Variant report

Variant	rs72958012
Chromosome Location	chr11:85351715-85351716
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:85337741..85343545-chr11:85345780..85354384,11	MCF-7	breast:
2	chr11:85347047..85348575-chr11:85349849..85352834,2	MCF-7	breast:
3	chr11:85338250..85341391-chr11:85347882..85353212,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000171204	Chromatin interaction
ENSG00000150672	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11234386	0.89[ASN][1000 genomes]
rs11234387	0.89[ASN][1000 genomes]
rs11234388	0.89[ASN][1000 genomes]
rs11234389	0.84[ASN][1000 genomes]
rs11234390	0.84[ASN][1000 genomes]
rs11234391	0.84[ASN][1000 genomes]
rs17148355	0.89[ASN][1000 genomes]
rs17208525	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17208602	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17208616	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17810701	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17810766	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17810802	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17810855	0.93[ASN][1000 genomes]
rs2276018	0.91[ASN][1000 genomes]
rs2304342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2374638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs494119	0.94[ASN][1000 genomes]
rs56695336	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57431471	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58631677	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59508078	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs616309	0.94[ASN][1000 genomes]
rs645798	0.94[ASN][1000 genomes]
rs72953967	0.85[ASN][1000 genomes]
rs72953982	0.89[ASN][1000 genomes]
rs72953991	0.89[ASN][1000 genomes]
rs72953995	0.94[ASN][1000 genomes]
rs72955904	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72955912	0.93[EUR][1000 genomes]
rs72955918	0.93[EUR][1000 genomes]
rs72955922	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72955939	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72958014	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72958027	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][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	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS 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 target site	64 gene(s)	inside rSNPs	diseases
3	nsv898047	chr11:85180409-85377707	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv898048	chr11:85206156-85404138	Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85340200-85351800	Weak transcription	Gastric	stomach
2	chr11:85340200-85352400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:85340600-85352800	Weak transcription	Fetal Brain Male	brain
4	chr11:85340600-85358200	Weak transcription	Aorta	Aorta
5	chr11:85340800-85358200	Weak transcription	Fetal Stomach	stomach
6	chr11:85340800-85358200	Weak transcription	Right Ventricle	heart
7	chr11:85340800-85358200	Weak transcription	HSMMtube	muscle
8	chr11:85341200-85354400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:85341200-85358000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr11:85341200-85358000	Weak transcription	NHLF	lung
11	chr11:85341200-85358200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:85341200-85358200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr11:85341200-85358200	Weak transcription	Spleen	Spleen
14	chr11:85341200-85358400	Weak transcription	Small Intestine	intestine
15	chr11:85341400-85354200	Weak transcription	Fetal Intestine Small	intestine
16	chr11:85341800-85353000	Weak transcription	Fetal Heart	heart
17	chr11:85342200-85358200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr11:85342400-85352600	Weak transcription	Psoas Muscle	Psoas
19	chr11:85342800-85352600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:85345800-85358000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr11:85346000-85354400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr11:85346000-85358000	Weak transcription	HMEC	breast
23	chr11:85346000-85358200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr11:85346000-85358200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr11:85346000-85358200	Weak transcription	Brain Angular Gyrus	brain
26	chr11:85346000-85358200	Weak transcription	Brain Substantia Nigra	brain
27	chr11:85346000-85358200	Weak transcription	Fetal Lung	lung
28	chr11:85346000-85358200	Weak transcription	NHEK	skin
29	chr11:85346400-85352600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr11:85346400-85354200	Weak transcription	Hela-S3	cervix
31	chr11:85346400-85358000	Weak transcription	HepG2	liver
32	chr11:85346400-85358200	Weak transcription	Lung	lung
33	chr11:85346600-85358200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr11:85346800-85358000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:85346800-85358200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr11:85347200-85357800	Weak transcription	GM12878-XiMat	blood
37	chr11:85347200-85358200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr11:85347400-85358000	Weak transcription	Colon Smooth Muscle	Colon
39	chr11:85347400-85358000	Weak transcription	Stomach Smooth Muscle	stomach
40	chr11:85347600-85354200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:85347600-85358000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:85347600-85358200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:85347600-85358200	Weak transcription	Brain Anterior Caudate	brain
44	chr11:85347800-85354400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr11:85347800-85358000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:85347800-85358200	Weak transcription	Placenta	Placenta
47	chr11:85348000-85352200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:85348000-85353200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:85348000-85358200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:85348200-85358200	Weak transcription	NHDF-Ad	bronchial

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