Variant report

Variant rs9384229
Chromosome Location chr6:150512677-150512678
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr6:150507000-150513200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr6:150508000-150513600 Weak transcription Lung lung
5 chr6:150508400-150517000 Weak transcription K562 blood
6 chr6:150510400-150513400 Enhancers Fetal Heart heart
7 chr6:150510600-150518000 Weak transcription Psoas Muscle Psoas
8 chr6:150510800-150514800 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived
9 chr6:150511000-150513800 Enhancers NHEK skin
10 chr6:150511200-150513800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr6:150512000-150512800 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:150512000-150514000 Enhancers HMEC breast
13 chr6:150512200-150513800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr6:150512400-150514000 Weak transcription Left Ventricle heart
15 chr6:150512600-150513200 Enhancers A549 lung
16 chr6:150512600-150514600 Weak transcription Right Atrium heart

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