Variant report

Variant	nsv614918
Chromosome Location	chr9:97380597-97412037
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:554)
CpG islands
(count:734)
Chromatin interactive
region (count:41)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:97411516-97411726	K562	blood:	n/a	n/a
2	ATF3	chr9:97385595-97385773	K562	blood:	n/a	n/a
3	ATF3	chr9:97385558-97385793	K562	blood:	n/a	n/a
4	BACH1	chr9:97402359-97402724	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr9:97385709-97385789	GM12878	blood:	n/a	n/a
6	CBX3	chr9:97385452-97385891	K562	blood:	n/a	n/a
7	CBX3	chr9:97385553-97385848	K562	blood:	n/a	n/a
8	CEBPB	chr9:97385596-97385889	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:97393714-97394265	MCF-7	breast:	n/a	n/a
10	CEBPB	chr9:97411347-97412134	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:97393900-97394051	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:97385602-97385841	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:97405513-97405692	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:97401295-97402332	MCF-7	breast:	n/a	n/a
15	CHD2	chr9:97411422-97412123	Hela-S3	cervix:	n/a	n/a
16	CTBP2	chr9:97402108-97403283	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr9:97385497-97385886	K562	blood:	n/a	n/a
18	CTCF	chr9:97385620-97385770	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr9:97385660-97385810	AG04449	skin:	n/a	n/a
20	CTCF	chr9:97385545-97385932	K562	blood:	n/a	n/a
21	CTCF	chr9:97385660-97385810	HPF	lung:	n/a	n/a
22	CTCF	chr9:97385634-97385840	MCF-7	breast:	n/a	n/a
23	CTCF	chr9:97385640-97385790	AG10803	skin:	n/a	n/a
24	CTCF	chr9:97410340-97410490	GM12867	blood:	n/a	n/a
25	CTCF	chr9:97392800-97392950	BE2_C	brain:	n/a	n/a
26	CTCF	chr9:97385660-97385810	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr9:97385651-97385818	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr9:97385473-97385990	K562	blood:	n/a	n/a
29	CTCF	chr9:97385640-97385790	HepG2	liver:	n/a	n/a
30	CTCF	chr9:97402100-97402250	GM12864	blood:	n/a	n/a
31	CTCF	chr9:97385640-97385831	ProgFib	skin:	n/a	n/a
32	CTCF	chr9:97392820-97392970	HepG2	liver:	n/a	n/a
33	CTCF	chr9:97385620-97385770	AG10803	skin:	n/a	n/a
34	CTCF	chr9:97385634-97385822	GM19239	blood:	n/a	n/a
35	CTCF	chr9:97385609-97385852	A549	lung:	n/a	n/a
36	CTCF	chr9:97385620-97385770	RPTEC	kidney:	n/a	n/a
37	CTCF	chr9:97385640-97385790	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr9:97385660-97385810	GM12873	blood:	n/a	n/a
39	CTCF	chr9:97385980-97386130	GM06990	blood:	n/a	n/a
40	CTCF	chr9:97385614-97385846	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:97385604-97385864	K562	blood:	n/a	n/a
42	CTCF	chr9:97392800-97392950	GM12871	blood:	n/a	n/a
43	CTCF	chr9:97385660-97385810	GM12878	blood:	n/a	n/a
44	CTCF	chr9:97392760-97392910	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:97392740-97392890	A549	lung:	n/a	n/a
46	CTCF	chr9:97385518-97385943	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:97385680-97385830	GM12869	blood:	n/a	n/a
48	CTCF	chr9:97385580-97385884	GM12892	blood:	n/a	n/a
49	CTCF	chr9:97385740-97385890	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr9:97389680-97389830	GM06990	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:97400833-97400883	MCF10A-Er-Src	breast:	n/a
2	chr9:97402166-97402216	GM12891	blood:	n/a
3	chr9:97400833-97400883	MCF10A-Er-Src	breast:	n/a
4	chr9:97402166-97402216	GM12891	blood:	n/a
5	chr9:97390853-97390903	HCM	heart:	n/a
6	chr9:97402555-97402605	H1-hESC	embryonic stem cell:	embryo
7	chr9:97402166-97402216	HCPEpiC	choroid plexus:	n/a
8	chr9:97402058-97402108	GM06990	blood:	n/a
9	chr9:97405553-97405603	SAEC	small airway:	n/a
10	chr9:97390853-97390903	T-47D	breast:	n/a
11	chr9:97400833-97400883	Hepatocyte	liver:	n/a
12	chr9:97403129-97403179	NH-A	brain:	n/a
13	chr9:97403668-97403718	HUVEC	blood vessel:	n/a
14	chr9:97402058-97402108	HAEpiC	amniotic membrane:	n/a
15	chr9:97402058-97402108	CMK	blood:	n/a
16	chr9:97405553-97405603	H1-hESC	embryonic stem cell:	embryo
17	chr9:97390853-97390903	HNPCEpiC	eye:	n/a
18	chr9:97402452-97402502	HNPCEpiC	eye:	n/a
19	chr9:97402452-97402502	NB4	blood:	n/a
20	chr9:97402555-97402605	HCT-116	colon:	n/a
21	chr9:97402166-97402216	HMEC	breast:	n/a
22	chr9:97400757-97400807	BE2_C	brain:	n/a
23	chr9:97400833-97400883	T-47D	breast:	n/a
24	chr9:97400757-97400807	HCPEpiC	choroid plexus:	n/a
25	chr9:97402058-97402108	K562	blood:	n/a
26	chr9:97402058-97402108	AG09319	gingival:	n/a
27	chr9:97403668-97403718	HAEpiC	amniotic membrane:	n/a
28	chr9:97401505-97401555	HEK293	kidney:	embryo
29	chr9:97401509-97401559	HL-60	blood:	n/a
30	chr9:97403668-97403718	NH-A	brain:	n/a
31	chr9:97390853-97390903	NT2-D1	testis:	n/a
32	chr9:97402058-97402108	Hepatocyte	liver:	n/a
33	chr9:97403668-97403718	AG04449	skin:	fetal
34	chr9:97405553-97405603	RPTEC	kidney:	n/a
35	chr9:97401505-97401555	T-47D	breast:	n/a
36	chr9:97405553-97405603	HEEpiC	esophagus:	n/a
37	chr9:97405553-97405603	SKMC	muscle:	n/a
38	chr9:97402555-97402605	NHDF-neo	bronchial:	n/a
39	chr9:97403129-97403179	HRE	kidney:	n/a
40	chr9:97402555-97402605	SKMC	muscle:	n/a
41	chr9:97401505-97401555	NH-A	brain:	n/a
42	chr9:97402058-97402108	AG04449	skin:	fetal
43	chr9:97401509-97401559	RPTEC	kidney:	n/a
44	chr9:97402166-97402216	HPAEpiC	pulmonary alveolar:	n/a
45	chr9:97402555-97402605	GM12892	blood:	n/a
46	chr9:97401505-97401555	SK-N-SH_RA	brain:	n/a
47	chr9:97401509-97401559	HCT-116	colon:	n/a
48	chr9:97402058-97402108	HEEpiC	esophagus:	n/a
49	chr9:97403668-97403718	MCF-7	breast:	n/a
50	chr9:97403129-97403179	LNCaP	prostate:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:97393231..97394953-chr9:97687496..97690303,2	MCF-7	breast:
2	chr2:70312789..70315252-chr9:97388486..97391200,2	MCF-7	breast:
3	chr9:97369469..97371530-chr9:97378423..97380826,2	K562	blood:
4	chr9:97389746..97395320-chr9:97854192..97858136,7	MCF-7	breast:
5	chr9:97373691..97376847-chr9:97393054..97396710,3	MCF-7	breast:
6	chr9:97399443..97401665-chr9:97771079..97774076,2	MCF-7	breast:
7	chr9:97360979..97363553-chr9:97393005..97395544,2	MCF-7	breast:
8	chr9:97375061..97375860-chr9:97384899..97385874,3	MCF-7	breast:
9	chr9:97388894..97390438-chr9:97391707..97394156,2	K562	blood:
10	chr9:97398090..97401026-chr9:97919610..97921770,2	MCF-7	breast:
11	chr9:97377917..97381579-chr9:97382484..97386312,5	MCF-7	breast:
12	chr9:97399286..97401961-chr9:97487355..97490023,2	MCF-7	breast:
13	chr9:97390244..97393079-chr9:97544131..97546613,2	MCF-7	breast:
14	chr9:97315886..97317442-chr9:97390408..97393191,2	MCF-7	breast:
15	chr9:97368983..97370788-chr9:97391157..97393414,2	MCF-7	breast:
16	chr9:97393498..97394166-chr9:97401048..97401667,2	MCF-7	breast:
17	chr9:97389422..97393205-chr9:97411609..97416128,4	MCF-7	breast:
18	chr9:97399795..97401859-chr9:97411374..97414324,3	MCF-7	breast:
19	chr9:96927010..96929542-chr9:97400485..97402088,2	MCF-7	breast:
20	chr9:97375440..97378542-chr9:97391725..97394611,4	MCF-7	breast:
21	chr9:97325572..97327725-chr9:97393482..97394985,2	MCF-7	breast:
22	chr9:97365715..97366434-chr9:97385051..97385749,2	MCF-7	breast:
23	chr9:97377917..97381579-chr9:97382484..97386312,5	MCF-7	breast:
24	chr9:97379626..97381399-chr9:97382615..97384650,2	K562	blood:
25	chr9:97393214..97394008-chr9:97401305..97401913,2	MCF-7	breast:
26	chr9:97379626..97381399-chr9:97382615..97384650,2	K562	blood:
27	chr9:97389422..97393205-chr9:97411609..97416128,4	MCF-7	breast:
28	chr9:97388894..97390438-chr9:97391707..97394156,2	K562	blood:
29	chr9:97393707..97398253-chr9:97766180..97769017,4	MCF-7	breast:
30	chr9:97316754..97318987-chr9:97400777..97403144,3	MCF-7	breast:
31	chr9:97397667..97400545-chr9:97634464..97636466,2	MCF-7	breast:
32	chr9:97375392..97377044-chr9:97391362..97392909,2	MCF-7	breast:
33	chr9:97393498..97394166-chr9:97401048..97401667,2	MCF-7	breast:
34	chr9:97315630..97317501-chr9:97398483..97401293,2	MCF-7	breast:
35	chr9:97393391..97395196-chr9:97892426..97894999,2	MCF-7	breast:
36	chr9:97392176..97395070-chr9:97431603..97433493,2	MCF-7	breast:
37	chr9:97366331..97367935-chr9:97380870..97383175,2	MCF-7	breast:
38	chr17:58637930..58639560-chr9:97403785..97405324,2	MCF-7	breast:
39	chr9:97391705..97394418-chr9:97757936..97760772,2	MCF-7	breast:
40	chr9:97334835..97337709-chr9:97386591..97389004,2	MCF-7	breast:
41	chr9:97406984..97409530-chr9:97419873..97421419,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBP1-1	chr9:97404074-97404262	NONHSAT133331
2	lnc-FBP1-1	chr9:97408325-97408389	NONHSAT133331
3	lnc-FBP1-1	chr9:97401648-97401788	NONHSAT133331

No data

Variant related genes	Relation type
FBP1	TF binding region
FBP1	CpG island
ENSG00000169564	chromatin interactions
ENSG00000231806	chromatin interactions
ENSG00000267678	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000148120	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000165140	chromatin interactions

Extended variants
information (count: 1214 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1214 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7867069	chr9:97380597-97380598	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11792428	chr9:97380631-97380632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569997235	chr9:97380645-97380646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555951456	chr9:97380680-97380681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs28369709	chr9:97380718-97380719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530085421	chr9:97380738-97380739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs59806476	chr9:97380768-97380769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148194074	chr9:97380769-97380770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538382256	chr9:97380825-97380826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13296485	chr9:97380859-97380860	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs28369707	chr9:97380878-97380879	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28369706	chr9:97380890-97380891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145293766	chr9:97380926-97380927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147569208	chr9:97380954-97380955	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140283066	chr9:97380967-97380968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375131927	chr9:97380989-97380990	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12380393	chr9:97381000-97381001	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs562779888	chr9:97381046-97381047	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28369705	chr9:97381049-97381050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs28369704	chr9:97381105-97381106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560270611	chr9:97381129-97381130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61708081	chr9:97381130-97381131	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs71498671	chr9:97381175-97381176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151175922	chr9:97381212-97381213	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140150076	chr9:97381233-97381234	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371322682	chr9:97381241-97381242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150458731	chr9:97381260-97381261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs28369703	chr9:97381269-97381270	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574341708	chr9:97381280-97381281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141477516	chr9:97381401-97381402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535221072	chr9:97381402-97381403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs28369702	chr9:97381445-97381446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34654698	chr9:97381471-97381472	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547524284	chr9:97381577-97381578	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28369701	chr9:97381632-97381633	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536476216	chr9:97381679-97381680	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4574908	chr9:97381711-97381712	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576273355	chr9:97381730-97381731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536975662	chr9:97381744-97381745	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556509332	chr9:97381770-97381771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138997140	chr9:97381819-97381820	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs3935327	chr9:97381821-97381822	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs141977034	chr9:97381845-97381846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373163415	chr9:97381853-97381854	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572271690	chr9:97381871-97381872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112721637	chr9:97381875-97381876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4075984	chr9:97381881-97381882	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561349917	chr9:97381885-97381886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10123016	chr9:97381923-97381924	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs369187619	chr9:97381931-97381932	Weak transcription Strong transcription Enhancers	n/a	n/a	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97364400-97382800	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr9:97364800-97382800	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr9:97366600-97384400	Weak transcription	Small Intestine	intestine
4	chr9:97370000-97382400	Weak transcription	Lung	lung
5	chr9:97371400-97401000	Weak transcription	Spleen	Spleen
6	chr9:97371600-97384200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:97372400-97384400	Weak transcription	Gastric	stomach
8	chr9:97373000-97381200	Weak transcription	Fetal Stomach	stomach
9	chr9:97374600-97380600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr9:97374600-97384400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:97374600-97392600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr9:97374600-97393400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr9:97374800-97381000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr9:97374800-97384200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr9:97375200-97385600	Weak transcription	Stomach Mucosa	stomach
16	chr9:97375400-97382800	Strong transcription	Duodenum Mucosa	Duodenum
17	chr9:97375400-97382800	Strong transcription	Fetal Intestine Large	intestine
18	chr9:97375400-97383000	Strong transcription	Fetal Intestine Small	intestine
19	chr9:97375800-97380600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr9:97375800-97381000	Weak transcription	Pancreas	Pancrea
21	chr9:97376200-97385800	Strong transcription	Liver	Liver
22	chr9:97380600-97381400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr9:97380800-97383000	Enhancers	Fetal Lung	lung
24	chr9:97381000-97381400	Enhancers	Aorta	Aorta
25	chr9:97381000-97381400	Enhancers	Pancreas	Pancrea
26	chr9:97381000-97381600	Strong transcription	Rectal Mucosa Donor 29	rectum
27	chr9:97381000-97381800	Enhancers	Fetal Heart	heart
28	chr9:97381000-97381800	Enhancers	Ovary	ovary
29	chr9:97381200-97381600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr9:97381200-97381600	Enhancers	Fetal Stomach	stomach
31	chr9:97381400-97381600	Enhancers	Right Atrium	heart
32	chr9:97381400-97389800	Weak transcription	Pancreas	Pancrea
33	chr9:97381400-97400400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr9:97381600-97382000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr9:97381600-97382400	Weak transcription	Fetal Stomach	stomach
36	chr9:97381600-97401000	Weak transcription	Right Atrium	heart
37	chr9:97381800-97382400	Weak transcription	Ovary	ovary
38	chr9:97382000-97382600	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr9:97382400-97382600	ZNF genes & repeats	Lung	lung
40	chr9:97382400-97382600	Enhancers	Ovary	ovary
41	chr9:97382400-97382800	Enhancers	Fetal Stomach	stomach
42	chr9:97382600-97392800	Weak transcription	Lung	lung
43	chr9:97382600-97393000	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr9:97382800-97384400	Weak transcription	Fetal Stomach	stomach
45	chr9:97382800-97387000	Weak transcription	Fetal Intestine Large	intestine
46	chr9:97382800-97387600	Weak transcription	Duodenum Mucosa	Duodenum
47	chr9:97382800-97388200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr9:97382800-97399400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr9:97383000-97383800	Weak transcription	Fetal Intestine Small	intestine
50	chr9:97383000-97384200	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links