| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41310133-41310207 | Rare:25 | ||||
| chr19:41363794-41363992 | Common:1; Rare:70; Clinvar:1 | ||||
| chr19:41364123-41364191 | Rare:23; Clinvar:1 | ||||
| chr19:41959282-41959466 | Common:1; Rare:59 | ||||
| chr19:42075782-42076235 | Common:4; Rare:130 | ||||
| chr19:42302318-42302722 | Rare:109 | ||||
| chr19:42325368-42325670 | Rare:88 | ||||
| chr19:43527182-43527302 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575477-43575818 | Common:2; Rare:89 | ||||
| chr19:43596045-43596429 | Common:3; Rare:119 | ||||
| chr19:43670140-43670309 | Common:2; Rare:39 | ||||
| chr19:43754901-43755102 | Common:3; Rare:69 | ||||
| chr19:43827186-43827424 | Common:2; Rare:47 | ||||
| chr19:43901736-43901916 | Common:3; Rare:38 | ||||
| chr19:43951119-43951283 | Common:1; Rare:46 |