Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:149406823-149406973 | Rare:27 | ||||
chr5:150534895-150535201 | Common:2; Rare:63; Clinvar (benign):1 | ||||
chr5:150626928-150627283 | Common:3; Rare:53 | ||||
chr5:150778579-150778906 | Common:6; Rare:111 | ||||
chr5:150790400-150790496 | Rare:19 | ||||
chr5:150946527-150946616 | Rare:21 | ||||
chr5:151005773-151005780 | Rare:2 | ||||
chr5:159100318-159100509 | Common:3; Rare:60 | ||||
chr5:168288344-168288613 | Rare:56 | ||||
chr5:172656724-172656874 | Common:1; Rare:28 | ||||
chr5:172767618-172767713 | Common:2; Rare:17 | ||||
chr5:172769843-172770103 | Common:2; Rare:52 | ||||
chr5:172873163-172873357 | Common:1; Rare:37 | ||||
chr5:172887064-172887226 | Common:3; Rare:38 | ||||
chr5:176066703-176066735 |