Variant report

Variant	rs577581818
Chromosome Location	chr8:100698354-100698355
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv524617	chr8:100032844-100717925	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1022914	chr8:100190356-100720313	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv539695	chr8:100190356-100720313	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv891226	chr8:100295634-100708595	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv891227	chr8:100295634-100743556	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1019256	chr8:100336249-100852803	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
7	nsv539698	chr8:100336249-100852803	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
8	esv2758167	chr8:100404151-100838624	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
9	esv2759633	chr8:100404151-100838624	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1029616	chr8:100442135-100796643	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1023922	chr8:100474230-100702005	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
12	nsv831408	chr8:100523523-100721507	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
13	esv20740	chr8:100698324-100701511	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100675400-100706000	Weak transcription	Left Ventricle	heart
2	chr8:100687000-100739800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:100688400-100708200	Weak transcription	HSMMtube	muscle
4	chr8:100688600-100705600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr8:100688800-100698400	Weak transcription	Aorta	Aorta
6	chr8:100688800-100698800	Weak transcription	Gastric	stomach
7	chr8:100688800-100704600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr8:100688800-100711400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr8:100688800-100716000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr8:100689000-100698800	Weak transcription	Thymus	Thymus
11	chr8:100692000-100698400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:100692000-100711800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:100692800-100698800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr8:100695200-100708200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:100695200-100709800	Weak transcription	Pancreas	Pancrea
16	chr8:100696000-100698400	ZNF genes & repeats	Fetal Lung	lung
17	chr8:100696000-100700000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:100697400-100698400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:100697600-100698400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
20	chr8:100697600-100698400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr8:100697600-100700800	Strong transcription	Primary T cells from cord blood	blood
22	chr8:100697800-100698400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr8:100697800-100698400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr8:100697800-100699000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr8:100697800-100700400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
26	chr8:100698000-100698400	Enhancers	HMEC	breast
27	chr8:100698000-100698600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:100698000-100698600	Weak transcription	Fetal Muscle Trunk	muscle
29	chr8:100698000-100698800	Enhancers	NHEK	skin
30	chr8:100698000-100699000	ZNF genes & repeats	Placenta	Placenta
31	chr8:100698000-100699000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
32	chr8:100698000-100699800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
33	chr8:100698000-100699800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:100698000-100716000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr8:100698200-100698400	ZNF genes & repeats	Fetal Intestine Large	intestine
36	chr8:100698200-100698600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
37	chr8:100698200-100698600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:100698200-100698600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:100698200-100698800	ZNF genes & repeats	Fetal Muscle Leg	muscle
40	chr8:100698200-100699000	Enhancers	K562	blood
41	chr8:100698200-100699200	Enhancers	Stomach Mucosa	stomach
42	chr8:100698200-100699600	Strong transcription	Ovary	ovary
43	chr8:100698200-100699800	Strong transcription	Primary B cells from peripheral blood	blood
44	chr8:100698200-100700000	Strong transcription	Primary B cells from cord blood	blood
45	chr8:100698200-100700000	Strong transcription	Duodenum Mucosa	Duodenum
46	chr8:100698200-100700000	ZNF genes & repeats	Fetal Stomach	stomach
47	chr8:100698200-100714600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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