Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:124538991-124539287 | Common:2; Rare:151; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr8:124728396-124728652 | Common:2; Rare:79 | ||||
chr8:125091702-125091914 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
chr8:127735866-127736092 | Rare:51 | ||||
chr8:127736119-127736328 | Common:3; Rare:52 | ||||
chr8:132675534-132675647 | Rare:32 | ||||
chr8:133297194-133297420 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
chr8:133571821-133572185 | Rare:89 | ||||
chr8:134713010-134713221 | Common:1; Rare:70 | ||||
chr8:140511270-140511502 | Common:1; Rare:94 | ||||
chr8:141001125-141001491 | Common:4; Rare:125 | ||||
chr8:141002071-141002132 | Rare:12 | ||||
chr8:141391888-141392046 | Common:1; Rare:55 | ||||
chr8:143018393-143018583 | Common:2; Rare:57 | ||||
chr8:143541424-143541663 | Common:3; Rare:78 |