Variant report

Variant rs1779174
Chromosome Location chr1:77694640-77694641
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77685800-77695600 Weak transcription Left Ventricle heart
2 chr1:77686000-77699200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:77686600-77694800 Weak transcription Brain Hippocampus Middle brain
4 chr1:77686600-77698200 Weak transcription Brain Angular Gyrus brain
5 chr1:77686800-77698000 Weak transcription HUVEC blood vessel
6 chr1:77687000-77695200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:77687000-77695200 Weak transcription NHDF-Ad bronchial
8 chr1:77687000-77695400 Weak transcription Muscle Satellite Cultured Cells --
9 chr1:77688400-77697600 Weak transcription Primary T cells from cord blood blood
10 chr1:77690800-77695400 Weak transcription HSMM muscle
11 chr1:77692800-77694800 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr1:77693000-77695600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr1:77693800-77697600 Weak transcription Primary hematopoietic stem cells blood
14 chr1:77694400-77695000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr1:77694600-77694800 Enhancers Brain Anterior Caudate brain
16 chr1:77694600-77694800 Enhancers Brain Cingulate Gyrus brain
17 chr1:77694600-77694800 Enhancers Fetal Kidney kidney
18 chr1:77694600-77696800 Enhancers A549 lung

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