Variant report

Variant rs4706765
Chromosome Location chr6:79979749-79979750
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:79976000-79979800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr6:79978600-79980400 Enhancers K562 blood
3 chr6:79978800-79980200 Enhancers Ovary ovary
4 chr6:79979000-79980400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr6:79979200-79980200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:79979400-79979800 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr6:79979400-79980200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr6:79979400-79980200 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr6:79979400-79980200 Enhancers Stomach Smooth Muscle stomach
10 chr6:79979600-79980000 Enhancers Cortex derived primary cultured neurospheres brain
11 chr6:79979600-79980000 Enhancers Fetal Intestine Small intestine
12 chr6:79979600-79980200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr6:79979600-79980200 Enhancers Fetal Heart heart
14 chr6:79979600-79980200 Enhancers Fetal Intestine Large intestine
15 chr6:79979600-79980400 Enhancers Colon Smooth Muscle Colon

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