Variant report

Variant	rs6862991
Chromosome Location	chr5:113509828-113509829
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10038304	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10041267	0.90[EUR][1000 genomes]
rs10043950	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10045558	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10463657	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10900693	0.90[EUR][1000 genomes]
rs11241267	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12153188	0.84[EUR][1000 genomes]
rs12521597	0.89[ASN][1000 genomes]
rs12523408	0.88[CEU][hapmap];0.89[CHB][hapmap];0.88[JPT][hapmap]
rs12652393	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4074169	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4131322	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4429843	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4460133	0.91[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.81[EUR][1000 genomes]
rs4482897	0.90[EUR][1000 genomes]
rs4505938	0.84[EUR][1000 genomes]
rs4615290	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61415455	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6594788	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6594797	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6594801	0.91[EUR][1000 genomes]
rs6859418	0.80[EUR][1000 genomes]
rs6872938	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6891422	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6894277	0.83[EUR][1000 genomes]
rs7701720	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7738011	0.87[ASN][1000 genomes]
rs9326913	0.93[EUR][1000 genomes];0.85[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	nsv882726	chr5:113404933-113555626	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2763899	chr5:113474771-113533857	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv599432	chr5:113486177-113561766	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv521754	chr5:113507154-113515807	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113505600-113511800	Weak transcription	Fetal Heart	heart
2	chr5:113509200-113510200	Weak transcription	HUVEC	blood vessel

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