Variant report

Variant	rs11226148
Chromosome Location	chr11:103953106-103953107
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10502025	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10895567	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11226131	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226137	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11226141	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11226151	0.91[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11604692	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17331117	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs17331385	0.81[ASN][1000 genomes]
rs17422384	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1827323	0.91[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs66580623	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs67420841	0.92[AMR][1000 genomes]
rs68152835	0.98[ASN][1000 genomes]
rs7930019	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7930348	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7935739	0.91[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7943604	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:103945000-103961600	Weak transcription	Left Ventricle	heart
2	chr11:103945000-103964400	Weak transcription	Aorta	Aorta
3	chr11:103945000-103965400	Weak transcription	Ovary	ovary

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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