Variant report

Variant	rs61790422
Chromosome Location	chr4:19950138-19950139
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10938784	1.00[ASN][1000 genomes]
rs12498777	0.95[ASN][1000 genomes]
rs12501642	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12504071	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12505951	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12507097	0.97[ASN][1000 genomes]
rs12509507	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12512771	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12648215	0.95[ASN][1000 genomes]
rs16868857	0.98[ASN][1000 genomes]
rs16868882	0.98[ASN][1000 genomes]
rs16868933	0.87[ASN][1000 genomes]
rs16868937	0.94[ASN][1000 genomes]
rs16868942	0.94[ASN][1000 genomes]
rs16868984	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4343723	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4349601	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4597829	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56207856	0.82[AFR][1000 genomes]
rs56287156	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56978174	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58812947	0.98[ASN][1000 genomes]
rs60621850	0.94[ASN][1000 genomes]
rs60791911	0.98[ASN][1000 genomes]
rs73801279	0.98[ASN][1000 genomes]
rs73801302	0.98[ASN][1000 genomes]
rs73803904	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73803906	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73803907	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs73803908	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73803915	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529290	chr4:19658583-20173839	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv593790	chr4:19740879-20142039	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2752044	chr4:19788263-20126804	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1003707	chr4:19898883-19963213	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
5	nsv1005430	chr4:19932874-20013705	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
6	nsv999227	chr4:19948910-19975405	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	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	chr4:19949800-19952000	Weak transcription	NHLF	lung

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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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