Variant report

Variant	rs67496128
Chromosome Location	chr2:76397508-76397509
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10188424	0.90[EUR][1000 genomes]
rs10205242	0.89[EUR][1000 genomes]
rs11673856	0.97[EUR][1000 genomes]
rs11678895	0.98[EUR][1000 genomes]
rs11679728	0.85[EUR][1000 genomes]
rs11690678	0.93[EUR][1000 genomes]
rs12713863	0.90[EUR][1000 genomes]
rs12987316	0.87[EUR][1000 genomes]
rs12996043	0.84[EUR][1000 genomes]
rs12997508	0.91[EUR][1000 genomes]
rs13002280	0.98[EUR][1000 genomes]
rs13030138	0.90[EUR][1000 genomes]
rs13409722	0.87[EUR][1000 genomes]
rs1608587	0.93[EUR][1000 genomes]
rs17700671	0.91[EUR][1000 genomes]
rs17750689	0.87[EUR][1000 genomes]
rs17750877	0.88[EUR][1000 genomes]
rs34236297	0.96[EUR][1000 genomes]
rs34743837	0.98[EUR][1000 genomes]
rs35475961	0.89[EUR][1000 genomes]
rs35787624	0.96[EUR][1000 genomes]
rs35861585	0.90[EUR][1000 genomes]
rs6547046	0.85[EUR][1000 genomes]
rs68152182	0.93[EUR][1000 genomes]
rs71418796	0.90[EUR][1000 genomes]
rs71418798	0.92[EUR][1000 genomes]
rs71420904	0.92[EUR][1000 genomes]
rs744235	0.93[EUR][1000 genomes]
rs7565818	0.83[EUR][1000 genomes]
rs7572341	0.97[EUR][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	nsv834265	chr2:76275611-76450728	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv999645	chr2:76317006-76451354	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv874311	chr2:76389455-76492999	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 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	chr2:76396800-76397600	Enhancers	Fetal Brain Male	brain
2	chr2:76396800-76397600	Weak transcription	K562	blood
3	chr2:76397400-76401400	Enhancers	HepG2	liver

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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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