Variant report

Variant	esv1813758
Chromosome Location	chr9:93557698-93573095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:427)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:93558128-93558701	GM12878	blood:	n/a	n/a
2	ATF2	chr9:93558086-93558762	GM12878	blood:	n/a	n/a
3	ATF2	chr9:93570958-93571504	GM12878	blood:	n/a	n/a
4	BATF	chr9:93558330-93558658	GM12878	blood:	n/a	n/a
5	BATF	chr9:93558312-93558666	GM12878	blood:	n/a	n/a
6	BATF	chr9:93562260-93562580	GM12878	blood:	n/a	n/a
7	BCLAF1	chr9:93557895-93558286	GM12878	blood:	n/a	n/a
8	BCLAF1	chr9:93558295-93558754	GM12878	blood:	n/a	n/a
9	BCLAF1	chr9:93563791-93564158	GM12878	blood:	n/a	chr9:93563897-93563910 chr9:93564106-93564119 chr9:93563994-93564007
10	BHLHE40	chr9:93563893-93564846	K562	blood:	n/a	chr9:93563900-93563916 chr9:93564075-93564091 chr9:93564103-93564119 chr9:93564079-93564095 chr9:93564100-93564116
11	BHLHE40	chr9:93564460-93564481	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:93557323-93557700	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:93562410-93562610	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:93563964-93564164	GM12878	blood:	n/a	chr9:93564075-93564091 chr9:93564103-93564119 chr9:93564079-93564095 chr9:93564100-93564116
15	BRCA1	chr9:93564267-93564283	GM12878	blood:	n/a	n/a
16	CCNT2	chr9:93563783-93564596	K562	blood:	n/a	n/a
17	CEBPB	chr9:93558076-93558339	K562	blood:	n/a	n/a
18	CEBPB	chr9:93569861-93570164	K562	blood:	n/a	chr9:93570002-93570019 chr9:93569935-93569946
19	CEBPB	chr9:93567249-93567449	K562	blood:	n/a	chr9:93567258-93567271
20	CEBPB	chr9:93558125-93558375	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr9:93562516-93562658	GM12878	blood:	n/a	n/a
22	CHD1	chr9:93564204-93565045	GM12878	blood:	n/a	n/a
23	CHD1	chr9:93563902-93564658	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr9:93564155-93564657	K562	blood:	n/a	n/a
25	CHD2	chr9:93564260-93564291	GM12878	blood:	n/a	n/a
26	CTBP2	chr9:93563441-93564584	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:93562380-93562530	GM06990	blood:	n/a	n/a
28	CTCF	chr9:93562440-93562590	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr9:93562460-93562610	HMEC	breast:	n/a	n/a
30	CTCF	chr9:93563902-93563912	MCF-7	breast:	n/a	n/a
31	CTCF	chr9:93562347-93562741	GM12878	blood:	n/a	n/a
32	CTCF	chr9:93562400-93562550	K562	blood:	n/a	n/a
33	CTCF	chr9:93562474-93562637	GM13977	blood:	n/a	n/a
34	CTCF	chr9:93562400-93562550	GM12869	blood:	n/a	n/a
35	CTCF	chr9:93562400-93562550	SAEC	small airway:	n/a	n/a
36	CTCF	chr9:93562420-93562570	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr9:93563840-93563990	GM12866	blood:	n/a	n/a
38	CTCF	chr9:93562431-93562617	GM19240	blood:	n/a	n/a
39	CTCF	chr9:93562470-93562603	Gliobla	brain:	n/a	n/a
40	CTCF	chr9:93562500-93562650	GM12867	blood:	n/a	n/a
41	CTCF	chr9:93562499-93562609	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr9:93562420-93562570	GM12875	blood:	n/a	n/a
43	CTCF	chr9:93562460-93562610	AG04449	skin:	n/a	n/a
44	CTCF	chr9:93563560-93563710	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr9:93563800-93563950	SAEC	small airway:	n/a	n/a
46	CTCF	chr9:93562380-93562530	HL-60	blood:	n/a	n/a
47	CTCF	chr9:93562448-93562595	HepG2	liver:	n/a	n/a
48	CTCF	chr9:93562420-93562570	SAEC	small airway:	n/a	n/a
49	CTCF	chr9:93562530-93562600	Medullo	brain:	n/a	n/a
50	CTCF	chr9:93562420-93562570	GM12872	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:93564603-93564653	HRE	kidney:	n/a
2	chr9:93564339-93564389	AG09319	gingival:	n/a
3	chr9:93564339-93564389	NH-A	brain:	n/a
4	chr9:93564028-93564078	SKMC	muscle:	n/a
5	chr9:93564149-93564199	HUVEC	blood vessel:	n/a
6	chr9:93564149-93564199	HRCEpiC	kidney:	n/a
7	chr9:93564603-93564653	SK-N-SH_RA	brain:	n/a
8	chr9:93564603-93564653	NHBE	bronchial:	n/a
9	chr9:93564603-93564653	Hepatocyte	liver:	n/a
10	chr9:93564149-93564199	NH-A	brain:	n/a
11	chr9:93564028-93564078	Hela-S3	cervix:	n/a
12	chr9:93564456-93564506	H1-hESC	embryonic stem cell:	embryo
13	chr9:93563776-93563826	HIPEpiC	eye:	n/a
14	chr9:93564339-93564389	HUVEC	blood vessel:	n/a
15	chr9:93563778-93563828	GM12892	blood:	n/a
16	chr9:93564603-93564653	GM12878	blood:	n/a
17	chr9:93564149-93564199	HCM	heart:	n/a
18	chr9:93564149-93564199	HCT-116	colon:	n/a
19	chr9:93564149-93564199	PFSK-1	brain:	n/a
20	chr9:93563778-93563828	HEK293	kidney:	embryo
21	chr9:93563776-93563826	K562	blood:	n/a
22	chr9:93563776-93563826	AG04450	lung:	fetal
23	chr9:93563778-93563828	LNCaP	prostate:	n/a
24	chr9:93564149-93564199	H1-hESC	embryonic stem cell:	embryo
25	chr9:93564339-93564389	HRE	kidney:	n/a
26	chr9:93564149-93564199	Jurkat	blood:	n/a
27	chr9:93563778-93563828	SAEC	small airway:	n/a
28	chr9:93564339-93564389	Caco-2	colon:	n/a
29	chr9:93564149-93564199	BJ	skin:	n/a
30	chr9:93564149-93564199	AG10803	skin:	n/a
31	chr9:93564456-93564506	HRPEpiC	eye:	n/a
32	chr9:93564456-93564506	Hepatocyte	liver:	n/a
33	chr9:93564339-93564389	AoSMC	blood vessel:	n/a
34	chr9:93563776-93563826	PrEC	prostate:	n/a
35	chr9:93564603-93564653	SK-N-MC	brain:	n/a
36	chr9:93563778-93563828	SKMC	muscle:	n/a
37	chr9:93564149-93564199	SKMC	muscle:	n/a
38	chr9:93564339-93564389	HRCEpiC	kidney:	n/a
39	chr9:93564603-93564653	NH-A	brain:	n/a
40	chr9:93563776-93563826	ECC-1	luminal epithelium:	n/a
41	chr9:93564339-93564389	Hela-S3	cervix:	n/a
42	chr9:93564028-93564078	U87	brain:	n/a
43	chr9:93564456-93564506	A549	lung:	n/a
44	chr9:93563776-93563826	T-47D	breast:	n/a
45	chr9:93563778-93563828	HL-60	blood:	n/a
46	chr9:93564603-93564653	U87	brain:	n/a
47	chr9:93563778-93563828	PFSK-1	brain:	n/a
48	chr9:93564149-93564199	PANC-1	pancreas:	n/a
49	chr9:93564603-93564653	GM12891	blood:	n/a
50	chr9:93563776-93563826	HCF	heart:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:93553805..93555797-chr9:93557563..93559338,2	MCF-7	breast:
2	chr9:93564315..93567256-chr9:93578660..93580228,2	MCF-7	breast:
3	chr9:93548131..93550213-chr9:93558299..93561058,2	MCF-7	breast:
4	chr9:93566130..93568297-chr9:93575356..93577751,2	K562	blood:
5	chr9:93562623..93567761-chr9:93568030..93571323,5	K562	blood:
6	chr9:93557495..93560173-chr9:93596413..93598052,2	MCF-7	breast:
7	chr9:93569248..93572925-chr9:93585588..93587867,3	K562	blood:
8	chr9:93571707..93573621-chr9:93620166..93622474,2	MCF-7	breast:
9	chr9:93561901..93563996-chr9:93577117..93579715,2	MCF-7	breast:
10	chr9:93556987..93560757-chr9:93560998..93566241,6	MCF-7	breast:
11	chr9:93569272..93571391-chr9:93577022..93579806,2	K562	blood:
12	chr9:93561656..93565893-chr9:93566155..93575937,12	MCF-7	breast:
13	chr9:93557618..93560728-chr9:93560879..93563311,3	K562	blood:
14	chr9:93557618..93560728-chr9:93560879..93563311,3	K562	blood:
15	chr9:93566479..93568925-chr9:93571004..93572513,2	MCF-7	breast:
16	chr9:93566139..93567654-chr9:93575721..93577420,2	MCF-7	breast:
17	chr9:93566479..93568925-chr9:93571004..93572513,2	MCF-7	breast:
18	chr9:93566333..93568000-chr9:93577767..93579301,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYK-3	chr9:93572886-93572918	ENSG00000249765

No data

Variant related genes	Relation type
SYK	TF binding region
SYK	CpG island
ENSG00000165025	chromatin interactions
HDLBP	miRNA target sites

Extended variants
information (count: 678 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10993693	chr9:93557698-93557699	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567825244	chr9:93557739-93557740	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373296560	chr9:93557743-93557744	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs536824937	chr9:93557755-93557756	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553530661	chr9:93557756-93557757	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573283153	chr9:93557760-93557761	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112539128	chr9:93557771-93557772	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558869694	chr9:93557808-93557809	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575450244	chr9:93557810-93557811	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373517502	chr9:93557811-93557812	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544071669	chr9:93557858-93557859	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141623975	chr9:93557908-93557909	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150100147	chr9:93557911-93557912	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191954131	chr9:93557979-93557980	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201858149	chr9:93557988-93557989	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560032910	chr9:93557998-93557999	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs1333638	chr9:93558010-93558011	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs138572624	chr9:93558080-93558081	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs370791275	chr9:93558100-93558101	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184093301	chr9:93558107-93558108	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551890955	chr9:93558120-93558121	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562477016	chr9:93558121-93558122	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs531247844	chr9:93558122-93558123	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141657286	chr9:93558182-93558183	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567938467	chr9:93558236-93558237	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs11399508	chr9:93558275-93558276	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs397956973	chr9:93558287-93558288	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112677362	chr9:93558295-93558296	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111318934	chr9:93558322-93558323	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2774237	chr9:93558346-93558347	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs375285895	chr9:93558355-93558356	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188189479	chr9:93558370-93558371	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566859233	chr9:93558376-93558377	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539073520	chr9:93558437-93558438	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139699084	chr9:93558451-93558452	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575558426	chr9:93558471-93558472	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537829900	chr9:93558475-93558476	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541695820	chr9:93558556-93558557	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4744502	chr9:93558575-93558576	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs112858117	chr9:93558600-93558601	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs149630103	chr9:93558615-93558616	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs191973419	chr9:93558639-93558640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544374466	chr9:93558650-93558651	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576887700	chr9:93558683-93558684	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545849304	chr9:93558694-93558695	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374168419	chr9:93558793-93558794	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs80123009	chr9:93558828-93558829	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116988088	chr9:93558845-93558846	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559062414	chr9:93558870-93558871	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561607828	chr9:93558872-93558873	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Glioma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr9:93556200-93559200	Enhancers	Primary B cells from peripheral blood	blood
5	chr9:93556600-93557800	Enhancers	Stomach Mucosa	stomach
6	chr9:93556600-93558600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr9:93556600-93559200	Flanking Active TSS	GM12878-XiMat	blood
8	chr9:93556800-93558600	Enhancers	Primary hematopoietic stem cells	blood
9	chr9:93557200-93558200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:93557200-93558600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr9:93557200-93559600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr9:93557400-93558000	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr9:93557400-93559200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr9:93557600-93559200	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr9:93557600-93562800	Weak transcription	Fetal Intestine Large	intestine
16	chr9:93557600-93563400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:93557600-93563400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr9:93557600-93563400	Weak transcription	Pancreas	Pancrea
19	chr9:93557800-93558800	Weak transcription	Stomach Mucosa	stomach
20	chr9:93558000-93558400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr9:93558000-93558800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr9:93558000-93559000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:93558200-93559200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:93558400-93558800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr9:93558600-93558800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr9:93558600-93558800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr9:93558600-93558800	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr9:93558600-93558800	Enhancers	Adipose Nuclei	Adipose
29	chr9:93558600-93559000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:93558600-93559000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr9:93558600-93559000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:93558600-93559000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:93558600-93559200	Enhancers	Small Intestine	intestine
34	chr9:93558800-93559000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr9:93558800-93559000	Enhancers	Primary hematopoietic stem cells	blood
36	chr9:93558800-93559000	Enhancers	Gastric	stomach
37	chr9:93558800-93559000	Bivalent Enhancer	Lung	lung
38	chr9:93558800-93559000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr9:93558800-93559200	Enhancers	Fetal Lung	lung
40	chr9:93558800-93559200	Enhancers	Fetal Thymus	thymus
41	chr9:93558800-93559200	Enhancers	Thymus	Thymus
42	chr9:93558800-93559400	Enhancers	Stomach Mucosa	stomach
43	chr9:93558800-93562800	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr9:93559000-93559200	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr9:93559000-93559400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr9:93559000-93559400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr9:93559000-93562400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:93559000-93563800	Weak transcription	Gastric	stomach
49	chr9:93559200-93559400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:93559200-93559400	Enhancers	GM12878-XiMat	blood

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