Variant report

Variant	rs11227628
Chromosome Location	chr11:66685356-66685357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:66679281..66682230-chr11:66683799..66685977,2	MCF-7	breast:

Extended variants
information (count: 26 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1077256	0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs10791894	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs10791896	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11227624	0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11227625	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11227630	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1530891	0.86[JPT][hapmap]
rs1901376	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4930394	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6591226	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs67156018	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7107498	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7110302	0.90[JPT][hapmap]
rs7119682	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs746018	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs746019	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7935749	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7936290	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7944999	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7952017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs966021	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv897794	chr11:66579572-66744119	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv555226	chr11:66579572-66845362	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
3	nsv428574	chr11:66619002-66804133	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv832194	chr11:66634462-66805980	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
5	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs11227628	CTD-3074O7.2	cis	Muscle Skeletal	GTEx
rs11227628	LRFN4	Cis_1M	lymphoblastoid	RTeQTL
rs11227628	ACTN3	cis	Muscle Skeletal	GTEx

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66674000-66687000	Weak transcription	HSMMtube	muscle
2	chr11:66674400-66689600	Weak transcription	NHLF	lung
3	chr11:66674600-66696400	Weak transcription	NHEK	skin
4	chr11:66675000-66696200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:66675600-66687000	Weak transcription	Osteobl	bone
6	chr11:66675600-66699800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:66676200-66688600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:66676800-66696400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:66677200-66692000	Weak transcription	Pancreas	Pancrea
10	chr11:66678000-66688600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:66680200-66686800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr11:66680600-66689000	Weak transcription	Brain Germinal Matrix	brain
13	chr11:66680800-66687000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr11:66682400-66685400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:66682600-66685400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr11:66682600-66687400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:66683000-66685600	Enhancers	A549	lung
18	chr11:66683200-66688600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:66683200-66698200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr11:66683400-66688600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr11:66683400-66688600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr11:66683600-66687200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr11:66683600-66687400	Weak transcription	Adipose Nuclei	Adipose
24	chr11:66683600-66687600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:66683600-66688400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:66683600-66688600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr11:66683800-66686000	Weak transcription	Gastric	stomach
28	chr11:66683800-66687000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:66683800-66687200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:66683800-66687400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr11:66683800-66687400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr11:66683800-66692400	Weak transcription	Fetal Intestine Small	intestine
33	chr11:66684000-66685600	Weak transcription	Stomach Mucosa	stomach
34	chr11:66684000-66686000	Weak transcription	Hela-S3	cervix
35	chr11:66684000-66686000	Weak transcription	K562	blood
36	chr11:66684000-66687000	Weak transcription	Brain Anterior Caudate	brain
37	chr11:66684000-66687000	Weak transcription	Brain Hippocampus Middle	brain
38	chr11:66684000-66687000	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr11:66684000-66687200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:66684000-66687400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr11:66684000-66688600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr11:66684000-66688600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr11:66684000-66688800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:66684200-66686800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:66684200-66687000	Weak transcription	Brain Angular Gyrus	brain
46	chr11:66684200-66687000	Weak transcription	Brain Substantia Nigra	brain
47	chr11:66684600-66686800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:66685000-66685400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr11:66685000-66686400	Weak transcription	Brain Cingulate Gyrus	brain
50	chr11:66685200-66685400	Strong transcription	Liver	Liver

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