Variant report

Variant	rs6772119
Chromosome Location	chr3:24514462-24514463
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:24503594..24506625-chr3:24513720..24517968,3	MCF-7	breast:
2	chr3:24514431..24517573-chr3:24535246..24537303,3	K562	blood:
3	chr3:24510050..24515409-chr3:24534368..24537620,7	MCF-7	breast:
4	chr3:24513307..24515783-chr3:24564000..24565708,2	MCF-7	breast:
5	chr3:24513555..24516625-chr3:24517777..24521528,3	MCF-7	breast:
6	chr3:24510569..24514476-chr3:24514887..24518486,4	K562	blood:

Variant related genes	Relation type
ENSG00000228791	Chromatin interaction
ENSG00000151090	Chromatin interaction

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

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

rs_ID	r²[population]
rs9816324	1.00[AMR][1000 genomes]
rs9845983	1.00[YRI][hapmap];1.00[AFR][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	nsv834641	chr3:24465862-24633738	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv834642	chr3:24475558-24640593	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
3	nsv1012975	chr3:24500706-24615644	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24499600-24526800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr3:24503200-24517200	Weak transcription	Colon Smooth Muscle	Colon
3	chr3:24504600-24517400	Weak transcription	Right Ventricle	heart
4	chr3:24509600-24531000	Weak transcription	Fetal Lung	lung
5	chr3:24510000-24517400	Weak transcription	NHDF-Ad	bronchial
6	chr3:24511000-24517400	Weak transcription	Fetal Intestine Small	intestine
7	chr3:24513200-24514600	Enhancers	HMEC	breast
8	chr3:24513600-24514600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:24513600-24514800	Enhancers	Hela-S3	cervix
10	chr3:24513600-24517400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:24513600-24517400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:24513600-24517400	Weak transcription	Adipose Nuclei	Adipose
13	chr3:24513800-24517400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr3:24514000-24517000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:24514000-24517400	Weak transcription	Liver	Liver
16	chr3:24514000-24517400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:24514200-24515800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:24514200-24517000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr3:24514200-24517400	Weak transcription	Psoas Muscle	Psoas
20	chr3:24514400-24517000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:24514400-24517000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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