Variant report

Variant	rs61660982
Chromosome Location	chr4:97472479-97472480
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10007670	0.84[AFR][1000 genomes]
rs10009216	0.84[AFR][1000 genomes]
rs10012373	0.84[AFR][1000 genomes]
rs10019459	0.84[AFR][1000 genomes]
rs10516992	0.84[AFR][1000 genomes]
rs12330946	0.84[AFR][1000 genomes]
rs12331222	0.84[AFR][1000 genomes]
rs12331232	0.84[AFR][1000 genomes]
rs12331799	0.84[AFR][1000 genomes]
rs17025663	0.84[AFR][1000 genomes]
rs28533304	0.84[AFR][1000 genomes]
rs28559835	0.84[AFR][1000 genomes]
rs28565234	0.84[AFR][1000 genomes]
rs28615709	0.84[AFR][1000 genomes]
rs28636778	0.84[AFR][1000 genomes]
rs28655209	0.84[AFR][1000 genomes]
rs28687059	0.84[AFR][1000 genomes]
rs28889126	0.84[AFR][1000 genomes]
rs55706248	0.84[AFR][1000 genomes]
rs57434387	0.80[AFR][1000 genomes]
rs58521019	0.82[AFR][1000 genomes]
rs59844377	0.84[AFR][1000 genomes]
rs60333423	0.82[AFR][1000 genomes]
rs60421343	0.84[AFR][1000 genomes]
rs60702817	0.84[AFR][1000 genomes]
rs60857678	0.84[AFR][1000 genomes]
rs61033100	0.84[AFR][1000 genomes]
rs6816546	0.84[AFR][1000 genomes]
rs6845274	0.84[AFR][1000 genomes]
rs72890904	0.84[AFR][1000 genomes]
rs9992776	0.84[AFR][1000 genomes]
rs9999916	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879634	chr4:97371381-97727113	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv879635	chr4:97389090-97591085	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1007650	chr4:97393803-97485770	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97472000-97472600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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