Variant report

Variant	rs11524180
Chromosome Location	chr9:8328459-8328460
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10758952	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10758954	0.81[ASN][1000 genomes]
rs10815822	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10976953	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10976960	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976962	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11521513	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11521514	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12551994	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12555185	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12682697	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12682993	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12684196	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12684395	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12684864	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12685966	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16927547	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2173711	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3739579	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3780336	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3847288	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3847291	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4008212	0.83[EUR][1000 genomes]
rs4008216	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60965360	0.80[ASN][1000 genomes]
rs7042854	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72710309	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7848455	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7848705	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7848818	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7854665	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][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	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	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
3	nsv892224	chr9:8263737-8338431	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8312200-8338200	Weak transcription	Brain Angular Gyrus	brain
2	chr9:8313800-8329400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:8316000-8329600	Weak transcription	Ovary	ovary
4	chr9:8318200-8329000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:8323400-8329000	Weak transcription	Fetal Lung	lung
6	chr9:8323400-8329400	Weak transcription	Brain Anterior Caudate	brain
7	chr9:8323400-8341600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:8323800-8329600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr9:8323800-8329600	Weak transcription	Brain Hippocampus Middle	brain
10	chr9:8323800-8329800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:8323800-8341600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:8324000-8345000	Weak transcription	Fetal Brain Male	brain
13	chr9:8324200-8328800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:8324200-8329400	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr9:8324400-8337400	Weak transcription	Brain Germinal Matrix	brain
16	chr9:8326400-8329200	Weak transcription	Fetal Brain Female	brain
17	chr9:8326400-8331000	Weak transcription	Fetal Kidney	kidney
18	chr9:8326800-8337400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr9:8327000-8329200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr9:8327200-8338000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr9:8327400-8329000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr9:8327600-8329200	Weak transcription	Fetal Stomach	stomach
23	chr9:8328000-8338000	Weak transcription	Dnd41	blood
24	chr9:8328200-8338600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:8328400-8329200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:8328400-8330200	Strong transcription	Fetal Muscle Leg	muscle
27	chr9:8328400-8330600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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