Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77128935-77129093 | Common:1; Rare:35 | ||||
chr1:83860993-83861065 | Rare:18 | ||||
chr1:86457109-86457386 | Common:2; Rare:49 | ||||
chr1:86517604-86517686 | Rare:10 | ||||
chr1:86549109-86549238 | Common:1; Rare:20 | ||||
chr1:86567156-86567517 | Common:1; Rare:71 | ||||
chr1:86646416-86646527 | Rare:19 | ||||
chr1:86648415-86648561 | Common:1; Rare:25 | ||||
chr1:92840502-92840751 | Common:2; Rare:75; Clinvar:1 | ||||
chr1:94864081-94864258 | Rare:29 | ||||
chr1:95743178-95743371 | Common:2; Rare:38 | ||||
chr1:108922253-108922511 | Rare:54; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr1:108923827-108924087 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:110340404-110340501 | Rare:30 | ||||
chr1:111188270-111188572 | Common:2; Rare:83 |