Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193059447-193059705 | Rare:133 | ||||
chr1:193186578-193186643 | Rare:8 | ||||
chr1:196651933-196652172 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
chr1:200042281-200042613 | Common:1; Rare:74 | ||||
chr1:200410027-200410234 | Rare:61 | ||||
chr1:200669876-200670102 | Common:11; Rare:79 | ||||
chr1:201154452-201154642 | Common:2; Rare:50 | ||||
chr1:201283449-201283553 | Rare:18 | ||||
chr1:201399302-201399674 | Common:1; Rare:137 | ||||
chr1:201829554-201829585 | Common:1 | ||||
chr1:201946065-201946214 | Rare:43 | ||||
chr1:201946243-201946329 | Rare:19 | ||||
chr1:201946440-201946813 | Common:2; Rare:61 | ||||
chr1:201955369-201955529 | Common:1; Rare:46 | ||||
chr1:202010307-202010642 | Common:4; Rare:77 |