Variant report

Variant	rs11133239
Chromosome Location	chr4:53848506-53848507
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:53414793..53417097-chr4:53846819..53849228,3	MCF-7	breast:
2	chr4:53576473..53578968-chr4:53847637..53849543,2	K562	blood:
3	chr4:53411349..53412285-chr4:53848309..53849353,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000226950	Chromatin interaction
ENSG00000264585	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs13340297	1.00[JPT][hapmap]
rs17645134	0.80[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	nsv1004889	chr4:53436500-54106281	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv537094	chr4:53436500-54106281	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv508280	chr4:53825060-53907661	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:53786600-53861400	Weak transcription	Primary B cells from cord blood	blood
2	chr4:53818200-53849800	Weak transcription	Primary T cells from cord blood	blood
3	chr4:53838800-53850200	Weak transcription	Aorta	Aorta
4	chr4:53844400-53849200	Weak transcription	Fetal Stomach	stomach
5	chr4:53844400-53850000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:53844400-53850200	Weak transcription	Ovary	ovary
7	chr4:53844600-53850000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:53844600-53850000	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:53846200-53850000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr4:53846800-53850000	Weak transcription	HMEC	breast
11	chr4:53846800-53850000	Weak transcription	NHEK	skin
12	chr4:53847000-53848600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:53847200-53849200	Weak transcription	Fetal Muscle Leg	muscle
14	chr4:53847400-53851200	Enhancers	Fetal Kidney	kidney
15	chr4:53847800-53850800	Enhancers	Fetal Heart	heart
16	chr4:53848000-53848800	Enhancers	Fetal Brain Female	brain
17	chr4:53848000-53849200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:53848000-53851400	Enhancers	NHDF-Ad	bronchial
19	chr4:53848000-53851600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:53848200-53850200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr4:53848400-53848600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr4:53848400-53848600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:53848400-53849200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:53848400-53850200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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