Variant report

Variant	rs1678528
Chromosome Location	chr12:58052294-58052295
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10082911	0.88[ASN][1000 genomes]
rs10783836	0.90[ASN][1000 genomes]
rs10783842	0.86[ASN][1000 genomes]
rs10783843	0.84[ASN][1000 genomes]
rs10783844	0.88[ASN][1000 genomes]
rs1082502	0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1082503	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10876993	0.91[ASN][1000 genomes]
rs10877001	0.89[ASN][1000 genomes]
rs10877006	0.89[ASN][1000 genomes]
rs10877007	0.86[ASN][1000 genomes]
rs10877008	0.89[ASN][1000 genomes]
rs1092472	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs11172277	0.87[ASN][1000 genomes]
rs11172306	0.85[ASN][1000 genomes]
rs11536137	0.82[ASN][1000 genomes]
rs12302351	0.90[ASN][1000 genomes]
rs12302451	0.80[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs12314562	0.94[ASN][1000 genomes]
rs12316021	0.94[ASN][1000 genomes]
rs12809742	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12813384	0.87[ASN][1000 genomes]
rs1585781	0.96[ASN][1000 genomes]
rs1628552	0.85[ASN][1000 genomes]
rs1629032	0.88[ASN][1000 genomes]
rs1633360	0.88[ASN][1000 genomes]
rs1678504	0.88[ASN][1000 genomes]
rs1678505	0.87[ASN][1000 genomes]
rs1678511	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1678512	0.94[ASN][1000 genomes]
rs1678513	0.95[ASN][1000 genomes]
rs1678515	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1678516	0.81[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1678519	0.87[ASN][1000 genomes]
rs1678520	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1678522	0.88[ASN][1000 genomes]
rs1678527	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1678529	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1678530	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1678531	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1678532	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1678534	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1678539	0.95[ASN][1000 genomes]
rs1689584	0.88[ASN][1000 genomes]
rs1689585	0.91[ASN][1000 genomes]
rs1689586	0.89[ASN][1000 genomes]
rs1689592	0.95[ASN][1000 genomes]
rs1689594	0.95[ASN][1000 genomes]
rs1689595	0.95[ASN][1000 genomes]
rs1689596	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1689597	0.88[AFR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1689600	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1689601	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1689603	0.81[ASN][1000 genomes]
rs1689604	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2619441	0.88[ASN][1000 genomes]
rs2619466	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2619471	0.86[ASN][1000 genomes]
rs2640630	0.93[ASN][1000 genomes]
rs2640631	0.94[ASN][1000 genomes]
rs2928053	0.95[ASN][1000 genomes]
rs2928054	0.91[ASN][1000 genomes]
rs2928055	0.92[ASN][1000 genomes]
rs2928061	0.89[ASN][1000 genomes]
rs2928062	0.88[ASN][1000 genomes]
rs2928064	0.89[ASN][1000 genomes]
rs3825078	0.88[ASN][1000 genomes]
rs4760164	0.88[ASN][1000 genomes]
rs4760165	0.95[ASN][1000 genomes]
rs4760168	0.88[ASN][1000 genomes]
rs701006	0.89[ASN][1000 genomes]
rs7136269	0.94[ASN][1000 genomes]
rs73123375	0.80[ASN][1000 genomes]
rs774887	0.83[ASN][1000 genomes]
rs774888	0.88[ASN][1000 genomes]
rs774891	0.95[ASN][1000 genomes]
rs7976852	0.87[ASN][1000 genomes]
rs7979246	0.88[ASN][1000 genomes]
rs799575	0.94[ASN][1000 genomes]
rs810204	0.95[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	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
2	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	nsv541504	chr12:57958701-58062311	Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv1802058	chr12:58028127-58062667	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
5	nsv559044	chr12:58028671-58065448	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
6	nsv975499	chr12:58034418-58068937	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv508676	chr12:58045136-58098538	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
8	esv3433378	chr12:58051277-58060854	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1678528	FAM119B	Cis_1M	lymphoblastoid	RTeQTL
rs1678528	TSFM	Cis_1M	lymphoblastoid	RTeQTL
rs1678528	SLC26A10	cis	Heart Left Ventricle	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58051800-58052800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr12:58052200-58054200	Enhancers	K562	blood

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