Variant report

Variant rs59074407
Chromosome Location chr1:73412701-73412702
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:73410200-73412800 Weak transcription iPS-18 Cell Line embryonic stem cell
2 chr1:73410200-73416200 Weak transcription H9 Cell Line embryonic stem cell
3 chr1:73412000-73413200 Enhancers H1 Cell Line embryonic stem cell
4 chr1:73412000-73413400 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr1:73412000-73413800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr1:73412200-73413200 Enhancers HUES6 Cell Line embryonic stem cell
7 chr1:73412200-73413400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr1:73412200-73413400 Enhancers HUES48 Cell Line embryonic stem cell
9 chr1:73412200-73413400 Enhancers HUES64 Cell Line embryonic stem cell
10 chr1:73412400-73413200 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr1:73412400-73413200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:73412400-73413200 Enhancers Fetal Heart heart
13 chr1:73412600-73413400 Enhancers Cortex derived primary cultured neurospheres brain

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