Variant report

Variant	rs1027112
Chromosome Location	chr11:104218854-104218855
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10791694	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10791696	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10791697	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10895617	0.86[JPT][hapmap]
rs10895657	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10895658	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10895665	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10895666	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10895667	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10895672	0.85[EUR][1000 genomes]
rs10895673	0.85[EUR][1000 genomes]
rs10895674	0.85[EUR][1000 genomes]
rs10895675	0.85[EUR][1000 genomes]
rs10895681	0.83[EUR][1000 genomes]
rs11226318	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11226319	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11226321	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11226334	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11226335	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11226341	0.88[EUR][1000 genomes]
rs11226343	0.85[EUR][1000 genomes]
rs11226346	0.83[EUR][1000 genomes]
rs11226348	0.83[EUR][1000 genomes]
rs11600376	0.83[EUR][1000 genomes]
rs11600631	0.85[EUR][1000 genomes]
rs11602456	0.85[EUR][1000 genomes]
rs11602492	0.81[EUR][1000 genomes]
rs11602527	0.83[EUR][1000 genomes]
rs11604356	0.83[EUR][1000 genomes]
rs11605911	0.83[EUR][1000 genomes]
rs11606581	0.81[EUR][1000 genomes]
rs11608063	0.89[EUR][1000 genomes]
rs12272804	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12361853	0.85[EUR][1000 genomes]
rs12362326	0.85[EUR][1000 genomes]
rs12362336	0.85[EUR][1000 genomes]
rs12362748	0.85[EUR][1000 genomes]
rs12787859	0.83[EUR][1000 genomes]
rs12787993	0.83[EUR][1000 genomes]
rs12794711	0.85[EUR][1000 genomes]
rs12795075	0.83[EUR][1000 genomes]
rs12803570	0.83[EUR][1000 genomes]
rs12807112	0.81[EUR][1000 genomes]
rs1471982	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1552535	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17102421	0.85[EUR][1000 genomes]
rs1825824	0.85[AMR][1000 genomes]
rs1873095	0.83[EUR][1000 genomes]
rs1873096	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1873097	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2012496	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34076835	0.83[EUR][1000 genomes]
rs34563542	0.88[EUR][1000 genomes]
rs34877813	0.89[EUR][1000 genomes]
rs36056538	0.83[EUR][1000 genomes]
rs4754111	0.88[EUR][1000 genomes]
rs4754112	0.83[EUR][1000 genomes]
rs4754114	0.83[EUR][1000 genomes]
rs4755021	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4755022	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4755023	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4755029	0.81[EUR][1000 genomes]
rs4755034	0.83[EUR][1000 genomes]
rs6591078	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7110594	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7121183	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7123854	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71484353	0.85[EUR][1000 genomes]
rs71484355	0.85[EUR][1000 genomes]
rs7947072	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760322	chr11:103760085-104374141	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1051448	chr11:103864766-104274112	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
3	nsv541157	chr11:103864766-104274112	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1043976	chr11:103881236-104526403	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1040367	chr11:103956747-104440470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1044271	chr11:104136156-104666252	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 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	chr11:104210000-104221800	Weak transcription	HMEC	breast
2	chr11:104216200-104220200	Weak transcription	Psoas Muscle	Psoas

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