Variant report

Variant	rs66916501
Chromosome Location	chr4:97522106-97522107
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs13101358	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13111155	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13112783	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13118705	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13118976	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13137303	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13138090	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13150748	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13150788	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13151319	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34562744	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34684469	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34804130	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34949655	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35433600	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35718009	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36008950	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36092553	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4130397	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4260614	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4269250	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4371697	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4443294	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6532639	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66496713	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs67022992	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67064822	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72688094	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7672470	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7672897	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7673132	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7673255	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7697527	0.98[AMR][1000 genomes];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	nsv879634	chr4:97371381-97727113	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv879635	chr4:97389090-97591085	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2757944	chr4:97509566-97809092	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2759268	chr4:97509566-97809092	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97520000-97523800	Weak transcription	Ovary	ovary
2	chr4:97520600-97523600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:97521000-97524800	Weak transcription	Fetal Heart	heart

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