Variant report

Variant	rs17153710
Chromosome Location	chr8:11603989-11603990
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11430194..11430977-chr8:11603626..11604340,2	MCF-7	breast:
2	chr8:11421842..11422772-chr8:11603355..11604431,7	MCF-7	breast:
3	chr8:11424667..11425261-chr8:11603180..11604185,3	MCF-7	breast:
4	chr8:11602490..11604038-chr8:11606565..11608594,2	K562	blood:
5	chr8:11594028..11596357-chr8:11603341..11605570,2	K562	blood:
6	chr8:11421781..11422781-chr8:11603539..11604516,9	K562	blood:
7	chr8:11603020..11605526-chr8:11757590..11759777,2	K562	blood:
8	chr8:11573922..11574562-chr8:11603556..11604064,2	MCF-7	breast:
9	chr8:11422237..11424811-chr8:11602615..11604781,2	MCF-7	breast:
10	chr8:11587887..11588889-chr8:11603840..11604789,8	MCF-7	breast:
11	chr8:11446870..11447723-chr8:11603904..11604616,2	K562	blood:
12	chr8:11587850..11588855-chr8:11603787..11604777,28	MCF-7	breast:
13	chr8:11587892..11588820-chr8:11603814..11604865,11	MCF-7	breast:

No data

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10089520	1.00[CHB][hapmap]
rs10095823	1.00[CHB][hapmap]
rs12545992	1.00[CHB][hapmap]
rs28622563	1.00[MEX][hapmap]
rs28665608	1.00[ASN][1000 genomes]
rs3207196	1.00[ASN][1000 genomes]
rs6601627	1.00[CHB][hapmap]
rs6601628	1.00[CHB][hapmap]
rs6601630	1.00[CHB][hapmap]
rs6998854	1.00[CHB][hapmap]
rs7000179	1.00[CHB][hapmap]
rs73666003	1.00[ASN][1000 genomes]
rs73666006	1.00[ASN][1000 genomes]
rs804259	1.00[JPT][hapmap]
rs8191535	1.00[JPT][hapmap]
rs8191555	1.00[JPT][hapmap]
rs8191595	1.00[CHB][hapmap]
rs9720275	1.00[CHB][hapmap]
rs9886596	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv916483	chr8:11590294-11672038	Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv890359	chr8:11599570-11617240	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11596200-11604000	Enhancers	Pancreas	Pancrea
2	chr8:11598400-11604200	Enhancers	Stomach Mucosa	stomach
3	chr8:11599200-11605000	Enhancers	Left Ventricle	heart
4	chr8:11601200-11604800	Enhancers	Liver	Liver
5	chr8:11602000-11604200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:11602000-11604200	Weak transcription	Gastric	stomach
7	chr8:11602000-11606600	Enhancers	Ovary	ovary
8	chr8:11602400-11604200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:11602400-11604400	Enhancers	Fetal Heart	heart
10	chr8:11602400-11606000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:11602400-11606200	Weak transcription	Right Ventricle	heart
12	chr8:11602600-11604600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:11603600-11604000	Enhancers	Right Atrium	heart
14	chr8:11603800-11604200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
15	chr8:11603800-11604200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:11603800-11604200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
17	chr8:11603800-11604200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
18	chr8:11603800-11604400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr8:11603800-11604400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
20	chr8:11603800-11604400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr8:11603800-11604400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr8:11603800-11604400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
23	chr8:11603800-11604400	Genic enhancers	Fetal Intestine Small	intestine
24	chr8:11603800-11604400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
25	chr8:11603800-11604400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
26	chr8:11603800-11604600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
27	chr8:11603800-11604600	Enhancers	Duodenum Mucosa	Duodenum
28	chr8:11603800-11604600	Enhancers	HepG2	liver

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