Variant report

Variant	rs17475694
Chromosome Location	chr8:118938914-118938915
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:118931174..118933770-chr8:118938914..118940644,2	K562	blood:
2	chr8:118928857..118930921-chr8:118936919..118939329,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10088632	1.00[CEU][hapmap]
rs10109062	1.00[CEU][hapmap]
rs11562671	0.85[YRI][hapmap]
rs11562730	1.00[CEU][hapmap]
rs11562757	1.00[CEU][hapmap]
rs11562766	1.00[CEU][hapmap]
rs17430749	0.85[YRI][hapmap]
rs17431152	0.85[YRI][hapmap]
rs17431215	0.85[YRI][hapmap]
rs17453567	0.85[YRI][hapmap]
rs17453602	0.85[YRI][hapmap]
rs17453651	0.85[YRI][hapmap]
rs17474839	1.00[CEU][hapmap]
rs17475323	1.00[CEU][hapmap]
rs17475358	1.00[CEU][hapmap]
rs17475365	1.00[CEU][hapmap]
rs17475659	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475666	0.85[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475673	0.85[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475687	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475722	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475743	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475785	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17475918	1.00[CEU][hapmap]
rs17476226	0.85[YRI][hapmap]
rs17476233	0.85[YRI][hapmap]
rs17476247	1.00[CEU][hapmap]
rs17476254	0.85[YRI][hapmap]
rs17476296	0.85[YRI][hapmap]
rs17477049	1.00[CEU][hapmap]
rs17504170	1.00[CEU][hapmap]
rs17504205	1.00[CEU][hapmap]
rs17504490	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17504568	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17504631	0.85[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17504743	1.00[CEU][hapmap]
rs17505079	1.00[CEU][hapmap]
rs2086008	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2086009	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4377987	1.00[CEU][hapmap]
rs4556109	1.00[CEU][hapmap]
rs6984750	1.00[CEU][hapmap]
rs7357537	1.00[CEU][hapmap]
rs7462118	1.00[CEU][hapmap]
rs9297572	1.00[CEU][hapmap]
rs9656924	1.00[CEU][hapmap]
rs9792392	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv933516	chr8:118764605-119009093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv831440	chr8:118871930-119052269	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv891411	chr8:118891896-118942698	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1032355	chr8:118896733-119003223	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv465785	chr8:118901928-118970300	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv612046	chr8:118901928-118970300	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118933200-118943800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:118933200-118946600	Weak transcription	Gastric	stomach
3	chr8:118933400-118940800	Enhancers	Osteobl	bone
4	chr8:118933600-118940000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:118933600-118941400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr8:118933600-118945600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr8:118933600-118945800	Weak transcription	Right Atrium	heart
8	chr8:118933600-118946200	Weak transcription	Ovary	ovary
9	chr8:118933600-118946600	Weak transcription	Brain Germinal Matrix	brain
10	chr8:118933800-118939400	Weak transcription	Adipose Nuclei	Adipose
11	chr8:118933800-118939400	Weak transcription	Fetal Brain Male	brain
12	chr8:118933800-118946000	Weak transcription	Fetal Intestine Large	intestine
13	chr8:118934000-118940600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:118934600-118940200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:118935000-118940000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr8:118935200-118939800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr8:118935200-118940200	Weak transcription	Right Ventricle	heart
18	chr8:118935200-118940400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr8:118935200-118942400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr8:118935200-118946200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:118935200-118949800	Weak transcription	Psoas Muscle	Psoas
22	chr8:118935200-118958600	Weak transcription	Esophagus	oesophagus
23	chr8:118935400-118939800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:118936600-118939200	Weak transcription	Fetal Heart	heart
25	chr8:118936600-118940200	Weak transcription	A549	lung
26	chr8:118936600-118942400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr8:118937000-118939200	Weak transcription	HMEC	breast
28	chr8:118937000-118939200	Weak transcription	NH-A	brain
29	chr8:118937200-118939800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:118937600-118939400	Weak transcription	NHLF	lung
31	chr8:118937800-118939200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:118937800-118939800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:118937800-118939800	Weak transcription	NHEK	skin
34	chr8:118937800-118942200	Enhancers	Liver	Liver
35	chr8:118938000-118949800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr8:118938200-118939400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:118938200-118940600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr8:118938400-118940400	Enhancers	Fetal Lung	lung
39	chr8:118938400-118940600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:118938400-118942400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:118938600-118939000	Enhancers	Brain Substantia Nigra	brain
42	chr8:118938600-118939200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:118938600-118939200	Enhancers	Small Intestine	intestine
44	chr8:118938600-118940200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr8:118938600-118940600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:118938600-118940600	Enhancers	HSMM	muscle
47	chr8:118938800-118939000	Enhancers	HepG2	liver
48	chr8:118938800-118939200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr8:118938800-118939400	Enhancers	Brain Angular Gyrus	brain
50	chr8:118938800-118939400	Enhancers	Fetal Muscle Leg	muscle

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