Variant report

Variant	rs6584896
Chromosome Location	chr10:110525352-110525353
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11194236	0.86[EUR][1000 genomes]
rs11194237	0.88[EUR][1000 genomes]
rs11194240	0.85[EUR][1000 genomes]
rs11593382	0.86[EUR][1000 genomes]
rs11818211	0.91[ASN][1000 genomes]
rs12268110	0.87[EUR][1000 genomes]
rs12570728	0.88[ASN][1000 genomes]
rs12570752	0.81[ASN][1000 genomes]
rs12571386	0.90[ASN][1000 genomes]
rs12572118	0.91[ASN][1000 genomes]
rs12573133	0.87[ASN][1000 genomes]
rs1415559	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1415560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1538123	0.98[EUR][1000 genomes]
rs1538125	0.85[ASN][1000 genomes]
rs1577855	0.91[ASN][1000 genomes]
rs1577857	0.90[EUR][1000 genomes]
rs17124956	0.88[ASN][1000 genomes]
rs17124959	0.88[ASN][1000 genomes]
rs17124963	0.88[ASN][1000 genomes]
rs17125119	0.97[EUR][1000 genomes]
rs17125159	0.89[ASN][1000 genomes]
rs1856167	1.00[ASN][1000 genomes]
rs2461318	0.86[ASN][1000 genomes]
rs2900789	0.88[EUR][1000 genomes]
rs3904798	0.87[ASN][1000 genomes]
rs4120666	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4333960	0.92[EUR][1000 genomes]
rs58662988	0.86[ASN][1000 genomes]
rs58878892	0.91[ASN][1000 genomes]
rs6584881	0.88[EUR][1000 genomes]
rs6584882	0.91[ASN][1000 genomes]
rs6584883	0.91[ASN][1000 genomes]
rs6584894	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7071972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7080507	0.88[EUR][1000 genomes]
rs7083224	0.84[ASN][1000 genomes]
rs7083647	0.97[EUR][1000 genomes]
rs7085179	0.97[EUR][1000 genomes]
rs7085695	0.97[EUR][1000 genomes]
rs7086707	0.90[EUR][1000 genomes]
rs7097391	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7100476	0.87[EUR][1000 genomes]
rs72828027	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7475718	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7893638	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7893734	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7893809	0.84[ASN][1000 genomes]
rs7898012	0.89[EUR][1000 genomes]
rs7901337	0.88[ASN][1000 genomes]
rs7901956	0.88[ASN][1000 genomes]
rs7906104	0.97[EUR][1000 genomes]
rs7909130	0.89[ASN][1000 genomes]
rs7914339	0.91[ASN][1000 genomes]
rs7914481	0.84[ASN][1000 genomes]
rs7918446	0.88[EUR][1000 genomes]
rs7920978	0.91[ASN][1000 genomes]
rs7923374	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050244	chr10:110279647-110779693	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv917125	chr10:110425573-111119776	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv492162	chr10:110440656-111089721	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1067661	chr10:110440715-111089466	Active TSS Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv529130	chr10:110440715-111089466	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	esv3429369	chr10:110454775-110753351	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	esv2758240	chr10:110458987-110643496	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2759782	chr10:110458987-110643496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv2750851	chr10:110503788-110905211	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6584896	ACSL5	cis	parietal	SCAN
rs6584896	ADD3	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:110524000-110525800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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