Variant report

Variant	rs893157
Chromosome Location	chr15:62378641-62378642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10047986	0.81[AMR][1000 genomes]
rs1030859	0.81[AMR][1000 genomes]
rs1030860	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1030861	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10519153	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10851707	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11630347	0.81[EUR][1000 genomes]
rs11632441	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11635977	0.81[AMR][1000 genomes]
rs11639147	0.80[EUR][1000 genomes]
rs12438690	0.81[AMR][1000 genomes]
rs12438803	0.81[AMR][1000 genomes]
rs12439356	0.89[CEU][hapmap];0.81[AMR][1000 genomes]
rs12442212	0.89[CEU][hapmap]
rs12442589	0.87[EUR][1000 genomes]
rs12442675	0.85[CEU][hapmap]
rs12592402	0.81[CEU][hapmap]
rs12592464	0.80[EUR][1000 genomes]
rs12594658	0.82[CEU][hapmap]
rs12898209	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs12900703	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12913951	0.81[AMR][1000 genomes]
rs1364810	0.82[CEU][hapmap]
rs1370177	0.82[CEU][hapmap]
rs1436961	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1436963	0.81[AMR][1000 genomes]
rs1436964	0.81[AMR][1000 genomes]
rs1534542	0.89[CEU][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17205407	0.81[AMR][1000 genomes]
rs17271403	0.80[AMR][1000 genomes]
rs17271438	0.80[AMR][1000 genomes]
rs1836996	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2414754	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs2414759	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34096515	0.81[AMR][1000 genomes]
rs3784445	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs3784633	0.84[CEU][hapmap]
rs4143841	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4143842	0.81[AMR][1000 genomes]
rs4564516	0.81[AMR][1000 genomes]
rs4775455	0.82[CEU][hapmap]
rs4775457	0.81[AMR][1000 genomes]
rs4775458	0.81[AMR][1000 genomes]
rs7161883	0.80[EUR][1000 genomes]
rs7162536	0.81[AMR][1000 genomes]
rs7168164	0.82[CEU][hapmap]
rs7177276	0.86[CEU][hapmap];0.81[AMR][1000 genomes]
rs7177711	0.86[CEU][hapmap];0.81[AMR][1000 genomes]
rs7178424	0.89[CEU][hapmap];0.81[AMR][1000 genomes]
rs7178540	0.89[CEU][hapmap];0.81[AMR][1000 genomes]
rs7178945	0.88[CEU][hapmap];0.81[AMR][1000 genomes]
rs7182842	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs731820	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8025877	0.85[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8026008	0.86[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8038932	0.81[AMR][1000 genomes]
rs8039651	0.85[CEU][hapmap]
rs893156	0.86[CEU][hapmap]
rs893158	0.86[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs933807	0.81[CEU][hapmap]
rs9989353	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9989354	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv457176	chr15:62178695-62519658	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv569643	chr15:62178695-62519658	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv471247	chr15:62202481-62519658	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv569646	chr15:62202482-62519658	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv1044748	chr15:62276183-62521856	Active TSS Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv542405	chr15:62276183-62521856	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv457178	chr15:62340126-62394324	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv569652	chr15:62340126-62394324	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
9	nsv1560	chr15:62354264-62399304	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv948606	chr15:62364932-63088916	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 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	chr15:62367800-62379800	Weak transcription	Pancreas	Pancrea
2	chr15:62373200-62379200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr15:62376000-62380400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:62378200-62379600	Weak transcription	Hela-S3	cervix
5	chr15:62378200-62379800	Weak transcription	Right Atrium	heart
6	chr15:62378200-62379800	Weak transcription	HUVEC	blood vessel
7	chr15:62378400-62380000	Weak transcription	Fetal Stomach	stomach
8	chr15:62378400-62380200	Weak transcription	Fetal Lung	lung
9	chr15:62378600-62379600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr15:62378600-62379600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr15:62378600-62379600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr15:62378600-62379800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr15:62378600-62379800	Weak transcription	Fetal Muscle Leg	muscle

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