Variant report

Variant	rs12578696
Chromosome Location	chr12:119449298-119449299
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11069228	0.92[CEU][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];0.90[MEX][hapmap];0.95[MKK][hapmap];0.96[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11069232	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11611681	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12580179	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12580370	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1405050	0.94[CHB][hapmap];0.84[CHD][hapmap];0.86[ASN][1000 genomes]
rs2393464	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61937960	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs61937964	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61937965	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61937967	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61937968	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7306404	0.81[CHB][hapmap];0.84[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv930978	chr12:118866332-119450600	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1046251	chr12:119353064-119467301	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv541615	chr12:119353064-119467301	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119447000-119450400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:119447000-119450600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:119447600-119449400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:119447600-119449600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:119447600-119450400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:119449000-119450600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:119449200-119451000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr12:119449200-119451200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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