Variant report

Variant	rs11150651
Chromosome Location	chr16:31936095-31936096
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:31930170..31932707-chr16:31934024..31936447,2	K562	blood:
2	chr16:31926461..31927983-chr16:31935855..31938647,2	K562	blood:
3	chr16:31929972..31932646-chr16:31933691..31936236,4	MCF-7	breast:
4	chr16:31932491..31936311-chr16:31936605..31941493,6	K562	blood:
5	chr16:31929792..31932707-chr16:31934299..31936447,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10871460	0.83[EUR][1000 genomes]
rs11150650	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12444740	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12599066	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12919368	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12924931	0.89[EUR][1000 genomes]
rs1827959	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1828131	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1857943	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2358778	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3843960	1.00[ASW][hapmap];0.98[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3843961	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3850114	0.87[LWK][hapmap];0.85[MKK][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3861268	1.00[ASW][hapmap];0.98[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3861270	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913868	1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913870	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913871	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4026652	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4026653	0.97[AFR][1000 genomes]
rs4026654	1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4402587	0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889517	1.00[ASW][hapmap];0.98[LWK][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889518	1.00[ASW][hapmap];0.98[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889563	0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4889565	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889567	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889568	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889569	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6565290	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6565291	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7185691	0.88[AFR][1000 genomes]
rs7197804	0.82[LWK][hapmap];0.84[MKK][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7200162	1.00[ASW][hapmap];0.80[LWK][hapmap];0.91[MKK][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7202831	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7203345	0.89[MKK][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7205034	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8048908	1.00[ASW][hapmap];0.98[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs8056158	0.86[EUR][1000 genomes]
rs8058598	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8059500	1.00[CHD][hapmap];0.86[LWK][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8060276	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9788838	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9921760	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9924259	0.82[ASW][hapmap];0.94[MKK][hapmap]
rs9928574	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9928704	1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv833196	chr16:31897381-32068953	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv1850460	chr16:31905688-32097085	Strong transcription ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv974735	chr16:31933472-31947343	ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1848653	chr16:31934245-32394874	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31931200-31936600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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