Variant report

Variant	rs6836018
Chromosome Location	chr4:75981612-75981613
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10006711	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10020755	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10049552	0.85[EUR][1000 genomes]
rs10049553	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs1062293	0.85[CHB][hapmap]
rs11098475	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11098644	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11725966	0.83[CHB][hapmap]
rs11727003	0.85[CHB][hapmap]
rs11730113	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11944489	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2114176	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3775527	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3822109	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4859938	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6836430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005324	chr4:75689880-76233555	Bivalent/Poised TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv537142	chr4:75689880-76233555	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75956800-75982800	Weak transcription	Pancreas	Pancrea
2	chr4:75974400-75982600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:75974800-75983800	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:75977800-75983600	Weak transcription	Right Ventricle	heart
5	chr4:75980800-75982200	Enhancers	Fetal Heart	heart
6	chr4:75981600-75981800	Enhancers	Left Ventricle	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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