Variant report

Variant	nsv1016120
Chromosome Location	chr4:187046337-187090478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:861)
CpG islands
(count:1404)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187058644-187058864	K562	blood:	n/a	n/a
2	ARID3A	chr4:187058552-187058902	HepG2	liver:	n/a	n/a
3	ATF2	chr4:187055315-187055866	GM12878	blood:	n/a	n/a
4	ATF2	chr4:187071057-187071421	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:187066156-187066584	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:187082521-187082663	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:187058431-187058728	GM12878	blood:	n/a	n/a
8	BATF	chr4:187058420-187058694	GM12878	blood:	n/a	n/a
9	BATF	chr4:187055371-187055785	GM12878	blood:	n/a	n/a
10	BATF	chr4:187055418-187055866	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:187055420-187055843	GM12878	blood:	n/a	n/a
12	BCL3	chr4:187055433-187055716	GM12878	blood:	n/a	n/a
13	BCL3	chr4:187059720-187060074	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:187055428-187055813	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:187055345-187055835	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:187059455-187059456	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:187055496-187055825	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:187082411-187082510	GM12878	blood:	n/a	n/a
19	CEBPB	chr4:187058752-187058939	K562	blood:	n/a	n/a
20	CEBPB	chr4:187067232-187067556	H1-hESC	embryonic stem cell:	n/a	chr4:187067399-187067412
21	CEBPB	chr4:187089147-187089328	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:187078910-187079176	K562	blood:	n/a	n/a
23	CEBPB	chr4:187078966-187079181	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:187078864-187079223	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:187078955-187079103	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:187078958-187079135	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:187058612-187058894	A549	lung:	n/a	n/a
28	CEBPB	chr4:187059932-187059959	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:187089187-187089327	A549	lung:	n/a	n/a
30	CHD1	chr4:187059861-187059865	GM12878	blood:	n/a	n/a
31	CHD2	chr4:187071137-187071471	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr4:187055449-187055790	GM12878	blood:	n/a	n/a
33	CHD2	chr4:187082399-187082540	HepG2	liver:	n/a	n/a
34	CTBP2	chr4:187065194-187065977	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:187054120-187054270	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr4:187065420-187065570	GM12865	blood:	n/a	n/a
37	CTCF	chr4:187065480-187065630	HMF	breast:	n/a	n/a
38	CTCF	chr4:187054120-187054270	HPF	lung:	n/a	n/a
39	CTCF	chr4:187054166-187054282	GM19240	blood:	n/a	n/a
40	CTCF	chr4:187054122-187054328	GM19239	blood:	n/a	n/a
41	CTCF	chr4:187065420-187065570	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr4:187058740-187058890	RPTEC	kidney:	n/a	chr4:187058771-187058792 chr4:187058776-187058794
43	CTCF	chr4:187058700-187058850	GM12874	blood:	n/a	chr4:187058771-187058792 chr4:187058776-187058794
44	CTCF	chr4:187071186-187071401	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr4:187071200-187071350	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:187071217-187071377	GM13976	blood:	n/a	n/a
47	CTCF	chr4:187058533-187058639	Fibrobl	skin:	n/a	chr4:187058610-187058628
48	CTCF	chr4:187080920-187081066	GM19239	blood:	n/a	n/a
49	CTCF	chr4:187058680-187058830	MCF-7	breast:	n/a	chr4:187058771-187058792 chr4:187058776-187058794
50	CTCF	chr4:187054160-187054310	GM12875	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187069057-187069107	HIPEpiC	eye:	n/a
2	chr4:187069057-187069107	HIPEpiC	eye:	n/a
3	chr4:187065417-187065467	A549	lung:	n/a
4	chr4:187078771-187078821	NHBE	bronchial:	n/a
5	chr4:187065516-187065566	HL-60	blood:	n/a
6	chr4:187070303-187070353	AG09319	gingival:	n/a
7	chr4:187070303-187070353	ECC-1	luminal epithelium:	n/a
8	chr4:187065846-187065896	T-47D	breast:	n/a
9	chr4:187069057-187069107	MCF10A-Er-Src	breast:	n/a
10	chr4:187071162-187071212	HCF	heart:	n/a
11	chr4:187088191-187088241	MCF-7	breast:	n/a
12	chr4:187053574-187053624	Caco-2	colon:	n/a
13	chr4:187065713-187065763	NHBE	bronchial:	n/a
14	chr4:187065417-187065467	HMEC	breast:	n/a
15	chr4:187065831-187065881	AG09309	skin:	n/a
16	chr4:187074031-187074081	K562	blood:	n/a
17	chr4:187066430-187066480	HEEpiC	esophagus:	n/a
18	chr4:187065831-187065881	GM12892	blood:	n/a
19	chr4:187065944-187065994	HCT-116	colon:	n/a
20	chr4:187070357-187070407	Hepatocyte	liver:	n/a
21	chr4:187053574-187053624	BE2_C	brain:	n/a
22	chr4:187065831-187065881	AoSMC	blood vessel:	n/a
23	chr4:187053574-187053624	HRPEpiC	eye:	n/a
24	chr4:187065417-187065467	MCF-7	breast:	n/a
25	chr4:187069057-187069107	Caco-2	colon:	n/a
26	chr4:187074031-187074081	AoSMC	blood vessel:	n/a
27	chr4:187065713-187065763	A549	lung:	n/a
28	chr4:187065940-187065990	HRE	kidney:	n/a
29	chr4:187065713-187065763	HCM	heart:	n/a
30	chr4:187088191-187088241	GM12878	blood:	n/a
31	chr4:187070357-187070407	HEK293	kidney:	embryo
32	chr4:187065417-187065467	HL-60	blood:	n/a
33	chr4:187074031-187074081	AG09319	gingival:	n/a
34	chr4:187065417-187065467	HEK293	kidney:	embryo
35	chr4:187065831-187065881	MCF-7	breast:	n/a
36	chr4:187066430-187066480	H1-hESC	embryonic stem cell:	embryo
37	chr4:187066279-187066329	HCT-116	colon:	n/a
38	chr4:187078828-187078878	MCF-7	breast:	n/a
39	chr4:187078828-187078878	A549	lung:	n/a
40	chr4:187065831-187065881	AG09319	gingival:	n/a
41	chr4:187066279-187066329	NB4	blood:	n/a
42	chr4:187053574-187053624	NT2-D1	testis:	n/a
43	chr4:187065950-187066000	RPTEC	kidney:	n/a
44	chr4:187066505-187066555	CMK	blood:	n/a
45	chr4:187065940-187065990	RPTEC	kidney:	n/a
46	chr4:187078771-187078821	K562	blood:	n/a
47	chr4:187071162-187071212	ProgFib	skin:	n/a
48	chr4:187065516-187065566	Jurkat	blood:	n/a
49	chr4:187066279-187066329	Hela-S3	cervix:	n/a
50	chr4:187078771-187078821	IMR90	lung:	fetal

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
2	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
3	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
4	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
5	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
6	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
7	chr4:187077276..187078819-chr4:187080715..187083352,2	K562	blood:
8	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:
9	chr4:187061612..187063617-chr4:187065011..187066705,2	K562	blood:
10	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
11	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
12	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
13	chr4:186953201..186953720-chr4:187058277..187058867,2	MCF-7	breast:
14	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
15	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
16	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
17	chr4:187077276..187078819-chr4:187080715..187083352,2	K562	blood:
18	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
19	chr4:187080678..187082912-chr4:187084577..187086317,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253013	TF binding region
ENSG00000250327	TF binding region
FAM149A	TF binding region
ENSG00000253013	CpG island
ENSG00000250327	CpG island
FAM149A	CpG island
ENSG00000269302	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000145476	chromatin interactions

Extended variants
information (count: 2051 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2051 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11730434	chr4:187046337-187046338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs201379637	chr4:187046370-187046371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373044914	chr4:187046378-187046379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114657445	chr4:187046408-187046409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557447597	chr4:187046453-187046454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1715060	chr4:187046469-187046470	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs79866125	chr4:187046470-187046471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533607110	chr4:187046487-187046488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114260776	chr4:187046524-187046525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576732712	chr4:187046573-187046574	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs181835692	chr4:187046596-187046597	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs186132046	chr4:187046597-187046598	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192397161	chr4:187046613-187046614	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs369972050	chr4:187046614-187046615	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576804450	chr4:187046618-187046619	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs536690427	chr4:187046623-187046624	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562100014	chr4:187046628-187046629	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs114897590	chr4:187046635-187046636	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541138072	chr4:187046640-187046641	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs74507004	chr4:187046658-187046659	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs375528947	chr4:187046668-187046669	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs146705687	chr4:187046669-187046670	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs180692065	chr4:187046704-187046705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554955127	chr4:187046724-187046725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1715061	chr4:187046744-187046745	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs186238399	chr4:187046761-187046762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6849187	chr4:187046762-187046763	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568136069	chr4:187046807-187046808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116810882	chr4:187046873-187046874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573467513	chr4:187046883-187046884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1715062	chr4:187046884-187046885	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs6849946	chr4:187046928-187046929	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191160110	chr4:187046958-187046959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182767533	chr4:187046959-187046960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1519316	chr4:187046962-187046963	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555949872	chr4:187046976-187046977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141902765	chr4:187046984-187046985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572513453	chr4:187046986-187046987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187456300	chr4:187047003-187047004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564470043	chr4:187047015-187047016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533244628	chr4:187047034-187047035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190501423	chr4:187047040-187047041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2055914	chr4:187047041-187047042	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs115717514	chr4:187047045-187047046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1519317	chr4:187047069-187047070	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs568331611	chr4:187047079-187047080	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144023303	chr4:187047137-187047138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183107024	chr4:187047157-187047158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533058448	chr4:187047261-187047262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547564396	chr4:187047310-187047311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187037200-187053600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:187039200-187053800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:187039200-187065000	Weak transcription	Fetal Brain Female	brain
4	chr4:187039400-187046600	Weak transcription	Gastric	stomach
5	chr4:187040600-187058200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr4:187043200-187053800	Weak transcription	Pancreas	Pancrea
7	chr4:187045000-187046400	Weak transcription	Fetal Stomach	stomach
8	chr4:187045000-187053200	Weak transcription	Fetal Intestine Large	intestine
9	chr4:187045200-187058400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr4:187046400-187047200	Strong transcription	Fetal Stomach	stomach
11	chr4:187046600-187047000	Strong transcription	Gastric	stomach
12	chr4:187047000-187050000	Weak transcription	Gastric	stomach
13	chr4:187047200-187053800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr4:187047200-187063200	Weak transcription	Fetal Stomach	stomach
15	chr4:187050000-187050400	Enhancers	Fetal Lung	lung
16	chr4:187050000-187050600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr4:187050000-187050600	Enhancers	Gastric	stomach
18	chr4:187050400-187053800	Weak transcription	Fetal Lung	lung
19	chr4:187050600-187065000	Weak transcription	Gastric	stomach
20	chr4:187052400-187053800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:187052600-187052800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:187052600-187053000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:187052600-187053000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr4:187052600-187053800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:187052600-187053800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:187052600-187054200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr4:187052600-187054200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:187052600-187054600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:187052600-187054600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:187052800-187054200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr4:187052800-187054600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:187053000-187053200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:187053000-187053400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr4:187053000-187053800	Enhancers	Brain Substantia Nigra	brain
35	chr4:187053000-187054600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr4:187053200-187054200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:187053200-187055000	Enhancers	Fetal Intestine Large	intestine
38	chr4:187053400-187054600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr4:187053600-187054000	Enhancers	Small Intestine	intestine
40	chr4:187053600-187054000	Enhancers	Stomach Mucosa	stomach
41	chr4:187053600-187054200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:187053600-187054400	Enhancers	Fetal Intestine Small	intestine
43	chr4:187053600-187054600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:187053800-187054000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:187053800-187054000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:187053800-187054200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:187053800-187054200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:187053800-187054200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:187053800-187054200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:187053800-187054200	Enhancers	Fetal Kidney	kidney

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