Variant report

Variant	nsv1030929
Chromosome Location	chr9:11659295-12196202
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	BACH1	chr9:12170667-12170713	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr9:12011400-12011402	GM12878	blood:	n/a	n/a
3	CBX3	chr9:12054451-12054644	K562	blood:	n/a	n/a
4	CEBPB	chr9:11946375-11946610	HepG2	liver:	n/a	chr9:11946481-11946492
5	CEBPB	chr9:11727949-11728190	A549	lung:	n/a	n/a
6	CEBPB	chr9:11660296-11660487	HepG2	liver:	n/a	chr9:11660442-11660453
7	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084
8	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
9	CEBPB	chr9:11784110-11784218	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr9:11663947-11664283	K562	blood:	n/a	chr9:11664111-11664122
11	CEBPB	chr9:11790686-11790886	HepG2	liver:	n/a	chr9:11790808-11790821 chr9:11790808-11790819
12	CEBPB	chr9:11779927-11780177	A549	lung:	n/a	n/a
13	CEBPB	chr9:11727974-11728209	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:11933909-11934318	Hela-S3	cervix:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
15	CEBPB	chr9:11959593-11959818	IMR90	lung:	n/a	chr9:11959657-11959668
16	CEBPB	chr9:11934067-11934195	HepG2	liver:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
17	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:11933995-11934266	ECC-1	luminal epithelium:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
19	CEBPB	chr9:11702589-11702913	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:12119993-12120079	A549	lung:	n/a	chr9:12120059-12120068 chr9:12120057-12120070 chr9:12120057-12120068
21	CEBPB	chr9:11704304-11704462	HepG2	liver:	n/a	chr9:11704344-11704355
22	CEBPB	chr9:11959508-11959839	HepG2	liver:	n/a	chr9:11959657-11959668
23	CEBPB	chr9:11743712-11743936	IMR90	lung:	n/a	chr9:11743800-11743811 chr9:11743833-11743844
24	CEBPB	chr9:12012267-12012412	A549	lung:	n/a	n/a
25	CEBPB	chr9:11663929-11664298	IMR90	lung:	n/a	chr9:11664111-11664122
26	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
27	CEBPB	chr9:11702572-11702971	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:11795605-11795828	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:11968269-11968582	A549	lung:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
30	CEBPB	chr9:11664029-11664280	ECC-1	luminal epithelium:	n/a	chr9:11664111-11664122
31	CEBPB	chr9:11933929-11934303	IMR90	lung:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
32	CEBPB	chr9:11968320-11968531	HepG2	liver:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
33	CEBPB	chr9:11899316-11899547	A549	lung:	n/a	n/a
34	CEBPB	chr9:12129071-12129335	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:11663959-11664285	A549	lung:	n/a	chr9:11664111-11664122
36	CEBPB	chr9:11663945-11664399	H1-hESC	embryonic stem cell:	n/a	chr9:11664111-11664122
37	CEBPB	chr9:11702581-11702905	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:11702576-11702894	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr9:11663947-11664294	HepG2	liver:	n/a	chr9:11664111-11664122
40	CEBPB	chr9:11702586-11702895	A549	lung:	n/a	n/a
41	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
42	CEBPB	chr9:11959566-11959766	K562	blood:	n/a	chr9:11959657-11959668
43	CEBPB	chr9:11743695-11743965	HepG2	liver:	n/a	chr9:11743800-11743811 chr9:11743833-11743844
44	CEBPB	chr9:11946400-11946627	IMR90	lung:	n/a	chr9:11946481-11946492
45	CEBPB	chr9:11702554-11702976	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
47	CHD1	chr9:11672402-11672403	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr9:11687520-11687670	GM12873	blood:	n/a	n/a
49	CTCF	chr9:11906644-11906673	GM13976	blood:	n/a	n/a
50	CTCF	chr9:11997160-11997310	HEK293	kidney:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:11701463..11703909-chr9:11703963..11706145,2	K562	blood:
2	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
3	chr9:11687941..11690802-chr9:11691495..11694345,3	K562	blood:
4	chr9:11701463..11703909-chr9:11703963..11706145,2	K562	blood:
5	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
6	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
7	chr9:11687941..11690802-chr9:11691495..11694345,3	K562	blood:
8	chr18:21570976..21573123-chr9:12145530..12147030,2	MCF-7	breast:
9	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-2	chr9:12159117-12159147	XLOC_007648
2	lnc-MPDZ-9	chr9:12149117-12149147	NONHSAT130219
3	lnc-MPDZ-2	chr9:12098660-12099015	XLOC_007648
4	lnc-MPDZ-9	chr9:12088660-12089015	NONHSAT130219
5	lnc-PTPRD-5	chr9:11829210-11829360	XLOC_007647
6	lnc-PTPRD-5	chr9:11829221-11829360	XLOC_007647
7	lnc-PTPRD-5	chr9:11834674-11834988	XLOC_007647
8	lnc-MPDZ-2	chr9:12146273-12146401	XLOC_007648
9	lnc-PTPRD-5	chr9:11822678-11822704	XLOC_007647
10	lnc-MPDZ-9	chr9:12106821-12106865	NONHSAT130219
11	lnc-PTPRD-5	chr9:11834674-11834959	XLOC_007647
12	lnc-MPDZ-9	chr9:12136273-12136401	NONHSAT130219
13	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
14	lnc-PTPRD-10	chr9:11816029-11816601	l_3733_chr9:11816028-11824988_testes
15	lnc-PTPRD-5	chr9:11834674-11834959	XLOC_007647
16	lnc-PTPRD-5	chr9:11829221-11829360	XLOC_007647
17	lnc-MPDZ-2	chr9:12098714-12099015	XLOC_007648
18	lnc-MPDZ-2	chr9:12139007-12139044	XLOC_007648
19	lnc-PTPRD-5	chr9:11826175-11826601	XLOC_007647
20	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
21	lnc-PTPRD-10	chr9:11819221-11819360	l_3733_chr9:11816028-11824988_testes
22	lnc-PTPRD-10	chr9:11824674-11824988	l_3733_chr9:11816028-11824988_testes

Variant related genes	Relation type
ENSG00000224935	TF binding region
ENSG00000168234	chromatin interactions
CUL5	miRNA target sites
FLOT2	miRNA target sites
CSF1	miRNA target sites

Extended variants
information (count: 6306 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:6306 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540029647	chr9:11686835-11686836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181971788	chr9:11686854-11686855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563947408	chr9:11686879-11686880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529355020	chr9:11686887-11686888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549527483	chr9:11686908-11686909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566199563	chr9:11686932-11686933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112943984	chr9:11686949-11686950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116075487	chr9:11686953-11686954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570712249	chr9:11686956-11686957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs61352891	chr9:11686963-11686964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190599309	chr9:11686965-11686966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78149581	chr9:11686970-11686971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576217596	chr9:11687098-11687099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530430981	chr9:11687099-11687100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114741777	chr9:11687130-11687131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372825330	chr9:11687173-11687174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145683118	chr9:11687175-11687176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543478332	chr9:11687176-11687177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562785223	chr9:11687192-11687193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151044790	chr9:11687202-11687203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs80001872	chr9:11687204-11687205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115321143	chr9:11687215-11687216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578180490	chr9:11687244-11687245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75505940	chr9:11687247-11687248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563710534	chr9:11687249-11687250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529460389	chr9:11687286-11687287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73401439	chr9:11687302-11687303	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559844031	chr9:11687314-11687315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528598937	chr9:11687341-11687342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551794045	chr9:11687342-11687343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568316051	chr9:11687369-11687370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186668257	chr9:11696406-11696407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558447790	chr9:11696445-11696446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs578193346	chr9:11696458-11696459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200671100	chr9:11696466-11696467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2821193	chr9:11696468-11696469	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563729313	chr9:11696478-11696479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574234340	chr9:11696487-11696488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542995820	chr9:11696488-11696489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559519403	chr9:11696491-11696492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568376901	chr9:11696549-11696550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547345037	chr9:11696556-11696557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183431542	chr9:11696613-11696614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532921372	chr9:11696639-11696640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139981227	chr9:11696646-11696647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549567384	chr9:11696650-11696651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527898633	chr9:11696657-11696658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2821192	chr9:11696698-11696699	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187915459	chr9:11696712-11696713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193182526	chr9:11696793-11696794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Schizophrenia	18511947	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chordoma	21215367	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11686800-11687400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:11696400-11696600	Enhancers	Fetal Brain Male	brain
3	chr9:11696600-11697800	Weak transcription	Fetal Brain Male	brain
4	chr9:11697800-11698400	Enhancers	Fetal Brain Male	brain
5	chr9:11698400-11701800	Weak transcription	Fetal Brain Male	brain
6	chr9:11698800-11701400	Enhancers	Fetal Brain Female	brain
7	chr9:11700600-11700800	Enhancers	Brain Angular Gyrus	brain
8	chr9:11700600-11701800	Enhancers	Brain Hippocampus Middle	brain
9	chr9:11700800-11701000	Enhancers	Brain Cingulate Gyrus	brain
10	chr9:11700800-11704400	Weak transcription	Brain Angular Gyrus	brain
11	chr9:11701000-11702000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr9:11701200-11701600	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr9:11701400-11704600	Weak transcription	Fetal Brain Female	brain
14	chr9:11701600-11702000	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr9:11701800-11702200	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr9:11701800-11702200	Active TSS	Brain Substantia Nigra	brain
17	chr9:11701800-11704800	Enhancers	Fetal Brain Male	brain
18	chr9:11702000-11703600	Enhancers	Brain Cingulate Gyrus	brain
19	chr9:11702000-11703800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr9:11702200-11702400	Weak transcription	Brain Substantia Nigra	brain
21	chr9:11702200-11702800	Enhancers	Brain Hippocampus Middle	brain
22	chr9:11702400-11703200	Enhancers	Brain Substantia Nigra	brain
23	chr9:11702800-11703800	Weak transcription	Brain Hippocampus Middle	brain
24	chr9:11703200-11703600	Weak transcription	Brain Substantia Nigra	brain
25	chr9:11703600-11704000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr9:11703600-11705000	Enhancers	Brain Substantia Nigra	brain
27	chr9:11703800-11705000	Enhancers	Brain Hippocampus Middle	brain
28	chr9:11703800-11705000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr9:11704000-11704800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:11704000-11705000	Enhancers	Brain Cingulate Gyrus	brain
31	chr9:11704000-11705200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:11704200-11705000	Enhancers	Brain Anterior Caudate	brain
33	chr9:11704400-11704800	Enhancers	Brain Angular Gyrus	brain
34	chr9:11704400-11705000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:11704600-11705000	Enhancers	Fetal Brain Female	brain
36	chr9:11705000-11707000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:11705200-11706400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:11705600-11706000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:11706400-11708800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:11707000-11708200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:11728600-11729400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr9:11728800-11729200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr9:11729000-11729400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr9:11743000-11743800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:11748800-11750000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:11775800-11776400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr9:11779600-11780800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr9:11788400-11788600	Enhancers	Pancreas	Pancrea
49	chr9:11795000-11795400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:11806000-11806600	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links