Variant report

Variant	rs17695026
Chromosome Location	chr9:27155031-27155032
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10511803	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10967734	0.82[EUR][1000 genomes]
rs12337860	0.94[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12340500	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs12343345	0.81[EUR][1000 genomes]
rs12350086	0.81[EUR][1000 genomes]
rs12352474	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17694796	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17756599	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17756667	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17756685	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4421433	1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4601425	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs62542752	0.81[AMR][1000 genomes]
rs62542753	0.81[AMR][1000 genomes]
rs62542755	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62542757	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62542758	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62544592	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62544599	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62544600	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62544601	0.86[AMR][1000 genomes]
rs62544602	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62544603	0.83[AMR][1000 genomes]
rs62544604	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62544652	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7854048	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs7856747	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892862	chr9:26956663-27190655	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	nsv892863	chr9:27138898-27170934	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27149600-27155400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:27150800-27158000	Weak transcription	Spleen	Spleen
3	chr9:27151000-27155800	Enhancers	Placenta Amnion	Placenta Amnion
4	chr9:27151000-27158000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:27151000-27172800	Weak transcription	Left Ventricle	heart
6	chr9:27151000-27229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:27151200-27164800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:27151800-27158000	Weak transcription	Lung	lung
9	chr9:27151800-27165000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr9:27152000-27174600	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:27152200-27165400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:27152400-27156600	Weak transcription	Hela-S3	cervix
13	chr9:27152400-27157800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr9:27152400-27181600	Weak transcription	Adipose Nuclei	Adipose
15	chr9:27153600-27155400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr9:27153600-27155600	Enhancers	HSMM	muscle
17	chr9:27154200-27155200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:27154200-27155400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:27154400-27155400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:27154400-27155400	Enhancers	HMEC	breast
21	chr9:27154400-27155600	Enhancers	NHEK	skin
22	chr9:27154400-27155800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr9:27154400-27155800	Enhancers	HSMMtube	muscle
24	chr9:27154400-27158000	Enhancers	Osteobl	bone
25	chr9:27154600-27155200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:27154600-27155200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr9:27154600-27155200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:27154600-27155200	Enhancers	NHLF	lung
29	chr9:27154600-27155400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:27154600-27155400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr9:27154600-27155400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr9:27154600-27155400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:27154600-27155400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr9:27154600-27155400	Enhancers	Colon Smooth Muscle	Colon
35	chr9:27154600-27155400	Enhancers	Rectal Smooth Muscle	rectum
36	chr9:27154600-27155400	Flanking Active TSS	HUVEC	blood vessel
37	chr9:27154600-27155600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:27154600-27155600	Enhancers	Fetal Heart	heart
39	chr9:27154600-27155800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:27154800-27155200	Enhancers	Placenta	Placenta
41	chr9:27154800-27155400	Enhancers	Fetal Stomach	stomach
42	chr9:27155000-27155200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:27155000-27155400	Enhancers	Aorta	Aorta
44	chr9:27155000-27155400	Enhancers	Fetal Lung	lung
45	chr9:27155000-27155600	Enhancers	NH-A	brain

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