Variant report

Variant	rs11937861
Chromosome Location	chr4:122680075-122680076
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:122675401..122678000-chr4:122678051..122680477,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10001422	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10011665	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10470915	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10471016	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11930525	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11947643	0.89[EUR][1000 genomes]
rs1574283	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17051397	0.88[EUR][1000 genomes]
rs17051398	0.90[EUR][1000 genomes]
rs28515183	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28676474	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3903026	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4077754	0.85[EUR][1000 genomes]
rs4309856	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4508913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4522884	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4571354	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56030020	0.81[EUR][1000 genomes]
rs56221685	0.87[EUR][1000 genomes]
rs57312551	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58127039	0.97[EUR][1000 genomes]
rs59796939	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61665948	0.85[EUR][1000 genomes]
rs6534322	0.86[EUR][1000 genomes]
rs6823340	0.87[EUR][1000 genomes]
rs6825926	0.94[GIH][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs6858061	0.87[EUR][1000 genomes]
rs72913994	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72915905	0.89[EUR][1000 genomes]
rs73844293	0.87[EUR][1000 genomes]
rs73844294	0.87[EUR][1000 genomes]
rs7661218	0.86[TSI][hapmap];0.87[EUR][1000 genomes]
rs7684547	0.85[EUR][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	nsv817261	chr4:122085173-123020068	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv997539	chr4:122544104-123274266	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv530157	chr4:122557302-123248756	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv461635	chr4:122633535-122720999	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv595357	chr4:122633535-122720999	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv508309	chr4:122663791-122680645	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122674000-122684800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:122679000-122682000	Weak transcription	Fetal Heart	heart
3	chr4:122679600-122680800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:122679600-122680800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:122679600-122681000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:122679800-122680800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:122680000-122680600	Enhancers	Osteobl	bone

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