Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91500568-91500901 | Common:3; Rare:82 | ||||
chr1:91886023-91886385 | Rare:139 | ||||
chr1:92298929-92299089 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
chr1:92784707-92784852 | Common:1; Rare:34 | ||||
chr1:92785043-92785268 | Common:3; Rare:90 | ||||
chr1:92831947-92832147 | Common:1; Rare:97; Clinvar:7; Clinvar (benign):7 | ||||
chr1:92832223-92832353 | Rare:42 | ||||
chr1:93079056-93079290 | Common:3; Rare:103 | ||||
chr1:93179859-93179954 | Common:1; Rare:24 | ||||
chr1:93180053-93180236 | Rare:65 | ||||
chr1:93180258-93180699 | Common:1; Rare:171 | ||||
chr1:93345738-93345904 | Common:4; Rare:64 | ||||
chr1:93846618-93846753 | Common:1; Rare:43 | ||||
chr1:93847218-93847250 | Rare:6 | ||||
chr1:93879124-93879279 | Common:1; Rare:57 |