| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166680207-166680443 | Common:1; Rare:59 | ||||
| chr6:166901149-166901747 | Common:1; Rare:155 | ||||
| chr6:166901768-166902128 | Common:7; Rare:118 | ||||
| chr6:167118109-167118211 | Rare:22 | ||||
| chr6:167141184-167141323 | Common:2; Rare:23 | ||||
| chr6:167241573-167241886 | Common:5; Rare:58 | ||||
| chr6:167531060-167531136 | Rare:16 | ||||
| chr6:167566043-167566148 | Common:1; Rare:10 | ||||
| chr6:167678101-167678232 | Common:2; Rare:28 | ||||
| chr6:167731307-167731446 | Common:2; Rare:46 | ||||
| chr6:168289277-168289448 | Common:5; Rare:47 | ||||
| chr6:168413081-168413410 | Common:7; Rare:96 | ||||
| chr6:168413564-168413629 | Rare:13 | ||||
| chr6:168598522-168598852 | Common:3; Rare:80; Clinvar (pathogenic):1 | ||||
| chr6:168860714-168860859 | Common:1; Rare:26 |