Variant report

Variant rs6600878
Chromosome Location chr4:69958336-69958337
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69955600-69959400 Weak transcription HepG2 liver
2 chr4:69957400-69959600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr4:69957400-69960000 Enhancers NHEK skin
4 chr4:69957600-69958400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr4:69957600-69958400 Enhancers Osteobl bone
6 chr4:69957600-69959800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr4:69957800-69958800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr4:69957800-69958800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr4:69958000-69958800 Weak transcription Muscle Satellite Cultured Cells --
10 chr4:69958000-69958800 Weak transcription NH-A brain
11 chr4:69958000-69959200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr4:69958000-69960800 Weak transcription HUVEC blood vessel
13 chr4:69958200-69958600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr4:69958200-69958600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr4:69958200-69961000 Weak transcription HMEC breast

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