| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691157-109691323 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179933-110180188 | Common:2; Rare:71 | ||||
| chr6:110874633-110874796 | Common:4; Rare:54 | ||||
| chr6:110958437-110958542 | Common:2; Rare:30 | ||||
| chr6:110958552-110959050 | Common:10; Rare:164 | ||||
| chr6:110981954-110982125 | Common:2; Rare:90 | ||||
| chr6:111259040-111259366 | Common:3; Rare:95 | ||||
| chr6:111483214-111483591 | Common:1; Rare:135 | ||||
| chr6:111483702-111483902 | Common:1; Rare:91 | ||||
| chr6:112087409-112087691 | Rare:91 | ||||
| chr6:112254478-112254695 | Rare:42 | ||||
| chr6:113971098-113971495 | Common:3; Rare:126 | ||||
| chr6:116100720-116100909 | Common:1; Rare:71 | ||||
| chr6:116254068-116254224 | Common:4; Rare:39 | ||||
| chr6:116279841-116280120 | Common:2; Rare:94 |