| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6373204-6373517 | Rare:50 | ||||
| chr19:6393385-6393769 | Common:5; Rare:114 | ||||
| chr19:6416839-6417071 | Common:1; Rare:80 | ||||
| chr19:6464152-6464340 | Rare:28 | ||||
| chr19:6710814-6711065 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6714164-6714442 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6737247-6737332 | Rare:23 | ||||
| chr19:6739476-6739779 | Common:6; Rare:87 | ||||
| chr19:6740627-6740791 | Common:1; Rare:37 | ||||
| chr19:6740842-6741136 | Rare:81 | ||||
| chr19:7395028-7395209 | Common:4; Rare:55 | ||||
| chr19:7488970-7489103 | Rare:65 | ||||
| chr19:7533930-7534213 | Common:3; Rare:65; Clinvar (benign):1 | ||||
| chr19:7535574-7535791 | Common:3; Rare:79 | ||||
| chr19:7629523-7629915 | Common:5; Rare:134; Clinvar (benign):2; Clinvar (pathogenic):1 |