Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:85048476-85048617 | Common:2; Rare:33 | ||||
chr1:85062207-85062352 | Common:2; Rare:34 | ||||
chr1:85259623-85259917 | Common:4; Rare:99 | ||||
chr1:85276338-85276774 | Common:6; Rare:137; Clinvar (benign):2 | ||||
chr1:85708306-85708558 | Common:4; Rare:92 | ||||
chr1:86396259-86396410 | Common:3; Rare:37 | ||||
chr1:86704469-86704657 | Rare:73 | ||||
chr1:86704785-86704932 | Common:2; Rare:60 | ||||
chr1:86914314-86914819 | Common:1; Rare:156 | ||||
chr1:88684065-88684435 | Common:3; Rare:96 | ||||
chr1:88992596-88993137 | Common:6; Rare:137 | ||||
chr1:89022854-89022934 | Rare:10 | ||||
chr1:89820931-89821228 | Common:1; Rare:92 | ||||
chr1:89821782-89821900 | Rare:34 | ||||
chr1:89843334-89843515 | Common:1; Rare:71 |