Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:15704175-15704458 | Common:1; Rare:59 | ||||
chr16:15708805-15708873 | Rare:37; Clinvar:8; Clinvar (benign):4 | ||||
chr16:15719218-15719440 | Common:1; Rare:69; Clinvar:6; Clinvar (benign):3 | ||||
chr16:15720232-15720589 | Common:1; Rare:91; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr16:15747576-15747855 | Rare:65; Clinvar:7; Clinvar (benign):2 | ||||
chr16:15747872-15748045 | Common:4; Rare:52; Clinvar:2; Clinvar (benign):4 | ||||
chr16:20308409-20308479 | Rare:18 | ||||
chr16:21502146-21502350 | Common:1; Rare:54 | ||||
chr16:21520420-21520704 | Common:1; Rare:30 | ||||
chr16:21820393-21820566 | Rare:52 | ||||
chr16:29595052-29595147 | Common:6; Rare:56 | ||||
chr16:29595323-29595521 | Common:3; Rare:93 | ||||
chr16:30527353-30527510 | Rare:43 | ||||
chr16:30875375-30875490 | Rare:38 | ||||
chr16:30892838-30893092 | Rare:70 |