Variant report

Variant	rs10832452
Chromosome Location	chr11:15518925-15518926
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:15512584..15515913-chr11:15518069..15521001,3	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10734236	0.93[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10766257	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10766258	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10766260	0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10766263	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10766267	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10766268	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10766269	0.80[AFR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10766271	0.83[EUR][1000 genomes]
rs10832444	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10832446	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10832466	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10832467	0.95[ASN][1000 genomes]
rs10832471	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10832472	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10832474	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11023593	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11023595	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11023596	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11023597	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11023598	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11023599	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11023600	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11023609	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11023612	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12270000	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12272473	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12278599	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12284635	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2351044	0.86[ASN][1000 genomes]
rs2351046	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2351050	0.84[EUR][1000 genomes]
rs2351057	0.82[EUR][1000 genomes]
rs4032487	0.83[EUR][1000 genomes]
rs4129900	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4388847	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6486249	0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6486250	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6486251	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7106201	0.83[EUR][1000 genomes]
rs7106594	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7118895	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7130722	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7479720	0.92[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7927872	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7950188	0.97[ASN][1000 genomes]
rs9651572	0.85[AFR][1000 genomes];0.92[ASN][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	esv1809270	chr11:15504338-15528140	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15512200-15520400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:15514600-15523200	Enhancers	Fetal Intestine Large	intestine
3	chr11:15514800-15520200	Enhancers	Liver	Liver
4	chr11:15514800-15522400	Enhancers	Fetal Intestine Small	intestine
5	chr11:15515800-15522000	Weak transcription	Placenta	Placenta
6	chr11:15516400-15519000	Weak transcription	Psoas Muscle	Psoas
7	chr11:15516600-15519000	Weak transcription	Esophagus	oesophagus
8	chr11:15518200-15520000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr11:15518400-15519200	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr11:15518600-15519200	Enhancers	Fetal Lung	lung
11	chr11:15518600-15519200	Enhancers	Pancreas	Pancrea
12	chr11:15518600-15519600	Enhancers	Duodenum Mucosa	Duodenum
13	chr11:15518800-15519400	Enhancers	Fetal Muscle Leg	muscle
14	chr11:15518800-15520000	Enhancers	Stomach Mucosa	stomach

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