Variant report

Variant rs9383712
Chromosome Location chr6:150510820-150510821
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150497800-150511000 Weak transcription NHEK skin
2 chr6:150499600-150519600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr6:150502400-150511800 Weak transcription Right Atrium heart
4 chr6:150506600-150512000 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr6:150506600-150515600 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr6:150506800-150512000 Weak transcription HMEC breast
7 chr6:150507000-150513200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr6:150507200-150511200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:150507600-150512000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:150508000-150511000 Weak transcription Left Ventricle heart
11 chr6:150508000-150513600 Weak transcription Lung lung
12 chr6:150508400-150517000 Weak transcription K562 blood
13 chr6:150510400-150511200 Enhancers Right Ventricle heart
14 chr6:150510400-150513400 Enhancers Fetal Heart heart
15 chr6:150510600-150512200 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr6:150510600-150518000 Weak transcription Psoas Muscle Psoas
17 chr6:150510800-150514800 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived

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