Variant report

Variant	rs7163325
Chromosome Location	chr15:58661680-58661681
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10518972	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12905748	0.85[JPT][hapmap]
rs1444940	0.85[JPT][hapmap]
rs16940092	0.80[EUR][1000 genomes]
rs192330	0.97[EUR][1000 genomes]
rs261308	0.93[EUR][1000 genomes]
rs448183	0.84[EUR][1000 genomes]
rs56030675	0.85[EUR][1000 genomes]
rs60819793	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61422286	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72740825	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8035357	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047246	chr15:58375607-58707158	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS 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 miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv529717	chr15:58519923-58756814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1042201	chr15:58520746-58780710	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv569598	chr15:58552606-58852463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv904266	chr15:58580921-58689187	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1041779	chr15:58634768-58662280	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58656000-58663600	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr15:58661200-58662400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:58661200-58662400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr15:58661200-58662400	Enhancers	Liver	Liver
5	chr15:58661400-58661800	Enhancers	Primary T cells fromperipheralblood	blood
6	chr15:58661400-58661800	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr15:58661400-58661800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr15:58661400-58661800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr15:58661400-58661800	Flanking Active TSS	Duodenum Mucosa	Duodenum
10	chr15:58661400-58662000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr15:58661400-58662000	Active TSS	GM12878-XiMat	blood
12	chr15:58661400-58662000	Active TSS	HepG2	liver
13	chr15:58661400-58662200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:58661400-58662200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr15:58661400-58662200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr15:58661400-58662200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr15:58661400-58662400	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr15:58661400-58662400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr15:58661400-58662400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr15:58661400-58662400	Enhancers	Fetal Thymus	thymus
21	chr15:58661400-58662400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr15:58661400-58662400	Enhancers	HSMMtube	muscle
23	chr15:58661400-58662800	Enhancers	HSMM	muscle
24	chr15:58661600-58661800	Active TSS	Osteobl	bone
25	chr15:58661600-58662000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr15:58661600-58662000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr15:58661600-58662200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr15:58661600-58662200	Active TSS	NHLF	lung
29	chr15:58661600-58662400	Enhancers	Primary T cells from cord blood	blood
30	chr15:58661600-58662400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr15:58661600-58662400	Enhancers	Fetal Kidney	kidney

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