Variant report

Variant	rs73987224
Chromosome Location	chr2:212942703-212942704
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13015590	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847650	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847714	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847732	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57924179	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60944259	0.83[AFR][1000 genomes]
rs73987225	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987226	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987229	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987231	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987234	0.83[AFR][1000 genomes]
rs73987235	0.81[AFR][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	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875798	chr2:212852669-212961992	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv875802	chr2:212867291-213004603	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv875803	chr2:212874828-212969560	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv875804	chr2:212891401-212997024	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212940600-212942800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:212941000-212942800	Enhancers	Dnd41	blood
3	chr2:212942600-212942800	Enhancers	GM12878-XiMat	blood

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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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