Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145823819-145824249 | Rare:159 | ||||
chr1:145845435-145845638 | Common:3; Rare:44 | ||||
chr1:145918676-145919022 | Common:2; Rare:81; Clinvar:1 | ||||
chr1:145927364-145927604 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958202 | Rare:47 | ||||
chr1:145964561-145964742 | Rare:46 | ||||
chr1:145994079-145994230 | Rare:52 | ||||
chr1:145995809-145995972 | Common:2; Rare:44 | ||||
chr1:145996291-145996902 | Common:2; Rare:212 | ||||
chr1:146228917-146229202 | Common:3; Rare:70 | ||||
chr1:147172427-147172823 | Common:1; Rare:102 | ||||
chr1:147225070-147225425 | Common:2; Rare:70 | ||||
chr1:147225510-147225773 | Rare:42 | ||||
chr1:147242541-147242738 | Common:3; Rare:82 | ||||
chr1:148151949-148152062 | Rare:34 |