| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39409438-39409839 | Common:3; Rare:121 | ||||
| chr19:39410145-39411975 | Common:14; Rare:626 | ||||
| chr19:39453170-39453800 | Common:4; Rare:237 | ||||
| chr19:39557903-39558064 | Common:1; Rare:25 | ||||
| chr19:39677968-39678252 | Common:7; Rare:75 | ||||
| chr19:39824270-39825050 | Common:8; Rare:286 | ||||
| chr19:39858510-39859030 | Common:16; Rare:160 | ||||
| chr19:40217074-40217328 | Common:2; Rare:97 | ||||
| chr19:40217400-40217740 | Rare:88 | ||||
| chr19:40249555-40249704 | Common:1; Rare:35 | ||||
| chr19:40323650-40324120 | Common:1; Rare:129 | ||||
| chr19:40360680-40360960 | Common:1; Rare:38 | ||||
| chr19:40392820-40393340 | Common:4; Rare:193 | ||||
| chr19:40403428-40403809 | Common:3; Rare:170; Clinvar:5; Clinvar (benign):3 | ||||
| chr19:40404199-40404356 | Rare:65 |