Variant report

Variant	nsv881399
Chromosome Location	chr4:165754241-165833645
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 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	ATF2	chr4:165797902-165798295	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:165819988-165820431	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:165820081-165820453	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:165815873-165816270	GM12878	blood:	n/a	n/a
5	BATF	chr4:165815851-165816286	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:165798206-165798475	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:165811702-165812242	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:165815953-165816206	GM12878	blood:	n/a	n/a
9	CEBPB	chr4:165826250-165826537	K562	blood:	n/a	chr4:165826399-165826410
10	CEBPB	chr4:165824559-165824582	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:165802030-165802424	MCF-7	breast:	n/a	n/a
12	CEBPB	chr4:165801600-165801995	H1-hESC	embryonic stem cell:	n/a	chr4:165801839-165801856 chr4:165801842-165801855 chr4:165801797-165801808
13	CEBPB	chr4:165787890-165788501	H1-hESC	embryonic stem cell:	n/a	chr4:165788490-165788498
14	CEBPB	chr4:165814888-165815064	K562	blood:	n/a	n/a
15	CEBPB	chr4:165826047-165826433	A549	lung:	n/a	chr4:165826085-165826098 chr4:165826399-165826410
16	CEBPB	chr4:165814884-165815014	A549	lung:	n/a	n/a
17	CEBPB	chr4:165824361-165824554	K562	blood:	n/a	n/a
18	CEBPB	chr4:165801664-165801932	HepG2	liver:	n/a	chr4:165801839-165801856 chr4:165801842-165801855 chr4:165801797-165801808
19	CEBPB	chr4:165814991-165815031	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:165826242-165826531	HepG2	liver:	n/a	chr4:165826399-165826410
21	CEBPB	chr4:165826081-165826493	H1-hESC	embryonic stem cell:	n/a	chr4:165826085-165826098 chr4:165826399-165826410
22	CHD1	chr4:165801109-165801557	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr4:165798069-165800388	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr4:165800716-165800843	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr4:165801727-165801927	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr4:165816236-165816280	GM12878	blood:	n/a	n/a
27	CHD2	chr4:165798043-165798606	GM12878	blood:	n/a	n/a
28	CTCF	chr4:165805360-165805510	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr4:165805348-165805542	LNCaP	prostate:	n/a	n/a
30	CTCF	chr4:165805360-165805510	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr4:165805360-165805510	GM12875	blood:	n/a	n/a
32	CTCF	chr4:165777016-165777089	ProgFib	skin:	n/a	n/a
33	CTCF	chr4:165805320-165805470	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr4:165805427-165805459	Fibrobl	skin:	n/a	n/a
35	CTCF	chr4:165805570-165805604	Lung_OC	lung:	n/a	n/a
36	CTCF	chr4:165805255-165805643	GM12878	blood:	n/a	n/a
37	CTCF	chr4:165805360-165805510	AG09319	gingival:	n/a	n/a
38	CTCF	chr4:165805316-165805682	SK-N-SH	brain:	n/a	n/a
39	CTCF	chr4:165805420-165805570	HVMF	connective:	n/a	n/a
40	CTCF	chr4:165805318-165805555	HepG2	liver:	n/a	n/a
41	CTCF	chr4:165805420-165805570	HCT-116	colon:	n/a	n/a
42	CTCF	chr4:165805360-165805510	SAEC	small airway:	n/a	n/a
43	CTCF	chr4:165805320-165805470	GM12871	blood:	n/a	n/a
44	CTCF	chr4:165773533-165773592	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:165805320-165805470	HepG2	liver:	n/a	n/a
46	CTCF	chr4:165805420-165805570	HAc	cerebellar:	n/a	n/a
47	CTCF	chr4:165808228-165808276	GM20000	blood:	n/a	n/a
48	CTCF	chr4:165798288-165798325	GM19239	blood:	n/a	n/a
49	CTCF	chr4:165805319-165805560	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:165805324-165805555	GM10266	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165770585-165770635	IMR90	lung:	fetal
2	chr4:165798316-165798366	GM12891	blood:	n/a
3	chr4:165798316-165798366	AG09319	gingival:	n/a
4	chr4:165798316-165798366	PANC-1	pancreas:	n/a
5	chr4:165770585-165770635	HL-60	blood:	n/a
6	chr4:165798316-165798366	SK-N-MC	brain:	n/a
7	chr4:165770585-165770635	HMEC	breast:	n/a
8	chr4:165798316-165798366	PFSK-1	brain:	n/a
9	chr4:165770585-165770635	A549	lung:	n/a
10	chr4:165798316-165798366	GM06990	blood:	n/a
11	chr4:165798316-165798366	HAEpiC	amniotic membrane:	n/a
12	chr4:165770585-165770635	SK-N-SH	brain:	n/a
13	chr4:165798316-165798366	HCF	heart:	n/a
14	chr4:165798316-165798366	SAEC	small airway:	n/a
15	chr4:165798316-165798366	AG10803	skin:	n/a
16	chr4:165798316-165798366	HL-60	blood:	n/a
17	chr4:165798316-165798366	HEK293	kidney:	embryo
18	chr4:165770585-165770635	NB4	blood:	n/a
19	chr4:165770585-165770635	NT2-D1	testis:	n/a
20	chr4:165770585-165770635	HRCEpiC	kidney:	n/a
21	chr4:165798316-165798366	MCF10A-Er-Src	breast:	n/a
22	chr4:165770585-165770635	HCT-116	colon:	n/a
23	chr4:165798316-165798366	HIPEpiC	eye:	n/a
24	chr4:165770585-165770635	NHDF-neo	bronchial:	n/a
25	chr4:165770585-165770635	HRPEpiC	eye:	n/a
26	chr4:165770585-165770635	AoSMC	blood vessel:	n/a
27	chr4:165798316-165798366	T-47D	breast:	n/a
28	chr4:165798316-165798366	SK-N-SH	brain:	n/a
29	chr4:165770585-165770635	NH-A	brain:	n/a
30	chr4:165798316-165798366	NT2-D1	testis:	n/a
31	chr4:165770585-165770635	AG09319	gingival:	n/a
32	chr4:165770585-165770635	HNPCEpiC	eye:	n/a
33	chr4:165798316-165798366	HCPEpiC	choroid plexus:	n/a
34	chr4:165798316-165798366	U87	brain:	n/a
35	chr4:165770585-165770635	MCF10A-Er-Src	breast:	n/a
36	chr4:165798316-165798366	HCT-116	colon:	n/a
37	chr4:165798316-165798366	GM19239	blood:	n/a
38	chr4:165798316-165798366	BJ	skin:	n/a
39	chr4:165770585-165770635	HEEpiC	esophagus:	n/a
40	chr4:165770585-165770635	AG10803	skin:	n/a
41	chr4:165798316-165798366	Caco-2	colon:	n/a
42	chr4:165798316-165798366	NHBE	bronchial:	n/a
43	chr4:165798316-165798366	AG04449	skin:	fetal
44	chr4:165798316-165798366	HUVEC	blood vessel:	n/a
45	chr4:165770585-165770635	RPTEC	kidney:	n/a
46	chr4:165770585-165770635	HCM	heart:	n/a
47	chr4:165798316-165798366	HepG2	liver:	n/a
48	chr4:165798316-165798366	IMR90	lung:	fetal
49	chr4:165770585-165770635	HepG2	liver:	n/a
50	chr4:165798316-165798366	A549	lung:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:165700661..165701216-chr4:165804953..165805488,2	MCF-7	breast:
2	chr4:165800303..165802984-chr4:165804742..165807562,2	K562	blood:
3	chr4:165772859..165774381-chr4:165791100..165793270,2	MCF-7	breast:
4	chr4:165830577..165832077-chr7:25164613..25166543,2	MCF-7	breast:
5	chr4:165800303..165802984-chr4:165804742..165807562,2	K562	blood:
6	chr4:165818735..165821525-chr4:166031427..166033920,2	K562	blood:
7	chr4:165833603..165835632-chr4:165838442..165840941,2	MCF-7	breast:
8	chr4:165786297..165787799-chr4:165799445..165800981,2	MCF-7	breast:
9	chr4:165700977..165701537-chr4:165804617..165805893,3	MCF-7	breast:
10	chr4:165786297..165787799-chr4:165799445..165800981,2	MCF-7	breast:
11	chr4:165772859..165774381-chr4:165791100..165793270,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-1	chr4:165817960-165818137	ENSG00000248329
2	lnc-C4orf39-1	chr4:165798156-165798559	ENSG00000248329
3	lnc-C4orf39-1	chr4:165800072-165800161	ENSG00000248329
4	lnc-C4orf39-1	chr4:165819878-165820117	ENSG00000248329
5	lnc-C4orf39-1	chr4:165816568-165818675	ENSG00000248329
6	lnc-C4orf39-1	chr4:165819878-165820117	ENSG00000248329
7	lnc-C4orf39-1	chr4:165800072-165800161	ENSG00000248329
8	lnc-C4orf39-1	chr4:165817616-165818137	ENSG00000248329
9	lnc-C4orf39-1	chr4:165816368-165818669	NONHSAT099084
10	lnc-C4orf39-1	chr4:165798346-165798559	ENSG00000248329
11	lnc-C4orf39-1	chr4:165798156-165798559	NONHSAT099080
12	lnc-C4orf39-1	chr4:165798394-165798559	ENSG00000248329
13	lnc-C4orf39-1	chr4:165816568-165818676	NONHSAT099080
14	lnc-C4orf39-1	chr4:165800023-165800066	FPKM1_group_24404_transcript_2
15	lnc-C4orf39-1	chr4:165800072-165800408	ENSG00000248329
16	lnc-C4orf39-1	chr4:165800072-165800161	NONHSAT099080
17	lnc-C4orf39-1	chr4:165798158-165798562	FPKM1_group_24404_transcript_2

No data

Variant related genes	Relation type
TRIM60P14	TF binding region
ENSG00000248329	TF binding region
TRIM60P14	CpG island
ENSG00000248329	CpG island
ENSG00000172115	chromatin interactions
VANGL1	miRNA target sites
TMEM63B	miRNA target sites
DNAJB4	miRNA target sites
NSF	miRNA target sites
EZH2	miRNA target sites
RNF149	miRNA target sites
FANCC	miRNA target sites
SAPS2	miRNA target sites
TRAIP	miRNA target sites
DENR	miRNA target sites

Extended variants
information (count: 3044 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3044 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10034282	chr4:165754241-165754242	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542140294	chr4:165754248-165754249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561978765	chr4:165754279-165754280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562817768	chr4:165754307-165754308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73871504	chr4:165754338-165754339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541196211	chr4:165754343-165754344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551754405	chr4:165754344-165754345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554583520	chr4:165754364-165754365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145463179	chr4:165754366-165754367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs28481651	chr4:165754370-165754371	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs567545394	chr4:165754467-165754468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73871505	chr4:165754481-165754482	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs80137910	chr4:165754522-165754523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147281787	chr4:165754531-165754532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77687191	chr4:165754536-165754537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538963254	chr4:165754545-165754546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113225298	chr4:165754567-165754568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557828635	chr4:165754594-165754595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570018217	chr4:165754666-165754667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7679273	chr4:165754705-165754706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs370049843	chr4:165754713-165754714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7678940	chr4:165754744-165754745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs567992043	chr4:165754750-165754751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573743741	chr4:165754778-165754779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184263035	chr4:165754781-165754782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116689929	chr4:165754805-165754806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577914075	chr4:165754878-165754879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544964476	chr4:165754885-165754886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560146624	chr4:165754914-165754915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533752345	chr4:165754948-165754949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527654641	chr4:165754973-165754974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377154642	chr4:165754976-165754977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369419381	chr4:165754977-165754978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7679373	chr4:165755004-165755005	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs572897423	chr4:165755005-165755006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531667983	chr4:165755015-165755016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7657848	chr4:165755042-165755043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7679551	chr4:165755081-165755082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs112951693	chr4:165755103-165755104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114296134	chr4:165755169-165755170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373147272	chr4:165755195-165755196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188550122	chr4:165755210-165755211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149114892	chr4:165755233-165755234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181001940	chr4:165755261-165755262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567356776	chr4:165755350-165755351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142195222	chr4:165755356-165755357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556362022	chr4:165755409-165755410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577746645	chr4:165755423-165755424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544928646	chr4:165755429-165755430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151149691	chr4:165755449-165755450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165749800-165765400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:165753800-165754600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:165764200-165765600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr4:165764600-165764800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr4:165764600-165765000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr4:165764600-165765000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:165764600-165765600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:165764600-165765800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:165764600-165765800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:165764600-165765800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:165764800-165765800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:165765000-165765400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr4:165765000-165765400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:165765400-165765600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr4:165765400-165765600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr4:165765400-165765600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:165765400-165765800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:165765600-165765800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:165765600-165767800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr4:165765600-165769800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr4:165765600-165770000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:165765800-165767400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr4:165765800-165767600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:165765800-165767800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:165765800-165769400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr4:165767400-165768200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:165767600-165768400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:165767600-165768600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:165767800-165768000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:165767800-165768000	Enhancers	Fetal Muscle Leg	muscle
31	chr4:165767800-165768200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr4:165767800-165768400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr4:165768400-165769400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:165768600-165768800	Enhancers	Fetal Muscle Leg	muscle
35	chr4:165769400-165770200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:165769600-165769800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr4:165770000-165770200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr4:165770000-165770200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:165770000-165770200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:165777000-165777200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:165777000-165777200	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:165777200-165780800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:165777600-165778000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr4:165782200-165787000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr4:165786000-165786200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:165786200-165787000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:165786400-165786600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr4:165786400-165786600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:165786600-165787800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:165786600-165787800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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