| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18918922-18919328 | Common:9; Rare:210 | ||||
| chr19:18919299-18919819 | Common:19; Rare:1093 | ||||
| chr19:18941030-18941530 | Common:6; Rare:137 | ||||
| chr19:19032386-19033141 | Common:7; Rare:142 | ||||
| chr19:19033349-19033776 | Common:14; Rare:666 | ||||
| chr19:19033773-19033941 | Common:5; Rare:167 | ||||
| chr19:19034263-19034690 | Common:12; Rare:160 | ||||
| chr19:19063384-19064064 | Common:6; Rare:777 | ||||
| chr19:19105030-19106101 | Common:14; Rare:1041; Clinvar (pathogenic):7 | ||||
| chr19:19120451-19120832 | Common:2; Rare:156 | ||||
| chr19:19138293-19138766 | Common:11; Rare:304 | ||||
| chr19:19170190-19170580 | Common:12; Rare:374 | ||||
| chr19:19191987-19192387 | Common:10; Rare:383; Clinvar (benign):2 | ||||
| chr19:19192496-19192996 | Common:16; Rare:762; Clinvar (benign):2 | ||||
| chr19:19192937-19193488 | Common:1; Rare:122; Clinvar (benign):1 |