Variant report

Variant	rs7827032
Chromosome Location	chr8:103779027-103779028
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:103769042..103771563-chr8:103778663..103780380,2	MCF-7	breast:
2	chr8:103775938..103779802-chr8:103800388..103802850,3	MCF-7	breast:
3	chr8:103760932..103779637-chr8:103816413..103823932,43	MCF-7	breast:
4	chr8:103768328..103770834-chr8:103776432..103779286,2	K562	blood:
5	chr8:103778765..103784253-chr8:103785133..103788553,5	MCF-7	breast:
6	chr8:103777223..103779993-chr8:103798108..103799875,2	MCF-7	breast:
7	chr8:103662477..103667937-chr8:103778259..103783622,7	MCF-7	breast:
8	chr8:103775757..103778292-chr8:103778774..103781669,2	K562	blood:
9	chr8:103751112..103752616-chr8:103777186..103780062,2	MCF-7	breast:
10	chr8:103664561..103669175-chr8:103777642..103782938,9	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253669	Chromatin interaction
ENSG00000155090	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10100951	1.00[CEU][hapmap]
rs1469767	1.00[EUR][1000 genomes]
rs16869801	1.00[CEU][hapmap]
rs2304350	1.00[CEU][hapmap]
rs28625448	1.00[EUR][1000 genomes]
rs28649644	1.00[EUR][1000 genomes]
rs28664674	1.00[EUR][1000 genomes]
rs56720100	1.00[EUR][1000 genomes]
rs56724276	1.00[EUR][1000 genomes]
rs60538892	1.00[EUR][1000 genomes]
rs60587672	1.00[EUR][1000 genomes]
rs73278866	1.00[EUR][1000 genomes]
rs73278868	1.00[EUR][1000 genomes]
rs73278884	1.00[EUR][1000 genomes]
rs73278887	1.00[EUR][1000 genomes]
rs7839128	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	esv1814245	chr8:103735804-103824566	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv1021898	chr8:103767324-103922482	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
4	nsv520922	chr8:103778809-103780586	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv519814	chr8:103778809-103806914	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103772400-103780200	Weak transcription	A549	lung
2	chr8:103774200-103779600	Weak transcription	Psoas Muscle	Psoas
3	chr8:103774400-103779200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:103774600-103779200	Weak transcription	Lung	lung
5	chr8:103774600-103779200	Weak transcription	Pancreas	Pancrea
6	chr8:103774600-103779600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:103774800-103780000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:103775000-103779600	Weak transcription	Fetal Lung	lung
9	chr8:103775000-103780000	Weak transcription	Brain Anterior Caudate	brain
10	chr8:103776600-103790600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr8:103776800-103779600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:103777000-103779600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:103777000-103780000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr8:103777200-103779200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:103777200-103780400	Weak transcription	Osteobl	bone
16	chr8:103777400-103779400	Weak transcription	Primary T cells from cord blood	blood
17	chr8:103777600-103779400	Weak transcription	Adipose Nuclei	Adipose
18	chr8:103777600-103779800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:103777600-103779800	Weak transcription	NHEK	skin
20	chr8:103778600-103779800	Enhancers	Colon Smooth Muscle	Colon
21	chr8:103778600-103781600	Enhancers	Fetal Muscle Leg	muscle
22	chr8:103778800-103780000	Bivalent Enhancer	HepG2	liver
23	chr8:103778800-103782600	Enhancers	Fetal Muscle Trunk	muscle
24	chr8:103778800-103783800	Enhancers	Fetal Thymus	thymus
25	chr8:103779000-103779600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr8:103779000-103779600	Enhancers	Stomach Smooth Muscle	stomach
27	chr8:103779000-103780000	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr8:103779000-103782600	Enhancers	Placenta	Placenta
29	chr8:103779000-103783600	Enhancers	Right Atrium	heart
30	chr8:103779000-103783800	Enhancers	Aorta	Aorta

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