Variant report

Variant	rs16927668
Chromosome Location	chr9:8369533-8369534
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10511491	0.91[CHB][hapmap]
rs10732364	0.82[CHB][hapmap]
rs10739157	0.96[CHB][hapmap];0.87[JPT][hapmap]
rs10739158	0.91[CHB][hapmap]
rs10739159	0.91[CHB][hapmap]
rs10739160	0.85[CHB][hapmap]
rs10758961	0.87[ASN][1000 genomes]
rs10758963	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10758964	0.95[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10758965	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10758966	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10758967	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10815823	0.87[CHB][hapmap]
rs10815827	0.83[CHB][hapmap]
rs10815828	0.91[CHB][hapmap]
rs10815832	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs10976987	1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10977006	0.95[CHB][hapmap]
rs10977014	0.81[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]
rs1156294	0.82[CHB][hapmap]
rs1392518	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1392519	0.82[CEU][hapmap];0.83[CHB][hapmap]
rs1500321	0.87[CHB][hapmap];0.80[JPT][hapmap]
rs1500322	0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1500323	0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs20513	0.81[CHB][hapmap]
rs2310	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2381741	0.82[CEU][hapmap];0.83[CHB][hapmap]
rs35972185	0.86[ASN][1000 genomes]
rs3736381	0.95[CHB][hapmap]
rs3765142	0.95[CHB][hapmap]
rs3847290	0.83[CHB][hapmap]
rs4740935	0.83[CHB][hapmap]
rs4740936	0.83[CHB][hapmap]
rs4740937	0.86[CHB][hapmap]
rs4740939	0.83[CHB][hapmap]
rs4740940	0.83[CHB][hapmap]
rs4740941	0.83[CHB][hapmap]
rs4742488	0.95[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs4742490	0.91[CHB][hapmap]
rs6477294	0.82[CHB][hapmap]
rs6477295	0.81[CHB][hapmap]
rs6477299	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs7018576	0.82[CHB][hapmap]
rs7022162	0.82[CHB][hapmap]
rs7032880	0.87[CHB][hapmap]
rs7038767	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs7851892	0.83[CHB][hapmap]
rs7853112	0.87[CHB][hapmap]
rs7856922	0.83[CHB][hapmap]
rs7857177	0.91[CHB][hapmap]
rs7864500	1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.88[ASN][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	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv892225	chr9:8345072-8379313	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8339600-8397600	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:8341800-8372600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr9:8350200-8372400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:8357200-8374200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:8357600-8381800	Weak transcription	Aorta	Aorta
6	chr9:8361400-8401600	Weak transcription	Fetal Muscle Trunk	muscle
7	chr9:8364600-8370400	Weak transcription	Fetal Lung	lung
8	chr9:8364600-8382200	Weak transcription	Ovary	ovary
9	chr9:8364800-8376000	Weak transcription	Fetal Brain Male	brain
10	chr9:8364800-8377200	Weak transcription	Fetal Brain Female	brain
11	chr9:8364800-8401600	Weak transcription	Brain Germinal Matrix	brain
12	chr9:8365000-8395400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr9:8365200-8386800	Weak transcription	Brain Anterior Caudate	brain
14	chr9:8365600-8376600	Weak transcription	Brain Substantia Nigra	brain
15	chr9:8365600-8386200	Weak transcription	Brain Angular Gyrus	brain
16	chr9:8365600-8386200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr9:8365800-8375800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:8366800-8370200	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr9:8366800-8373000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:8366800-8383000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr9:8367000-8371600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:8367200-8394600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr9:8367200-8399800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:8367600-8376200	Weak transcription	Brain Hippocampus Middle	brain

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