Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:124474555-124474738 | Rare:65 | ||||
chr8:124474953-124475105 | Rare:49 | ||||
chr8:124539040-124539204 | Common:2; Rare:90; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:124727959-124728095 | Common:1; Rare:40 | ||||
chr8:125091730-125091923 | Common:2; Rare:66; Clinvar (benign):2 | ||||
chr8:126558362-126558628 | Common:1; Rare:100 | ||||
chr8:127735890-127736092 | Rare:47 | ||||
chr8:129939752-129939835 | Rare:27 | ||||
chr8:133571824-133572255 | Rare:113 | ||||
chr8:134713029-134713152 | Common:1; Rare:44 | ||||
chr8:140511264-140511494 | Common:1; Rare:95 | ||||
chr8:140718341-140718459 | Common:1; Rare:33 | ||||
chr8:143018403-143018582 | Common:2; Rare:52 | ||||
chr8:143541430-143541648 | Common:2; Rare:72 | ||||
chr8:143558269-143558410 | Common:1; Rare:59 |