Variant report

Variant rs17019732
Chromosome Location chr4:93557816-93557817
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:93550000-93574800 Weak transcription H1 Cell Line embryonic stem cell
2 chr4:93552000-93579000 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr4:93554400-93570400 Weak transcription HUES48 Cell Line embryonic stem cell
4 chr4:93555200-93559200 Enhancers Cortex derived primary cultured neurospheres brain
5 chr4:93556800-93559200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr4:93557000-93558000 Enhancers Fetal Brain Female brain
7 chr4:93557200-93558000 Enhancers Brain Germinal Matrix brain
8 chr4:93557200-93558000 Active TSS Brain Inferior Temporal Lobe brain
9 chr4:93557200-93558000 Enhancers Fetal Brain Male brain
10 chr4:93557400-93558000 Enhancers Brain Anterior Caudate brain
11 chr4:93557400-93558000 Enhancers Fetal Intestine Small intestine
12 chr4:93557600-93558000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr4:93557600-93558000 Flanking Active TSS Brain Cingulate Gyrus brain
14 chr4:93557800-93558000 Enhancers Brain Substantia Nigra brain
15 chr4:93557800-93558200 Enhancers Brain Angular Gyrus brain
16 chr4:93557800-93560600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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