Variant report

Variant rs6752
Chromosome Location chr1:209908100-209908101
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209902400-209915000 Weak transcription Brain Substantia Nigra brain
2 chr1:209902400-209915400 Weak transcription Brain Angular Gyrus brain
3 chr1:209903000-209915200 Weak transcription Brain Inferior Temporal Lobe brain
4 chr1:209906200-209909200 Genic enhancers Liver Liver
5 chr1:209906400-209914200 Weak transcription Left Ventricle heart
6 chr1:209906600-209909400 Weak transcription Fetal Heart heart
7 chr1:209906600-209914800 Weak transcription Right Atrium heart
8 chr1:209906800-209908600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:209907600-209914800 Weak transcription Spleen Spleen
10 chr1:209907600-209920800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:209907800-209914600 Weak transcription Right Ventricle heart
12 chr1:209908000-209909000 Weak transcription Ovary ovary
13 chr1:209908000-209909400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr1:209908000-209909600 Weak transcription Primary monocytes fromperipheralblood blood
15 chr1:209908000-209909600 Weak transcription Monocytes-CD14+_RO01746 blood

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