Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:5237984-5238135 | Common:1; Rare:58 | ||||
chr18:8704572-8704680 | Common:2; Rare:17 | ||||
chr18:12330745-12330890 | Rare:23 | ||||
chr18:31724625-31724787 | Rare:16 | ||||
chr18:46087204-46087455 | Rare:60; Clinvar (pathogenic):1 | ||||
chr18:57630183-57630384 | Common:1; Rare:54 | ||||
chr18:57802020-57802260 | Common:2; Rare:62 | ||||
chr18:76491475-76491651 | Common:3; Rare:77 | ||||
chr19:311935-312217 | Common:9; Rare:142 | ||||
chr19:1876164-1876312 | Common:1; Rare:54 | ||||
chr19:2115224-2115607 | Common:4; Rare:139 | ||||
chr19:3361161-3361205 | Rare:10 | ||||
chr19:3409578-3409923 | Common:1; Rare:85 | ||||
chr19:3977213-3977612 | Common:4; Rare:130; Clinvar (benign):8 | ||||
chr19:4513656-4513903 | Rare:77 |