Variant report

Variant	nsv893690
Chromosome Location	chr9:107992706-108083485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1795)
CpG islands
(count:488)
Chromatin interactive
region (count:111)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1795 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	chr9:108052906-108054144	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:108025287-108025472	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:108014051-108014936	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:108080904-108082219	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:108043003-108043135	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:108059091-108059446	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:108006571-108006804	K562	blood:	n/a	n/a
9	ATF1	chr9:108013454-108013793	K562	blood:	n/a	n/a
10	ATF1	chr9:108059178-108059447	K562	blood:	n/a	n/a
11	ATF1	chr9:108061593-108062088	K562	blood:	n/a	n/a
12	ATF1	chr9:108005463-108005931	K562	blood:	n/a	n/a
13	ATF2	chr9:108006351-108006826	GM12878	blood:	n/a	n/a
14	ATF2	chr9:108006462-108006810	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr9:108006222-108006848	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr9:108068660-108069420	GM12878	blood:	n/a	n/a
17	ATF2	chr9:108006290-108006898	GM12878	blood:	n/a	n/a
18	ATF3	chr9:108006379-108006912	A549	lung:	n/a	chr9:108006752-108006761
19	ATF3	chr9:108061628-108062035	K562	blood:	n/a	chr9:108061812-108061823
20	ATF3	chr9:108006253-108006974	A549	lung:	n/a	chr9:108006752-108006761
21	BACH1	chr9:108007355-108008138	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr9:108059138-108059634	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr9:108055802-108055826	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr9:108006452-108006840	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr9:108006600-108006691	K562	blood:	n/a	n/a
26	BATF	chr9:108069811-108070156	GM12878	blood:	n/a	n/a
27	BATF	chr9:108061700-108061945	GM12878	blood:	n/a	n/a
28	BATF	chr9:108069173-108069422	GM12878	blood:	n/a	n/a
29	BATF	chr9:108006468-108006793	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:108075518-108075805	GM12878	blood:	n/a	n/a
31	BCL3	chr9:108006483-108006930	GM12878	blood:	n/a	chr9:108006667-108006680
32	BCL3	chr9:108006330-108006927	A549	lung:	n/a	chr9:108006667-108006680
33	BCL3	chr9:108006255-108006860	A549	lung:	n/a	chr9:108006667-108006680
34	BCLAF1	chr9:108006323-108007446	GM12878	blood:	n/a	chr9:108006667-108006680 chr9:108007203-108007216
35	BCLAF1	chr9:108006279-108006939	GM12878	blood:	n/a	chr9:108006667-108006680
36	BCLAF1	chr9:108006464-108006994	K562	blood:	n/a	chr9:108006667-108006680
37	BCLAF1	chr9:108006399-108006886	K562	blood:	n/a	chr9:108006667-108006680
38	BHLHE40	chr9:108006378-108007331	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:108009006-108009021	K562	blood:	n/a	n/a
40	BHLHE40	chr9:108006335-108006860	K562	blood:	n/a	n/a
41	BHLHE40	chr9:108006183-108007382	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:108061670-108062055	K562	blood:	n/a	n/a
43	BHLHE40	chr9:108082945-108083463	GM12878	blood:	n/a	n/a
44	BRCA1	chr9:108058952-108059647	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr9:108007494-108008290	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr9:108006458-108006869	HepG2	liver:	n/a	n/a
47	BRCA1	chr9:108006434-108006821	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr9:108007462-108007698	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr9:108006372-108006849	GM12878	blood:	n/a	n/a
50	BRCA1	chr9:108061595-108062082	Hela-S3	cervix:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:108006776-108006826	HRPEpiC	eye:	n/a
2	chr9:108006776-108006826	NB4	blood:	n/a
3	chr9:108006974-108007024	GM06990	blood:	n/a
4	chr9:108008079-108008129	HMEC	breast:	n/a
5	chr9:108003927-108003977	HCM	heart:	n/a
6	chr9:108008079-108008129	PrEC	prostate:	n/a
7	chr9:108006611-108006661	ovcar-3	ovarian:	n/a
8	chr9:108053809-108053859	IMR90	lung:	fetal
9	chr9:108053809-108053859	GM06990	blood:	n/a
10	chr9:108053809-108053859	SKMC	muscle:	n/a
11	chr9:108005349-108005399	HEEpiC	esophagus:	n/a
12	chr9:108003927-108003977	NH-A	brain:	n/a
13	chr9:108007124-108007174	MCF10A-Er-Src	breast:	n/a
14	chr9:108003927-108003977	HNPCEpiC	eye:	n/a
15	chr9:108007124-108007174	PFSK-1	brain:	n/a
16	chr9:108007124-108007174	U87	brain:	n/a
17	chr9:108007124-108007174	AG09309	skin:	n/a
18	chr9:108007124-108007174	SKMC	muscle:	n/a
19	chr9:108006611-108006661	BJ	skin:	n/a
20	chr9:108006776-108006826	MCF10A-Er-Src	breast:	n/a
21	chr9:108008079-108008129	NB4	blood:	n/a
22	chr9:108007124-108007174	Hela-S3	cervix:	n/a
23	chr9:108005349-108005399	PrEC	prostate:	n/a
24	chr9:108007124-108007174	HepG2	liver:	n/a
25	chr9:108007124-108007174	NH-A	brain:	n/a
26	chr9:108005349-108005399	HCF	heart:	n/a
27	chr9:108006776-108006826	A549	lung:	n/a
28	chr9:108005349-108005399	HL-60	blood:	n/a
29	chr9:108006611-108006661	PANC-1	pancreas:	n/a
30	chr9:108053809-108053859	SK-N-MC	brain:	n/a
31	chr9:108008079-108008129	AG09309	skin:	n/a
32	chr9:108006776-108006826	SKMC	muscle:	n/a
33	chr9:108006611-108006661	HL-60	blood:	n/a
34	chr9:108008079-108008129	A549	lung:	n/a
35	chr9:108006611-108006661	Caco-2	colon:	n/a
36	chr9:108007124-108007174	AG04450	lung:	fetal
37	chr9:108006974-108007024	Caco-2	colon:	n/a
38	chr9:108006611-108006661	T-47D	breast:	n/a
39	chr9:108003927-108003977	PANC-1	pancreas:	n/a
40	chr9:108005349-108005399	HepG2	liver:	n/a
41	chr9:108008079-108008129	HepG2	liver:	n/a
42	chr9:108005349-108005399	HCM	heart:	n/a
43	chr9:108008079-108008129	SK-N-SH	brain:	n/a
44	chr9:108006611-108006661	GM12892	blood:	n/a
45	chr9:108008079-108008129	NT2-D1	testis:	n/a
46	chr9:108006974-108007024	HNPCEpiC	eye:	n/a
47	chr9:108006611-108006661	NH-A	brain:	n/a
48	chr9:108008079-108008129	SK-N-SH_RA	brain:	n/a
49	chr9:108007124-108007174	LNCaP	prostate:	n/a
50	chr9:108006974-108007024	HPAEpiC	pulmonary alveolar:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:108005803..108008854-chr9:108078704..108081931,3	MCF-7	breast:
2	chr2:8821577..8823173-chr9:108072270..108073804,2	MCF-7	breast:
3	chr9:108011346..108013959-chr9:108015569..108017411,2	MCF-7	breast:
4	chr9:107993075..107994603-chr9:107998043..108000828,2	MCF-7	breast:
5	chr9:108053038..108054954-chr9:108056839..108058571,2	K562	blood:
6	chr9:108005319..108006844-chr9:108176651..108179101,2	MCF-7	breast:
7	chr9:108007262..108007998-chr9:108175454..108176410,3	MCF-7	breast:
8	chr9:108052363..108054677-chr9:108071523..108074219,3	MCF-7	breast:
9	chr9:108044800..108047623-chr9:108061922..108064222,3	MCF-7	breast:
10	chr9:108031908..108033818-chr9:108035186..108036701,2	MCF-7	breast:
11	chr10:130522788..130523540-chr9:108078431..108079374,2	MCF-7	breast:
12	chr9:108020140..108022569-chr9:108023419..108024993,2	K562	blood:
13	chr9:108020140..108022569-chr9:108023419..108024993,2	K562	blood:
14	chr9:108006089..108008759-chr9:108057985..108062385,6	MCF-7	breast:
15	chr9:108052363..108054677-chr9:108071523..108074219,3	MCF-7	breast:
16	chr9:108024809..108030231-chr9:108032274..108037301,6	MCF-7	breast:
17	chr9:107940503..107943393-chr9:108000733..108002997,2	MCF-7	breast:
18	chr9:107971630..107974403-chr9:107994725..107996879,2	MCF-7	breast:
19	chr9:107990853..107992925-chr9:108005176..108007091,2	MCF-7	breast:
20	chr15:72764720..72766890-chr9:108036384..108038851,2	MCF-7	breast:
21	chr9:108006564..108010979-chr9:108011940..108017474,8	MCF-7	breast:
22	chr9:108059299..108061602-chr9:108067206..108069690,2	K562	blood:
23	chr9:108056287..108057910-chr9:108057918..108060484,2	MCF-7	breast:
24	chr9:108024809..108030231-chr9:108032274..108037301,6	MCF-7	breast:
25	chr9:108005738..108008360-chr9:108117762..108120177,2	MCF-7	breast:
26	chr9:108048778..108051200-chr9:108054042..108056380,2	MCF-7	breast:
27	chr9:108048778..108051200-chr9:108054042..108056380,2	MCF-7	breast:
28	chr9:108006964..108008816-chr9:108165166..108168105,2	MCF-7	breast:
29	chr9:107986434..107988530-chr9:108007277..108010113,2	MCF-7	breast:
30	chr9:107993075..107994603-chr9:107998043..108000828,2	MCF-7	breast:
31	chr9:108006932..108009449-chr9:108036462..108038843,2	MCF-7	breast:
32	chr9:108034840..108036346-chr9:108041989..108044497,2	MCF-7	breast:
33	chr9:108024187..108026293-chr9:108029663..108031698,2	MCF-7	breast:
34	chr9:108031908..108033818-chr9:108035186..108036701,2	MCF-7	breast:
35	chr6:26031886..26032421-chr9:108007272..108008250,2	Hela-S3	cervix:
36	chr9:108005360..108008304-chr9:108034590..108036365,2	MCF-7	breast:
37	chr9:108029737..108031595-chr9:108037318..108040481,4	MCF-7	breast:
38	chr9:108011346..108013959-chr9:108015569..108017411,2	MCF-7	breast:
39	chr9:108031908..108034745-chr9:108037571..108039465,2	MCF-7	breast:
40	chr9:108003331..108004862-chr9:108007062..108008730,2	MCF-7	breast:
41	chr9:108052475..108054719-chr9:108057760..108060481,3	MCF-7	breast:
42	chr9:108011317..108013962-chr9:108054613..108056350,2	MCF-7	breast:
43	chr9:108013957..108014924-chr9:108175549..108176493,3	MCF-7	breast:
44	chr9:108080682..108083667-chr9:108087313..108089895,3	MCF-7	breast:
45	chr9:108004369..108006903-chr9:108106116..108108591,2	MCF-7	breast:
46	chr9:108061298..108064082-chr9:108078853..108080505,2	K562	blood:
47	chr9:108053113..108055212-chr9:108060978..108062866,2	MCF-7	breast:
48	chr9:107993056..107995506-chr9:107999251..108000803,2	MCF-7	breast:
49	chr9:108017304..108019990-chr9:108021859..108023819,2	MCF-7	breast:
50	chr9:108006620..108008569-chr9:108021985..108025100,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKTN-1	chr9:108081203-108081292	NONHSAT133814
2	lnc-FKTN-1	chr9:108080494-108080574	NONHSAT133814
3	lnc-FSD1L-3	chr9:108006929-108007185	NONHSAT133813

No data

Variant related genes	Relation type
SLC44A1	TF binding region
SLC44A1	CpG island
ENSG00000124693	chromatin interactions
ENSG00000070214	chromatin interactions
ENSG00000230013	chromatin interactions
ENSG00000165029	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000238208	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000115738	chromatin interactions
ENSG00000235092	chromatin interactions
ENSG00000152082	chromatin interactions
ENSG00000226334	chromatin interactions

Extended variants
information (count: 3371 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10120869	chr9:107992706-107992707	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573014347	chr9:107992710-107992711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540662725	chr9:107992737-107992738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141759074	chr9:107992739-107992740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532669537	chr9:107992762-107992763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368203199	chr9:107992783-107992784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550647056	chr9:107992806-107992807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187075552	chr9:107992842-107992843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs11453301	chr9:107992872-107992873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35584270	chr9:107992873-107992874	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530233480	chr9:107992877-107992878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548331817	chr9:107992939-107992940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543483012	chr9:107992944-107992945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374948896	chr9:107992999-107993000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73508576	chr9:107993062-107993063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1705490	chr9:107993162-107993163	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546602577	chr9:107993164-107993165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532527541	chr9:107993167-107993168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1705491	chr9:107993182-107993183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs571142684	chr9:107993214-107993215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191569670	chr9:107993216-107993217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538752273	chr9:107993232-107993233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143533526	chr9:107993234-107993235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183901535	chr9:107993266-107993267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148066838	chr9:107993275-107993276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554794820	chr9:107993288-107993289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573141940	chr9:107993332-107993333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574960829	chr9:107993335-107993336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189314194	chr9:107993366-107993367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565317570	chr9:107993394-107993395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141777162	chr9:107993419-107993420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544151965	chr9:107993430-107993431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370978331	chr9:107993431-107993432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192700730	chr9:107993453-107993454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530122903	chr9:107993461-107993462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185753713	chr9:107993462-107993463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55838049	chr9:107993465-107993466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56016847	chr9:107993466-107993467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2441214	chr9:107993492-107993493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs7036235	chr9:107993497-107993498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4742944	chr9:107993502-107993503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369027120	chr9:107993527-107993528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190453953	chr9:107993583-107993584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147274660	chr9:107993616-107993617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113748779	chr9:107993688-107993689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373959816	chr9:107993772-107993773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550555892	chr9:107993795-107993796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569014231	chr9:107993796-107993797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536350202	chr9:107993826-107993827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7860049	chr9:107993861-107993862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2694 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

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	chr9:107994400-107994600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:107994400-107994600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:107994400-107995200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr9:107994600-107995200	Enhancers	HSMM	muscle
8	chr9:107994800-107996000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:107994800-107996000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:107995000-107995200	Enhancers	Fetal Lung	lung
11	chr9:107995200-107996200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:107995200-107996200	Weak transcription	Fetal Lung	lung
13	chr9:107995600-107996400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:107995600-107996400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr9:107995600-107996600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr9:107995600-107996600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:107995600-107996800	Enhancers	Hela-S3	cervix
18	chr9:107995800-107996200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:107996000-107996400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:107996000-107996400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:107996000-107996400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr9:107996200-107996400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr9:107996200-107996600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:107996200-107996600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr9:107996200-107996600	Enhancers	Fetal Lung	lung
26	chr9:107996400-108003400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:107996600-108002000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr9:107996600-108002800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr9:107996800-107997200	Enhancers	Psoas Muscle	Psoas
30	chr9:107998200-107999400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr9:107998600-107999200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr9:107999000-108000000	Enhancers	Fetal Intestine Small	intestine
33	chr9:107999000-108001200	Enhancers	Fetal Intestine Large	intestine
34	chr9:107999200-108000400	Enhancers	HepG2	liver
35	chr9:107999600-107999800	Enhancers	Stomach Mucosa	stomach
36	chr9:108000000-108005200	Weak transcription	Stomach Mucosa	stomach
37	chr9:108000000-108006000	Weak transcription	Fetal Intestine Small	intestine
38	chr9:108000400-108000800	Weak transcription	HepG2	liver
39	chr9:108000800-108001000	Enhancers	HepG2	liver
40	chr9:108000800-108001200	Enhancers	Liver	Liver
41	chr9:108000800-108001600	Enhancers	Pancreas	Pancrea
42	chr9:108001000-108003600	Weak transcription	HepG2	liver
43	chr9:108001200-108006000	Weak transcription	Liver	Liver
44	chr9:108001200-108006000	Weak transcription	Fetal Intestine Large	intestine
45	chr9:108001400-108001600	Enhancers	Fetal Brain Male	brain
46	chr9:108001800-108003000	Weak transcription	Fetal Brain Male	brain
47	chr9:108002000-108002200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr9:108002200-108003000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr9:108002400-108002600	Enhancers	Left Ventricle	heart
50	chr9:108002400-108004200	Enhancers	H1 Cell Line	embryonic stem cell

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