| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:104941274-104941635 | Common:2; Rare:116 | ||||
| chr6:107046281-107046605 | Common:1; Rare:51 | ||||
| chr6:107154660-107154949 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:107488818-107488971 | Rare:31 | ||||
| chr6:107511671-107511697 | Rare:4 | ||||
| chr6:108558415-108558696 | Common:1; Rare:91 | ||||
| chr6:109454877-109455126 | Common:4; Rare:52 | ||||
| chr6:113854944-113855359 | Common:1; Rare:47 | ||||
| chr6:113858041-113858322 | Common:3; Rare:60 | ||||
| chr6:116681777-116681986 | Rare:33 | ||||
| chr6:127267765-127267814 | Rare:6 | ||||
| chr6:127267836-127267920 | Rare:14 | ||||
| chr6:127267960-127268121 | Common:5; Rare:29 | ||||
| chr6:135498412-135498461 | Rare:12 | ||||
| chr6:136113849-136114057 | Common:1; Rare:39 |