Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44495582..44498780-chr10:44499655..44502319,3	K562	blood:

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

rs_ID	r²[population]
rs10793515	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10793516	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10793517	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10899963	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10899965	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10899973	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11238808	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11238817	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11238818	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12570314	0.88[CEU][hapmap];0.82[TSI][hapmap]
rs1472168	0.84[AMR][1000 genomes]
rs2047009	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4412714	0.81[AMR][1000 genomes]
rs4948591	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4948815	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4948818	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7090343	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7091447	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7478408	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7903121	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9332446	0.86[AMR][1000 genomes];0.80[EUR][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:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44494200-44502600	Weak transcription	Right Atrium	heart
2	chr10:44495800-44504400	Weak transcription	Pancreas	Pancrea
3	chr10:44500000-44500600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:44500000-44501000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr10:44500000-44501200	Enhancers	Placenta	Placenta
6	chr10:44500000-44502600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr10:44500000-44503200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr10:44500200-44500600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:44500200-44500600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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