Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9910163-9910613 | Common:4; Rare:153 | ||||
chr1:9910653-9910987 | Common:3; Rare:71 | ||||
chr1:9942925-9943145 | Common:2; Rare:59 | ||||
chr1:9943182-9943518 | Common:3; Rare:95 | ||||
chr1:10032524-10032998 | Common:3; Rare:129 | ||||
chr1:10033118-10033249 | Rare:27 | ||||
chr1:10210263-10210615 | Common:6; Rare:103 | ||||
chr1:10398857-10399105 | Common:2; Rare:94 | ||||
chr1:10399260-10399560 | Common:3; Rare:65 | ||||
chr1:10430443-10430802 | Common:8; Rare:123 | ||||
chr1:10430962-10431269 | Common:2; Rare:79 | ||||
chr1:10472414-10472768 | Rare:86 | ||||
chr1:10474787-10475219 | Common:1; Rare:137; Clinvar:4; Clinvar (benign):1 | ||||
chr1:10694435-10694706 | Common:1; Rare:89 | ||||
chr1:10796567-10796879 | Common:3; Rare:89 |