| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:112087424-112087684 | Rare:85 | ||||
| chr6:116100695-116100911 | Common:1; Rare:82 | ||||
| chr6:116253982-116254242 | Common:6; Rare:80 | ||||
| chr6:116278899-116279004 | Rare:30 | ||||
| chr6:116279086-116279405 | Common:2; Rare:121 | ||||
| chr6:116279846-116280086 | Common:1; Rare:83 | ||||
| chr6:116370717-116371093 | Common:1; Rare:91 | ||||
| chr6:116571202-116571563 | Common:2; Rare:101 | ||||
| chr6:117602431-117602641 | Common:4; Rare:58 | ||||
| chr6:117675314-117675498 | Common:3; Rare:51 | ||||
| chr6:118548097-118548328 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:118651531-118651779 | Common:4; Rare:82 | ||||
| chr6:118893919-118894302 | Common:3; Rare:115 | ||||
| chr6:118934978-118935048 | Common:3; Rare:19 | ||||
| chr6:119349705-119349940 | Common:3; Rare:82 |