Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648138-119648350 | Common:3; Rare:77 | ||||
chr1:144461589-144461825 | Common:4; Rare:93 | ||||
chr1:145214907-145215018 | Rare:16 | ||||
chr1:145673786-145674079 | Rare:61 | ||||
chr1:145707321-145707516 | Common:1; Rare:30 | ||||
chr1:145823870-145824296 | Rare:146 | ||||
chr1:145918657-145919034 | Common:2; Rare:93; Clinvar:1 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958204 | Rare:48 | ||||
chr1:145964505-145964742 | Rare:59 | ||||
chr1:145995162-145995479 | Rare:122 | ||||
chr1:145995989-145996217 | Rare:98 | ||||
chr1:145996412-145996790 | Common:1; Rare:136 | ||||
chr1:146938362-146938496 | Common:2; Rare:31 | ||||
chr1:147172056-147172252 | Rare:55 |