Variant report

Variant	rs7034702
Chromosome Location	chr9:108226302-108226303
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:108222226..108224417-chr9:108226079..108228119,2	K562	blood:
2	chr9:108221322..108223726-chr9:108225722..108228119,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10991660	0.80[CEU][hapmap];0.86[GIH][hapmap];0.94[LWK][hapmap];0.89[MKK][hapmap];0.85[TSI][hapmap];0.84[AFR][1000 genomes]
rs10991682	0.80[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs11999966	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];0.97[LWK][hapmap];0.93[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12002748	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12004019	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12004886	1.00[CEU][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12342071	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];0.98[MKK][hapmap];0.92[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12342465	0.86[AFR][1000 genomes]
rs13362922	0.94[AFR][1000 genomes]
rs1808155	0.87[AFR][1000 genomes]
rs1854124	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs2149592	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.92[LWK][hapmap];0.98[MKK][hapmap];0.92[TSI][hapmap];0.84[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2149593	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.84[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2417627	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41277781	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs66820447	0.83[EUR][1000 genomes]
rs7033452	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs7034699	0.89[AFR][1000 genomes]
rs7042000	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7858616	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7867012	1.00[ASW][hapmap];0.80[CEU][hapmap];0.86[GIH][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs7870485	0.99[AFR][1000 genomes]
rs7872832	1.00[ASW][hapmap];0.80[CEU][hapmap];0.86[GIH][hapmap];0.89[LWK][hapmap];1.00[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs9657645	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9969773	0.86[AFR][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	nsv1037750	chr9:108027692-108251733	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1053973	chr9:108199177-108300186	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv615115	chr9:108205262-108298183	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv893692	chr9:108218852-108320988	ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a
5	nsv1050141	chr9:108219667-108317424	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108211000-108248000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr9:108211800-108227000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr9:108212200-108234800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:108212800-108226600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:108214400-108227200	Weak transcription	Fetal Kidney	kidney
6	chr9:108214600-108309800	Weak transcription	HUVEC	blood vessel
7	chr9:108220200-108243400	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:108220400-108227600	Weak transcription	Liver	Liver
9	chr9:108220400-108237400	Weak transcription	Brain Hippocampus Middle	brain
10	chr9:108220400-108252600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr9:108220600-108226600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:108220600-108227000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr9:108220600-108227600	Weak transcription	HMEC	breast
14	chr9:108220600-108231000	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:108220600-108237000	Weak transcription	Pancreas	Pancrea
16	chr9:108220600-108237400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr9:108220800-108226600	Weak transcription	Hela-S3	cervix
18	chr9:108220800-108227000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr9:108220800-108229200	Weak transcription	NHLF	lung
20	chr9:108220800-108237000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:108220800-108237600	Weak transcription	Aorta	Aorta
22	chr9:108221000-108226400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:108221000-108226600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr9:108221000-108226600	Weak transcription	NHDF-Ad	bronchial
25	chr9:108221000-108226800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:108221000-108226800	Weak transcription	HSMM	muscle
27	chr9:108221000-108227000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr9:108221000-108227000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:108221000-108227000	Weak transcription	Fetal Lung	lung
30	chr9:108221000-108227000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr9:108221000-108227000	Weak transcription	Dnd41	blood
32	chr9:108221000-108227200	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:108221000-108229000	Weak transcription	Lung	lung
34	chr9:108221000-108233200	Weak transcription	Stomach Smooth Muscle	stomach
35	chr9:108221000-108235400	Weak transcription	Gastric	stomach
36	chr9:108221000-108236200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr9:108221000-108237400	Weak transcription	Brain Substantia Nigra	brain
38	chr9:108221000-108257000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr9:108221000-108257200	Weak transcription	Fetal Stomach	stomach
40	chr9:108221000-108266000	Weak transcription	NHEK	skin
41	chr9:108221000-108277200	Weak transcription	Left Ventricle	heart
42	chr9:108221200-108226400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr9:108221200-108226400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:108221200-108226800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr9:108221200-108226800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:108221200-108226800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr9:108221200-108226800	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr9:108221200-108226800	Weak transcription	Fetal Brain Female	brain
49	chr9:108221200-108227000	Weak transcription	Primary B cells from cord blood	blood
50	chr9:108221200-108227000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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