| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:121334440-121334549 | Common:2; Rare:51 | ||||
| chr6:121334709-121334828 | Common:2; Rare:27 | ||||
| chr6:121435497-121435761 | Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:122399351-122399715 | Common:6; Rare:138 | ||||
| chr6:122471739-122471937 | Common:3; Rare:65 | ||||
| chr6:124962869-124963252 | Common:1; Rare:139 | ||||
| chr6:125301847-125302173 | Common:7; Rare:98 | ||||
| chr6:125780818-125780874 | Common:1; Rare:11 | ||||
| chr6:125780887-125781370 | Common:2; Rare:85 | ||||
| chr6:125918551-125918912 | Rare:53 | ||||
| chr6:125919148-125919439 | Rare:73 | ||||
| chr6:125956651-125956983 | Common:1; Rare:91 | ||||
| chr6:125986365-125986698 | Rare:122 | ||||
| chr6:127266785-127266901 | Common:1; Rare:43 | ||||
| chr6:127343327-127343446 | Rare:24 |