| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:797127-797471 | Rare:147 | ||||
| chr19:804634-805180 | Common:2; Rare:204 | ||||
| chr19:821923-822143 | Rare:64 | ||||
| chr19:893143-893484 | Common:3; Rare:147 | ||||
| chr19:913144-913264 | Rare:39 | ||||
| chr19:928888-929059 | Rare:51 | ||||
| chr19:984205-984348 | Common:4; Rare:53 | ||||
| chr19:1020770-1021193 | Common:2; Rare:113 | ||||
| chr19:1021254-1021522 | Common:10; Rare:115 | ||||
| chr19:1039943-1040112 | Common:2; Rare:50 | ||||
| chr19:1067099-1067187 | Common:1; Rare:25 | ||||
| chr19:1103794-1104119 | Common:4; Rare:137 | ||||
| chr19:1105462-1105804 | Common:3; Rare:151 | ||||
| chr19:1174225-1174344 | Common:1; Rare:60 | ||||
| chr19:1220277-1220439 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):12 |