Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:97920570-97920690 | Rare:32 | ||||
chr1:97920862-97921211 | Common:2; Rare:130; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:97921450-97921538 | Common:2; Rare:16 | ||||
chr1:98661285-98661372 | Common:2; Rare:17 | ||||
chr1:98661454-98661918 | Common:4; Rare:150 | ||||
chr1:98661923-98662062 | Rare:23 | ||||
chr1:98662064-98662325 | Rare:59 | ||||
chr1:99645274-99645460 | Common:1; Rare:42 | ||||
chr1:99646053-99646081 | |||||
chr1:99646091-99646422 | Common:1; Rare:78 | ||||
chr1:99765726-99766041 | Rare:47 | ||||
chr1:99849640-99850398 | Common:2; Rare:185; Clinvar:2 | ||||
chr1:99969433-99969518 | Rare:13 | ||||
chr1:99969678-99969854 | Common:1; Rare:37 | ||||
chr1:99969861-99970221 | Common:3; Rare:82 |