Variant report
Variant | rs57716863 |
---|---|
Chromosome Location | chr19:51433398-51433399 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr19:51429800-51433400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
2 | chr19:51429800-51433400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
3 | chr19:51430400-51435200 | Weak transcription | Hela-S3 | cervix |
4 | chr19:51432400-51433400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr19:51432800-51433600 | Enhancers | Brain Hippocampus Middle | brain |
6 | chr19:51432800-51435400 | Weak transcription | Esophagus | oesophagus |
7 | chr19:51432800-51437400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr19:51433200-51433400 | Bivalent Enhancer | Primary T cells fromperipheralblood | blood |
9 | chr19:51433200-51433400 | Bivalent Enhancer | Stomach Smooth Muscle | stomach |
10 | chr19:51433200-51433600 | Bivalent/Poised TSS | HUES6 Cell Line | embryonic stem cell |
11 | chr19:51433200-51433600 | Bivalent Enhancer | Primary T helper cells PMA-I stimulated | -- |
12 | chr19:51433200-51433600 | Bivalent Enhancer | Foreskin Melanocyte Primary Cells skin01 | Skin |
13 | chr19:51433200-51433600 | Enhancers | A549 | lung |
14 | chr19:51433200-51433800 | Bivalent/Poised TSS | iPS-15b Cell Line | embryonic stem cell |
15 | chr19:51433200-51434000 | Enhancers | NHEK | skin |
16 | chr19:51433200-51437600 | Enhancers | HMEC | breast |