Variant report

Variant	rs11947605
Chromosome Location	chr4:119036131-119036132
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10002892	0.91[AFR][1000 genomes]
rs10004800	0.98[AFR][1000 genomes]
rs10007381	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10007959	0.91[AFR][1000 genomes]
rs10012359	0.95[AFR][1000 genomes]
rs10015485	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10025979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10030449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10213202	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11933537	0.91[AFR][1000 genomes]
rs11943650	0.91[AFR][1000 genomes]
rs11944865	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28507472	0.91[AFR][1000 genomes]
rs28723489	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28753894	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28768382	0.95[AFR][1000 genomes]
rs6842651	0.87[AFR][1000 genomes]
rs72907180	0.86[AFR][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	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1009076	chr4:118949490-119269424	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1001236	chr4:118949490-119271243	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1008236	chr4:118989467-119154024	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv999152	chr4:119001143-119138322	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv34038	chr4:119035124-119455391	Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 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	chr4:119034800-119039800	Strong transcription	Dnd41	blood
2	chr4:119036000-119036200	Enhancers	HMEC	breast

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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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