Variant report

Variant	rs12823071
Chromosome Location	chr12:39446349-39446350
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11169908	0.84[CEU][hapmap]
rs11170524	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11170641	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11170818	0.85[EUR][1000 genomes]
rs11561416	0.93[EUR][1000 genomes]
rs11611490	0.83[ASN][1000 genomes]
rs12230119	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12230277	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12812262	0.85[CHB][hapmap]
rs12826889	0.93[EUR][1000 genomes]
rs1463212	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1562727	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17465893	0.80[CEU][hapmap];0.85[CHB][hapmap]
rs1900991	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2388060	0.84[CEU][hapmap]
rs2388173	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34529174	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4768548	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7300430	0.93[EUR][1000 genomes]
rs7967776	0.80[CEU][hapmap]
rs7972629	0.84[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	nsv1047623	chr12:39187817-39539939	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv3389115	chr12:39221256-39448458	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39437200-39452400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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