Variant report

Variant	rs4734294
Chromosome Location	chr8:95979997-95979998
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95972771..95975327-chr8:95979134..95982751,4	MCF-7	breast:
2	chr8:95958611..95965751-chr8:95975918..95982196,8	MCF-7	breast:
3	chr8:95977560..95980300-chr8:96031568..96033219,2	MCF-7	breast:
4	chr8:95979420..95981585-chr8:96022909..96025497,2	MCF-7	breast:
5	chr8:95979244..95983291-chr8:95999970..96003553,4	MCF-7	breast:
6	chr8:95977216..95979367-chr8:95979972..95982886,3	K562	blood:
7	chr8:95959560..95963083-chr8:95975054..95981497,8	MCF-7	breast:
8	chr8:95979576..95981944-chr8:95985170..95988290,3	MCF-7	breast:
9	chr8:95975782..95977350-chr8:95979734..95982719,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000164938	Chromatin interaction
ENSG00000156170	Chromatin interaction
ENSG00000253878	Chromatin interaction
ENSG00000253528	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10081596	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10086284	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10112447	0.92[ASN][1000 genomes]
rs1011795	0.90[ASN][1000 genomes]
rs1011796	0.91[ASN][1000 genomes]
rs10956932	0.81[ASN][1000 genomes]
rs12549003	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1349763	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1453379	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2013597	0.91[ASN][1000 genomes]
rs2084968	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2904893	0.91[ASN][1000 genomes]
rs2956210	0.91[ASN][1000 genomes]
rs3019175	0.82[ASN][1000 genomes]
rs3802193	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4734293	0.89[ASN][1000 genomes]
rs4735334	0.92[ASN][1000 genomes]
rs6993278	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7007935	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7823366	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7827478	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7835379	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs896850	0.91[ASN][1000 genomes]
rs896851	0.91[ASN][1000 genomes]
rs9643353	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers 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	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95962800-95980200	Weak transcription	Ovary	ovary
2	chr8:95962800-95980600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:95963000-95980400	Weak transcription	HSMM	muscle
4	chr8:95964400-95980000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:95964400-96002200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:95964600-95980200	Weak transcription	Brain Substantia Nigra	brain
7	chr8:95964600-95980600	Weak transcription	Fetal Brain Female	brain
8	chr8:95964600-95992800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:95964800-95980400	Weak transcription	Brain Anterior Caudate	brain
10	chr8:95964800-95981800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:95964800-95999000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:95964800-95999600	Weak transcription	Brain Hippocampus Middle	brain
13	chr8:95964800-95999600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr8:95965000-95999600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr8:95966000-95986800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:95966000-95993000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr8:95970600-96000800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:95971400-95986800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr8:95971400-95987400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:95971600-95983800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:95971600-95987000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:95971600-95987000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr8:95971600-95987200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:95971600-96000400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:95971800-95986800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:95972400-95980800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:95972400-95994800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr8:95972600-95987600	Weak transcription	HMEC	breast
29	chr8:95972800-95980200	Weak transcription	Fetal Lung	lung
30	chr8:95973000-95980200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr8:95973000-95987000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr8:95973200-95980200	Weak transcription	HSMMtube	muscle
33	chr8:95973600-95980200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr8:95973600-95981800	Enhancers	Pancreas	Pancrea
35	chr8:95974400-95980200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr8:95974400-95980200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr8:95974400-96002000	Weak transcription	Esophagus	oesophagus
38	chr8:95974600-95980200	Weak transcription	Gastric	stomach
39	chr8:95974600-95980600	Weak transcription	Colonic Mucosa	Colon
40	chr8:95974600-95987000	Weak transcription	Thymus	Thymus
41	chr8:95975800-95981000	Enhancers	Osteobl	bone
42	chr8:95976000-95980200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr8:95976000-95980400	Weak transcription	HepG2	liver
44	chr8:95976200-95980000	Weak transcription	Fetal Heart	heart
45	chr8:95976200-95980400	Weak transcription	Right Ventricle	heart
46	chr8:95976200-95990000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr8:95976400-95980000	Weak transcription	Fetal Muscle Leg	muscle
48	chr8:95976400-95980200	Weak transcription	Lung	lung
49	chr8:95976600-95981000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr8:95976600-95993200	Weak transcription	Primary T cells from cord blood	blood

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