| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4182495-4182710 | Common:1; Rare:82; Clinvar:1 | ||||
| chr19:4831668-4832044 | Common:3; Rare:79 | ||||
| chr19:4867621-4867853 | Common:3; Rare:71 | ||||
| chr19:5293204-5293421 | Common:1; Rare:98 | ||||
| chr19:5340700-5341033 | Common:1; Rare:125 | ||||
| chr19:5622737-5623188 | Common:5; Rare:177 | ||||
| chr19:5791140-5791343 | Common:5; Rare:64 | ||||
| chr19:5903655-5903848 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):4 | ||||
| chr19:5978063-5978383 | Common:3; Rare:120 | ||||
| chr19:6393125-6393250 | Common:2; Rare:29 | ||||
| chr19:6737276-6737319 | Rare:12 | ||||
| chr19:7395022-7395215 | Common:4; Rare:59 | ||||
| chr19:7489006-7489103 | Rare:44 | ||||
| chr19:7534054-7534199 | Common:3; Rare:36; Clinvar (benign):1 | ||||
| chr19:7629520-7629844 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 |