Variant report

Variant	esv2647558
Chromosome Location	chr4:3572478-3605989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:857)
Chromatin interactive
region (count:20)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:3600326-3600440	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:3591938-3592292	K562	blood:	n/a	n/a
3	BACH1	chr4:3591953-3592306	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr4:3590653-3590888	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:3576432-3576518	K562	blood:	n/a	n/a
6	BHLHE40	chr4:3592078-3592121	K562	blood:	n/a	n/a
7	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
8	BHLHE40	chr4:3587360-3587604	K562	blood:	n/a	n/a
9	BHLHE40	chr4:3586629-3586990	HepG2	liver:	n/a	n/a
10	BRCA1	chr4:3576365-3576373	HepG2	liver:	n/a	n/a
11	BRCA1	chr4:3578147-3578290	HepG2	liver:	n/a	n/a
12	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
13	CEBPB	chr4:3576042-3576167	HepG2	liver:	n/a	chr4:3576093-3576104
14	CEBPB	chr4:3578250-3578520	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:3578297-3578444	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:3592195-3592197	K562	blood:	n/a	n/a
17	CHD2	chr4:3577950-3577961	K562	blood:	n/a	n/a
18	CHD2	chr4:3578272-3578287	HepG2	liver:	n/a	n/a
19	CHD2	chr4:3605527-3605779	HepG2	liver:	n/a	n/a
20	CHD2	chr4:3575147-3575242	HepG2	liver:	n/a	n/a
21	CTCF	chr4:3574200-3574350	HepG2	liver:	n/a	n/a
22	CTCF	chr4:3604680-3604830	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr4:3575913-3576104	K562	blood:	n/a	n/a
24	CTCF	chr4:3574260-3574410	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:3582500-3582650	BE2_C	brain:	n/a	n/a
26	CTCF	chr4:3597459-3597550	HepG2	liver:	n/a	n/a
27	CTCF	chr4:3574160-3574310	AG10803	skin:	n/a	n/a
28	CTCF	chr4:3574271-3574364	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:3595698-3595703	GM19239	blood:	n/a	n/a
30	CTCF	chr4:3574280-3574430	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr4:3574173-3574378	HepG2	liver:	n/a	n/a
32	CTCF	chr4:3600479-3600866	GM19239	blood:	n/a	n/a
33	CTCF	chr4:3574240-3574390	HepG2	liver:	n/a	n/a
34	CTCF	chr4:3597640-3597790	K562	blood:	n/a	n/a
35	CTCF	chr4:3585797-3585872	GM19239	blood:	n/a	n/a
36	CTCF	chr4:3574220-3574370	HAc	cerebellar:	n/a	n/a
37	CTCF	chr4:3592820-3592970	BE2_C	brain:	n/a	n/a
38	CTCF	chr4:3582720-3582870	BE2_C	brain:	n/a	n/a
39	CTCF	chr4:3590140-3590290	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr4:3597680-3597830	A549	lung:	n/a	n/a
41	CTCF	chr4:3597380-3597530	HEK293	kidney:	n/a	n/a
42	CTCF	chr4:3574160-3574310	K562	blood:	n/a	n/a
43	CTCF	chr4:3574354-3574358	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:3574240-3574390	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr4:3592339-3592356	K562	blood:	n/a	n/a
46	CTCF	chr4:3600950-3601118	GM19239	blood:	n/a	n/a
47	CTCF	chr4:3574140-3574290	HEK293	kidney:	n/a	n/a
48	CTCF	chr4:3575560-3575710	GM12872	blood:	n/a	n/a
49	CTCF	chr4:3574220-3574370	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:3600865-3600922	H1-hESC	embryonic stem cell:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3576273-3576323	BJ	skin:	n/a
2	chr4:3597739-3597789	HEEpiC	esophagus:	n/a
3	chr4:3591253-3591303	HCM	heart:	n/a
4	chr4:3576273-3576323	BJ	skin:	n/a
5	chr4:3597739-3597789	HEEpiC	esophagus:	n/a
6	chr4:3591253-3591303	HCM	heart:	n/a
7	chr4:3597739-3597789	U87	brain:	n/a
8	chr4:3572794-3572844	Hela-S3	cervix:	n/a
9	chr4:3577650-3577700	GM12892	blood:	n/a
10	chr4:3577496-3577546	NHBE	bronchial:	n/a
11	chr4:3572794-3572844	HIPEpiC	eye:	n/a
12	chr4:3577650-3577700	GM19239	blood:	n/a
13	chr4:3578583-3578633	LNCaP	prostate:	n/a
14	chr4:3578583-3578633	NB4	blood:	n/a
15	chr4:3576489-3576539	PrEC	prostate:	n/a
16	chr4:3591253-3591303	HAEpiC	amniotic membrane:	n/a
17	chr4:3597859-3597909	IMR90	lung:	fetal
18	chr4:3576489-3576539	ProgFib	skin:	n/a
19	chr4:3591216-3591266	HMEC	breast:	n/a
20	chr4:3578583-3578633	BE2_C	brain:	n/a
21	chr4:3597859-3597909	MCF-7	breast:	n/a
22	chr4:3572794-3572844	NT2-D1	testis:	n/a
23	chr4:3591253-3591303	HMEC	breast:	n/a
24	chr4:3572794-3572844	ProgFib	skin:	n/a
25	chr4:3577650-3577700	HCT-116	colon:	n/a
26	chr4:3591253-3591303	RPTEC	kidney:	n/a
27	chr4:3597739-3597789	NT2-D1	testis:	n/a
28	chr4:3597739-3597789	HCT-116	colon:	n/a
29	chr4:3576273-3576323	PANC-1	pancreas:	n/a
30	chr4:3576489-3576539	AG04449	skin:	fetal
31	chr4:3576273-3576323	NT2-D1	testis:	n/a
32	chr4:3591243-3591293	SK-N-MC	brain:	n/a
33	chr4:3578432-3578482	HAEpiC	amniotic membrane:	n/a
34	chr4:3597580-3597630	BJ	skin:	n/a
35	chr4:3591253-3591303	HCF	heart:	n/a
36	chr4:3597739-3597789	HEK293	kidney:	embryo
37	chr4:3591216-3591266	SK-N-MC	brain:	n/a
38	chr4:3578432-3578482	NT2-D1	testis:	n/a
39	chr4:3591243-3591293	H1-hESC	embryonic stem cell:	embryo
40	chr4:3597859-3597909	HRE	kidney:	n/a
41	chr4:3572794-3572844	LNCaP	prostate:	n/a
42	chr4:3591253-3591303	GM12878	blood:	n/a
43	chr4:3577496-3577546	LNCaP	prostate:	n/a
44	chr4:3572794-3572844	K562	blood:	n/a
45	chr4:3591216-3591266	HRPEpiC	eye:	n/a
46	chr4:3576273-3576323	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:3597739-3597789	Hela-S3	cervix:	n/a
48	chr4:3591243-3591293	K562	blood:	n/a
49	chr4:3576489-3576539	NT2-D1	testis:	n/a
50	chr4:3577650-3577700	HL-60	blood:	n/a

(count:20 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 2573 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2573 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4110464	chr4:3572484-3572485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561694797	chr4:3572486-3572487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182747387	chr4:3572494-3572495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547326425	chr4:3572504-3572505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572299364	chr4:3572510-3572511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58317230	chr4:3572511-3572512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539086369	chr4:3572540-3572541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200221443	chr4:3572544-3572545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549363214	chr4:3572560-3572561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71636724	chr4:3572578-3572579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569440383	chr4:3572589-3572590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535186409	chr4:3572648-3572649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58586227	chr4:3572673-3572674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555943806	chr4:3572693-3572694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187993988	chr4:3572703-3572704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145568758	chr4:3572704-3572705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535331330	chr4:3572724-3572725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558452803	chr4:3572725-3572726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578248425	chr4:3572734-3572735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149472866	chr4:3572741-3572742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369174980	chr4:3572743-3572744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543887697	chr4:3572745-3572746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13106128	chr4:3572762-3572763	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs59655376	chr4:3572768-3572769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563655741	chr4:3572779-3572780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574092883	chr4:3572784-3572785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60905545	chr4:3572795-3572796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542724567	chr4:3572800-3572801	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs10049521	chr4:3572803-3572804	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs561921100	chr4:3572846-3572847	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs73796116	chr4:3572854-3572855	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs73084733	chr4:3572866-3572867	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs66591121	chr4:3572887-3572888	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs527453211	chr4:3572918-3572919	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs547559092	chr4:3572940-3572941	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs73084736	chr4:3572941-3572942	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs564086208	chr4:3572970-3572971	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs4989442	chr4:3572975-3572976	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs4989443	chr4:3572984-3572985	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs4989444	chr4:3572993-3572994	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs533035027	chr4:3573016-3573017	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs79392131	chr4:3573021-3573022	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs549399794	chr4:3573037-3573038	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs569276859	chr4:3573052-3573053	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs4989445	chr4:3573061-3573062	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs4989446	chr4:3573076-3573077	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs4999852	chr4:3573094-3573095	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs4999853	chr4:3573108-3573109	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs4999854	chr4:3573111-3573112	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs566273460	chr4:3573131-3573132	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	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:241 , 50 per page) page: 1 2 3 4 5

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	chr4:3572000-3573000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:3572800-3573600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr4:3573000-3573400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
6	chr4:3573000-3575600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:3573000-3580200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:3573800-3574200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
9	chr4:3573800-3574800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr4:3573800-3578200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:3574000-3574400	ZNF genes & repeats	Spleen	Spleen
12	chr4:3574200-3574600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:3574200-3574800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
14	chr4:3574400-3574800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
15	chr4:3574600-3575200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:3575200-3576400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:3575600-3575800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr4:3576000-3579600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:3576400-3576600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:3576400-3576600	Enhancers	Gastric	stomach
21	chr4:3576600-3577600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr4:3576600-3580200	Weak transcription	Gastric	stomach
23	chr4:3576800-3578600	Enhancers	Fetal Intestine Large	intestine
24	chr4:3577000-3577200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:3577000-3577200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:3577000-3578600	Enhancers	Fetal Intestine Small	intestine
27	chr4:3577200-3577400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:3577200-3577400	Bivalent Enhancer	HepG2	liver
29	chr4:3577400-3577600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:3577400-3577800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr4:3577400-3578000	Flanking Bivalent TSS/Enh	HepG2	liver
32	chr4:3577600-3577800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:3577600-3577800	Bivalent Enhancer	Right Ventricle	heart
34	chr4:3577600-3578800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:3577800-3578200	Enhancers	Duodenum Mucosa	Duodenum
36	chr4:3578000-3578400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
37	chr4:3578000-3578600	Flanking Active TSS	HepG2	liver
38	chr4:3578200-3578400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr4:3578200-3578400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr4:3578400-3578800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
41	chr4:3578400-3579000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr4:3578600-3578800	Active TSS	Fetal Intestine Large	intestine
43	chr4:3578600-3578800	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr4:3578600-3579200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
45	chr4:3578600-3579400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:3578600-3579400	Enhancers	HepG2	liver
47	chr4:3578600-3579600	Flanking Active TSS	Fetal Intestine Small	intestine
48	chr4:3578800-3579000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:3578800-3579000	Flanking Active TSS	Fetal Intestine Large	intestine
50	chr4:3578800-3579400	Active TSS	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links