Variant report

Variant	rs11155311
Chromosome Location	chr6:143936061-143936062
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:143926590..143928506-chr6:143934076..143936971,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11155314	0.83[MEX][hapmap]
rs12193494	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12200809	0.81[EUR][1000 genomes]
rs12524982	0.89[JPT][hapmap]
rs12525281	0.89[JPT][hapmap]
rs12525974	0.89[JPT][hapmap]
rs12527275	0.89[JPT][hapmap]
rs13191026	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13192672	0.89[JPT][hapmap]
rs13195900	0.95[ASN][1000 genomes]
rs13199393	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13214196	0.89[JPT][hapmap]
rs1338535	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17291151	0.89[JPT][hapmap]
rs1884172	0.89[JPT][hapmap]
rs2328506	0.82[ASN][1000 genomes]
rs35296418	0.82[ASN][1000 genomes]
rs67470559	0.92[ASN][1000 genomes]
rs6911970	1.00[CHB][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs6932482	0.89[JPT][hapmap]
rs6937798	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7745970	0.95[ASN][1000 genomes]
rs7757372	0.90[JPT][hapmap]
rs9484795	0.89[JPT][hapmap]
rs9496699	0.89[CHB][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs9496740	0.89[JPT][hapmap]

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	esv2758084	chr6:143916621-144079976	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759476	chr6:143916621-144079976	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1032369	chr6:143925374-144007513	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv604805	chr6:143930404-144005949	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143917000-143973600	Weak transcription	Fetal Intestine Small	intestine
2	chr6:143917200-143941400	Weak transcription	Fetal Intestine Large	intestine
3	chr6:143929600-143938600	Weak transcription	Fetal Heart	heart
4	chr6:143929600-143941800	Weak transcription	Esophagus	oesophagus
5	chr6:143929600-143943400	Weak transcription	Left Ventricle	heart
6	chr6:143930200-143937800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:143930400-143949400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:143930800-143946600	Weak transcription	Primary T cells from cord blood	blood
9	chr6:143934800-143936400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:143935200-143936200	Enhancers	GM12878-XiMat	blood
11	chr6:143935200-143936400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr6:143935400-143937000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr6:143935400-143937600	Weak transcription	Placenta	Placenta
14	chr6:143935400-143938000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr6:143935600-143936200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr6:143935600-143941000	Weak transcription	Stomach Smooth Muscle	stomach
17	chr6:143935600-143942400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr6:143935600-143946600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr6:143935800-143936200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr6:143935800-143936400	Enhancers	Stomach Mucosa	stomach
21	chr6:143936000-143936800	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr6:143936000-143938800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:143936000-143939000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:143936000-143941000	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr6:143936000-143941400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:143936000-143941400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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