Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:121639159-121639384 | Common:1; Rare:54 | ||||
chr8:145002881-145003029 | Common:1; Rare:45 | ||||
chr9:738043-738272 | Common:3; Rare:74 | ||||
chr9:9441795-9442069 | Common:4; Rare:70 | ||||
chr9:19378369-19378629 | Common:1; Rare:76 | ||||
chr9:35681893-35682042 | Rare:34 | ||||
chr9:40991988-40992379 | Common:7; Rare:28 | ||||
chr9:68357861-68357941 | Common:1 | ||||
chr9:70413950-70414061 | Rare:19 | ||||
chr9:83979604-83979681 | Rare:29 | ||||
chr9:129320826-129321012 | Rare:28 | ||||
chr9:134811334-134811599 | Rare:80; Clinvar:7; Clinvar (benign):4 | ||||
chr9:136847680-136847995 | Rare:84 | ||||
chrM:404-561 | |||||
chrM:623-1392 |