| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6372520-6372827 | Common:5; Rare:105 | ||||
| chr19:6381152-6381382 | Common:3; Rare:91 | ||||
| chr19:6393097-6393231 | Common:2; Rare:33 | ||||
| chr19:6393371-6393769 | Common:5; Rare:117 | ||||
| chr19:6737233-6737314 | Rare:24 | ||||
| chr19:7069653-7069741 | Common:1; Rare:27 | ||||
| chr19:7395032-7395185 | Common:4; Rare:47 | ||||
| chr19:7488988-7489103 | Rare:52 | ||||
| chr19:7534023-7534208 | Common:3; Rare:48; Clinvar (benign):1 | ||||
| chr19:7535574-7535763 | Common:3; Rare:68 | ||||
| chr19:7551114-7551220 | Common:1; Rare:40 | ||||
| chr19:7629500-7629871 | Common:7; Rare:137; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636997-7637143 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr19:7680706-7680889 | Common:1; Rare:60 | ||||
| chr19:7903501-7903861 | Common:2; Rare:112 |