| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109094262-109094384 | Rare:20 | ||||
| chr6:109094810-109095188 | Common:4; Rare:112 | ||||
| chr6:109095433-109095567 | Rare:26 | ||||
| chr6:109382066-109382517 | Common:7; Rare:202; Clinvar (benign):2 | ||||
| chr6:109691151-109691339 | Common:3; Rare:45; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179947-110180188 | Common:2; Rare:66 | ||||
| chr6:110415505-110415701 | Rare:47 | ||||
| chr6:110874633-110874798 | Common:4; Rare:54 | ||||
| chr6:110958437-110958554 | Common:3; Rare:32 | ||||
| chr6:110958600-110958788 | Common:5; Rare:69 | ||||
| chr6:110981966-110982115 | Common:2; Rare:80 | ||||
| chr6:111483145-111483545 | Common:1; Rare:138 | ||||
| chr6:111483707-111483775 | Common:1; Rare:31 | ||||
| chr6:112087409-112087684 | Rare:91 | ||||
| chr6:113971195-113971495 | Common:3; Rare:90 |