Variant report

Variant	rs7721198
Chromosome Location	chr5:89975085-89975086
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10036258	0.84[EUR][1000 genomes]
rs10036980	0.83[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10043836	0.84[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10045236	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10045394	0.85[EUR][1000 genomes]
rs10058765	0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10060427	0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10062714	0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10062924	0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10067181	1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs10068473	1.00[JPT][hapmap]
rs10072105	0.92[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1014750	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1028191	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1028192	0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1033290	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10462342	0.91[JPT][hapmap]
rs10514327	0.91[JPT][hapmap]
rs10514333	1.00[JPT][hapmap]
rs10942596	0.83[JPT][hapmap]
rs10942597	0.82[JPT][hapmap]
rs10942605	1.00[JPT][hapmap]
rs10942606	0.83[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1160121	1.00[JPT][hapmap]
rs12188928	1.00[JPT][hapmap]
rs12516985	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12652606	0.86[EUR][1000 genomes]
rs12655180	0.81[JPT][hapmap]
rs12657264	0.87[EUR][1000 genomes]
rs13167491	0.91[EUR][1000 genomes]
rs13185955	0.82[JPT][hapmap]
rs1533603	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap]
rs1673378	0.83[JPT][hapmap]
rs1673379	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs16868957	0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1700510	0.92[CHB][hapmap];0.81[JPT][hapmap]
rs1700511	0.84[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes]
rs1878878	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1993474	1.00[JPT][hapmap]
rs2176624	0.81[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2222242	0.80[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs2366771	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs2366773	0.91[CHB][hapmap];0.89[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2366774	0.92[CHB][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2366777	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28517617	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28550273	0.83[ASN][1000 genomes]
rs28587199	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3805483	0.90[JPT][hapmap]
rs3927265	0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4379236	0.83[ASN][1000 genomes]
rs490812	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs491241	0.80[EUR][1000 genomes]
rs4916681	0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs4916682	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4916684	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4916686	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4916813	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4916814	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4916815	1.00[JPT][hapmap]
rs498491	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs499148	0.82[JPT][hapmap]
rs502596	0.83[CHB][hapmap];0.90[JPT][hapmap];0.81[EUR][1000 genomes]
rs603015	0.82[JPT][hapmap]
rs617379	0.92[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes]
rs637442	0.84[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes]
rs6452904	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6452905	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6452906	0.83[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs645652	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs648430	0.82[JPT][hapmap]
rs6861525	0.89[ASN][1000 genomes]
rs6863710	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6878917	0.92[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6881412	0.83[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6883872	0.92[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6888355	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs688956	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs688960	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs6898209	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7703530	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7703588	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7714506	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7723259	0.84[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7724806	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes]
rs7726624	0.92[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs7729703	0.84[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7732169	1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs9293550	0.84[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs963866	0.84[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs977906	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9790907	0.92[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes];0.82[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	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv933668	chr5:89854253-89999672	Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv531965	chr5:89886550-90145002	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	nsv1029970	chr5:89940489-89986831	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	nsv1032225	chr5:89940489-89999954	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv1025391	chr5:89943364-89995164	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
9	nsv537805	chr5:89943364-89995164	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	nsv882367	chr5:89956991-90209824	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
11	nsv934323	chr5:89968158-90111853	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
12	nsv1015449	chr5:89968626-90219398	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89936800-89994200	Weak transcription	Brain Germinal Matrix	brain
2	chr5:89950200-89981600	Weak transcription	Fetal Brain Female	brain
3	chr5:89950400-90033400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:89964400-89993400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr5:89964600-89994800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:89965000-89993600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr5:89967200-89979000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:89967200-89992000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:89968000-89980400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr5:89968000-89982000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:89968400-89982000	Strong transcription	K562	blood
12	chr5:89968600-89982000	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr5:89968600-89982000	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr5:89971600-89978000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr5:89971600-89978000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr5:89971800-89979400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr5:89972000-89985600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr5:89972800-89978000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:89973800-89976800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:89974200-89976600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:89974600-89976600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr5:89975000-89975800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:89975000-89976000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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