Variant report

Variant	rs59586361
Chromosome Location	chr4:21552770-21552771
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs13131360	0.81[ASN][1000 genomes]
rs16871492	0.93[EUR][1000 genomes]
rs16871505	0.89[EUR][1000 genomes]
rs16871508	0.89[EUR][1000 genomes]
rs16871511	0.89[EUR][1000 genomes]
rs16871514	0.89[EUR][1000 genomes]
rs3049994	0.81[EUR][1000 genomes]
rs41397149	0.93[EUR][1000 genomes]
rs41500944	0.93[EUR][1000 genomes]
rs56155919	0.89[EUR][1000 genomes]
rs56186155	0.96[EUR][1000 genomes]
rs56408419	0.92[EUR][1000 genomes]
rs57501870	0.93[ASN][1000 genomes]
rs60492426	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6813304	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6824316	0.83[EUR][1000 genomes]
rs6824702	0.89[EUR][1000 genomes]
rs6824711	0.89[EUR][1000 genomes]
rs6836213	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6843752	0.93[EUR][1000 genomes]
rs6843837	0.93[EUR][1000 genomes]
rs6844068	0.93[EUR][1000 genomes]
rs6848885	0.93[EUR][1000 genomes]
rs6849321	0.93[EUR][1000 genomes]
rs73252231	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73252235	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73252236	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73252249	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73252255	0.96[EUR][1000 genomes]
rs73252256	0.96[EUR][1000 genomes]
rs73252257	0.96[EUR][1000 genomes]
rs73252260	0.93[EUR][1000 genomes]
rs73252261	0.93[EUR][1000 genomes]
rs73252264	0.93[EUR][1000 genomes]
rs73252265	0.93[EUR][1000 genomes]
rs73252266	0.93[EUR][1000 genomes]
rs73252267	0.93[EUR][1000 genomes]
rs73252268	0.93[EUR][1000 genomes]
rs73252269	0.93[EUR][1000 genomes]
rs73252271	0.93[EUR][1000 genomes]
rs73252272	0.93[EUR][1000 genomes]
rs73252288	0.96[EUR][1000 genomes]
rs73252289	0.96[EUR][1000 genomes]
rs73252290	0.93[EUR][1000 genomes]
rs73254304	0.89[EUR][1000 genomes]
rs73254305	0.89[EUR][1000 genomes]
rs73254306	0.89[EUR][1000 genomes]
rs73254307	0.92[EUR][1000 genomes]
rs73254310	0.89[EUR][1000 genomes]
rs73254311	0.92[EUR][1000 genomes]
rs73254313	0.92[EUR][1000 genomes]
rs73254386	0.96[EUR][1000 genomes]
rs73254387	0.96[EUR][1000 genomes]
rs73256510	0.82[EUR][1000 genomes]
rs7657287	0.93[EUR][1000 genomes]
rs7657482	0.93[EUR][1000 genomes]
rs7679874	0.89[EUR][1000 genomes]
rs7681243	0.93[EUR][1000 genomes]
rs7681823	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv829879	chr4:21418568-21611002	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv998481	chr4:21421945-21608805	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv829880	chr4:21492426-21693816	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv997742	chr4:21515920-21575213	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1002353	chr4:21518045-21575213	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
7	nsv1001219	chr4:21518045-21580423	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
8	esv2760860	chr4:21518045-21580435	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
9	nsv525271	chr4:21519577-21575623	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
10	nsv470019	chr4:21519577-21576754	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
11	nsv593805	chr4:21519577-21576754	Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
12	nsv1009425	chr4:21542141-21566178	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
13	nsv593806	chr4:21546537-21566178	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21547000-21553800	Weak transcription	Fetal Heart	heart

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