Variant report
Variant | rs60289981 |
---|---|
Chromosome Location | chr6:64443127-64443128 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:64423600-64444400 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
2 | chr6:64424200-64450400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
3 | chr6:64436400-64444600 | Weak transcription | HepG2 | liver |
4 | chr6:64436800-64445400 | Weak transcription | Primary T cells from cord blood | blood |
5 | chr6:64437400-64459600 | Weak transcription | Aorta | Aorta |
6 | chr6:64437800-64445000 | Weak transcription | Primary hematopoietic stem cells | blood |
7 | chr6:64441200-64443200 | Enhancers | Muscle Satellite Cultured Cells | -- |
8 | chr6:64441200-64443200 | Enhancers | HUVEC | blood vessel |
9 | chr6:64441400-64443600 | Enhancers | Hela-S3 | cervix |
10 | chr6:64441600-64443200 | Enhancers | HMEC | breast |
11 | chr6:64441600-64443800 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
12 | chr6:64441800-64443200 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
13 | chr6:64441800-64443400 | Enhancers | NHDF-Ad | bronchial |
14 | chr6:64442000-64451800 | Weak transcription | Fetal Intestine Small | intestine |
15 | chr6:64442000-64451800 | Weak transcription | Small Intestine | intestine |
16 | chr6:64442200-64444600 | Weak transcription | NHEK | skin |
17 | chr6:64442400-64445400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
18 | chr6:64442400-64450200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
19 | chr6:64443000-64444600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |