Variant report

Variant rs145364461
Chromosome Location chr2:50918641-50918642
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50915800-50918800 Weak transcription H9 Cell Line embryonic stem cell
2 chr2:50916000-50918800 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr2:50916000-50948000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:50916200-50923800 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr2:50918200-50918800 Weak transcription Brain Substantia Nigra brain
6 chr2:50918400-50918800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:50918400-50919200 Active TSS Brain Angular Gyrus brain
8 chr2:50918400-50919600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr2:50918600-50918800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr2:50918600-50919200 Enhancers HUES48 Cell Line embryonic stem cell
11 chr2:50918600-50919200 Enhancers HUES64 Cell Line embryonic stem cell
12 chr2:50918600-50919200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr2:50918600-50919200 Active TSS Brain Anterior Caudate brain
14 chr2:50918600-50919200 Active TSS Brain Cingulate Gyrus brain
15 chr2:50918600-50919400 Active TSS Brain Hippocampus Middle brain
16 chr2:50918600-50919400 Active TSS Brain Inferior Temporal Lobe brain
17 chr2:50918600-50919800 Enhancers Cortex derived primary cultured neurospheres brain

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