| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:109426042-109426203 | Rare:32 | ||||
| chr1:109426314-109426621 | Common:1; Rare:108 | ||||
| chr1:109426632-109426925 | Common:2; Rare:84 | ||||
| chr1:109466449-109466603 | Common:2; Rare:37 | ||||
| chr1:109483870-109484078 | Common:2; Rare:78 | ||||
| chr1:109484084-109484316 | Common:1; Rare:70 | ||||
| chr1:109493890-109494191 | Common:2; Rare:89 | ||||
| chr1:109494233-109494385 | Common:2; Rare:36 | ||||
| chr1:109509649-109509893 | Common:1; Rare:77 | ||||
| chr1:109548422-109548841 | Common:5; Rare:141; Clinvar (pathogenic):1 | ||||
| chr1:109619717-109619922 | Rare:45 | ||||
| chr1:109620937-109621169 | Rare:67 | ||||
| chr1:109655511-109655780 | Common:2; Rare:44 | ||||
| chr1:109655930-109656220 | Common:3; Rare:75 | ||||
| chr1:109667826-109668096 | Common:2; Rare:77 |