Variant report

Variant	rs2202703
Chromosome Location	chr17:17338020-17338021
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:17335195..17342131-chr17:17347291..17351486,7	MCF-7	breast:
2	chr17:17337262..17338945-chr17:17347016..17349151,2	MCF-7	breast:
3	chr17:17336920..17339471-chr17:17342851..17344452,2	MCF-7	breast:
4	chr17:17335771..17338449-chr17:17342663..17345052,2	MCF-7	breast:
5	chr17:17324473..17327302-chr17:17336395..17338556,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000227158	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1123297	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11650117	0.88[EUR][1000 genomes]
rs11654572	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12449517	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12453750	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13341175	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1605450	0.81[ASN][1000 genomes]
rs2012886	0.81[ASN][1000 genomes]
rs4924834	0.81[ASN][1000 genomes]
rs4925141	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6502596	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7209348	0.81[ASN][1000 genomes]
rs7209715	0.81[ASN][1000 genomes]
rs7209929	0.81[ASN][1000 genomes]
rs7210546	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7212942	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7215510	0.81[ASN][1000 genomes]
rs7216896	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7217126	0.81[ASN][1000 genomes]
rs7501994	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8075087	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs925095	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9893203	0.83[ASN][1000 genomes]
rs9899529	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]

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	nsv1058849	chr17:17308009-17348548	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1058804	chr17:17308984-17348548	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1062207	chr17:17310099-17344599	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv543234	chr17:17310099-17344599	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv574523	chr17:17310886-17347995	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1056137	chr17:17311017-17348939	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv543235	chr17:17311017-17348939	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv482648	chr17:17315268-17455442	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
9	nsv515800	chr17:17322196-17344653	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1065710	chr17:17328111-17391443	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17326200-17343400	Weak transcription	Right Atrium	heart
2	chr17:17330200-17350000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr17:17334800-17339200	Enhancers	Thymus	Thymus
4	chr17:17334800-17339400	Enhancers	HepG2	liver
5	chr17:17334800-17340400	Enhancers	Fetal Thymus	thymus
6	chr17:17335400-17348800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr17:17335800-17338200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr17:17335800-17338200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr17:17336000-17338400	Enhancers	Hela-S3	cervix
10	chr17:17336200-17338200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr17:17336200-17338600	Weak transcription	Brain Germinal Matrix	brain
12	chr17:17336400-17341400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr17:17336800-17338600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr17:17337000-17343400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr17:17337200-17339200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr17:17337400-17338400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr17:17337600-17343600	Weak transcription	Dnd41	blood
18	chr17:17337800-17340800	Enhancers	A549	lung
19	chr17:17338000-17338400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr17:17338000-17338800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr17:17338000-17339400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr17:17338000-17339400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr17:17338000-17339600	Enhancers	NHDF-Ad	bronchial

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