Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30634265-30634553 | Common:1; Rare:72 | ||||
chr16:30875299-30875478 | Common:1; Rare:63 | ||||
chr16:31700473-31700619 | Common:2; Rare:30 | ||||
chr16:46743437-46743536 | Rare:20 | ||||
chr16:53070798-53070922 | Rare:11 | ||||
chr16:53094192-53094307 | Rare:15 | ||||
chr16:54898098-54898312 | Common:1; Rare:26 | ||||
chr16:56708539-56708697 | Common:1; Rare:22 | ||||
chr16:56911929-56912023 | Rare:16 | ||||
chr16:56917164-56917284 | Rare:19 | ||||
chr16:56971367-56971557 | Common:3; Rare:40; Clinvar (benign):1 | ||||
chr16:57039188-57039459 | Rare:36 | ||||
chr16:57039658-57039835 | Common:1; Rare:44 | ||||
chr16:57042706-57042998 | Common:2; Rare:61 | ||||
chr16:57086614-57086733 | Common:2; Rare:22 |