| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:112095585-112095908 | Common:8; Rare:50 | ||||
| chr6:112114661-112114851 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:112689618-112689789 | Common:4; Rare:71 | ||||
| chr6:113167966-113168075 | Rare:20 | ||||
| chr6:113184386-113184538 | Rare:24 | ||||
| chr6:113358148-113358350 | Rare:38 | ||||
| chr6:114084449-114084551 | Common:4; Rare:30 | ||||
| chr6:114341949-114342268 | Common:4; Rare:70 | ||||
| chr6:114545307-114545399 | Common:1; Rare:8 | ||||
| chr6:114997921-114998167 | Common:2; Rare:55 | ||||
| chr6:115643870-115643998 | Common:1; Rare:20 | ||||
| chr6:115716384-115716526 | Common:2; Rare:28 | ||||
| chr6:116038747-116038842 | Common:1; Rare:31 | ||||
| chr6:116229415-116229490 | Rare:23 | ||||
| chr6:117015531-117015685 | Common:2; Rare:33 |