Variant report

Variant rs191741152
Chromosome Location chr1:73381737-73381738
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:73378600-73382600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr1:73380200-73382000 Enhancers HUES48 Cell Line embryonic stem cell
3 chr1:73381000-73382000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr1:73381000-73382600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:73381200-73381800 Active TSS ES-I3 Cell Line embryonic stem cell
6 chr1:73381200-73381800 Flanking Active TSS HUES6 Cell Line embryonic stem cell
7 chr1:73381200-73381800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:73381200-73381800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr1:73381400-73381800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr1:73381400-73381800 Enhancers Fetal Brain Male brain
11 chr1:73381400-73382000 Flanking Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr1:73381400-73382000 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
13 chr1:73381600-73381800 Active TSS iPS-20b Cell Line embryonic stem cell

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