Variant report

Variant	rs12295506
Chromosome Location	chr11:16531705-16531706
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:16527461..16531095-chr11:16531624..16535473,5	K562	blood:
2	chr11:16498104..16500817-chr11:16530790..16532770,2	K562	blood:

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10766326	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10766329	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10766331	0.92[EUR][1000 genomes]
rs10766337	0.83[EUR][1000 genomes]
rs10832613	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832614	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832615	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832622	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10832627	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10832628	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10832629	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10832635	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10832637	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10832639	0.92[EUR][1000 genomes]
rs10832640	0.92[EUR][1000 genomes]
rs10832642	0.90[EUR][1000 genomes]
rs10832643	0.86[EUR][1000 genomes]
rs10832647	0.85[EUR][1000 genomes]
rs10832648	0.84[EUR][1000 genomes]
rs11023948	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11023959	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11023960	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11023962	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11023981	0.92[EUR][1000 genomes]
rs11023988	0.86[EUR][1000 genomes]
rs11529132	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11529582	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12270317	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12271656	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12276256	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12283896	0.85[EUR][1000 genomes]
rs12289091	0.86[EUR][1000 genomes]
rs12289093	0.83[EUR][1000 genomes]
rs12574185	0.85[EUR][1000 genomes]
rs12575840	0.81[EUR][1000 genomes]
rs12576360	0.85[EUR][1000 genomes]
rs12794400	0.85[EUR][1000 genomes]
rs12806064	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34138863	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34840028	0.86[EUR][1000 genomes]
rs35223308	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4492775	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4511252	0.88[EUR][1000 genomes]
rs4525190	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4536174	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4603269	0.86[EUR][1000 genomes]
rs56965201	0.85[EUR][1000 genomes]
rs57248274	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60439454	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6486296	0.85[EUR][1000 genomes]
rs6486298	0.86[EUR][1000 genomes]
rs6486300	0.85[EUR][1000 genomes]
rs7103094	0.85[EUR][1000 genomes]
rs7112327	0.81[EUR][1000 genomes]
rs7115099	0.83[EUR][1000 genomes]
rs7117636	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7118874	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7126577	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7127280	0.83[EUR][1000 genomes]
rs7129286	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7924787	0.92[EUR][1000 genomes]
rs7927904	0.85[EUR][1000 genomes]
rs7928885	0.84[EUR][1000 genomes]
rs7935041	0.86[EUR][1000 genomes]
rs7937139	0.92[EUR][1000 genomes]
rs7942856	0.88[EUR][1000 genomes]
rs7943712	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7945295	0.90[EUR][1000 genomes]
rs7945898	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7948110	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9988855	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897016	chr11:16455794-16691743	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1035768	chr11:16530440-16578566	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2761650	chr11:16530452-16541623	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16510400-16533000	Weak transcription	Fetal Heart	heart
2	chr11:16528000-16533400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr11:16530800-16531800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:16530800-16531800	Enhancers	NHEK	skin
5	chr11:16531600-16532000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr11:16531600-16533000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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