Variant report

Variant	rs13216349
Chromosome Location	chr6:75151471-75151472
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13193570	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13196531	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13196893	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13198156	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13212917	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16884759	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34952449	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34984274	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35307888	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35756548	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36053338	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs41360849	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs71555246	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71555257	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7744201	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744739	0.81[AFR][1000 genomes]
rs7768066	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9352116	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	esv2759442	chr6:74961996-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv35015	chr6:75031337-75154143	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2757178	chr6:75060947-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv886166	chr6:75082067-75155303	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv886167	chr6:75102625-75175449	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv886168	chr6:75112715-75166715	Enhancers Weak transcription Active TSS	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	chr6:75149800-75155800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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