Variant report

Variant	rs11236063
Chromosome Location	chr11:74063485-74063486
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F4	chr11:74063313-74063749	MCF10A-Er-Src	breast:	n/a	chr11:74063655-74063664

Variant related genes	Relation type
HNRNPA1P40	TF binding region

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10431176	0.83[CEU][hapmap]
rs10459047	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1053021	0.83[YRI][hapmap]
rs10793072	0.83[YRI][hapmap]
rs10793073	0.81[YRI][hapmap]
rs10793074	0.83[YRI][hapmap]
rs10898962	0.83[CEU][hapmap]
rs10898966	0.83[CEU][hapmap]
rs10898973	0.82[EUR][1000 genomes]
rs10898974	0.92[CEU][hapmap];0.85[JPT][hapmap];0.92[EUR][1000 genomes]
rs10898975	1.00[CEU][hapmap];0.85[JPT][hapmap];0.92[EUR][1000 genomes]
rs10898976	1.00[CEU][hapmap];0.85[JPT][hapmap];0.92[EUR][1000 genomes]
rs10898980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10898984	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236029	0.83[CEU][hapmap]
rs11236042	1.00[CEU][hapmap];0.85[JPT][hapmap];0.92[EUR][1000 genomes]
rs11236043	1.00[CEU][hapmap];0.85[JPT][hapmap];0.92[EUR][1000 genomes]
rs11236044	0.92[EUR][1000 genomes]
rs11236052	1.00[CEU][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11236053	1.00[CEU][hapmap];0.92[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11236054	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11236055	0.84[EUR][1000 genomes]
rs11236060	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11236071	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11236072	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11236077	1.00[CEU][hapmap];0.89[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11236081	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11236082	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11236083	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11236091	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236092	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236093	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12049823	0.85[CEU][hapmap]
rs12225215	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12225446	1.00[CEU][hapmap];0.92[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1279293	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs17132964	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1944971	0.83[CEU][hapmap]
rs2282488	1.00[CEU][hapmap];0.84[JPT][hapmap];0.92[EUR][1000 genomes]
rs3741130	0.83[YRI][hapmap]
rs3741132	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs3741133	0.83[CEU][hapmap]
rs3867270	0.83[YRI][hapmap]
rs3867271	0.83[YRI][hapmap]
rs3867272	0.83[YRI][hapmap]
rs3888908	0.83[EUR][1000 genomes]
rs3894652	0.83[EUR][1000 genomes]
rs4121668	0.92[CEU][hapmap]
rs515924	0.85[CEU][hapmap];0.90[YRI][hapmap]
rs550552	0.85[CEU][hapmap]
rs58852370	0.83[EUR][1000 genomes]
rs588725	0.85[CEU][hapmap]
rs61258589	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61288268	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61902380	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61902404	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs625532	0.84[CEU][hapmap]
rs630078	0.85[CEU][hapmap]
rs639228	0.92[CEU][hapmap]
rs658976	0.92[CEU][hapmap]
rs676103	0.85[CEU][hapmap];0.90[YRI][hapmap]
rs7117465	0.92[CEU][hapmap]
rs7924914	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7926851	0.81[YRI][hapmap]
rs7940145	0.81[YRI][hapmap]
rs7941916	0.83[YRI][hapmap]
rs7945908	0.83[YRI][hapmap]
rs7951617	1.00[CEU][hapmap];0.85[JPT][hapmap];0.92[EUR][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	esv2757451	chr11:73842609-74545888	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv2759837	chr11:73842609-74557597	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	esv34979	chr11:73878688-74533452	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
4	esv2758277	chr11:73887567-74557597	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
5	nsv825994	chr11:73936667-74534455	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
6	nsv1049915	chr11:74052264-74126319	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74031200-74071200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:74037400-74078800	Weak transcription	Small Intestine	intestine
3	chr11:74037800-74086200	Weak transcription	Brain Anterior Caudate	brain
4	chr11:74038000-74071200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr11:74038000-74077400	Weak transcription	Psoas Muscle	Psoas
6	chr11:74038000-74077600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr11:74038000-74084400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr11:74038200-74065000	Weak transcription	Aorta	Aorta
9	chr11:74038200-74071000	Weak transcription	Fetal Stomach	stomach
10	chr11:74038200-74071400	Weak transcription	Left Ventricle	heart
11	chr11:74038200-74071400	Weak transcription	Lung	lung
12	chr11:74038200-74082000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:74038200-74084400	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:74038400-74084400	Weak transcription	Liver	Liver
15	chr11:74038400-74086200	Weak transcription	Adipose Nuclei	Adipose
16	chr11:74038600-74071400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:74038800-74070600	Weak transcription	Fetal Brain Male	brain
18	chr11:74039400-74071400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:74039800-74066200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr11:74041800-74071200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:74041800-74071400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:74042000-74077600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr11:74042200-74065600	Weak transcription	Fetal Heart	heart
24	chr11:74042200-74081200	Weak transcription	Hela-S3	cervix
25	chr11:74044800-74079200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr11:74045800-74071400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr11:74045800-74073200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr11:74046000-74071800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr11:74047200-74071200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr11:74047800-74068400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr11:74047800-74077600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr11:74048000-74070800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:74048400-74077800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:74049400-74071800	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:74049400-74080400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr11:74049600-74070800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr11:74049800-74077400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:74050400-74070800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr11:74050800-74071000	Weak transcription	Fetal Intestine Small	intestine
40	chr11:74050800-74085800	Weak transcription	Colonic Mucosa	Colon
41	chr11:74051000-74071400	Weak transcription	Gastric	stomach
42	chr11:74051000-74071400	Weak transcription	Pancreas	Pancrea
43	chr11:74051200-74067200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr11:74051200-74070800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr11:74052400-74064600	Weak transcription	Brain Angular Gyrus	brain
46	chr11:74052400-74071000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr11:74052400-74071200	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr11:74053200-74070400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr11:74053200-74071400	Weak transcription	Ovary	ovary
50	chr11:74053400-74071600	Weak transcription	Fetal Muscle Leg	muscle

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