123612269 | Rare:36 | ||||
| chr7:128828302-128828348 | Common:1; Rare:8 | ||||
| chr7:128837391-128837752 | Common:3; Rare:103; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr7:128838263-128838693 | Common:1; Rare:132; Clinvar:19; Clinvar (benign):8 | ||||
| chr7:128847689-128848068 | Common:1; Rare:130; Clinvar:16; Clinvar (benign):12 | ||||
| chr7:128848558-128848982 | Common:2; Rare:132; Clinvar:19; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr7:128852586-128853031 | Common:4; Rare:132; Clinvar:15; Clinvar (benign):11 | ||||
| chr7:128853969-128854580 | Common:1; Rare:180; Clinvar:14; Clinvar (benign):13; Clinvar (pathogenic):1 |