Variant report
Variant | rs2606069 |
---|---|
Chromosome Location | chr2:173494525-173494526 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:173461400-173504200 | Weak transcription | NHEK | skin |
2 | chr2:173462200-173507400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr2:173465600-173495200 | Weak transcription | Ovary | ovary |
4 | chr2:173471800-173495600 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
5 | chr2:173472600-173504600 | Weak transcription | Adipose Nuclei | Adipose |
6 | chr2:173474600-173504400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr2:173478800-173496800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
8 | chr2:173479600-173495800 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
9 | chr2:173479600-173496200 | Weak transcription | Thymus | Thymus |
10 | chr2:173479800-173494600 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
11 | chr2:173479800-173496000 | Weak transcription | Placenta Amnion | Placenta Amnion |
12 | chr2:173480000-173495000 | Weak transcription | Primary B cells from peripheral blood | blood |
13 | chr2:173480000-173495200 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
14 | chr2:173480000-173496000 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
15 | chr2:173480200-173495800 | Weak transcription | GM12878-XiMat | blood |
16 | chr2:173480200-173499200 | Weak transcription | HepG2 | liver |
17 | chr2:173485800-173497200 | Weak transcription | Brain Hippocampus Middle | brain |
18 | chr2:173489200-173496200 | Weak transcription | Fetal Thymus | thymus |
19 | chr2:173489200-173507200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
20 | chr2:173489400-173500400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
21 | chr2:173489400-173504200 | Weak transcription | NHLF | lung |
22 | chr2:173490200-173500600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
23 | chr2:173490400-173497200 | Weak transcription | HSMM | muscle |
24 | chr2:173491400-173494800 | Strong transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
25 | chr2:173491800-173494600 | Strong transcription | Primary T cells from cord blood | blood |
26 | chr2:173491800-173494800 | Strong transcription | Primary B cells from cord blood | blood |
27 | chr2:173491800-173494800 | Strong transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
28 | chr2:173492000-173494800 | Strong transcription | Dnd41 | blood |
29 | chr2:173492200-173494800 | Strong transcription | Primary T helper naive cells fromperipheralblood | blood |
30 | chr2:173492800-173494600 | Strong transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
31 | chr2:173492800-173494600 | Strong transcription | Fetal Stomach | stomach |
32 | chr2:173492800-173497600 | Weak transcription | Fetal Brain Female | brain |
33 | chr2:173493000-173494600 | Strong transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
34 | chr2:173494000-173494600 | Enhancers | Fetal Brain Male | brain |
35 | chr2:173494200-173494600 | Strong transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
36 | chr2:173494200-173494600 | ZNF genes & repeats | Aorta | Aorta |
37 | chr2:173494200-173494600 | ZNF genes & repeats | Esophagus | oesophagus |
38 | chr2:173494200-173494600 | ZNF genes & repeats | Lung | lung |
39 | chr2:173494200-173494600 | ZNF genes & repeats | Spleen | Spleen |
40 | chr2:173494400-173494600 | Enhancers | Fetal Muscle Leg | muscle |