Variant report

Variant	nsv1049133
Chromosome Location	chr9:108292302-108356068
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:644)
CpG islands
(count:366)
Chromatin interactive
region (count:21)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:108311704-108311937	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:108301809-108301901	HepG2	liver:	n/a	n/a
3	ATF1	chr9:108318907-108318917	K562	blood:	n/a	n/a
4	ATF2	chr9:108320020-108320564	GM12878	blood:	n/a	n/a
5	ATF2	chr9:108320060-108320482	GM12878	blood:	n/a	n/a
6	ATF2	chr9:108304063-108304566	GM12878	blood:	n/a	n/a
7	ATF2	chr9:108297869-108298796	GM12878	blood:	n/a	n/a
8	ATF2	chr9:108297994-108298741	GM12878	blood:	n/a	n/a
9	ATF2	chr9:108320072-108320500	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr9:108320242-108320603	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr9:108320284-108320464	GM12878	blood:	n/a	n/a
12	ATF3	chr9:108319873-108320659	GM12878	blood:	n/a	n/a
13	ATF3	chr9:108320004-108320583	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr9:108320209-108320585	K562	blood:	n/a	n/a
15	ATF3	chr9:108320276-108320648	K562	blood:	n/a	n/a
16	ATF3	chr9:108320138-108320695	HepG2	liver:	n/a	n/a
17	ATF3	chr9:108320157-108320554	HepG2	liver:	n/a	n/a
18	BATF	chr9:108297171-108297470	GM12878	blood:	n/a	chr9:108297311-108297322 chr9:108297297-108297308 chr9:108297312-108297322
19	BATF	chr9:108304158-108304497	GM12878	blood:	n/a	n/a
20	BATF	chr9:108297131-108297508	GM12878	blood:	n/a	chr9:108297311-108297322 chr9:108297297-108297308 chr9:108297312-108297322
21	BATF	chr9:108304115-108304509	GM12878	blood:	n/a	n/a
22	BATF	chr9:108298333-108298628	GM12878	blood:	n/a	n/a
23	BATF	chr9:108298082-108298866	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:108298203-108298684	GM12878	blood:	n/a	chr9:108298235-108298244 chr9:108298265-108298274 chr9:108298266-108298275 chr9:108298234-108298243
25	BCL11A	chr9:108304214-108304468	GM12878	blood:	n/a	n/a
26	BCL3	chr9:108319860-108320714	A549	lung:	n/a	chr9:108320358-108320367
27	BCL3	chr9:108304118-108304532	GM12878	blood:	n/a	n/a
28	BCL3	chr9:108298065-108298669	GM12878	blood:	n/a	chr9:108298235-108298244 chr9:108298265-108298274 chr9:108298266-108298275 chr9:108298234-108298243
29	BCL3	chr9:108319759-108320618	A549	lung:	n/a	chr9:108320358-108320367
30	BCLAF1	chr9:108298201-108298541	GM12878	blood:	n/a	chr9:108298235-108298244 chr9:108298265-108298274 chr9:108298266-108298275 chr9:108298234-108298243
31	BCLAF1	chr9:108319932-108320744	GM12878	blood:	n/a	chr9:108320358-108320367
32	BCLAF1	chr9:108303939-108304472	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:108319969-108320707	K562	blood:	n/a	n/a
34	BHLHE40	chr9:108298149-108298556	GM12878	blood:	n/a	n/a
35	BRCA1	chr9:108320258-108320458	HepG2	liver:	n/a	n/a
36	BRCA1	chr9:108319992-108320797	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr9:108354007-108354203	K562	blood:	n/a	n/a
38	CBX3	chr9:108353880-108354218	K562	blood:	n/a	n/a
39	CCNT2	chr9:108320233-108320656	K562	blood:	n/a	n/a
40	CEBPB	chr9:108353350-108353664	HepG2	liver:	n/a	chr9:108353491-108353502
41	CEBPB	chr9:108331790-108332133	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:108331852-108332108	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:108301811-108302217	HCT-116	colon:	n/a	n/a
44	CEBPB	chr9:108320052-108320569	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr9:108331788-108332132	A549	lung:	n/a	n/a
46	CEBPB	chr9:108320151-108320467	K562	blood:	n/a	n/a
47	CEBPB	chr9:108297491-108297770	HepG2	liver:	n/a	chr9:108297621-108297632
48	CEBPB	chr9:108297527-108297740	K562	blood:	n/a	chr9:108297621-108297632
49	CEBPB	chr9:108331804-108332138	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:108320278-108320502	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:108323097-108323147	CMK	blood:	n/a
2	chr9:108320327-108320377	BJ	skin:	n/a
3	chr9:108320518-108320568	IMR90	lung:	fetal
4	chr9:108320518-108320568	Hela-S3	cervix:	n/a
5	chr9:108320178-108320228	GM12891	blood:	n/a
6	chr9:108320518-108320568	LNCaP	prostate:	n/a
7	chr9:108320507-108320557	GM12878	blood:	n/a
8	chr9:108311111-108311161	K562	blood:	n/a
9	chr9:108323097-108323147	HRCEpiC	kidney:	n/a
10	chr9:108311111-108311161	AoSMC	blood vessel:	n/a
11	chr9:108320327-108320377	HCM	heart:	n/a
12	chr9:108323097-108323147	SK-N-SH_RA	brain:	n/a
13	chr9:108320178-108320228	NT2-D1	testis:	n/a
14	chr9:108320178-108320228	HepG2	liver:	n/a
15	chr9:108320327-108320377	AG10803	skin:	n/a
16	chr9:108323097-108323147	PFSK-1	brain:	n/a
17	chr9:108320507-108320557	Hepatocyte	liver:	n/a
18	chr9:108311111-108311161	HCM	heart:	n/a
19	chr9:108323097-108323147	MCF-7	breast:	n/a
20	chr9:108320178-108320228	PFSK-1	brain:	n/a
21	chr9:108320507-108320557	HEK293	kidney:	embryo
22	chr9:108320327-108320377	HIPEpiC	eye:	n/a
23	chr9:108320178-108320228	RPTEC	kidney:	n/a
24	chr9:108320518-108320568	HEEpiC	esophagus:	n/a
25	chr9:108320507-108320557	PANC-1	pancreas:	n/a
26	chr9:108323097-108323147	HIPEpiC	eye:	n/a
27	chr9:108311111-108311161	HEK293	kidney:	embryo
28	chr9:108320178-108320228	H1-hESC	embryonic stem cell:	embryo
29	chr9:108311111-108311161	HUVEC	blood vessel:	n/a
30	chr9:108320178-108320228	PANC-1	pancreas:	n/a
31	chr9:108311111-108311161	MCF10A-Er-Src	breast:	n/a
32	chr9:108323097-108323147	GM19239	blood:	n/a
33	chr9:108320507-108320557	HRCEpiC	kidney:	n/a
34	chr9:108323097-108323147	HRE	kidney:	n/a
35	chr9:108320178-108320228	AG09319	gingival:	n/a
36	chr9:108320327-108320377	PANC-1	pancreas:	n/a
37	chr9:108323097-108323147	SAEC	small airway:	n/a
38	chr9:108323097-108323147	GM12891	blood:	n/a
39	chr9:108320507-108320557	Caco-2	colon:	n/a
40	chr9:108320518-108320568	HCF	heart:	n/a
41	chr9:108320327-108320377	HCF	heart:	n/a
42	chr9:108320518-108320568	SK-N-SH_RA	brain:	n/a
43	chr9:108323097-108323147	PANC-1	pancreas:	n/a
44	chr9:108320507-108320557	HCPEpiC	choroid plexus:	n/a
45	chr9:108320518-108320568	SKMC	muscle:	n/a
46	chr9:108311111-108311161	SAEC	small airway:	n/a
47	chr9:108311111-108311161	SK-N-MC	brain:	n/a
48	chr9:108311111-108311161	GM06990	blood:	n/a
49	chr9:108320327-108320377	AG09319	gingival:	n/a
50	chr9:108320507-108320557	H1-hESC	embryonic stem cell:	embryo

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:108295821..108298820-chr9:108299705..108303201,3	MCF-7	breast:
2	chr9:108293123..108295259-chr9:108297045..108298602,2	K562	blood:
3	chr9:108351411..108353757-chr9:108354344..108356561,3	K562	blood:
4	chr9:108294400..108296396-chr9:108300252..108301863,2	K562	blood:
5	chr9:108293123..108295259-chr9:108297045..108298602,2	K562	blood:
6	chr9:108295821..108298820-chr9:108299705..108303201,3	MCF-7	breast:
7	chr9:108311203..108313649-chr9:108317166..108319459,2	K562	blood:
8	chr6:26020975..26022487-chr9:108293972..108296238,2	MCF-7	breast:
9	chr9:108311203..108313649-chr9:108317166..108319459,2	K562	blood:
10	chr2:187349629..187352498-chr9:108293568..108295157,2	MCF-7	breast:
11	chr9:108294400..108296396-chr9:108300252..108301863,2	K562	blood:
12	chr9:108314759..108316945-chr9:108319984..108322234,2	K562	blood:
13	chr9:108303576..108305468-chr9:108318629..108320964,2	MCF-7	breast:
14	chr9:108330989..108333120-chr9:108334347..108336541,2	K562	blood:
15	chr9:108285609..108287326-chr9:108292970..108295032,2	K562	blood:
16	chr9:108351411..108353757-chr9:108354344..108356561,3	K562	blood:
17	chr9:108330989..108333120-chr9:108334347..108336541,2	K562	blood:
18	chr9:108319265..108321879-chr9:108349827..108352014,2	MCF-7	breast:
19	chr9:108313005..108314954-chr9:108320273..108321938,2	MCF-7	breast:
20	chr9:108312149..108315123-chr9:108317166..108320384,3	K562	blood:
21	chr9:108310997..108313277-chr9:108319909..108321430,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKTN-1	chr9:108302459-108302607	NONHSAT133814
2	lnc-FSD1L-2	chr9:108337226-108337299	NONHSAT133821
3	lnc-FSD1L-2	chr9:108320422-108320446	NONHSAT133820
4	lnc-ABCA1-2	chr9:108319395-108319456	NONHSAT133817
5	lnc-ABCA1-2	chr9:108316326-108316624	NONHSAT133819
6	lnc-FSD1L-2	chr9:108336479-108336613	NONHSAT133821
7	lnc-ABCA1-2	chr9:108319395-108319456	NONHSAT133819
8	lnc-ABCA1-2	chr9:108320051-108320362	NONHSAT133817
9	lnc-FSD1L-2	chr9:108320431-108320446	NONHSAT133821
10	lnc-ABCA1-2	chr9:108320475-108320746	NONHSAT133818
11	lnc-ABCA1-2	chr9:108316326-108316624	NONHSAT133818
12	lnc-FSD1L-2	chr9:108337226-108337418	NONHSAT133820
13	lnc-ABCA1-2	chr9:108319395-108319456	NONHSAT133818
14	lnc-ABCA1-2	chr9:108316316-108316624	ENSG00000228317.1
15	lnc-ABCA1-2	chr9:108320051-108320310	ENSG00000228317.1
16	lnc-ABCA1-2	chr9:108319395-108319456	ENSG00000228317.1
17	lnc-FKTN-1	chr9:108301589-108301714	NONHSAT133814
18	lnc-ABCA1-2	chr9:108320531-108320583	NONHSAT133819
19	lnc-FSD1L-2	chr9:108335936-108336027	NONHSAT133821
20	lnc-ABCA1-2	chr9:108316326-108316624	NONHSAT133817

No data

Variant related genes	Relation type
ENSG00000228317	TF binding region
FKTN	TF binding region
ENSG00000228317	CpG island
FKTN	CpG island
ENSG00000228317	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000106692	chromatin interactions
ENSG00000065548	chromatin interactions

Extended variants
information (count: 2639 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2639 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191432534	chr9:108292338-108292339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532835897	chr9:108292357-108292358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572900422	chr9:108292370-108292371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117551014	chr9:108292377-108292378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80014286	chr9:108292430-108292431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577033420	chr9:108292457-108292458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2768296	chr9:108292482-108292483	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs77268599	chr9:108292501-108292502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76553976	chr9:108292526-108292527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1327354	chr9:108292554-108292555	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs560344139	chr9:108292588-108292589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527802466	chr9:108292604-108292605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79091371	chr9:108292623-108292624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182975723	chr9:108292625-108292626	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531644559	chr9:108292657-108292658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141207844	chr9:108292691-108292692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186236375	chr9:108292695-108292696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138275117	chr9:108292764-108292765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149627197	chr9:108292782-108292783	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201115063	chr9:108292857-108292858	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78269364	chr9:108292884-108292885	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143948317	chr9:108292896-108292897	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539889215	chr9:108292923-108292924	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189646072	chr9:108292945-108292946	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371275183	chr9:108292968-108292969	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558395614	chr9:108292971-108292972	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75450160	chr9:108292974-108292975	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537880182	chr9:108293004-108293005	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556493815	chr9:108293005-108293006	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2768278	chr9:108293042-108293043	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs542011592	chr9:108293069-108293070	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560318465	chr9:108293079-108293080	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77438506	chr9:108293097-108293098	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183380012	chr9:108293130-108293131	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564465813	chr9:108293137-108293138	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115727831	chr9:108293140-108293141	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549769786	chr9:108293144-108293145	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149470570	chr9:108293150-108293151	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374692192	chr9:108293152-108293153	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562006624	chr9:108293162-108293163	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529555074	chr9:108293194-108293195	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374029270	chr9:108293208-108293209	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2768279	chr9:108293223-108293224	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539677808	chr9:108293264-108293265	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7856617	chr9:108293284-108293285	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570500157	chr9:108293308-108293309	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537793462	chr9:108293314-108293315	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7870562	chr9:108293316-108293317	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574757738	chr9:108293338-108293339	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6477448	chr9:108293437-108293438	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD

Chromatin state (count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108214600-108309800	Weak transcription	HUVEC	blood vessel
2	chr9:108222600-108311400	Weak transcription	Fetal Heart	heart
3	chr9:108231800-108296800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:108242600-108300000	Weak transcription	Brain Anterior Caudate	brain
5	chr9:108268200-108306000	Weak transcription	Brain Angular Gyrus	brain
6	chr9:108272800-108304600	Weak transcription	NHEK	skin
7	chr9:108274400-108299800	Weak transcription	Fetal Lung	lung
8	chr9:108276200-108309200	Weak transcription	Lung	lung
9	chr9:108278000-108292800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:108278800-108296600	Weak transcription	A549	lung
11	chr9:108278800-108297000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:108278800-108305800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr9:108279000-108293200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr9:108279000-108296000	Weak transcription	Fetal Muscle Leg	muscle
15	chr9:108279000-108311400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:108279000-108317600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:108279200-108297400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr9:108279200-108313000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr9:108279400-108296800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:108279600-108294800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:108279600-108296800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:108280200-108297200	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr9:108282400-108293200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:108282400-108294200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:108282400-108294800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr9:108282400-108294800	Weak transcription	NH-A	brain
27	chr9:108282400-108296400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr9:108282400-108296800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr9:108282400-108296800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr9:108282400-108297600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:108282400-108299600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr9:108282400-108300000	Weak transcription	HSMMtube	muscle
33	chr9:108282400-108302800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:108282400-108302800	Weak transcription	HSMM	muscle
35	chr9:108282400-108312400	Weak transcription	HepG2	liver
36	chr9:108282400-108319800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr9:108282400-108319800	Weak transcription	Left Ventricle	heart
38	chr9:108282400-108319800	Weak transcription	Psoas Muscle	Psoas
39	chr9:108282600-108319800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr9:108285200-108296800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr9:108289200-108306200	Weak transcription	Fetal Brain Male	brain
42	chr9:108289800-108309800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr9:108290000-108298800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr9:108290800-108296400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr9:108291000-108292600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr9:108291000-108294200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:108291000-108296200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:108291000-108296400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:108291400-108297200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:108291800-108310200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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