Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119768792-119769020 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
chr1:145607915-145608069 | Rare:51 | ||||
chr1:145707323-145707484 | Common:1; Rare:23 | ||||
chr1:145823885-145824238 | Rare:125 | ||||
chr1:145859009-145859193 | Rare:50 | ||||
chr1:145918676-145919044 | Common:2; Rare:85; Clinvar:1 | ||||
chr1:145927422-145927634 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
chr1:145964571-145964731 | Rare:40 | ||||
chr1:145996455-145996808 | Common:1; Rare:135 | ||||
chr1:146228968-146229209 | Common:2; Rare:50 | ||||
chr1:147172427-147172823 | Common:1; Rare:102 | ||||
chr1:147225035-147225436 | Common:2; Rare:80 | ||||
chr1:147225525-147225651 | Rare:21 | ||||
chr1:148458680-148458967 | Common:2; Rare:76 | ||||
chr1:148951806-148952178 | Common:5; Rare:83 |