Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185156675-185157303 | Common:3; Rare:191 | ||||
chr1:185157422-185157534 | Common:1; Rare:37 | ||||
chr1:185317071-185317469 | Common:1; Rare:109 | ||||
chr1:186375061-186375944 | Common:1; Rare:252 | ||||
chr1:186680297-186680696 | Common:3; Rare:90 | ||||
chr1:192808788-192809175 | Common:4; Rare:159; Clinvar:1 | ||||
chr1:193059314-193059705 | Rare:182 | ||||
chr1:193105381-193105523 | Common:2; Rare:58 | ||||
chr1:193121743-193122216 | Common:2; Rare:171; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193186576-193186677 | Rare:14 | ||||
chr1:196608863-196609168 | Common:2; Rare:53 | ||||
chr1:197902551-197902651 | Common:1; Rare:34 | ||||
chr1:197917133-197917379 | Common:1; Rare:67 | ||||
chr1:200669842-200670130 | Common:12; Rare:93 | ||||
chr1:201399307-201399633 | Common:1; Rare:128 |