Variant report

Variant	rs566248693
Chromosome Location	chr9:93563004-93563005
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr9:93562794-93563112	GM12878	blood:	n/a	n/a
2	SPI1	chr9:93562844-93563059	K562	blood:	n/a	n/a
3	POLR2A	chr9:93562803-93565322	GM12891	blood:	n/a	n/a
4	POLR2A	chr9:93562865-93564666	GM19193	blood:	n/a	n/a
5	SPI1	chr9:93562689-93563135	GM12891	blood:	n/a	n/a
6	SPI1	chr9:93562849-93563064	GM12878	blood:	n/a	n/a
7	POLR2A	chr9:93562858-93564727	GM12878	blood:	n/a	n/a
8	POLR2A	chr9:93562373-93564761	GM19099	blood:	n/a	n/a
9	SPI1	chr9:93562859-93563206	HL-60	blood:	n/a	n/a
10	POLR2A	chr9:93562921-93564604	GM15510	blood:	n/a	n/a
11	POLR2A	chr9:93562377-93564915	Raji	blood:	n/a	n/a
12	SPI1	chr9:93562491-93563422	GM12878	blood:	n/a	n/a
13	SPI1	chr9:93562741-93563130	GM12891	blood:	n/a	n/a
14	FOXM1	chr9:93562259-93563114	GM12878	blood:	n/a	n/a
15	SPI1	chr9:93562799-93563062	K562	blood:	n/a	n/a
16	NFYB	chr9:93562757-93563357	GM12878	blood:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:93557618..93560728-chr9:93560879..93563311,3	K562	blood:
2	chr9:93561901..93563996-chr9:93577117..93579715,2	MCF-7	breast:

No data

Variant related genes	Relation type
SYK	TF binding region

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893567	chr9:93519280-93609668	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831652	chr9:93527411-93696923	Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv893569	chr9:93552550-93587089	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1038685	chr9:93556174-93685729	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv1813758	chr9:93557698-93573095	Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv3387417	chr9:93562956-93565504	Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93551800-93563400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:93552000-93563400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:93556000-93563400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:93557600-93563400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:93557600-93563400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr9:93557600-93563400	Weak transcription	Pancreas	Pancrea
7	chr9:93559000-93563800	Weak transcription	Gastric	stomach
8	chr9:93559200-93563200	Weak transcription	Thymus	Thymus
9	chr9:93559400-93563200	Weak transcription	Stomach Mucosa	stomach
10	chr9:93561200-93564000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr9:93561400-93563200	Enhancers	Primary B cells from cord blood	blood
12	chr9:93561800-93563400	Enhancers	Primary B cells from peripheral blood	blood
13	chr9:93561800-93563400	Enhancers	GM12878-XiMat	blood
14	chr9:93562400-93563200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:93562600-93563200	Enhancers	Primary hematopoietic stem cells	blood
16	chr9:93562600-93563200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:93562800-93563400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr9:93562800-93563400	Enhancers	Fetal Intestine Large	intestine
19	chr9:93562800-93563400	Enhancers	Fetal Thymus	thymus
20	chr9:93562800-93563400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr9:93562800-93563400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr9:93562800-93563400	Enhancers	K562	blood
23	chr9:93562800-93563800	Enhancers	Spleen	Spleen
24	chr9:93563000-93563800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr9:93563000-93563800	Bivalent Enhancer	Brain Hippocampus Middle	brain

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