Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193121773-193122145 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
chr1:193122146-193122308 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:193186561-193186880 | Rare:55 | ||||
chr1:197146586-197146701 | Rare:24; Clinvar:3 | ||||
chr1:197902556-197902650 | Rare:32 | ||||
chr1:200409941-200410359 | Rare:119 | ||||
chr1:200669804-200670110 | Common:12; Rare:97 | ||||
chr1:201492638-201492965 | Common:4; Rare:46 | ||||
chr1:201648079-201648185 | Rare:21 | ||||
chr1:201648329-201648674 | Common:1; Rare:87 | ||||
chr1:201946079-201946261 | Rare:56 | ||||
chr1:201946377-201946802 | Common:3; Rare:70 | ||||
chr1:201955250-201955541 | Common:1; Rare:82 | ||||
chr1:201982744-201983111 | Rare:101 | ||||
chr1:202927090-202927387 | Common:5; Rare:126 |