Variant report

Variant rs17368567
Chromosome Location chr5:92684177-92684178
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:92672600-92684400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr5:92677000-92685400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr5:92678800-92684200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr5:92683600-92684200 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr5:92683600-92684200 Bivalent Enhancer HepG2 liver
6 chr5:92683600-92684800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr5:92683600-92684800 Enhancers Fetal Muscle Trunk muscle
8 chr5:92683600-92685600 Enhancers Muscle Satellite Cultured Cells --
9 chr5:92683800-92685000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr5:92683800-92686400 Enhancers HMEC breast
11 chr5:92684000-92684400 Enhancers HUES64 Cell Line embryonic stem cell
12 chr5:92684000-92684400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr5:92684000-92684600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr5:92684000-92684600 Enhancers Fetal Muscle Leg muscle
15 chr5:92684000-92684800 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr5:92684000-92686400 Enhancers HSMM muscle

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