Variant report

Variant rs57701631
Chromosome Location chr11:102656980-102656981
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:102651600-102667600 Weak transcription NHDF-Ad bronchial
2 chr11:102652000-102661200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr11:102652000-102661200 Weak transcription NHLF lung
4 chr11:102655000-102657200 Weak transcription Stomach Mucosa stomach
5 chr11:102655200-102660600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:102655600-102659000 Weak transcription NHEK skin
7 chr11:102655600-102668600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:102656600-102657400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr11:102656800-102657000 Enhancers Fetal Stomach stomach
10 chr11:102656800-102657200 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr11:102656800-102657400 Enhancers iPS-20b Cell Line embryonic stem cell

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