Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
chr12:131711036-131711101 | Rare:16 | ||||
chr13:20232204-20232359 | Common:2; Rare:47 | ||||
chr13:21140412-21140615 | Rare:99 | ||||
chr13:21176522-21176704 | Common:1; Rare:85 | ||||
chr13:25301502-25301686 | Common:1; Rare:73 | ||||
chr13:26221798-26221972 | Rare:51 | ||||
chr13:27424485-27424711 | Common:4; Rare:72 | ||||
chr13:28659055-28659187 | Rare:55; Clinvar (pathogenic):1 | ||||
chr13:30465828-30466111 | Common:1; Rare:88 | ||||
chr13:33285719-33285884 | Rare:38 | ||||
chr13:37000757-37000805 | Rare:23 | ||||
chr13:39655627-39655724 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):3 | ||||
chr13:41060927-41061024 | Common:9; Rare:57 | ||||
chr13:41061226-41061580 | Common:3; Rare:119 |