Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207032721-207032942 | Common:3; Rare:39 | ||||
chr1:207050942-207051076 | Common:1; Rare:65 | ||||
chr1:207052957-207053100 | Rare:34 | ||||
chr1:207053103-207053330 | Common:1; Rare:63 | ||||
chr1:207321424-207321571 | Common:1; Rare:41 | ||||
chr1:207321598-207321873 | Rare:65 | ||||
chr1:207322127-207322599 | Rare:145; Clinvar:1 | ||||
chr1:207751915-207752601 | Common:3; Rare:189; Clinvar:1 | ||||
chr1:207890237-207890384 | Common:1; Rare:27 | ||||
chr1:207911029-207911403 | Common:1; Rare:90 | ||||
chr1:208244236-208244532 | Common:1; Rare:85 | ||||
chr1:209651097-209651472 | Common:2; Rare:68 | ||||
chr1:209675139-209675557 | Common:3; Rare:105 | ||||
chr1:209802208-209802379 | Rare:23 | ||||
chr1:209806117-209806291 | Common:5; Rare:62; Clinvar:2; Clinvar (benign):2 |