Variant report

Variant	rs11731007
Chromosome Location	chr4:55278299-55278300
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11133321	0.81[ASN][1000 genomes]
rs11133324	0.95[ASN][1000 genomes]
rs1124924	0.95[ASN][1000 genomes]
rs1156181	0.83[ASN][1000 genomes]
rs11725646	0.96[ASN][1000 genomes]
rs11730655	0.96[ASN][1000 genomes]
rs11732321	0.83[ASN][1000 genomes]
rs12108487	0.96[ASN][1000 genomes]
rs12507641	0.95[ASN][1000 genomes]
rs12647796	0.96[ASN][1000 genomes]
rs13122614	0.95[ASN][1000 genomes]
rs13146383	0.95[ASN][1000 genomes]
rs1507949	0.95[ASN][1000 genomes]
rs1553663	0.82[AFR][1000 genomes]
rs2009664	0.95[ASN][1000 genomes]
rs2120497	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2412581	0.96[ASN][1000 genomes]
rs6554175	0.87[ASN][1000 genomes]
rs6554176	0.87[ASN][1000 genomes]
rs6811402	0.95[ASN][1000 genomes]
rs6841717	0.96[ASN][1000 genomes]
rs7658884	0.87[ASN][1000 genomes]
rs7670201	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008793	chr4:55060925-55535807	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv537098	chr4:55060925-55535807	Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv999400	chr4:55143598-55776995	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv997430	chr4:55253397-55529288	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv4344	chr4:55260607-55305235	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55275400-55282600	Weak transcription	Placenta	Placenta

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