| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6110328-6111001 | Common:27; Rare:950 | ||||
| chr19:6161230-6161430 | Common:2; Rare:72 | ||||
| chr19:6161350-6161805 | Common:16; Rare:159 | ||||
| chr19:6199438-6199955 | Common:66; Rare:649 | ||||
| chr19:6279101-6279513 | Rare:202 | ||||
| chr19:6279530-6279840 | Common:3; Rare:91 | ||||
| chr19:6279800-6280381 | Common:18; Rare:459 | ||||
| chr19:6361170-6362204 | Common:23; Rare:969; Clinvar:11; Clinvar (benign):30; Clinvar (pathogenic):1 | ||||
| chr19:6372038-6372438 | Common:6; Rare:134 | ||||
| chr19:6372389-6372893 | Common:36; Rare:855 | ||||
| chr19:6372905-6373554 | Common:2; Rare:371 | ||||
| chr19:6373698-6374098 | Common:1; Rare:162 | ||||
| chr19:6381120-6381450 | Common:3; Rare:131 | ||||
| chr19:6381629-6382029 | Common:4; Rare:173 | ||||
| chr19:6392194-6392594 | Common:1; Rare:159 |