| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:113873321-113873439 | Common:1; Rare:23 | ||||
| chr6:116277387-116277481 | Rare:16 | ||||
| chr6:116277554-116277755 | Common:3; Rare:46 | ||||
| chr6:117999195-117999313 | Common:3; Rare:32 | ||||
| chr6:118895097-118895249 | Rare:43 | ||||
| chr6:119011402-119011507 | Common:2; Rare:29 | ||||
| chr6:119201293-119201552 | Common:1; Rare:43 | ||||
| chr6:119350586-119350722 | Common:2; Rare:29 | ||||
| chr6:125790179-125790241 | Common:1; Rare:10 | ||||
| chr6:127290107-127290416 | Rare:98 | ||||
| chr6:127515063-127515290 | Common:1; Rare:55 | ||||
| chr6:129391203-129391499 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:129460035-129460324 | Common:1; Rare:73; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr6:129464093-129464351 | Common:3; Rare:58; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr6:129481017-129481364 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |