Variant report

Variant	esv2759670
Chromosome Location	chr9:11793343-12197607
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	chr9:12119993-12120079	A549	lung:	n/a	chr9:12120059-12120068 chr9:12120057-12120070 chr9:12120057-12120068
5	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084
6	CEBPB	chr9:11899316-11899547	A549	lung:	n/a	n/a
7	CEBPB	chr9:11959593-11959818	IMR90	lung:	n/a	chr9:11959657-11959668
8	CEBPB	chr9:11946400-11946627	IMR90	lung:	n/a	chr9:11946481-11946492
9	CEBPB	chr9:12129071-12129335	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:11968320-11968531	HepG2	liver:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
11	CEBPB	chr9:11968269-11968582	A549	lung:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
12	CEBPB	chr9:11959566-11959766	K562	blood:	n/a	chr9:11959657-11959668
13	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
14	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
16	CEBPB	chr9:11933995-11934266	ECC-1	luminal epithelium:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
17	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
18	CEBPB	chr9:11959508-11959839	HepG2	liver:	n/a	chr9:11959657-11959668
19	CEBPB	chr9:11934067-11934195	HepG2	liver:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
20	CEBPB	chr9:12012267-12012412	A549	lung:	n/a	n/a
21	CEBPB	chr9:11933929-11934303	IMR90	lung:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
22	CEBPB	chr9:11933909-11934318	Hela-S3	cervix:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
23	CEBPB	chr9:11946375-11946610	HepG2	liver:	n/a	chr9:11946481-11946492
24	CEBPB	chr9:11795605-11795828	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
26	CTCF	chr9:12078782-12078864	LNCaP	prostate:	n/a	n/a
27	CTCF	chr9:12092280-12092430	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr9:12142395-12142451	LNCaP	prostate:	n/a	n/a
29	CTCF	chr9:12092315-12092389	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:12101680-12101830	GM12869	blood:	n/a	n/a
31	CTCF	chr9:11906644-11906673	GM13976	blood:	n/a	n/a
32	CTCF	chr9:12076206-12076321	GM10266	blood:	n/a	n/a
33	CTCF	chr9:12041004-12041085	GM20000	blood:	n/a	n/a
34	CTCF	chr9:12100160-12100310	NB4	blood:	n/a	n/a
35	CTCF	chr9:12180880-12181030	HEK293	kidney:	n/a	n/a
36	CTCF	chr9:12055107-12055140	GM13976	blood:	n/a	n/a
37	CTCF	chr9:12041600-12041634	GM20000	blood:	n/a	n/a
38	CTCF	chr9:12195560-12195710	HMF	breast:	n/a	n/a
39	CTCF	chr9:12045540-12045690	HPF	lung:	n/a	n/a
40	CTCF	chr9:12076187-12076204	GM10248	blood:	n/a	n/a
41	CTCF	chr9:12195520-12195670	HMF	breast:	n/a	n/a
42	CTCF	chr9:12053853-12053871	GM20000	blood:	n/a	n/a
43	CTCF	chr9:11952660-11952810	AG09319	gingival:	n/a	n/a
44	CTCF	chr9:11944302-11944336	GM13977	blood:	n/a	n/a
45	CTCF	chr9:12195600-12195750	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr9:11997160-11997310	HEK293	kidney:	n/a	n/a
47	CTCF	chr9:11893413-11893434	Fibrobl	skin:	n/a	n/a
48	CTCF	chr9:12195600-12195750	NHEK	skin:	n/a	n/a
49	CTCF	chr9:12195560-12195710	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr9:12092304-12092357	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
2	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
3	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
4	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
5	chr18:21570976..21573123-chr9:12145530..12147030,2	MCF-7	breast:

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

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: 5385 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:5385 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181654104	chr9:11795021-11795022	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs577721433	chr9:11795023-11795024	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs185937398	chr9:11795034-11795035	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs556956209	chr9:11795045-11795046	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs575908579	chr9:11795047-11795048	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs575511803	chr9:11795072-11795073	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs79970777	chr9:11795080-11795081	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs148796208	chr9:11795086-11795087	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs141544302	chr9:11795111-11795112	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs540880706	chr9:11795133-11795134	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs543822294	chr9:11795164-11795165	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs564174503	chr9:11795219-11795220	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs191976981	chr9:11795223-11795224	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs549781926	chr9:11795270-11795271	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs569704483	chr9:11795271-11795272	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs529601427	chr9:11795272-11795273	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs35657213	chr9:11795274-11795275	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs549697253	chr9:11795275-11795276	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs146360106	chr9:11795291-11795292	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs10960237	chr9:11795313-11795314	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs546711710	chr9:11795367-11795368	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs560325475	chr9:11795376-11795377	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs10960254	chr9:11806018-11806019	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs143757815	chr9:11806026-11806027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375658575	chr9:11806027-11806028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188892719	chr9:11806038-11806039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551583873	chr9:11806039-11806040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571241266	chr9:11806049-11806050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528055488	chr9:11806053-11806054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192650732	chr9:11806069-11806070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369867602	chr9:11806074-11806075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548877597	chr9:11806089-11806090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12341074	chr9:11806107-11806108	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs138046931	chr9:11806152-11806153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553217229	chr9:11806170-11806171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184634573	chr9:11806208-11806209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564795027	chr9:11806213-11806214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189224588	chr9:11806242-11806243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143500169	chr9:11806276-11806277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180913868	chr9:11806284-11806285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs4551461	chr9:11806285-11806286	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs111901581	chr9:11806287-11806288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550741969	chr9:11806312-11806313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530078849	chr9:11806335-11806336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547034899	chr9:11806339-11806340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559667870	chr9:11806358-11806359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138676731	chr9:11806424-11806425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185795203	chr9:11806448-11806449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571468074	chr9:11806514-11806515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536857306	chr9:11806538-11806539	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Schizophrenia	18511947	CNVD
Schizophrenia	23813976	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	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:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11795000-11795400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:11806000-11806600	Enhancers	Fetal Heart	heart
3	chr9:11812600-11813000	Enhancers	Fetal Brain Male	brain
4	chr9:11819200-11820000	Weak transcription	Fetal Brain Male	brain
5	chr9:11820000-11820200	Enhancers	Fetal Brain Male	brain
6	chr9:11820000-11821400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:11820200-11821000	Weak transcription	Fetal Brain Male	brain
8	chr9:11820600-11822600	Enhancers	Fetal Heart	heart
9	chr9:11820800-11821800	Enhancers	Fetal Brain Female	brain
10	chr9:11820800-11822600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:11821000-11823400	Enhancers	Fetal Brain Male	brain
12	chr9:11821400-11821800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:11821400-11821800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:11821400-11821800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:11821400-11821800	Enhancers	Pancreas	Pancrea
16	chr9:11821600-11822000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr9:11821800-11823000	Weak transcription	Fetal Brain Female	brain
18	chr9:11821800-11823200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:11823000-11823200	Enhancers	Fetal Brain Female	brain
20	chr9:11823400-11832200	Weak transcription	Fetal Brain Male	brain
21	chr9:11831800-11833000	Enhancers	Fetal Brain Female	brain
22	chr9:11832200-11832600	Enhancers	Fetal Brain Male	brain
23	chr9:11832600-11833600	Weak transcription	Fetal Brain Male	brain
24	chr9:11833600-11833800	Enhancers	Fetal Brain Male	brain
25	chr9:11867200-11868000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr9:11867200-11868000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr9:11867400-11867800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr9:11868800-11869000	Enhancers	Fetal Brain Female	brain
29	chr9:11869000-11871800	Weak transcription	Fetal Brain Female	brain
30	chr9:11871600-11871800	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr9:11871800-11872400	Enhancers	Fetal Brain Male	brain
32	chr9:11871800-11872600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr9:11871800-11872800	Enhancers	Fetal Brain Female	brain
34	chr9:11874000-11874600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr9:11874000-11874600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:11874200-11874600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr9:11874200-11874600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr9:11874200-11874600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr9:11874200-11874600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:11874200-11874600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr9:11874200-11874800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr9:11874200-11875000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr9:11874200-11875400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr9:11874600-11875800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr9:11876000-11876200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr9:11892600-11893200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr9:11892600-11893200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:11892800-11893600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:11892800-11894200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:11893000-11893400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links