Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44478479..44480901-chr10:44492659..44495293,2	K562	blood:

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

rs_ID	r²[population]
rs10793515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10793516	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10793517	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10899963	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10899965	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10899973	0.90[AMR][1000 genomes]
rs11238808	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11238817	0.90[AMR][1000 genomes]
rs11238818	0.90[AMR][1000 genomes]
rs12570314	0.88[CEU][hapmap];0.84[TSI][hapmap]
rs1472168	0.86[AMR][1000 genomes]
rs1873756	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2047009	0.90[AMR][1000 genomes]
rs4412714	0.83[AMR][1000 genomes]
rs4948591	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4948815	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4948818	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7090343	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7478408	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7903121	0.90[AMR][1000 genomes]
rs9332446	0.88[AMR][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	nsv466884	chr10:44473036-44515130	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv550698	chr10:44473036-44515130	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44492400-44494800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr10:44494200-44502600	Weak transcription	Right Atrium	heart
3	chr10:44494600-44495600	Weak transcription	Pancreas	Pancrea
4	chr10:44494600-44499200	Weak transcription	NHDF-Ad	bronchial

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