| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110981959-110982113 | Common:2; Rare:78 | ||||
| chr6:111483139-111483591 | Common:1; Rare:160 | ||||
| chr6:111483707-111483769 | Common:1; Rare:30 | ||||
| chr6:112087409-112087688 | Rare:91 | ||||
| chr6:113971106-113971427 | Common:3; Rare:102 | ||||
| chr6:116100695-116100913 | Common:1; Rare:84 | ||||
| chr6:116254058-116254242 | Common:4; Rare:49 | ||||
| chr6:116278727-116279038 | Rare:94 | ||||
| chr6:116279138-116279500 | Common:3; Rare:146 | ||||
| chr6:116279510-116279662 | Common:2; Rare:51 | ||||
| chr6:116279672-116279996 | Common:1; Rare:123 | ||||
| chr6:116765590-116765873 | Common:1; Rare:76 | ||||
| chr6:117602414-117602641 | Common:4; Rare:63 | ||||
| chr6:117675318-117675505 | Common:3; Rare:50 | ||||
| chr6:118548043-118548390 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):2 |