| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:96321286-96321540 | Common:2; Rare:62 | ||||
| chr7:99392377-99392793 | Common:1; Rare:117 | ||||
| chr7:100335870-100336146 | Common:1; Rare:90 | ||||
| chr7:101223495-101223842 | Rare:118 | ||||
| chr7:102822436-102822506 | Common:1; Rare:9 | ||||
| chr7:105013018-105013207 | Common:1; Rare:69 | ||||
| chr7:105110213-105110315 | Rare:25 | ||||
| chr7:107935647-107935804 | Common:2; Rare:29 | ||||
| chr7:112205590-112205685 | Rare:24 | ||||
| chr7:116211430-116211666 | Common:3; Rare:44 | ||||
| chr7:128530382-128530590 | Rare:42 | ||||
| chr7:128591846-128591928 | Common:1; Rare:15 | ||||
| chr7:128837425-128837707 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr7:128842618-128842954 | Common:4; Rare:120; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr7:128843226-128843533 | Common:1; Rare:95; Clinvar:12; Clinvar (benign):3 |