Variant report

Variant	rs11570222
Chromosome Location	chr11:57582908-57582909
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	chr11:57439349..57441484-chr11:57580748..57583529,2	MCF-7	breast:
2	chr11:57530276..57533156-chr11:57582774..57585188,2	K562	blood:

Variant related genes	Relation type
ENSG00000156599	Chromatin interaction
ENSG00000198561	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10896641	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11570214	0.95[AFR][1000 genomes]
rs12284270	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1704778	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2911726	1.00[ASW][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[YRI][hapmap]
rs2926652	1.00[YRI][hapmap]
rs2926657	1.00[ASW][hapmap];1.00[LWK][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2969934	1.00[ASW][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[YRI][hapmap]
rs2969940	1.00[ASW][hapmap];1.00[LWK][hapmap];0.84[MKK][hapmap];1.00[YRI][hapmap]
rs2969946	1.00[YRI][hapmap]
rs613152	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs620450	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs637770	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs686459	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][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	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv530621	chr11:57139699-57703639	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	nsv1040913	chr11:57315006-57696122	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
5	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11570222	CTNND1	cis	multi-tissue	Pritchard

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57556400-57587800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:57568200-57585800	Strong transcription	Fetal Muscle Trunk	muscle
3	chr11:57568200-57586000	Strong transcription	Fetal Muscle Leg	muscle
4	chr11:57568200-57588200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:57568400-57586600	Strong transcription	Placenta	Placenta
6	chr11:57568600-57585800	Strong transcription	Sigmoid Colon	Sigmoid Colon
7	chr11:57568600-57586000	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr11:57568600-57586000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:57568600-57586400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:57568600-57586600	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr11:57568600-57587000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr11:57568600-57587200	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:57568600-57589000	Strong transcription	NHLF	lung
14	chr11:57568800-57585200	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr11:57568800-57585600	Strong transcription	Fetal Intestine Large	intestine
16	chr11:57568800-57589000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:57568800-57589000	Strong transcription	NH-A	brain
18	chr11:57569000-57583800	Strong transcription	NHDF-Ad	bronchial
19	chr11:57569000-57584800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
20	chr11:57569000-57584800	Strong transcription	HMEC	breast
21	chr11:57569000-57585000	Strong transcription	HepG2	liver
22	chr11:57569000-57585800	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr11:57569000-57586000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr11:57569000-57586400	Strong transcription	Brain Germinal Matrix	brain
25	chr11:57569000-57587000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr11:57569000-57587000	Strong transcription	NHEK	skin
27	chr11:57569000-57587200	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr11:57569000-57587400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr11:57569000-57587800	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr11:57569000-57588800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:57569000-57589200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:57569200-57583200	Strong transcription	Fetal Brain Male	brain
33	chr11:57569200-57584800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:57569200-57584800	Strong transcription	A549	lung
35	chr11:57569200-57585000	Strong transcription	Ovary	ovary
36	chr11:57569200-57585200	Strong transcription	Fetal Intestine Small	intestine
37	chr11:57569200-57585400	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr11:57569200-57585400	Strong transcription	Stomach Smooth Muscle	stomach
39	chr11:57569200-57585800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:57569200-57585800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:57569200-57585800	Strong transcription	Fetal Stomach	stomach
42	chr11:57569200-57585800	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr11:57569200-57586000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:57569200-57586200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:57569200-57586200	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr11:57569200-57586400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:57569200-57586600	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr11:57569200-57586600	Strong transcription	Fetal Brain Female	brain
49	chr11:57569200-57587200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:57569200-57589000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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