Variant report
Variant | rs1564706 |
---|---|
Chromosome Location | chr2:111792518-111792519 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:111786000-111795800 | Enhancers | Primary monocytes fromperipheralblood | blood |
2 | chr2:111786800-111792800 | Enhancers | Fetal Intestine Small | intestine |
3 | chr2:111787000-111792800 | Enhancers | Fetal Intestine Large | intestine |
4 | chr2:111787400-111795600 | Weak transcription | H1 Cell Line | embryonic stem cell |
5 | chr2:111787800-111825400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr2:111788200-111792600 | Weak transcription | H9 Cell Line | embryonic stem cell |
7 | chr2:111788200-111793400 | Weak transcription | Fetal Thymus | thymus |
8 | chr2:111788200-111799200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
9 | chr2:111790800-111793600 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
10 | chr2:111790800-111799200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
11 | chr2:111790800-111800200 | Weak transcription | Spleen | Spleen |
12 | chr2:111791200-111792600 | Enhancers | Duodenum Mucosa | Duodenum |
13 | chr2:111791200-111794600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
14 | chr2:111791200-111795600 | Weak transcription | Gastric | stomach |
15 | chr2:111791200-111795800 | Enhancers | Monocytes-CD14+_RO01746 | blood |
16 | chr2:111791400-111793400 | Weak transcription | Primary B cells from cord blood | blood |
17 | chr2:111792200-111793000 | Enhancers | Fetal Kidney | kidney |
18 | chr2:111792400-111796600 | Weak transcription | Fetal Lung | lung |
19 | chr2:111792400-111797200 | Weak transcription | Fetal Heart | heart |