Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:14598391-14598691 | Common:1; Rare:90 | ||||
chr1:15344974-15345213 | Common:1; Rare:62 | ||||
chr1:15409803-15409906 | Rare:32 | ||||
chr1:15524170-15524511 | Common:2; Rare:99 | ||||
chr1:15526536-15526917 | Common:2; Rare:125 | ||||
chr1:15617215-15617451 | Common:1; Rare:69 | ||||
chr1:15736023-15736296 | Common:2; Rare:53 | ||||
chr1:16018010-16018367 | Common:7; Rare:105 | ||||
chr1:16048557-16048789 | Common:5; Rare:82; Clinvar (benign):2 | ||||
chr1:16048915-16049021 | Common:1; Rare:48; Clinvar (benign):1 | ||||
chr1:16352392-16352598 | Common:3; Rare:114 | ||||
chr1:16613449-16613653 | Common:1 | ||||
chr1:17053946-17054317 | Common:3; Rare:120; Clinvar:16; Clinvar (benign):12 | ||||
chr1:17439669-17439900 | Rare:79 | ||||
chr1:18480795-18481041 | Common:2; Rare:52 |