| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118652514-118652548 | Rare:12 | ||||
| chr6:118893913-118894313 | Common:3; Rare:122 | ||||
| chr6:118894588-118894656 | Common:1; Rare:20 | ||||
| chr6:118894666-118894707 | Rare:14 | ||||
| chr6:118934457-118934641 | Rare:66 | ||||
| chr6:118934978-118935074 | Common:4; Rare:31 | ||||
| chr6:119349759-119349936 | Common:2; Rare:63 | ||||
| chr6:121334403-121334561 | Common:4; Rare:67 | ||||
| chr6:121334666-121334792 | Common:1; Rare:18 | ||||
| chr6:121435383-121435827 | Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122399427-122399818 | Common:5; Rare:141 | ||||
| chr6:122400034-122400142 | Rare:24 | ||||
| chr6:122471706-122471962 | Common:4; Rare:96 | ||||
| chr6:122788929-122789331 | Common:1; Rare:80 | ||||
| chr6:122789491-122789819 | Common:1; Rare:84 |