Variant report

Variant	rs2762059
Chromosome Location	chr13:50893509-50893510
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:50854880..50857569-chr13:50892767..50895281,2	MCF-7	breast:
2	chr13:50699045..50701986-chr13:50891820..50895192,4	K562	blood:
3	chr13:50891858..50893890-chr13:50960724..50962841,2	K562	blood:
4	chr13:50885994..50888094-chr13:50892337..50894524,2	MCF-7	breast:
5	chr13:50893025..50895334-chr13:50896388..50898768,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000231607	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1149858	0.91[EUR][1000 genomes]
rs1262865	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1326125	0.83[GIH][hapmap];0.80[TSI][hapmap]
rs2159440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2532967	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2532969	0.91[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2532970	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2580183	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2703079	0.81[CHB][hapmap]
rs2740531	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2740534	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2740535	1.00[ASW][hapmap];0.92[CEU][hapmap];0.93[GIH][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2740538	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2740540	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2740541	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2762057	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2762061	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2812212	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs3990215	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4942914	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2752608	chr13:50550099-51054499	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1249 gene(s)	inside rSNPs	diseases
5	nsv900076	chr13:50710579-50912578	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv561632	chr13:50874346-50912578	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50892400-50895600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr13:50892600-50894200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr13:50892600-50895400	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr13:50892600-50895600	Enhancers	Primary T cells from cord blood	blood
5	chr13:50892600-50896200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr13:50892800-50894400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr13:50892800-50894800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr13:50892800-50895000	Enhancers	Primary T cells fromperipheralblood	blood
9	chr13:50892800-50895000	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr13:50892800-50895000	Enhancers	Fetal Thymus	thymus
11	chr13:50892800-50895200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr13:50892800-50895200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr13:50892800-50895400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr13:50892800-50896000	Enhancers	HepG2	liver
15	chr13:50893000-50893600	Enhancers	A549	lung
16	chr13:50893000-50893800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr13:50893000-50893800	Flanking Active TSS	K562	blood
18	chr13:50893000-50895000	Enhancers	Thymus	Thymus
19	chr13:50893000-50895200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr13:50893000-50895400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr13:50893200-50893600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr13:50893200-50894600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr13:50893200-50894800	Enhancers	Primary hematopoietic stem cells	blood
24	chr13:50893200-50894800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr13:50893200-50895000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr13:50893200-50895200	Enhancers	Stomach Mucosa	stomach
27	chr13:50893400-50893600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr13:50893400-50893800	Weak transcription	Pancreas	Pancrea
29	chr13:50893400-50894200	Flanking Active TSS	Dnd41	blood
30	chr13:50893400-50895200	Enhancers	Hela-S3	cervix
31	chr13:50893400-50898200	Weak transcription	Left Ventricle	heart

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