Variant report

Variant	rs10897009
Chromosome Location	chr11:59923194-59923195
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs107903	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10897011	0.82[EUR][1000 genomes]
rs11230147	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11230153	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11230155	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11230180	0.82[EUR][1000 genomes]
rs1125357	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11600716	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11605427	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12226022	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12453	0.85[EUR][1000 genomes]
rs1303615	0.85[EUR][1000 genomes]
rs1303621	0.86[EUR][1000 genomes]
rs17528859	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17529983	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17602572	0.84[EUR][1000 genomes]
rs1786137	0.80[EUR][1000 genomes]
rs1813217	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1820430	0.82[EUR][1000 genomes]
rs1834549	0.82[EUR][1000 genomes]
rs1834550	0.82[EUR][1000 genomes]
rs1834551	0.82[EUR][1000 genomes]
rs1834557	0.81[EUR][1000 genomes]
rs2070970	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2081545	0.82[EUR][1000 genomes]
rs2165525	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2278867	0.85[EUR][1000 genomes]
rs2583471	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2583476	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2847655	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2847663	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2847664	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2847666	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2847667	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2847668	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2855017	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs483629	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs487997	0.81[EUR][1000 genomes]
rs4939311	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4939312	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4939314	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs502419	0.81[EUR][1000 genomes]
rs502581	0.81[EUR][1000 genomes]
rs504272	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs510518	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs512495	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs514266	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs516478	0.81[EUR][1000 genomes]
rs521952	0.80[EUR][1000 genomes]
rs525794	0.87[EUR][1000 genomes]
rs534273	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs540170	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs555635	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs556917	0.81[EUR][1000 genomes]
rs55847558	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56189574	0.86[ASN][1000 genomes]
rs56201148	0.82[EUR][1000 genomes]
rs563803	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs564912	0.86[EUR][1000 genomes]
rs569046	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs574695	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs574704	0.81[EUR][1000 genomes]
rs574798	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs580817	0.81[EUR][1000 genomes]
rs581133	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs602396	0.85[EUR][1000 genomes]
rs61901691	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs652354	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7124974	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72918674	0.85[EUR][1000 genomes]
rs7926344	0.80[EUR][1000 genomes]
rs7926354	0.80[EUR][1000 genomes]
rs7926729	0.80[EUR][1000 genomes]
rs7926954	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7933202	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7935829	0.85[EUR][1000 genomes]
rs7946992	0.84[EUR][1000 genomes]
rs920573	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs983392	0.88[AMR][1000 genomes];0.96[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	nsv832173	chr11:59788884-59940560	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv468579	chr11:59814287-59975400	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv555150	chr11:59814287-59975400	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv33843	chr11:59908131-59945334	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv832174	chr11:59909267-60073908	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
6	nsv825936	chr11:59922944-59923621	Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59923000-59923200	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr11:59923000-59923800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:59923000-59924000	Enhancers	Primary monocytes fromperipheralblood	blood

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