Variant report

Variant	nsv428542
Chromosome Location	chr9:103709079-103878127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:103824845-103825458	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:103790867-103791286	HepG2	liver:	n/a	n/a
3	ATF2	chr9:103860655-103861126	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:103790580-103790837	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:103791645-103791808	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:103791051-103791349	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr9:103860719-103861010	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr9:103813501-103813803	GM12878	blood:	n/a	n/a
9	BRCA1	chr9:103790826-103790927	HepG2	liver:	n/a	n/a
10	CCNT2	chr9:103848435-103848635	K562	blood:	n/a	n/a
11	CCNT2	chr9:103824903-103825103	K562	blood:	n/a	n/a
12	CEBPB	chr9:103770352-103770590	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:103793753-103794100	HepG2	liver:	n/a	chr9:103793913-103793924
14	CEBPB	chr9:103877751-103878043	HepG2	liver:	n/a	chr9:103877878-103877891 chr9:103877878-103877891 chr9:103877878-103877889
15	CEBPB	chr9:103770373-103770497	A549	lung:	n/a	n/a
16	CEBPB	chr9:103750188-103750390	A549	lung:	n/a	chr9:103750266-103750279 chr9:103750266-103750277
17	CEBPB	chr9:103872528-103872728	A549	lung:	n/a	n/a
18	CEBPB	chr9:103763259-103763321	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:103877825-103878025	IMR90	lung:	n/a	chr9:103877878-103877891 chr9:103877878-103877891 chr9:103877878-103877889
20	CEBPB	chr9:103870588-103870909	IMR90	lung:	n/a	chr9:103870732-103870743 chr9:103870733-103870744 chr9:103870732-103870745 chr9:103870732-103870745
21	CEBPB	chr9:103862488-103862688	H1-hESC	embryonic stem cell:	n/a	chr9:103862570-103862581 chr9:103862570-103862583 chr9:103862570-103862581
22	CEBPB	chr9:103722721-103722992	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:103845364-103845615	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr9:103870703-103870840	A549	lung:	n/a	chr9:103870732-103870743 chr9:103870733-103870744 chr9:103870732-103870745 chr9:103870732-103870745
25	CEBPB	chr9:103835415-103835721	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:103793776-103794093	A549	lung:	n/a	chr9:103793913-103793924
27	CEBPB	chr9:103872512-103872686	K562	blood:	n/a	n/a
28	CEBPB	chr9:103858495-103858799	A549	lung:	n/a	n/a
29	CEBPB	chr9:103793774-103794094	IMR90	lung:	n/a	chr9:103793913-103793924
30	CEBPB	chr9:103870583-103870883	HepG2	liver:	n/a	chr9:103870732-103870743 chr9:103870733-103870744 chr9:103870732-103870745 chr9:103870732-103870745
31	CEBPB	chr9:103824989-103825338	HepG2	liver:	n/a	chr9:103825109-103825122
32	CEBPB	chr9:103825002-103825319	HepG2	liver:	n/a	chr9:103825109-103825122
33	CEBPB	chr9:103825019-103825252	HepG2	liver:	n/a	chr9:103825109-103825122
34	CEBPB	chr9:103824952-103825358	HepG2	liver:	n/a	chr9:103825109-103825122
35	CEBPB	chr9:103877842-103878034	A549	lung:	n/a	chr9:103877878-103877891 chr9:103877878-103877891 chr9:103877878-103877889
36	CEBPB	chr9:103833114-103833399	HepG2	liver:	n/a	chr9:103833254-103833265 chr9:103833255-103833266 chr9:103833254-103833267
37	CEBPB	chr9:103790732-103791222	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:103858281-103858791	HepG2	liver:	n/a	chr9:103858378-103858389
39	CEBPB	chr9:103750113-103750651	HepG2	liver:	n/a	chr9:103750266-103750279 chr9:103750266-103750277
40	CEBPB	chr9:103845411-103845542	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:103776981-103777213	HepG2	liver:	n/a	chr9:103777089-103777100
42	CEBPB	chr9:103722690-103722902	A549	lung:	n/a	n/a
43	CHD1	chr9:103860934-103861134	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr9:103791334-103791520	HepG2	liver:	n/a	n/a
45	CHD2	chr9:103790634-103791021	HepG2	liver:	n/a	n/a
46	CREB1	chr9:103824889-103825403	HepG2	liver:	n/a	n/a
47	CTBP2	chr9:103790495-103792277	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr9:103791013-103791345	MCF-7	breast:	n/a	chr9:103791080-103791093 chr9:103791077-103791095
49	CTCF	chr9:103791000-103791150	SK-N-SH_RA	brain:	n/a	chr9:103791080-103791093 chr9:103791077-103791095
50	CTCF	chr9:103791120-103791270	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:103791078-103791128	HEEpiC	esophagus:	n/a
2	chr9:103788959-103789009	LNCaP	prostate:	n/a
3	chr9:103791078-103791128	HEEpiC	esophagus:	n/a
4	chr9:103788959-103789009	LNCaP	prostate:	n/a
5	chr9:103793011-103793061	GM12891	blood:	n/a
6	chr9:103829627-103829677	NT2-D1	testis:	n/a
7	chr9:103792172-103792222	HepG2	liver:	n/a
8	chr9:103792059-103792109	NHDF-neo	bronchial:	n/a
9	chr9:103792059-103792109	HNPCEpiC	eye:	n/a
10	chr9:103789186-103789236	GM12891	blood:	n/a
11	chr9:103788959-103789009	HNPCEpiC	eye:	n/a
12	chr9:103793011-103793061	GM12878	blood:	n/a
13	chr9:103829627-103829677	HUVEC	blood vessel:	n/a
14	chr9:103790959-103791009	HCPEpiC	choroid plexus:	n/a
15	chr9:103790197-103790247	LNCaP	prostate:	n/a
16	chr9:103793011-103793061	AG10803	skin:	n/a
17	chr9:103790959-103791009	HEEpiC	esophagus:	n/a
18	chr9:103788959-103789009	HAEpiC	amniotic membrane:	n/a
19	chr9:103829627-103829677	AG09309	skin:	n/a
20	chr9:103791078-103791128	ProgFib	skin:	n/a
21	chr9:103788959-103789009	HMEC	breast:	n/a
22	chr9:103792172-103792222	BE2_C	brain:	n/a
23	chr9:103793011-103793061	NT2-D1	testis:	n/a
24	chr9:103788959-103789009	T-47D	breast:	n/a
25	chr9:103793011-103793061	ECC-1	luminal epithelium:	n/a
26	chr9:103790197-103790247	PrEC	prostate:	n/a
27	chr9:103790959-103791009	GM12891	blood:	n/a
28	chr9:103792172-103792222	GM06990	blood:	n/a
29	chr9:103793011-103793061	HCPEpiC	choroid plexus:	n/a
30	chr9:103792172-103792222	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:103829627-103829677	HIPEpiC	eye:	n/a
32	chr9:103793011-103793061	HEK293	kidney:	embryo
33	chr9:103792059-103792109	K562	blood:	n/a
34	chr9:103792059-103792109	BE2_C	brain:	n/a
35	chr9:103792172-103792222	HMEC	breast:	n/a
36	chr9:103790197-103790247	HL-60	blood:	n/a
37	chr9:103790959-103791009	Caco-2	colon:	n/a
38	chr9:103829627-103829677	AG04449	skin:	fetal
39	chr9:103788959-103789009	HCPEpiC	choroid plexus:	n/a
40	chr9:103790959-103791009	IMR90	lung:	fetal
41	chr9:103829627-103829677	LNCaP	prostate:	n/a
42	chr9:103792172-103792222	NT2-D1	testis:	n/a
43	chr9:103789186-103789236	HCM	heart:	n/a
44	chr9:103792172-103792222	ECC-1	luminal epithelium:	n/a
45	chr9:103791078-103791128	AG04449	skin:	fetal
46	chr9:103789186-103789236	HCT-116	colon:	n/a
47	chr9:103829627-103829677	MCF-7	breast:	n/a
48	chr9:103790197-103790247	GM12878	blood:	n/a
49	chr9:103792172-103792222	NHBE	bronchial:	n/a
50	chr9:103791078-103791128	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:103784494..103787314-chr9:103788511..103790366,2	MCF-7	breast:
2	chr3:64008841..64009357-chr9:103859409..103859996,2	MCF-7	breast:
3	chr9:103805241..103807580-chr9:103810302..103812299,2	K562	blood:
4	chr9:103774298..103776723-chr9:103778438..103781005,2	MCF-7	breast:
5	chr9:103805241..103807580-chr9:103810302..103812299,2	K562	blood:
6	chr9:103774298..103776723-chr9:103778438..103781005,2	MCF-7	breast:
7	chr9:103705431..103707617-chr9:103715386..103717085,2	K562	blood:
8	chr9:103784494..103787314-chr9:103788511..103790366,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF189-5	chr9:103802630-103803168	NONHSAT133721

Variant related genes	Relation type
ENSG00000148123	TF binding region
GAPDHP26	TF binding region
ENSG00000148123	CpG island
GAPDHP26	CpG island
ENSG00000163636	chromatin interactions

Extended variants
information (count: 3748 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3748 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534965174	chr9:103720232-103720233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557536606	chr9:103720268-103720269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147470193	chr9:103720270-103720271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73504748	chr9:103720339-103720340	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553109201	chr9:103720352-103720353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572277442	chr9:103720356-103720357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117992829	chr9:103721263-103721264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191519772	chr9:103721274-103721275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73656412	chr9:103721305-103721306	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534597295	chr9:103721326-103721327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs71507702	chr9:103721327-103721328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531075531	chr9:103721330-103721331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116915254	chr9:103721345-103721346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574273506	chr9:103721350-103721351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182619541	chr9:103721365-103721366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554589035	chr9:103721393-103721394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189778952	chr9:103722616-103722617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146431302	chr9:103722623-103722624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140868515	chr9:103722625-103722626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs578114983	chr9:103722653-103722654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540428951	chr9:103722695-103722696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560314041	chr9:103722730-103722731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529315890	chr9:103722731-103722732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181215833	chr9:103722781-103722782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573848172	chr9:103733193-103733194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs536190557	chr9:103733198-103733199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556304569	chr9:103733213-103733214	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs78153502	chr9:103734419-103734420	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs190191648	chr9:103734435-103734436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs574481550	chr9:103734520-103734521	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534711387	chr9:103734528-103734529	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs181531833	chr9:103734583-103734584	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs187388288	chr9:103734584-103734585	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142945716	chr9:103734586-103734587	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs146136789	chr9:103734598-103734599	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs528722946	chr9:103734619-103734620	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs190215955	chr9:103734667-103734668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140169549	chr9:103734676-103734677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs180988927	chr9:103734724-103734725	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs552979891	chr9:103734731-103734732	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs577599854	chr9:103734741-103734742	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550528283	chr9:103734754-103734755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs538700507	chr9:103734761-103734762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs545138513	chr9:103734767-103734768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs532251337	chr9:103734786-103734787	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs142279948	chr9:103734819-103734820	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs565857875	chr9:103734843-103734844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs534477919	chr9:103734856-103734857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs552361858	chr9:103734869-103734870	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568032265	chr9:103734899-103734900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Gastrointestinal stromal cancer	20877625	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
Acute lymphoblastic leukemia	21339820	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103720200-103720400	Enhancers	Fetal Brain Female	brain
2	chr9:103721200-103721400	Enhancers	Fetal Brain Female	brain
3	chr9:103722600-103722800	Enhancers	Fetal Brain Female	brain
4	chr9:103750800-103751000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr9:103751200-103752200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:103752000-103752600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:103752200-103752400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr9:103752200-103752600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:103752200-103753000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:103752400-103753000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:103752400-103753000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr9:103753000-103753600	Enhancers	HepG2	liver
13	chr9:103753200-103753400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr9:103753200-103753600	Enhancers	Fetal Heart	heart
15	chr9:103762000-103763000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr9:103762000-103763000	Enhancers	HMEC	breast
17	chr9:103776400-103777200	Enhancers	HepG2	liver
18	chr9:103776800-103777800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr9:103777800-103778800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr9:103778800-103779000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr9:103779000-103780800	Weak transcription	Right Atrium	heart
22	chr9:103779400-103779800	Enhancers	Fetal Muscle Leg	muscle
23	chr9:103779800-103780200	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:103780200-103781200	Enhancers	Fetal Muscle Leg	muscle
25	chr9:103780400-103781800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr9:103780600-103781000	Enhancers	Brain Germinal Matrix	brain
27	chr9:103780600-103781200	Enhancers	Brain Cingulate Gyrus	brain
28	chr9:103780600-103781200	Enhancers	Brain Substantia Nigra	brain
29	chr9:103780600-103781400	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr9:103780600-103781400	Enhancers	Fetal Brain Female	brain
31	chr9:103780600-103781600	Enhancers	Brain Hippocampus Middle	brain
32	chr9:103780600-103781600	Enhancers	Fetal Heart	heart
33	chr9:103780600-103782000	Enhancers	Fetal Brain Male	brain
34	chr9:103780800-103781000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:103780800-103781000	Enhancers	Right Atrium	heart
36	chr9:103780800-103781200	Enhancers	Fetal Muscle Trunk	muscle
37	chr9:103780800-103781200	Enhancers	Fetal Stomach	stomach
38	chr9:103780800-103781200	Enhancers	Psoas Muscle	Psoas
39	chr9:103780800-103781200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr9:103780800-103781400	Enhancers	Brain Anterior Caudate	brain
41	chr9:103781200-103785200	Weak transcription	Fetal Muscle Leg	muscle
42	chr9:103781600-103781800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:103782000-103788600	Weak transcription	Fetal Brain Male	brain
44	chr9:103785200-103786000	Enhancers	Fetal Muscle Leg	muscle
45	chr9:103788000-103789800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr9:103788000-103790000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:103788000-103790200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr9:103788200-103788400	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr9:103788200-103789600	Enhancers	Brain Substantia Nigra	brain
50	chr9:103788200-103790200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links