Variant report

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

rs_ID	r²[population]
rs12069481	1.00[CEU][hapmap]
rs12091733	0.91[EUR][1000 genomes]
rs1545007	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs16856811	0.93[EUR][1000 genomes]
rs16856830	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs1901357	0.99[EUR][1000 genomes]
rs2116517	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2568102	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2599511	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2599512	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2798414	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2798415	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2798418	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3813991	0.93[EUR][1000 genomes]
rs55968043	0.97[EUR][1000 genomes]
rs60031791	0.97[EUR][1000 genomes]
rs6681161	1.00[CEU][hapmap]
rs6681310	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs7524473	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap]
rs919678	0.97[ASN][1000 genomes]
rs919679	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv3332610	chr1:166111288-166282689	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166241400-166243400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:166242000-166243600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:166242200-166243400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:166242200-166243400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:166242400-166246000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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