Variant report

Variant	rs7765368
Chromosome Location	chr6:119678456-119678457
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:119668152..119672285-chr6:119673337..119678807,6	MCF-7	breast:
2	chr6:119668855..119673733-chr6:119677455..119681608,7	K562	blood:
3	chr6:119673474..119675079-chr6:119676928..119679552,2	K562	blood:

Variant related genes	Relation type
ENSG00000111885	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11153813	0.98[ASN][1000 genomes]
rs12529667	0.89[MEX][hapmap]
rs12530171	0.89[MEX][hapmap]
rs12664079	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1295374	0.82[AFR][1000 genomes]
rs1295375	0.82[AFR][1000 genomes]
rs1295379	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1295380	0.80[YRI][hapmap]
rs1295386	0.83[CHD][hapmap];0.85[ASN][1000 genomes]
rs1295390	1.00[CEU][hapmap];0.97[LWK][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1295394	0.82[AFR][1000 genomes]
rs1797064	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs195057	0.84[MEX][hapmap]
rs195062	0.81[ASN][1000 genomes]
rs195063	0.97[CHD][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs195071	0.83[CHD][hapmap];0.80[ASN][1000 genomes]
rs195076	0.90[ASN][1000 genomes]
rs195077	0.89[MEX][hapmap]
rs195078	0.83[CHD][hapmap];0.81[ASN][1000 genomes]
rs195079	0.81[ASN][1000 genomes]
rs195081	0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs195083	0.81[ASN][1000 genomes]
rs195085	0.84[ASN][1000 genomes]
rs195086	0.93[ASN][1000 genomes]
rs4946409	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6569074	0.81[CHB][hapmap];0.87[ASN][1000 genomes]
rs6569075	0.88[ASN][1000 genomes]
rs6921356	0.86[ASN][1000 genomes]
rs6924723	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7773367	0.86[ASN][1000 genomes]
rs9372529	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9374789	0.89[MEX][hapmap]
rs9387646	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9398506	0.89[MEX][hapmap]
rs9401139	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	esv1802628	chr6:119647135-119678881	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119671800-119689200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:119673400-119690000	Weak transcription	K562	blood
3	chr6:119673600-119680800	Weak transcription	Fetal Heart	heart
4	chr6:119673600-119687200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:119675200-119688800	Weak transcription	Brain Anterior Caudate	brain
6	chr6:119675400-119679200	Weak transcription	Dnd41	blood
7	chr6:119677000-119680200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:119677000-119681000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr6:119677000-119686000	Weak transcription	Primary B cells from cord blood	blood
10	chr6:119677000-119691800	Weak transcription	Adipose Nuclei	Adipose
11	chr6:119677600-119679800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr6:119677600-119680200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:119677600-119681400	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr6:119677800-119680400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:119678000-119680200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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