| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109455613-109455788 | Common:3; Rare:49 | ||||
| chr6:109691150-109691322 | Common:3; Rare:44; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179962-110180170 | Common:2; Rare:62 | ||||
| chr6:110874633-110874798 | Common:4; Rare:54 | ||||
| chr6:110958600-110958788 | Common:5; Rare:69 | ||||
| chr6:110981861-110982116 | Common:3; Rare:114 | ||||
| chr6:111483165-111483562 | Common:1; Rare:138 | ||||
| chr6:111605824-111606150 | Common:2; Rare:58 | ||||
| chr6:112087414-112087678 | Rare:88 | ||||
| chr6:113857262-113857425 | Common:1; Rare:36 | ||||
| chr6:113970604-113970817 | Rare:68 | ||||
| chr6:113971074-113971521 | Common:3; Rare:146 | ||||
| chr6:116100695-116100897 | Common:1; Rare:72 | ||||
| chr6:116254046-116254242 | Common:4; Rare:55 | ||||
| chr6:116279846-116280086 | Common:1; Rare:83 |