Variant report

Variant	rs583782
Chromosome Location	chr6:4110810-4110811
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs101418	0.80[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs11751668	0.82[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs11755877	0.80[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs1204951	0.84[ASN][1000 genomes]
rs2326408	0.91[ASN][1000 genomes]
rs2745455	0.82[ASN][1000 genomes]
rs2783063	0.80[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2783073	0.91[ASN][1000 genomes]
rs28878015	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4443542	0.83[EUR][1000 genomes]
rs4959271	0.98[ASN][1000 genomes]
rs582008	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs583881	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs584585	0.84[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs592953	0.81[CHB][hapmap]
rs593291	0.80[CHB][hapmap]
rs594662	0.80[CHB][hapmap]
rs595413	0.80[CHB][hapmap]
rs608195	0.80[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs611500	0.91[ASN][1000 genomes]
rs612022	0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs612477	0.86[ASN][1000 genomes]
rs613028	0.88[ASN][1000 genomes]
rs613260	0.91[ASN][1000 genomes]
rs613709	0.91[ASN][1000 genomes]
rs617604	0.82[ASN][1000 genomes]
rs617790	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs619439	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs619483	0.81[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs619873	0.91[ASN][1000 genomes]
rs620484	0.85[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs621205	0.99[ASN][1000 genomes]
rs626080	0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs627259	0.86[ASN][1000 genomes]
rs629362	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs633290	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs634114	0.80[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs634698	0.89[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs634970	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs638329	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[ASN][1000 genomes]
rs639905	0.80[CHB][hapmap]
rs643232	0.80[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs646385	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs648900	0.91[ASN][1000 genomes]
rs649725	0.85[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs654982	0.83[JPT][hapmap]
rs659025	0.84[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs659051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs659305	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs660560	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs660957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs661404	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs661657	0.84[ASN][1000 genomes]
rs662834	0.80[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs664299	0.89[ASN][1000 genomes]
rs664635	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs664898	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs665894	0.82[ASN][1000 genomes]
rs666254	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs668070	0.81[ASN][1000 genomes]
rs671364	0.81[CHB][hapmap]
rs674543	0.81[ASN][1000 genomes]
rs676683	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs678285	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs679303	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs688176	0.80[CHB][hapmap]
rs689308	0.91[ASN][1000 genomes]
rs694058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs694903	0.86[ASN][1000 genomes]
rs707991	0.80[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs7166	0.91[ASN][1000 genomes]
rs7744628	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs7757606	0.91[ASN][1000 genomes]
rs853416	0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs853417	0.91[ASN][1000 genomes]
rs853418	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9328220	0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs9378831	1.00[YRI][hapmap]
rs9392560	1.00[YRI][hapmap]
rs9405214	1.00[YRI][hapmap]
rs9405219	0.84[ASN][1000 genomes]
rs9405701	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs942475	0.80[CHB][hapmap]

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	nsv532020	chr6:3417520-4140257	Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1022968	chr6:3862744-4272502	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv538106	chr6:3862744-4272502	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv1030104	chr6:4062894-4240269	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	esv2422231	chr6:4100333-4233454	Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription 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 target site	23 gene(s)	inside rSNPs	diseases
6	esv2422457	chr6:4100333-4377396	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4102600-4113800	Weak transcription	Psoas Muscle	Psoas
2	chr6:4103400-4115400	Weak transcription	Fetal Brain Male	brain
3	chr6:4103400-4115600	Weak transcription	Fetal Stomach	stomach
4	chr6:4103400-4115600	Weak transcription	Gastric	stomach
5	chr6:4104600-4115600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:4104600-4115600	Weak transcription	Pancreas	Pancrea
7	chr6:4104800-4115000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:4104800-4115200	Weak transcription	HMEC	breast
9	chr6:4105000-4113600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:4105400-4111000	Enhancers	HepG2	liver
11	chr6:4107200-4114800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr6:4109000-4115600	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:4109200-4115600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:4110200-4113800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:4110200-4114600	Weak transcription	Brain Germinal Matrix	brain
16	chr6:4110400-4113200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr6:4110400-4115400	Weak transcription	Fetal Kidney	kidney
18	chr6:4110400-4115600	Weak transcription	Ovary	ovary
19	chr6:4110400-4118400	Weak transcription	A549	lung
20	chr6:4110400-4124400	Weak transcription	Fetal Heart	heart
21	chr6:4110600-4113200	Weak transcription	Left Ventricle	heart
22	chr6:4110600-4115400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:4110600-4115400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr6:4110600-4115600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:4110600-4115600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:4110600-4115600	Weak transcription	Fetal Intestine Large	intestine
27	chr6:4110600-4115600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr6:4110600-4115800	Weak transcription	Small Intestine	intestine
29	chr6:4110800-4111000	Enhancers	Stomach Mucosa	stomach
30	chr6:4110800-4113400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr6:4110800-4115200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr6:4110800-4115600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr6:4110800-4115600	Weak transcription	HUVEC	blood vessel

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