Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:109785437-109785613 | Common:1; Rare:65 | ||||
chr13:112995769-112995794 | Rare:2 | ||||
chr13:112996906-112997125 | Common:1; Rare:59 | ||||
chr13:113008540-113008865 | Common:2; Rare:55 | ||||
chr13:113014476-113014755 | Common:2; Rare:69 | ||||
chr13:113022850-113023002 | Common:3; Rare:29 | ||||
chr13:113822068-113822326 | Common:2; Rare:84 | ||||
chr13:113834658-113834892 | Common:7; Rare:80 | ||||
chr13:113837938-113837955 | Rare:3 | ||||
chr14:21495064-21495313 | Common:1; Rare:63 | ||||
chr14:22980677-22980854 | Common:1; Rare:39 | ||||
chr14:23364675-23364746 | Rare:12 | ||||
chr14:24251855-24251921 | Rare:15 | ||||
chr14:24258285-24258564 | Rare:63; Clinvar:2; Clinvar (pathogenic):3 | ||||
chr14:31248592-31248758 | Common:2; Rare:26 |