Variant report

Variant	rs6726820
Chromosome Location	chr2:67181166-67181167
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10174577	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10175701	0.87[ASN][1000 genomes]
rs10180582	0.87[ASN][1000 genomes]
rs10210389	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10496138	0.95[ASN][1000 genomes]
rs12467586	1.00[JPT][hapmap]
rs13409540	0.95[ASN][1000 genomes]
rs1362484	0.87[ASN][1000 genomes]
rs58683753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6721312	0.96[ASN][1000 genomes]
rs67764531	0.93[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7419773	0.96[ASN][1000 genomes]
rs7591850	1.00[JPT][hapmap]
rs868373	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 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	chr2:67179600-67182600	Weak transcription	Fetal Lung	lung
2	chr2:67180800-67184200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr2:67180800-67186400	Weak transcription	Colon Smooth Muscle	Colon

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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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