Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:22206556-22206591 | Rare:10 | ||||
chr16:22436949-22437071 | Rare:46 | ||||
chr16:22437160-22437326 | Rare:52 | ||||
chr16:22437505-22437701 | Common:2; Rare:51 | ||||
chr16:23557333-23557456 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641246-23641536 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24540241-24540728 | Rare:128 | ||||
chr16:25111537-25111852 | Common:2; Rare:95 | ||||
chr16:27268724-27268850 | Common:1; Rare:39 | ||||
chr16:27549882-27550168 | Common:2; Rare:108 | ||||
chr16:28538796-28539165 | Common:2; Rare:89 | ||||
chr16:28846216-28846463 | Common:2; Rare:103; Clinvar:7; Clinvar (benign):6 | ||||
chr16:28925156-28925266 | Rare:29 | ||||
chr16:28974532-28974792 | Common:2; Rare:84 | ||||
chr16:29995566-29995707 | Common:1; Rare:68 |