Variant report

Variant	nsv972783
Chromosome Location	chr9:96104996-96108763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:96108635-96109071	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr9:96108654-96108656	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:96105793-96105794	A549	lung:	n/a	n/a
4	CHD2	chr9:96108248-96108795	H1-hESC	embryonic stem cell:	n/a	chr9:96108730-96108740
5	CTBP2	chr9:96107924-96109053	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr9:96108600-96108750	HCM	heart:	n/a	n/a
7	CTCF	chr9:96108720-96108870	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr9:96108078-96108166	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr9:96108020-96108170	HepG2	liver:	n/a	n/a
10	CTCF	chr9:96107963-96108224	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:96108740-96108890	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr9:96107951-96108152	K562	blood:	n/a	n/a
13	CTCF	chr9:96108100-96108350	HCFaa	heart:	n/a	n/a
14	CTCF	chr9:96108680-96108830	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr9:96108660-96108810	AG09319	gingival:	n/a	n/a
16	CTCF	chr9:96107950-96108187	K562	blood:	n/a	n/a
17	E2F6	chr9:96107898-96109269	H1-hESC	embryonic stem cell:	n/a	chr9:96108619-96108628 chr9:96108056-96108068 chr9:96108696-96108708
18	E2F6	chr9:96108269-96109198	H1-hESC	embryonic stem cell:	n/a	chr9:96108619-96108628 chr9:96108696-96108708
19	GATA3	chr9:96104693-96105030	MCF-7	breast:	n/a	n/a
20	GTF2F1	chr9:96108594-96108963	H1-hESC	embryonic stem cell:	n/a	n/a
21	HA-E2F1	chr9:96104713-96105158	MCF-7	breast:	n/a	n/a
22	MAX	chr9:96104663-96105036	MCF-7	breast:	n/a	chr9:96104757-96104766
23	MAX	chr9:96108073-96108479	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAX	chr9:96104556-96105042	MCF-7	breast:	n/a	chr9:96104757-96104766
25	MAX	chr9:96107900-96109154	H1-hESC	embryonic stem cell:	n/a	chr9:96108823-96108832 chr9:96108823-96108833
26	MAX	chr9:96104620-96105068	ECC-1	luminal epithelium:	n/a	chr9:96104757-96104766
27	MAX	chr9:96107960-96109158	H1-hESC	embryonic stem cell:	n/a	chr9:96108823-96108832 chr9:96108823-96108833
28	MAX	chr9:96104678-96105017	ECC-1	luminal epithelium:	n/a	chr9:96104757-96104766
29	MXI1	chr9:96108041-96108592	H1-hESC	embryonic stem cell:	n/a	n/a
30	MYC	chr9:96107111-96107215	H1-hESC	embryonic stem cell:	n/a	n/a
31	MYC	chr9:96108632-96108703	H1-hESC	embryonic stem cell:	n/a	n/a
32	MYC	chr9:96108116-96108429	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr9:96104731-96105002	MCF-7	breast:	n/a	chr9:96104757-96104766
34	NFIC	chr9:96104660-96105072	ECC-1	luminal epithelium:	n/a	chr9:96105007-96105023
35	NR2F2	chr9:96104668-96105068	MCF-7	breast:	n/a	n/a
36	POLR2A	chr9:96108675-96109086	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr9:96108150-96109141	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr9:96108143-96108230	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr9:96108284-96108293	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr9:96108324-96109010	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr9:96108556-96109113	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr9:96105319-96105344	GM12878	blood:	n/a	n/a
43	POLR2A	chr9:96105349-96105511	GM12878	blood:	n/a	n/a
44	POLR2A	chr9:96105270-96105299	HUVEC	blood vessel:	n/a	n/a
45	RAD21	chr9:96107950-96108314	H1-hESC	embryonic stem cell:	n/a	chr9:96108039-96108052
46	RAD21	chr9:96107989-96108227	H1-hESC	embryonic stem cell:	n/a	chr9:96108039-96108052
47	SIN3A	chr9:96107940-96109179	H1-hESC	embryonic stem cell:	n/a	chr9:96108544-96108557
48	SIN3AK20	chr9:96104591-96105065	MCF-7	breast:	n/a	n/a
49	TAF1	chr9:96108591-96108916	H1-hESC	embryonic stem cell:	n/a	n/a
50	TBP	chr9:96108398-96109146	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96106281-96106331	RPTEC	kidney:	n/a
2	chr9:96108467-96108517	PFSK-1	brain:	n/a
3	chr9:96106281-96106331	CMK	blood:	n/a
4	chr9:96106281-96106331	K562	blood:	n/a
5	chr9:96108319-96108369	LNCaP	prostate:	n/a
6	chr9:96108467-96108517	Hela-S3	cervix:	n/a
7	chr9:96106281-96106331	AG10803	skin:	n/a
8	chr9:96108319-96108369	Jurkat	blood:	n/a
9	chr9:96108467-96108517	RPTEC	kidney:	n/a
10	chr9:96108319-96108369	PrEC	prostate:	n/a
11	chr9:96108319-96108369	HRCEpiC	kidney:	n/a
12	chr9:96108319-96108369	HAEpiC	amniotic membrane:	n/a
13	chr9:96108319-96108369	Hela-S3	cervix:	n/a
14	chr9:96106281-96106331	SAEC	small airway:	n/a
15	chr9:96108319-96108369	SKMC	muscle:	n/a
16	chr9:96108467-96108517	GM12892	blood:	n/a
17	chr9:96108467-96108517	NH-A	brain:	n/a
18	chr9:96106281-96106331	ProgFib	skin:	n/a
19	chr9:96108467-96108517	PANC-1	pancreas:	n/a
20	chr9:96108467-96108517	K562	blood:	n/a
21	chr9:96108319-96108369	H1-hESC	embryonic stem cell:	embryo
22	chr9:96108319-96108369	AG09319	gingival:	n/a
23	chr9:96108467-96108517	SK-N-SH_RA	brain:	n/a
24	chr9:96108467-96108517	GM06990	blood:	n/a
25	chr9:96106281-96106331	AoSMC	blood vessel:	n/a
26	chr9:96108319-96108369	NHDF-neo	bronchial:	n/a
27	chr9:96108319-96108369	AoSMC	blood vessel:	n/a
28	chr9:96108319-96108369	HEEpiC	esophagus:	n/a
29	chr9:96106281-96106331	HCPEpiC	choroid plexus:	n/a
30	chr9:96108319-96108369	HCT-116	colon:	n/a
31	chr9:96108467-96108517	HCF	heart:	n/a
32	chr9:96108319-96108369	T-47D	breast:	n/a
33	chr9:96108319-96108369	HPAEpiC	pulmonary alveolar:	n/a
34	chr9:96108467-96108517	NB4	blood:	n/a
35	chr9:96108467-96108517	AG10803	skin:	n/a
36	chr9:96106281-96106331	AG04450	lung:	fetal
37	chr9:96108467-96108517	HCM	heart:	n/a
38	chr9:96106281-96106331	HCF	heart:	n/a
39	chr9:96108319-96108369	AG04449	skin:	fetal
40	chr9:96108319-96108369	GM12892	blood:	n/a
41	chr9:96106281-96106331	H1-hESC	embryonic stem cell:	embryo
42	chr9:96106281-96106331	HRPEpiC	eye:	n/a
43	chr9:96108467-96108517	A549	lung:	n/a
44	chr9:96108319-96108369	NB4	blood:	n/a
45	chr9:96108319-96108369	MCF10A-Er-Src	breast:	n/a
46	chr9:96108319-96108369	HIPEpiC	eye:	n/a
47	chr9:96108467-96108517	AG04449	skin:	fetal
48	chr9:96108319-96108369	PFSK-1	brain:	n/a
49	chr9:96108319-96108369	BE2_C	brain:	n/a
50	chr9:96108319-96108369	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:96102856..96105406-chr9:96141051..96143168,2	MCF-7	breast:
2	chr9:96102234..96103753-chr9:96106109..96107624,2	K562	blood:

No data

Variant related genes	Relation type
C9orf129	TF binding region
C9orf129	CpG island

Extended variants
information (count: 170 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547605807	chr9:96105041-96105042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2494781	chr9:96105043-96105044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs373742707	chr9:96105059-96105060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368726588	chr9:96105063-96105064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530300521	chr9:96105075-96105076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2258451	chr9:96105124-96105125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548629167	chr9:96105147-96105148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570326907	chr9:96105166-96105167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369984590	chr9:96105173-96105174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149117751	chr9:96105193-96105194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552565388	chr9:96105194-96105195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572391689	chr9:96105211-96105212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535084390	chr9:96105254-96105255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553413108	chr9:96105325-96105326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186552304	chr9:96105347-96105348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2258457	chr9:96105375-96105376	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554606797	chr9:96105413-96105414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575891182	chr9:96105414-96105415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543017624	chr9:96105421-96105422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs9696550	chr9:96105431-96105432	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs2258459	chr9:96105436-96105437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372977467	chr9:96105438-96105439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189274259	chr9:96105440-96105441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2258460	chr9:96105441-96105442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2494779	chr9:96105448-96105449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540803081	chr9:96105492-96105493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187234092	chr9:96105519-96105520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35342696	chr9:96105560-96105561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548756252	chr9:96105568-96105569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190915981	chr9:96105608-96105609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201370384	chr9:96105617-96105618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531186886	chr9:96105625-96105626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552627701	chr9:96105663-96105664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2258469	chr9:96105677-96105678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202057406	chr9:96105695-96105696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149259653	chr9:96105699-96105700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534991841	chr9:96105728-96105729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183044403	chr9:96105732-96105733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377190163	chr9:96105760-96105761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568529963	chr9:96105824-96105825	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs79887866	chr9:96105862-96105863	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs554701501	chr9:96105884-96105885	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs185933216	chr9:96105918-96105919	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs536913543	chr9:96106009-96106010	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs114480138	chr9:96106016-96106017	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs138915564	chr9:96106043-96106044	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs576458894	chr9:96106075-96106076	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs541019325	chr9:96106084-96106085	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs562051949	chr9:96106096-96106097	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs190595499	chr9:96106100-96106101	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96098600-96108000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:96098800-96105000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr9:96101400-96107200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr9:96102600-96106000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:96102600-96107600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:96102800-96105800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:96102800-96106000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr9:96102800-96106000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:96102800-96106200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr9:96102800-96107200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr9:96102800-96107800	Weak transcription	Fetal Brain Male	brain
12	chr9:96102800-96108200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:96103000-96106000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr9:96103200-96106200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:96103400-96106000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:96104600-96105000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:96104800-96105000	Enhancers	Gastric	stomach
18	chr9:96104800-96105000	Enhancers	Left Ventricle	heart
19	chr9:96104800-96105200	Enhancers	Esophagus	oesophagus
20	chr9:96104800-96106800	Enhancers	Placenta	Placenta
21	chr9:96105000-96105800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr9:96105000-96107800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:96105200-96106400	Weak transcription	Esophagus	oesophagus
24	chr9:96105800-96106800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr9:96105800-96106800	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
26	chr9:96105800-96108400	Weak transcription	Right Atrium	heart
27	chr9:96106000-96106400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr9:96106000-96106800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr9:96106000-96106800	Active TSS	Brain Cingulate Gyrus	brain
30	chr9:96106000-96107200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr9:96106000-96107600	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr9:96106000-96107800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr9:96106200-96106400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:96106200-96106600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr9:96106200-96106600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr9:96106200-96106800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr9:96106200-96107200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr9:96106400-96106600	Enhancers	Esophagus	oesophagus
39	chr9:96106400-96107200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr9:96106400-96107200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr9:96106600-96106800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr9:96106600-96106800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr9:96106600-96107400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr9:96106800-96107000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr9:96106800-96107600	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr9:96106800-96107800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr9:96106800-96108000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr9:96106800-96108000	Weak transcription	Placenta	Placenta
49	chr9:96106800-96108200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr9:96106800-96108200	Active TSS	HUES6 Cell Line	embryonic stem cell

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