Variant report

Variant	rs4735637
Chromosome Location	chr8:100742996-100742997
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

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	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1349244	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1349245	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1449786	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1449790	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1449791	0.89[AMR][1000 genomes];0.94[EUR][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]
rs16897656	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897662	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897666	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897685	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897701	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897702	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897708	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897713	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897726	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897728	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17331148	1.00[EUR][1000 genomes]
rs1979115	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1979117	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2067529	0.85[EUR][1000 genomes]
rs2084554	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2084555	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2100220	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2122341	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2167101	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28372694	0.82[EUR][1000 genomes]
rs2871953	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28847009	0.88[EUR][1000 genomes]
rs4288349	0.88[EUR][1000 genomes]
rs4342557	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4531021	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734434	0.88[EUR][1000 genomes]
rs4734435	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4734436	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4734437	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734438	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734439	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735616	0.88[EUR][1000 genomes]
rs4735622	0.88[EUR][1000 genomes]
rs4735623	0.88[EUR][1000 genomes]
rs4735624	0.88[EUR][1000 genomes]
rs4735631	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4735632	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735634	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735635	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735636	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4735638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735639	0.90[ASN][1000 genomes]
rs4735642	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735644	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735645	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4735646	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56912854	0.94[AMR][1000 genomes]
rs57753543	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61753724	0.89[AMR][1000 genomes];1.00[EUR][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]
rs7832916	0.88[EUR][1000 genomes]
rs7833256	0.88[EUR][1000 genomes]
rs7833870	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7841162	0.82[EUR][1000 genomes]
rs921313	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	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
2	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
3	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
4	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
5	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
6	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
7	nsv1033944	chr8:100737321-100916345	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100710200-100785000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:100713200-100746800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr8:100716800-100744400	Weak transcription	Aorta	Aorta
4	chr8:100719600-100750600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:100725600-100779800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:100727000-100779000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr8:100727600-100746200	Weak transcription	Liver	Liver
8	chr8:100727600-100751800	Weak transcription	HSMM	muscle
9	chr8:100728000-100744000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr8:100728400-100765600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr8:100728800-100746200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr8:100728800-100747200	Weak transcription	Dnd41	blood
13	chr8:100729600-100744800	Weak transcription	Lung	lung
14	chr8:100730000-100745800	Weak transcription	Brain Angular Gyrus	brain
15	chr8:100730200-100750000	Weak transcription	GM12878-XiMat	blood
16	chr8:100731600-100745800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr8:100732800-100753200	Weak transcription	Right Ventricle	heart
18	chr8:100734200-100744400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:100734200-100745600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr8:100734200-100752000	Weak transcription	Placenta	Placenta
21	chr8:100734200-100779200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr8:100734400-100746000	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr8:100734400-100749200	Weak transcription	Esophagus	oesophagus
24	chr8:100734400-100750000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr8:100734600-100761600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr8:100734600-100767200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:100734600-100796600	Weak transcription	Pancreas	Pancrea
28	chr8:100735400-100746200	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr8:100736200-100751600	Weak transcription	Fetal Stomach	stomach
30	chr8:100736400-100758600	Weak transcription	Fetal Lung	lung
31	chr8:100736600-100743800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr8:100736600-100743800	Weak transcription	Fetal Muscle Trunk	muscle
33	chr8:100736600-100744400	Weak transcription	Ovary	ovary
34	chr8:100736600-100746400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr8:100736600-100746400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr8:100736600-100749600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr8:100737600-100744600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr8:100737800-100766000	Weak transcription	Thymus	Thymus
39	chr8:100737800-100779000	Weak transcription	Left Ventricle	heart
40	chr8:100738000-100743000	Weak transcription	Primary hematopoietic stem cells	blood
41	chr8:100738000-100747200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr8:100738000-100751000	Weak transcription	Fetal Intestine Large	intestine
43	chr8:100738200-100745800	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr8:100738200-100749800	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr8:100738600-100744200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr8:100740200-100746400	Weak transcription	Fetal Intestine Small	intestine
47	chr8:100740400-100743200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:100740600-100744600	Weak transcription	Osteobl	bone
49	chr8:100740600-100747600	Weak transcription	HSMMtube	muscle
50	chr8:100740600-100767400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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