Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrM:11189-11600 | |||||
chrX:1392100-1392367 | Common:6; Rare:115 | ||||
chrX:11111136-11111356 | Common:3; Rare:47 | ||||
chrX:13734596-13734821 | Common:3; Rare:71; Clinvar (benign):1 | ||||
chrX:16719426-16719683 | Rare:71 | ||||
chrX:19670880-19670959 | Rare:17 | ||||
chrX:20141740-20142086 | Common:1; Rare:80 | ||||
chrX:21940613-21940759 | Common:2; Rare:39 | ||||
chrX:24054626-24055000 | Common:1; Rare:87 | ||||
chrX:40580742-40581021 | Common:4; Rare:68; Clinvar (benign):1 | ||||
chrX:43656146-43656390 | Rare:52 | ||||
chrX:46545385-46545540 | Rare:31 | ||||
chrX:47144668-47144837 | Common:1; Rare:27 | ||||
chrX:47145005-47145273 | Rare:35 | ||||
chrX:47482586-47482665 | Common:5; Rare:18; Clinvar:2 |