Variant report

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

rs_ID	r²[population]
rs10131053	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10131334	0.89[ASN][1000 genomes]
rs10144393	0.92[ASN][1000 genomes]
rs12431750	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12432589	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12434928	0.84[EUR][1000 genomes]
rs12879664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12880194	0.92[ASN][1000 genomes]
rs12891714	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4243672	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4259973	0.96[ASN][1000 genomes]
rs4328366	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4350506	0.91[ASN][1000 genomes]
rs4386065	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4410004	0.92[ASN][1000 genomes]
rs4489939	0.92[ASN][1000 genomes]
rs4500652	0.86[ASN][1000 genomes]
rs4904174	0.85[EUR][1000 genomes]
rs55682233	0.95[ASN][1000 genomes]
rs7148496	0.92[ASN][1000 genomes]
rs7148700	0.94[ASN][1000 genomes]
rs7151303	0.89[ASN][1000 genomes]
rs7158947	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7160613	0.96[ASN][1000 genomes]
rs71908900	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs8003576	0.91[ASN][1000 genomes]
rs8008906	0.85[EUR][1000 genomes]
rs8012447	0.84[EUR][1000 genomes]
rs8012777	0.84[EUR][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	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
3	esv3375849	chr14:84841699-84843697	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84839000-84843600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:84841200-84842200	Enhancers	HUVEC	blood vessel
3	chr14:84841200-84842400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:84841400-84842200	Enhancers	NH-A	brain
5	chr14:84841600-84842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:84841600-84842200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr14:84841600-84842200	Enhancers	HSMMtube	muscle

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