Variant report

Variant	rs6831352
Chromosome Location	chr4:100063525-100063526
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 136 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:128)

rs_ID	r²[population]
rs10017466	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1042364	0.85[EUR][1000 genomes]
rs1042365	0.85[EUR][1000 genomes]
rs1126670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1126671	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1126672	0.86[EUR][1000 genomes]
rs1126673	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1139490	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1230154	0.86[AMR][1000 genomes]
rs1230156	0.86[AMR][1000 genomes]
rs13102874	0.86[EUR][1000 genomes]
rs13110176	0.86[EUR][1000 genomes]
rs13110764	0.86[EUR][1000 genomes]
rs13112176	0.86[EUR][1000 genomes]
rs13112733	0.86[EUR][1000 genomes]
rs13113166	0.86[EUR][1000 genomes]
rs13127153	0.86[EUR][1000 genomes]
rs13127582	0.86[EUR][1000 genomes]
rs13129488	0.86[EUR][1000 genomes]
rs13132776	0.83[EUR][1000 genomes]
rs13132999	0.86[EUR][1000 genomes]
rs13133633	0.86[EUR][1000 genomes]
rs13133647	0.86[EUR][1000 genomes]
rs13138294	0.86[EUR][1000 genomes]
rs13140423	0.86[EUR][1000 genomes]
rs13143133	0.86[EUR][1000 genomes]
rs17217949	0.86[EUR][1000 genomes]
rs17218003	0.86[EUR][1000 genomes]
rs17218073	0.86[EUR][1000 genomes]
rs17218108	0.86[EUR][1000 genomes]
rs17218141	0.86[EUR][1000 genomes]
rs17218162	0.86[EUR][1000 genomes]
rs17218239	0.86[EUR][1000 genomes]
rs17218288	0.86[EUR][1000 genomes]
rs17218560	0.86[EUR][1000 genomes]
rs17218602	0.86[EUR][1000 genomes]
rs17817359	0.86[EUR][1000 genomes]
rs17817868	0.86[EUR][1000 genomes]
rs17817958	0.86[EUR][1000 genomes]
rs1984362	0.85[EUR][1000 genomes]
rs1984364	0.84[EUR][1000 genomes]
rs2213035	0.86[EUR][1000 genomes]
rs2602891	0.84[EUR][1000 genomes]
rs2602893	0.84[EUR][1000 genomes]
rs2602894	0.85[EUR][1000 genomes]
rs2602895	0.84[EUR][1000 genomes]
rs2602896	0.85[EUR][1000 genomes]
rs2602897	0.85[EUR][1000 genomes]
rs2851246	0.85[EUR][1000 genomes]
rs2851247	0.85[EUR][1000 genomes]
rs2851248	0.85[EUR][1000 genomes]
rs2851249	0.85[EUR][1000 genomes]
rs2851252	0.84[EUR][1000 genomes]
rs2851253	0.84[EUR][1000 genomes]
rs2851255	0.80[EUR][1000 genomes]
rs2851270	0.81[AMR][1000 genomes]
rs2851274	0.81[AMR][1000 genomes]
rs28987088	0.86[EUR][1000 genomes]
rs28987097	0.86[EUR][1000 genomes]
rs28987098	0.86[EUR][1000 genomes]
rs28987100	0.86[EUR][1000 genomes]
rs28987101	0.85[EUR][1000 genomes]
rs28987102	0.86[EUR][1000 genomes]
rs29001183	0.86[EUR][1000 genomes]
rs29001194	0.86[EUR][1000 genomes]
rs29001195	0.86[EUR][1000 genomes]
rs29001196	0.86[EUR][1000 genomes]
rs29001199	0.86[EUR][1000 genomes]
rs29001201	0.86[EUR][1000 genomes]
rs29001202	0.85[EUR][1000 genomes]
rs29001203	0.86[EUR][1000 genomes]
rs29001208	0.86[EUR][1000 genomes]
rs29001209	0.86[EUR][1000 genomes]
rs29001211	0.86[EUR][1000 genomes]
rs29001212	0.86[EUR][1000 genomes]
rs29001214	0.86[EUR][1000 genomes]
rs29001215	0.86[EUR][1000 genomes]
rs29001216	0.86[EUR][1000 genomes]
rs29001223	0.86[EUR][1000 genomes]
rs29001224	0.86[EUR][1000 genomes]
rs29001229	0.85[EUR][1000 genomes]
rs29001231	0.85[EUR][1000 genomes]
rs29001232	0.85[EUR][1000 genomes]
rs2924583	0.85[EUR][1000 genomes]
rs34071486	0.86[EUR][1000 genomes]
rs34118841	0.83[EUR][1000 genomes]
rs34360292	0.86[EUR][1000 genomes]
rs34634551	0.85[EUR][1000 genomes]
rs34805407	0.86[EUR][1000 genomes]
rs34876213	0.86[EUR][1000 genomes]
rs34936974	0.86[EUR][1000 genomes]
rs35062722	0.84[EUR][1000 genomes]
rs35073321	0.86[EUR][1000 genomes]
rs35146617	0.84[EUR][1000 genomes]
rs35361391	0.85[EUR][1000 genomes]
rs35491981	0.85[EUR][1000 genomes]
rs35662508	0.86[EUR][1000 genomes]
rs35784540	0.86[EUR][1000 genomes]
rs35797419	0.85[EUR][1000 genomes]
rs35988291	0.86[EUR][1000 genomes]
rs36034266	0.86[EUR][1000 genomes]
rs3919370	0.86[EUR][1000 genomes]
rs4699710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4699712	0.86[EUR][1000 genomes]
rs4699713	0.86[EUR][1000 genomes]
rs4699714	0.86[EUR][1000 genomes]
rs4699716	0.85[EUR][1000 genomes]
rs4699717	0.84[EUR][1000 genomes]
rs4699718	0.85[EUR][1000 genomes]
rs56222233	0.85[EUR][1000 genomes]
rs56272995	0.86[EUR][1000 genomes]
rs56295995	0.86[EUR][1000 genomes]
rs6532795	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6532796	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6532798	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs67311928	0.86[EUR][1000 genomes]
rs6813415	0.86[EUR][1000 genomes]
rs6822348	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6837685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6848050	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7434491	0.85[EUR][1000 genomes]
rs7669636	0.86[EUR][1000 genomes]
rs7670060	0.86[EUR][1000 genomes]
rs7670241	0.85[EUR][1000 genomes]
rs7670638	0.86[EUR][1000 genomes]
rs7672728	0.86[EUR][1000 genomes]
rs7689753	0.86[EUR][1000 genomes]
rs7694646	0.86[EUR][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	nsv1009017	chr4:99669441-100406394	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1002927	chr4:99952472-100148690	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1005446	chr4:99988287-100121669	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv537196	chr4:99988287-100121669	Strong transcription ZNF genes & repeats Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv1002574	chr4:100023999-100133693	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv3528915	chr4:100025155-100096234	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3528916	chr4:100025155-100096234	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6831352	ADH5	cis	Whole Blood	GTEx

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100012800-100063800	Weak transcription	Aorta	Aorta
2	chr4:100035000-100098200	Weak transcription	Ovary	ovary
3	chr4:100039800-100064800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:100044400-100063600	Weak transcription	Fetal Intestine Small	intestine
5	chr4:100048800-100063800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr4:100051400-100063600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:100056800-100082600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:100057800-100065200	Weak transcription	Fetal Lung	lung
9	chr4:100062400-100063800	Transcr. at gene 5' and 3'	Liver	Liver
10	chr4:100062600-100065800	Active TSS	Duodenum Mucosa	Duodenum
11	chr4:100063000-100064200	Enhancers	HepG2	liver
12	chr4:100063200-100063600	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr4:100063200-100064000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:100063400-100064000	Enhancers	H1 Cell Line	embryonic stem cell

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