Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27212581-27212701 | Common:1; Rare:26 | ||||
chr13:27432618-27432784 | Rare:33 | ||||
chr13:29849085-29849142 | Rare:13 | ||||
chr13:29849422-29849522 | Rare:27 | ||||
chr13:30108862-30109178 | Common:3; Rare:59 | ||||
chr13:33015323-33015505 | Common:1; Rare:33 | ||||
chr13:33017009-33017166 | Rare:51; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr13:33200567-33200730 | Rare:32 | ||||
chr13:37007917-37008173 | Rare:64 | ||||
chr13:37091010-37091141 | Rare:22 | ||||
chr13:40172289-40172418 | Common:2; Rare:35 | ||||
chr13:40664732-40664890 | Common:3; Rare:42 | ||||
chr13:41060127-41060275 | Common:2; Rare:45 | ||||
chr13:41458275-41458791 | Common:2; Rare:128 | ||||
chr13:41458816-41459063 | Rare:39 |