Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927362-145927654 | Common:1; Rare:75; Clinvar (pathogenic):1 | ||||
chr1:145957992-145958225 | Rare:54 | ||||
chr1:145964558-145964754 | Rare:49 | ||||
chr1:145995277-145995449 | Rare:69 | ||||
chr1:145996503-145996882 | Common:1; Rare:151 | ||||
chr1:146228968-146229180 | Common:2; Rare:46 | ||||
chr1:146938297-146938374 | Rare:34 | ||||
chr1:147172310-147172797 | Common:1; Rare:132 | ||||
chr1:147242533-147242799 | Common:5; Rare:112 | ||||
chr1:147541205-147541576 | Common:2; Rare:59 | ||||
chr1:147670211-147670282 | Rare:16 | ||||
chr1:147670439-147670674 | Common:2; Rare:49 | ||||
chr1:147928274-147928478 | Common:2; Rare:74 | ||||
chr1:148152146-148152381 | Common:2; Rare:83 | ||||
chr1:148458802-148459006 | Common:1; Rare:59 |