Variant report
Variant | rs7678087 |
---|---|
Chromosome Location | chr4:101855022-101855023 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:101853400-101855800 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
2 | chr4:101853800-101855200 | Active TSS | Brain Hippocampus Middle | brain |
3 | chr4:101854400-101855200 | Enhancers | Brain Cingulate Gyrus | brain |
4 | chr4:101854400-101855200 | Flanking Active TSS | NHDF-Ad | bronchial |
5 | chr4:101854400-101855400 | Flanking Active TSS | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
6 | chr4:101854600-101855200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
7 | chr4:101854600-101855400 | Flanking Active TSS | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
8 | chr4:101854800-101855200 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
9 | chr4:101854800-101855200 | Enhancers | Ovary | ovary |
10 | chr4:101854800-101855400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
11 | chr4:101854800-101855400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
12 | chr4:101854800-101857800 | Weak transcription | Fetal Brain Female | brain |
13 | chr4:101855000-101855200 | Enhancers | Primary T helper memory cells from peripheral blood 1 | blood |
14 | chr4:101855000-101855400 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
15 | chr4:101855000-101855400 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
16 | chr4:101855000-101855400 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
17 | chr4:101855000-101855400 | Enhancers | Adipose Nuclei | Adipose |
18 | chr4:101855000-101855400 | Enhancers | Placenta | Placenta |