Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596703-19597096 | Common:3; Rare:137 | ||||
chr1:20486203-20486384 | Rare:42 | ||||
chr1:20508028-20508194 | Common:2; Rare:59 | ||||
chr1:20661320-20661730 | Common:3; Rare:150; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786591-20786870 | Rare:104 | ||||
chr1:20787238-20787406 | Rare:88 | ||||
chr1:21176860-21177069 | Rare:53 | ||||
chr1:21345467-21345640 | Common:2; Rare:68 | ||||
chr1:21783086-21783285 | Common:2; Rare:72 | ||||
chr1:23019316-23019493 | Rare:50 | ||||
chr1:23194788-23194961 | Common:1; Rare:39 | ||||
chr1:23368854-23368974 | Common:1; Rare:42 | ||||
chr1:23559413-23559671 | Common:2; Rare:113 | ||||
chr1:23743302-23743506 | Rare:79 | ||||
chr1:23791089-23791231 | Rare:42 |