Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:157022820..157026060-chr3:157027403..157031164,3	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1027603	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12496879	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12629552	0.88[ASN][1000 genomes]
rs1500916	0.86[ASN][1000 genomes]
rs1500919	0.96[ASN][1000 genomes]
rs1500920	0.96[ASN][1000 genomes]
rs1546261	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1568609	0.96[ASN][1000 genomes]
rs1568612	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2047649	0.88[ASN][1000 genomes]
rs2088810	0.84[AMR][1000 genomes]
rs4680351	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4680358	0.96[ASN][1000 genomes]
rs6441124	0.84[ASN][1000 genomes]
rs6771109	0.81[AMR][1000 genomes]
rs6776647	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6801110	0.88[ASN][1000 genomes]
rs7614339	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7631556	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs885094	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9857875	0.96[ASN][1000 genomes]
rs988587	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs988588	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9990136	0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877687	chr3:156924793-157044184	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157004800-157028200	Weak transcription	HUVEC	blood vessel
2	chr3:157013000-157032600	Weak transcription	NH-A	brain
3	chr3:157015600-157048400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:157019000-157029000	Weak transcription	NHLF	lung
5	chr3:157019200-157028200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:157019200-157028400	Weak transcription	Osteobl	bone
7	chr3:157019400-157028200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:157021800-157035400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:157023800-157028200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:157024000-157028400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:157024200-157028600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:157025800-157026200	Enhancers	Fetal Heart	heart

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