| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:112619726-112619875 | Common:2; Rare:55 | ||||
| chr1:112956178-112956461 | Common:5; Rare:124; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113073081-113073255 | Common:1; Rare:69 | ||||
| chr1:113390180-113390501 | Common:1; Rare:80 | ||||
| chr1:113759120-113759194 | Rare:18 | ||||
| chr1:113811999-113812075 | Common:1; Rare:25 | ||||
| chr1:113812246-113812608 | Common:2; Rare:143 | ||||
| chr1:113904797-113905445 | Common:7; Rare:185; Clinvar (benign):1 | ||||
| chr1:114511237-114511317 | Common:2; Rare:30 | ||||
| chr1:114757925-114758103 | Common:3; Rare:58 | ||||
| chr1:116373025-116373459 | Common:1; Rare:147 | ||||
| chr1:116400625-116400878 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
| chr1:117060153-117060346 | Common:2; Rare:42 | ||||
| chr1:117929546-117929806 | Common:4; Rare:77 | ||||
| chr1:119140573-119140787 | Common:1; Rare:80; Clinvar (pathogenic):1 |