| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42255053-42255230 | Common:2; Rare:93 | ||||
| chr19:42268170-42268557 | Rare:151 | ||||
| chr19:42268670-42269060 | Rare:183 | ||||
| chr19:42280357-42280614 | Common:2; Rare:119 | ||||
| chr19:42283749-42284090 | Rare:226 | ||||
| chr19:42302240-42302696 | Rare:181 | ||||
| chr19:42325260-42325695 | Rare:215 | ||||
| chr19:43463620-43464200 | Common:3; Rare:267 | ||||
| chr19:43504018-43504501 | Common:14; Rare:244 | ||||
| chr19:43525390-43525840 | Common:2; Rare:118 | ||||
| chr19:43527163-43527310 | Common:5; Rare:57; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575451-43575830 | Common:4; Rare:189 | ||||
| chr19:43595997-43596466 | Common:6; Rare:250 | ||||
| chr19:43618840-43619200 | Rare:142 | ||||
| chr19:43619220-43619400 | Rare:70 |