Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84574413-84574561 | Common:1; Rare:47 | ||||
chr1:85276480-85276706 | Common:2; Rare:77 | ||||
chr1:86396246-86396413 | Common:3; Rare:39 | ||||
chr1:86704481-86704966 | Common:3; Rare:173 | ||||
chr1:86914300-86914752 | Common:3; Rare:131 | ||||
chr1:88684110-88684374 | Common:2; Rare:70 | ||||
chr1:88992600-88992988 | Common:3; Rare:102 | ||||
chr1:89198913-89199057 | Rare:16 | ||||
chr1:89632897-89633188 | Common:1; Rare:80 | ||||
chr1:89821727-89821857 | Rare:41 | ||||
chr1:89994981-89995213 | Common:2; Rare:87 | ||||
chr1:92075330-92075605 | Common:1; Rare:47 | ||||
chr1:92298933-92299066 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr1:92831924-92832105 | Common:1; Rare:87; Clinvar:6; Clinvar (benign):4 | ||||
chr1:92961405-92961592 | Rare:72 |