| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5978078-5978393 | Common:3; Rare:117 | ||||
| chr19:6110471-6110854 | Common:3; Rare:116 | ||||
| chr19:6199495-6199846 | Common:13; Rare:114 | ||||
| chr19:6361733-6361843 | Rare:46; Clinvar:1 | ||||
| chr19:6372479-6372827 | Common:5; Rare:114 | ||||
| chr19:6393119-6393528 | Common:4; Rare:115 | ||||
| chr19:6502270-6502411 | Rare:35; Clinvar (benign):1 | ||||
| chr19:6737547-6737908 | Common:4; Rare:114 | ||||
| chr19:7069653-7069742 | Common:1; Rare:28 | ||||
| chr19:7395014-7395188 | Common:6; Rare:53 | ||||
| chr19:7489006-7489103 | Rare:44 | ||||
| chr19:7535599-7535749 | Common:3; Rare:50 | ||||
| chr19:7629523-7629837 | Common:5; Rare:112; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636989-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7903569-7903923 | Rare:112 |