Variant report

Variant	rs12645359
Chromosome Location	chr4:21553882-21553883
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10516393	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs11940371	0.88[EUR][1000 genomes]
rs12648125	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs12651393	0.81[CEU][hapmap];0.84[EUR][1000 genomes]
rs12651530	0.81[EUR][1000 genomes]
rs13104108	0.87[CEU][hapmap];0.89[EUR][1000 genomes]
rs13115047	0.83[CEU][hapmap]
rs13128455	0.87[EUR][1000 genomes]
rs1350716	0.89[EUR][1000 genomes]
rs1350717	0.89[EUR][1000 genomes]
rs1460476	0.88[EUR][1000 genomes]
rs1460477	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs1503985	0.86[EUR][1000 genomes]
rs1503986	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs1503987	0.88[EUR][1000 genomes]
rs1812151	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs1817323	0.88[EUR][1000 genomes]
rs1817324	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs1841373	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs59768023	0.88[EUR][1000 genomes]
rs67250899	0.89[EUR][1000 genomes]
rs6813482	0.89[EUR][1000 genomes]
rs6832481	0.82[CEU][hapmap]
rs6836186	0.89[EUR][1000 genomes]
rs6836515	0.89[EUR][1000 genomes]
rs905627	0.95[CEU][hapmap];0.88[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	chr4:21553800-21557000	Enhancers	Fetal Heart	heart

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