Variant report

Variant	rs72779664
Chromosome Location	chr5:97176188-97176189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs12653428	1.00[ASN][1000 genomes]
rs12654021	1.00[ASN][1000 genomes]
rs12655508	1.00[ASN][1000 genomes]
rs12655548	1.00[ASN][1000 genomes]
rs12656172	1.00[ASN][1000 genomes]
rs4327612	1.00[ASN][1000 genomes]
rs4379225	1.00[ASN][1000 genomes]
rs4440387	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4551099	0.91[ASN][1000 genomes]
rs55706044	0.95[EUR][1000 genomes]
rs55725155	0.90[EUR][1000 genomes]
rs55743944	1.00[ASN][1000 genomes]
rs55817884	0.90[EUR][1000 genomes]
rs55937002	1.00[ASN][1000 genomes]
rs56074649	1.00[ASN][1000 genomes]
rs56152369	0.93[EUR][1000 genomes]
rs56260839	0.92[EUR][1000 genomes]
rs56313368	1.00[ASN][1000 genomes]
rs56336851	1.00[ASN][1000 genomes]
rs56666656	1.00[ASN][1000 genomes]
rs58700659	0.88[EUR][1000 genomes]
rs59931467	0.95[EUR][1000 genomes]
rs61166915	1.00[ASN][1000 genomes]
rs61545180	1.00[ASN][1000 genomes]
rs6557009	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6557011	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66476007	0.93[EUR][1000 genomes]
rs66774764	0.93[EUR][1000 genomes]
rs67435821	0.87[EUR][1000 genomes]
rs67922319	0.93[EUR][1000 genomes]
rs67935527	0.93[EUR][1000 genomes]
rs68166390	0.95[EUR][1000 genomes]
rs6859489	0.87[EUR][1000 genomes]
rs6882744	0.97[ASN][1000 genomes]
rs6884205	0.87[EUR][1000 genomes]
rs6890322	1.00[ASN][1000 genomes]
rs72779661	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72779662	1.00[ASN][1000 genomes]
rs72779665	1.00[ASN][1000 genomes]
rs72779667	1.00[ASN][1000 genomes]
rs72779669	1.00[ASN][1000 genomes]
rs72779670	1.00[ASN][1000 genomes]
rs72779671	1.00[ASN][1000 genomes]
rs72779673	1.00[ASN][1000 genomes]
rs72779675	1.00[ASN][1000 genomes]
rs72779676	1.00[ASN][1000 genomes]
rs72779677	1.00[ASN][1000 genomes]
rs72779680	1.00[ASN][1000 genomes]
rs72779683	1.00[ASN][1000 genomes]
rs72779685	1.00[ASN][1000 genomes]
rs72779686	1.00[ASN][1000 genomes]
rs72779690	1.00[ASN][1000 genomes]
rs72779691	1.00[ASN][1000 genomes]
rs72781505	1.00[ASN][1000 genomes]
rs72781506	1.00[ASN][1000 genomes]
rs72781508	1.00[ASN][1000 genomes]
rs72781509	1.00[ASN][1000 genomes]
rs72781511	1.00[ASN][1000 genomes]
rs72781512	1.00[ASN][1000 genomes]
rs72781514	1.00[ASN][1000 genomes]
rs72781515	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72781520	1.00[ASN][1000 genomes]
rs72781522	1.00[ASN][1000 genomes]
rs72781524	1.00[ASN][1000 genomes]
rs72781525	1.00[ASN][1000 genomes]
rs72781527	1.00[ASN][1000 genomes]
rs7701490	1.00[ASN][1000 genomes]
rs7714125	1.00[ASN][1000 genomes]
rs7719818	1.00[ASN][1000 genomes]
rs7724005	1.00[ASN][1000 genomes]
rs7729626	1.00[ASN][1000 genomes]
rs7732992	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534326	chr5:96531217-97283481	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1031429	chr5:96777286-97269498	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv527650	chr5:96783726-97260358	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1028224	chr5:96791214-97258383	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv537814	chr5:96791214-97258383	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1020125	chr5:96937248-97350644	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv432757	chr5:97006304-97213768	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	esv2754965	chr5:97013452-97296147	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1027714	chr5:97034552-97211333	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv471024	chr5:97048466-97187183	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1034347	chr5:97062961-97241450	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv830418	chr5:97139371-97326878	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97173600-97176800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:97173600-97176800	Enhancers	Hela-S3	cervix
3	chr5:97173600-97176800	Enhancers	HSMM	muscle
4	chr5:97173600-97176800	Enhancers	NH-A	brain
5	chr5:97173600-97176800	Enhancers	NHDF-Ad	bronchial
6	chr5:97173600-97177000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr5:97173600-97177000	Enhancers	Osteobl	bone
8	chr5:97173800-97176600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:97173800-97176600	Enhancers	Adipose Nuclei	Adipose
10	chr5:97173800-97176600	Enhancers	NHEK	skin
11	chr5:97173800-97176600	Enhancers	NHLF	lung
12	chr5:97173800-97176800	Enhancers	Fetal Lung	lung
13	chr5:97173800-97176800	Enhancers	HMEC	breast
14	chr5:97174000-97177000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:97174000-97177400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr5:97174200-97176400	Weak transcription	Ovary	ovary
17	chr5:97174200-97176800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:97174400-97176800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:97174400-97176800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:97174600-97176600	Weak transcription	Colon Smooth Muscle	Colon
21	chr5:97174600-97177000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr5:97175000-97176600	Enhancers	Rectal Smooth Muscle	rectum
23	chr5:97175200-97176800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:97175200-97178200	Weak transcription	Fetal Muscle Leg	muscle
25	chr5:97175400-97176400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:97175400-97176400	Weak transcription	HSMMtube	muscle
27	chr5:97175400-97176800	Flanking Active TSS	HUVEC	blood vessel
28	chr5:97175600-97178000	Weak transcription	Dnd41	blood
29	chr5:97175800-97176600	Weak transcription	Fetal Stomach	stomach
30	chr5:97175800-97179600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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