Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:197902524-197902652 | Common:1; Rare:43 | ||||
chr1:198156920-198157305 | Common:1; Rare:128 | ||||
chr1:200042266-200042626 | Common:1; Rare:84 | ||||
chr1:200409986-200410119 | Rare:44 | ||||
chr1:200669842-200670243 | Common:12; Rare:117 | ||||
chr1:201363057-201363415 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:201366759-201366952 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):4 | ||||
chr1:201368143-201368548 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):7 | ||||
chr1:201372754-201372806 | Rare:8 | ||||
chr1:201374818-201374915 | Common:1; Rare:15 | ||||
chr1:201375026-201375119 | Rare:21 | ||||
chr1:201377606-201378017 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
chr1:201648018-201648191 | Rare:33 | ||||
chr1:201739127-201739385 | Common:2; Rare:39 | ||||
chr1:201739537-201739704 | Common:4; Rare:34 |