Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:58235091-58235395 | Common:2; Rare:64 | ||||
chr18:58307392-58307438 | Rare:7 | ||||
chr18:58370178-58370465 | Common:2; Rare:68; Clinvar (benign):1 | ||||
chr18:61858685-61858938 | Rare:46 | ||||
chr18:63159035-63159148 | Common:1; Rare:17 | ||||
chr18:74598571-74598661 | Rare:25 | ||||
chr18:76491475-76491665 | Common:3; Rare:78 | ||||
chr19:290098-290396 | Common:3; Rare:54 | ||||
chr19:748249-748490 | Common:1; Rare:63 | ||||
chr19:751880-752105 | Rare:47 | ||||
chr19:752697-753045 | Common:4; Rare:83 | ||||
chr19:867271-867475 | Common:4; Rare:73 | ||||
chr19:1108897-1109115 | Rare:94 | ||||
chr19:1410523-1410734 | Common:1; Rare:52 | ||||
chr19:1839974-1840235 | Common:1; Rare:69 |