Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:248906080-248906275 | Rare:76 | ||||
chr10:988302-988490 | Common:1; Rare:74 | ||||
chr10:1048881-1049095 | Common:2; Rare:110 | ||||
chr10:1056306-1056424 | Rare:16 | ||||
chr10:1056688-1056836 | Common:2; Rare:58 | ||||
chr10:3785160-3785590 | Common:4; Rare:178 | ||||
chr10:5684664-5684886 | Common:5; Rare:85 | ||||
chr10:5813364-5813673 | Common:3; Rare:127 | ||||
chr10:5889872-5890288 | Common:5; Rare:147 | ||||
chr10:5917303-5917484 | Rare:54 | ||||
chr10:7787863-7788258 | Common:1; Rare:162 | ||||
chr10:7799771-7800088 | Rare:84 | ||||
chr10:12195797-12195992 | Rare:51 | ||||
chr10:13099706-13100298 | Common:5; Rare:138; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13300054-13300189 | Rare:46; Clinvar:1 |