Variant report

Variant rs58353759
Chromosome Location chr6:150513778-150513779
allele A/C
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 chr6:150511000-150513800 Enhancers NHEK skin
7 chr6:150511200-150513800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr6:150512000-150514000 Enhancers HMEC breast
9 chr6:150512200-150513800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr6:150512400-150514000 Weak transcription Left Ventricle heart
11 chr6:150512600-150514600 Weak transcription Right Atrium heart
12 chr6:150512800-150514000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:150513200-150513800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr6:150513400-150514200 Weak transcription Fetal Heart heart
15 chr6:150513600-150517200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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