Variant report

Variant	rs2374052
Chromosome Location	chr12:103743752-103743753
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10778228	0.90[CEU][hapmap]
rs10778231	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10778232	0.95[CEU][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10778236	0.95[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10778237	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10778238	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10860977	0.90[CEU][hapmap];0.83[EUR][1000 genomes]
rs10860989	0.81[CEU][hapmap]
rs10860990	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11111537	0.80[CEU][hapmap]
rs11111540	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12301542	0.94[CEU][hapmap]
rs12305336	0.81[CEU][hapmap]
rs1343868	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1879621	0.95[CEU][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1996749	0.90[CEU][hapmap];0.86[EUR][1000 genomes]
rs2374060	0.95[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2374061	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs4764732	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4764733	0.80[CEU][hapmap]
rs4764949	0.90[CEU][hapmap]
rs4764952	0.87[EUR][1000 genomes]
rs4764955	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6539066	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs6539069	0.95[CEU][hapmap];0.93[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6539070	0.94[CEU][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6539071	0.82[AMR][1000 genomes]
rs7137989	0.90[CEU][hapmap];0.84[EUR][1000 genomes]
rs7969597	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7970479	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7970531	0.95[CEU][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7971321	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs8181626	0.94[EUR][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	nsv455703	chr12:103692799-103818049	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv560037	chr12:103692799-103818049	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103707200-103786400	Weak transcription	Primary B cells from cord blood	blood
2	chr12:103741600-103745800	Weak transcription	Primary B cells from peripheral blood	blood

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