Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:45841159..45843943-chr3:45848484..45850929,2	MCF-7	breast:
2	chr3:45842115..45844572-chr3:45845458..45847855,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10490770	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13071258	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13078854	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13081482	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17712877	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17713054	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17763537	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17763742	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34288077	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34326463	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34668658	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35044562	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35081325	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35508621	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35624553	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35652899	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35731912	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35896106	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67959919	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71325088	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72893671	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73064425	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv834678	chr3:45804294-46010256	Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:45838400-45860000	Weak transcription	Gastric	stomach
2	chr3:45841000-45847600	Weak transcription	Primary T cells from cord blood	blood
3	chr3:45842000-45849400	Strong transcription	Dnd41	blood
4	chr3:45842400-45843600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:45842400-45843600	Weak transcription	Fetal Intestine Small	intestine
6	chr3:45842400-45857400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr3:45842400-45859200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr3:45842400-45859800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:45842600-45854400	Weak transcription	Fetal Intestine Large	intestine
10	chr3:45843000-45846800	Weak transcription	Brain Anterior Caudate	brain
11	chr3:45843200-45843600	Strong transcription	Fetal Thymus	thymus
12	chr3:45843200-45846400	Strong transcription	Thymus	Thymus
13	chr3:45843400-45843800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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