Variant report

Variant	rs7655622
Chromosome Location	chr4:99231913-99231914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10001137	0.91[AMR][1000 genomes]
rs10003061	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10003496	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10006734	0.91[AMR][1000 genomes]
rs10010260	0.91[AMR][1000 genomes]
rs10013248	1.00[ASW][hapmap];1.00[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.94[YRI][hapmap];0.91[AMR][1000 genomes]
rs10015953	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10017075	0.91[AMR][1000 genomes]
rs10017827	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10022073	1.00[YRI][hapmap];0.91[AMR][1000 genomes]
rs10025311	0.94[YRI][hapmap];0.91[AMR][1000 genomes]
rs10026222	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10027925	0.91[AMR][1000 genomes]
rs10029895	1.00[ASW][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes]
rs10032785	0.82[AMR][1000 genomes]
rs10034649	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10212883	0.91[AMR][1000 genomes]
rs1024127	1.00[GIH][hapmap];0.82[AMR][1000 genomes]
rs10470953	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs12331722	0.82[AMR][1000 genomes]
rs13353633	0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs16996571	0.82[AMR][1000 genomes]
rs17027388	0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs17027393	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs17027526	0.87[ASW][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap];0.91[AMR][1000 genomes]
rs17027538	1.00[ASW][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs17027559	0.82[AMR][1000 genomes]
rs17027597	0.82[AMR][1000 genomes]
rs17027617	1.00[GIH][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.84[YRI][hapmap];0.91[AMR][1000 genomes]
rs28374939	0.91[AMR][1000 genomes]
rs28407050	0.91[AMR][1000 genomes]
rs28438716	0.91[AMR][1000 genomes]
rs28446845	0.91[AMR][1000 genomes]
rs28451188	0.82[AMR][1000 genomes]
rs28455818	0.91[AMR][1000 genomes]
rs28459325	0.82[AMR][1000 genomes]
rs28472340	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28478192	1.00[ASW][hapmap];1.00[GIH][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28494643	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28497963	0.82[AMR][1000 genomes]
rs28529663	0.91[AMR][1000 genomes]
rs28558542	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28564255	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28589745	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28647503	0.91[AMR][1000 genomes]
rs28649922	0.91[AMR][1000 genomes]
rs28651612	0.91[AMR][1000 genomes]
rs2866009	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs28664868	0.91[AMR][1000 genomes]
rs28705201	0.84[AFR][1000 genomes]
rs28731135	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28786730	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28806635	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28807427	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28840158	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28883979	0.82[AMR][1000 genomes]
rs28893208	0.91[AMR][1000 genomes]
rs41275691	0.82[AMR][1000 genomes]
rs41275693	0.91[AMR][1000 genomes]
rs41525749	0.91[AMR][1000 genomes]
rs56805018	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs59725407	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs6831386	0.86[YRI][hapmap];0.91[AMR][1000 genomes]
rs6834495	0.91[AMR][1000 genomes]
rs6858042	0.91[AMR][1000 genomes]
rs73834403	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73834404	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73834429	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73834444	0.91[AMR][1000 genomes]
rs73834475	0.82[AMR][1000 genomes]
rs73834479	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73834489	0.82[AMR][1000 genomes]
rs7656868	0.91[AMR][1000 genomes]
rs7658383	1.00[ASW][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.94[YRI][hapmap];0.91[AMR][1000 genomes]
rs9307226	0.82[AMR][1000 genomes]
rs9991668	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs9994467	0.91[AMR][1000 genomes]
rs9995184	1.00[GIH][hapmap];0.82[AMR][1000 genomes]
rs9997337	1.00[GIH][hapmap];0.82[AMR][1000 genomes]
rs9998801	0.82[AMR][1000 genomes]
rs9999779	1.00[GIH][hapmap];0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529623	chr4:98501338-99460166	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv1001570	chr4:98976239-99239838	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1004616	chr4:99085875-99308901	Genic enhancers Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv2763801	chr4:99094892-99413853	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	esv2754250	chr4:99094922-99527122	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv879651	chr4:99105055-99441349	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv879652	chr4:99125659-99303633	Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv879653	chr4:99152631-99260423	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv1004181	chr4:99208152-99529576	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99184000-99239600	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:99184200-99242200	Weak transcription	A549	lung
3	chr4:99185400-99239400	Weak transcription	NHEK	skin
4	chr4:99206000-99234800	Weak transcription	Pancreas	Pancrea
5	chr4:99206200-99232800	Weak transcription	Gastric	stomach
6	chr4:99206200-99234000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr4:99206200-99239800	Weak transcription	Aorta	Aorta
8	chr4:99210200-99250800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr4:99212400-99239800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr4:99212400-99287800	Weak transcription	Thymus	Thymus
11	chr4:99214200-99240800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr4:99215000-99235400	Weak transcription	HSMMtube	muscle
13	chr4:99215000-99235600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:99215000-99317000	Weak transcription	Left Ventricle	heart
15	chr4:99216800-99236000	Weak transcription	HUVEC	blood vessel
16	chr4:99216800-99236000	Weak transcription	NH-A	brain
17	chr4:99216800-99236000	Weak transcription	NHDF-Ad	bronchial
18	chr4:99216800-99239200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr4:99217000-99237400	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr4:99217000-99239400	Weak transcription	HMEC	breast
21	chr4:99217600-99235800	Weak transcription	HSMM	muscle
22	chr4:99219000-99252000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:99219600-99236400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:99219600-99244600	Weak transcription	Fetal Thymus	thymus
25	chr4:99221400-99234800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:99223800-99234400	Weak transcription	Dnd41	blood
27	chr4:99223800-99288000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr4:99224400-99240000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:99224400-99247400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:99225200-99253400	Weak transcription	Fetal Lung	lung
31	chr4:99225400-99240600	Weak transcription	Primary B cells from cord blood	blood
32	chr4:99225600-99236000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:99226400-99232800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr4:99226400-99238800	Weak transcription	Fetal Intestine Small	intestine
35	chr4:99226600-99239200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr4:99227000-99243000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr4:99227200-99238000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr4:99227400-99236400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:99227600-99234400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:99227800-99236200	Weak transcription	Primary T cells from cord blood	blood
41	chr4:99229000-99232800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:99229200-99239600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:99229800-99241000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr4:99231200-99249000	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr4:99231600-99235200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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