Variant report

Variant	rs537459978
Chromosome Location	chr1:85204062-85204063
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413749	chr1:85203614-85205762	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85203400-85204200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:85203600-85204200	Enhancers	H1 Cell Line	embryonic stem cell
3	chr1:85203800-85204400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:85204000-85204200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:85204000-85204200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr1:85204000-85204200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:85204000-85204200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:85204000-85204400	Enhancers	iPS-18 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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