Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:58254998-58255398 | Common:5; Rare:102 | ||||
chr13:58618276-58618430 | Rare:22 | ||||
chr13:58619468-58620251 | Common:1; Rare:204 | ||||
chr13:58620205-58620509 | Common:1; Rare:88 | ||||
chr13:59099473-59099674 | Common:1; Rare:33 | ||||
chr13:59111909-59112709 | Common:3; Rare:237 | ||||
chr13:59211355-59211835 | Common:7; Rare:127 | ||||
chr13:59679330-59679630 | Common:1; Rare:52 | ||||
chr13:59750885-59751206 | Rare:71 | ||||
chr13:59774753-59774936 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr13:60585001-60585551 | Common:13; Rare:235 | ||||
chr13:60603020-60603330 | Common:3; Rare:53 | ||||
chr13:60758295-60758695 | Common:1; Rare:122 | ||||
chr13:60759518-60760107 | Common:2; Rare:129 | ||||
chr13:61495605-61496005 | Common:6; Rare:113 |