Variant report

Variant	rs71507372
Chromosome Location	chr9:13281032-13281033
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:13033734..13035793-chr9:13280439..13283221,2	K562	blood:
2	chr9:13278089..13282078-chr9:14313109..14316114,3	MCF-7	breast:
3	chr9:13275549..13278427-chr9:13279998..13281670,2	K562	blood:

Variant related genes	Relation type
ENSG00000147862	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10809923	1.00[ASN][1000 genomes]
rs10809926	1.00[ASN][1000 genomes]
rs11790299	1.00[ASN][1000 genomes]
rs13290727	1.00[ASN][1000 genomes]
rs13297131	1.00[ASN][1000 genomes]
rs1854665	1.00[ASN][1000 genomes]
rs1888150	1.00[ASN][1000 genomes]
rs1980994	1.00[ASN][1000 genomes]
rs2149988	1.00[ASN][1000 genomes]
rs34101279	1.00[ASN][1000 genomes]
rs34161313	0.83[AMR][1000 genomes]
rs34306347	0.86[AMR][1000 genomes]
rs34423860	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34504254	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34714632	1.00[ASN][1000 genomes]
rs34862901	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4392997	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7047995	1.00[ASN][1000 genomes]
rs713497	0.83[AMR][1000 genomes]
rs71507376	0.83[AMR][1000 genomes]
rs7866658	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892578	chr9:12942956-13485035	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv892583	chr9:13166139-13350478	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv892584	chr9:13214871-13350478	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS 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
4	nsv427838	chr9:13229753-13393890	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13278800-13281200	Weak transcription	Fetal Heart	heart
2	chr9:13279800-13284200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:13280200-13281200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:13280200-13281800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:13280200-13282000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:13280200-13282400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:13280200-13282400	Weak transcription	NH-A	brain
8	chr9:13280200-13282600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:13280200-13282600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr9:13280200-13282600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:13280200-13282600	Weak transcription	NHDF-Ad	bronchial
12	chr9:13280200-13283000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:13280200-13283200	Weak transcription	Fetal Lung	lung
14	chr9:13280200-13283400	Weak transcription	Rectal Smooth Muscle	rectum
15	chr9:13280200-13283600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr9:13280200-13284000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:13280200-13284000	Enhancers	Colon Smooth Muscle	Colon
18	chr9:13280200-13284000	Weak transcription	Fetal Kidney	kidney
19	chr9:13280200-13284000	Weak transcription	NHLF	lung
20	chr9:13280200-13284400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:13280200-13285200	Weak transcription	Ovary	ovary
22	chr9:13280200-13295600	Weak transcription	Aorta	Aorta
23	chr9:13280400-13281200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:13280400-13281600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:13280400-13282600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:13280800-13281400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr9:13281000-13281200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr9:13281000-13281200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr9:13281000-13282400	Weak transcription	Fetal Stomach	stomach
30	chr9:13281000-13283800	Enhancers	Osteobl	bone

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