Variant report

Variant	rs73815167
Chromosome Location	chr4:31038905-31038906
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs13120823	0.82[EUR][1000 genomes]
rs13147117	0.82[EUR][1000 genomes]
rs2307	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28571043	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34189753	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs55707833	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56393119	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs59848134	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6847526	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6847757	0.82[EUR][1000 genomes]
rs73812504	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73812506	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73812507	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73812508	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73812512	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73812515	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73812516	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]

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	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:31033000-31042400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:31034200-31043000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr4:31036800-31042000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:31036800-31042200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:31036800-31042200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:31036800-31042600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:31037200-31041800	Weak transcription	ES-UCSF4 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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