Variant report

Variant	rs4735632
Chromosome Location	chr8:100698499-100698500
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10504990	0.88[EUR][1000 genomes]
rs10504991	0.88[EUR][1000 genomes]
rs10504992	0.88[EUR][1000 genomes]
rs11984855	0.82[EUR][1000 genomes]
rs11987013	0.88[EUR][1000 genomes]
rs11987034	0.88[EUR][1000 genomes]
rs11988133	0.88[EUR][1000 genomes]
rs11989649	0.85[EUR][1000 genomes]
rs11992778	0.88[EUR][1000 genomes]
rs11994623	0.88[EUR][1000 genomes]
rs11996543	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1349244	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1349245	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1449786	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1449790	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1449791	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1552443	0.88[EUR][1000 genomes]
rs16897410	0.88[EUR][1000 genomes]
rs16897439	0.88[EUR][1000 genomes]
rs16897488	0.88[EUR][1000 genomes]
rs16897504	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs16897573	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs16897581	0.92[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs16897656	1.00[EUR][1000 genomes]
rs16897662	1.00[EUR][1000 genomes]
rs16897666	1.00[EUR][1000 genomes]
rs16897685	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16897701	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16897702	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16897708	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16897713	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16897726	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16897728	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17331148	1.00[EUR][1000 genomes]
rs1979115	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1979117	1.00[EUR][1000 genomes]
rs2067529	0.85[EUR][1000 genomes]
rs2084554	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2084555	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2100220	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2122341	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2167101	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28372694	0.82[EUR][1000 genomes]
rs2871953	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28847009	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4288349	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4342557	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4531021	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4734434	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4734435	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734436	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4734437	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4734438	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4734439	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735616	0.88[EUR][1000 genomes]
rs4735622	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4735623	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4735624	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4735631	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4735633	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4735634	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735635	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735636	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4735637	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735638	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735642	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4735644	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735645	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735646	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56912854	0.89[AMR][1000 genomes]
rs57753543	1.00[EUR][1000 genomes]
rs61753724	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7003135	0.97[EUR][1000 genomes]
rs73271394	0.94[EUR][1000 genomes]
rs73273207	0.97[EUR][1000 genomes]
rs7387462	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7832916	0.88[EUR][1000 genomes]
rs7833256	0.88[EUR][1000 genomes]
rs7833870	1.00[EUR][1000 genomes]
rs7841162	0.82[EUR][1000 genomes]
rs921313	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv524617	chr8:100032844-100717925	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1022914	chr8:100190356-100720313	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv539695	chr8:100190356-100720313	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv891226	chr8:100295634-100708595	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv891227	chr8:100295634-100743556	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1019256	chr8:100336249-100852803	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
7	nsv539698	chr8:100336249-100852803	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
8	esv2758167	chr8:100404151-100838624	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
9	esv2759633	chr8:100404151-100838624	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1029616	chr8:100442135-100796643	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1023922	chr8:100474230-100702005	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
12	nsv831408	chr8:100523523-100721507	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
13	esv20740	chr8:100698324-100701511	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3480575	chr8:100698424-100701711	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3480576	chr8:100698424-100701711	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100675400-100706000	Weak transcription	Left Ventricle	heart
2	chr8:100687000-100739800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:100688400-100708200	Weak transcription	HSMMtube	muscle
4	chr8:100688600-100705600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr8:100688800-100698800	Weak transcription	Gastric	stomach
6	chr8:100688800-100704600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr8:100688800-100711400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr8:100688800-100716000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr8:100689000-100698800	Weak transcription	Thymus	Thymus
10	chr8:100692000-100711800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr8:100692800-100698800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:100695200-100708200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:100695200-100709800	Weak transcription	Pancreas	Pancrea
14	chr8:100696000-100700000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:100697600-100700800	Strong transcription	Primary T cells from cord blood	blood
16	chr8:100697800-100699000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr8:100697800-100700400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
18	chr8:100698000-100698600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:100698000-100698600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr8:100698000-100698800	Enhancers	NHEK	skin
21	chr8:100698000-100699000	ZNF genes & repeats	Placenta	Placenta
22	chr8:100698000-100699000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
23	chr8:100698000-100699800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chr8:100698000-100699800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:100698000-100716000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr8:100698200-100698600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
27	chr8:100698200-100698600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:100698200-100698600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:100698200-100698800	ZNF genes & repeats	Fetal Muscle Leg	muscle
30	chr8:100698200-100699000	Enhancers	K562	blood
31	chr8:100698200-100699200	Enhancers	Stomach Mucosa	stomach
32	chr8:100698200-100699600	Strong transcription	Ovary	ovary
33	chr8:100698200-100699800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr8:100698200-100700000	Strong transcription	Primary B cells from cord blood	blood
35	chr8:100698200-100700000	Strong transcription	Duodenum Mucosa	Duodenum
36	chr8:100698200-100700000	ZNF genes & repeats	Fetal Stomach	stomach
37	chr8:100698200-100714600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:100698400-100698600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr8:100698400-100698800	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr8:100698400-100698800	Weak transcription	Adipose Nuclei	Adipose
41	chr8:100698400-100699000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr8:100698400-100699200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:100698400-100699400	Strong transcription	Aorta	Aorta
44	chr8:100698400-100699400	Strong transcription	Fetal Lung	lung
45	chr8:100698400-100699600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
46	chr8:100698400-100699600	Strong transcription	Fetal Intestine Large	intestine
47	chr8:100698400-100699800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr8:100698400-100699800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr8:100698400-100699800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr8:100698400-100699800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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