Variant report

Variant	rs7258562
Chromosome Location	chr19:21514564-21514565
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	chr19:21511256..21513599-chr19:21513725..21515814,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182141	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10414834	0.87[EUR][1000 genomes]
rs10424079	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11666213	0.87[EUR][1000 genomes]
rs11666447	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11666525	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11666540	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11667103	0.95[EUR][1000 genomes]
rs11667361	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11667392	0.89[EUR][1000 genomes]
rs11669033	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11669790	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11670815	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11670868	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11672341	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11672583	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11673320	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11879901	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13346641	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1621154	0.95[EUR][1000 genomes]
rs1626404	0.95[EUR][1000 genomes]
rs1762578	0.95[EUR][1000 genomes]
rs17680605	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1781867	0.95[EUR][1000 genomes]
rs1781872	0.95[EUR][1000 genomes]
rs1967182	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2061916	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2154302	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2358993	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2359144	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2359145	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2562405	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2562411	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2562413	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2562416	0.86[EUR][1000 genomes]
rs2650776	0.86[EUR][1000 genomes]
rs2650844	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2650848	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs279807	0.90[EUR][1000 genomes]
rs279809	0.91[EUR][1000 genomes]
rs2928211	0.81[EUR][1000 genomes]
rs3853837	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3853838	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4321312	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4327181	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4359573	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4544364	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4638726	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55756795	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55790393	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55875743	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs55899865	0.95[EUR][1000 genomes]
rs57299552	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58412280	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60173523	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61035285	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62107465	0.93[EUR][1000 genomes]
rs62107468	0.84[EUR][1000 genomes]
rs62107469	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62107472	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62107479	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62107531	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62107532	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62107534	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62107536	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62107539	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62107540	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62107541	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62109225	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62109226	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62109227	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62109228	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62109229	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62110071	0.91[EUR][1000 genomes]
rs62110367	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62110377	0.88[EUR][1000 genomes]
rs62110416	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62110420	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62110424	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62110426	0.91[EUR][1000 genomes]
rs62110428	0.87[EUR][1000 genomes]
rs62110429	0.87[EUR][1000 genomes]
rs7246339	0.95[EUR][1000 genomes]
rs7251135	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7258099	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7258473	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73537884	0.93[AMR][1000 genomes];0.97[EUR][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	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv911416	chr19:21388995-21548211	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv911417	chr19:21388995-21564001	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv911420	chr19:21454672-21613397	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	esv2751783	chr19:21465822-21726337	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	esv3363678	chr19:21483148-21756908	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv963023	chr19:21491992-21570395	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	esv3415719	chr19:21511760-21519079	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7258562	ZNF708	cis	Skin Sun Exposed Lower leg	GTEx
rs7258562	RP11-678G14.2	cis	Whole Blood	GTEx
rs7258562	ZNF708	cis	lung	GTEx
rs7258562	ZNF708	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21512400-21515000	Weak transcription	H9 Cell Line	embryonic stem cell

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