Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:132669936-132670040 | Common:1; Rare:50 | ||||
chr9:132878308-132878374 | Common:1; Rare:20 | ||||
chr9:133348043-133348266 | Common:2; Rare:90 | ||||
chr9:133356452-133356593 | Common:1; Rare:64; Clinvar (benign):2 | ||||
chr9:133375999-133376366 | Common:1; Rare:133 | ||||
chr9:134641551-134641771 | Common:1; Rare:64 | ||||
chr9:136410609-136410668 | Rare:29 | ||||
chr9:137188547-137188711 | Common:2; Rare:77 | ||||
chr9:137618809-137619029 | Common:1; Rare:99 | ||||
chrM:2468-3110 | |||||
chrM:3163-3437 | |||||
chrM:5304-5590 | |||||
chrM:5895-5996 | |||||
chrM:7292-7592 | |||||
chrM:7984-8073 |