Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1037250	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1037251	0.89[ASN][1000 genomes]
rs11847513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17120161	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17120171	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17120173	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17120175	0.81[EUR][1000 genomes]
rs17120180	0.81[EUR][1000 genomes]
rs2922651	0.89[ASN][1000 genomes]
rs3008504	0.89[ASN][1000 genomes]
rs3008505	0.89[ASN][1000 genomes]
rs57651825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150499	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73372005	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73377471	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73381138	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73387324	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73387326	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73389279	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74071320	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs986734	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046875	chr14:84993510-85193250	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1052415	chr14:85001891-85078853	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85036600-85046200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr14:85037000-85045000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:85040200-85041200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:85040400-85041200	Enhancers	Brain Germinal Matrix	brain

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