| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691158-109691329 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179962-110180179 | Common:2; Rare:64 | ||||
| chr6:110958583-110958788 | Common:5; Rare:73 | ||||
| chr6:110981954-110982113 | Common:2; Rare:81 | ||||
| chr6:111259210-111259346 | Rare:44 | ||||
| chr6:111483400-111483544 | Rare:60 | ||||
| chr6:112087446-112087684 | Rare:74 | ||||
| chr6:116100726-116100886 | Rare:59 | ||||
| chr6:116254058-116254242 | Common:4; Rare:49 | ||||
| chr6:116279841-116280108 | Common:2; Rare:91 | ||||
| chr6:116571202-116571569 | Common:2; Rare:103 | ||||
| chr6:117602460-117602660 | Common:3; Rare:58 | ||||
| chr6:118893885-118894300 | Common:4; Rare:127 | ||||
| chr6:124963126-124963219 | Common:1; Rare:34 | ||||
| chr6:125781058-125781156 | Rare:18 |