Variant report

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

rs_ID	r²[population]
rs10131334	0.91[AFR][1000 genomes]
rs10132716	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10144393	0.81[AFR][1000 genomes]
rs12431750	0.89[AFR][1000 genomes]
rs12432108	0.89[ASN][1000 genomes]
rs12434928	0.94[ASN][1000 genomes]
rs12435926	0.97[ASN][1000 genomes]
rs12436244	0.99[ASN][1000 genomes]
rs12880081	0.99[ASN][1000 genomes]
rs12880194	0.87[AFR][1000 genomes]
rs12880837	0.98[ASN][1000 genomes]
rs12891609	0.98[ASN][1000 genomes]
rs12892327	0.97[ASN][1000 genomes]
rs12893690	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12895750	0.99[ASN][1000 genomes]
rs12898135	0.97[ASN][1000 genomes]
rs3924098	0.99[ASN][1000 genomes]
rs4259973	0.89[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4299082	0.81[AFR][1000 genomes]
rs4350506	0.88[AFR][1000 genomes]
rs4410004	0.87[AFR][1000 genomes]
rs4418993	0.89[AFR][1000 genomes]
rs4489939	0.87[AFR][1000 genomes]
rs4500652	0.87[AFR][1000 genomes]
rs4635264	0.99[ASN][1000 genomes]
rs4904174	0.95[ASN][1000 genomes]
rs7141228	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7141801	0.99[ASN][1000 genomes]
rs7147801	0.99[ASN][1000 genomes]
rs7148496	0.87[AFR][1000 genomes]
rs7148700	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7151303	0.87[AFR][1000 genomes]
rs7159902	0.97[ASN][1000 genomes]
rs7160613	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs8003576	0.87[AFR][1000 genomes]
rs8008906	0.95[ASN][1000 genomes]
rs8012447	0.94[ASN][1000 genomes]
rs8012777	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84865000-84876000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:84867600-84868000	Enhancers	Fetal Lung	lung
3	chr14:84867600-84869800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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