Variant report

Variant	esv3447097
Chromosome Location	chr4:3571554-3614352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:1037)
Chromatin interactive
region (count:23)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:3591953-3592306	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:3591938-3592292	K562	blood:	n/a	n/a
3	BACH1	chr4:3600326-3600440	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr4:3590653-3590888	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
6	BHLHE40	chr4:3587360-3587604	K562	blood:	n/a	n/a
7	BHLHE40	chr4:3592078-3592121	K562	blood:	n/a	n/a
8	BHLHE40	chr4:3576432-3576518	K562	blood:	n/a	n/a
9	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
10	BHLHE40	chr4:3586629-3586990	HepG2	liver:	n/a	n/a
11	BRCA1	chr4:3576365-3576373	HepG2	liver:	n/a	n/a
12	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
13	BRCA1	chr4:3578147-3578290	HepG2	liver:	n/a	n/a
14	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
15	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
17	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
18	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
19	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
20	CEBPB	chr4:3592195-3592197	K562	blood:	n/a	n/a
21	CEBPB	chr4:3608707-3609063	HepG2	liver:	n/a	chr4:3608890-3608901
22	CEBPB	chr4:3608690-3609116	K562	blood:	n/a	chr4:3608890-3608901
23	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
24	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:3576042-3576167	HepG2	liver:	n/a	chr4:3576093-3576104
26	CEBPB	chr4:3608726-3609033	IMR90	lung:	n/a	chr4:3608890-3608901
27	CEBPB	chr4:3578250-3578520	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:3608606-3609111	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
29	CEBPB	chr4:3608675-3609108	MCF-7	breast:	n/a	chr4:3608890-3608901
30	CEBPB	chr4:3578297-3578444	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
32	CEBPB	chr4:3608709-3609077	Hela-S3	cervix:	n/a	chr4:3608890-3608901
33	CEBPB	chr4:3608726-3609020	A549	lung:	n/a	chr4:3608890-3608901
34	CEBPD	chr4:3608662-3609107	K562	blood:	n/a	n/a
35	CEBPZ	chr4:3610104-3610260	HepG2	liver:	n/a	n/a
36	CHD2	chr4:3605527-3605779	HepG2	liver:	n/a	n/a
37	CHD2	chr4:3577950-3577961	K562	blood:	n/a	n/a
38	CHD2	chr4:3578272-3578287	HepG2	liver:	n/a	n/a
39	CHD2	chr4:3608550-3608560	GM12878	blood:	n/a	n/a
40	CHD2	chr4:3606516-3606589	HepG2	liver:	n/a	n/a
41	CHD2	chr4:3575147-3575242	HepG2	liver:	n/a	n/a
42	CTCF	chr4:3588329-3588359	GM13976	blood:	n/a	n/a
43	CTCF	chr4:3574296-3574353	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:3609840-3609990	HepG2	liver:	n/a	n/a
45	CTCF	chr4:3609840-3609990	Caco-2	colon:	n/a	n/a
46	CTCF	chr4:3582760-3582910	HepG2	liver:	n/a	n/a
47	CTCF	chr4:3574123-3574508	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:3591820-3591970	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:3597440-3597590	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr4:3574240-3574390	HBMEC	blood vessel:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3591216-3591266	SAEC	small airway:	n/a
2	chr4:3572794-3572844	NB4	blood:	n/a
3	chr4:3591243-3591293	HRPEpiC	eye:	n/a
4	chr4:3597859-3597909	BE2_C	brain:	n/a
5	chr4:3597580-3597630	SK-N-MC	brain:	n/a
6	chr4:3576489-3576539	NB4	blood:	n/a
7	chr4:3571919-3571969	PrEC	prostate:	n/a
8	chr4:3578583-3578633	Hepatocyte	liver:	n/a
9	chr4:3591243-3591293	RPTEC	kidney:	n/a
10	chr4:3576336-3576386	ovcar-3	ovarian:	n/a
11	chr4:3576489-3576539	HepG2	liver:	n/a
12	chr4:3576336-3576386	AG09319	gingival:	n/a
13	chr4:3576489-3576539	CMK	blood:	n/a
14	chr4:3597739-3597789	U87	brain:	n/a
15	chr4:3576489-3576539	IMR90	lung:	fetal
16	chr4:3597859-3597909	U87	brain:	n/a
17	chr4:3571857-3571907	AG09309	skin:	n/a
18	chr4:3576273-3576323	Hepatocyte	liver:	n/a
19	chr4:3591243-3591293	NB4	blood:	n/a
20	chr4:3571527-3571577	RPTEC	kidney:	n/a
21	chr4:3571857-3571907	GM06990	blood:	n/a
22	chr4:3591216-3591266	HNPCEpiC	eye:	n/a
23	chr4:3577650-3577700	HMEC	breast:	n/a
24	chr4:3571919-3571969	AoSMC	blood vessel:	n/a
25	chr4:3577496-3577546	PANC-1	pancreas:	n/a
26	chr4:3591243-3591293	HUVEC	blood vessel:	n/a
27	chr4:3571527-3571577	BE2_C	brain:	n/a
28	chr4:3576336-3576386	CMK	blood:	n/a
29	chr4:3576273-3576323	GM12878	blood:	n/a
30	chr4:3571527-3571577	HCPEpiC	choroid plexus:	n/a
31	chr4:3576273-3576323	NHDF-neo	bronchial:	n/a
32	chr4:3577496-3577546	IMR90	lung:	fetal
33	chr4:3591243-3591293	SAEC	small airway:	n/a
34	chr4:3597580-3597630	NHDF-neo	bronchial:	n/a
35	chr4:3571527-3571577	PrEC	prostate:	n/a
36	chr4:3597859-3597909	AG10803	skin:	n/a
37	chr4:3597859-3597909	HAEpiC	amniotic membrane:	n/a
38	chr4:3571527-3571577	T-47D	breast:	n/a
39	chr4:3576273-3576323	RPTEC	kidney:	n/a
40	chr4:3571857-3571907	MCF-7	breast:	n/a
41	chr4:3591253-3591303	MCF-7	breast:	n/a
42	chr4:3597739-3597789	SK-N-SH_RA	brain:	n/a
43	chr4:3597739-3597789	GM12878	blood:	n/a
44	chr4:3576336-3576386	HNPCEpiC	eye:	n/a
45	chr4:3576273-3576323	ProgFib	skin:	n/a
46	chr4:3576489-3576539	HEEpiC	esophagus:	n/a
47	chr4:3572794-3572844	NT2-D1	testis:	n/a
48	chr4:3578432-3578482	HUVEC	blood vessel:	n/a
49	chr4:3578432-3578482	SK-N-MC	brain:	n/a
50	chr4:3591253-3591303	AG04450	lung:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
2	chr12:94805847..94806347-chr4:3589447..3589978,2	K562	blood:
3	chr4:3574894..3577613-chr4:3578076..3580368,2	K562	blood:
4	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
5	chr4:3532775..3535041-chr4:3574379..3576145,2	K562	blood:
6	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
7	chr4:3532636..3535397-chr4:3592609..3595369,2	K562	blood:
8	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
9	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
10	chr4:3596211..3598668-chr4:3781245..3783965,2	K562	blood:
11	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
12	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
13	chr4:3573176..3575691-chr4:3650301..3652396,2	MCF-7	breast:
14	chr4:3608635..3609305-chr8:108914123..108914952,2	MCF-7	breast:
15	chr4:3577226..3578815-chr4:3583775..3586576,2	K562	blood:
16	chr4:3576753..3579179-chr4:3579407..3585070,6	K562	blood:
17	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
18	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
19	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
20	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
21	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
22	chr4:3533888..3535501-chr4:3581402..3583969,2	MCF-7	breast:
23	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	XLOC_003428
2	lnc-LRPAP1-5	chr4:3600844-3601755	NONHSAT094890
3	lnc-RP3-368B9.1.1-1	chr4:3590661-3592166	XLOC_003428
4	lnc-RP3-368B9.1.1-1	chr4:3590661-3592712	NR_040045
5	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	XLOC_003428
6	lnc-RP3-368B9.1.1-1	chr4:3591991-3592438	XLOC_003428
7	lnc-RP3-368B9.1.1-1	chr4:3589778-3589914	XLOC_003428
8	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	NR_040045
9	lnc-LRPAP1-5	chr4:3600324-3600789	NONHSAT094890
10	lnc-RP3-368B9.1.1-1	chr4:3590661-3590741	XLOC_003428
11	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	XLOC_003428
12	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	NR_040045

No data

Variant related genes	Relation type
LINC00955	TF binding region
LINC00955	CpG island
ENSG00000216560	chromatin interactions
ENSG00000173588	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
TMEM2	miRNA target sites

Extended variants
information (count: 3411 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3411 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539957969	chr4:3571556-3571557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1741563	chr4:3571557-3571558	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150513459	chr4:3571576-3571577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537890638	chr4:3571579-3571580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562725403	chr4:3571580-3571581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199527895	chr4:3571633-3571634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1741562	chr4:3571641-3571642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184700655	chr4:3571654-3571655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561939391	chr4:3571662-3571663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527644254	chr4:3571663-3571664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112049608	chr4:3571672-3571673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146704609	chr4:3571673-3571674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189682971	chr4:3571693-3571694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533443972	chr4:3571712-3571713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552436658	chr4:3571713-3571714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73796115	chr4:3571731-3571732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs67074573	chr4:3571738-3571739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144388094	chr4:3571765-3571766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554803840	chr4:3571769-3571770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567975906	chr4:3571784-3571785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533827769	chr4:3571794-3571795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180859165	chr4:3571802-3571803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576561270	chr4:3571818-3571819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545456650	chr4:3571832-3571833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140334993	chr4:3571834-3571835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372185364	chr4:3571852-3571853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144120612	chr4:3571853-3571854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562444615	chr4:3571857-3571858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200866810	chr4:3571859-3571860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527973935	chr4:3571905-3571906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201433834	chr4:3571906-3571907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35571101	chr4:3571917-3571918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199912020	chr4:3571922-3571923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541443893	chr4:3571935-3571936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1741561	chr4:3571936-3571937	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369894956	chr4:3571939-3571940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533481113	chr4:3571961-3571962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185963031	chr4:3571981-3571982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192084494	chr4:3572030-3572031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181072533	chr4:3572033-3572034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373086177	chr4:3572044-3572045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113567046	chr4:3572058-3572059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570122049	chr4:3572059-3572060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531496630	chr4:3572062-3572063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548076127	chr4:3572071-3572072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1730800	chr4:3572087-3572088	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs533826446	chr4:3572091-3572092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553743517	chr4:3572108-3572109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181821997	chr4:3572125-3572126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186056578	chr4:3572159-3572160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3550600-3580400	Weak transcription	Right Atrium	heart
2	chr4:3558800-3574600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:3571800-3572000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:3572000-3573000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3572800-3573600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr4:3573000-3573400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
7	chr4:3573000-3575600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:3573000-3580200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:3573800-3574200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr4:3573800-3574800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr4:3573800-3578200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:3574000-3574400	ZNF genes & repeats	Spleen	Spleen
13	chr4:3574200-3574600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:3574200-3574800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
15	chr4:3574400-3574800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
16	chr4:3574600-3575200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:3575200-3576400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:3575600-3575800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr4:3576000-3579600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:3576400-3576600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr4:3576400-3576600	Enhancers	Gastric	stomach
22	chr4:3576600-3577600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr4:3576600-3580200	Weak transcription	Gastric	stomach
24	chr4:3576800-3578600	Enhancers	Fetal Intestine Large	intestine
25	chr4:3577000-3577200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:3577000-3577200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:3577000-3578600	Enhancers	Fetal Intestine Small	intestine
28	chr4:3577200-3577400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:3577200-3577400	Bivalent Enhancer	HepG2	liver
30	chr4:3577400-3577600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:3577400-3577800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr4:3577400-3578000	Flanking Bivalent TSS/Enh	HepG2	liver
33	chr4:3577600-3577800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:3577600-3577800	Bivalent Enhancer	Right Ventricle	heart
35	chr4:3577600-3578800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:3577800-3578200	Enhancers	Duodenum Mucosa	Duodenum
37	chr4:3578000-3578400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
38	chr4:3578000-3578600	Flanking Active TSS	HepG2	liver
39	chr4:3578200-3578400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:3578200-3578400	Weak transcription	Duodenum Mucosa	Duodenum
41	chr4:3578400-3578800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
42	chr4:3578400-3579000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
43	chr4:3578600-3578800	Active TSS	Fetal Intestine Large	intestine
44	chr4:3578600-3578800	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr4:3578600-3579200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
46	chr4:3578600-3579400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:3578600-3579400	Enhancers	HepG2	liver
48	chr4:3578600-3579600	Flanking Active TSS	Fetal Intestine Small	intestine
49	chr4:3578800-3579000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:3578800-3579000	Flanking Active TSS	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links