Variant report

Variant	rs4721360
Chromosome Location	chr7:14743734-14743735
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10228891	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10259838	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10278975	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10950534	0.81[AMR][1000 genomes]
rs11971649	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12154366	0.84[EUR][1000 genomes]
rs12536592	0.83[ASN][1000 genomes]
rs12537147	0.83[ASN][1000 genomes]
rs12539208	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12669997	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12699654	0.81[ASN][1000 genomes]
rs1357856	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1357871	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1404615	0.83[AMR][1000 genomes]
rs1404616	0.83[AMR][1000 genomes]
rs1525078	0.80[AMR][1000 genomes]
rs1525099	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1568846	0.83[ASN][1000 genomes]
rs1568847	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17606181	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17668635	0.81[ASN][1000 genomes]
rs17668761	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1830028	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4719417	0.83[ASN][1000 genomes]
rs62448684	0.84[EUR][1000 genomes]
rs6944222	0.81[AMR][1000 genomes]
rs6947566	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6954517	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6956435	0.80[AMR][1000 genomes]
rs6965637	0.83[ASN][1000 genomes]
rs6966274	0.83[ASN][1000 genomes]
rs7784799	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7785767	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs885438	0.80[AMR][1000 genomes]
rs9639212	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9639213	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9691103	0.82[AMR][1000 genomes]
rs9784967	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887712	chr7:14717872-14829858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 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	chr7:14712800-14775200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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