Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37574396-37574690 | Rare:63 | ||||
chr1:46302022-46302253 | Common:1; Rare:58 | ||||
chr1:53071577-53071836 | Common:4; Rare:61 | ||||
chr1:67831948-67832276 | Common:1; Rare:73 | ||||
chr1:70232166-70232352 | Rare:45 | ||||
chr1:70250371-70250840 | Rare:116 | ||||
chr1:77964646-77964929 | Rare:71 | ||||
chr1:85500654-85500948 | Common:6; Rare:46 | ||||
chr1:85582234-85582389 | Rare:42 | ||||
chr1:93154683-93155084 | Common:3; Rare:115 | ||||
chr1:94532239-94532342 | Rare:21 | ||||
chr1:114708012-114708163 | Rare:18; Clinvar (benign):1 | ||||
chr1:114730321-114730621 | Common:1; Rare:46 | ||||
chr1:148522519-148522657 | Common:3; Rare:74 | ||||
chr1:150966528-150966797 | Common:1; Rare:70 |