Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62688271-62688510 | Common:1; Rare:96 | ||||
chr1:62784053-62784180 | Rare:48 | ||||
chr1:63523179-63523563 | Common:3; Rare:97 | ||||
chr1:66533403-66533624 | Common:2; Rare:32 | ||||
chr1:66924810-66925023 | Rare:91 | ||||
chr1:70205534-70205764 | Rare:77 | ||||
chr1:70221302-70221506 | Rare:87 | ||||
chr1:70354697-70354852 | Rare:55 | ||||
chr1:70411078-70411291 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080972-71081359 | Rare:107 | ||||
chr1:74198148-74198270 | Common:1; Rare:63 | ||||
chr1:74732994-74733266 | Common:5; Rare:86 | ||||
chr1:77219385-77219482 | Rare:46 | ||||
chr1:77888462-77888695 | Rare:53; Clinvar:2 | ||||
chr1:77979013-77979291 | Common:2; Rare:97 |