Variant report

Variant	rs73600091
Chromosome Location	chr6:149499457-149499458
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11155626	0.96[ASN][1000 genomes]
rs11155628	0.87[EUR][1000 genomes]
rs11155630	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12190751	0.96[ASN][1000 genomes]
rs12195850	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196284	0.96[ASN][1000 genomes]
rs12196893	0.96[ASN][1000 genomes]
rs12200379	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12210317	0.96[ASN][1000 genomes]
rs12213636	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4073251	0.96[ASN][1000 genomes]
rs4470876	0.88[ASN][1000 genomes]
rs58638760	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6900527	0.92[ASN][1000 genomes]
rs6909527	0.96[ASN][1000 genomes]
rs72989962	0.96[ASN][1000 genomes]
rs72989978	0.96[ASN][1000 genomes]
rs72993821	0.96[ASN][1000 genomes]
rs73004281	0.96[ASN][1000 genomes]
rs73779024	0.96[ASN][1000 genomes]
rs7743674	0.96[ASN][1000 genomes]
rs7751665	0.90[EUR][1000 genomes]
rs7774537	0.88[ASN][1000 genomes]
rs7776204	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390657	0.96[ASN][1000 genomes]
rs9918331	0.96[ASN][1000 genomes]
rs9918332	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv3407275	chr6:149498209-149500207	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv2466757	chr6:149498326-149499898	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149492200-149503600	Weak transcription	Right Atrium	heart

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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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