| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3118355-3118376 | Rare:13 | ||||
| chr6:3118572-3118743 | Common:2; Rare:56 | ||||
| chr6:3157445-3157642 | Common:6; Rare:74; Clinvar (benign):1 | ||||
| chr6:3227648-3227809 | Rare:44 | ||||
| chr6:3231730-3231838 | Rare:18 | ||||
| chr6:3259115-3259189 | Rare:19 | ||||
| chr6:3324051-3324530 | Rare:111 | ||||
| chr6:3752131-3752282 | Common:2; Rare:46 | ||||
| chr6:3849161-3849428 | Common:3; Rare:74 | ||||
| chr6:4021187-4021465 | Rare:120 | ||||
| chr6:5003646-5003843 | Common:5; Rare:62 | ||||
| chr6:5003978-5004126 | Common:2; Rare:67 | ||||
| chr6:5260661-5261060 | Common:6; Rare:144; Clinvar (benign):4 | ||||
| chr6:5261238-5261603 | Common:9; Rare:102 | ||||
| chr6:6006793-6007004 | Common:1; Rare:49 |