Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:125091709-125091934 | Common:2; Rare:80; Clinvar (benign):3 | ||||
chr8:127735922-127736076 | Rare:32 | ||||
chr8:127736134-127736257 | Common:3; Rare:24 | ||||
chr8:132675540-132675647 | Rare:30 | ||||
chr8:134713010-134713239 | Common:1; Rare:78 | ||||
chr8:140511210-140511502 | Common:3; Rare:110 | ||||
chr8:142777819-142777873 | Rare:17 | ||||
chr8:143018393-143018558 | Common:2; Rare:50 | ||||
chr8:143558267-143558354 | Common:1; Rare:33 | ||||
chr8:143597123-143597313 | Common:1; Rare:49 | ||||
chr8:143635912-143636069 | Common:2; Rare:63 | ||||
chr8:143829306-143829502 | Rare:77 | ||||
chr8:143944703-143944962 | Common:2; Rare:71 | ||||
chr8:144078530-144078722 | Common:1; Rare:58 | ||||
chr8:144104163-144104519 | Common:3; Rare:117 |