Variant report

Variant	nsv893569
Chromosome Location	chr9:93552550-93587089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:427)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:93577646-93578062	K562	blood:	n/a	n/a
2	ATF1	chr9:93577680-93577987	K562	blood:	n/a	n/a
3	ATF1	chr9:93584043-93584326	K562	blood:	n/a	n/a
4	ATF2	chr9:93558128-93558701	GM12878	blood:	n/a	n/a
5	ATF2	chr9:93555884-93556513	GM12878	blood:	n/a	n/a
6	ATF2	chr9:93570958-93571504	GM12878	blood:	n/a	n/a
7	ATF2	chr9:93558086-93558762	GM12878	blood:	n/a	n/a
8	ATF2	chr9:93555851-93556401	GM12878	blood:	n/a	n/a
9	ATF3	chr9:93577707-93577947	K562	blood:	n/a	n/a
10	ATF3	chr9:93577612-93578074	GM12878	blood:	n/a	n/a
11	BATF	chr9:93555879-93556434	GM12878	blood:	n/a	n/a
12	BATF	chr9:93558330-93558658	GM12878	blood:	n/a	n/a
13	BATF	chr9:93555938-93556401	GM12878	blood:	n/a	n/a
14	BATF	chr9:93558312-93558666	GM12878	blood:	n/a	n/a
15	BATF	chr9:93562260-93562580	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:93556018-93556304	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:93555930-93556381	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:93563791-93564158	GM12878	blood:	n/a	chr9:93563897-93563910 chr9:93564106-93564119 chr9:93563994-93564007
19	BCLAF1	chr9:93558295-93558754	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:93557895-93558286	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:93555883-93556413	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:93562410-93562610	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:93577676-93578076	GM12878	blood:	n/a	chr9:93577834-93577843 chr9:93577835-93577844 chr9:93577833-93577846 chr9:93577829-93577850 chr9:93577835-93577844
24	BHLHE40	chr9:93563964-93564164	GM12878	blood:	n/a	chr9:93564075-93564091 chr9:93564103-93564119 chr9:93564079-93564095 chr9:93564100-93564116
25	BHLHE40	chr9:93577607-93578299	K562	blood:	n/a	chr9:93577834-93577843 chr9:93577835-93577844 chr9:93577833-93577846 chr9:93577829-93577850 chr9:93577835-93577844
26	BHLHE40	chr9:93564460-93564481	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:93557381-93557616	K562	blood:	n/a	n/a
28	BHLHE40	chr9:93563893-93564846	K562	blood:	n/a	chr9:93563900-93563916 chr9:93564075-93564091 chr9:93564103-93564119 chr9:93564079-93564095 chr9:93564100-93564116
29	BHLHE40	chr9:93577132-93577217	K562	blood:	n/a	n/a
30	BHLHE40	chr9:93557323-93557700	GM12878	blood:	n/a	n/a
31	BRCA1	chr9:93564267-93564283	GM12878	blood:	n/a	n/a
32	CBX3	chr9:93577559-93578039	K562	blood:	n/a	n/a
33	CCNT2	chr9:93577556-93578063	K562	blood:	n/a	n/a
34	CCNT2	chr9:93574670-93574870	K562	blood:	n/a	n/a
35	CCNT2	chr9:93563783-93564596	K562	blood:	n/a	n/a
36	CEBPB	chr9:93569861-93570164	K562	blood:	n/a	chr9:93570002-93570019 chr9:93569935-93569946
37	CEBPB	chr9:93558076-93558339	K562	blood:	n/a	n/a
38	CEBPB	chr9:93567249-93567449	K562	blood:	n/a	chr9:93567258-93567271
39	CEBPB	chr9:93558125-93558375	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr9:93563902-93564658	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr9:93564204-93565045	GM12878	blood:	n/a	n/a
42	CHD1	chr9:93562516-93562658	GM12878	blood:	n/a	n/a
43	CHD2	chr9:93564260-93564291	GM12878	blood:	n/a	n/a
44	CHD2	chr9:93564155-93564657	K562	blood:	n/a	n/a
45	CHD2	chr9:93557385-93557629	GM12878	blood:	n/a	n/a
46	CTBP2	chr9:93563441-93564584	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:93562560-93562710	HVMF	connective:	n/a	n/a
48	CTCF	chr9:93562460-93562610	GM12878	blood:	n/a	n/a
49	CTCF	chr9:93562400-93562550	RPTEC	kidney:	n/a	n/a
50	CTCF	chr9:93563914-93563923	MCF-7	breast:	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	chr9:93564149-93564199	HMEC	breast:	n/a
2	chr9:93563776-93563826	MCF-7	breast:	n/a
3	chr9:93564149-93564199	Hepatocyte	liver:	n/a
4	chr9:93564603-93564653	PrEC	prostate:	n/a
5	chr9:93564339-93564389	NH-A	brain:	n/a
6	chr9:93564028-93564078	NB4	blood:	n/a
7	chr9:93564149-93564199	HL-60	blood:	n/a
8	chr9:93564028-93564078	AoSMC	blood vessel:	n/a
9	chr9:93564456-93564506	PFSK-1	brain:	n/a
10	chr9:93563776-93563826	Jurkat	blood:	n/a
11	chr9:93564603-93564653	RPTEC	kidney:	n/a
12	chr9:93564603-93564653	U87	brain:	n/a
13	chr9:93564028-93564078	PrEC	prostate:	n/a
14	chr9:93564028-93564078	MCF-7	breast:	n/a
15	chr9:93564603-93564653	CMK	blood:	n/a
16	chr9:93563778-93563828	AG10803	skin:	n/a
17	chr9:93563778-93563828	ECC-1	luminal epithelium:	n/a
18	chr9:93564149-93564199	AG10803	skin:	n/a
19	chr9:93563778-93563828	U87	brain:	n/a
20	chr9:93564149-93564199	HRE	kidney:	n/a
21	chr9:93564339-93564389	Hela-S3	cervix:	n/a
22	chr9:93564603-93564653	Jurkat	blood:	n/a
23	chr9:93564339-93564389	T-47D	breast:	n/a
24	chr9:93564028-93564078	HPAEpiC	pulmonary alveolar:	n/a
25	chr9:93563778-93563828	HCM	heart:	n/a
26	chr9:93564149-93564199	HCM	heart:	n/a
27	chr9:93564149-93564199	GM12892	blood:	n/a
28	chr9:93563776-93563826	GM12891	blood:	n/a
29	chr9:93564456-93564506	HRCEpiC	kidney:	n/a
30	chr9:93564339-93564389	BJ	skin:	n/a
31	chr9:93564149-93564199	BE2_C	brain:	n/a
32	chr9:93564456-93564506	HCT-116	colon:	n/a
33	chr9:93564149-93564199	HAEpiC	amniotic membrane:	n/a
34	chr9:93563776-93563826	AG04450	lung:	fetal
35	chr9:93563776-93563826	CMK	blood:	n/a
36	chr9:93563776-93563826	PrEC	prostate:	n/a
37	chr9:93564603-93564653	HUVEC	blood vessel:	n/a
38	chr9:93564339-93564389	ECC-1	luminal epithelium:	n/a
39	chr9:93564603-93564653	AG09309	skin:	n/a
40	chr9:93564028-93564078	AG09309	skin:	n/a
41	chr9:93564603-93564653	SK-N-SH_RA	brain:	n/a
42	chr9:93564603-93564653	HL-60	blood:	n/a
43	chr9:93563778-93563828	HCF	heart:	n/a
44	chr9:93564149-93564199	A549	lung:	n/a
45	chr9:93564339-93564389	H1-hESC	embryonic stem cell:	embryo
46	chr9:93563776-93563826	Hepatocyte	liver:	n/a
47	chr9:93563776-93563826	SAEC	small airway:	n/a
48	chr9:93564603-93564653	NH-A	brain:	n/a
49	chr9:93563778-93563828	BE2_C	brain:	n/a
50	chr9:93564603-93564653	Hepatocyte	liver:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:93564315..93567256-chr9:93578660..93580228,2	MCF-7	breast:
2	chr9:93553805..93555797-chr9:93557563..93559338,2	MCF-7	breast:
3	chr9:93563428..93565399-chr9:93578384..93582187,4	MCF-7	breast:
4	chr9:93566139..93567654-chr9:93575721..93577420,2	MCF-7	breast:
5	chr9:93562623..93567761-chr9:93568030..93571323,5	K562	blood:
6	chr9:93560904..93565448-chr9:93577148..93580132,4	K562	blood:
7	chr9:93548131..93550213-chr9:93558299..93561058,2	MCF-7	breast:
8	chr9:93569248..93572925-chr9:93585588..93587867,3	K562	blood:
9	chr9:93566479..93568925-chr9:93571004..93572513,2	MCF-7	breast:
10	chr9:93556987..93560757-chr9:93560998..93566241,6	MCF-7	breast:
11	chr9:93564315..93567256-chr9:93578660..93580228,2	MCF-7	breast:
12	chr9:93569248..93572925-chr9:93585588..93587867,3	K562	blood:
13	chr9:93561656..93565893-chr9:93566155..93575937,12	MCF-7	breast:
14	chr9:93569272..93571391-chr9:93577022..93579806,2	K562	blood:
15	chr9:93571707..93573621-chr9:93620166..93622474,2	MCF-7	breast:
16	chr9:93566130..93568297-chr9:93575356..93577751,2	K562	blood:
17	chr9:93557618..93560728-chr9:93560879..93563311,3	K562	blood:
18	chr9:93561901..93563996-chr9:93577117..93579715,2	MCF-7	breast:
19	chr9:93566479..93568925-chr9:93571004..93572513,2	MCF-7	breast:
20	chr9:93566130..93568297-chr9:93575356..93577751,2	K562	blood:
21	chr9:93569272..93571391-chr9:93577022..93579806,2	K562	blood:
22	chr9:93553805..93555797-chr9:93557563..93559338,2	MCF-7	breast:
23	chr9:93560904..93565448-chr9:93577288..93580605,5	K562	blood:
24	chr9:93561901..93563996-chr9:93577117..93579715,2	MCF-7	breast:
25	chr9:93573891..93575434-chr9:93575492..93578203,2	MCF-7	breast:
26	chr9:93566333..93568000-chr9:93577767..93579301,2	MCF-7	breast:
27	chr9:93566139..93567654-chr9:93575721..93577420,2	MCF-7	breast:
28	chr9:93557618..93560728-chr9:93560879..93563311,3	K562	blood:
29	chr9:93566333..93568000-chr9:93577767..93579301,2	MCF-7	breast:
30	chr9:93557495..93560173-chr9:93596413..93598052,2	MCF-7	breast:
31	chr9:93573891..93575434-chr9:93575492..93578203,2	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: 1358 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs290267	chr9:93552550-93552551	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553696220	chr9:93552615-93552616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181682028	chr9:93552619-93552620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545714569	chr9:93552657-93552658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187098645	chr9:93552674-93552675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142160060	chr9:93552698-93552699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567797222	chr9:93552702-93552703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115935632	chr9:93552723-93552724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561678779	chr9:93552746-93552747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527326446	chr9:93552765-93552766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146052826	chr9:93552774-93552775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562092565	chr9:93552778-93552779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138907020	chr9:93552803-93552804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552516993	chr9:93552810-93552811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550300096	chr9:93552811-93552812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191178702	chr9:93552828-93552829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183420700	chr9:93552843-93552844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548315652	chr9:93552873-93552874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568211100	chr9:93552933-93552934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184907815	chr9:93552964-93552965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10821500	chr9:93552970-93552971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150287815	chr9:93553032-93553033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189718439	chr9:93553047-93553048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556088721	chr9:93553103-93553104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201532322	chr9:93553117-93553118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4744009	chr9:93553213-93553214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs541651468	chr9:93553242-93553243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114470081	chr9:93553249-93553250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112100045	chr9:93553264-93553265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541040978	chr9:93553312-93553313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559219014	chr9:93553358-93553359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532695561	chr9:93553377-93553378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546434741	chr9:93553378-93553379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563030333	chr9:93553387-93553388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183135432	chr9:93553413-93553414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548352068	chr9:93553428-93553429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76737939	chr9:93553443-93553444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572644848	chr9:93553471-93553472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527746807	chr9:93553475-93553476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533301231	chr9:93553558-93553559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs167080	chr9:93553577-93553578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs167079	chr9:93553665-93553666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs544220148	chr9:93553682-93553683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369841222	chr9:93553683-93553684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570779278	chr9:93553695-93553696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187814485	chr9:93553706-93553707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192434807	chr9:93553769-93553770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78117529	chr9:93553826-93553827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72742780	chr9:93553840-93553841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141134086	chr9:93553976-93553977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93550000-93557400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr9:93550800-93552800	Enhancers	Primary B cells from peripheral blood	blood
3	chr9:93551400-93552600	Enhancers	Primary B cells from cord blood	blood
4	chr9:93551800-93552600	Enhancers	Placenta	Placenta
5	chr9:93551800-93552800	Enhancers	Fetal Stomach	stomach
6	chr9:93551800-93563400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:93552000-93552600	Enhancers	Fetal Kidney	kidney
8	chr9:93552000-93552800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:93552000-93563400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr9:93552200-93552600	Enhancers	Fetal Muscle Leg	muscle
11	chr9:93552400-93552600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr9:93552400-93552600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:93552400-93555600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr9:93552400-93556000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr9:93552600-93555600	Weak transcription	Primary B cells from cord blood	blood
16	chr9:93552600-93556800	Weak transcription	Fetal Kidney	kidney
17	chr9:93552800-93556200	Weak transcription	Primary B cells from peripheral blood	blood
18	chr9:93555600-93556200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr9:93555600-93556600	ZNF genes & repeats	GM12878-XiMat	blood
20	chr9:93555600-93557600	Enhancers	Primary B cells from cord blood	blood
21	chr9:93556000-93557400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr9:93556000-93563400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:93556200-93556600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr9:93556200-93559200	Enhancers	Primary B cells from peripheral blood	blood
25	chr9:93556600-93557200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr9:93556600-93557800	Enhancers	Stomach Mucosa	stomach
27	chr9:93556600-93558600	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr9:93556600-93559200	Flanking Active TSS	GM12878-XiMat	blood
29	chr9:93556800-93557400	Enhancers	Fetal Kidney	kidney
30	chr9:93556800-93558600	Enhancers	Primary hematopoietic stem cells	blood
31	chr9:93557200-93557600	Enhancers	Fetal Intestine Large	intestine
32	chr9:93557200-93558200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:93557200-93558600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr9:93557200-93559600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr9:93557400-93557600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:93557400-93557600	Enhancers	Adipose Nuclei	Adipose
37	chr9:93557400-93557600	Enhancers	Duodenum Mucosa	Duodenum
38	chr9:93557400-93557600	Enhancers	Pancreas	Pancrea
39	chr9:93557400-93557600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr9:93557400-93558000	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr9:93557400-93559200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr9:93557600-93559200	Flanking Active TSS	Primary B cells from cord blood	blood
43	chr9:93557600-93562800	Weak transcription	Fetal Intestine Large	intestine
44	chr9:93557600-93563400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:93557600-93563400	Weak transcription	Duodenum Mucosa	Duodenum
46	chr9:93557600-93563400	Weak transcription	Pancreas	Pancrea
47	chr9:93557800-93558800	Weak transcription	Stomach Mucosa	stomach
48	chr9:93558000-93558400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr9:93558000-93558800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr9:93558000-93559000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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