| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118651497-118651787 | Common:4; Rare:99 | ||||
| chr6:118710073-118710212 | Rare:35 | ||||
| chr6:118893904-118894346 | Common:3; Rare:138 | ||||
| chr6:118934978-118935274 | Common:7; Rare:101 | ||||
| chr6:119349705-119349940 | Common:3; Rare:82 | ||||
| chr6:121334454-121334606 | Common:4; Rare:58 | ||||
| chr6:121334699-121334792 | Common:1; Rare:16 | ||||
| chr6:121435534-121435761 | Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:122399351-122399814 | Common:6; Rare:166 | ||||
| chr6:122471733-122471950 | Common:4; Rare:76 | ||||
| chr6:122779572-122779781 | Rare:45 | ||||
| chr6:122789146-122789308 | Common:1; Rare:36 | ||||
| chr6:122789311-122789404 | Common:1; Rare:33 | ||||
| chr6:122789467-122789594 | Common:1; Rare:49 | ||||
| chr6:123636800-123637415 | Common:4; Rare:115; Clinvar:1; Clinvar (benign):1 |