| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:62186960-62187320 | Common:5; Rare:100 | ||||
| chr18:63422392-63422687 | Common:2; Rare:81 | ||||
| chr18:68714987-68715250 | Common:5; Rare:120 | ||||
| chr18:74597810-74597881 | Common:1; Rare:20 | ||||
| chr18:79988280-79988608 | Common:2; Rare:110; Clinvar:1 | ||||
| chr19:572237-572628 | Common:3; Rare:192 | ||||
| chr19:893165-893484 | Common:3; Rare:133 | ||||
| chr19:1103799-1104115 | Common:4; Rare:131 | ||||
| chr19:1132115-1132373 | Common:1; Rare:116 | ||||
| chr19:1354808-1354990 | Rare:74 | ||||
| chr19:2096263-2096407 | Rare:51 | ||||
| chr19:2328554-2328703 | Common:2; Rare:71 | ||||
| chr19:2785241-2785578 | Common:5; Rare:103 | ||||
| chr19:3982805-3983194 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:4229242-4229535 | Common:2; Rare:88 |