Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48233071-48233475 | Common:3; Rare:140 | ||||
chr13:48303667-48303896 | Rare:77; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48533050-48533106 | Common:1; Rare:17 | ||||
chr13:48975603-48975934 | Common:2; Rare:103 | ||||
chr13:48976147-48976260 | Rare:30 | ||||
chr13:48976495-48976656 | Common:2; Rare:55 | ||||
chr13:49247800-49247984 | Rare:51 | ||||
chr13:49444005-49444484 | Common:1; Rare:153 | ||||
chr13:49495902-49496185 | Common:3; Rare:70 | ||||
chr13:49585527-49585658 | Common:1; Rare:47 | ||||
chr13:49936238-49936574 | Common:1; Rare:100 | ||||
chr13:50081933-50082341 | Common:1; Rare:116 | ||||
chr13:51452443-51452592 | Rare:54 | ||||
chr13:51452603-51452638 | Common:1; Rare:3 | ||||
chr13:51453013-51453377 | Rare:138 |