| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45464627-45465055 | Common:1; Rare:103 | ||||
| chr13:45465279-45465366 | Rare:19 | ||||
| chr13:45701580-45701869 | Rare:43 | ||||
| chr13:46052621-46052905 | Common:2; Rare:77 | ||||
| chr13:46181897-46182464 | Common:3; Rare:95 | ||||
| chr13:46211844-46211977 | Common:2; Rare:43 | ||||
| chr13:46386516-46386772 | Rare:56 | ||||
| chr13:46387217-46387382 | Rare:47 | ||||
| chr13:46552953-46553316 | Common:2; Rare:116 | ||||
| chr13:46679930-46679945 | |||||
| chr13:46796540-46796729 | Common:1; Rare:57 | ||||
| chr13:46797036-46797430 | Common:4; Rare:114 | ||||
| chr13:48001208-48001491 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):7 | ||||
| chr13:48037333-48037816 | Common:5; Rare:174; Clinvar:2 | ||||
| chr13:48037915-48038211 | Common:6; Rare:86 |