Variant report

Variant rs6685627
Chromosome Location chr1:185238201-185238202
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:185193800-185263600 Weak transcription Brain Inferior Temporal Lobe brain
2 chr1:185210600-185250400 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr1:185218800-185269400 Weak transcription Pancreas Pancrea
4 chr1:185227000-185247400 Weak transcription Primary hematopoietic stem cells blood
5 chr1:185227800-185262000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:185228800-185250400 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr1:185230400-185247000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:185231000-185263400 Weak transcription Fetal Kidney kidney
9 chr1:185231800-185249200 Weak transcription Primary T cells from cord blood blood
10 chr1:185234000-185253200 Weak transcription Fetal Heart heart
11 chr1:185235000-185261800 Weak transcription Duodenum Mucosa Duodenum
12 chr1:185235200-185256800 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr1:185235400-185265400 Weak transcription Brain Substantia Nigra brain
14 chr1:185236600-185265600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
15 chr1:185237000-185248000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
16 chr1:185237800-185240800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
17 chr1:185237800-185241000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr1:185238200-185238600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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