| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116680934-116681259 | Common:3; Rare:101 | ||||
| chr6:116765625-116765828 | Rare:57 | ||||
| chr6:117602176-117602361 | Rare:71 | ||||
| chr6:117602400-117602650 | Common:4; Rare:67 | ||||
| chr6:118548158-118548418 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:118893913-118894251 | Common:3; Rare:100 | ||||
| chr6:118934981-118935097 | Common:4; Rare:41 | ||||
| chr6:119349759-119349963 | Common:2; Rare:77 | ||||
| chr6:121334448-121334549 | Common:2; Rare:44 | ||||
| chr6:121334706-121334780 | Common:1; Rare:13 | ||||
| chr6:121435497-121435833 | Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122399357-122399745 | Common:6; Rare:145 | ||||
| chr6:122471715-122471931 | Common:3; Rare:72 | ||||
| chr6:123636811-123637082 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:123637216-123637426 | Common:2; Rare:42 |