Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241519699-241519977 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:241848094-241848266 | Common:2; Rare:32 | ||||
chr1:243255741-243256111 | Rare:99; Clinvar:4 | ||||
chr1:244451866-244452161 | Common:1; Rare:106 | ||||
chr1:244835530-244835734 | Common:3; Rare:92; Clinvar (benign):4 | ||||
chr1:244970251-244970411 | Common:3; Rare:76 | ||||
chr1:246566209-246566514 | Common:1; Rare:101 | ||||
chr10:988234-988470 | Common:3; Rare:86 | ||||
chr10:1048882-1049092 | Common:2; Rare:108 | ||||
chr10:7787938-7788222 | Common:1; Rare:119 | ||||
chr10:12068753-12068974 | Common:2; Rare:75 | ||||
chr10:12195793-12196241 | Rare:122 | ||||
chr10:13099949-13100205 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):4 | ||||
chr10:13348023-13348370 | Rare:120 | ||||
chr10:14008426-14008541 | Common:1; Rare:23 |