Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:134176925-134177257 | Common:2; Rare:102 | ||||
chr5:134371000-134371184 | Common:1; Rare:48 | ||||
chr5:134411855-134411990 | Rare:41 | ||||
chr5:134648685-134648840 | Rare:46 | ||||
chr5:134845802-134846094 | Rare:131 | ||||
chr5:135578923-135579198 | Common:2; Rare:80 | ||||
chr5:137889323-137889457 | Common:1; Rare:43 | ||||
chr5:138033039-138033164 | Common:1; Rare:45 | ||||
chr5:138178941-138179154 | Common:2; Rare:46 | ||||
chr5:138465728-138465875 | Rare:54 | ||||
chr5:138543104-138543523 | Common:2; Rare:130 | ||||
chr5:138753273-138753503 | Common:2; Rare:79 | ||||
chr5:139198284-139198531 | Rare:83; Clinvar (benign):1 | ||||
chr5:139561100-139561359 | Common:1; Rare:102 | ||||
chr5:139561739-139561812 | Rare:25 |