Variant report

Variant	nsv881590
Chromosome Location	chr4:187021315-187107849
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	chr4:187058552-187058902	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187058644-187058864	K562	blood:	n/a	n/a
3	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
4	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:187055315-187055866	GM12878	blood:	n/a	n/a
6	ATF2	chr4:187071057-187071421	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:187066156-187066584	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:187025719-187026243	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:187082521-187082663	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:187026701-187026862	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:187058420-187058694	GM12878	blood:	n/a	n/a
12	BATF	chr4:187055371-187055785	GM12878	blood:	n/a	n/a
13	BATF	chr4:187055418-187055866	GM12878	blood:	n/a	n/a
14	BATF	chr4:187058431-187058728	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:187055420-187055843	GM12878	blood:	n/a	n/a
16	BCL3	chr4:187055433-187055716	GM12878	blood:	n/a	n/a
17	BCL3	chr4:187059720-187060074	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:187055345-187055835	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:187055428-187055813	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:187059455-187059456	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:187055496-187055825	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:187090880-187090890	K562	blood:	n/a	n/a
23	BHLHE40	chr4:187039012-187039026	K562	blood:	n/a	n/a
24	BRCA1	chr4:187082411-187082510	GM12878	blood:	n/a	n/a
25	CEBPB	chr4:187037881-187038220	Hela-S3	cervix:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
26	CEBPB	chr4:187037849-187038207	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
27	CEBPB	chr4:187037865-187038243	K562	blood:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
28	CEBPB	chr4:187089187-187089327	A549	lung:	n/a	n/a
29	CEBPB	chr4:187078966-187079181	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:187037847-187038225	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
31	CEBPB	chr4:187078958-187079135	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:187078910-187079176	K562	blood:	n/a	n/a
33	CEBPB	chr4:187067232-187067556	H1-hESC	embryonic stem cell:	n/a	chr4:187067399-187067412
34	CEBPB	chr4:187037872-187038236	IMR90	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
35	CEBPB	chr4:187058752-187058939	K562	blood:	n/a	n/a
36	CEBPB	chr4:187089147-187089328	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:187037868-187038236	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
38	CEBPB	chr4:187037874-187038237	H1-hESC	embryonic stem cell:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
39	CEBPB	chr4:187059932-187059959	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:187078955-187079103	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:187078864-187079223	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:187037845-187038266	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
43	CEBPB	chr4:187037900-187038225	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
44	CEBPB	chr4:187037867-187038233	HepG2	liver:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
45	CEBPB	chr4:187037859-187038158	MCF-7	breast:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
46	CEBPB	chr4:187058612-187058894	A549	lung:	n/a	n/a
47	CHD1	chr4:187059861-187059865	GM12878	blood:	n/a	n/a
48	CHD1	chr4:187026105-187026212	H1-hESC	embryonic stem cell:	n/a	chr4:187026142-187026152
49	CHD2	chr4:187071137-187071471	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:187055449-187055790	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187039516-187039566	Jurkat	blood:	n/a
2	chr4:187070303-187070353	HUVEC	blood vessel:	n/a
3	chr4:187025897-187025947	HRCEpiC	kidney:	n/a
4	chr4:187074031-187074081	K562	blood:	n/a
5	chr4:187065955-187066005	HCM	heart:	n/a
6	chr4:187039516-187039566	Jurkat	blood:	n/a
7	chr4:187070303-187070353	HUVEC	blood vessel:	n/a
8	chr4:187025897-187025947	HRCEpiC	kidney:	n/a
9	chr4:187074031-187074081	K562	blood:	n/a
10	chr4:187065955-187066005	HCM	heart:	n/a
11	chr4:187039516-187039566	A549	lung:	n/a
12	chr4:187026872-187026922	GM12878	blood:	n/a
13	chr4:187065516-187065566	MCF-7	breast:	n/a
14	chr4:187039516-187039566	GM06990	blood:	n/a
15	chr4:187065950-187066000	MCF10A-Er-Src	breast:	n/a
16	chr4:187078828-187078878	HRCEpiC	kidney:	n/a
17	chr4:187065831-187065881	U87	brain:	n/a
18	chr4:187078828-187078878	ovcar-3	ovarian:	n/a
19	chr4:187065516-187065566	HNPCEpiC	eye:	n/a
20	chr4:187026278-187026328	BJ	skin:	n/a
21	chr4:187065417-187065467	GM12891	blood:	n/a
22	chr4:187088191-187088241	T-47D	breast:	n/a
23	chr4:187063756-187063806	NHBE	bronchial:	n/a
24	chr4:187037318-187037368	PrEC	prostate:	n/a
25	chr4:187037256-187037306	SK-N-SH	brain:	n/a
26	chr4:187065944-187065994	ovcar-3	ovarian:	n/a
27	chr4:187065940-187065990	PFSK-1	brain:	n/a
28	chr4:187026225-187026275	CMK	blood:	n/a
29	chr4:187026710-187026760	T-47D	breast:	n/a
30	chr4:187026970-187027020	HEK293	kidney:	embryo
31	chr4:187065955-187066005	BE2_C	brain:	n/a
32	chr4:187026225-187026275	GM19239	blood:	n/a
33	chr4:187026225-187026275	SK-N-MC	brain:	n/a
34	chr4:187053574-187053624	LNCaP	prostate:	n/a
35	chr4:187078828-187078878	HCPEpiC	choroid plexus:	n/a
36	chr4:187088169-187088219	ProgFib	skin:	n/a
37	chr4:187078828-187078878	AG09319	gingival:	n/a
38	chr4:187026872-187026922	AoSMC	blood vessel:	n/a
39	chr4:187063756-187063806	BJ	skin:	n/a
40	chr4:187065950-187066000	HAEpiC	amniotic membrane:	n/a
41	chr4:187025886-187025936	NB4	blood:	n/a
42	chr4:187070303-187070353	HCPEpiC	choroid plexus:	n/a
43	chr4:187065713-187065763	ECC-1	luminal epithelium:	n/a
44	chr4:187026872-187026922	PFSK-1	brain:	n/a
45	chr4:187026872-187026922	K562	blood:	n/a
46	chr4:187025420-187025470	IMR90	lung:	fetal
47	chr4:187025654-187025704	AG09309	skin:	n/a
48	chr4:187025420-187025470	Jurkat	blood:	n/a
49	chr4:187078771-187078821	NHBE	bronchial:	n/a
50	chr4:187025654-187025704	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187080678..187082912-chr4:187084577..187086317,2	K562	blood:
2	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
3	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
4	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
5	chr4:187106383..187110529-chr4:187110531..187113610,6	K562	blood:
6	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
7	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:
8	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
9	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
10	chr4:187061612..187063617-chr4:187065011..187066705,2	K562	blood:
11	chr4:187077276..187078819-chr4:187080715..187083352,2	K562	blood:
12	chr4:187077276..187078819-chr4:187080715..187083352,2	K562	blood:
13	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
14	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:
15	chr4:187092198..187094078-chr4:187111646..187113279,2	MCF-7	breast:
16	chr4:186953201..186953720-chr4:187058277..187058867,2	MCF-7	breast:
17	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
18	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
19	chr4:187091730..187094624-chr4:187097179..187100415,3	MCF-7	breast:
20	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
21	chr4:187106828..187109765-chr4:187110186..187112854,4	K562	blood:
22	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
23	chr4:187098304..187101860-chr4:187110284..187112773,3	K562	blood:
24	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:
25	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
26	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
27	chr4:187023730..187026664-chr4:187030524..187032198,2	MCF-7	breast:
28	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
29	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:

Variant related genes	Relation type
CYP4V2	TF binding region
ENSG00000253013	TF binding region
ENSG00000250327	TF binding region
FAM149A	TF binding region
ORAOV1P1	TF binding region
CYP4V2	CpG island
ENSG00000253013	CpG island
ENSG00000250327	CpG island
FAM149A	CpG island
ORAOV1P1	CpG island
ENSG00000204424	chromatin interactions
ENSG00000145476	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000250641	chromatin interactions
ENSG00000251008	chromatin interactions

Extended variants
information (count: 3645 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3645 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9312342	chr4:187021315-187021316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77926359	chr4:187021319-187021320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77009325	chr4:187021321-187021322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79770429	chr4:187021323-187021324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75549026	chr4:187021326-187021327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529603406	chr4:187021409-187021410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191156058	chr4:187021419-187021420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115406847	chr4:187021442-187021443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs55797065	chr4:187021447-187021448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536143428	chr4:187021453-187021454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551819744	chr4:187021484-187021485	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571575387	chr4:187021505-187021506	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs142061156	chr4:187021512-187021513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs62347991	chr4:187021538-187021539	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182637399	chr4:187021572-187021573	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535340311	chr4:187021577-187021578	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555304887	chr4:187021604-187021605	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs572168414	chr4:187021614-187021615	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540790521	chr4:187021645-187021646	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs6824238	chr4:187021652-187021653	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs62347992	chr4:187021694-187021695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs188159292	chr4:187021697-187021698	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563270694	chr4:187021698-187021699	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs542230572	chr4:187021753-187021754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575382087	chr4:187021760-187021761	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373839072	chr4:187021798-187021799	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544222243	chr4:187021831-187021832	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554253031	chr4:187021840-187021841	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147936334	chr4:187021913-187021914	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191802214	chr4:187021949-187021950	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140048954	chr4:187021954-187021955	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs9312343	chr4:187021989-187021990	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571369876	chr4:187022067-187022068	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530905511	chr4:187022072-187022073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542949449	chr4:187022086-187022087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145671605	chr4:187022102-187022103	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567303937	chr4:187022132-187022133	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs535398663	chr4:187022186-187022187	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs555605754	chr4:187022258-187022259	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs565738660	chr4:187022303-187022304	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs534775081	chr4:187022305-187022306	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs62347993	chr4:187022362-187022363	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs143576216	chr4:187022364-187022365	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs112061210	chr4:187022375-187022376	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs112778441	chr4:187022379-187022380	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs78871969	chr4:187022380-187022381	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs79245175	chr4:187022417-187022418	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182896066	chr4:187022429-187022430	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs545165156	chr4:187022458-187022459	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs187656344	chr4:187022498-187022499	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187009600-187025400	Weak transcription	Ovary	ovary
2	chr4:187014600-187024000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:187018600-187025400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr4:187023400-187024400	Weak transcription	Pancreas	Pancrea
5	chr4:187024400-187024600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:187024400-187024600	Enhancers	Gastric	stomach
7	chr4:187024400-187024600	Enhancers	Pancreas	Pancrea
8	chr4:187024600-187025400	Weak transcription	Gastric	stomach
9	chr4:187024600-187025400	Weak transcription	Pancreas	Pancrea
10	chr4:187025000-187025400	Enhancers	Fetal Intestine Small	intestine
11	chr4:187025200-187025400	Enhancers	Fetal Intestine Large	intestine
12	chr4:187025200-187025400	Enhancers	Fetal Kidney	kidney
13	chr4:187025200-187025400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr4:187025200-187025400	Bivalent Enhancer	Stomach Mucosa	stomach
15	chr4:187025200-187026000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
16	chr4:187025400-187025600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
17	chr4:187025400-187025600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:187025400-187025600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
19	chr4:187025400-187025600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:187025400-187025600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
21	chr4:187025400-187025600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr4:187025400-187025600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
23	chr4:187025400-187025600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
24	chr4:187025400-187025600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
25	chr4:187025400-187025600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:187025400-187025600	Enhancers	Liver	Liver
27	chr4:187025400-187025600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr4:187025400-187025600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr4:187025400-187025600	Bivalent Enhancer	Fetal Muscle Leg	muscle
30	chr4:187025400-187025600	Bivalent Enhancer	Placenta	Placenta
31	chr4:187025400-187025600	Bivalent Enhancer	Fetal Thymus	thymus
32	chr4:187025400-187025600	Enhancers	Gastric	stomach
33	chr4:187025400-187025600	Enhancers	Lung	lung
34	chr4:187025400-187025600	Enhancers	Ovary	ovary
35	chr4:187025400-187025600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr4:187025400-187025600	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
37	chr4:187025400-187025600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
38	chr4:187025400-187025600	Bivalent Enhancer	NH-A	brain
39	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
40	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
42	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:187025400-187025800	Active TSS	Fetal Brain Male	brain
44	chr4:187025400-187025800	Flanking Active TSS	Fetal Intestine Large	intestine
45	chr4:187025400-187025800	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	Fetal Lung	lung
47	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
48	chr4:187025400-187025800	Flanking Active TSS	Pancreas	Pancrea
49	chr4:187025400-187025800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
50	chr4:187025400-187025800	Flanking Active TSS	Rectal Smooth Muscle	rectum

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