Variant report

Variant rs184737498
Chromosome Location chr2:50848979-50848980
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50838800-50849400 Weak transcription Fetal Brain Female brain
2 chr2:50839000-50851800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
3 chr2:50843000-50853600 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr2:50847000-50849400 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:50847800-50849400 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr2:50848000-50850400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr2:50848200-50851800 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr2:50848400-50850200 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr2:50848600-50849000 Enhancers Brain Substantia Nigra brain
10 chr2:50848600-50849400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr2:50848600-50850600 Strong transcription Brain Germinal Matrix brain
12 chr2:50848800-50849400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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