Variant report

Variant	rs73813021
Chromosome Location	chr4:45207631-45207632
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1500495	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16858147	0.84[AFR][1000 genomes]
rs16858373	1.00[AMR][1000 genomes]
rs41502944	1.00[AMR][1000 genomes]
rs56316722	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57284288	0.87[AFR][1000 genomes]
rs57338164	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57933080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59366613	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61049347	0.84[AFR][1000 genomes]
rs61175363	0.82[AFR][1000 genomes]
rs61308768	1.00[AMR][1000 genomes]
rs61700072	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73813018	0.87[AFR][1000 genomes]
rs73813019	0.87[AFR][1000 genomes]
rs73813035	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73813038	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73813039	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73813040	1.00[AMR][1000 genomes]
rs73813042	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73813044	1.00[AMR][1000 genomes]
rs73813049	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7656155	0.85[AFR][1000 genomes];1.00[AMR][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	nsv1014327	chr4:44735209-45218149	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829919	chr4:45069901-45253808	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv594104	chr4:45105210-45665828	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv461349	chr4:45175691-45265046	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv594105	chr4:45175691-45265046	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv878984	chr4:45191856-45321022	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:45202000-45214600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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