Variant report

Variant	rs57431896
Chromosome Location	chr3:94777269-94777270
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:94776805..94778652-chr3:94799142..94801105,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs13317670	1.00[EUR][1000 genomes]
rs13433996	1.00[EUR][1000 genomes]
rs1579543	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16853923	1.00[EUR][1000 genomes]
rs28682536	1.00[EUR][1000 genomes]
rs4384951	1.00[EUR][1000 genomes]
rs58014210	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58086527	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58204392	1.00[AMR][1000 genomes]
rs59975236	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60472824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6414229	1.00[EUR][1000 genomes]
rs73846915	1.00[EUR][1000 genomes]
rs73847062	1.00[AMR][1000 genomes]
rs73847071	1.00[AMR][1000 genomes]
rs73847076	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73847077	1.00[AMR][1000 genomes]
rs73847080	1.00[AMR][1000 genomes]
rs73847085	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73847088	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73847092	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73847093	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73848726	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73848727	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73848734	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73850322	1.00[EUR][1000 genomes]
rs7628702	1.00[EUR][1000 genomes]
rs9288849	1.00[EUR][1000 genomes]
rs973259	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9823394	1.00[EUR][1000 genomes]
rs9861253	1.00[EUR][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	nsv877169	chr3:94675697-94840854	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv590993	chr3:94759504-94841342	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1012191	chr3:94769139-94854973	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv536652	chr3:94769139-94854973	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94777200-94778000	Enhancers	Fetal Heart	heart

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