Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:75555978-75555994 | Rare:7 | ||||
chr16:75556167-75556412 | Common:3; Rare:97; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr16:75566179-75566512 | Common:3; Rare:149 | ||||
chr16:75623222-75623442 | Common:3; Rare:79 | ||||
chr16:75647595-75647873 | Common:4; Rare:140; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr16:75648482-75648624 | Rare:57 | ||||
chr16:75648628-75648731 | Rare:43 | ||||
chr16:76277106-76277597 | Common:2; Rare:101 | ||||
chr16:77190686-77191034 | Common:10; Rare:112 | ||||
chr16:77191115-77191246 | Common:1; Rare:57 | ||||
chr16:77212170-77212289 | Common:2; Rare:47 | ||||
chr16:77722314-77722560 | Common:3; Rare:83 | ||||
chr16:77788280-77788659 | Common:3; Rare:140 | ||||
chr16:78099339-78099731 | Common:2; Rare:155 | ||||
chr16:80540869-80541067 | Common:3; Rare:82 |