Variant report

Variant rs9989031
Chromosome Location chr12:83041884-83041885
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:83039800-83044200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr12:83040000-83043600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr12:83040000-83044200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr12:83040000-83044200 Weak transcription NHEK skin
5 chr12:83040200-83043600 Weak transcription HMEC breast
6 chr12:83041400-83042400 Enhancers Cortex derived primary cultured neurospheres brain
7 chr12:83041600-83042400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr12:83041600-83042400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr12:83041600-83042400 Active TSS Brain Anterior Caudate brain
10 chr12:83041600-83042600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr12:83041600-83042600 Enhancers Brain Substantia Nigra brain
12 chr12:83041600-83042800 Enhancers HUES48 Cell Line embryonic stem cell
13 chr12:83041800-83042000 Enhancers Brain Cingulate Gyrus brain
14 chr12:83041800-83042000 Enhancers Brain Hippocampus Middle brain
15 chr12:83041800-83042400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr12:83041800-83042400 Active TSS Brain Inferior Temporal Lobe brain
17 chr12:83041800-83042600 Active TSS Brain Angular Gyrus brain

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