Variant report

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

rs_ID	r²[population]
rs10427172	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11888548	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11901831	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12619707	0.87[ASN][1000 genomes]
rs16845944	1.00[ASN][1000 genomes]
rs17744862	0.91[EUR][1000 genomes]
rs1821661	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1836739	0.86[ASN][1000 genomes]
rs34588906	0.89[ASN][1000 genomes]
rs55985613	0.84[EUR][1000 genomes]
rs56172792	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58735954	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59224996	0.93[ASN][1000 genomes]
rs60254210	1.00[ASN][1000 genomes]
rs61031475	0.80[EUR][1000 genomes]
rs66471203	1.00[ASN][1000 genomes]
rs66600814	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67103742	0.98[ASN][1000 genomes]
rs72947641	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72947669	0.91[ASN][1000 genomes]
rs72947685	0.87[ASN][1000 genomes]
rs73083812	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73083814	0.80[AFR][1000 genomes]
rs73083815	0.80[AFR][1000 genomes]
rs73985404	0.88[AFR][1000 genomes]
rs73985405	0.80[AFR][1000 genomes]
rs7571041	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[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	nsv834523	chr2:212163236-212331393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv875776	chr2:212196908-212264818	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212214200-212232000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:212225800-212229800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:212225800-212232000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:212227200-212229400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:212227200-212232400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr2:212228800-212229600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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