Variant report

Variant rs73678239
Chromosome Location chr8:49053396-49053397
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49050000-49053400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr8:49050000-49053400 Weak transcription NHEK skin
3 chr8:49050000-49056400 Weak transcription H9 Cell Line embryonic stem cell
4 chr8:49050200-49055800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr8:49051200-49053800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:49051600-49054200 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr8:49051800-49054000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr8:49051800-49058000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr8:49051800-49065800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr8:49052000-49055800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr8:49052800-49054400 Enhancers Fetal Lung lung
12 chr8:49052800-49054800 Enhancers HSMM muscle
13 chr8:49053000-49054000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr8:49053200-49053600 Enhancers Muscle Satellite Cultured Cells --
15 chr8:49053200-49053800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr8:49053200-49054600 Enhancers NH-A brain

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