Variant report

Variant	nsv879914
Chromosome Location	chr4:128005362-128123638
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	chr4:128061186-128061295	K562	blood:	n/a	n/a
2	BRCA1	chr4:128061453-128061744	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr4:128007689-128008011	K562	blood:	n/a	n/a
4	CEBPB	chr4:128083951-128084257	HepG2	liver:	n/a	chr4:128084088-128084101 chr4:128084093-128084105 chr4:128084090-128084101 chr4:128084088-128084099
5	CEBPB	chr4:128083970-128084189	A549	lung:	n/a	chr4:128084088-128084101 chr4:128084093-128084105 chr4:128084090-128084101 chr4:128084088-128084099
6	CEBPB	chr4:128061493-128061835	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr4:128064957-128065268	Hela-S3	cervix:	n/a	chr4:128065138-128065155 chr4:128065139-128065150
8	CEBPB	chr4:128063078-128063355	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:128116705-128116951	A549	lung:	n/a	chr4:128116892-128116909 chr4:128116893-128116906 chr4:128116802-128116813
10	CEBPB	chr4:128015624-128015727	A549	lung:	n/a	n/a
11	CEBPB	chr4:128116652-128116984	HepG2	liver:	n/a	chr4:128116892-128116909 chr4:128116893-128116906 chr4:128116802-128116813
12	CEBPB	chr4:128041093-128041154	IMR90	lung:	n/a	chr4:128041105-128041116
13	CEBPB	chr4:128083884-128084299	IMR90	lung:	n/a	chr4:128084088-128084101 chr4:128084093-128084105 chr4:128084090-128084101 chr4:128084088-128084099
14	CEBPB	chr4:128041100-128041186	HepG2	liver:	n/a	chr4:128041105-128041116
15	CEBPB	chr4:128053350-128053544	HepG2	liver:	n/a	chr4:128053500-128053511
16	CEBPB	chr4:128053395-128053574	K562	blood:	n/a	chr4:128053500-128053511
17	CEBPB	chr4:128083875-128084354	Hela-S3	cervix:	n/a	chr4:128084088-128084101 chr4:128084093-128084105 chr4:128084090-128084101 chr4:128084088-128084099
18	CEBPB	chr4:128064990-128065286	IMR90	lung:	n/a	chr4:128065138-128065155 chr4:128065139-128065150
19	CEBPB	chr4:128063031-128063428	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:128087147-128087531	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:128116667-128116980	IMR90	lung:	n/a	chr4:128116892-128116909 chr4:128116893-128116906 chr4:128116802-128116813
22	CREB1	chr4:128024855-128025166	GM12878	blood:	n/a	n/a
23	CREB1	chr4:128055645-128055953	GM12878	blood:	n/a	n/a
24	CTCF	chr4:128046140-128046290	HCT-116	colon:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
25	CTCF	chr4:128110120-128110270	AG04450	lung:	n/a	n/a
26	CTCF	chr4:128046201-128046384	MCF-7	breast:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
27	CTCF	chr4:128046096-128046435	GM12878	blood:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
28	CTCF	chr4:128046200-128046350	HCPEpiC	choroid plexus:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
29	CTCF	chr4:128046520-128046670	AG09309	skin:	n/a	n/a
30	CTCF	chr4:128110066-128110328	Medullo	brain:	n/a	n/a
31	CTCF	chr4:128046180-128046330	AG04450	lung:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
32	CTCF	chr4:128110143-128110213	LNCaP	prostate:	n/a	n/a
33	CTCF	chr4:128046240-128046390	MCF-7	breast:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
34	CTCF	chr4:128046154-128046436	H1-hESC	embryonic stem cell:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
35	CTCF	chr4:128110100-128110250	HRE	kidney:	n/a	n/a
36	CTCF	chr4:128046140-128046290	GM06990	blood:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
37	CTCF	chr4:128110093-128110374	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:128046140-128046290	HAc	cerebellar:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
39	CTCF	chr4:128041740-128041890	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr4:128110113-128110255	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr4:128046200-128046350	AoAF	blood vessel:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
42	CTCF	chr4:128049520-128049670	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr4:128051991-128052024	MCF-7	breast:	n/a	chr4:128052005-128052013 chr4:128052002-128052020
44	CTCF	chr4:128049560-128049710	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:128109980-128110130	GM06990	blood:	n/a	n/a
46	CTCF	chr4:128061100-128061250	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:128046180-128046330	HBMEC	blood vessel:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
48	CTCF	chr4:128046060-128046330	HFF-Myc	foreskin:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272
49	CTCF	chr4:128110140-128110290	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:128046200-128046350	HVMF	connective:	n/a	chr4:128046255-128046271 chr4:128046249-128046270 chr4:128046259-128046267 chr4:128046254-128046272

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128048177-128048227	HMEC	breast:	n/a
2	chr4:128048177-128048227	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:128062757-128062807	HEK293	kidney:	embryo
4	chr4:128062757-128062807	RPTEC	kidney:	n/a
5	chr4:128062757-128062807	HRCEpiC	kidney:	n/a
6	chr4:128048177-128048227	NH-A	brain:	n/a
7	chr4:128048177-128048227	PFSK-1	brain:	n/a
8	chr4:128062757-128062807	T-47D	breast:	n/a
9	chr4:128064781-128064831	HNPCEpiC	eye:	n/a
10	chr4:128062757-128062807	HCT-116	colon:	n/a
11	chr4:128048177-128048227	RPTEC	kidney:	n/a
12	chr4:128062757-128062807	AG10803	skin:	n/a
13	chr4:128064781-128064831	Jurkat	blood:	n/a
14	chr4:128062757-128062807	HAEpiC	amniotic membrane:	n/a
15	chr4:128062757-128062807	AG09309	skin:	n/a
16	chr4:128048177-128048227	HCF	heart:	n/a
17	chr4:128064781-128064831	HRPEpiC	eye:	n/a
18	chr4:128048177-128048227	GM12891	blood:	n/a
19	chr4:128064781-128064831	AG09319	gingival:	n/a
20	chr4:128048177-128048227	HIPEpiC	eye:	n/a
21	chr4:128064781-128064831	Hela-S3	cervix:	n/a
22	chr4:128064781-128064831	AoSMC	blood vessel:	n/a
23	chr4:128048177-128048227	AG09319	gingival:	n/a
24	chr4:128062757-128062807	HepG2	liver:	n/a
25	chr4:128048177-128048227	PANC-1	pancreas:	n/a
26	chr4:128064781-128064831	AG04450	lung:	fetal
27	chr4:128064781-128064831	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:128048177-128048227	HCT-116	colon:	n/a
29	chr4:128064781-128064831	PANC-1	pancreas:	n/a
30	chr4:128048177-128048227	GM19239	blood:	n/a
31	chr4:128062757-128062807	PrEC	prostate:	n/a
32	chr4:128064781-128064831	IMR90	lung:	fetal
33	chr4:128064781-128064831	CMK	blood:	n/a
34	chr4:128064781-128064831	HIPEpiC	eye:	n/a
35	chr4:128048177-128048227	MCF-7	breast:	n/a
36	chr4:128064781-128064831	HMEC	breast:	n/a
37	chr4:128064781-128064831	HCF	heart:	n/a
38	chr4:128064781-128064831	GM12892	blood:	n/a
39	chr4:128048177-128048227	HCM	heart:	n/a
40	chr4:128062757-128062807	ECC-1	luminal epithelium:	n/a
41	chr4:128048177-128048227	SKMC	muscle:	n/a
42	chr4:128064781-128064831	AG10803	skin:	n/a
43	chr4:128064781-128064831	U87	brain:	n/a
44	chr4:128048177-128048227	AG04449	skin:	fetal
45	chr4:128048177-128048227	NHBE	bronchial:	n/a
46	chr4:128062757-128062807	AG09319	gingival:	n/a
47	chr4:128064781-128064831	SK-N-SH_RA	brain:	n/a
48	chr4:128064781-128064831	T-47D	breast:	n/a
49	chr4:128062757-128062807	ProgFib	skin:	n/a
50	chr4:128064781-128064831	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:128112105..128114057-chr4:128114987..128117110,2	K562	blood:
2	chr4:128049381..128052250-chr4:128052874..128054495,2	K562	blood:
3	chr4:127876797..127878682-chr4:128046816..128049745,2	K562	blood:
4	chr4:128049162..128050116-chr4:128321706..128322303,2	MCF-7	breast:
5	chr4:128114466..128117078-chr4:128117654..128119344,2	K562	blood:
6	chr4:128050087..128052250-chr4:128052874..128054936,2	K562	blood:
7	chr4:127513096..127513892-chr4:128045874..128046732,3	MCF-7	breast:
8	chr4:128112105..128114057-chr4:128114987..128117110,2	K562	blood:
9	chr4:128093003..128095000-chr4:128096462..128098842,3	K562	blood:
10	chr4:127612459..127613544-chr4:128045619..128046731,4	MCF-7	breast:
11	chr4:128050087..128052250-chr4:128052874..128054936,2	K562	blood:
12	chr4:128093003..128095000-chr4:128096462..128098842,3	K562	blood:
13	chr4:128049381..128052250-chr4:128052874..128054495,2	K562	blood:
14	chr4:128111026..128111538-chr4:128400100..128400873,2	MCF-7	breast:
15	chr4:127548164..127549529-chr4:128045945..128046997,5	MCF-7	breast:
16	chr4:128061832..128064365-chr4:128065851..128068645,2	K562	blood:
17	chr4:128114466..128117078-chr4:128117654..128119344,2	K562	blood:
18	chr4:128061832..128064365-chr4:128065851..128068645,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFSD8-4	chr4:128015586-128015631	XLOC_004067
2	lnc-MFSD8-4	chr4:128017487-128017878	XLOC_004067
3	lnc-MFSD8-4	chr4:128016259-128016421	XLOC_004067
4	lnc-MFSD8-3	chr4:128018253-128018414	ENSG00000248491
5	lnc-MFSD8-3	chr4:128115534-128115648	ENSG00000248491
6	lnc-MFSD8-4	chr4:128016259-128016504	XLOC_004067
7	lnc-MFSD8-4	chr4:128015620-128015631	XLOC_004067
8	lnc-MFSD8-3	chr4:128027790-128027926	ENSG00000248491
9	lnc-MFSD8-3	chr4:128018046-128018414	ENSG00000248491

Variant related genes	Relation type
ENSG00000248491	TF binding region
ENSG00000248491	CpG island
PIK3CA	miRNA target sites
ITGA5	miRNA target sites

Extended variants
information (count: 2500 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2500 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6852817	chr4:128005362-128005363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551184155	chr4:128005446-128005447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13116630	chr4:128005468-128005469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536634083	chr4:128005476-128005477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555655566	chr4:128005654-128005655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34688603	chr4:128005668-128005669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567590458	chr4:128005673-128005674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369492357	chr4:128005711-128005712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374001033	chr4:128005823-128005824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534906655	chr4:128005848-128005849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553488641	chr4:128005857-128005858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138181263	chr4:128005862-128005863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148780937	chr4:128005892-128005893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545515799	chr4:128005905-128005906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377647531	chr4:128005918-128005919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552717878	chr4:128005937-128005938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571005084	chr4:128005938-128005939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192017750	chr4:128005942-128005943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114505274	chr4:128006002-128006003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543017124	chr4:128006058-128006059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561967993	chr4:128006071-128006072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529161637	chr4:128006077-128006078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540958427	chr4:128006090-128006091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373863171	chr4:128006138-128006139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559546823	chr4:128006165-128006166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532960719	chr4:128006170-128006171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551487201	chr4:128006186-128006187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569376139	chr4:128006194-128006195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10010552	chr4:128006216-128006217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548522119	chr4:128006300-128006301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12651138	chr4:128006439-128006440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535366843	chr4:128006466-128006467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77090132	chr4:128006497-128006498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28366863	chr4:128006523-128006524	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538825756	chr4:128006593-128006594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78487155	chr4:128006660-128006661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139310149	chr4:128006674-128006675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543054078	chr4:128006703-128006704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555044450	chr4:128006725-128006726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573271481	chr4:128006726-128006727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144253888	chr4:128006761-128006762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377551268	chr4:128006765-128006766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185229750	chr4:128006800-128006801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72925322	chr4:128006822-128006823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554176124	chr4:128006835-128006836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190517132	chr4:128006845-128006846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530479964	chr4:128006865-128006866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548656965	chr4:128006870-128006871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193100211	chr4:128006882-128006883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184282343	chr4:128006906-128006907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	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
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128004800-128007600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:128007400-128007800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:128007600-128008000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:128007600-128008200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr4:128009000-128009200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:128009200-128011000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:128009800-128010200	Enhancers	Lung	lung
8	chr4:128018200-128018800	Enhancers	Fetal Lung	lung
9	chr4:128018600-128019000	Enhancers	Fetal Brain Male	brain
10	chr4:128018800-128023200	Weak transcription	Fetal Lung	lung
11	chr4:128019000-128024200	Weak transcription	Fetal Brain Male	brain
12	chr4:128023200-128025800	Enhancers	Fetal Lung	lung
13	chr4:128024000-128025800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr4:128024200-128024400	Enhancers	Fetal Brain Male	brain
15	chr4:128024400-128024800	Weak transcription	Fetal Brain Male	brain
16	chr4:128024600-128025000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:128024600-128025000	Enhancers	Brain Hippocampus Middle	brain
18	chr4:128024800-128025200	Enhancers	Brain Angular Gyrus	brain
19	chr4:128024800-128025600	Enhancers	Brain Cingulate Gyrus	brain
20	chr4:128024800-128025600	Enhancers	Colon Smooth Muscle	Colon
21	chr4:128024800-128025600	Enhancers	Fetal Brain Male	brain
22	chr4:128025800-128028000	Weak transcription	Fetal Lung	lung
23	chr4:128028000-128028800	ZNF genes & repeats	Fetal Lung	lung
24	chr4:128035400-128036000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:128038600-128042000	Weak transcription	Fetal Brain Male	brain
26	chr4:128039200-128042200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:128039400-128039800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:128039800-128040200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:128039800-128040400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:128039800-128040600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:128039800-128040600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:128039800-128040800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:128040000-128040400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:128040000-128040400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:128040000-128040400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:128040000-128040400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:128040000-128040600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr4:128040000-128040600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:128040000-128040600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:128040200-128040400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:128040400-128040600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:128040400-128041600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr4:128040400-128041600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:128040400-128043800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr4:128040600-128041400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:128040600-128041600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr4:128040600-128041600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:128040600-128044400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr4:128040600-128046400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr4:128040800-128041400	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links