Variant report

Variant	rs11224644
Chromosome Location	chr11:101096711-101096712
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10466630	1.00[AMR][1000 genomes]
rs10466631	1.00[AMR][1000 genomes]
rs10466632	1.00[AMR][1000 genomes]
rs10466633	1.00[AMR][1000 genomes]
rs11224622	1.00[AMR][1000 genomes]
rs11224623	1.00[AMR][1000 genomes]
rs12270775	1.00[AMR][1000 genomes]
rs12279240	1.00[AMR][1000 genomes]
rs12280167	1.00[AMR][1000 genomes]
rs12281137	1.00[AMR][1000 genomes]
rs12284507	1.00[AMR][1000 genomes]
rs12287094	1.00[AMR][1000 genomes]
rs12289458	1.00[AMR][1000 genomes]
rs60766012	1.00[AMR][1000 genomes]
rs73579728	1.00[AMR][1000 genomes]
rs73583806	1.00[AMR][1000 genomes]
rs73583818	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv556131	chr11:100985777-101480017	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv530644	chr11:101010088-101486038	Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	esv2753322	chr11:101052790-101311790	Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr11:101092400-101102000	Weak transcription	Aorta	Aorta
2	chr11:101095200-101105400	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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