Variant report

Variant	rs7695963
Chromosome Location	chr4:7975053-7975054
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:7938506..7945813-chr4:7968503..7977501,21	MCF-7	breast:
2	chr4:7943385..7945490-chr4:7973996..7976275,2	MCF-7	breast:
3	chr4:7974598..7977296-chr4:7995967..7999387,3	MCF-7	breast:
4	chr4:7940228..7942732-chr4:7972694..7975678,3	MCF-7	breast:
5	chr4:7973238..7976056-chr4:7980066..7981632,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196526	Chromatin interaction
ENSG00000228919	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12644791	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1317283	0.86[ASN][1000 genomes]
rs1317284	0.86[ASN][1000 genomes]
rs1317285	0.94[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1574393	0.94[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs28447132	0.92[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28461913	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28480985	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28653042	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28712356	0.88[AMR][1000 genomes]
rs4696724	0.90[AMR][1000 genomes]
rs4696725	0.87[AMR][1000 genomes]
rs4696927	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4696930	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6818752	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6824006	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6830083	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9685030	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv34140	chr4:7787936-8172491	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats 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	18 gene(s)	inside rSNPs	diseases
3	esv2754386	chr4:7822449-7992909	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2756298	chr4:7822449-7992909	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv829851	chr4:7958698-8049060	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
6	nsv469779	chr4:7965253-8177646	Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv482448	chr4:7965253-8177646	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv878579	chr4:7969594-8011696	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7963400-7975400	Weak transcription	Aorta	Aorta
2	chr4:7967000-7987600	Weak transcription	Psoas Muscle	Psoas
3	chr4:7969000-7975600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
4	chr4:7969200-7975600	Enhancers	Fetal Thymus	thymus
5	chr4:7969200-7975800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:7969400-7975800	Enhancers	Stomach Smooth Muscle	stomach
7	chr4:7969400-7976000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:7969600-7975800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr4:7970400-7980200	Weak transcription	HSMM	muscle
10	chr4:7970800-7975800	Enhancers	NH-A	brain
11	chr4:7971000-7976000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:7971000-7976000	Enhancers	HMEC	breast
13	chr4:7971200-7976000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:7971600-7975800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:7972000-7975200	Weak transcription	HSMMtube	muscle
16	chr4:7972200-7975400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr4:7972200-7976200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:7972200-7979600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr4:7972200-7980600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:7972400-7975200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:7972400-7975400	Weak transcription	Brain Anterior Caudate	brain
22	chr4:7972400-7975600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr4:7972400-7975600	Enhancers	Esophagus	oesophagus
24	chr4:7972400-7975800	Weak transcription	Colon Smooth Muscle	Colon
25	chr4:7972400-7976000	Enhancers	NHEK	skin
26	chr4:7972400-7978400	Weak transcription	Fetal Kidney	kidney
27	chr4:7972400-7980200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr4:7972600-7975400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr4:7972600-7975400	Weak transcription	Left Ventricle	heart
30	chr4:7972600-7976000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:7972600-7976000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:7972800-7975400	Weak transcription	Right Atrium	heart
33	chr4:7972800-7975600	Enhancers	Fetal Intestine Large	intestine
34	chr4:7972800-7975600	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr4:7973000-7975200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:7973000-7975600	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr4:7973000-7975600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr4:7973000-7975600	Enhancers	Stomach Mucosa	stomach
39	chr4:7973000-7976000	Enhancers	Placenta	Placenta
40	chr4:7973000-7978400	Weak transcription	Fetal Lung	lung
41	chr4:7973000-7980000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:7973000-7980200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:7973000-7980200	Weak transcription	Adipose Nuclei	Adipose
44	chr4:7973200-7975600	Enhancers	A549	lung
45	chr4:7973200-7975600	Enhancers	GM12878-XiMat	blood
46	chr4:7973400-7978400	Weak transcription	Fetal Brain Male	brain
47	chr4:7973400-7978400	Weak transcription	Fetal Heart	heart
48	chr4:7973600-7975400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr4:7973600-7975600	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr4:7973600-7975800	Enhancers	NHLF	lung

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