Variant report

Variant rs187269696
Chromosome Location chr2:50914793-50914794
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50913600-50914800 Enhancers HUES48 Cell Line embryonic stem cell
2 chr2:50913600-50916000 Enhancers HUES6 Cell Line embryonic stem cell
3 chr2:50913600-50916200 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr2:50913800-50915800 Enhancers Brain Anterior Caudate brain
5 chr2:50913800-50916200 Enhancers H1 Cell Line embryonic stem cell
6 chr2:50914000-50917800 Weak transcription Brain Angular Gyrus brain
7 chr2:50914200-50915200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr2:50914200-50916000 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr2:50914200-50918600 Weak transcription Brain Cingulate Gyrus brain
10 chr2:50914400-50918400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:50914600-50914800 Enhancers H9 Cell Line embryonic stem cell
12 chr2:50914600-50914800 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
13 chr2:50914600-50915200 Enhancers Fetal Heart heart

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