| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6392938-6393745 | Common:35; Rare:838 | ||||
| chr19:6393780-6394140 | Common:3; Rare:243 | ||||
| chr19:6423442-6423876 | Common:2; Rare:274 | ||||
| chr19:6424717-6425601 | Common:14; Rare:963 | ||||
| chr19:6459656-6460056 | Common:11; Rare:204 | ||||
| chr19:6460090-6460436 | Common:6; Rare:162 | ||||
| chr19:6476201-6476424 | Rare:63 | ||||
| chr19:6476525-6476925 | Common:20; Rare:298 | ||||
| chr19:6481917-6482317 | Rare:96 | ||||
| chr19:6502180-6502651 | Common:3; Rare:329; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr19:6530744-6531250 | Common:20; Rare:696 | ||||
| chr19:6603972-6604350 | Common:6; Rare:132 | ||||
| chr19:6670084-6670484 | Common:1; Rare:90 | ||||
| chr19:6677867-6678267 | Common:3; Rare:361; Clinvar:9; Clinvar (benign):7 | ||||
| chr19:6697217-6697617 | Common:7; Rare:193; Clinvar:2; Clinvar (benign):4 |