Variant report

Variant	nsv880626
Chromosome Location	chr4:188829088-188962325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:881)
CpG islands
(count:2510)
Chromatin interactive
region (count:13)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:881 , 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	ATF2	chr4:188916749-188917170	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:188926433-188926974	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:188916764-188917071	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:188915055-188915396	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:188953244-188953886	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:188917657-188917951	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:188916526-188917174	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:188952989-188953975	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:188936288-188936488	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
12	BCL11A	chr4:188953306-188953649	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr4:188929455-188929456	HepG2	liver:	n/a	n/a
14	BHLHE40	chr4:188923505-188923772	K562	blood:	n/a	n/a
15	BRCA1	chr4:188909297-188909449	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr4:188923496-188923905	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr4:188936021-188936859	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:188917816-188917938	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:188929371-188929912	A549	lung:	n/a	n/a
20	CEBPB	chr4:188875669-188875935	HepG2	liver:	n/a	chr4:188875825-188875836
21	CEBPB	chr4:188873586-188873809	IMR90	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
22	CEBPB	chr4:188936053-188937221	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:188923470-188923960	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr4:188829199-188829608	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:188875779-188875862	H1-hESC	embryonic stem cell:	n/a	chr4:188875825-188875836
26	CEBPB	chr4:188898167-188898421	HepG2	liver:	n/a	chr4:188898278-188898291 chr4:188898279-188898290
27	CEBPB	chr4:188929383-188929936	A549	lung:	n/a	n/a
28	CEBPB	chr4:188929463-188929848	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:188936139-188936670	A549	lung:	n/a	n/a
30	CEBPB	chr4:188936262-188936771	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:188873544-188873823	HepG2	liver:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
32	CEBPB	chr4:188936268-188936828	A549	lung:	n/a	n/a
33	CEBPB	chr4:188936287-188936507	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr4:188929269-188929961	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:188873517-188873689	Hela-S3	cervix:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
36	CEBPB	chr4:188916852-188917179	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:188839840-188839977	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:188873512-188873759	A549	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
39	CHD1	chr4:188919719-188919955	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr4:188952977-188953947	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr4:188916853-188919438	H1-hESC	embryonic stem cell:	n/a	chr4:188918682-188918692 chr4:188918099-188918109
42	CHD1	chr4:188828998-188830029	IMR90	lung:	n/a	n/a
43	CHD2	chr4:188923470-188923823	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr4:188936198-188936867	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr4:188937818-188938313	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:188850337-188850446	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr4:188914155-188915309	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:188917776-188918281	H1-hESC	embryonic stem cell:	n/a	chr4:188918099-188918109
49	CHD2	chr4:188952861-188953856	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:188929422-188929870	Hela-S3	cervix:	n/a	n/a

(count:2510 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188829287-188829337	HRPEpiC	eye:	n/a
2	chr4:188891490-188891540	GM12891	blood:	n/a
3	chr4:188917173-188917223	HNPCEpiC	eye:	n/a
4	chr4:188916867-188916917	U87	brain:	n/a
5	chr4:188953906-188953956	SAEC	small airway:	n/a
6	chr4:188829287-188829337	HL-60	blood:	n/a
7	chr4:188918218-188918268	AG04450	lung:	fetal
8	chr4:188953677-188953727	GM06990	blood:	n/a
9	chr4:188953906-188953956	NT2-D1	testis:	n/a
10	chr4:188829287-188829337	HRPEpiC	eye:	n/a
11	chr4:188891490-188891540	GM12891	blood:	n/a
12	chr4:188917173-188917223	HNPCEpiC	eye:	n/a
13	chr4:188916867-188916917	U87	brain:	n/a
14	chr4:188953906-188953956	SAEC	small airway:	n/a
15	chr4:188829287-188829337	HL-60	blood:	n/a
16	chr4:188918218-188918268	AG04450	lung:	fetal
17	chr4:188953677-188953727	GM06990	blood:	n/a
18	chr4:188953906-188953956	NT2-D1	testis:	n/a
19	chr4:188858971-188859021	HMEC	breast:	n/a
20	chr4:188952355-188952405	Hepatocyte	liver:	n/a
21	chr4:188916726-188916776	LNCaP	prostate:	n/a
22	chr4:188916668-188916718	NB4	blood:	n/a
23	chr4:188918072-188918122	GM12892	blood:	n/a
24	chr4:188916865-188916915	SK-N-SH_RA	brain:	n/a
25	chr4:188858709-188858759	NHDF-neo	bronchial:	n/a
26	chr4:188916875-188916925	HRE	kidney:	n/a
27	chr4:188843522-188843572	Caco-2	colon:	n/a
28	chr4:188916867-188916917	SAEC	small airway:	n/a
29	chr4:188924717-188924767	MCF-7	breast:	n/a
30	chr4:188953092-188953142	K562	blood:	n/a
31	chr4:188917173-188917223	SK-N-MC	brain:	n/a
32	chr4:188953527-188953577	HL-60	blood:	n/a
33	chr4:188829287-188829337	HEEpiC	esophagus:	n/a
34	chr4:188916496-188916546	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:188924752-188924802	ECC-1	luminal epithelium:	n/a
36	chr4:188924717-188924767	AoSMC	blood vessel:	n/a
37	chr4:188843522-188843572	HL-60	blood:	n/a
38	chr4:188854221-188854271	HRPEpiC	eye:	n/a
39	chr4:188924717-188924767	H1-hESC	embryonic stem cell:	embryo
40	chr4:188916709-188916759	RPTEC	kidney:	n/a
41	chr4:188953677-188953727	BE2_C	brain:	n/a
42	chr4:188917251-188917301	GM12892	blood:	n/a
43	chr4:188916814-188916864	PrEC	prostate:	n/a
44	chr4:188953969-188954019	HUVEC	blood vessel:	n/a
45	chr4:188917173-188917223	GM12891	blood:	n/a
46	chr4:188916875-188916925	BE2_C	brain:	n/a
47	chr4:188944412-188944462	GM12892	blood:	n/a
48	chr4:188916724-188916774	MCF-7	breast:	n/a
49	chr4:188858971-188859021	GM12892	blood:	n/a
50	chr4:188916867-188916917	HPAEpiC	pulmonary alveolar:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188914670..188915671-chr4:189167438..189168869,4	MCF-7	breast:
2	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
3	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
4	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
5	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
6	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
7	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
8	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
9	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
10	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
11	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
12	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
13	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-2	chr4:188881466-188881648	XLOC_004222
2	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
3	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099726
4	lnc-TRIML2-2	chr4:188881466-188881649	NONHSAT099725
5	lnc-TRIML2-2	chr4:188866817-188867016	NONHSAT099725
6	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
7	lnc-ZFP42-8	chr4:188869892-188870239	l_2822_chr4:188790794-188818331_testes
8	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099725
9	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
10	lnc-TRIML2-2	chr4:188908697-188908733	NONHSAT099726

No data

Variant related genes	Relation type
ZFP42	TF binding region
ENSG00000213331	TF binding region
ZFP42	CpG island
ENSG00000213331	CpG island

Extended variants
information (count: 4145 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4145 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10866303	chr4:188829088-188829089	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs77854935	chr4:188829117-188829118	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs573921660	chr4:188829158-188829159	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573526812	chr4:188829170-188829171	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs75342728	chr4:188829229-188829230	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs572968810	chr4:188829232-188829233	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540848430	chr4:188829243-188829244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs140732612	chr4:188829282-188829283	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs559246757	chr4:188829284-188829285	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs182770540	chr4:188829291-188829292	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs73874725	chr4:188829293-188829294	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563531054	chr4:188829306-188829307	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs59895541	chr4:188829307-188829308	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188141693	chr4:188829311-188829312	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs34432950	chr4:188829361-188829362	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs150455520	chr4:188829362-188829363	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs79887388	chr4:188829432-188829433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551984740	chr4:188829455-188829456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192908665	chr4:188829493-188829494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184351978	chr4:188829498-188829499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367838229	chr4:188829649-188829650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541167946	chr4:188829669-188829670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533638361	chr4:188829694-188829695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556967057	chr4:188829766-188829767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572034263	chr4:188829791-188829792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567158091	chr4:188829796-188829797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187242034	chr4:188829813-188829814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553013470	chr4:188829814-188829815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573069109	chr4:188829857-188829858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538479429	chr4:188829875-188829876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558322176	chr4:188829934-188829935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558373909	chr4:188829974-188829975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577764140	chr4:188830029-188830030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552753692	chr4:188830079-188830080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192573375	chr4:188830182-188830183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563763099	chr4:188830192-188830193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573968673	chr4:188830253-188830254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542983279	chr4:188830259-188830260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184608390	chr4:188830292-188830293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145375513	chr4:188830331-188830332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202138608	chr4:188830339-188830340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6841763	chr4:188830340-188830341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35469814	chr4:188830347-188830348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190559813	chr4:188830355-188830356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376344649	chr4:188830359-188830360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6841942	chr4:188830382-188830383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs370150790	chr4:188830422-188830423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6841977	chr4:188830424-188830425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34928945	chr4:188830432-188830433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565478781	chr4:188830434-188830435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188825000-188829600	Weak transcription	NH-A	brain
2	chr4:188828200-188830200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:188828800-188829400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:188828800-188830000	Enhancers	Fetal Muscle Leg	muscle
5	chr4:188828800-188830000	Enhancers	Fetal Stomach	stomach
6	chr4:188829000-188829400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:188829000-188829400	Flanking Active TSS	Osteobl	bone
8	chr4:188829000-188829600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:188829000-188829600	Enhancers	Aorta	Aorta
10	chr4:188829000-188829600	Enhancers	Fetal Lung	lung
11	chr4:188829000-188829800	Enhancers	Ovary	ovary
12	chr4:188829000-188830000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:188829000-188830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:188829000-188830000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:188829000-188830000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr4:188829000-188830000	Enhancers	Fetal Brain Male	brain
17	chr4:188829000-188830000	Enhancers	NHDF-Ad	bronchial
18	chr4:188829000-188830000	Enhancers	NHLF	lung
19	chr4:188829000-188830200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:188829000-188830200	Enhancers	A549	lung
21	chr4:188829200-188829800	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr4:188829400-188830200	Enhancers	Osteobl	bone
23	chr4:188829600-188830000	Enhancers	NH-A	brain
24	chr4:188830000-188832000	Weak transcription	Fetal Muscle Leg	muscle
25	chr4:188830000-188833800	Weak transcription	NHDF-Ad	bronchial
26	chr4:188832000-188832200	Bivalent Enhancer	Fetal Brain Male	brain
27	chr4:188832000-188832400	Enhancers	Fetal Muscle Leg	muscle
28	chr4:188832400-188833400	Weak transcription	Fetal Muscle Leg	muscle
29	chr4:188833400-188833600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:188833600-188833800	Enhancers	Fetal Muscle Leg	muscle
31	chr4:188842000-188844400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:188842600-188843600	Enhancers	Brain Germinal Matrix	brain
33	chr4:188843200-188843400	Bivalent Enhancer	Fetal Brain Male	brain
34	chr4:188843400-188843800	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr4:188843400-188843800	Enhancers	Fetal Lung	lung
36	chr4:188843800-188844200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:188849800-188850000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:188850000-188850200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:188850000-188850600	Enhancers	Lung	lung
40	chr4:188850200-188850400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:188850200-188850800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:188850400-188851000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:188850600-188850800	ZNF genes & repeats	Lung	lung
44	chr4:188850600-188850800	Bivalent Enhancer	Right Ventricle	heart
45	chr4:188850600-188851000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:188851000-188851400	ZNF genes & repeats	Fetal Stomach	stomach
47	chr4:188851000-188853200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:188851400-188856000	Weak transcription	Fetal Stomach	stomach
49	chr4:188853200-188854800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:188854200-188856200	Enhancers	Ovary	ovary

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