Variant report

Variant	rs73940047
Chromosome Location	chr2:76988548-76988549
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs56944364	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59473135	1.00[EUR][1000 genomes]
rs6752009	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73940045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7590874	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv582235	chr2:76881210-76997763	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv874320	chr2:76971709-77013724	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv458263	chr2:76976626-76994984	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	nsv1011401	chr2:76982546-77068714	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island 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	chr2:76973400-76989200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:76984200-76988600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:76987600-76989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:76987800-76988600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:76987800-76988600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr2:76988000-76989000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:76988000-76998400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:76988200-76990400	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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