Variant report

Variant rs6957485
Chromosome Location chr7:17048810-17048811
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17033400-17052600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr7:17045600-17049200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr7:17045600-17049200 Weak transcription Adipose Nuclei Adipose
4 chr7:17045600-17056200 Weak transcription Stomach Mucosa stomach
5 chr7:17047800-17052400 Weak transcription Osteobl bone
6 chr7:17048000-17049400 Weak transcription HMEC breast
7 chr7:17048000-17049600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:17048200-17050400 Weak transcription NHEK skin
9 chr7:17048400-17051400 Enhancers Primary monocytes fromperipheralblood blood
10 chr7:17048600-17049800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr7:17048600-17049800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr7:17048600-17050800 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr7:17048600-17050800 Enhancers Primary T helper cells PMA-I stimulated --
14 chr7:17048600-17050800 Enhancers Primary T helper 17 cells PMA-I stimulated --
15 chr7:17048800-17049400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr7:17048800-17050400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr7:17048800-17050800 Enhancers Primary T helper memory cells from peripheral blood 1 blood

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