Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247412-25247638 | Common:4; Rare:151 | ||||
chr1:25267680-25268020 | Common:7; Rare:79 | ||||
chr1:25338113-25338453 | Common:1; Rare:112 | ||||
chr1:25430167-25430344 | Common:8; Rare:114 | ||||
chr1:25430598-25430965 | Common:3; Rare:104 | ||||
chr1:25800002-25800259 | Rare:156; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:25819872-25820040 | Common:6; Rare:100 | ||||
chr1:25859288-25859583 | Common:6; Rare:219 | ||||
chr1:25892451-25892951 | Common:17; Rare:253 | ||||
chr1:25906388-25906588 | Rare:132 | ||||
chr1:25998028-25998390 | Common:4; Rare:177 | ||||
chr1:26110820-26111210 | Common:5; Rare:156 | ||||
chr1:26111588-26111860 | Common:2; Rare:165 | ||||
chr1:26112159-26112298 | Rare:37 | ||||
chr1:26177400-26177550 | Common:2; Rare:45 |