Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:807769-808002 | Rare:67 | ||||
chr16:1207024-1207311 | Common:2; Rare:131; Clinvar:2; Clinvar (benign):3 | ||||
chr16:1213975-1214025 | Common:1; Rare:16 | ||||
chr16:1216342-1216533 | Common:3; Rare:59 | ||||
chr16:1219330-1219419 | Rare:34 | ||||
chr16:2524674-2524785 | Rare:26 | ||||
chr16:2576902-2577090 | Common:2; Rare:15 | ||||
chr16:2603332-2603473 | Common:1; Rare:58 | ||||
chr16:2673334-2673736 | Common:10; Rare:139 | ||||
chr16:3029345-3029557 | Rare:85 | ||||
chr16:3031120-3031381 | Common:3; Rare:61 | ||||
chr16:3087081-3087131 | Rare:10 | ||||
chr16:3143814-3144017 | Common:1; Rare:44 | ||||
chr16:3144149-3144324 | Common:1; Rare:38 | ||||
chr16:3147283-3147350 | Rare:20 |