| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6710318-6711110 | Common:13; Rare:286; Clinvar:1; Clinvar (benign):6 | ||||
| chr19:6714170-6714600 | Common:1; Rare:162; Clinvar (benign):3 | ||||
| chr19:6720462-6720992 | Common:4; Rare:225; Clinvar (benign):4 | ||||
| chr19:6730430-6730830 | Common:9; Rare:126 | ||||
| chr19:6736464-6736915 | Common:2; Rare:212 | ||||
| chr19:6737362-6738090 | Common:15; Rare:349 | ||||
| chr19:6739452-6739786 | Common:12; Rare:181 | ||||
| chr19:7294197-7294537 | Common:12; Rare:148 | ||||
| chr19:7395021-7395210 | Common:4; Rare:58 | ||||
| chr19:7515770-7516224 | Common:2; Rare:166 | ||||
| chr19:7535500-7535830 | Common:6; Rare:168; Clinvar:3 | ||||
| chr19:7595704-7595934 | Common:2; Rare:84 | ||||
| chr19:7629511-7629854 | Common:10; Rare:238; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:7636989-7637172 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr19:7680724-7680898 | Common:2; Rare:110 |