| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54115286-54115364 | Rare:21 | ||||
| chr19:54115560-54115836 | Common:3; Rare:72; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:54136952-54137364 | Common:5; Rare:110 | ||||
| chr19:54137686-54137836 | Common:1; Rare:53 | ||||
| chr19:54138267-54138339 | Rare:14 | ||||
| chr19:54159396-54159552 | Common:1; Rare:65 | ||||
| chr19:54159608-54160196 | Common:1; Rare:192 | ||||
| chr19:54189290-54189529 | Common:2; Rare:70 | ||||
| chr19:54189538-54189609 | Common:1; Rare:29 | ||||
| chr19:54189803-54190093 | Common:2; Rare:77 | ||||
| chr19:54190236-54190590 | Common:4; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:54190892-54191054 | Rare:54 | ||||
| chr19:54191137-54191402 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:54200437-54201144 | Common:10; Rare:214 | ||||
| chr19:54369123-54369284 | Common:1; Rare:27 |