| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39480731-39480909 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
| chr19:39846296-39846473 | Common:1; Rare:82 | ||||
| chr19:39970918-39971238 | Common:4; Rare:90 | ||||
| chr19:39979594-39979981 | Rare:71 | ||||
| chr19:39996925-39997118 | Common:5; Rare:62 | ||||
| chr19:40056135-40056284 | Rare:19 | ||||
| chr19:40090864-40090999 | Common:1; Rare:38 | ||||
| chr19:40285238-40285572 | Common:1; Rare:121 | ||||
| chr19:40348388-40348739 | Common:4; Rare:117 | ||||
| chr19:40377813-40378058 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr19:40413365-40413521 | Rare:44 | ||||
| chr19:40425990-40426141 | Common:1; Rare:43 | ||||
| chr19:40444263-40444525 | Common:3; Rare:83 | ||||
| chr19:40465735-40466098 | Common:3; Rare:105 | ||||
| chr19:40715074-40715167 | Rare:27 |