Variant report

Variant	nsv961134
Chromosome Location	chr18:28612225-28625943
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	chr18:28625753-28625790	K562	blood:	n/a	n/a
2	BACH1	chr18:28622505-28622509	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:28622835-28622968	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:28621452-28621945	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr18:28625576-28625946	HepG2	liver:	n/a	chr18:28625756-28625769 chr18:28625615-28625626 chr18:28625758-28625769
6	CEBPB	chr18:28625504-28625872	HepG2	liver:	n/a	chr18:28625756-28625769 chr18:28625615-28625626 chr18:28625758-28625769
7	CEBPB	chr18:28625640-28625827	HepG2	liver:	n/a	chr18:28625756-28625769 chr18:28625758-28625769
8	CEBPB	chr18:28625673-28625844	K562	blood:	n/a	chr18:28625756-28625769 chr18:28625758-28625769
9	CEBPB	chr18:28616397-28616528	K562	blood:	n/a	chr18:28616408-28616421
10	CEBPB	chr18:28622860-28622958	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr18:28622506-28622672	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr18:28623090-28623182	HepG2	liver:	n/a	n/a
13	CHD2	chr18:28621029-28621033	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr18:28621489-28621739	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr18:28620948-28623230	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr18:28622160-28622310	HEK293	kidney:	n/a	chr18:28622231-28622240
17	CTCF	chr18:28623000-28623150	HMEC	breast:	n/a	n/a
18	CTCF	chr18:28622960-28623110	NHEK	skin:	n/a	n/a
19	CTCF	chr18:28622205-28622278	NHEK	skin:	n/a	chr18:28622231-28622240
20	CTCF	chr18:28623060-28623210	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr18:28622940-28623090	HMEC	breast:	n/a	n/a
22	CTCF	chr18:28623020-28623170	HEK293	kidney:	n/a	n/a
23	CTCF	chr18:28622999-28623144	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr18:28623700-28623850	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr18:28621660-28621810	HMEC	breast:	n/a	n/a
26	CTCF	chr18:28623020-28623170	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr18:28623060-28623210	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr18:28622100-28622250	WERI-Rb-1	eye:	n/a	chr18:28622231-28622240
29	CTCF	chr18:28623600-28623750	HEK293	kidney:	n/a	n/a
30	CTCF	chr18:28623200-28623350	HMEC	breast:	n/a	n/a
31	CTCF	chr18:28623100-28623250	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr18:28622140-28622290	HMEC	breast:	n/a	chr18:28622231-28622240
33	CTCF	chr18:28623040-28623190	SAEC	small airway:	n/a	n/a
34	CTCF	chr18:28623060-28623210	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr18:28623000-28623150	HepG2	liver:	n/a	n/a
36	E2F4	chr18:28622598-28623101	MCF10A-Er-Src	breast:	n/a	chr18:28622853-28622862
37	E2F4	chr18:28620936-28621408	MCF10A-Er-Src	breast:	n/a	chr18:28621326-28621340
38	E2F4	chr18:28621908-28622224	MCF10A-Er-Src	breast:	n/a	chr18:28621932-28621939 chr18:28621932-28621939 chr18:28622195-28622202 chr18:28621931-28621943 chr18:28621932-28621939
39	E2F6	chr18:28621612-28622058	H1-hESC	embryonic stem cell:	n/a	chr18:28621645-28621654 chr18:28621932-28621939 chr18:28621932-28621939 chr18:28621931-28621943 chr18:28621932-28621939
40	E2F6	chr18:28622087-28622816	H1-hESC	embryonic stem cell:	n/a	chr18:28622195-28622202
41	E2F6	chr18:28620912-28623325	H1-hESC	embryonic stem cell:	n/a	chr18:28621645-28621654 chr18:28621932-28621939 chr18:28621326-28621340 chr18:28621932-28621939 chr18:28622853-28622862 chr18:28622195-28622202 chr18:28621931-28621943 chr18:28621932-28621939
42	EP300	chr18:28619311-28619859	ECC-1	luminal epithelium:	n/a	chr18:28619687-28619695
43	EP300	chr18:28619456-28619516	GM12878	blood:	n/a	n/a
44	EP300	chr18:28622735-28622837	HepG2	liver:	n/a	n/a
45	FOS	chr18:28619464-28619862	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr18:28624919-28625261	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr18:28620450-28620475	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr18:28619428-28619864	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr18:28620766-28620966	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr18:28624888-28625292	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:28622811-28622861	LNCaP	prostate:	n/a
2	chr18:28623040-28623090	NB4	blood:	n/a
3	chr18:28622811-28622861	LNCaP	prostate:	n/a
4	chr18:28623040-28623090	NB4	blood:	n/a
5	chr18:28622912-28622962	T-47D	breast:	n/a
6	chr18:28622876-28622926	U87	brain:	n/a
7	chr18:28622474-28622524	NHBE	bronchial:	n/a
8	chr18:28623874-28623924	K562	blood:	n/a
9	chr18:28623874-28623924	CMK	blood:	n/a
10	chr18:28622876-28622926	LNCaP	prostate:	n/a
11	chr18:28622918-28622968	HCT-116	colon:	n/a
12	chr18:28622200-28622250	HEK293	kidney:	embryo
13	chr18:28623040-28623090	Hepatocyte	liver:	n/a
14	chr18:28622593-28622643	CMK	blood:	n/a
15	chr18:28623874-28623924	U87	brain:	n/a
16	chr18:28622940-28622990	HCF	heart:	n/a
17	chr18:28621490-28621540	U87	brain:	n/a
18	chr18:28622024-28622074	HAEpiC	amniotic membrane:	n/a
19	chr18:28623159-28623209	NT2-D1	testis:	n/a
20	chr18:28621651-28621701	AG10803	skin:	n/a
21	chr18:28622200-28622250	HNPCEpiC	eye:	n/a
22	chr18:28623060-28623110	HL-60	blood:	n/a
23	chr18:28622474-28622524	AG09309	skin:	n/a
24	chr18:28621651-28621701	K562	blood:	n/a
25	chr18:28622024-28622074	HEEpiC	esophagus:	n/a
26	chr18:28621985-28622035	Hepatocyte	liver:	n/a
27	chr18:28622811-28622861	AG04450	lung:	fetal
28	chr18:28621985-28622035	AoSMC	blood vessel:	n/a
29	chr18:28621490-28621540	NB4	blood:	n/a
30	chr18:28622024-28622074	Caco-2	colon:	n/a
31	chr18:28620915-28620965	A549	lung:	n/a
32	chr18:28622811-28622861	HCF	heart:	n/a
33	chr18:28623159-28623209	HCF	heart:	n/a
34	chr18:28622918-28622968	HRCEpiC	kidney:	n/a
35	chr18:28622811-28622861	HRE	kidney:	n/a
36	chr18:28622813-28622863	AG04450	lung:	fetal
37	chr18:28624074-28624124	SAEC	small airway:	n/a
38	chr18:28621651-28621701	HepG2	liver:	n/a
39	chr18:28624074-28624124	Caco-2	colon:	n/a
40	chr18:28621985-28622035	PANC-1	pancreas:	n/a
41	chr18:28624074-28624124	AG09319	gingival:	n/a
42	chr18:28622474-28622524	MCF10A-Er-Src	breast:	n/a
43	chr18:28622024-28622074	PrEC	prostate:	n/a
44	chr18:28622918-28622968	SAEC	small airway:	n/a
45	chr18:28623874-28623924	HRCEpiC	kidney:	n/a
46	chr18:28623874-28623924	AG09319	gingival:	n/a
47	chr18:28622876-28622926	HPAEpiC	pulmonary alveolar:	n/a
48	chr18:28622811-28622861	HCPEpiC	choroid plexus:	n/a
49	chr18:28622918-28622968	HL-60	blood:	n/a
50	chr18:28622876-28622926	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr18:28614001..28615580-chr18:28618945..28620521,2	K562	blood:
2	chr18:28614001..28615580-chr18:28618945..28620521,2	K562	blood:
3	chr18:28594117..28596433-chr18:28615710..28618191,2	MCF-7	breast:
4	chr18:28622482..28623001-chrX:152864333..152864870,2	MCF-7	breast:

Variant related genes	Relation type
DSC3	TF binding region
DSC3	CpG island
ENSG00000147382	chromatin interactions
ENSG00000260081	chromatin interactions

Extended variants
information (count: 528 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369729390	chr18:28612227-28612228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2852003	chr18:28612229-28612230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145242863	chr18:28612232-28612233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114988341	chr18:28612233-28612234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199839758	chr18:28612262-28612263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201289822	chr18:28612287-28612288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144672222	chr18:28612307-28612308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151272810	chr18:28612344-28612345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116639442	chr18:28612351-28612352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573334254	chr18:28612357-28612358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540372873	chr18:28612358-28612359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548424109	chr18:28612417-28612418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201746783	chr18:28612517-28612518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200277943	chr18:28612519-28612520	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60371736	chr18:28612520-28612521	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12968143	chr18:28612551-28612552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201632814	chr18:28612554-28612555	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141259232	chr18:28612556-28612557	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59431301	chr18:28612557-28612558	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62087290	chr18:28612563-28612564	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532386707	chr18:28612618-28612619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2577061	chr18:28612678-28612679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544475357	chr18:28612695-28612696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184474585	chr18:28612706-28612707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530213133	chr18:28612711-28612712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537250200	chr18:28612753-28612754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114203680	chr18:28612777-28612778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116467185	chr18:28612832-28612833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369107234	chr18:28612860-28612861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115787862	chr18:28612891-28612892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570401869	chr18:28612919-28612920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537871765	chr18:28612922-28612923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556481722	chr18:28612926-28612927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568405148	chr18:28612951-28612952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535643831	chr18:28612994-28612995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35744973	chr18:28612997-28612998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114097400	chr18:28613064-28613065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552530202	chr18:28613115-28613116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188876212	chr18:28613135-28613136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373633409	chr18:28613171-28613172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115114836	chr18:28613198-28613199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76313124	chr18:28613206-28613207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140570854	chr18:28613267-28613268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563253845	chr18:28613283-28613284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192619393	chr18:28613316-28613317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544231231	chr18:28613377-28613378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185629232	chr18:28613400-28613401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35798316	chr18:28613449-28613450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557472954	chr18:28613533-28613534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550339638	chr18:28613620-28613621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28592600-28614800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:28601000-28613800	Weak transcription	Esophagus	oesophagus
3	chr18:28601000-28620800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr18:28609000-28619400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr18:28609800-28612400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr18:28610400-28613800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr18:28611800-28614200	Weak transcription	NHEK	skin
8	chr18:28611800-28619200	Weak transcription	HMEC	breast
9	chr18:28612200-28616000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr18:28612400-28612600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr18:28613800-28614000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr18:28613800-28614000	ZNF genes & repeats	Esophagus	oesophagus
13	chr18:28614000-28615600	Weak transcription	Esophagus	oesophagus
14	chr18:28614000-28617600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr18:28614200-28614600	Active TSS	NHEK	skin
16	chr18:28614600-28614800	Flanking Active TSS	NHEK	skin
17	chr18:28614800-28615200	Enhancers	NHEK	skin
18	chr18:28614800-28619800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr18:28615200-28615600	Weak transcription	NHEK	skin
20	chr18:28615600-28617600	Enhancers	NHEK	skin
21	chr18:28616000-28616400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr18:28616400-28617400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr18:28617400-28618200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr18:28617600-28617800	Flanking Active TSS	NHEK	skin
25	chr18:28617600-28618000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr18:28617800-28618000	Enhancers	NHEK	skin
27	chr18:28618000-28618200	Flanking Active TSS	NHEK	skin
28	chr18:28618000-28619200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:28618200-28618600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr18:28618200-28619200	Enhancers	NHEK	skin
31	chr18:28618600-28621800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr18:28619200-28619400	Enhancers	HMEC	breast
33	chr18:28619200-28620600	Flanking Active TSS	NHEK	skin
34	chr18:28619200-28621400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr18:28619400-28619800	Flanking Active TSS	HMEC	breast
36	chr18:28619400-28623200	Active TSS	Placenta Amnion	Placenta Amnion
37	chr18:28619600-28619800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr18:28619800-28620000	Active TSS	HMEC	breast
39	chr18:28619800-28623200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr18:28620000-28620200	Flanking Active TSS	HMEC	breast
41	chr18:28620200-28620800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
42	chr18:28620200-28623000	Active TSS	HMEC	breast
43	chr18:28620400-28620600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
44	chr18:28620400-28620600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr18:28620400-28620600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr18:28620400-28620600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
47	chr18:28620400-28620800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr18:28620400-28620800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
49	chr18:28620400-28622400	Active TSS	Right Atrium	heart
50	chr18:28620400-28623400	Active TSS	Breast Myoepithelial Primary Cells	Breast

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