Variant report

Variant	rs4906412
Chromosome Location	chr14:104519525-104519526
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:104504865..104507694-chr14:104518320..104521249,2	MCF-7	breast:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10130042	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10131031	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10131231	1.00[ASN][1000 genomes]
rs10133836	0.81[YRI][hapmap]
rs10137517	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10137676	1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10137889	1.00[ASN][1000 genomes]
rs10139210	1.00[ASN][1000 genomes]
rs10140292	1.00[JPT][hapmap]
rs10140436	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10141374	1.00[ASN][1000 genomes]
rs10142956	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10145882	1.00[JPT][hapmap]
rs10149898	1.00[ASN][1000 genomes]
rs10151165	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11160781	0.83[YRI][hapmap]
rs1187452	0.81[YRI][hapmap]
rs1187453	0.81[YRI][hapmap]
rs12436665	1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12437404	1.00[JPT][hapmap]
rs17101922	1.00[JPT][hapmap]
rs1885596	0.81[YRI][hapmap]
rs1951583	0.86[YRI][hapmap]
rs2295662	1.00[ASN][1000 genomes]
rs2368996	1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2368997	0.83[YRI][hapmap]
rs28416628	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28439019	1.00[ASN][1000 genomes]
rs28514602	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28555097	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28593161	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28715405	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28841005	0.87[AMR][1000 genomes]
rs4900603	1.00[JPT][hapmap]
rs4900606	1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906386	1.00[JPT][hapmap]
rs4906388	1.00[ASN][1000 genomes]
rs4906393	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906394	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906400	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906403	1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906407	1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906414	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55746000	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55866217	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56050561	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56279366	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56872578	1.00[ASN][1000 genomes]
rs58128911	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs58220415	1.00[ASN][1000 genomes]
rs59838226	1.00[ASN][1000 genomes]
rs7150795	1.00[JPT][hapmap];0.95[YRI][hapmap];0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7161153	0.81[YRI][hapmap]
rs74086783	1.00[ASN][1000 genomes]
rs74086977	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8004485	1.00[ASN][1000 genomes]
rs8007491	0.91[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8020110	1.00[JPT][hapmap]
rs9324070	1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9671924	1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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	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
5	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
6	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
7	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
8	nsv542209	chr14:104497447-104540729	Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv1050479	chr14:104500427-104805738	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	esv1806632	chr14:104516262-104640011	Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104496400-104520800	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr14:104509200-104520600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:104510800-104521000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:104514200-104520000	Enhancers	HSMMtube	muscle
5	chr14:104516400-104521200	Weak transcription	Fetal Brain Male	brain
6	chr14:104516800-104521400	Weak transcription	Spleen	Spleen
7	chr14:104517400-104520000	Weak transcription	Brain Anterior Caudate	brain
8	chr14:104518200-104519800	Enhancers	HSMM	muscle
9	chr14:104518400-104520800	Strong transcription	Monocytes-CD14+_RO01746	blood

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