Variant report

Variant	rs3015982
Chromosome Location	chr11:77157188-77157189
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:77149888..77152231-chr11:77155646..77157419,2	MCF-7	breast:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1225478	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1237490	0.86[EUR][1000 genomes]
rs2154754	0.86[EUR][1000 genomes]
rs2602476	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2602487	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3015983	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3015985	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3015986	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3015988	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3015990	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3015992	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3019233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3019234	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3019235	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3019236	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3019249	0.91[EUR][1000 genomes]
rs3019257	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34025917	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34880271	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs472691	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs476258	0.86[EUR][1000 genomes]
rs479104	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs493256	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs494289	0.88[EUR][1000 genomes]
rs503406	0.94[EUR][1000 genomes]
rs505841	0.85[EUR][1000 genomes]
rs508662	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs51500	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs520938	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs522015	0.94[EUR][1000 genomes]
rs523481	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs531638	0.90[EUR][1000 genomes]
rs535008	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs552323	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs557484	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs558470	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs560571	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs561386	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs562845	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs563731	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs572485	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs576220	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs580624	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs592602	0.88[EUR][1000 genomes]
rs595654	0.90[EUR][1000 genomes]
rs598801	0.92[EUR][1000 genomes]
rs644551	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs649040	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs653792	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs657269	0.80[EUR][1000 genomes]
rs674259	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs683455	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs683762	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs684793	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs686068	0.92[EUR][1000 genomes]
rs689108	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7934230	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7949721	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048360	chr11:76900813-77387933	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv541089	chr11:76900813-77387933	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1049603	chr11:76900813-77520411	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv541090	chr11:76900813-77520411	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	esv3424135	chr11:76961603-77277087	Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1037724	chr11:77061945-77250391	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv541091	chr11:77061945-77250391	Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3437433	chr11:77101280-77291686	Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77142200-77164800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:77147200-77160200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:77147200-77160800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:77149200-77165400	Weak transcription	Ovary	ovary
5	chr11:77149400-77158200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr11:77150200-77157200	Weak transcription	Fetal Thymus	thymus
7	chr11:77150200-77158000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:77152200-77162600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr11:77152800-77157600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr11:77152800-77166400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:77153600-77168600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr11:77153800-77160400	Weak transcription	Brain Anterior Caudate	brain
13	chr11:77154600-77157400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:77154600-77157800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr11:77154800-77159600	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr11:77155200-77157200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr11:77155200-77158600	Enhancers	Fetal Intestine Small	intestine
18	chr11:77155400-77157400	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr11:77155400-77158400	Enhancers	Fetal Intestine Large	intestine
20	chr11:77155400-77181400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:77156000-77157200	Flanking Active TSS	GM12878-XiMat	blood
22	chr11:77156000-77158200	Enhancers	Stomach Mucosa	stomach
23	chr11:77156000-77159200	Enhancers	Duodenum Mucosa	Duodenum
24	chr11:77156200-77157400	Enhancers	Primary hematopoietic stem cells	blood
25	chr11:77156400-77157600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr11:77156600-77157200	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr11:77156600-77157400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr11:77156600-77157600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr11:77156600-77158000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:77156600-77158200	Enhancers	HepG2	liver
31	chr11:77156600-77160200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr11:77156800-77157200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:77156800-77157800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:77156800-77158200	Enhancers	NHEK	skin
35	chr11:77156800-77158800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr11:77157000-77158000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr11:77157000-77158000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr11:77157000-77158000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr11:77157000-77159600	Weak transcription	Primary B cells from cord blood	blood
40	chr11:77157000-77160000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr11:77157000-77160000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:77157000-77160200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:77157000-77160200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr11:77157000-77168400	Weak transcription	Small Intestine	intestine

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