Variant report

Variant rs9383717
Chromosome Location chr6:150514280-150514281
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr6:150508400-150517000 Weak transcription K562 blood
4 chr6:150510600-150518000 Weak transcription Psoas Muscle Psoas
5 chr6:150510800-150514800 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived
6 chr6:150512600-150514600 Weak transcription Right Atrium heart
7 chr6:150513600-150517200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr6:150513800-150516800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:150513800-150517000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr6:150513800-150517000 Weak transcription NHEK skin
11 chr6:150514000-150514800 Weak transcription Lung lung
12 chr6:150514000-150517000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:150514000-150517000 Weak transcription HMEC breast
14 chr6:150514200-150515600 Enhancers Fetal Heart heart
15 chr6:150514200-150517000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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