Variant report

Variant	rs11627578
Chromosome Location	chr14:66234448-66234449
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10130526	1.00[YRI][hapmap]
rs10483785	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1075566	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11158611	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11622271	0.82[EUR][1000 genomes]
rs11622829	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs11624104	0.89[CEU][hapmap];0.84[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];0.89[JPT][hapmap];0.83[MEX][hapmap];0.84[TSI][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11625362	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11625882	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11627067	0.88[CEU][hapmap];0.89[CHB][hapmap];0.89[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11627184	0.89[CEU][hapmap];0.83[GIH][hapmap];0.80[MEX][hapmap];0.80[TSI][hapmap]
rs11627185	0.88[CEU][hapmap]
rs11627605	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11628765	0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11628840	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11848443	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11848444	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11848463	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12050182	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12050231	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12586842	0.83[EUR][1000 genomes]
rs12588838	0.89[CEU][hapmap];0.89[CHB][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12882200	0.83[EUR][1000 genomes]
rs12883382	0.82[EUR][1000 genomes]
rs12887134	0.85[CEU][hapmap]
rs12887673	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12887957	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12888212	0.87[EUR][1000 genomes]
rs12889002	0.88[CEU][hapmap];0.84[CHB][hapmap]
rs12890902	0.89[CEU][hapmap];0.83[CHB][hapmap]
rs12894034	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12894466	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12894902	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1535173	0.89[CEU][hapmap];0.83[GIH][hapmap];0.88[MEX][hapmap];0.84[TSI][hapmap];0.87[EUR][1000 genomes]
rs1958561	0.89[CEU][hapmap]
rs1998036	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs2064694	0.89[CEU][hapmap];0.84[CHB][hapmap];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2268961	0.89[CEU][hapmap];0.84[CHB][hapmap];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2268962	0.89[CEU][hapmap];0.84[CHB][hapmap];0.80[CHD][hapmap];0.93[GIH][hapmap];0.80[MEX][hapmap];0.80[TSI][hapmap];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2300865	0.88[CEU][hapmap];0.84[CHB][hapmap]
rs2411351	0.89[CEU][hapmap];0.83[GIH][hapmap];0.80[MEX][hapmap];0.84[EUR][1000 genomes]
rs2411404	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2411405	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28459012	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28616692	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3783709	0.89[CEU][hapmap]
rs4073415	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4581615	0.89[CEU][hapmap]
rs4902415	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902416	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56720460	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56922569	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59636756	0.84[EUR][1000 genomes]
rs61988977	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61988978	0.82[AMR][1000 genomes]
rs6573624	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6573626	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67957534	0.80[EUR][1000 genomes]
rs7142018	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7142165	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7142219	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7142651	0.89[CEU][hapmap];0.89[CHB][hapmap];0.83[EUR][1000 genomes]
rs7146829	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7149301	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7151846	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7155541	0.85[CEU][hapmap]
rs7157449	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7161123	0.88[CEU][hapmap];0.83[CHB][hapmap];0.93[GIH][hapmap]
rs730807	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs743084	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs743085	0.85[CEU][hapmap];0.80[CHD][hapmap];0.90[GIH][hapmap];0.80[MEX][hapmap];0.80[TSI][hapmap]
rs7493004	0.81[EUR][1000 genomes]
rs761831	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8007846	0.82[ASN][1000 genomes]
rs8010876	0.88[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8012278	0.85[CEU][hapmap];0.80[CHD][hapmap];0.93[GIH][hapmap];0.80[MEX][hapmap];0.80[TSI][hapmap]
rs8018278	0.89[CEU][hapmap];0.89[CHB][hapmap];0.89[JPT][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8018379	0.83[ASN][1000 genomes]
rs8022764	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs927004	0.89[CEU][hapmap];0.88[EUR][1000 genomes]
rs9323465	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs968540	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv1039168	chr14:65811750-66308343	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
4	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11627578	ZFP36L1	cis	parietal	SCAN
rs11627578	FUT8	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66215600-66239800	Weak transcription	Primary T cells from cord blood	blood
2	chr14:66229000-66239200	Weak transcription	Right Atrium	heart

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