Variant report

Variant	rs7108339
Chromosome Location	chr11:32434626-32434627
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32431985..32434925-chr11:32436480..32438156,2	K562	blood:
2	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10767935	0.94[CEU][hapmap];0.82[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10835894	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10835896	0.80[CEU][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10835900	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10835901	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10835903	0.94[CEU][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10835905	0.95[CEU][hapmap];0.84[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10835906	0.95[CEU][hapmap];0.84[JPT][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10835907	0.95[CEU][hapmap];0.84[JPT][hapmap]
rs11031757	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11031760	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11031761	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11031762	0.80[CEU][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11031767	0.83[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs11031769	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11031770	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11824258	0.88[EUR][1000 genomes]
rs12574749	0.82[JPT][hapmap]
rs16923242	0.95[CEU][hapmap];0.84[JPT][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1799937	0.87[EUR][1000 genomes]
rs2234587	0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2295081	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2295082	0.83[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3858440	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3858441	0.94[CEU][hapmap];0.82[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3858442	0.95[CEU][hapmap];0.83[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3858443	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3858445	0.82[EUR][1000 genomes]
rs3901671	0.94[CEU][hapmap];0.82[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3932463	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs5030201	0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs5030207	0.83[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs5030218	0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs5030241	0.88[AFR][1000 genomes]
rs58222320	0.81[EUR][1000 genomes]
rs58736369	0.81[EUR][1000 genomes]
rs61889206	0.82[AMR][1000 genomes]
rs7107082	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7116169	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7125543	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7125816	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7925851	0.80[CEU][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7926521	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7926620	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7938016	0.94[CEU][hapmap];0.82[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7939496	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7946388	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7951745	0.87[AMR][1000 genomes];0.83[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	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1038188	chr11:32410305-32449799	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32427800-32435000	Weak transcription	K562	blood
2	chr11:32433400-32437200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:32434000-32442400	Weak transcription	Right Ventricle	heart
4	chr11:32434200-32438000	Weak transcription	Ovary	ovary
5	chr11:32434400-32435400	Strong transcription	Fetal Kidney	kidney

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