Variant report

Variant	rs35732576
Chromosome Location	chr15:58759537-58759538
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:58758492..58760005-chr15:58885829..58888502,2	MCF-7	breast:
2	chr15:58624699..58626357-chr15:58758259..58760422,2	MCF-7	breast:
3	chr15:58754820..58757599-chr15:58758355..58762013,3	K562	blood:
4	chr15:58681878..58684869-chr15:58759181..58760747,2	MCF-7	breast:
5	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:
6	chr15:58758655..58760808-chr15:58812229..58814183,2	MCF-7	breast:
7	chr15:58758547..58760128-chr15:58777523..58780209,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259476	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10518978	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634902	0.87[ASN][1000 genomes]
rs12591216	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12591624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12592407	0.85[ASN][1000 genomes]
rs12593736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12593880	0.83[ASN][1000 genomes]
rs12594222	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12595191	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12900891	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12902119	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12903955	0.81[ASN][1000 genomes]
rs12904507	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12906459	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12908427	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12910028	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12910602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12913605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16940338	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17190580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17190587	0.87[ASN][1000 genomes]
rs2414581	0.85[ASN][1000 genomes]
rs28478642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28713618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2899630	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34053638	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34225834	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34297592	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34570549	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34577128	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34744603	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35633916	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35771822	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35795657	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4775053	0.87[ASN][1000 genomes]
rs6494009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6494010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6494011	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71478667	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71478668	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs71478670	0.81[ASN][1000 genomes]
rs71478671	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71478672	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7162384	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7162603	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7165752	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7169744	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7172556	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7174539	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8029592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8029837	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8041525	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][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	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
2	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
3	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
4	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
5	nsv904267	chr15:58699010-58769583	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1047048	chr15:58701400-58784800	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv3362898	chr15:58705732-58850860	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv457173	chr15:58731567-58779039	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv569600	chr15:58731567-58779039	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1043041	chr15:58744505-58876327	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58737400-58761800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:58743800-58770400	Enhancers	Fetal Thymus	thymus
3	chr15:58752400-58761800	Weak transcription	Right Atrium	heart
4	chr15:58752600-58760200	Weak transcription	Hela-S3	cervix
5	chr15:58752800-58765000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:58753000-58760400	Weak transcription	Pancreas	Pancrea
7	chr15:58754000-58760000	Weak transcription	Spleen	Spleen
8	chr15:58755000-58759600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr15:58755400-58760400	Weak transcription	Fetal Intestine Small	intestine
10	chr15:58755400-58765000	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr15:58755400-58765000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr15:58755600-58759800	Enhancers	GM12878-XiMat	blood
13	chr15:58755600-58759800	Weak transcription	NH-A	brain
14	chr15:58755600-58760400	Weak transcription	NHEK	skin
15	chr15:58755600-58760800	Weak transcription	HMEC	breast
16	chr15:58755600-58761400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:58755600-58763600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr15:58755800-58761000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr15:58755800-58761400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:58755800-58762200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr15:58755800-58765800	Weak transcription	Gastric	stomach
22	chr15:58756800-58761400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr15:58757000-58760000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:58757000-58760200	Weak transcription	A549	lung
25	chr15:58757200-58763000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:58757600-58761000	Enhancers	HSMMtube	muscle
27	chr15:58757800-58759600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr15:58757800-58761600	Enhancers	HSMM	muscle
29	chr15:58758000-58761800	Weak transcription	Dnd41	blood
30	chr15:58758200-58761400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:58758200-58761600	Weak transcription	Osteobl	bone
32	chr15:58758400-58761600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr15:58758600-58761000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:58758600-58761400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr15:58758600-58764000	Weak transcription	Thymus	Thymus
36	chr15:58758800-58759800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:58759000-58760400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:58759000-58761400	Weak transcription	NHDF-Ad	bronchial
39	chr15:58759000-58761400	Weak transcription	NHLF	lung
40	chr15:58759400-58759600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr15:58759400-58759600	Enhancers	H9 Cell Line	embryonic stem cell
42	chr15:58759400-58759600	Flanking Active TSS	Fetal Kidney	kidney
43	chr15:58759400-58759600	Enhancers	Fetal Lung	lung
44	chr15:58759400-58759600	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr15:58759400-58759800	Flanking Active TSS	Ovary	ovary
46	chr15:58759400-58760000	Flanking Active TSS	Liver	Liver
47	chr15:58759400-58760200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:58759400-58760600	Enhancers	Duodenum Mucosa	Duodenum
49	chr15:58759400-58760600	Enhancers	Fetal Intestine Large	intestine
50	chr15:58759400-58760600	Enhancers	K562	blood

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