Variant report

Variant	rs74133635
Chromosome Location	chr1:196204912-196204913
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11802442	0.94[AFR][1000 genomes]
rs11802997	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11803170	1.00[AFR][1000 genomes]
rs11805373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11806027	1.00[AFR][1000 genomes]
rs11806585	1.00[AFR][1000 genomes]
rs11809793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35084486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55797122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56287411	0.84[AFR][1000 genomes]
rs57962893	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58760665	0.84[AFR][1000 genomes]
rs60185937	1.00[AFR][1000 genomes]
rs74133630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133636	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133644	0.97[AFR][1000 genomes]
rs74133650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74136503	1.00[AFR][1000 genomes]
rs74136506	1.00[AFR][1000 genomes]
rs74136508	0.91[AFR][1000 genomes]
rs74136511	1.00[AFR][1000 genomes]
rs74136514	1.00[AFR][1000 genomes]
rs74136530	0.97[AFR][1000 genomes]
rs74136531	0.87[AFR][1000 genomes]
rs74136532	0.84[AFR][1000 genomes]
rs74136534	0.84[AFR][1000 genomes]
rs74136536	0.84[AFR][1000 genomes]
rs74136537	0.84[AFR][1000 genomes]
rs74136538	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872948	chr1:195872295-196236425	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv534209	chr1:196011881-196208885	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv872952	chr1:196174790-196304223	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv548741	chr1:196186750-196293493	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196194800-196205200	Strong transcription	Liver	Liver
2	chr1:196195600-196210600	Weak transcription	Fetal Brain Male	brain
3	chr1:196197400-196213000	Weak transcription	Ovary	ovary
4	chr1:196197800-196218400	Weak transcription	Fetal Muscle Trunk	muscle

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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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