| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44094203-44094410 | Common:1; Rare:49 | ||||
| chr19:44113131-44113451 | Common:4; Rare:73 | ||||
| chr19:44141410-44141615 | Common:3; Rare:27 | ||||
| chr19:44165012-44165146 | Common:1; Rare:32 | ||||
| chr19:44305001-44305117 | Rare:31 | ||||
| chr19:44500468-44500560 | Rare:31 | ||||
| chr19:44643787-44643902 | Rare:41 | ||||
| chr19:44813342-44813452 | Common:1; Rare:39 | ||||
| chr19:44819113-44819625 | Common:2; Rare:163; Clinvar (benign):1 | ||||
| chr19:44955247-44955420 | Common:2; Rare:51 | ||||
| chr19:45079120-45079296 | Common:1; Rare:48 | ||||
| chr19:45091583-45091782 | Common:1; Rare:53 | ||||
| chr19:45406340-45406687 | Common:2; Rare:86 | ||||
| chr19:45507228-45507568 | Common:1; Rare:93 | ||||
| chr19:45691909-45692053 | Rare:50 |