| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19170242-19170434 | Common:4; Rare:95 | ||||
| chr19:19192106-19192298 | Common:2; Rare:106 | ||||
| chr19:19192541-19192991 | Common:4; Rare:230 | ||||
| chr19:19320472-19320870 | Common:8; Rare:288 | ||||
| chr19:19385456-19386079 | Rare:285 | ||||
| chr19:19405350-19405868 | Common:8; Rare:270 | ||||
| chr19:19516110-19516297 | Rare:203; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:19663492-19663739 | Rare:83 | ||||
| chr19:19668534-19668909 | Common:4; Rare:180 | ||||
| chr19:19865726-19865950 | Common:1; Rare:59 | ||||
| chr19:21020478-21020717 | Common:3; Rare:52 | ||||
| chr19:21082016-21082293 | Rare:102 | ||||
| chr19:21141886-21142109 | Rare:60 | ||||
| chr19:21329271-21329508 | Common:2; Rare:51 | ||||
| chr19:21396943-21397149 | Rare:89 |