Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119414767-119415227 | Rare:72; Clinvar:1 | ||||
chr1:119415584-119415908 | Rare:63 | ||||
chr1:119648114-119648367 | Common:3; Rare:85 | ||||
chr1:120914053-120914181 | Rare:11 | ||||
chr1:121184774-121185088 | Common:1; Rare:105 | ||||
chr1:144461597-144461724 | Common:3; Rare:56 | ||||
chr1:145214903-145215021 | Rare:17 | ||||
chr1:145607875-145608049 | Common:2; Rare:52 | ||||
chr1:145823869-145824249 | Rare:132 | ||||
chr1:145858996-145859068 | Rare:26 | ||||
chr1:145859070-145859159 | Rare:20 | ||||
chr1:145918680-145919034 | Common:2; Rare:80 | ||||
chr1:145927394-145927644 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145957983-145958202 | Rare:51 | ||||
chr1:145964548-145964768 | Rare:52 |