Variant report

Variant	rs10967787
Chromosome Location	chr9:27227229-27227230
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10121367	0.89[ASN][1000 genomes]
rs10812539	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10967780	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10967781	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10967782	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10967783	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10967784	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10967786	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12337434	0.88[ASN][1000 genomes]
rs12338101	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12341363	0.92[ASN][1000 genomes]
rs12348510	0.82[AFR][1000 genomes]
rs12350032	0.94[ASN][1000 genomes]
rs12352222	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1322048	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1885381	0.90[ASN][1000 genomes]
rs2273715	0.88[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2273719	0.80[ASN][1000 genomes]
rs2275083	0.86[ASN][1000 genomes]
rs2756901	0.87[ASN][1000 genomes]
rs473205	0.84[AMR][1000 genomes]
rs4878366	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4879268	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs561708	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6475977	0.87[ASN][1000 genomes]
rs7874391	0.89[ASN][1000 genomes]
rs7874514	0.89[ASN][1000 genomes]
rs9886732	0.88[AFR][1000 genomes]
rs9886857	0.85[AFR][1000 genomes]
rs9987817	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016733	chr9:27073650-27264576	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1022313	chr9:27083369-27250505	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1017802	chr9:27088160-27262682	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1019104	chr9:27088160-27358206	Enhancers Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv892864	chr9:27176554-27296705	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv466335	chr9:27179244-27234029	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv613946	chr9:27179244-27234029	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1027482	chr9:27195840-27233157	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1018864	chr9:27195840-27294815	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv2761268	chr9:27195852-27291261	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv466336	chr9:27196119-27292703	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv471294	chr9:27196119-27292703	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv613947	chr9:27196119-27292703	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1033002	chr9:27199373-27232601	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv892865	chr9:27217992-27258216	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27151000-27229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:27166200-27229000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:27180800-27230600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr9:27196800-27228800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr9:27211800-27231600	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr9:27213000-27232800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:27215600-27229400	Weak transcription	Osteobl	bone
8	chr9:27219000-27231600	Weak transcription	Fetal Lung	lung
9	chr9:27219400-27230400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr9:27220800-27230000	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:27221000-27227600	Weak transcription	Liver	Liver
12	chr9:27221200-27229000	Weak transcription	Lung	lung
13	chr9:27221400-27230200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr9:27221600-27228800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:27221800-27229000	Weak transcription	Fetal Stomach	stomach
16	chr9:27222000-27230800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr9:27222800-27227400	Weak transcription	Left Ventricle	heart
18	chr9:27222800-27227600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:27223000-27230600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr9:27223200-27229000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:27226000-27231200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr9:27226200-27230600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:27226400-27227600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:27226400-27229200	Strong transcription	Ovary	ovary
25	chr9:27226800-27227800	Enhancers	Hela-S3	cervix
26	chr9:27226800-27228200	Enhancers	Placenta	Placenta
27	chr9:27227000-27228000	Genic enhancers	Adipose Nuclei	Adipose
28	chr9:27227000-27229400	ZNF genes & repeats	Aorta	Aorta
29	chr9:27227200-27229400	Strong transcription	HUVEC	blood vessel
30	chr9:27227200-27230000	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr9:27227200-27230000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:27227200-27230600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung

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