Variant report

Variant	rs62576045
Chromosome Location	chr9:136387366-136387367
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:136379966..136383646-chr9:136385055..136389168,4	MCF-7	breast:
2	chr9:136373550..136375691-chr9:136386455..136388624,2	MCF-7	breast:
3	chr9:136373965..136376176-chr9:136385397..136387787,2	K562	blood:
4	chr9:136342275..136345674-chr9:136385583..136388033,3	MCF-7	breast:
5	chr9:136386828..136388992-chr9:136391212..136394090,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000187616	Chromatin interaction
ENSG00000160326	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17150637	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2073871	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28433594	0.87[ASN][1000 genomes]
rs28521969	0.89[ASN][1000 genomes]
rs3763650	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62576048	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62576049	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62576050	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62576051	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9802272	0.91[ASN][1000 genomes]
rs9802273	0.98[ASN][1000 genomes]
rs9802318	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894059	chr9:136123840-136486929	Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv894077	chr9:136166346-136515297	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv894078	chr9:136194595-136484292	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
4	nsv933226	chr9:136224559-136407071	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv894081	chr9:136227260-136678954	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv894083	chr9:136281753-136452144	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv894084	chr9:136281753-136458311	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv894085	chr9:136281753-136478442	Bivalent Enhancer Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv894086	chr9:136281753-136657960	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	nsv894092	chr9:136311679-136452144	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv894093	chr9:136311679-136458311	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv894094	chr9:136311679-136528721	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
13	nsv530972	chr9:136324358-136643044	Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
14	nsv894097	chr9:136333356-136407208	Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv894098	chr9:136335824-136452144	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
16	nsv894099	chr9:136337168-136459543	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
17	nsv894100	chr9:136371224-136547602	Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv894101	chr9:136378650-136458311	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136377800-136388200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:136377800-136391400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:136378000-136388400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:136380000-136388800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr9:136380400-136390600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr9:136380400-136391000	Weak transcription	Right Atrium	heart
7	chr9:136380600-136390600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:136382000-136391400	Weak transcription	Ovary	ovary
9	chr9:136382400-136393400	Weak transcription	Spleen	Spleen
10	chr9:136384800-136387400	Enhancers	Brain Cingulate Gyrus	brain
11	chr9:136384800-136387600	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr9:136385000-136388400	Enhancers	Brain Substantia Nigra	brain
13	chr9:136385400-136387400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:136385400-136388600	Enhancers	Brain Hippocampus Middle	brain
15	chr9:136385400-136390600	Weak transcription	Fetal Kidney	kidney
16	chr9:136386000-136387400	Enhancers	Pancreas	Pancrea
17	chr9:136386000-136387800	Enhancers	Fetal Muscle Leg	muscle
18	chr9:136386200-136387600	Enhancers	Fetal Brain Male	brain
19	chr9:136386400-136391200	Weak transcription	Brain Angular Gyrus	brain
20	chr9:136386600-136387400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:136386800-136387400	Enhancers	Fetal Brain Female	brain
22	chr9:136386800-136387600	Enhancers	Primary T cells from cord blood	blood
23	chr9:136386800-136388400	Weak transcription	Fetal Lung	lung
24	chr9:136387000-136387400	Enhancers	Liver	Liver
25	chr9:136387000-136387800	Flanking Active TSS	Fetal Muscle Trunk	muscle
26	chr9:136387000-136387800	Enhancers	HSMM	muscle
27	chr9:136387000-136388600	Enhancers	Fetal Thymus	thymus
28	chr9:136387000-136389200	Enhancers	Placenta	Placenta
29	chr9:136387200-136387400	Flanking Active TSS	HSMMtube	muscle
30	chr9:136387200-136387800	Enhancers	Thymus	Thymus
31	chr9:136387200-136388000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr9:136387200-136388000	Bivalent Enhancer	HepG2	liver
33	chr9:136387200-136391400	Weak transcription	Brain Anterior Caudate	brain

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