Variant report

Variant	rs74086977
Chromosome Location	chr14:104456992-104456993
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10129730	0.86[AMR][1000 genomes]
rs10130042	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10131031	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10131231	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10137517	0.93[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10137676	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10137889	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10139210	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10140436	0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10141374	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10142229	0.82[AFR][1000 genomes]
rs10142365	0.86[AMR][1000 genomes]
rs10142956	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10144271	0.96[AFR][1000 genomes]
rs10149898	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10151165	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12436665	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2295662	1.00[ASN][1000 genomes]
rs2368996	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28416628	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28439019	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28514602	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28542749	0.89[AFR][1000 genomes]
rs28545507	0.96[AFR][1000 genomes]
rs28555097	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28563863	0.86[AMR][1000 genomes]
rs28593161	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28715405	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28841005	0.95[AMR][1000 genomes]
rs4900606	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906388	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906393	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906394	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906400	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906403	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906407	0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906412	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906414	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55746000	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55866217	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56050561	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56279366	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56872578	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58128911	0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs58220415	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59838226	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7150795	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74086761	0.86[AMR][1000 genomes]
rs74086783	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8004485	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8007491	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8020110	0.83[AMR][1000 genomes]
rs9324070	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9671924	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv902318	chr14:104255083-104464809	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
5	nsv1048353	chr14:104361402-104483286	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
6	nsv902322	chr14:104365310-104464809	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv902323	chr14:104381687-104464809	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv902324	chr14:104399640-104464809	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1049690	chr14:104411621-104575838	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv542208	chr14:104411621-104575838	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv526680	chr14:104427043-104568472	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104456000-104457000	ZNF genes & repeats	Spleen	Spleen
2	chr14:104456000-104465200	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr14:104456400-104471600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:104456600-104470000	Weak transcription	Pancreas	Pancrea
5	chr14:104456600-104471400	Weak transcription	Primary monocytes fromperipheralblood	blood

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