| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41364068-41364164 | Common:1; Rare:28; Clinvar:4 | ||||
| chr19:41397318-41397826 | Common:11; Rare:155; Clinvar (benign):4 | ||||
| chr19:41438877-41439089 | Common:5; Rare:38 | ||||
| chr19:41439503-41439669 | Rare:51 | ||||
| chr19:41860123-41860670 | Common:6; Rare:195; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41882916-41883267 | Common:1; Rare:66 | ||||
| chr19:41904957-41905264 | Common:1; Rare:71 | ||||
| chr19:41957381-41957693 | Rare:49 | ||||
| chr19:41959157-41959493 | Common:1; Rare:124 | ||||
| chr19:42075785-42076290 | Common:4; Rare:141 | ||||
| chr19:42132383-42132568 | Rare:36 | ||||
| chr19:42217667-42218086 | Common:2; Rare:131 | ||||
| chr19:42220110-42220382 | Common:2; Rare:70 | ||||
| chr19:42249691-42249873 | Rare:56; Clinvar (benign):1 | ||||
| chr19:42293313-42293564 | Common:1; Rare:70 |