Variant report

Variant	esv11788
Chromosome Location	chr4:3535452-3572824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:1161)
Chromatin interactive
region (count:4)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr4:3538736-3538904	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:3570059-3570293	GM12878	blood:	n/a	n/a
3	BCL3	chr4:3565347-3565556	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:3558900-3559131	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:3561241-3561607	HepG2	liver:	n/a	n/a
6	BHLHE40	chr4:3558966-3559121	K562	blood:	n/a	n/a
7	BHLHE40	chr4:3565199-3565519	K562	blood:	n/a	n/a
8	CEBPB	chr4:3551360-3551570	HepG2	liver:	n/a	chr4:3551516-3551529
9	CEBPB	chr4:3558808-3559129	IMR90	lung:	n/a	chr4:3558956-3558967
10	CEBPB	chr4:3558847-3559069	HepG2	liver:	n/a	chr4:3558956-3558967
11	CEBPB	chr4:3551405-3551575	IMR90	lung:	n/a	chr4:3551516-3551529
12	CEBPB	chr4:3558850-3559038	K562	blood:	n/a	chr4:3558956-3558967
13	CEBPB	chr4:3558857-3559121	K562	blood:	n/a	chr4:3558956-3558967
14	CEBPB	chr4:3551364-3551634	K562	blood:	n/a	chr4:3551516-3551529
15	CEBPB	chr4:3558947-3558991	A549	lung:	n/a	chr4:3558956-3558967
16	CEBPB	chr4:3551376-3551680	K562	blood:	n/a	chr4:3551516-3551529
17	CEBPB	chr4:3558850-3559034	K562	blood:	n/a	chr4:3558956-3558967
18	CEBPB	chr4:3560092-3560217	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:3558839-3559070	HepG2	liver:	n/a	chr4:3558956-3558967
20	CEBPB	chr4:3558772-3559159	HepG2	liver:	n/a	chr4:3558956-3558967
21	CEBPB	chr4:3558770-3559163	HepG2	liver:	n/a	chr4:3558956-3558967
22	CEBPD	chr4:3558802-3559114	HepG2	liver:	n/a	n/a
23	CTCF	chr4:3568080-3568230	HepG2	liver:	n/a	n/a
24	CTCF	chr4:3558024-3558307	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:3561455-3561511	LNCaP	prostate:	n/a	n/a
26	CTCF	chr4:3543428-3543512	GM13976	blood:	n/a	n/a
27	CTCF	chr4:3558120-3558270	HCT-116	colon:	n/a	n/a
28	CTCF	chr4:3568248-3568370	ProgFib	skin:	n/a	n/a
29	CTCF	chr4:3568146-3568416	K562	blood:	n/a	n/a
30	CTCF	chr4:3568183-3568428	A549	lung:	n/a	n/a
31	CTCF	chr4:3558060-3558210	BJ	skin:	n/a	n/a
32	CTCF	chr4:3568380-3568530	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr4:3558065-3558260	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr4:3568196-3568394	A549	lung:	n/a	n/a
35	CTCF	chr4:3558040-3558190	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr4:3558060-3558210	AG09309	skin:	n/a	n/a
37	CTCF	chr4:3568080-3568230	BE2_C	brain:	n/a	n/a
38	CTCF	chr4:3568060-3568210	BJ	skin:	n/a	n/a
39	CTCF	chr4:3558090-3558249	HepG2	liver:	n/a	n/a
40	CTCF	chr4:3558080-3558230	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr4:3558100-3558250	A549	lung:	n/a	n/a
42	CTCF	chr4:3558080-3558230	K562	blood:	n/a	n/a
43	CTCF	chr4:3568060-3568210	K562	blood:	n/a	n/a
44	CTCF	chr4:3568244-3568369	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:3568138-3568449	LNCaP	prostate:	n/a	n/a
46	CTCF	chr4:3568230-3568371	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:3537323-3537378	GM13976	blood:	n/a	n/a
48	CTCF	chr4:3558080-3558230	GM12878	blood:	n/a	n/a
49	CTCF	chr4:3558134-3558215	GM12891	blood:	n/a	n/a
50	CTCF	chr4:3558060-3558210	K562	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3567533-3567583	ovcar-3	ovarian:	n/a
2	chr4:3568034-3568084	AG04450	lung:	fetal
3	chr4:3567533-3567583	ovcar-3	ovarian:	n/a
4	chr4:3568034-3568084	AG04450	lung:	fetal
5	chr4:3568236-3568286	A549	lung:	n/a
6	chr4:3569189-3569239	AG04449	skin:	fetal
7	chr4:3571857-3571907	MCF10A-Er-Src	breast:	n/a
8	chr4:3567670-3567720	NHDF-neo	bronchial:	n/a
9	chr4:3572794-3572844	SKMC	muscle:	n/a
10	chr4:3567445-3567495	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:3567958-3568008	SAEC	small airway:	n/a
12	chr4:3567958-3568008	HAEpiC	amniotic membrane:	n/a
13	chr4:3567445-3567495	GM12891	blood:	n/a
14	chr4:3568520-3568570	AG09319	gingival:	n/a
15	chr4:3565646-3565696	BE2_C	brain:	n/a
16	chr4:3565893-3565943	GM12878	blood:	n/a
17	chr4:3563357-3563407	PFSK-1	brain:	n/a
18	chr4:3566660-3566710	Jurkat	blood:	n/a
19	chr4:3568236-3568286	NHBE	bronchial:	n/a
20	chr4:3561751-3561801	HL-60	blood:	n/a
21	chr4:3568520-3568570	RPTEC	kidney:	n/a
22	chr4:3565646-3565696	A549	lung:	n/a
23	chr4:3568236-3568286	GM06990	blood:	n/a
24	chr4:3571857-3571907	MCF-7	breast:	n/a
25	chr4:3565893-3565943	HRE	kidney:	n/a
26	chr4:3572794-3572844	Jurkat	blood:	n/a
27	chr4:3568236-3568286	ECC-1	luminal epithelium:	n/a
28	chr4:3572794-3572844	NT2-D1	testis:	n/a
29	chr4:3566660-3566710	AG04450	lung:	fetal
30	chr4:3567958-3568008	HRE	kidney:	n/a
31	chr4:3568520-3568570	AoSMC	blood vessel:	n/a
32	chr4:3567958-3568008	ovcar-3	ovarian:	n/a
33	chr4:3568034-3568084	HEK293	kidney:	embryo
34	chr4:3569189-3569239	PFSK-1	brain:	n/a
35	chr4:3569189-3569239	BE2_C	brain:	n/a
36	chr4:3565893-3565943	NHDF-neo	bronchial:	n/a
37	chr4:3565646-3565696	IMR90	lung:	fetal
38	chr4:3536906-3536956	HCM	heart:	n/a
39	chr4:3567533-3567583	U87	brain:	n/a
40	chr4:3567670-3567720	NT2-D1	testis:	n/a
41	chr4:3567670-3567720	PANC-1	pancreas:	n/a
42	chr4:3568034-3568084	CMK	blood:	n/a
43	chr4:3571527-3571577	SK-N-SH	brain:	n/a
44	chr4:3566660-3566710	U87	brain:	n/a
45	chr4:3571857-3571907	PFSK-1	brain:	n/a
46	chr4:3567670-3567720	BE2_C	brain:	n/a
47	chr4:3571527-3571577	SKMC	muscle:	n/a
48	chr4:3569189-3569239	GM19239	blood:	n/a
49	chr4:3567533-3567583	Hela-S3	cervix:	n/a
50	chr4:3567958-3568008	NB4	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3557568..3561232-chr4:3567417..3570129,3	K562	blood:
2	chr4:3532686..3534345-chr4:3544776..3546772,2	MCF-7	breast:
3	chr4:3557568..3561232-chr4:3567417..3570129,3	K562	blood:
4	chr4:3485927..3488368-chr4:3533732..3536345,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-2	chr4:3550401-3550523	NONHSAT094884
2	lnc-RP3-368B9.1.1-6	chr4:3561789-3562236	ucscGeneNc_uc003ghk_1
3	lnc-RP3-368B9.1.1-2	chr4:3546615-3546650	XLOC_003427
4	lnc-RP3-368B9.1.1-2	chr4:3546822-3546956	XLOC_003427
5	lnc-RP3-368B9.1.1-2	chr4:3546433-3547467	NONHSAT094884
6	lnc-RP3-368B9.1.1-6	chr4:3548394-3548648	ucscGeneNc_uc003ghk_1
7	lnc-RP3-368B9.1.1-2	chr4:3546822-3546956	ENSG00000270090.1
8	lnc-RP3-368B9.1.1-2	chr4:3546282-3546650	ENSG00000270090.1
9	lnc-RP3-368B9.1.1-2	chr4:3547897-3548075	XLOC_003427
10	lnc-RP3-368B9.1.1-2	chr4:3547241-3547393	XLOC_003427
11	lnc-RP3-368B9.1.1-2	chr4:3550402-3550523	XLOC_003427
12	lnc-RP3-368B9.1.1-2	chr4:3547897-3548077	XLOC_003427
13	lnc-RP3-368B9.1.1-2	chr4:3550188-3550315	ENSG00000270090.1
14	lnc-RP3-368B9.1.1-2	chr4:3547896-3548077	NONHSAT094884
15	lnc-RP3-368B9.1.1-2	chr4:3550188-3550309	XLOC_003427
16	lnc-RP3-368B9.1.1-2	chr4:3546822-3546956	XLOC_003427
17	lnc-RP3-368B9.1.1-2	chr4:3546453-3546650	XLOC_003427
18	lnc-RP3-368B9.1.1-6	chr4:3560459-3560539	ucscGeneNc_uc003ghk_1
19	lnc-RP3-368B9.1.1-2	chr4:3550187-3550309	NONHSAT094884
20	lnc-RP3-368B9.1.1-2	chr4:3546666-3547063	XLOC_003427
21	lnc-RP3-368B9.1.1-6	chr4:3559576-3559712	ucscGeneNc_uc003ghk_1

No data

Variant related genes	Relation type
ENSG00000270090	TF binding region
LRPAP1	TF binding region
ENSG00000270090	CpG island
LRPAP1	CpG island
ENSG00000175920	chromatin interactions
ENSG00000163956	chromatin interactions
TGFB2	miRNA target sites
TGFBI	miRNA target sites
TGFA	miRNA target sites

Extended variants
information (count: 1915 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1915 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148923471	chr4:3535476-3535477	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548936572	chr4:3535524-3535525	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569004892	chr4:3535564-3535565	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73793999	chr4:3535606-3535607	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs184510423	chr4:3535619-3535620	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551051721	chr4:3535631-3535632	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147301953	chr4:3535684-3535685	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140976823	chr4:3535703-3535704	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373190647	chr4:3535751-3535752	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557402678	chr4:3535802-3535803	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567912292	chr4:3535811-3535812	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142470081	chr4:3535814-3535815	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs1620149	chr4:3535875-3535876	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs35886504	chr4:3535914-3535915	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2073501	chr4:3535927-3535928	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs1741541	chr4:3535941-3535942	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557824010	chr4:3535957-3535958	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543571530	chr4:3535963-3535964	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189133058	chr4:3535994-3535995	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs193299792	chr4:3535997-3535998	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7672287	chr4:3536002-3536003	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs558964897	chr4:3536029-3536030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528071656	chr4:3536034-3536035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368838714	chr4:3536070-3536071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563931147	chr4:3536095-3536096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2073502	chr4:3536112-3536113	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs544263291	chr4:3536118-3536119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs151134666	chr4:3536146-3536147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531024789	chr4:3536161-3536162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185471753	chr4:3536162-3536163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2073503	chr4:3536176-3536177	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs536906747	chr4:3536180-3536181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200994626	chr4:3536193-3536194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566902014	chr4:3536240-3536241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539022969	chr4:3536253-3536254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs367708522	chr4:3536265-3536266	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs1794431	chr4:3536329-3536330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs10937932	chr4:3536505-3536506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189209774	chr4:3536506-3536507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374980323	chr4:3536514-3536515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369180359	chr4:3536531-3536532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573746539	chr4:3536538-3536539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181654264	chr4:3536564-3536565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs559199685	chr4:3536573-3536574	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs572539456	chr4:3536574-3536575	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs62272719	chr4:3536575-3536576	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs564658160	chr4:3536576-3536577	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs3108671	chr4:3536588-3536589	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530579413	chr4:3536629-3536630	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs550901662	chr4:3536635-3536636	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Lung cancer	18438408	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3535000-3535600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
2	chr4:3535000-3535800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:3535000-3535800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr4:3535000-3535800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:3535000-3536000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
6	chr4:3535000-3536800	Weak transcription	Lung	lung
7	chr4:3535400-3535600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr4:3535400-3535800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr4:3535400-3536000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:3535400-3537000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:3537000-3537200	Enhancers	Lung	lung
12	chr4:3537000-3537400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:3546000-3546200	Bivalent/Poised TSS	HepG2	liver
14	chr4:3546000-3546600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr4:3546000-3546600	Enhancers	HUVEC	blood vessel
16	chr4:3546000-3546800	Enhancers	Lung	lung
17	chr4:3548400-3549200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:3548400-3549200	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr4:3548400-3549200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr4:3548400-3550000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:3548600-3549000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:3548800-3549200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:3548800-3549400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:3548800-3549600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr4:3550600-3580400	Weak transcription	Right Atrium	heart
26	chr4:3554800-3557200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr4:3555000-3560600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr4:3555200-3555400	Enhancers	HepG2	liver
29	chr4:3555200-3558000	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr4:3555600-3558200	Weak transcription	HepG2	liver
31	chr4:3555800-3556200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:3556000-3560800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr4:3556400-3556800	Enhancers	Primary B cells from cord blood	blood
34	chr4:3556800-3557000	Weak transcription	Primary B cells from cord blood	blood
35	chr4:3557000-3557400	Enhancers	Primary B cells from cord blood	blood
36	chr4:3557200-3557400	Enhancers	Spleen	Spleen
37	chr4:3557200-3557800	Bivalent Enhancer	K562	blood
38	chr4:3557200-3558400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:3557200-3559400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr4:3557400-3558000	Bivalent Enhancer	Placenta	Placenta
41	chr4:3557400-3558200	Weak transcription	Primary B cells from cord blood	blood
42	chr4:3557400-3562000	Weak transcription	Spleen	Spleen
43	chr4:3557800-3558400	Enhancers	K562	blood
44	chr4:3558000-3558400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr4:3558000-3559000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr4:3558200-3558600	Enhancers	Primary B cells from cord blood	blood
47	chr4:3558200-3559000	Enhancers	HepG2	liver
48	chr4:3558200-3559200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:3558400-3559000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:3558400-3565200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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