Variant report

Variant rs3737681
Chromosome Location chr1:169138868-169138869
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169100800-169141400 Weak transcription Fetal Muscle Leg muscle
2 chr1:169104800-169142800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr1:169116400-169139400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr1:169121000-169140800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:169121200-169141200 Weak transcription Left Ventricle heart
6 chr1:169121800-169143000 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:169130400-169195200 Weak transcription Pancreas Pancrea
8 chr1:169131000-169139000 Weak transcription Fetal Intestine Small intestine
9 chr1:169131400-169139000 Weak transcription Ovary ovary
10 chr1:169131400-169149400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr1:169132800-169139000 Weak transcription Brain Hippocampus Middle brain
12 chr1:169135600-169139800 Weak transcription Primary T cells fromperipheralblood blood
13 chr1:169137600-169139000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:169137600-169158000 Weak transcription Primary T cells from cord blood blood
15 chr1:169137800-169141800 Weak transcription Primary T helper cells fromperipheralblood blood
16 chr1:169138000-169140200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --

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