Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11900092	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13018061	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1471887	0.88[JPT][hapmap]
rs1486969	1.00[MEX][hapmap];0.91[TSI][hapmap]
rs1518439	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16843745	0.88[JPT][hapmap]
rs17470100	0.88[JPT][hapmap]
rs17477262	0.84[EUR][1000 genomes]
rs1829364	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1968910	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2129483	1.00[MEX][hapmap];0.82[TSI][hapmap]
rs2931465	0.82[CEU][hapmap];0.92[TSI][hapmap]
rs35546150	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4954836	0.95[ASN][1000 genomes]
rs59982045	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs610276	1.00[MEX][hapmap];0.91[TSI][hapmap]
rs631497	0.83[YRI][hapmap]
rs649083	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs670617	0.85[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72894082	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72894090	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72896235	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896239	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896256	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72898260	1.00[ASN][1000 genomes]
rs72898263	1.00[ASN][1000 genomes]
rs901524	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754266	chr2:141023643-141270786	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875185	chr2:141055080-141179257	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv1002168	chr2:141056296-141157971	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv875186	chr2:141123496-141217244	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv459507	chr2:141130097-141170340	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv583190	chr2:141130097-141170340	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv470488	chr2:141133405-141170339	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141152200-141157600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:141153200-141159000	Weak transcription	Fetal Intestine Large	intestine

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