Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63367471-63367696 | Rare:143; Clinvar (benign):2 | ||||
chr1:63523139-63523602 | Common:6; Rare:241 | ||||
chr1:63592957-63593572 | Rare:279; Clinvar (benign):4 | ||||
chr1:63594214-63594407 | Common:2; Rare:44 | ||||
chr1:63594440-63594820 | Common:8; Rare:141 | ||||
chr1:64744795-64745159 | Common:2; Rare:183 | ||||
chr1:65147310-65147700 | Common:1; Rare:159 | ||||
chr1:65147981-65148204 | Common:6; Rare:84 | ||||
chr1:65254359-65254471 | Common:2; Rare:87 | ||||
chr1:65420110-65420690 | Common:9; Rare:249; Clinvar:1 | ||||
chr1:66924771-66925023 | Common:2; Rare:205 | ||||
chr1:66925090-66925535 | Common:4; Rare:265 | ||||
chr1:66930009-66930408 | Rare:230 | ||||
chr1:67053929-67054217 | Common:2; Rare:120 | ||||
chr1:67054350-67054650 | Common:7; Rare:96 |