Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91885887-91886317 | Rare:163 | ||||
chr1:92298958-92299086 | Common:1; Rare:67; Clinvar:1 | ||||
chr1:92832000-92832333 | Rare:148; Clinvar:7; Clinvar (benign):7 | ||||
chr1:93079069-93079394 | Common:4; Rare:126 | ||||
chr1:93180051-93180152 | Rare:38 | ||||
chr1:93180252-93180699 | Common:1; Rare:174 | ||||
chr1:93345619-93346137 | Common:6; Rare:173 | ||||
chr1:93447968-93448217 | Common:2; Rare:87 | ||||
chr1:93614085-93614353 | Common:2; Rare:36 | ||||
chr1:93847218-93847292 | Common:1; Rare:15 | ||||
chr1:93879124-93879370 | Common:3; Rare:89 | ||||
chr1:94237517-94237759 | Rare:91 | ||||
chr1:94418238-94418470 | Common:2; Rare:83 | ||||
chr1:94541081-94541390 | Common:1; Rare:68 | ||||
chr1:94541622-94541991 | Common:1; Rare:108 |