Variant report

Variant	rs10832712
Chromosome Location	chr11:17017080-17017081
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10741719	0.81[AFR][1000 genomes]
rs10741720	0.81[AFR][1000 genomes]
rs10766366	0.90[EUR][1000 genomes]
rs10766367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10766368	0.84[ASN][1000 genomes]
rs10766370	0.81[AFR][1000 genomes]
rs10832707	0.92[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10832709	0.93[AFR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10832710	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10832713	0.90[AFR][1000 genomes]
rs10832716	0.80[AFR][1000 genomes]
rs10832717	0.81[AFR][1000 genomes]
rs11024101	0.80[ASN][1000 genomes]
rs11024102	0.80[ASN][1000 genomes]
rs11024103	0.92[ASN][1000 genomes]
rs11024110	0.81[ASN][1000 genomes]
rs11529141	0.92[EUR][1000 genomes]
rs12575487	0.84[ASN][1000 genomes]
rs1468489	0.90[AFR][1000 genomes]
rs2302207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2353369	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4237715	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4237716	0.91[EUR][1000 genomes]
rs4469869	0.91[EUR][1000 genomes]
rs4562807	0.81[AFR][1000 genomes]
rs4756882	0.84[AFR][1000 genomes]
rs4756883	0.81[AFR][1000 genomes]
rs4757468	0.90[EUR][1000 genomes]
rs4757470	0.90[EUR][1000 genomes]
rs4757472	0.94[AFR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4757473	0.91[EUR][1000 genomes]
rs4757474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757475	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757476	0.92[EUR][1000 genomes]
rs4757479	0.81[AFR][1000 genomes]
rs4757482	0.84[AFR][1000 genomes]
rs4757484	0.84[AFR][1000 genomes]
rs6486332	0.81[AFR][1000 genomes]
rs6486333	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6486334	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6486335	0.88[AFR][1000 genomes]
rs7118307	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7122802	0.92[EUR][1000 genomes]
rs7928955	0.80[AFR][1000 genomes]
rs7930890	0.88[AFR][1000 genomes]
rs7931025	0.84[AFR][1000 genomes]
rs7933984	0.81[AFR][1000 genomes]
rs7934567	0.92[EUR][1000 genomes]
rs7937479	0.84[AFR][1000 genomes]
rs7940499	0.90[AFR][1000 genomes]
rs7944490	0.92[EUR][1000 genomes]
rs7947297	0.81[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832077	chr11:16834545-17059176	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17004800-17034200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:17006400-17034000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:17009400-17032600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:17009600-17017600	Weak transcription	Ovary	ovary
5	chr11:17009800-17018000	Weak transcription	Spleen	Spleen
6	chr11:17009800-17018800	Weak transcription	A549	lung
7	chr11:17009800-17030000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr11:17009800-17032600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr11:17009800-17032600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr11:17010000-17019000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:17010000-17023000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:17012400-17024200	Enhancers	Stomach Mucosa	stomach
13	chr11:17013400-17018000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr11:17013400-17033800	Weak transcription	Brain Substantia Nigra	brain
15	chr11:17014000-17017600	Weak transcription	Brain Anterior Caudate	brain
16	chr11:17014000-17023400	Weak transcription	Fetal Stomach	stomach
17	chr11:17014000-17025000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:17014200-17019200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:17014200-17021200	Genic enhancers	Fetal Intestine Small	intestine
20	chr11:17014200-17021400	Enhancers	Fetal Intestine Large	intestine
21	chr11:17014400-17018600	Enhancers	Duodenum Mucosa	Duodenum
22	chr11:17014400-17019000	Enhancers	Liver	Liver
23	chr11:17014600-17017800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:17014600-17019000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:17014600-17021000	Enhancers	Pancreas	Pancrea
26	chr11:17014800-17018600	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr11:17015000-17024800	Enhancers	Gastric	stomach
28	chr11:17015200-17017800	Weak transcription	Small Intestine	intestine
29	chr11:17015600-17018600	Enhancers	Colonic Mucosa	Colon
30	chr11:17015800-17017800	Weak transcription	Right Atrium	heart
31	chr11:17016000-17017200	Weak transcription	Fetal Heart	heart
32	chr11:17016000-17022600	Weak transcription	Esophagus	oesophagus
33	chr11:17016200-17017600	Weak transcription	Left Ventricle	heart
34	chr11:17016400-17017800	Weak transcription	HepG2	liver
35	chr11:17016400-17019400	Enhancers	Adipose Nuclei	Adipose
36	chr11:17016400-17034600	Weak transcription	Aorta	Aorta
37	chr11:17016600-17017800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr11:17016600-17030800	Weak transcription	Fetal Kidney	kidney
39	chr11:17016800-17017800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr11:17017000-17017400	Weak transcription	Right Ventricle	heart
41	chr11:17017000-17017600	Enhancers	Brain Hippocampus Middle	brain
42	chr11:17017000-17017800	Weak transcription	Lung	lung

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