Variant report

Variant	rs183896428
Chromosome Location	chr8:119080174-119080175
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:119073070..119075037-chr8:119078486..119081201,2	MCF-7	breast:
2	chr8:119078696..119080896-chr8:119086138..119088865,2	MCF-7	breast:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv612047	chr8:118939094-119468609	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1015380	chr8:118948652-119418389	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv539736	chr8:118948652-119418389	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv831441	chr8:119055370-119262970	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	esv2752195	chr8:119058819-119139819	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv526044	chr8:119079196-119082204	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119062200-119083600	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:119062800-119085000	Weak transcription	Fetal Stomach	stomach
3	chr8:119068000-119085600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr8:119069000-119081200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:119069200-119081200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr8:119069200-119091600	Weak transcription	Primary T cells from cord blood	blood
7	chr8:119069800-119080200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:119072800-119080400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr8:119073400-119083400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr8:119074000-119086200	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:119074000-119087200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr8:119074800-119086400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:119074800-119088600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:119075000-119102000	Weak transcription	Spleen	Spleen
15	chr8:119075600-119086000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr8:119075800-119081200	Weak transcription	Adipose Nuclei	Adipose
17	chr8:119075800-119081200	Weak transcription	Psoas Muscle	Psoas
18	chr8:119075800-119081400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:119075800-119083600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:119075800-119085800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:119075800-119086200	Weak transcription	Right Atrium	heart
22	chr8:119075800-119086400	Weak transcription	Brain Anterior Caudate	brain
23	chr8:119076000-119081200	Weak transcription	Fetal Lung	lung
24	chr8:119076000-119081200	Weak transcription	Small Intestine	intestine
25	chr8:119076000-119081200	Weak transcription	NHDF-Ad	bronchial
26	chr8:119076000-119086200	Weak transcription	Right Ventricle	heart
27	chr8:119076400-119086200	Weak transcription	Left Ventricle	heart
28	chr8:119076400-119086200	Weak transcription	Lung	lung
29	chr8:119077400-119080600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:119077400-119082000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:119078000-119080200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:119078000-119081400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:119078000-119099000	Weak transcription	Dnd41	blood
34	chr8:119078200-119080600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:119078200-119081000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr8:119078200-119083600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr8:119078200-119085200	Weak transcription	Fetal Brain Male	brain
38	chr8:119078400-119081200	Weak transcription	HUVEC	blood vessel
39	chr8:119078400-119085800	Weak transcription	Fetal Heart	heart
40	chr8:119078400-119086600	Weak transcription	Pancreas	Pancrea
41	chr8:119078400-119088400	Weak transcription	Hela-S3	cervix
42	chr8:119078400-119091600	Weak transcription	Gastric	stomach
43	chr8:119078600-119080200	Weak transcription	HepG2	liver
44	chr8:119078600-119081400	Weak transcription	Fetal Intestine Large	intestine
45	chr8:119079000-119081200	Weak transcription	Fetal Intestine Small	intestine
46	chr8:119079200-119086200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:119079200-119086400	Weak transcription	Brain Substantia Nigra	brain
48	chr8:119079400-119080200	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:119079400-119080200	Enhancers	Aorta	Aorta
50	chr8:119079400-119080200	Strong transcription	Liver	Liver

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