Variant report

Variant	rs3852255
Chromosome Location	chr7:18866447-18866448
allele	C/T
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:16)

rs_ID	r²[population]
rs10228341	0.81[CHB][hapmap]
rs10247184	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10441039	0.81[CHB][hapmap]
rs12056184	1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs12056282	1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs12113191	0.81[CHB][hapmap]
rs13230142	0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs13234562	0.86[ASN][1000 genomes]
rs17140086	1.00[CHB][hapmap];0.80[CHD][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs17140133	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs17140138	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs35936891	0.81[ASN][1000 genomes]
rs3852253	0.82[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.82[TSI][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3852254	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55930836	0.81[ASN][1000 genomes]
rs73312680	0.91[ASN][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	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv887814	chr7:18751998-18886177	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18854000-18874400	Weak transcription	Aorta	Aorta
2	chr7:18866200-18869000	Weak transcription	Osteobl	bone

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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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