Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161201817-161202667 | Common:8; Rare:406; Clinvar:10; Clinvar (benign):20 | ||||
chr1:161225750-161226094 | Common:20; Rare:99 | ||||
chr1:161314246-161314446 | Common:7; Rare:147; Clinvar:20; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
chr1:161749632-161749835 | Rare:69 | ||||
chr1:161750180-161750580 | Common:1; Rare:110 | ||||
chr1:161766133-161766576 | Common:10; Rare:243; Clinvar (pathogenic):2 | ||||
chr1:162069581-162069825 | Common:2; Rare:103 | ||||
chr1:162381485-162381768 | Common:3; Rare:53 | ||||
chr1:162497755-162497898 | Common:4; Rare:104 | ||||
chr1:162561309-162561734 | Common:9; Rare:276 | ||||
chr1:162790516-162790827 | Common:8; Rare:180 | ||||
chr1:163321691-163322121 | Common:2; Rare:210 | ||||
chr1:163322130-163322340 | Common:2; Rare:74 | ||||
chr1:164558794-164559250 | Common:2; Rare:224 | ||||
chr1:164559259-164559590 | Rare:142 |