Variant report

Variant	rs58518119
Chromosome Location	chr8:107685944-107685945
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:107679723..107681395-chr8:107684179..107686589,2	MCF-7	breast:
2	chr8:107685113..107687431-chr8:107693590..107695570,2	K562	blood:
3	chr8:107680913..107683388-chr8:107685068..107687950,2	K562	blood:

Variant related genes	Relation type
ENSG00000164830	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs28921388	1.00[AMR][1000 genomes]
rs28921415	1.00[AMR][1000 genomes]
rs28924672	1.00[AMR][1000 genomes]
rs28924685	1.00[AMR][1000 genomes]
rs36061217	1.00[AMR][1000 genomes]
rs6991117	1.00[AMR][1000 genomes]
rs7845537	1.00[AMR][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	nsv831419	chr8:107624709-107827801	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers 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	7 gene(s)	inside rSNPs	diseases
2	nsv6342	chr8:107644092-107688898	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv1799660	chr8:107679505-107689755	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107671200-107697200	Weak transcription	HSMM	muscle
2	chr8:107672200-107718800	Weak transcription	Psoas Muscle	Psoas
3	chr8:107672400-107718600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr8:107672600-107686000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:107672600-107696000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:107672800-107696000	Weak transcription	Fetal Kidney	kidney
7	chr8:107674400-107696000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr8:107676200-107697400	Weak transcription	Left Ventricle	heart
9	chr8:107677600-107709400	Weak transcription	Pancreas	Pancrea
10	chr8:107677600-107718800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr8:107679200-107738200	Weak transcription	Right Ventricle	heart
12	chr8:107681200-107730200	Weak transcription	Small Intestine	intestine
13	chr8:107681600-107696600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr8:107682200-107696600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:107683000-107686000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:107683600-107692800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr8:107683800-107718800	Weak transcription	Hela-S3	cervix
18	chr8:107684800-107686600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr8:107684800-107687000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
20	chr8:107684800-107687200	ZNF genes & repeats	Primary B cells from cord blood	blood
21	chr8:107684800-107688800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:107685400-107687200	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr8:107685600-107686400	ZNF genes & repeats	Primary T cells from cord blood	blood
24	chr8:107685600-107686600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
25	chr8:107685600-107686600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr8:107685800-107686000	ZNF genes & repeats	Gastric	stomach
27	chr8:107685800-107686000	Enhancers	Stomach Smooth Muscle	stomach
28	chr8:107685800-107686200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:107685800-107686400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
30	chr8:107685800-107686400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
31	chr8:107685800-107686400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:107685800-107686400	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr8:107685800-107686400	ZNF genes & repeats	Liver	Liver
34	chr8:107685800-107686400	Enhancers	Esophagus	oesophagus
35	chr8:107685800-107686400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr8:107685800-107686400	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
37	chr8:107685800-107686600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:107685800-107686600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr8:107685800-107686600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:107685800-107686600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
41	chr8:107685800-107686600	ZNF genes & repeats	Fetal Stomach	stomach
42	chr8:107685800-107687200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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