Variant report

Variant	rs2732522
Chromosome Location	chr11:35051943-35051944
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35039461..35041795-chr11:35050641..35052600,2	K562	blood:
2	chr11:35021693..35023212-chr11:35050497..35053250,2	MCF-7	breast:
3	chr11:35050379..35055023-chr11:35058548..35063780,5	MCF-7	breast:
4	chr11:35050517..35052677-chr11:35065091..35067302,2	K562	blood:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1035731	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1425804	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1477562	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1477563	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1559756	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2433161	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2433162	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2467603	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2469910	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2553787	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2553788	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2553789	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2553790	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2553791	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2553792	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2553793	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2553794	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2553795	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2553797	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2553800	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2553801	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2553802	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2553803	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2553805	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2553806	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2732520	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2732521	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732524	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2732526	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2732527	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2732528	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2732529	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2785153	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2785154	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2785155	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2785156	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2785157	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2785159	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2785160	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2785161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2785162	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2785163	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2785166	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2785167	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2785168	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2785169	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs471450	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs496623	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs497476	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs532282	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs536864	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs603820	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs622235	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs663993	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs666197	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs678137	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7479679	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][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	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv430371	chr11:34975067-35111292	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	esv1826391	chr11:35000983-35098193	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv540999	chr11:35021936-35185471	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	esv2758263	chr11:35029933-35226784	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	esv2759818	chr11:35029933-35238578	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35039800-35059200	Weak transcription	Pancreas	Pancrea
2	chr11:35049600-35054800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:35050600-35052000	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr11:35050600-35052000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:35050600-35053200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:35050600-35053200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr11:35050600-35053400	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr11:35050600-35054400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:35051000-35053200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:35051000-35053800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:35051000-35055400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr11:35051200-35052000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:35051200-35052200	Enhancers	Primary B cells from cord blood	blood
14	chr11:35051200-35053000	Enhancers	Primary B cells from peripheral blood	blood
15	chr11:35051200-35053000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr11:35051200-35054200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:35051200-35055400	Enhancers	Primary T cells from cord blood	blood
18	chr11:35051200-35056000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:35051400-35052200	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr11:35051400-35052800	Enhancers	Small Intestine	intestine
21	chr11:35051400-35053000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr11:35051400-35053000	Flanking Active TSS	A549	lung
23	chr11:35051400-35053000	Flanking Active TSS	Hela-S3	cervix
24	chr11:35051400-35053600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:35051400-35053800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr11:35051400-35053800	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr11:35051400-35054000	Enhancers	NHLF	lung
28	chr11:35051600-35052200	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr11:35051600-35052200	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr11:35051600-35052200	Enhancers	HSMMtube	muscle
31	chr11:35051600-35052200	Flanking Active TSS	K562	blood
32	chr11:35051600-35052200	Flanking Active TSS	NHEK	skin
33	chr11:35051600-35052400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr11:35051600-35052400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr11:35051600-35052400	Enhancers	Lung	lung
36	chr11:35051600-35052400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr11:35051600-35052600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr11:35051600-35052600	Flanking Active TSS	GM12878-XiMat	blood
39	chr11:35051600-35052800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr11:35051600-35052800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:35051600-35053000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:35051600-35053000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr11:35051600-35053000	Enhancers	Fetal Muscle Leg	muscle
44	chr11:35051600-35053800	Enhancers	HSMM	muscle
45	chr11:35051600-35053800	Enhancers	HUVEC	blood vessel
46	chr11:35051600-35054000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr11:35051600-35054200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:35051600-35054200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr11:35051600-35054600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr11:35051600-35054600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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