Variant report

Variant	rs484563
Chromosome Location	chr6:49284676-49284677
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs472168	0.98[AFR][1000 genomes]
rs473800	0.86[AFR][1000 genomes]
rs476657	1.00[AFR][1000 genomes]
rs482046	0.94[AFR][1000 genomes]
rs484612	1.00[AFR][1000 genomes]
rs486435	1.00[AFR][1000 genomes]
rs487363	1.00[AFR][1000 genomes]
rs488497	0.98[AFR][1000 genomes]
rs489459	0.81[AFR][1000 genomes]
rs493691	0.96[AFR][1000 genomes]
rs495233	0.98[AFR][1000 genomes]
rs496080	0.98[AFR][1000 genomes]
rs497390	0.98[AFR][1000 genomes]
rs498048	0.98[AFR][1000 genomes]
rs498264	0.96[AFR][1000 genomes]
rs498367	1.00[AFR][1000 genomes]
rs498400	0.81[AFR][1000 genomes]
rs501968	0.98[AFR][1000 genomes]
rs502868	0.96[AFR][1000 genomes]
rs505273	1.00[AFR][1000 genomes]
rs516988	0.96[AFR][1000 genomes]
rs517774	0.98[AFR][1000 genomes]
rs522061	0.98[AFR][1000 genomes]
rs523897	1.00[AFR][1000 genomes]
rs524822	0.98[AFR][1000 genomes]
rs525892	0.98[AFR][1000 genomes]
rs526635	0.90[AFR][1000 genomes]
rs529393	1.00[AFR][1000 genomes]
rs546248	0.96[AFR][1000 genomes]
rs547609	0.94[AFR][1000 genomes]
rs550645	0.98[AFR][1000 genomes]
rs552336	0.94[AFR][1000 genomes]
rs553567	0.98[AFR][1000 genomes]
rs554083	0.98[AFR][1000 genomes]
rs558669	1.00[AFR][1000 genomes]
rs559706	0.94[AFR][1000 genomes]
rs560700	1.00[AFR][1000 genomes]
rs563878	0.98[AFR][1000 genomes]
rs565793	0.94[AFR][1000 genomes]
rs567539	0.86[AFR][1000 genomes]
rs578848	0.98[AFR][1000 genomes]
rs579011	0.98[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949690	chr6:48595821-49289855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2755862	chr6:49081541-49298041	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv3434790	chr6:49281547-49295228	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription	n/a	n/a	inside rSNPs	n/a
4	esv3472555	chr6:49281568-49295231	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
5	esv3472556	chr6:49281633-49295152	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	inside rSNPs	n/a
6	esv3472557	chr6:49281695-49295113	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	inside rSNPs	n/a
7	esv13429	chr6:49281885-49295108	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49283400-49285000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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