Variant report

Variant	rs9905503
Chromosome Location	chr17:18184626-18184627
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:18178546..18181267-chr17:18181551..18184917,3	MCF-7	breast:
2	chr17:18164802..18166593-chr17:18182871..18185713,2	MCF-7	breast:
3	chr17:18150956..18154641-chr17:18182536..18186839,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000177731	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1001303	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28650333	1.00[EUR][1000 genomes]
rs28684992	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4924848	1.00[CEU][hapmap]
rs4924860	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4925152	1.00[EUR][1000 genomes]
rs4925154	1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4925155	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs4925156	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4925158	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4925161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4925164	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4925165	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4925168	1.00[EUR][1000 genomes]
rs61741784	1.00[EUR][1000 genomes]
rs7215491	1.00[CEU][hapmap]
rs72550754	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8070162	1.00[YRI][hapmap]
rs8071001	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8072977	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8075915	1.00[CEU][hapmap];0.84[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8078015	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9890722	1.00[CEU][hapmap];0.85[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9891934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9892072	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9893649	1.00[EUR][1000 genomes]
rs9898323	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9899244	0.81[AFR][1000 genomes]
rs9900996	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9902011	1.00[CEU][hapmap]
rs9903847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9904235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9905161	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9907938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9909530	0.92[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9911412	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9916721	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv492305	chr17:17980441-18424702	Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
6	nsv907773	chr17:18099962-18206234	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv907774	chr17:18103907-18206234	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	nsv907775	chr17:18108496-18206234	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv833386	chr17:18170261-18332726	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv1057081	chr17:18171516-18256347	Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
11	nsv543247	chr17:18171516-18256347	Weak transcription Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
12	nsv1062368	chr17:18180747-18259234	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18167000-18188200	Weak transcription	Stomach Mucosa	stomach
2	chr17:18172200-18217400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:18172400-18201000	Strong transcription	Fetal Stomach	stomach
4	chr17:18172800-18198400	Strong transcription	Thymus	Thymus
5	chr17:18173000-18198400	Strong transcription	Fetal Thymus	thymus
6	chr17:18173000-18199000	Strong transcription	Primary T cells from cord blood	blood
7	chr17:18173000-18200400	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr17:18173000-18213800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr17:18173200-18198400	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr17:18173200-18200200	Strong transcription	Placenta	Placenta
11	chr17:18173400-18198200	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr17:18173400-18198400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr17:18173400-18198800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr17:18173400-18200200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr17:18173400-18200800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:18173400-18201000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr17:18173400-18201000	Strong transcription	Fetal Intestine Small	intestine
18	chr17:18173600-18190800	Strong transcription	A549	lung
19	chr17:18173600-18198200	Strong transcription	Stomach Smooth Muscle	stomach
20	chr17:18173600-18200200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr17:18173600-18200800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr17:18174000-18200600	Strong transcription	Dnd41	blood
23	chr17:18174200-18200600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr17:18174800-18190600	Strong transcription	Duodenum Mucosa	Duodenum
25	chr17:18174800-18198600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr17:18174800-18200600	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr17:18175400-18189400	Strong transcription	NHLF	lung
28	chr17:18175600-18189200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr17:18175600-18196600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr17:18175600-18200800	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr17:18175800-18190200	Strong transcription	Brain Germinal Matrix	brain
32	chr17:18175800-18198600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr17:18175800-18199000	Strong transcription	H9 Cell Line	embryonic stem cell
34	chr17:18175800-18200800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr17:18175800-18201000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr17:18176200-18190800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr17:18176200-18190800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr17:18176200-18198200	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr17:18176200-18198400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr17:18176200-18198600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr17:18176200-18200800	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr17:18176400-18189200	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr17:18176400-18189400	Strong transcription	Spleen	Spleen
44	chr17:18176400-18190200	Strong transcription	Muscle Satellite Cultured Cells	--
45	chr17:18176400-18190200	Strong transcription	Osteobl	bone
46	chr17:18176400-18190400	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr17:18176400-18196600	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr17:18176400-18197000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr17:18176400-18198400	Strong transcription	Adipose Nuclei	Adipose
50	chr17:18176400-18199000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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