Variant report

Variant	rs34568491
Chromosome Location	chr9:118131944-118131945
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs13284742	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13286646	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs13287390	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs13290701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13293715	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13298466	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13300423	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs13301268	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13301972	1.00[AFR][1000 genomes]
rs2188042	1.00[AFR][1000 genomes]
rs34302658	1.00[AFR][1000 genomes]
rs34313216	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs34321307	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs34466382	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34471912	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs34581742	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34705596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34728021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34748014	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34816653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34900397	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs34928792	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34938648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35132145	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35203429	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35259015	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs35365687	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35433621	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35468444	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs35483504	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs35643606	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs35770937	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35976675	1.00[AFR][1000 genomes]
rs36001303	0.95[AMR][1000 genomes]
rs36007561	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36078239	1.00[AFR][1000 genomes]
rs4344149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56199075	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs57096760	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs60262778	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71505542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71505544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71505545	0.86[ASN][1000 genomes]
rs71505548	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv948346	chr9:118107565-118718197	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv2761552	chr9:118113846-118157488	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118119600-118135800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:118128600-118132200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:118129400-118132200	Enhancers	Osteobl	bone
4	chr9:118129800-118132200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:118129800-118132200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:118129800-118132400	Enhancers	NHLF	lung
7	chr9:118129800-118133200	Enhancers	NHDF-Ad	bronchial
8	chr9:118130000-118135200	Weak transcription	Stomach Mucosa	stomach
9	chr9:118130400-118132200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr9:118130400-118132200	Enhancers	HMEC	breast
11	chr9:118130600-118134600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:118130600-118142400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr9:118130800-118134600	Weak transcription	NH-A	brain
14	chr9:118130800-118135200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:118131000-118132200	Enhancers	NHEK	skin
16	chr9:118131000-118135200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:118131200-118132200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr9:118131200-118132200	Enhancers	Fetal Muscle Leg	muscle
19	chr9:118131200-118132200	Enhancers	Fetal Stomach	stomach
20	chr9:118131200-118133200	Enhancers	Fetal Lung	lung
21	chr9:118131200-118135200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:118131400-118132000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr9:118131400-118132000	Enhancers	Fetal Kidney	kidney
24	chr9:118131400-118132200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr9:118131400-118132400	Enhancers	Fetal Brain Male	brain
26	chr9:118131400-118132600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr9:118131600-118132200	Enhancers	Colon Smooth Muscle	Colon
28	chr9:118131600-118132200	Enhancers	HSMM	muscle
29	chr9:118131600-118132200	Enhancers	HSMMtube	muscle
30	chr9:118131600-118132400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:118131800-118132200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:118131800-118132200	Enhancers	Adipose Nuclei	Adipose
33	chr9:118131800-118132200	Enhancers	Fetal Brain Female	brain
34	chr9:118131800-118132400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:118131800-118132800	Enhancers	A549	lung

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