Variant report

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

rs_ID	r²[population]
rs1166721	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12324408	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12439384	0.83[ASN][1000 genomes]
rs12591862	0.82[EUR][1000 genomes]
rs12595664	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1491625	0.88[EUR][1000 genomes]
rs1602543	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16969786	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1906162	0.82[EUR][1000 genomes]
rs1906163	0.89[ASN][1000 genomes]
rs1906164	0.89[ASN][1000 genomes]
rs1906165	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2638012	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60676466	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6492913	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6492916	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67248221	0.85[ASN][1000 genomes]
rs67895637	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7168010	0.86[EUR][1000 genomes]
rs7169027	0.94[EUR][1000 genomes]
rs72727074	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72727076	0.96[ASN][1000 genomes]
rs8028323	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8182052	0.88[ASN][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	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 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	chr15:40021800-40038000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:40029000-40037200	Weak transcription	Right Atrium	heart
3	chr15:40029200-40040200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:40029600-40038600	Weak transcription	NHDF-Ad	bronchial
5	chr15:40033600-40040200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr15:40034400-40038400	Weak transcription	Osteobl	bone
7	chr15:40034600-40038400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr15:40034800-40038600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr15:40035000-40036200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr15:40035000-40040400	Weak transcription	Adipose Nuclei	Adipose
11	chr15:40035200-40036200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:40035200-40038400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr15:40035600-40036800	Enhancers	Hela-S3	cervix
14	chr15:40035600-40050000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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