Variant report

Variant	rs6495011
Chromosome Location	chr15:72880682-72880683
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:72880288-72882010	A549	lung:	n/a	n/a
2	POLR2A	chr15:72875838-72883343	K562	blood:	n/a	n/a
3	POLR2A	chr15:72880632-72880715	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:72880166..72881914-chr15:73065144..73067658,2	K562	blood:
2	chr15:72523201..72524932-chr15:72878327..72881016,2	MCF-7	breast:
3	chr15:72788089..72790886-chr15:72879625..72881509,2	K562	blood:

Variant related genes	Relation type
ENSG00000260534	TF binding region
ENSG00000067225	Chromatin interaction
ENSG00000159322	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10438370	0.82[AMR][1000 genomes]
rs10775206	0.82[AMR][1000 genomes]
rs10851858	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11072365	0.81[ASN][1000 genomes]
rs11072376	0.82[AMR][1000 genomes]
rs11072379	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1133316	0.83[AMR][1000 genomes]
rs1160608	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11631125	0.83[EUR][1000 genomes]
rs11636825	0.82[AMR][1000 genomes]
rs11637103	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11855682	0.83[EUR][1000 genomes]
rs12439018	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12900846	0.81[AMR][1000 genomes]
rs12901966	0.82[AMR][1000 genomes]
rs12908610	0.81[EUR][1000 genomes]
rs12910393	0.81[EUR][1000 genomes]
rs1374092	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1562250	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2278694	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2415135	0.81[AMR][1000 genomes]
rs2415139	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2415141	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3842946	0.81[AMR][1000 genomes]
rs4146286	0.81[AMR][1000 genomes]
rs4776601	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4776602	0.82[AMR][1000 genomes]
rs4776603	0.82[AMR][1000 genomes]
rs4777512	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4777514	0.82[AMR][1000 genomes]
rs4777517	0.86[AMR][1000 genomes]
rs4777520	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7177472	0.81[AMR][1000 genomes]
rs7496556	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7497390	0.82[AMR][1000 genomes]
rs7497793	0.82[AMR][1000 genomes]
rs8037282	0.82[AMR][1000 genomes]
rs8038734	0.81[AMR][1000 genomes]
rs8038934	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534037	chr15:72659210-72964029	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats 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 miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv2758386	chr15:72819785-73120560	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	esv2760039	chr15:72819785-73120560	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
4	nsv428307	chr15:72819785-73120560	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	esv3430383	chr15:72821093-73035167	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72829200-72880800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:72841000-72909000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr15:72850200-72880800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr15:72857400-72881000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr15:72870400-72881600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr15:72870800-72887800	Weak transcription	Right Ventricle	heart
7	chr15:72870800-72896400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:72870800-72902200	Weak transcription	Gastric	stomach
9	chr15:72871600-72889400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:72873400-72883800	Weak transcription	Aorta	Aorta
11	chr15:72873600-72884400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:72874800-72882200	Weak transcription	Small Intestine	intestine
13	chr15:72874800-72899800	Weak transcription	Fetal Stomach	stomach
14	chr15:72876000-72883600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr15:72876200-72882000	Weak transcription	Fetal Brain Male	brain
16	chr15:72876200-72903400	Weak transcription	Brain Germinal Matrix	brain
17	chr15:72876200-72907800	Weak transcription	Brain Substantia Nigra	brain
18	chr15:72876400-72903800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr15:72876600-72883800	Weak transcription	HSMMtube	muscle
20	chr15:72876800-72880800	Weak transcription	Psoas Muscle	Psoas
21	chr15:72876800-72882000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:72876800-72882600	Weak transcription	Pancreas	Pancrea
23	chr15:72876800-72883000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr15:72876800-72883400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:72876800-72907600	Weak transcription	Lung	lung
26	chr15:72877200-72881400	Weak transcription	HUVEC	blood vessel
27	chr15:72877200-72883200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr15:72877400-72881000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:72877400-72881800	Weak transcription	Dnd41	blood
30	chr15:72877400-72881800	Weak transcription	NHEK	skin
31	chr15:72877600-72882400	Weak transcription	Brain Hippocampus Middle	brain
32	chr15:72877600-72883200	Weak transcription	Fetal Lung	lung
33	chr15:72877600-72889400	Weak transcription	Rectal Smooth Muscle	rectum
34	chr15:72877800-72882000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr15:72877800-72883200	Weak transcription	Brain Anterior Caudate	brain
36	chr15:72877800-72910000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr15:72878000-72882600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr15:72878200-72880800	Weak transcription	Brain Cingulate Gyrus	brain
39	chr15:72878200-72884800	Weak transcription	Primary T cells from cord blood	blood
40	chr15:72878400-72880800	Weak transcription	Primary B cells from cord blood	blood
41	chr15:72878400-72880800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr15:72878400-72880800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr15:72878400-72881400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr15:72878400-72881400	Weak transcription	HepG2	liver
45	chr15:72878400-72881600	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr15:72878400-72882000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr15:72878400-72882400	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr15:72878400-72882800	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr15:72878400-72883200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr15:72878400-72883400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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