| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4723755-4723902 | Common:2; Rare:45 | ||||
| chr19:4831691-4831846 | Common:1; Rare:37 | ||||
| chr19:4867619-4867886 | Common:4; Rare:78 | ||||
| chr19:5622759-5623188 | Common:5; Rare:161 | ||||
| chr19:5680892-5681048 | Rare:39 | ||||
| chr19:5720135-5720330 | Rare:69 | ||||
| chr19:5978078-5978358 | Common:3; Rare:104 | ||||
| chr19:7395045-7395185 | Common:3; Rare:45 | ||||
| chr19:7629515-7629864 | Common:5; Rare:126; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636969-7637143 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr19:8321316-8321563 | Common:2; Rare:113 | ||||
| chr19:8363823-8364191 | Common:4; Rare:80 | ||||
| chr19:8390077-8390427 | Common:1; Rare:101 | ||||
| chr19:9538594-9538707 | Common:1; Rare:32 | ||||
| chr19:9621192-9621493 | Common:3; Rare:86 |