Variant report

Variant	rs11236060
Chromosome Location	chr11:74042667-74042668
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:74041592..74044323-chr11:74054058..74056372,2	MCF-7	breast:
2	chr11:74037228..74038762-chr11:74040686..74043088,2	K562	blood:
3	chr11:74041581..74043351-chr11:74050387..74052312,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10459047	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10898966	0.81[EUR][1000 genomes]
rs10898973	0.87[EUR][1000 genomes]
rs10898974	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10898975	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10898976	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10898980	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11236042	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11236043	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11236044	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11236052	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236053	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236054	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236055	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11236063	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11236071	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11236072	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11236077	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11236081	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11236082	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11236083	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12225215	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12225446	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1279293	0.86[AFR][1000 genomes]
rs17132964	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2282488	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2302508	0.82[EUR][1000 genomes]
rs3741132	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3888908	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3894652	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4121668	0.82[EUR][1000 genomes]
rs58852370	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61288268	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61902380	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61902404	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7949639	0.84[EUR][1000 genomes]
rs7951617	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:87 , 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	chr11:74033200-74047200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr11:74037000-74042800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr11:74037000-74046800	Weak transcription	Fetal Thymus	thymus
5	chr11:74037000-74055400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr11:74037200-74046800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr11:74037200-74050000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr11:74037400-74042800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr11:74037400-74051600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr11:74037400-74052200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:74037400-74078800	Weak transcription	Small Intestine	intestine
12	chr11:74037600-74051600	Weak transcription	Brain Angular Gyrus	brain
13	chr11:74037600-74052800	Weak transcription	A549	lung
14	chr11:74037800-74046800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr11:74037800-74086200	Weak transcription	Brain Anterior Caudate	brain
16	chr11:74038000-74044800	Weak transcription	Right Atrium	heart
17	chr11:74038000-74047000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr11:74038000-74047200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr11:74038000-74047200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr11:74038000-74047400	Weak transcription	Brain Germinal Matrix	brain
21	chr11:74038000-74050400	Weak transcription	Gastric	stomach
22	chr11:74038000-74071200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:74038000-74077400	Weak transcription	Psoas Muscle	Psoas
24	chr11:74038000-74077600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr11:74038000-74084400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr11:74038200-74043200	Weak transcription	Fetal Brain Female	brain
27	chr11:74038200-74047000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:74038200-74049000	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr11:74038200-74050400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:74038200-74052800	Weak transcription	Ovary	ovary
31	chr11:74038200-74053600	Weak transcription	Spleen	Spleen
32	chr11:74038200-74058200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr11:74038200-74065000	Weak transcription	Aorta	Aorta
34	chr11:74038200-74071000	Weak transcription	Fetal Stomach	stomach
35	chr11:74038200-74071400	Weak transcription	Left Ventricle	heart
36	chr11:74038200-74071400	Weak transcription	Lung	lung
37	chr11:74038200-74082000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr11:74038200-74084400	Weak transcription	Colon Smooth Muscle	Colon
39	chr11:74038400-74044800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:74038400-74046800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr11:74038400-74051800	Weak transcription	Fetal Muscle Leg	muscle
42	chr11:74038400-74052800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr11:74038400-74084400	Weak transcription	Liver	Liver
44	chr11:74038400-74086200	Weak transcription	Adipose Nuclei	Adipose
45	chr11:74038600-74051600	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr11:74038600-74071400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr11:74038800-74048200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:74038800-74070600	Weak transcription	Fetal Brain Male	brain
49	chr11:74039000-74053000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr11:74039200-74055200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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