Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:197776474-197776641 | Rare:26 | ||||
chr1:198156274-198156379 | Rare:22 | ||||
chr1:198159101-198159273 | Common:2; Rare:58 | ||||
chr1:198443359-198443681 | Common:2; Rare:51 | ||||
chr1:198699490-198699800 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr1:198932373-198932480 | Rare:17 | ||||
chr1:198935531-198935700 | Rare:30 | ||||
chr1:198937370-198937640 | Common:2; Rare:53 | ||||
chr1:199272753-199272872 | Rare:29 | ||||
chr1:199759194-199759356 | Rare:28 | ||||
chr1:199759460-199760060 | Common:2; Rare:103 | ||||
chr1:199948987-199949182 | Common:1; Rare:30 | ||||
chr1:200029079-200029249 | Common:2; Rare:65 | ||||
chr1:200039150-200039510 | Common:2; Rare:92 | ||||
chr1:200039515-200039650 | Rare:43 |