| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79988309-79988693 | Common:4; Rare:129; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572235-572644 | Common:3; Rare:205 | ||||
| chr19:633481-633733 | Common:8; Rare:122 | ||||
| chr19:663098-663425 | Common:3; Rare:126 | ||||
| chr19:893158-893506 | Common:3; Rare:159 | ||||
| chr19:913162-913308 | Rare:50 | ||||
| chr19:984230-984392 | Rare:61 | ||||
| chr19:1021253-1021522 | Common:10; Rare:115 | ||||
| chr19:1103749-1104119 | Common:7; Rare:155 | ||||
| chr19:1105515-1105804 | Common:3; Rare:132 | ||||
| chr19:1132109-1132452 | Common:2; Rare:136 | ||||
| chr19:1155107-1155314 | Rare:63 | ||||
| chr19:1174218-1174388 | Common:1; Rare:77 | ||||
| chr19:1222901-1223002 | Rare:31; Clinvar:3; Clinvar (benign):6 | ||||
| chr19:1248453-1248593 | Common:1; Rare:50 |