Variant report

Variant	rs28406061
Chromosome Location	chr7:96910642-96910643
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96909000-96911400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:96909600-96911000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:96910200-96910800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:96910200-96910800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:96910400-96910800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr7:96910400-96911000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr7:96910400-96911200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:96910400-96911200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:96910600-96910800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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