Variant report

Variant rs9384231
Chromosome Location chr6:150513356-150513357
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150499600-150519600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr6:150506600-150515600 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr6:150508000-150513600 Weak transcription Lung lung
4 chr6:150508400-150517000 Weak transcription K562 blood
5 chr6:150510400-150513400 Enhancers Fetal Heart heart
6 chr6:150510600-150518000 Weak transcription Psoas Muscle Psoas
7 chr6:150510800-150514800 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived
8 chr6:150511000-150513800 Enhancers NHEK skin
9 chr6:150511200-150513800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr6:150512000-150514000 Enhancers HMEC breast
11 chr6:150512200-150513800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr6:150512400-150514000 Weak transcription Left Ventricle heart
13 chr6:150512600-150514600 Weak transcription Right Atrium heart
14 chr6:150512800-150513600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr6:150512800-150514000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr6:150513000-150513600 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr6:150513200-150513800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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