Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1384743	0.85[EUR][1000 genomes]
rs1384744	0.85[EUR][1000 genomes]
rs17603029	0.85[EUR][1000 genomes]
rs2170703	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4274583	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4605358	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56880806	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58349979	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62156538	0.85[EUR][1000 genomes]
rs62156540	0.85[EUR][1000 genomes]
rs62156541	0.85[EUR][1000 genomes]
rs62156542	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs62156547	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62158280	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62158281	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62158282	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6741192	0.89[EUR][1000 genomes]
rs7573357	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7606736	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs874236	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv834249	chr2:67515471-67691605	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67532000-67538800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:67535400-67539400	Enhancers	NHDF-Ad	bronchial
3	chr2:67535800-67538400	Enhancers	Fetal Lung	lung
4	chr2:67536400-67539200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr2:67536400-67539400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:67536600-67538200	Weak transcription	NHLF	lung
7	chr2:67536800-67538200	Weak transcription	NH-A	brain
8	chr2:67536800-67538600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:67536800-67538600	Weak transcription	Hela-S3	cervix
10	chr2:67537000-67538600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr2:67537000-67538800	Weak transcription	A549	lung
12	chr2:67537200-67538800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:67537400-67538600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:67537600-67538200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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