Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86704469-86704622 | Rare:57 | ||||
chr1:86704732-86704918 | Common:2; Rare:70 | ||||
chr1:86914387-86914815 | Rare:133 | ||||
chr1:88684091-88684355 | Common:2; Rare:69 | ||||
chr1:88992605-88992871 | Common:3; Rare:58 | ||||
chr1:89065185-89065461 | Common:1; Rare:42 | ||||
chr1:89198851-89199001 | Rare:22 | ||||
chr1:89994987-89995178 | Common:2; Rare:73 | ||||
chr1:91021963-91022152 | Rare:54 | ||||
chr1:91500808-91500890 | Common:2; Rare:31 | ||||
chr1:91886012-91886340 | Rare:133 | ||||
chr1:92298945-92299078 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079089-93079308 | Common:2; Rare:92 | ||||
chr1:93179831-93179922 | Common:1; Rare:16 | ||||
chr1:93180300-93180751 | Common:2; Rare:180 |