Variant report

Variant	rs72700365
Chromosome Location	chr9:8691371-8691372
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1337807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55651018	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55664033	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55789848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55803510	1.00[AMR][1000 genomes]
rs56032582	1.00[EUR][1000 genomes]
rs56055933	1.00[EUR][1000 genomes]
rs56236902	1.00[EUR][1000 genomes]
rs56272971	1.00[EUR][1000 genomes]
rs56349253	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72696673	1.00[AMR][1000 genomes]
rs72696686	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72698226	1.00[EUR][1000 genomes]
rs72698230	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72698242	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72698248	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72698252	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72698257	1.00[EUR][1000 genomes]
rs72698260	1.00[EUR][1000 genomes]
rs72698261	1.00[EUR][1000 genomes]
rs72698262	1.00[EUR][1000 genomes]
rs72698266	1.00[EUR][1000 genomes]
rs72698268	1.00[EUR][1000 genomes]
rs72698270	1.00[EUR][1000 genomes]
rs72698271	1.00[EUR][1000 genomes]
rs72698274	1.00[EUR][1000 genomes]
rs72698277	1.00[EUR][1000 genomes]
rs72698280	1.00[EUR][1000 genomes]
rs72698282	1.00[EUR][1000 genomes]
rs72698283	1.00[EUR][1000 genomes]
rs72698285	1.00[EUR][1000 genomes]
rs72698286	1.00[EUR][1000 genomes]
rs72698287	1.00[EUR][1000 genomes]
rs72698288	1.00[EUR][1000 genomes]
rs72698289	1.00[EUR][1000 genomes]
rs72698296	1.00[EUR][1000 genomes]
rs72698299	1.00[EUR][1000 genomes]
rs72698302	1.00[EUR][1000 genomes]
rs72700303	1.00[EUR][1000 genomes]
rs72700310	1.00[EUR][1000 genomes]
rs72700312	1.00[EUR][1000 genomes]
rs72700315	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72700317	1.00[EUR][1000 genomes]
rs72700319	1.00[EUR][1000 genomes]
rs72700321	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72700323	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72700327	1.00[EUR][1000 genomes]
rs72700338	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72700346	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72700348	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv892228	chr9:8482778-8703733	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv892232	chr9:8645448-8698875	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv892233	chr9:8645448-8702964	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv892234	chr9:8645448-8703733	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8679800-8696400	Weak transcription	Ovary	ovary
2	chr9:8680000-8693000	Weak transcription	Fetal Brain Female	brain
3	chr9:8680000-8694800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr9:8682000-8694800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr9:8683000-8706000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr9:8683400-8696000	Weak transcription	Fetal Lung	lung
7	chr9:8683600-8693000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr9:8684200-8693000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:8686400-8693600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:8690000-8693000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:8690000-8693000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:8690400-8695000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:8691000-8691400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr9:8691000-8691400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr9:8691000-8691400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr9:8691000-8691600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr9:8691000-8692000	Enhancers	Brain Anterior Caudate	brain
18	chr9:8691000-8692200	Enhancers	Brain Angular Gyrus	brain
19	chr9:8691000-8693800	Enhancers	Brain Substantia Nigra	brain
20	chr9:8691200-8691400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr9:8691200-8693800	Enhancers	Brain Cingulate Gyrus	brain
22	chr9:8691200-8693800	Enhancers	Brain Hippocampus Middle	brain

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