Variant report

Variant	nsv893691
Chromosome Location	chr9:107994629-108020284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1174)
CpG islands
(count:428)
Chromatin interactive
region (count:42)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:108006506-108006916	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:108006571-108006804	K562	blood:	n/a	n/a
3	ARID3A	chr9:108014051-108014936	HepG2	liver:	n/a	n/a
4	ATF1	chr9:108013454-108013793	K562	blood:	n/a	n/a
5	ATF1	chr9:108005463-108005931	K562	blood:	n/a	n/a
6	ATF2	chr9:108006462-108006810	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:108006351-108006826	GM12878	blood:	n/a	n/a
8	ATF2	chr9:108006290-108006898	GM12878	blood:	n/a	n/a
9	ATF2	chr9:108006222-108006848	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr9:108006379-108006912	A549	lung:	n/a	chr9:108006752-108006761
11	ATF3	chr9:108006253-108006974	A549	lung:	n/a	chr9:108006752-108006761
12	BACH1	chr9:108006600-108006691	K562	blood:	n/a	n/a
13	BACH1	chr9:108006452-108006840	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:108007355-108008138	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr9:108006468-108006793	GM12878	blood:	n/a	n/a
16	BCL3	chr9:108006330-108006927	A549	lung:	n/a	chr9:108006667-108006680
17	BCL3	chr9:108006483-108006930	GM12878	blood:	n/a	chr9:108006667-108006680
18	BCL3	chr9:108006255-108006860	A549	lung:	n/a	chr9:108006667-108006680
19	BCLAF1	chr9:108006323-108007446	GM12878	blood:	n/a	chr9:108006667-108006680 chr9:108007203-108007216
20	BCLAF1	chr9:108006279-108006939	GM12878	blood:	n/a	chr9:108006667-108006680
21	BCLAF1	chr9:108006464-108006994	K562	blood:	n/a	chr9:108006667-108006680
22	BCLAF1	chr9:108006399-108006886	K562	blood:	n/a	chr9:108006667-108006680
23	BHLHE40	chr9:108006378-108007331	HepG2	liver:	n/a	n/a
24	BHLHE40	chr9:108006183-108007382	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:108006335-108006860	K562	blood:	n/a	n/a
26	BHLHE40	chr9:108009006-108009021	K562	blood:	n/a	n/a
27	BRCA1	chr9:108006458-108006869	HepG2	liver:	n/a	n/a
28	BRCA1	chr9:108006153-108006835	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr9:108006372-108006849	GM12878	blood:	n/a	n/a
30	BRCA1	chr9:108006434-108006821	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr9:108007462-108007698	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr9:108007494-108008290	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr9:108006467-108006812	K562	blood:	n/a	n/a
34	CBX3	chr9:108006154-108007059	HCT-116	colon:	n/a	n/a
35	CBX3	chr9:108006125-108007159	HCT-116	colon:	n/a	n/a
36	CBX3	chr9:108006169-108006907	K562	blood:	n/a	n/a
37	CCNT2	chr9:108006550-108007369	K562	blood:	n/a	chr9:108006752-108006761
38	CEBPB	chr9:107995472-107995676	K562	blood:	n/a	chr9:107995547-107995558
39	CEBPB	chr9:108004054-108004241	HepG2	liver:	n/a	chr9:108004143-108004156 chr9:108004144-108004155 chr9:108004143-108004156
40	CEBPB	chr9:107995408-107995705	HepG2	liver:	n/a	chr9:107995547-107995558
41	CEBPB	chr9:108007843-108008312	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr9:108006335-108006825	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:108004011-108004284	Hela-S3	cervix:	n/a	chr9:108004143-108004156 chr9:108004144-108004155 chr9:108004143-108004156
44	CEBPB	chr9:108006652-108006685	K562	blood:	n/a	n/a
45	CEBPB	chr9:107995434-107995695	IMR90	lung:	n/a	chr9:107995547-107995558
46	CEBPB	chr9:108006478-108006917	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr9:108006323-108006966	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:108014372-108014550	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:108003980-108004309	HepG2	liver:	n/a	chr9:108004143-108004156 chr9:108004144-108004155 chr9:108004143-108004156
50	CEBPB	chr9:107995429-107995678	Hela-S3	cervix:	n/a	chr9:107995547-107995558

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:108005349-108005399	SKMC	muscle:	n/a
2	chr9:108005349-108005399	SKMC	muscle:	n/a
3	chr9:108005349-108005399	HIPEpiC	eye:	n/a
4	chr9:108003927-108003977	HRPEpiC	eye:	n/a
5	chr9:108005349-108005399	NHBE	bronchial:	n/a
6	chr9:108006776-108006826	ECC-1	luminal epithelium:	n/a
7	chr9:108006776-108006826	Jurkat	blood:	n/a
8	chr9:108007124-108007174	ProgFib	skin:	n/a
9	chr9:108003927-108003977	H1-hESC	embryonic stem cell:	embryo
10	chr9:108006776-108006826	NH-A	brain:	n/a
11	chr9:108006776-108006826	LNCaP	prostate:	n/a
12	chr9:108005349-108005399	GM19239	blood:	n/a
13	chr9:108003927-108003977	Caco-2	colon:	n/a
14	chr9:108006776-108006826	H1-hESC	embryonic stem cell:	embryo
15	chr9:108008079-108008129	HRE	kidney:	n/a
16	chr9:108003927-108003977	ECC-1	luminal epithelium:	n/a
17	chr9:108007124-108007174	AG04450	lung:	fetal
18	chr9:108003927-108003977	Hepatocyte	liver:	n/a
19	chr9:108007124-108007174	CMK	blood:	n/a
20	chr9:108006974-108007024	GM12892	blood:	n/a
21	chr9:108008079-108008129	SKMC	muscle:	n/a
22	chr9:108006776-108006826	MCF10A-Er-Src	breast:	n/a
23	chr9:108005349-108005399	HL-60	blood:	n/a
24	chr9:108008079-108008129	SK-N-MC	brain:	n/a
25	chr9:108003927-108003977	HRE	kidney:	n/a
26	chr9:108005349-108005399	HRCEpiC	kidney:	n/a
27	chr9:108003927-108003977	HRCEpiC	kidney:	n/a
28	chr9:108005349-108005399	SK-N-SH	brain:	n/a
29	chr9:108005349-108005399	RPTEC	kidney:	n/a
30	chr9:108006611-108006661	HEEpiC	esophagus:	n/a
31	chr9:108006974-108007024	HEK293	kidney:	embryo
32	chr9:108006974-108007024	HRE	kidney:	n/a
33	chr9:108006974-108007024	HNPCEpiC	eye:	n/a
34	chr9:108006611-108006661	SK-N-MC	brain:	n/a
35	chr9:108003927-108003977	PANC-1	pancreas:	n/a
36	chr9:108006776-108006826	HEK293	kidney:	embryo
37	chr9:108006611-108006661	SAEC	small airway:	n/a
38	chr9:108007124-108007174	IMR90	lung:	fetal
39	chr9:108008079-108008129	Jurkat	blood:	n/a
40	chr9:108006974-108007024	PFSK-1	brain:	n/a
41	chr9:108003927-108003977	GM12892	blood:	n/a
42	chr9:108006974-108007024	CMK	blood:	n/a
43	chr9:108006776-108006826	A549	lung:	n/a
44	chr9:108003927-108003977	K562	blood:	n/a
45	chr9:108005349-108005399	GM12878	blood:	n/a
46	chr9:108006974-108007024	Hepatocyte	liver:	n/a
47	chr9:108006974-108007024	SK-N-SH_RA	brain:	n/a
48	chr9:108005349-108005399	HepG2	liver:	n/a
49	chr9:108006611-108006661	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:108006611-108006661	GM12891	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:107687369..107691649-chr9:108006197..108009884,7	MCF-7	breast:
2	chr9:108020140..108022569-chr9:108023419..108024993,2	K562	blood:
3	chr9:107993056..107995506-chr9:107999251..108000803,2	MCF-7	breast:
4	chr9:108007121..108007988-chr9:108175578..108176396,3	MCF-7	breast:
5	chr9:107986788..107989562-chr9:108004560..108006596,2	K562	blood:
6	chr9:108006932..108009449-chr9:108036462..108038843,2	MCF-7	breast:
7	chr9:107999147..108002971-chr9:108003945..108007816,6	MCF-7	breast:
8	chr9:107989785..107992485-chr9:107999468..108001014,2	MCF-7	breast:
9	chr9:107993075..107994603-chr9:107998043..108000828,2	MCF-7	breast:
10	chr9:107948857..107951560-chr9:108005097..108008240,3	MCF-7	breast:
11	chr9:107631539..107633067-chr9:108007173..108009446,2	MCF-7	breast:
12	chr9:107993056..107995506-chr9:107999251..108000803,2	MCF-7	breast:
13	chr9:108005955..108009044-chr9:108014921..108018676,7	MCF-7	breast:
14	chr9:108007303..108009573-chr9:108053805..108056055,2	MCF-7	breast:
15	chr9:107997912..108002258-chr9:108004974..108009513,7	MCF-7	breast:
16	chr9:108003331..108004862-chr9:108007062..108008730,2	MCF-7	breast:
17	chr9:108004369..108006903-chr9:108106116..108108591,2	MCF-7	breast:
18	chr9:107964013..107966115-chr9:108007069..108009049,2	MCF-7	breast:
19	chr2:130939236..130940096-chr9:108006055..108006614,2	NB4	blood:
20	chr9:108003331..108004862-chr9:108007062..108008730,2	MCF-7	breast:
21	chr9:108007022..108007998-chr9:108122682..108123316,3	MCF-7	breast:
22	chr9:108007148..108008877-chr9:108174581..108177913,4	MCF-7	breast:
23	chr9:107904194..107906765-chr9:108007305..108010272,2	MCF-7	breast:
24	chr9:108013957..108014924-chr9:108175549..108176493,3	MCF-7	breast:
25	chr9:108008269..108008775-chr9:108052722..108053326,2	MCF-7	breast:
26	chr9:108005558..108008995-chr9:108010064..108014248,9	MCF-7	breast:
27	chr9:108006963..108009238-chr9:108022447..108024092,2	MCF-7	breast:
28	chr9:108005738..108008360-chr9:108117762..108120177,2	MCF-7	breast:
29	chr9:108006964..108008816-chr9:108165166..108168105,2	MCF-7	breast:
30	chr9:108006564..108010979-chr9:108011940..108017474,8	MCF-7	breast:
31	chr9:108011346..108013959-chr9:108015569..108017411,2	MCF-7	breast:
32	chr9:108011317..108013962-chr9:108054613..108056350,2	MCF-7	breast:
33	chr9:108005319..108006844-chr9:108176651..108179101,2	MCF-7	breast:
34	chr9:107753703..107756289-chr9:108016783..108019094,2	MCF-7	breast:
35	chr6:26031886..26032421-chr9:108007272..108008250,2	Hela-S3	cervix:
36	chr9:107986434..107988530-chr9:108007277..108010113,2	MCF-7	breast:
37	chr9:108017304..108019990-chr9:108021859..108023819,2	MCF-7	breast:
38	chr9:108011346..108013959-chr9:108015569..108017411,2	MCF-7	breast:
39	chr9:108007262..108007998-chr9:108175454..108176410,3	MCF-7	breast:
40	chr9:108006717..108009348-chr9:108018755..108022219,3	MCF-7	breast:
41	chr9:107940503..107943393-chr9:108000733..108002997,2	MCF-7	breast:
42	chr9:107971630..107974403-chr9:107994725..107996879,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSD1L-3	chr9:108006929-108007185	NONHSAT133813

No data

Variant related genes	Relation type
SLC44A1	TF binding region
SLC44A1	CpG island
ENSG00000165029	chromatin interactions
ENSG00000238208	chromatin interactions
ENSG00000226334	chromatin interactions
ENSG00000152082	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000230013	chromatin interactions
ENSG00000070214	chromatin interactions

Extended variants
information (count: 905 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:905 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7866947	chr9:107994629-107994630	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375439667	chr9:107994686-107994687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146149340	chr9:107994694-107994695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs419443	chr9:107994721-107994722	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs543183443	chr9:107994731-107994732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546122131	chr9:107994733-107994734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564700216	chr9:107994735-107994736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs388679	chr9:107994781-107994782	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs188751569	chr9:107994794-107994795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56668999	chr9:107994850-107994851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529738610	chr9:107994898-107994899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541586743	chr9:107994918-107994919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138881400	chr9:107994960-107994961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566484746	chr9:107994973-107994974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398454	chr9:107995006-107995007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs370565128	chr9:107995021-107995022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7849463	chr9:107995089-107995090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542513888	chr9:107995106-107995107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572929899	chr9:107995152-107995153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77949757	chr9:107995163-107995164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570294781	chr9:107995218-107995219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537615308	chr9:107995222-107995223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35333045	chr9:107995244-107995245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371961384	chr9:107995274-107995275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114397928	chr9:107995298-107995299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535465546	chr9:107995374-107995375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143848248	chr9:107995486-107995487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77386759	chr9:107995578-107995579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539900236	chr9:107995667-107995668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147237768	chr9:107995670-107995671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181359752	chr9:107995758-107995759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139169510	chr9:107995780-107995781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562373757	chr9:107995795-107995796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186436991	chr9:107995816-107995817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141459954	chr9:107995859-107995860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11787900	chr9:107995875-107995876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190939320	chr9:107995879-107995880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201604595	chr9:107995907-107995908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13286790	chr9:107995916-107995917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556995187	chr9:107995943-107995944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563666362	chr9:107995980-107995981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575752241	chr9:107995989-107995990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543131034	chr9:107996000-107996001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527426601	chr9:107996037-107996038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552264258	chr9:107996064-107996065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374029424	chr9:107996074-107996075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11788342	chr9:107996125-107996126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs327961	chr9:107996143-107996144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs180882867	chr9:107996147-107996148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150888136	chr9:107996215-107996216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
T-cell acute lymphoblastic leukemia	18185524	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
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:107987800-108002400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr9:107993600-107995200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:107994200-107997400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:107994400-107995200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr9:107994600-107995200	Enhancers	HSMM	muscle
6	chr9:107994800-107996000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:107994800-107996000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:107995000-107995200	Enhancers	Fetal Lung	lung
9	chr9:107995200-107996200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr9:107995200-107996200	Weak transcription	Fetal Lung	lung
11	chr9:107995600-107996400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:107995600-107996400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr9:107995600-107996600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr9:107995600-107996600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:107995600-107996800	Enhancers	Hela-S3	cervix
16	chr9:107995800-107996200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr9:107996000-107996400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:107996000-107996400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:107996000-107996400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:107996200-107996400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:107996200-107996600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr9:107996200-107996600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr9:107996200-107996600	Enhancers	Fetal Lung	lung
24	chr9:107996400-108003400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:107996600-108002000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr9:107996600-108002800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr9:107996800-107997200	Enhancers	Psoas Muscle	Psoas
28	chr9:107998200-107999400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr9:107998600-107999200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr9:107999000-108000000	Enhancers	Fetal Intestine Small	intestine
31	chr9:107999000-108001200	Enhancers	Fetal Intestine Large	intestine
32	chr9:107999200-108000400	Enhancers	HepG2	liver
33	chr9:107999600-107999800	Enhancers	Stomach Mucosa	stomach
34	chr9:108000000-108005200	Weak transcription	Stomach Mucosa	stomach
35	chr9:108000000-108006000	Weak transcription	Fetal Intestine Small	intestine
36	chr9:108000400-108000800	Weak transcription	HepG2	liver
37	chr9:108000800-108001000	Enhancers	HepG2	liver
38	chr9:108000800-108001200	Enhancers	Liver	Liver
39	chr9:108000800-108001600	Enhancers	Pancreas	Pancrea
40	chr9:108001000-108003600	Weak transcription	HepG2	liver
41	chr9:108001200-108006000	Weak transcription	Liver	Liver
42	chr9:108001200-108006000	Weak transcription	Fetal Intestine Large	intestine
43	chr9:108001400-108001600	Enhancers	Fetal Brain Male	brain
44	chr9:108001800-108003000	Weak transcription	Fetal Brain Male	brain
45	chr9:108002000-108002200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr9:108002200-108003000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr9:108002400-108002600	Enhancers	Left Ventricle	heart
48	chr9:108002400-108004200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr9:108002400-108006200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr9:108002600-108006200	Weak transcription	Left Ventricle	heart

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