| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116279471-116279503 | Rare:11 | ||||
| chr6:116279524-116279592 | Rare:18 | ||||
| chr6:116279676-116279716 | Rare:15 | ||||
| chr6:116279834-116280136 | Common:3; Rare:101 | ||||
| chr6:116571183-116571638 | Common:3; Rare:132 | ||||
| chr6:116616281-116616568 | Common:3; Rare:64; Clinvar:1 | ||||
| chr6:117602185-117602235 | Rare:19 | ||||
| chr6:117602460-117602648 | Common:3; Rare:55 | ||||
| chr6:118548175-118548354 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:118574095-118574397 | Common:2; Rare:63 | ||||
| chr6:118651531-118651754 | Common:4; Rare:73 | ||||
| chr6:118893922-118894302 | Common:2; Rare:115 | ||||
| chr6:119349705-119349936 | Common:3; Rare:81 | ||||
| chr6:121334454-121334561 | Common:3; Rare:42 | ||||
| chr6:121334687-121334783 | Common:1; Rare:14 |