Variant report

Variant	esv1824573
Chromosome Location	chr4:3754366-3769411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:855)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:3768564-3769140	H1-hESC	embryonic stem cell:	n/a	chr4:3768787-3768801
2	ATF3	chr4:3758036-3758482	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr4:3758109-3758373	K562	blood:	n/a	n/a
4	ATF3	chr4:3758099-3758431	GM12878	blood:	n/a	n/a
5	ATF3	chr4:3758020-3758360	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:3769358-3769598	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3768715-3769081	H1-hESC	embryonic stem cell:	n/a	n/a
8	CCNT2	chr4:3767173-3768168	K562	blood:	n/a	chr4:3768060-3768069
9	CEBPB	chr4:3755791-3756185	H1-hESC	embryonic stem cell:	n/a	chr4:3755959-3755976
10	CEBPD	chr4:3767448-3767956	HepG2	liver:	n/a	n/a
11	CEBPD	chr4:3768042-3768292	HepG2	liver:	n/a	n/a
12	CHD2	chr4:3758121-3758413	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr4:3769391-3769621	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr4:3767139-3767236	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr4:3768617-3769097	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr4:3768574-3769520	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr4:3767309-3767561	A549	lung:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
18	CTCF	chr4:3768840-3768990	Caco-2	colon:	n/a	n/a
19	CTCF	chr4:3769360-3769510	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr4:3767300-3767450	HEK293	kidney:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
21	CTCF	chr4:3767365-3767537	A549	lung:	n/a	n/a
22	CTCF	chr4:3767240-3767470	HFF	foreskin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
23	CTCF	chr4:3769356-3769544	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:3764973-3765001	GM12891	blood:	n/a	n/a
25	CTCF	chr4:3767332-3767536	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:3767695-3767759	HepG2	liver:	n/a	n/a
27	CTCF	chr4:3767341-3767530	NHEK	skin:	n/a	n/a
28	CTCF	chr4:3767328-3767507	Fibrobl	skin:	n/a	n/a
29	CTCF	chr4:3768810-3769086	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:3769360-3769510	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr4:3767660-3767810	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr4:3767340-3767490	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:3767418-3767487	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr4:3768820-3768970	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr4:3768866-3769001	GM19239	blood:	n/a	n/a
36	CTCF	chr4:3768093-3768198	LNCaP	prostate:	n/a	n/a
37	CTCF	chr4:3767360-3767510	GM12866	blood:	n/a	n/a
38	CTCF	chr4:3767403-3767472	GM10266	blood:	n/a	n/a
39	CTCF	chr4:3767320-3767470	NHEK	skin:	n/a	n/a
40	CTCF	chr4:3767300-3767450	AG04449	skin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
41	CTCF	chr4:3768840-3768990	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr4:3769380-3769530	GM12874	blood:	n/a	n/a
43	CTCF	chr4:3769340-3769490	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr4:3767660-3767810	GM12875	blood:	n/a	n/a
45	CTCF	chr4:3767320-3767470	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:3769400-3769550	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:3767380-3767530	GM12868	blood:	n/a	n/a
48	CTCF	chr4:3769356-3769535	Medullo	brain:	n/a	n/a
49	CTCF	chr4:3767290-3767843	K562	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
50	CTCF	chr4:3767260-3767570	HepG2	liver:	n/a	chr4:3767314-3767327 chr4:3767312-3767325

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3767169-3767219	CMK	blood:	n/a
2	chr4:3767169-3767219	CMK	blood:	n/a
3	chr4:3767169-3767219	NH-A	brain:	n/a
4	chr4:3768097-3768147	K562	blood:	n/a
5	chr4:3767073-3767123	GM12878	blood:	n/a
6	chr4:3768555-3768605	HCM	heart:	n/a
7	chr4:3766656-3766706	HCT-116	colon:	n/a
8	chr4:3766875-3766925	HRPEpiC	eye:	n/a
9	chr4:3766151-3766201	AG09319	gingival:	n/a
10	chr4:3765047-3765097	HCPEpiC	choroid plexus:	n/a
11	chr4:3765047-3765097	HCF	heart:	n/a
12	chr4:3767169-3767219	HRPEpiC	eye:	n/a
13	chr4:3768638-3768688	Hela-S3	cervix:	n/a
14	chr4:3768097-3768147	SAEC	small airway:	n/a
15	chr4:3766151-3766201	GM12891	blood:	n/a
16	chr4:3768081-3768131	HCT-116	colon:	n/a
17	chr4:3768078-3768128	HEEpiC	esophagus:	n/a
18	chr4:3767402-3767452	Hela-S3	cervix:	n/a
19	chr4:3767073-3767123	Hepatocyte	liver:	n/a
20	chr4:3766875-3766925	AG09319	gingival:	n/a
21	chr4:3768078-3768128	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:3766656-3766706	HEEpiC	esophagus:	n/a
23	chr4:3766656-3766706	GM06990	blood:	n/a
24	chr4:3767073-3767123	K562	blood:	n/a
25	chr4:3766875-3766925	HNPCEpiC	eye:	n/a
26	chr4:3768555-3768605	HCF	heart:	n/a
27	chr4:3768081-3768131	NT2-D1	testis:	n/a
28	chr4:3756001-3756051	PANC-1	pancreas:	n/a
29	chr4:3768078-3768128	HMEC	breast:	n/a
30	chr4:3768097-3768147	Caco-2	colon:	n/a
31	chr4:3768097-3768147	GM12892	blood:	n/a
32	chr4:3766656-3766706	MCF-7	breast:	n/a
33	chr4:3767073-3767123	HEK293	kidney:	embryo
34	chr4:3765047-3765097	HCM	heart:	n/a
35	chr4:3768555-3768605	NT2-D1	testis:	n/a
36	chr4:3768638-3768688	Caco-2	colon:	n/a
37	chr4:3767169-3767219	HIPEpiC	eye:	n/a
38	chr4:3768078-3768128	SKMC	muscle:	n/a
39	chr4:3768458-3768508	AG04449	skin:	fetal
40	chr4:3767169-3767219	HRCEpiC	kidney:	n/a
41	chr4:3767169-3767219	AG04449	skin:	fetal
42	chr4:3767402-3767452	HUVEC	blood vessel:	n/a
43	chr4:3756001-3756051	AoSMC	blood vessel:	n/a
44	chr4:3766151-3766201	AG10803	skin:	n/a
45	chr4:3767169-3767219	NB4	blood:	n/a
46	chr4:3756001-3756051	AG10803	skin:	n/a
47	chr4:3767169-3767219	U87	brain:	n/a
48	chr4:3766151-3766201	NHBE	bronchial:	n/a
49	chr4:3768078-3768128	AG09319	gingival:	n/a
50	chr4:3766151-3766201	RPTEC	kidney:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3769000..3769555-chr4:3785283..3786137,2	MCF-7	breast:
2	chr4:3747628..3750191-chr4:3756565..3759403,2	K562	blood:
3	chr4:3757965..3759799-chr4:3762426..3765280,2	MCF-7	breast:
4	chr4:3750242..3752537-chr4:3756049..3758500,3	K562	blood:
5	chr4:3767101..3767926-chr4:3787451..3788371,3	MCF-7	breast:
6	chr4:3768745..3771580-chr4:3802446..3805073,2	MCF-7	breast:
7	chr4:3741522..3743412-chr4:3768536..3771001,2	MCF-7	breast:
8	chr4:3754355..3758397-chr4:3760571..3763729,4	K562	blood:
9	chr4:3766468..3768028-chr4:3774128..3775785,2	MCF-7	breast:
10	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:
11	chr4:3767078..3767943-chr4:3882124..3882913,2	MCF-7	breast:
12	chr4:3532933..3534970-chr4:3765784..3768236,2	MCF-7	breast:
13	chr4:3754355..3758397-chr4:3760571..3763729,4	K562	blood:
14	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
15	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
16	chr4:3750756..3752825-chr4:3753589..3756091,2	MCF-7	breast:
17	chr4:3750111..3752894-chr4:3765280..3767505,2	MCF-7	breast:
18	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
19	chr4:3757289..3759766-chr4:3767491..3769392,2	MCF-7	breast:
20	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:
21	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
22	chr4:3767262..3767834-chr4:3882421..3882953,2	K562	blood:
23	chr19:54974695..54977436-chr4:3766258..3768919,2	MCF-7	breast:
24	chr4:3750945..3752537-chr4:3756085..3758500,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-3	chr4:3761872-3765117	XLOC_003862
2	lnc-LRPAP1-3	chr4:3760475-3761753	XLOC_003862

No data

Variant related genes	Relation type
ENSG00000250986	TF binding region
ADRA2C	TF binding region
ENSG00000250986	CpG island
ADRA2C	CpG island
ENSG00000184160	chromatin interactions
ENSG00000250986	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000182909	chromatin interactions

Extended variants
information (count: 696 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16844858	chr4:3754366-3754367	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114740023	chr4:3754370-3754371	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs540775320	chr4:3754374-3754375	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs188953758	chr4:3754382-3754383	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs61169848	chr4:3754398-3754399	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565689475	chr4:3754411-3754412	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs12645890	chr4:3754427-3754428	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs574093818	chr4:3754435-3754436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs374288404	chr4:3754443-3754444	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs542113812	chr4:3754466-3754467	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs549916787	chr4:3754480-3754481	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs569703972	chr4:3754539-3754540	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs377010911	chr4:3754564-3754565	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs535698486	chr4:3754594-3754595	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs181445553	chr4:3754634-3754635	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs566282058	chr4:3754650-3754651	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs138568770	chr4:3754661-3754662	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs557980845	chr4:3754662-3754663	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs185534176	chr4:3754666-3754667	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs140296692	chr4:3754668-3754669	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs115241133	chr4:3754671-3754672	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs145407453	chr4:3754705-3754706	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs541701465	chr4:3754714-3754715	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs17813250	chr4:3754715-3754716	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs138035542	chr4:3754725-3754726	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs541342857	chr4:3754736-3754737	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs564339709	chr4:3754802-3754803	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs9291156	chr4:3754818-3754819	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs549779865	chr4:3754823-3754824	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs9761424	chr4:3754834-3754835	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs528971625	chr4:3754847-3754848	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs9291157	chr4:3754853-3754854	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs149535299	chr4:3754870-3754871	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs534848082	chr4:3754878-3754879	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs374310094	chr4:3754894-3754895	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs9761431	chr4:3754923-3754924	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs571588805	chr4:3754931-3754932	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs567682686	chr4:3754932-3754933	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs60006358	chr4:3754951-3754952	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557317208	chr4:3754965-3754966	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs567701530	chr4:3754985-3754986	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs536754071	chr4:3755000-3755001	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs553152414	chr4:3755001-3755002	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs572286815	chr4:3755023-3755024	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs28684669	chr4:3755024-3755025	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs528880102	chr4:3755041-3755042	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs550188527	chr4:3755072-3755073	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs558111115	chr4:3755089-3755090	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs569431783	chr4:3755105-3755106	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs376681047	chr4:3755144-3755145	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3746400-3754800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:3748200-3758200	Weak transcription	Aorta	Aorta
3	chr4:3750000-3763200	Weak transcription	Pancreas	Pancrea
4	chr4:3752400-3755600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr4:3753000-3756600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:3753200-3755000	Bivalent Enhancer	HepG2	liver
7	chr4:3753600-3755200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr4:3753800-3756600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:3753800-3756800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:3754400-3757000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:3754600-3755400	Bivalent Enhancer	Right Ventricle	heart
12	chr4:3754800-3755000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:3754800-3756400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:3754800-3757000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:3755000-3755400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
16	chr4:3755000-3756600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:3755200-3755400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr4:3755200-3755600	Bivalent Enhancer	Adipose Nuclei	Adipose
19	chr4:3755200-3755800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
20	chr4:3755200-3756600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr4:3755200-3756800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr4:3755600-3756200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr4:3755600-3756400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:3755800-3756200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr4:3755800-3756200	Enhancers	Fetal Kidney	kidney
26	chr4:3755800-3756800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:3756200-3756600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:3756200-3756800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:3756200-3756800	Bivalent Enhancer	Adipose Nuclei	Adipose
30	chr4:3756200-3757200	Enhancers	Right Ventricle	heart
31	chr4:3756200-3757400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr4:3756200-3764000	Weak transcription	Fetal Kidney	kidney
33	chr4:3756600-3756800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:3756600-3757200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr4:3756800-3757000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr4:3756800-3757000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr4:3756800-3757200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:3756800-3758000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:3757000-3757600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:3757200-3757400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:3757400-3757600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:3757600-3762000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:3758000-3760200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:3758200-3758600	ZNF genes & repeats	Aorta	Aorta
45	chr4:3758600-3761000	Weak transcription	Aorta	Aorta
46	chr4:3759600-3761400	Weak transcription	Spleen	Spleen
47	chr4:3760200-3761400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:3760800-3761200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr4:3761000-3762000	Strong transcription	Aorta	Aorta
50	chr4:3761400-3762200	ZNF genes & repeats	Spleen	Spleen

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