Variant report

Variant rs7759053
Chromosome Location chr6:140981842-140981843
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:140948600-140991200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:140981200-140982000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr6:140981200-140982000 Enhancers Fetal Intestine Small intestine
4 chr6:140981400-140982000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr6:140981400-140982000 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr6:140981400-140982000 Enhancers Fetal Intestine Large intestine
7 chr6:140981400-140982000 Enhancers NHDF-Ad bronchial
8 chr6:140981400-140982200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:140981600-140982600 Weak transcription Osteobl bone
10 chr6:140981600-140982800 Weak transcription Muscle Satellite Cultured Cells --
11 chr6:140981600-140983400 Enhancers HSMM muscle
12 chr6:140981800-140982800 Active TSS Ovary ovary
13 chr6:140981800-140983600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr6:140981800-140990600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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