Variant report

Variant	rs571391416
Chromosome Location	chr8:11017346-11017347
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	esv1815171	chr8:10940039-11128712	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1025426	chr8:10942929-11037903	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1026331	chr8:10955941-11046394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv519941	chr8:11016889-11039816	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10966400-11026200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:10997200-11021000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr8:10997400-11017400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr8:10999400-11021000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:11001600-11021000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr8:11002800-11022000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:11006800-11026200	Weak transcription	HSMM	muscle
8	chr8:11009200-11021000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:11009200-11024800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:11009800-11021400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:11012000-11021400	Weak transcription	Gastric	stomach
12	chr8:11012000-11022400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:11013200-11021000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr8:11013400-11026400	Weak transcription	Esophagus	oesophagus
15	chr8:11013600-11028800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:11014800-11017400	Weak transcription	Fetal Intestine Large	intestine
17	chr8:11014800-11021400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:11015400-11021600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:11015600-11021200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr8:11015600-11022400	Enhancers	Primary B cells from peripheral blood	blood
21	chr8:11016000-11021800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:11016600-11021400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr8:11016600-11032200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:11016800-11017400	Enhancers	HSMMtube	muscle
25	chr8:11017000-11017400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr8:11017000-11017400	Enhancers	GM12878-XiMat	blood
27	chr8:11017000-11017800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:11017200-11021000	Weak transcription	Pancreas	Pancrea
29	chr8:11017200-11021400	Weak transcription	Spleen	Spleen

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