Variant report

Variant	rs6901804
Chromosome Location	chr6:141868870-141868871
allele	G/T
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:19)

rs_ID	r²[population]
rs10223657	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58761168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6933512	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6933872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7759070	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484513	0.91[YRI][hapmap]
rs9484515	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484526	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496022	0.82[YRI][hapmap]
rs9496032	0.83[YRI][hapmap]
rs9496041	0.92[YRI][hapmap]
rs9496046	1.00[AMR][1000 genomes]
rs9496047	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496048	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496051	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496052	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496060	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496073	1.00[AFR][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	nsv1029550	chr6:141372610-142029669	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1015835	chr6:141713451-142233317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv538455	chr6:141713451-142233317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv2755719	chr6:141721907-142123546	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv3416837	chr6:141866859-141870357	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141827800-141870200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:141863400-141870400	Weak transcription	Muscle Satellite Cultured Cells	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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