Variant report

Variant	rs9889186
Chromosome Location	chr16:81449737-81449738
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1075353	1.00[ASW][hapmap]
rs11861861	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11866931	1.00[EUR][1000 genomes]
rs13335052	1.00[EUR][1000 genomes]
rs16955319	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34441922	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34797363	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4613060	1.00[EUR][1000 genomes]
rs7186064	0.89[EUR][1000 genomes]
rs7186540	0.89[EUR][1000 genomes]
rs7188374	1.00[EUR][1000 genomes]
rs7191231	0.89[EUR][1000 genomes]
rs7191804	0.89[EUR][1000 genomes]
rs7201488	0.89[EUR][1000 genomes]
rs7205597	1.00[EUR][1000 genomes]
rs72835160	1.00[EUR][1000 genomes]
rs72835164	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72835165	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72835171	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72835178	0.89[EUR][1000 genomes]
rs8046466	0.89[EUR][1000 genomes]
rs9888977	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9889135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9889175	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9889196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9927898	0.89[EUR][1000 genomes]
rs9935485	1.00[EUR][1000 genomes]
rs9940535	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532569	chr16:80980356-81700149	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1058519	chr16:81177767-81735333	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	nsv948448	chr16:81198147-81906766	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
4	nsv1061359	chr16:81349826-81471867	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
5	nsv542992	chr16:81349826-81471867	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81447800-81449800	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr16:81447800-81450000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr16:81447800-81450000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr16:81447800-81451200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr16:81448000-81449800	Enhancers	Fetal Brain Male	brain
6	chr16:81448000-81450000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:81448000-81450000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr16:81448000-81450200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr16:81448000-81450600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr16:81448400-81451000	Enhancers	A549	lung
11	chr16:81448600-81451000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:81448600-81453200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr16:81449200-81449800	Flanking Active TSS	Fetal Brain Female	brain
14	chr16:81449200-81450600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr16:81449200-81451200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr16:81449400-81449800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr16:81449400-81449800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:81449400-81449800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr16:81449400-81449800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr16:81449400-81449800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr16:81449400-81449800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr16:81449400-81449800	Enhancers	Brain Angular Gyrus	brain
23	chr16:81449400-81449800	Enhancers	Brain Anterior Caudate	brain
24	chr16:81449400-81449800	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr16:81449400-81450000	Bivalent Enhancer	Fetal Stomach	stomach
26	chr16:81449400-81451000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr16:81449600-81449800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr16:81449600-81449800	Enhancers	Brain Cingulate Gyrus	brain
29	chr16:81449600-81449800	Enhancers	Brain Germinal Matrix	brain
30	chr16:81449600-81449800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr16:81449600-81449800	Enhancers	NH-A	brain

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