Variant report

Variant rs17146453
Chromosome Location chr7:64904606-64904607
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:64902400-64904800 Weak transcription HepG2 liver
2 chr7:64902800-64904800 Enhancers NHDF-Ad bronchial
3 chr7:64902800-64906600 Enhancers NHEK skin
4 chr7:64902800-64907200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr7:64902800-64907200 Enhancers HMEC breast
6 chr7:64903000-64906800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:64903200-64907400 Enhancers NH-A brain
8 chr7:64903600-64904800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr7:64904000-64905400 Weak transcription Osteobl bone
10 chr7:64904200-64905200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr7:64904200-64905200 Weak transcription HSMM muscle
12 chr7:64904200-64905400 Weak transcription Muscle Satellite Cultured Cells --
13 chr7:64904200-64905600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr7:64904200-64905600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr7:64904200-64905600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr7:64904200-64905600 Weak transcription NHLF lung
17 chr7:64904400-64905400 Weak transcription HUVEC blood vessel

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