Variant report

Variant	rs1486021
Chromosome Location	chr4:81535277-81535278
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10033938	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1038530	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1038531	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11940084	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12650380	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1352077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1486015	0.81[AFR][1000 genomes]
rs1486027	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1486030	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1601512	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1601513	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2132264	0.85[AMR][1000 genomes]
rs2867780	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2867782	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs329402	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs329403	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34306570	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs34975597	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs396273	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4146323	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4283653	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs444023	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs444680	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4693062	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4693510	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4693531	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs544526	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs59789768	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6535031	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6535040	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6535041	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72864881	0.83[EUR][1000 genomes]
rs72874049	0.85[AMR][1000 genomes]
rs72874070	0.82[AMR][1000 genomes]
rs72874077	0.85[AMR][1000 genomes]
rs72874089	0.85[AMR][1000 genomes]
rs72874098	0.85[AMR][1000 genomes]
rs72879935	0.82[EUR][1000 genomes]
rs7668590	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7675185	0.82[EUR][1000 genomes]
rs7696162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs923178	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs971728	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002776	chr4:81480374-81802614	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv537154	chr4:81480374-81802614	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3518601	chr4:81523238-81831941	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3518602	chr4:81523354-81831976	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv1804420	chr4:81529088-81535393	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv1815074	chr4:81529088-81535393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3507556	chr4:81529778-81537026	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1815120	chr4:81529855-81535393	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1814776	chr4:81529867-81535393	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3488564	chr4:81529978-81537076	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3488566	chr4:81530910-81536366	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3467223	chr4:81531064-81536054	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	esv3467224	chr4:81531064-81536054	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
14	esv3467222	chr4:81531081-81536062	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
15	esv3488561	chr4:81531104-81536047	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
16	esv3488567	chr4:81531107-81536026	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
17	esv3488568	chr4:81531126-81535976	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
18	esv3488565	chr4:81531158-81535986	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3488562	chr4:81531161-81535991	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
20	esv3507557	chr4:81531161-81535991	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
21	esv3488560	chr4:81531216-81535947	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
22	esv3488569	chr4:81531221-81535942	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
23	esv18350	chr4:81531281-81535875	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
24	esv1805022	chr4:81531478-81535393	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
25	esv1808245	chr4:81531478-81535393	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
26	esv1811696	chr4:81531478-81535393	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81533200-81536800	Weak transcription	Fetal Intestine Large	intestine
2	chr4:81534200-81535800	Enhancers	Stomach Mucosa	stomach
3	chr4:81534600-81536000	Enhancers	HUES48 Cell Line	embryonic stem cell

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