Variant report

Variant	rs12139929
Chromosome Location	chr1:102350086-102350087
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10874521	0.84[EUR][1000 genomes]
rs10874524	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11164314	0.90[ASN][1000 genomes]
rs11164316	0.87[ASN][1000 genomes]
rs11164317	0.87[ASN][1000 genomes]
rs11164324	0.95[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1120398	0.87[ASN][1000 genomes]
rs12025533	0.90[ASN][1000 genomes]
rs12026338	0.90[ASN][1000 genomes]
rs12028754	0.90[ASN][1000 genomes]
rs12033269	0.90[ASN][1000 genomes]
rs12035099	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12041588	0.89[ASN][1000 genomes]
rs12117918	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12136252	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs12730585	0.89[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1319726	0.88[ASN][1000 genomes]
rs1336792	0.87[ASN][1000 genomes]
rs1415098	0.87[ASN][1000 genomes]
rs1415100	0.87[ASN][1000 genomes]
rs1415103	0.90[ASN][1000 genomes]
rs1415105	0.90[ASN][1000 genomes]
rs1591591	0.87[ASN][1000 genomes]
rs1856036	0.90[ASN][1000 genomes]
rs2050571	0.87[ASN][1000 genomes]
rs2050572	0.87[ASN][1000 genomes]
rs4642900	0.87[ASN][1000 genomes]
rs56883975	0.90[ASN][1000 genomes]
rs6577276	0.86[ASN][1000 genomes]
rs6577278	0.87[ASN][1000 genomes]
rs6659134	0.87[ASN][1000 genomes]
rs6661052	0.87[ASN][1000 genomes]
rs6693196	0.87[ASN][1000 genomes]
rs6694755	0.87[ASN][1000 genomes]
rs6702995	0.85[ASN][1000 genomes]
rs74107956	0.90[ASN][1000 genomes]
rs74107958	0.90[ASN][1000 genomes]
rs7543929	0.90[ASN][1000 genomes]
rs962901	0.90[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	nsv522921	chr1:102170295-102876392	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv522156	chr1:102309649-102421714	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102350000-102351200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:102350000-102351600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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