Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69339548-69339801 | Rare:100; Clinvar (benign):1 | ||||
chr16:69424489-69424678 | Rare:53 | ||||
chr16:69726489-69727026 | Common:3; Rare:134 | ||||
chr16:70299093-70299205 | Common:1; Rare:20 | ||||
chr16:70523539-70523837 | Common:3; Rare:92 | ||||
chr16:71895234-71895550 | Common:2; Rare:122 | ||||
chr16:72093602-72093929 | Rare:76 | ||||
chr16:74296512-74296902 | Common:1; Rare:136 | ||||
chr16:74666853-74667166 | Common:4; Rare:102 | ||||
chr16:75433408-75433812 | Common:4; Rare:121 | ||||
chr16:75647643-75647763 | Common:1; Rare:59; Clinvar:2 | ||||
chr16:77190707-77190980 | Common:8; Rare:88 | ||||
chr16:81006809-81007272 | Common:4; Rare:157 | ||||
chr16:82170160-82170358 | Common:5; Rare:105 | ||||
chr16:84116833-84117061 | Common:3; Rare:89 |