Variant report

Variant rs17092157
Chromosome Location chr12:43252742-43252743
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:43248400-43253000 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr12:43248400-43254000 Weak transcription Psoas Muscle Psoas
3 chr12:43248600-43252800 Weak transcription Fetal Lung lung
4 chr12:43248800-43253200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr12:43248800-43254000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr12:43249200-43254000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr12:43251600-43253800 Enhancers Fetal Kidney kidney
8 chr12:43252200-43254400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr12:43252200-43254600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr12:43252400-43253000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr12:43252600-43252800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr12:43252600-43253800 Enhancers Osteobl bone
13 chr12:43252600-43254400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr12:43252600-43254400 Enhancers Fetal Stomach stomach

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