Variant report

Variant	nsv593466
Chromosome Location	chr4:3753417-3767556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:488)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:3758020-3758360	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr4:3758099-3758431	GM12878	blood:	n/a	n/a
3	ATF3	chr4:3758036-3758482	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:3758109-3758373	K562	blood:	n/a	n/a
5	CCNT2	chr4:3767173-3768168	K562	blood:	n/a	chr4:3768060-3768069
6	CEBPB	chr4:3755791-3756185	H1-hESC	embryonic stem cell:	n/a	chr4:3755959-3755976
7	CEBPD	chr4:3767448-3767956	HepG2	liver:	n/a	n/a
8	CHD2	chr4:3767139-3767236	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr4:3758121-3758413	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr4:3767366-3767479	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:3767320-3767470	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr4:3767380-3767524	GM13977	blood:	n/a	n/a
13	CTCF	chr4:3767309-3767561	A549	lung:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
14	CTCF	chr4:3767380-3767458	GM12878	blood:	n/a	n/a
15	CTCF	chr4:3767320-3767470	HFF-Myc	foreskin:	n/a	n/a
16	CTCF	chr4:3767320-3767470	AG10803	skin:	n/a	n/a
17	CTCF	chr4:3767288-3767472	K562	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
18	CTCF	chr4:3767300-3767450	Caco-2	colon:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
19	CTCF	chr4:3767180-3767330	GM12867	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
20	CTCF	chr4:3767290-3767843	K562	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
21	CTCF	chr4:3767360-3767510	GM12870	blood:	n/a	n/a
22	CTCF	chr4:3767400-3767550	SAEC	small airway:	n/a	n/a
23	CTCF	chr4:3767320-3767470	NHEK	skin:	n/a	n/a
24	CTCF	chr4:3767323-3767542	LNCaP	prostate:	n/a	n/a
25	CTCF	chr4:3767240-3767470	HFF	foreskin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
26	CTCF	chr4:3767340-3767490	HMEC	breast:	n/a	n/a
27	CTCF	chr4:3767180-3767605	H1-hESC	embryonic stem cell:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
28	CTCF	chr4:3767326-3767549	K562	blood:	n/a	n/a
29	CTCF	chr4:3767340-3767490	HVMF	connective:	n/a	n/a
30	CTCF	chr4:3767340-3767519	ProgFib	skin:	n/a	n/a
31	CTCF	chr4:3767260-3767570	HepG2	liver:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
32	CTCF	chr4:3767320-3767470	GM12871	blood:	n/a	n/a
33	CTCF	chr4:3767340-3767490	HCT-116	colon:	n/a	n/a
34	CTCF	chr4:3767396-3767451	GM19240	blood:	n/a	n/a
35	CTCF	chr4:3767300-3767450	AG04449	skin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
36	CTCF	chr4:3767320-3767470	GM12874	blood:	n/a	n/a
37	CTCF	chr4:3767360-3767510	GM12866	blood:	n/a	n/a
38	CTCF	chr4:3767220-3767614	H1-hESC	embryonic stem cell:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
39	CTCF	chr4:3767320-3767470	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr4:3764973-3765001	GM12891	blood:	n/a	n/a
41	CTCF	chr4:3767263-3767870	K562	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
42	CTCF	chr4:3767330-3767529	A549	lung:	n/a	n/a
43	CTCF	chr4:3767320-3767470	GM12869	blood:	n/a	n/a
44	CTCF	chr4:3767300-3767450	HEK293	kidney:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
45	CTCF	chr4:3767380-3767530	GM12872	blood:	n/a	n/a
46	CTCF	chr4:3767140-3767290	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:3767380-3767530	GM12864	blood:	n/a	n/a
48	CTCF	chr4:3767340-3767537	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:3767300-3767450	HRE	kidney:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
50	CTCF	chr4:3767300-3767450	AG09319	gingival:	n/a	chr4:3767314-3767327 chr4:3767312-3767325

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3765047-3765097	NHDF-neo	bronchial:	n/a
2	chr4:3765047-3765097	AG04450	lung:	fetal
3	chr4:3765047-3765097	BE2_C	brain:	n/a
4	chr4:3767073-3767123	GM19239	blood:	n/a
5	chr4:3766875-3766925	RPTEC	kidney:	n/a
6	chr4:3766656-3766706	HL-60	blood:	n/a
7	chr4:3766875-3766925	ECC-1	luminal epithelium:	n/a
8	chr4:3766875-3766925	AG09309	skin:	n/a
9	chr4:3767169-3767219	SK-N-SH	brain:	n/a
10	chr4:3765047-3765097	HEEpiC	esophagus:	n/a
11	chr4:3766656-3766706	HIPEpiC	eye:	n/a
12	chr4:3766875-3766925	NT2-D1	testis:	n/a
13	chr4:3766656-3766706	AoSMC	blood vessel:	n/a
14	chr4:3767169-3767219	HIPEpiC	eye:	n/a
15	chr4:3766656-3766706	HCF	heart:	n/a
16	chr4:3766875-3766925	HEEpiC	esophagus:	n/a
17	chr4:3765047-3765097	H1-hESC	embryonic stem cell:	embryo
18	chr4:3766875-3766925	CMK	blood:	n/a
19	chr4:3767402-3767452	BJ	skin:	n/a
20	chr4:3765047-3765097	ProgFib	skin:	n/a
21	chr4:3766151-3766201	NHBE	bronchial:	n/a
22	chr4:3766656-3766706	Caco-2	colon:	n/a
23	chr4:3767169-3767219	GM12892	blood:	n/a
24	chr4:3756001-3756051	HepG2	liver:	n/a
25	chr4:3767402-3767452	SK-N-SH	brain:	n/a
26	chr4:3767169-3767219	Hela-S3	cervix:	n/a
27	chr4:3767073-3767123	PrEC	prostate:	n/a
28	chr4:3767169-3767219	SK-N-SH_RA	brain:	n/a
29	chr4:3767169-3767219	HNPCEpiC	eye:	n/a
30	chr4:3766875-3766925	PFSK-1	brain:	n/a
31	chr4:3766151-3766201	HCT-116	colon:	n/a
32	chr4:3766875-3766925	HL-60	blood:	n/a
33	chr4:3756001-3756051	BE2_C	brain:	n/a
34	chr4:3766656-3766706	HNPCEpiC	eye:	n/a
35	chr4:3767402-3767452	AoSMC	blood vessel:	n/a
36	chr4:3767073-3767123	SKMC	muscle:	n/a
37	chr4:3767402-3767452	AG09309	skin:	n/a
38	chr4:3767169-3767219	HEEpiC	esophagus:	n/a
39	chr4:3767169-3767219	K562	blood:	n/a
40	chr4:3767402-3767452	GM12891	blood:	n/a
41	chr4:3766875-3766925	NB4	blood:	n/a
42	chr4:3766656-3766706	HUVEC	blood vessel:	n/a
43	chr4:3766151-3766201	SK-N-SH_RA	brain:	n/a
44	chr4:3756001-3756051	ovcar-3	ovarian:	n/a
45	chr4:3766151-3766201	NT2-D1	testis:	n/a
46	chr4:3766151-3766201	NH-A	brain:	n/a
47	chr4:3766656-3766706	CMK	blood:	n/a
48	chr4:3766875-3766925	HMEC	breast:	n/a
49	chr4:3766875-3766925	HRE	kidney:	n/a
50	chr4:3766151-3766201	AoSMC	blood vessel:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3766468..3768028-chr4:3774128..3775785,2	MCF-7	breast:
2	chr4:3750111..3752894-chr4:3765280..3767505,2	MCF-7	breast:
3	chr4:3747628..3750191-chr4:3756565..3759403,2	K562	blood:
4	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
5	chr4:3767101..3767926-chr4:3787451..3788371,3	MCF-7	breast:
6	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:
7	chr4:3532933..3534970-chr4:3765784..3768236,2	MCF-7	breast:
8	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
9	chr4:3757289..3759766-chr4:3767491..3769392,2	MCF-7	breast:
10	chr4:3750945..3752537-chr4:3756085..3758500,2	K562	blood:
11	chr4:3767078..3767943-chr4:3882124..3882913,2	MCF-7	breast:
12	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:
13	chr4:3757965..3759799-chr4:3762426..3765280,2	MCF-7	breast:
14	chr4:3767262..3767834-chr4:3882421..3882953,2	K562	blood:
15	chr4:3750242..3752537-chr4:3756049..3758500,3	K562	blood:
16	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
17	chr19:54974695..54977436-chr4:3766258..3768919,2	MCF-7	breast:
18	chr4:3750756..3752825-chr4:3753589..3756091,2	MCF-7	breast:
19	chr4:3754355..3758397-chr4:3760571..3763729,4	K562	blood:
20	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
21	chr4:3754355..3758397-chr4:3760571..3763729,4	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
ENSG00000182909	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000250986	chromatin interactions

Extended variants
information (count: 678 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:678 , 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	rs10013535	chr4:3753417-3753418	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs77722736	chr4:3753432-3753433	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs570542772	chr4:3753463-3753464	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs540073840	chr4:3753479-3753480	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs535710201	chr4:3753528-3753529	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs576856607	chr4:3753558-3753559	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs542163621	chr4:3753561-3753562	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs4916613	chr4:3753586-3753587	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572925053	chr4:3753614-3753615	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs540016606	chr4:3753641-3753642	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs575765227	chr4:3753668-3753669	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs541388468	chr4:3753669-3753670	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs564268563	chr4:3753749-3753750	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs539621912	chr4:3753775-3753776	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs140741814	chr4:3753804-3753805	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs34779659	chr4:3753822-3753823	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs558362348	chr4:3753865-3753866	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs545631404	chr4:3753866-3753867	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs562338958	chr4:3753874-3753875	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs144651339	chr4:3753888-3753889	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs367676114	chr4:3753901-3753902	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs184389307	chr4:3753942-3753943	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs563273613	chr4:3753955-3753956	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs547402801	chr4:3753969-3753970	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs530857916	chr4:3753979-3753980	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs570601668	chr4:3754113-3754114	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs376136265	chr4:3754124-3754125	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs545747515	chr4:3754139-3754140	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs190585658	chr4:3754141-3754142	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs570165093	chr4:3754171-3754172	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs536012051	chr4:3754187-3754188	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs193245938	chr4:3754200-3754201	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs572676735	chr4:3754211-3754212	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs534740051	chr4:3754216-3754217	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs73792652	chr4:3754238-3754239	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs577760268	chr4:3754253-3754254	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs367925454	chr4:3754266-3754267	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs573245860	chr4:3754293-3754294	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs55658541	chr4:3754338-3754339	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184559945	chr4:3754340-3754341	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs16844857	chr4:3754348-3754349	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs16844858	chr4:3754366-3754367	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs114740023	chr4:3754370-3754371	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs540775320	chr4:3754374-3754375	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs188953758	chr4:3754382-3754383	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs61169848	chr4:3754398-3754399	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565689475	chr4:3754411-3754412	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs12645890	chr4:3754427-3754428	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574093818	chr4:3754435-3754436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs374288404	chr4:3754443-3754444	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:283 , 50 per page) page: 1 2 3 4 5 6

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	chr4:3752000-3753800	Enhancers	Brain Germinal Matrix	brain
5	chr4:3752400-3755600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr4:3752600-3754000	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:3753000-3753800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:3753000-3756600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:3753200-3755000	Bivalent Enhancer	HepG2	liver
10	chr4:3753600-3755200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr4:3753800-3756600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:3753800-3756800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:3754400-3757000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr4:3754600-3755400	Bivalent Enhancer	Right Ventricle	heart
15	chr4:3754800-3755000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:3754800-3756400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:3754800-3757000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:3755000-3755400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr4:3755000-3756600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:3755200-3755400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
21	chr4:3755200-3755600	Bivalent Enhancer	Adipose Nuclei	Adipose
22	chr4:3755200-3755800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr4:3755200-3756600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr4:3755200-3756800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr4:3755600-3756200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr4:3755600-3756400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:3755800-3756200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr4:3755800-3756200	Enhancers	Fetal Kidney	kidney
29	chr4:3755800-3756800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr4:3756200-3756600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:3756200-3756800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:3756200-3756800	Bivalent Enhancer	Adipose Nuclei	Adipose
33	chr4:3756200-3757200	Enhancers	Right Ventricle	heart
34	chr4:3756200-3757400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
35	chr4:3756200-3764000	Weak transcription	Fetal Kidney	kidney
36	chr4:3756600-3756800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:3756600-3757200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr4:3756800-3757000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr4:3756800-3757000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr4:3756800-3757200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:3756800-3758000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:3757000-3757600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:3757200-3757400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:3757400-3757600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:3757600-3762000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:3758000-3760200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:3758200-3758600	ZNF genes & repeats	Aorta	Aorta
48	chr4:3758600-3761000	Weak transcription	Aorta	Aorta
49	chr4:3759600-3761400	Weak transcription	Spleen	Spleen
50	chr4:3760200-3761400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links