Variant report

Variant	rs4696695
Chromosome Location	chr4:8538177-8538178
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:8473542..8475287-chr4:8537371..8538949,2	MCF-7	breast:
2	chr4:8537532..8539229-chr4:8550769..8552595,2	MCF-7	breast:
3	chr4:8534354..8538693-chr4:8538746..8544060,9	MCF-7	breast:
4	chr4:8531043..8532660-chr4:8536787..8539068,2	K562	blood:

Variant related genes	Relation type
ENSG00000155275	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs13139429	0.85[AMR][1000 genomes]
rs13140128	0.91[ASN][1000 genomes]
rs16842480	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs16842483	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16842486	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16842498	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16842557	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs16842560	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs16842563	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs16842567	0.82[ASN][1000 genomes]
rs3103082	0.96[ASN][1000 genomes]
rs4247232	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4247233	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4259044	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4358384	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4619877	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4696692	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4696693	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4696696	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4696838	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55765509	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55789011	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55977448	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs56053534	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs61258495	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62287446	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62287455	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs869600	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs869602	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs883607	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1002680	chr4:8357163-8721214	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv4224	chr4:8503727-8546462	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv461221	chr4:8534283-8554894	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv593640	chr4:8534283-8554894	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv878612	chr4:8534283-8618916	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv980117	chr4:8535043-8545141	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8532600-8542800	Enhancers	Placenta	Placenta
2	chr4:8533200-8542800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:8535000-8541600	Enhancers	Pancreas	Pancrea
4	chr4:8535200-8538600	Enhancers	Colon Smooth Muscle	Colon
5	chr4:8535800-8540400	Enhancers	Lung	lung
6	chr4:8536000-8538200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:8536000-8538600	Weak transcription	Fetal Lung	lung
8	chr4:8536000-8538600	Weak transcription	Fetal Stomach	stomach
9	chr4:8536000-8538600	Weak transcription	Gastric	stomach
10	chr4:8536000-8538600	Weak transcription	Ovary	ovary
11	chr4:8536000-8538800	Weak transcription	Colonic Mucosa	Colon
12	chr4:8536000-8541400	Enhancers	Stomach Mucosa	stomach
13	chr4:8536400-8538400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:8536600-8538200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:8536600-8538400	Weak transcription	HSMMtube	muscle
16	chr4:8536600-8538600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:8536600-8538600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:8536600-8538600	Weak transcription	NHEK	skin
19	chr4:8536600-8538800	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr4:8536600-8541400	Enhancers	Esophagus	oesophagus
21	chr4:8536800-8538200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:8536800-8538200	Weak transcription	HMEC	breast
23	chr4:8536800-8538600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:8536800-8538800	Weak transcription	Duodenum Mucosa	Duodenum
25	chr4:8536800-8538800	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr4:8536800-8539600	Enhancers	Fetal Thymus	thymus
27	chr4:8537000-8538800	Enhancers	Stomach Smooth Muscle	stomach
28	chr4:8537200-8538800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr4:8537400-8538600	Weak transcription	Fetal Intestine Large	intestine
30	chr4:8537400-8538800	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr4:8537400-8539800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr4:8537400-8542200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:8537600-8542600	Enhancers	GM12878-XiMat	blood
34	chr4:8537800-8538400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr4:8537800-8538600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:8537800-8539200	Enhancers	Fetal Muscle Leg	muscle
37	chr4:8538000-8538400	Weak transcription	Rectal Smooth Muscle	rectum
38	chr4:8538000-8539000	Weak transcription	Fetal Kidney	kidney

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