Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648131-119648372 | Common:3; Rare:81 | ||||
chr1:120176310-120176553 | Rare:52 | ||||
chr1:145214736-145215034 | Rare:34 | ||||
chr1:145823839-145824336 | Rare:169 | ||||
chr1:145836753-145836866 | Rare:36 | ||||
chr1:145845441-145845654 | Common:3; Rare:54 | ||||
chr1:145858945-145859179 | Rare:74 | ||||
chr1:145918658-145919052 | Common:2; Rare:96; Clinvar:1 | ||||
chr1:145927364-145927648 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958223 | Rare:53 | ||||
chr1:145964567-145964754 | Rare:47 | ||||
chr1:145995137-145995521 | Common:1; Rare:157 | ||||
chr1:145995742-145996412 | Common:2; Rare:247 | ||||
chr1:145996417-145996790 | Common:1; Rare:136 | ||||
chr1:146938542-146938759 | Rare:57 |