Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:48405154..48407904-chr3:48408057..48410443,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10780032	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11706626	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11915428	1.00[EUR][1000 genomes]
rs3731495	1.00[EUR][1000 genomes]
rs3731539	1.00[EUR][1000 genomes]
rs3731547	1.00[EUR][1000 genomes]
rs3924179	1.00[EUR][1000 genomes]
rs4858818	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs55782175	1.00[EUR][1000 genomes]
rs58835493	1.00[EUR][1000 genomes]
rs59352296	1.00[EUR][1000 genomes]
rs6442103	1.00[EUR][1000 genomes]
rs6442122	1.00[EUR][1000 genomes]
rs6791777	1.00[EUR][1000 genomes]
rs6793732	1.00[EUR][1000 genomes]
rs6801348	0.88[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73830466	1.00[EUR][1000 genomes]
rs73831562	1.00[EUR][1000 genomes]
rs73831565	1.00[EUR][1000 genomes]
rs73831572	1.00[EUR][1000 genomes]
rs73831577	1.00[EUR][1000 genomes]
rs73831579	1.00[EUR][1000 genomes]
rs7633433	1.00[EUR][1000 genomes]
rs898226	1.00[EUR][1000 genomes]
rs9852211	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs9917799	1.00[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	nsv834683	chr3:48301504-48493261	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv834684	chr3:48385699-48589323	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 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	chr3:48406800-48412800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr3:48408800-48411400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:48409200-48410800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:48409200-48411200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr3:48409200-48411400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:48409200-48414000	Weak transcription	Fetal Heart	heart
7	chr3:48409200-48414600	Weak transcription	K562	blood
8	chr3:48409400-48411200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:48409600-48411200	Weak transcription	Pancreas	Pancrea

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