Variant report

Variant rs296729
Chromosome Location chr9:93749394-93749395
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93747000-93751000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr9:93747600-93750600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr9:93747600-93750800 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr9:93747600-93751000 Enhancers HMEC breast
5 chr9:93747600-93751200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:93748200-93749800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr9:93748200-93750200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr9:93748200-93750400 Weak transcription NHDF-Ad bronchial
9 chr9:93748200-93750800 Enhancers NHEK skin
10 chr9:93748200-93753800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr9:93748200-93753800 Weak transcription Hela-S3 cervix
12 chr9:93748600-93749800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr9:93748800-93750400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr9:93748800-93750600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:93748800-93754000 Weak transcription HUVEC blood vessel

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