Variant report

Variant	rs7761085
Chromosome Location	chr6:33519058-33519059
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11964131	1.00[AMR][1000 genomes]
rs3846856	1.00[AMR][1000 genomes]
rs3846857	1.00[AMR][1000 genomes]
rs3846858	1.00[AMR][1000 genomes]
rs3846859	1.00[AMR][1000 genomes]
rs3857560	1.00[AMR][1000 genomes]
rs4460206	1.00[AMR][1000 genomes]
rs5745578	1.00[AMR][1000 genomes]
rs5745579	1.00[AMR][1000 genomes]
rs5745580	1.00[AMR][1000 genomes]
rs5745597	1.00[AMR][1000 genomes]
rs60691479	1.00[AMR][1000 genomes]
rs6903143	1.00[AMR][1000 genomes]
rs6909769	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6928531	1.00[AMR][1000 genomes]
rs7739493	0.85[AFR][1000 genomes]
rs7739507	0.85[AFR][1000 genomes]
rs7739510	0.85[AFR][1000 genomes]
rs7739857	0.93[AFR][1000 genomes]
rs7744691	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7752282	0.85[AFR][1000 genomes]
rs7762586	1.00[AMR][1000 genomes]
rs7765464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7769914	1.00[AMR][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	nsv602832	chr6:33382241-33520221	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv2763548	chr6:33496201-33524779	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33514000-33519800	Enhancers	Placenta	Placenta
2	chr6:33516000-33523800	Weak transcription	GM12878-XiMat	blood
3	chr6:33516600-33521800	Weak transcription	Primary T cells from cord blood	blood
4	chr6:33516800-33537600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr6:33517800-33524800	Weak transcription	Esophagus	oesophagus
6	chr6:33518000-33520200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:33518000-33520800	Weak transcription	NHEK	skin
8	chr6:33519000-33519600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:33519000-33519800	Enhancers	Fetal Muscle Leg	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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