Variant report

Variant	rs10137676
Chromosome Location	chr14:104466652-104466653
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:104465698..104467426-chr14:104468975..104470525,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10129730	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10130042	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10131031	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10131231	1.00[ASN][1000 genomes]
rs10131792	0.94[AFR][1000 genomes]
rs10137517	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10137889	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10139210	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10140292	1.00[JPT][hapmap]
rs10140436	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10141374	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10142365	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10142956	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10145882	1.00[JPT][hapmap]
rs10149898	1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10151165	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12436665	1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12437404	1.00[JPT][hapmap]
rs17101922	1.00[JPT][hapmap]
rs2295662	1.00[ASN][1000 genomes]
rs2368996	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28416628	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28439019	1.00[ASN][1000 genomes]
rs28514602	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28555097	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28563863	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs28593161	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28715405	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28841005	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4900603	1.00[JPT][hapmap]
rs4900606	1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906386	1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs4906388	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906393	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906394	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906400	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906403	1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906407	1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906412	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906414	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55746000	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55866217	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56050561	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56279366	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56872578	1.00[ASN][1000 genomes]
rs58128911	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs58220415	1.00[ASN][1000 genomes]
rs59838226	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7150795	1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74086761	0.81[AMR][1000 genomes]
rs74086783	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74086977	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8004485	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8007491	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8020110	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9324070	1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9671924	1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	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
4	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
5	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
6	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
7	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
8	nsv1047990	chr14:104460605-104556463	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr14:104456400-104471600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr14:104456600-104470000	Weak transcription	Pancreas	Pancrea
3	chr14:104456600-104471400	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr14:104457000-104476400	Weak transcription	Spleen	Spleen
5	chr14:104465200-104471400	Weak transcription	Monocytes-CD14+_RO01746	blood

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