Variant report
Variant | rs67309224 |
---|---|
Chromosome Location | chr7:98823702-98823703 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:98811000-98827600 | Weak transcription | Right Atrium | heart |
2 | chr7:98821400-98824600 | Enhancers | Stomach Mucosa | stomach |
3 | chr7:98822600-98826800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr7:98822600-98827000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr7:98822800-98823800 | Enhancers | Hela-S3 | cervix |
6 | chr7:98822800-98824200 | Weak transcription | HepG2 | liver |
7 | chr7:98822800-98826800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr7:98823200-98824600 | Weak transcription | A549 | lung |
9 | chr7:98823400-98823800 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
10 | chr7:98823400-98823800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
11 | chr7:98823400-98826800 | Weak transcription | NHEK | skin |
12 | chr7:98823600-98824200 | Enhancers | K562 | blood |