Variant report

Variant	rs7001461
Chromosome Location	chr8:58293886-58293887
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-12	chr8:58293308-58294764	l_3602_chr8:58277926-58304841_testes

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs11990740	0.97[ASN][1000 genomes]
rs11991955	0.95[ASN][1000 genomes]
rs11994423	0.97[ASN][1000 genomes]
rs11994454	0.97[ASN][1000 genomes]
rs11994487	0.97[ASN][1000 genomes]
rs11997856	0.97[ASN][1000 genomes]
rs1317835	0.93[AFR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16922090	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16922102	0.95[ASN][1000 genomes]
rs16922104	0.95[ASN][1000 genomes]
rs4738588	0.97[ASN][1000 genomes]
rs4738591	0.97[ASN][1000 genomes]
rs4738593	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs55960888	0.99[ASN][1000 genomes]
rs56121699	0.99[ASN][1000 genomes]
rs56690481	0.90[ASN][1000 genomes]
rs56832078	0.99[ASN][1000 genomes]
rs57744550	0.99[ASN][1000 genomes]
rs57829000	0.97[ASN][1000 genomes]
rs58748161	0.96[ASN][1000 genomes]
rs59643894	0.97[ASN][1000 genomes]
rs60129174	0.97[ASN][1000 genomes]
rs60999477	0.96[ASN][1000 genomes]
rs6471602	0.92[ASN][1000 genomes]
rs6980863	0.89[ASN][1000 genomes]
rs6980975	0.93[ASN][1000 genomes]
rs6981267	0.99[ASN][1000 genomes]
rs6981437	0.99[ASN][1000 genomes]
rs6981568	0.99[ASN][1000 genomes]
rs6982211	0.99[ASN][1000 genomes]
rs6985947	0.99[ASN][1000 genomes]
rs6986207	0.99[ASN][1000 genomes]
rs6995433	0.87[ASN][1000 genomes]
rs6996802	0.99[ASN][1000 genomes]
rs6996833	0.97[ASN][1000 genomes]
rs6997730	0.97[ASN][1000 genomes]
rs7002746	0.97[ASN][1000 genomes]
rs7018061	0.97[ASN][1000 genomes]
rs7018443	0.99[ASN][1000 genomes]
rs72652956	0.99[ASN][1000 genomes]
rs72652957	0.99[ASN][1000 genomes]
rs72652989	0.95[ASN][1000 genomes]
rs72652991	0.95[ASN][1000 genomes]
rs72652997	0.92[ASN][1000 genomes]
rs72652998	0.90[ASN][1000 genomes]
rs72652999	0.92[ASN][1000 genomes]
rs72653000	0.92[ASN][1000 genomes]
rs72654805	0.95[ASN][1000 genomes]
rs7814333	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7826185	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7831519	0.87[ASN][1000 genomes]
rs7840258	0.96[ASN][1000 genomes]
rs9694509	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9694545	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758161	chr8:57930392-58474449	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2759618	chr8:57930392-58474449	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv890936	chr8:58266339-58564501	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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