Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:35290199-35290372 | Common:2; Rare:64 | ||||
chr18:36129229-36129523 | Common:4; Rare:92 | ||||
chr18:36187419-36187517 | Common:2; Rare:40 | ||||
chr18:36828754-36829140 | Common:3; Rare:142 | ||||
chr18:46104135-46104386 | Common:3; Rare:69; Clinvar (benign):1 | ||||
chr18:47150452-47150546 | Common:2; Rare:34 | ||||
chr18:49813835-49814199 | Common:1; Rare:153 | ||||
chr18:56651133-56651379 | Common:3; Rare:62 | ||||
chr18:57621718-57621959 | Common:3; Rare:86 | ||||
chr18:62186955-62187305 | Common:5; Rare:97 | ||||
chr18:63367151-63367328 | Common:1; Rare:61 | ||||
chr18:63422391-63422616 | Common:1; Rare:61 | ||||
chr18:66604083-66604377 | Common:4; Rare:55 | ||||
chr18:68714987-68715254 | Common:5; Rare:121 | ||||
chr18:70205650-70205748 | Common:2; Rare:47; Clinvar (benign):2 |