Variant report

Variant	nsv879850
Chromosome Location	chr4:120898509-120969089
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	chr4:120964875-120964999	HepG2	liver:	n/a	n/a
2	ATF2	chr4:120926115-120927036	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:120925034-120925381	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:120924730-120925731	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:120929305-120929507	GM12878	blood:	n/a	n/a
6	BCL3	chr4:120930925-120931351	GM12878	blood:	n/a	n/a
7	BCL3	chr4:120930881-120931214	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:120901457-120901478	GM12878	blood:	n/a	n/a
9	BRCA1	chr4:120925181-120925772	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:120939460-120939828	HepG2	liver:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
11	CEBPB	chr4:120922065-120922388	Hela-S3	cervix:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
12	CEBPB	chr4:120928222-120929097	Hela-S3	cervix:	n/a	chr4:120928880-120928888
13	CEBPB	chr4:120939413-120939869	MCF-7	breast:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
14	CEBPB	chr4:120930902-120931245	MCF-7	breast:	n/a	chr4:120930977-120930990
15	CEBPB	chr4:120922133-120922389	A549	lung:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
16	CEBPB	chr4:120939475-120939821	K562	blood:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
17	CEBPB	chr4:120922126-120922326	K562	blood:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
18	CEBPB	chr4:120922073-120922396	IMR90	lung:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
19	CEBPB	chr4:120953850-120954085	HepG2	liver:	n/a	chr4:120953995-120954012
20	CEBPB	chr4:120955314-120955502	HepG2	liver:	n/a	chr4:120955329-120955340
21	CEBPB	chr4:120922073-120922387	HepG2	liver:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
22	CEBPB	chr4:120928203-120929050	IMR90	lung:	n/a	chr4:120928880-120928888
23	CEBPB	chr4:120939477-120939828	H1-hESC	embryonic stem cell:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
24	CEBPB	chr4:120930805-120931370	IMR90	lung:	n/a	chr4:120930977-120930990
25	CEBPB	chr4:120922082-120922311	H1-hESC	embryonic stem cell:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
26	CEBPB	chr4:120939469-120940140	IMR90	lung:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
27	CEBPB	chr4:120939475-120939836	A549	lung:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
28	CEBPB	chr4:120956410-120956619	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:120939462-120939829	Hela-S3	cervix:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
30	CEBPB	chr4:120922026-120922449	MCF-7	breast:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
31	CEBPB	chr4:120939427-120939922	MCF-7	breast:	n/a	chr4:120939641-120939650 chr4:120939639-120939652 chr4:120939641-120939650 chr4:120939641-120939650
32	CHD1	chr4:120921737-120921912	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr4:120915931-120916139	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr4:120926578-120926606	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:120928347-120928389	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr4:120924468-120927590	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:120945840-120945990	AG04450	lung:	n/a	n/a
38	CTCF	chr4:120964100-120964250	NHEK	skin:	n/a	n/a
39	CTCF	chr4:120945933-120946027	IMR90	lung:	n/a	n/a
40	CTCF	chr4:120945919-120946022	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:120945860-120946010	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr4:120945840-120945990	HAc	cerebellar:	n/a	n/a
43	CTCF	chr4:120945940-120946090	GM12875	blood:	n/a	n/a
44	CTCF	chr4:120945840-120945990	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:120945840-120945990	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:120945972-120945978	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr4:120945860-120946010	HEK293	kidney:	n/a	n/a
48	CTCF	chr4:120945840-120945990	GM12866	blood:	n/a	n/a
49	CTCF	chr4:120945840-120945990	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:120945860-120946010	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120930379-120930429	Jurkat	blood:	n/a
2	chr4:120915594-120915644	Hepatocyte	liver:	n/a
3	chr4:120915594-120915644	A549	lung:	n/a
4	chr4:120930379-120930429	SK-N-MC	brain:	n/a
5	chr4:120915594-120915644	GM06990	blood:	n/a
6	chr4:120915594-120915644	IMR90	lung:	fetal
7	chr4:120898808-120898858	HCF	heart:	n/a
8	chr4:120930379-120930429	NHDF-neo	bronchial:	n/a
9	chr4:120930379-120930429	GM06990	blood:	n/a
10	chr4:120930379-120930429	HepG2	liver:	n/a
11	chr4:120915594-120915644	NHDF-neo	bronchial:	n/a
12	chr4:120898808-120898858	PFSK-1	brain:	n/a
13	chr4:120930379-120930429	A549	lung:	n/a
14	chr4:120915594-120915644	SAEC	small airway:	n/a
15	chr4:120930379-120930429	RPTEC	kidney:	n/a
16	chr4:120915594-120915644	SK-N-MC	brain:	n/a
17	chr4:120915594-120915644	HCPEpiC	choroid plexus:	n/a
18	chr4:120915594-120915644	LNCaP	prostate:	n/a
19	chr4:120930379-120930429	AG04450	lung:	fetal
20	chr4:120930379-120930429	IMR90	lung:	fetal
21	chr4:120930379-120930429	GM19239	blood:	n/a
22	chr4:120915594-120915644	AG09309	skin:	n/a
23	chr4:120930379-120930429	ECC-1	luminal epithelium:	n/a
24	chr4:120930379-120930429	HMEC	breast:	n/a
25	chr4:120898808-120898858	HEK293	kidney:	embryo
26	chr4:120898808-120898858	HRE	kidney:	n/a
27	chr4:120930379-120930429	MCF-7	breast:	n/a
28	chr4:120898808-120898858	Caco-2	colon:	n/a
29	chr4:120915594-120915644	Hela-S3	cervix:	n/a
30	chr4:120915594-120915644	SK-N-SH_RA	brain:	n/a
31	chr4:120915594-120915644	HCF	heart:	n/a
32	chr4:120915594-120915644	U87	brain:	n/a
33	chr4:120930379-120930429	PFSK-1	brain:	n/a
34	chr4:120930379-120930429	NH-A	brain:	n/a
35	chr4:120930379-120930429	MCF10A-Er-Src	breast:	n/a
36	chr4:120930379-120930429	Hepatocyte	liver:	n/a
37	chr4:120930379-120930429	HEEpiC	esophagus:	n/a
38	chr4:120915594-120915644	HCM	heart:	n/a
39	chr4:120898808-120898858	HCM	heart:	n/a
40	chr4:120930379-120930429	AoSMC	blood vessel:	n/a
41	chr4:120915594-120915644	BJ	skin:	n/a
42	chr4:120898808-120898858	HRCEpiC	kidney:	n/a
43	chr4:120898808-120898858	AoSMC	blood vessel:	n/a
44	chr4:120898808-120898858	CMK	blood:	n/a
45	chr4:120915594-120915644	GM12891	blood:	n/a
46	chr4:120898808-120898858	SK-N-SH	brain:	n/a
47	chr4:120898808-120898858	RPTEC	kidney:	n/a
48	chr4:120930379-120930429	SK-N-SH_RA	brain:	n/a
49	chr4:120898808-120898858	AG09319	gingival:	n/a
50	chr4:120898808-120898858	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:120956553..120960562-chr4:120961898..120965735,4	K562	blood:
2	chr4:120898790..120900807-chr4:120905834..120908765,2	K562	blood:
3	chr4:120956553..120960562-chr4:120961898..120965735,4	K562	blood:
4	chr4:120958158..120959809-chr4:120965003..120967800,2	K562	blood:
5	chr4:120921343..120923138-chr4:120927262..120929036,2	K562	blood:
6	chr4:120692868..120695733-chr4:120948622..120950761,2	K562	blood:
7	chr4:120955421..120958256-chr4:120958733..120960538,2	K562	blood:
8	chr4:120966303..120968314-chr4:120969694..120972264,2	K562	blood:
9	chr4:120964367..120966016-chr4:120972622..120975603,2	K562	blood:
10	chr4:120965543..120968090-chr4:120982539..120985159,2	K562	blood:
11	chr4:120958158..120959809-chr4:120965003..120967800,2	K562	blood:
12	chr4:120931283..120933611-chr4:120937604..120939144,2	MCF-7	breast:
13	chr4:120965102..120968292-chr4:120969292..120973289,4	K562	blood:
14	chr4:120898790..120900807-chr4:120905834..120908765,2	K562	blood:
15	chr4:120921343..120923138-chr4:120927262..120929036,2	K562	blood:
16	chr4:120955421..120958256-chr4:120958733..120960538,2	K562	blood:
17	chr4:120892542..120895411-chr4:120896318..120898714,2	MCF-7	breast:
18	chr4:120899347..120901114-chr4:120901609..120903898,2	MCF-7	breast:
19	chr4:120931283..120933611-chr4:120937604..120939144,2	MCF-7	breast:
20	chr4:120899347..120901114-chr4:120901609..120903898,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-11	chr4:120923406-120924078	NONHSAT098112
2	lnc-MAD2L1-1	chr4:120961463-120961770	ENSG00000253825
3	lnc-MAD2L1-1	chr4:120956188-120956353	ENSG00000253825
4	lnc-MAD2L1-3	chr4:120943327-120943495	ucscGeneNc_uc003idk_1
5	lnc-MAD2L1-3	chr4:120941240-120941365	ucscGeneNc_uc003idk_1
6	lnc-MAD2L1-3	chr4:120941955-120941997	ucscGeneNc_uc003idk_1
7	lnc-MAD2L1-3	chr4:120939709-120939839	ucscGeneNc_uc003idk_1
8	lnc-MAD2L1-3	chr4:120945055-120945118	ucscGeneNc_uc003idk_1

Variant related genes	Relation type
ENSG00000253825	TF binding region
ENSG00000253825	CpG island

Extended variants
information (count: 1879 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1879 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1503535	chr4:120898509-120898510	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs181857707	chr4:120898522-120898523	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs553931354	chr4:120898533-120898534	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs372817722	chr4:120898549-120898550	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs115197995	chr4:120898551-120898552	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554463927	chr4:120898552-120898553	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs568039474	chr4:120898596-120898597	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567549496	chr4:120898612-120898613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533152963	chr4:120898648-120898649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72684588	chr4:120898674-120898675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs370656926	chr4:120898752-120898753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185100813	chr4:120898763-120898764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545893868	chr4:120898778-120898779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374562247	chr4:120898808-120898809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570752377	chr4:120898817-120898818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552970817	chr4:120898832-120898833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563846416	chr4:120898843-120898844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572899396	chr4:120898853-120898854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541876481	chr4:120898878-120898879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138141054	chr4:120898882-120898883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190884959	chr4:120898914-120898915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544478328	chr4:120898918-120898919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183074973	chr4:120899075-120899076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533226444	chr4:120899082-120899083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73842785	chr4:120899101-120899102	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566499532	chr4:120899118-120899119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373723588	chr4:120899164-120899165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188161507	chr4:120899285-120899286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10012352	chr4:120899287-120899288	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs142635797	chr4:120899314-120899315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532311634	chr4:120899345-120899346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537398180	chr4:120899411-120899412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556831100	chr4:120899521-120899522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570642712	chr4:120899606-120899607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191096000	chr4:120899658-120899659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143177949	chr4:120899724-120899725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374508222	chr4:120899732-120899733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553083470	chr4:120899771-120899772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73842786	chr4:120899831-120899832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541839712	chr4:120899888-120899889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558747787	chr4:120899916-120899917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200436650	chr4:120899918-120899919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551489884	chr4:120899952-120899953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183160698	chr4:120899965-120899966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187491322	chr4:120899977-120899978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146034198	chr4:120900061-120900062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544901741	chr4:120900075-120900076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564486214	chr4:120900114-120900115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533593188	chr4:120900118-120900119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540452388	chr4:120900160-120900161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Myelodysplastic syndrome	18508791	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120883400-120903400	Weak transcription	Left Ventricle	heart
2	chr4:120897000-120900600	Enhancers	Rectal Smooth Muscle	rectum
3	chr4:120897600-120898800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:120897600-120902000	Enhancers	Colon Smooth Muscle	Colon
5	chr4:120897800-120898600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:120898000-120898800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:120898000-120898800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:120898200-120898600	Flanking Active TSS	Stomach Smooth Muscle	stomach
9	chr4:120898200-120898800	Enhancers	Fetal Kidney	kidney
10	chr4:120898200-120899000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:120898200-120899000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:120898200-120899400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr4:120898400-120898800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr4:120898400-120898800	Enhancers	Fetal Stomach	stomach
15	chr4:120898400-120899000	Enhancers	Fetal Muscle Leg	muscle
16	chr4:120898400-120899000	Enhancers	Right Atrium	heart
17	chr4:120898600-120899200	Enhancers	Stomach Smooth Muscle	stomach
18	chr4:120898600-120905800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr4:120898800-120901600	Weak transcription	Fetal Kidney	kidney
20	chr4:120900600-120901600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:120901400-120901800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr4:120901600-120901800	Enhancers	Fetal Lung	lung
23	chr4:120901600-120902600	Enhancers	Fetal Kidney	kidney
24	chr4:120901600-120902800	Enhancers	Rectal Smooth Muscle	rectum
25	chr4:120901800-120902400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:120901800-120902600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:120901800-120902600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr4:120902600-120903800	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr4:120902800-120905800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr4:120903800-120904400	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr4:120903800-120906200	Enhancers	Fetal Lung	lung
32	chr4:120904400-120904800	Enhancers	Aorta	Aorta
33	chr4:120904800-120905600	Weak transcription	Aorta	Aorta
34	chr4:120905600-120906000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:120905600-120906000	Enhancers	Aorta	Aorta
36	chr4:120905600-120906200	Enhancers	Fetal Stomach	stomach
37	chr4:120905600-120906400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr4:120905600-120906400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:120905800-120906200	Enhancers	Fetal Muscle Leg	muscle
40	chr4:120905800-120906200	Enhancers	Rectal Smooth Muscle	rectum
41	chr4:120905800-120906400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr4:120905800-120906400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:120905800-120906400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:120906400-120911000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:120911000-120913800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:120911400-120911600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:120911600-120912600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr4:120911600-120914400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:120912200-120912400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:120912200-120912600	Enhancers	HUES64 Cell Line	embryonic stem cell

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