Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108199957-108200043 | Common:2; Rare:17 | ||||
chr1:108200126-108200451 | Common:9; Rare:101 | ||||
chr1:108200878-108200980 | Common:1; Rare:28 | ||||
chr1:108692186-108692365 | Common:1; Rare:70 | ||||
chr1:108692649-108692866 | Rare:62 | ||||
chr1:108697485-108697549 | Common:1; Rare:12 | ||||
chr1:108746434-108746783 | Common:3; Rare:123 | ||||
chr1:108830628-108830886 | Common:3; Rare:74 | ||||
chr1:108914133-108914420 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
chr1:108949858-108950116 | Rare:43 | ||||
chr1:108963362-108963574 | Common:1; Rare:79 | ||||
chr1:109075889-109076112 | Rare:87 | ||||
chr1:109090576-109090868 | Common:4; Rare:75 | ||||
chr1:109090888-109091025 | Rare:39 | ||||
chr1:109213842-109214143 | Rare:94 |