Variant report

Variant	rs11234966
Chromosome Location	chr11:86813178-86813179
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10792897	0.81[EUR][1000 genomes]
rs10792906	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792908	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10792909	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10792910	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898580	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10898586	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10898587	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10898588	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10898590	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10898593	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898594	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898595	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898600	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10898603	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898604	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898605	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10898606	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10898607	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898608	0.87[ASN][1000 genomes]
rs10898609	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898610	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898613	0.87[ASN][1000 genomes]
rs11234907	0.83[EUR][1000 genomes]
rs11234911	0.86[EUR][1000 genomes]
rs11234923	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11234925	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11234930	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11234932	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11234933	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11234937	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11234940	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234941	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234945	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234946	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234950	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234952	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234958	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234961	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234962	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234965	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234968	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234969	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234972	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234976	0.98[EUR][1000 genomes]
rs11234977	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234982	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234989	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234991	0.84[ASN][1000 genomes]
rs11234993	0.85[ASN][1000 genomes]
rs11234996	0.87[ASN][1000 genomes]
rs11533276	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11820668	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12223784	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12360980	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12363760	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1531144	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1968741	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6592334	0.99[ASN][1000 genomes]
rs67946471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7117731	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7124448	0.80[ASN][1000 genomes]
rs7127557	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9666468	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv1037042	chr11:86586876-86978492	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv541119	chr11:86586876-86978492	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv898058	chr11:86754948-86889284	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv898059	chr11:86754948-86949369	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv1046288	chr11:86757573-87158571	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
10	esv1844274	chr11:86776992-86872908	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv468776	chr11:86788716-86826422	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv555706	chr11:86788716-86826422	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1045057	chr11:86794670-87033779	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv541121	chr11:86794670-87033779	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
15	nsv468777	chr11:86794856-86985581	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv555707	chr11:86794856-86985581	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86776600-86815600	Weak transcription	HSMMtube	muscle
2	chr11:86783000-86814000	Weak transcription	Hela-S3	cervix
3	chr11:86787400-86819600	Weak transcription	NH-A	brain
4	chr11:86787600-86825200	Weak transcription	Brain Substantia Nigra	brain
5	chr11:86787800-86817400	Weak transcription	Colon Smooth Muscle	Colon
6	chr11:86787800-86819400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:86788200-86817800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:86788200-86824600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr11:86788200-86830400	Weak transcription	Right Ventricle	heart
10	chr11:86788600-86836400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:86798000-86820000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:86798200-86817800	Weak transcription	Fetal Thymus	thymus
13	chr11:86798400-86821600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:86799400-86817800	Weak transcription	Psoas Muscle	Psoas
15	chr11:86799600-86821000	Weak transcription	Primary B cells from cord blood	blood
16	chr11:86801000-86816200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:86801600-86817800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:86803600-86817800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr11:86803600-86817800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr11:86804400-86814600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr11:86804400-86824800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:86804600-86813600	Weak transcription	GM12878-XiMat	blood
23	chr11:86804600-86817400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:86804600-86824600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:86804600-86839400	Weak transcription	Fetal Kidney	kidney
26	chr11:86804800-86817800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr11:86805000-86814600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr11:86805000-86818000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:86806400-86816200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:86806600-86816200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr11:86806800-86815800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:86806800-86817800	Weak transcription	Aorta	Aorta
33	chr11:86806800-86829600	Weak transcription	Primary T cells from cord blood	blood
34	chr11:86806800-86835800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:86808200-86816200	Weak transcription	Fetal Stomach	stomach
36	chr11:86808800-86817800	Weak transcription	Fetal Muscle Leg	muscle
37	chr11:86808800-86819400	Weak transcription	Dnd41	blood
38	chr11:86808800-86819600	Weak transcription	Fetal Muscle Trunk	muscle
39	chr11:86808800-86824600	Weak transcription	Adipose Nuclei	Adipose
40	chr11:86809000-86814600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr11:86809000-86816200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:86809000-86817800	Weak transcription	Gastric	stomach
43	chr11:86809000-86819400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr11:86809000-86819400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr11:86809000-86819600	Weak transcription	Stomach Mucosa	stomach
46	chr11:86809000-86844000	Weak transcription	Ovary	ovary
47	chr11:86809000-86876000	Weak transcription	Left Ventricle	heart
48	chr11:86809200-86814600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr11:86809200-86818000	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr11:86809400-86813200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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