Variant report

Variant	rs1084769
Chromosome Location	chr6:93272153-93272154
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1084765	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1084767	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1084768	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1328488	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1328489	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1574819	0.85[EUR][1000 genomes]
rs2770127	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2770130	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs332949	1.00[EUR][1000 genomes]
rs332950	1.00[EUR][1000 genomes]
rs6454900	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6454901	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7762219	1.00[EUR][1000 genomes]
rs783848	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs783858	1.00[ASN][1000 genomes]
rs783864	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9351324	1.00[EUR][1000 genomes];1.00[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	esv1845487	chr6:93099906-93306808	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886355	chr6:93166766-93530757	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1018402	chr6:93173579-93855804	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv886356	chr6:93179624-93293303	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3427169	chr6:93268331-93272329	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:93269200-93273600	Weak transcription	Fetal Heart	heart

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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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