Variant report

Variant	rs265076
Chromosome Location	chr9:71151234-71151235
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:71150643..71152948-chr9:71155677..71157843,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181778	Chromatin interaction
ENSG00000226337	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10120859	0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs10746875	0.80[YRI][hapmap]
rs10780986	0.92[GIH][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs10868961	0.92[EUR][1000 genomes]
rs10869020	0.81[GIH][hapmap]
rs11142697	0.92[EUR][1000 genomes]
rs11789244	1.00[MEX][hapmap]
rs12238439	1.00[MEX][hapmap]
rs265073	0.97[GIH][hapmap]
rs265077	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs265078	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs265079	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs265083	0.88[TSI][hapmap]
rs398222	0.87[ASN][1000 genomes]
rs404994	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6560203	0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs7034863	0.92[EUR][1000 genomes]
rs7861495	0.81[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427847	chr9:70318730-71153527	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv893413	chr9:71130848-71196984	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv893411	chr9:71130848-71199545	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv893412	chr9:71130848-71199545	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1024967	chr9:71130848-71210031	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv482506	chr9:71130848-71280888	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv466392	chr9:71130848-71318817	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv614546	chr9:71130848-71318817	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1026962	chr9:71130848-71357605	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1032210	chr9:71130848-71511987	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
11	nsv893414	chr9:71139378-71320732	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr9:71131000-71152600	Weak transcription	NHLF	lung
2	chr9:71137600-71156000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:71139600-71161600	Weak transcription	Spleen	Spleen
4	chr9:71141400-71151800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:71145800-71151800	Weak transcription	Aorta	Aorta
6	chr9:71145800-71161600	Weak transcription	Gastric	stomach
7	chr9:71146200-71155400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr9:71146400-71151600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:71146400-71151800	Weak transcription	Placenta	Placenta
10	chr9:71146400-71151800	Weak transcription	Stomach Mucosa	stomach
11	chr9:71146400-71156000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr9:71146600-71151800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr9:71148000-71153800	Enhancers	Colon Smooth Muscle	Colon
14	chr9:71148000-71153800	Enhancers	Rectal Smooth Muscle	rectum
15	chr9:71148800-71151600	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr9:71148800-71152000	Weak transcription	Psoas Muscle	Psoas
17	chr9:71148800-71152000	Weak transcription	Right Atrium	heart
18	chr9:71148800-71156400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:71149000-71151600	Weak transcription	Fetal Intestine Large	intestine
20	chr9:71149000-71151600	Weak transcription	Fetal Stomach	stomach
21	chr9:71149000-71151800	Weak transcription	Fetal Lung	lung
22	chr9:71149000-71151800	Weak transcription	Left Ventricle	heart
23	chr9:71149200-71151800	Weak transcription	Fetal Intestine Small	intestine
24	chr9:71149200-71152000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:71149200-71154400	Weak transcription	Fetal Kidney	kidney
26	chr9:71149400-71155400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr9:71150200-71153800	Enhancers	HSMMtube	muscle
28	chr9:71150400-71153800	Enhancers	Fetal Muscle Leg	muscle
29	chr9:71150800-71153800	Enhancers	Fetal Heart	heart
30	chr9:71151000-71151400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr9:71151000-71151600	Weak transcription	Right Ventricle	heart

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