Variant report

Variant	rs1440866
Chromosome Location	chr4:80466159-80466160
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10004226	0.84[ASN][1000 genomes]
rs10021556	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10022309	1.00[ASN][1000 genomes]
rs10022314	1.00[ASN][1000 genomes]
rs10022663	0.85[ASN][1000 genomes]
rs10025630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10027904	0.82[ASN][1000 genomes]
rs10033410	1.00[ASN][1000 genomes]
rs1074134	0.82[ASN][1000 genomes]
rs11098741	1.00[ASN][1000 genomes]
rs11098742	1.00[ASN][1000 genomes]
rs11098762	0.84[ASN][1000 genomes]
rs11098764	0.84[ASN][1000 genomes]
rs11098766	0.84[ASN][1000 genomes]
rs11728755	0.84[ASN][1000 genomes]
rs11736348	0.82[ASN][1000 genomes]
rs11736369	0.85[ASN][1000 genomes]
rs11936123	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11941782	0.88[ASN][1000 genomes]
rs12500146	0.84[ASN][1000 genomes]
rs12502224	1.00[ASN][1000 genomes]
rs12506212	0.86[ASN][1000 genomes]
rs12507160	0.84[ASN][1000 genomes]
rs12507375	0.84[ASN][1000 genomes]
rs12510204	1.00[ASN][1000 genomes]
rs12510243	1.00[ASN][1000 genomes]
rs12511646	0.84[ASN][1000 genomes]
rs12511890	0.82[ASN][1000 genomes]
rs12513177	1.00[ASN][1000 genomes]
rs12639996	1.00[ASN][1000 genomes]
rs12640638	1.00[ASN][1000 genomes]
rs13111877	0.82[ASN][1000 genomes]
rs13112067	0.88[ASN][1000 genomes]
rs13112577	0.88[ASN][1000 genomes]
rs13118924	0.80[ASN][1000 genomes]
rs13127970	0.80[ASN][1000 genomes]
rs13128134	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13144408	0.95[ASN][1000 genomes]
rs1371993	0.88[ASN][1000 genomes]
rs1371996	0.99[ASN][1000 genomes]
rs1440852	0.84[ASN][1000 genomes]
rs1440853	0.84[ASN][1000 genomes]
rs1440854	0.84[ASN][1000 genomes]
rs1440860	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1440861	0.82[ASN][1000 genomes]
rs1440862	0.82[ASN][1000 genomes]
rs1440863	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1440864	0.84[ASN][1000 genomes]
rs1440865	1.00[ASN][1000 genomes]
rs1561638	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1561639	0.82[ASN][1000 genomes]
rs1561640	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1595966	1.00[ASN][1000 genomes]
rs1837645	0.88[ASN][1000 genomes]
rs1837646	0.88[ASN][1000 genomes]
rs1837647	0.96[ASN][1000 genomes]
rs1899232	0.82[ASN][1000 genomes]
rs1971838	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1975399	0.84[ASN][1000 genomes]
rs1992367	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2119419	0.87[ASN][1000 genomes]
rs2119420	0.87[ASN][1000 genomes]
rs2119421	0.98[ASN][1000 genomes]
rs2165386	0.84[ASN][1000 genomes]
rs2165387	0.85[ASN][1000 genomes]
rs2165388	0.97[ASN][1000 genomes]
rs4389603	0.85[ASN][1000 genomes]
rs4443312	0.88[ASN][1000 genomes]
rs4583785	0.84[ASN][1000 genomes]
rs4975052	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4975053	1.00[ASN][1000 genomes]
rs4975054	1.00[ASN][1000 genomes]
rs4975055	1.00[ASN][1000 genomes]
rs4975056	0.87[ASN][1000 genomes]
rs4975057	0.85[ASN][1000 genomes]
rs6812760	0.88[ASN][1000 genomes]
rs6850999	0.84[ASN][1000 genomes]
rs6852514	0.84[ASN][1000 genomes]
rs723243	0.82[ASN][1000 genomes]
rs723245	0.81[ASN][1000 genomes]
rs7655446	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7663844	0.82[ASN][1000 genomes]
rs7667469	0.84[ASN][1000 genomes]
rs7670107	0.82[ASN][1000 genomes]
rs7684683	0.82[ASN][1000 genomes]
rs7690520	0.84[ASN][1000 genomes]
rs7691021	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7691868	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7691918	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7697359	1.00[ASN][1000 genomes]
rs880988	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9307532	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs968176	0.84[ASN][1000 genomes]
rs998437	0.84[ASN][1000 genomes]
rs9993773	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999174	chr4:80212935-80512356	Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv879506	chr4:80316417-80604625	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv879507	chr4:80365765-80552199	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv879508	chr4:80398708-80552199	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv829980	chr4:80442108-80468775	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	lncRNA	n/a	inside rSNPs	diseases
6	nsv1002031	chr4:80459528-80759113	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1440866	LINC00989	cis	Skin Sun Exposed Lower leg	GTEx
rs1440866	LINC00989	cis	Adipose Subcutaneous	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80465000-80478200	Weak transcription	H9 Cell Line	embryonic stem cell

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