Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42577682-42577856 | Common:1; Rare:82 | ||||
chr17:42609320-42609683 | Common:8; Rare:144 | ||||
chr17:42773371-42773470 | Rare:27 | ||||
chr17:42833236-42833475 | Rare:76 | ||||
chr17:42964428-42964503 | Rare:32 | ||||
chr17:43171003-43171240 | Rare:75 | ||||
chr17:43778907-43779048 | Rare:32 | ||||
chr17:44186699-44186998 | Rare:98 | ||||
chr17:44187171-44187274 | Rare:29 | ||||
chr17:44324777-44324955 | Common:2; Rare:64 | ||||
chr17:44350506-44350793 | Rare:101; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503377-44503711 | Rare:132 | ||||
chr17:44899383-44899736 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45061119-45061347 | Common:1; Rare:67 | ||||
chr17:45132346-45132623 | Common:2; Rare:80 |