Variant report

Variant	rs12058102
Chromosome Location	chr1:170322055-170322056
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10494488	1.00[EUR][1000 genomes]
rs10919380	1.00[EUR][1000 genomes]
rs10919385	1.00[EUR][1000 genomes]
rs12059763	1.00[EUR][1000 genomes]
rs12067967	1.00[EUR][1000 genomes]
rs12071682	1.00[EUR][1000 genomes]
rs12088917	1.00[EUR][1000 genomes]
rs12091696	1.00[EUR][1000 genomes]
rs12096909	1.00[EUR][1000 genomes]
rs12097499	1.00[EUR][1000 genomes]
rs13375039	1.00[EUR][1000 genomes]
rs13375419	1.00[EUR][1000 genomes]
rs13376452	1.00[EUR][1000 genomes]
rs1556499	1.00[EUR][1000 genomes]
rs16863293	1.00[EUR][1000 genomes]
rs2095136	1.00[EUR][1000 genomes]
rs28545641	1.00[EUR][1000 genomes]
rs58151495	1.00[EUR][1000 genomes]
rs6701383	1.00[EUR][1000 genomes]
rs7518635	1.00[EUR][1000 genomes]
rs7554519	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014033	chr1:169968488-170453021	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	nsv535200	chr1:169968488-170453021	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	esv2756870	chr1:170315081-170413292	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	esv2758977	chr1:170315081-170413292	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	5 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	chr1:170317600-170323400	Weak transcription	Pancreas	Pancrea
2	chr1:170320600-170323400	Weak transcription	Fetal Heart	heart
3	chr1:170320800-170323400	Weak transcription	Left Ventricle	heart
4	chr1:170321000-170323400	Weak transcription	Psoas Muscle	Psoas
5	chr1:170321400-170323400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:170321600-170323400	Weak transcription	Right Atrium	heart

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