Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:47177448-47177748 | Common:2; Rare:35 | ||||
chrX:47180338-47180504 | Common:1; Rare:24 | ||||
chrX:47195644-47195670 | Rare:5 | ||||
chrX:47195950-47196144 | Rare:29 | ||||
chrX:47196147-47196595 | Rare:55 | ||||
chrX:47199085-47199566 | Common:1; Rare:110; Clinvar (benign):10 | ||||
chrX:47205960-47206447 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):6 | ||||
chrX:47210840-47211402 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):5 | ||||
chrX:47211436-47211659 | Common:1; Rare:39 | ||||
chrX:47212419-47213130 | Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
chrX:47224862-47225093 | Common:1; Rare:35 | ||||
chrX:47247621-47248010 | Common:2; Rare:118 | ||||
chrX:47566638-47567111 | Common:1; Rare:125 | ||||
chrX:47583122-47583536 | Rare:49 | ||||
chrX:48989623-48989875 | Rare:39 |