Variant report

Variant	rs4407485
Chromosome Location	chr4:120020195-120020196
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:119967207..119969277-chr4:120017510..120021674,3	MCF-7	breast:
2	chr4:120015958..120018191-chr4:120019171..120021900,2	MCF-7	breast:
3	chr4:120018111..120021033-chr4:120132660..120135354,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000145390	Chromatin interaction
ENSG00000178636	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs17272604	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17332199	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1903108	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1982571	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4240323	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4261975	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4320121	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4320122	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4374608	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4420962	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4420963	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4440202	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4508865	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4565063	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4572857	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4629433	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4637382	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4834747	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4834748	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs5008976	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs5008977	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6813730	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6819075	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6845990	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6851886	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6852072	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6852315	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7669848	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv948802	chr4:119844269-120208926	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv1007214	chr4:120007913-120112460	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1008115	chr4:120007913-120143849	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv1003827	chr4:120008227-120112460	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv522386	chr4:120009147-120115379	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
8	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
9	nsv1007619	chr4:120014898-120112460	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4407485	USP53	cis	lung	GTEx

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120014800-120022800	Weak transcription	NHEK	skin
2	chr4:120014800-120045000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:120015000-120020200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:120015000-120020200	Weak transcription	HSMM	muscle
5	chr4:120015000-120020200	Weak transcription	NH-A	brain
6	chr4:120015000-120021800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr4:120015000-120027800	Weak transcription	Right Atrium	heart
8	chr4:120015600-120020200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:120015800-120020200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:120017000-120027600	Weak transcription	Left Ventricle	heart
11	chr4:120018600-120022000	Enhancers	A549	lung
12	chr4:120018800-120020200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:120018800-120021000	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:120018800-120022400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:120019000-120020200	Enhancers	NHDF-Ad	bronchial
16	chr4:120019000-120020600	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr4:120019000-120020800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:120019200-120020600	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr4:120019400-120020600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr4:120019400-120025000	Weak transcription	Colon Smooth Muscle	Colon
21	chr4:120019600-120020800	Enhancers	Osteobl	bone
22	chr4:120019800-120020200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr4:120019800-120020400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr4:120020000-120021000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:120020000-120021000	Enhancers	Hela-S3	cervix
26	chr4:120020000-120021000	Enhancers	HSMMtube	muscle
27	chr4:120020000-120021200	Enhancers	Muscle Satellite Cultured Cells	--

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