Variant report

Variant	esv2760864
Chromosome Location	chr4:165771791-165835433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 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	chr4:165819988-165820431	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:165820081-165820453	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:165797902-165798295	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:165815851-165816286	GM12878	blood:	n/a	n/a
5	BATF	chr4:165815873-165816270	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:165798206-165798475	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:165815953-165816206	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:165811702-165812242	GM12878	blood:	n/a	n/a
9	CEBPB	chr4:165814991-165815031	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:165826081-165826493	H1-hESC	embryonic stem cell:	n/a	chr4:165826085-165826098 chr4:165826399-165826410
11	CEBPB	chr4:165814888-165815064	K562	blood:	n/a	n/a
12	CEBPB	chr4:165826242-165826531	HepG2	liver:	n/a	chr4:165826399-165826410
13	CEBPB	chr4:165826047-165826433	A549	lung:	n/a	chr4:165826085-165826098 chr4:165826399-165826410
14	CEBPB	chr4:165824559-165824582	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:165826250-165826537	K562	blood:	n/a	chr4:165826399-165826410
16	CEBPB	chr4:165802030-165802424	MCF-7	breast:	n/a	n/a
17	CEBPB	chr4:165834764-165834970	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:165787890-165788501	H1-hESC	embryonic stem cell:	n/a	chr4:165788490-165788498
19	CEBPB	chr4:165824361-165824554	K562	blood:	n/a	n/a
20	CEBPB	chr4:165801600-165801995	H1-hESC	embryonic stem cell:	n/a	chr4:165801839-165801856 chr4:165801842-165801855 chr4:165801797-165801808
21	CEBPB	chr4:165814884-165815014	A549	lung:	n/a	n/a
22	CEBPB	chr4:165834769-165834969	K562	blood:	n/a	n/a
23	CEBPB	chr4:165801664-165801932	HepG2	liver:	n/a	chr4:165801839-165801856 chr4:165801842-165801855 chr4:165801797-165801808
24	CHD1	chr4:165801109-165801557	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr4:165800716-165800843	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr4:165798069-165800388	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr4:165801727-165801927	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:165816236-165816280	GM12878	blood:	n/a	n/a
29	CHD2	chr4:165798043-165798606	GM12878	blood:	n/a	n/a
30	CTCF	chr4:165805440-165805590	GM12869	blood:	n/a	n/a
31	CTCF	chr4:165834794-165834943	GM13977	blood:	n/a	n/a
32	CTCF	chr4:165834747-165834912	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr4:165834760-165834910	GM12878	blood:	n/a	n/a
34	CTCF	chr4:165805320-165805470	GM12866	blood:	n/a	n/a
35	CTCF	chr4:165834920-165835070	GM12864	blood:	n/a	n/a
36	CTCF	chr4:165805340-165805490	GM12867	blood:	n/a	n/a
37	CTCF	chr4:165805360-165805510	GM12869	blood:	n/a	n/a
38	CTCF	chr4:165805336-165805508	HepG2	liver:	n/a	n/a
39	CTCF	chr4:165805358-165805521	GM13976	blood:	n/a	n/a
40	CTCF	chr4:165805360-165805510	Caco-2	colon:	n/a	n/a
41	CTCF	chr4:165805324-165805560	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:165805308-165805544	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:165805420-165805570	BJ	skin:	n/a	n/a
44	CTCF	chr4:165805340-165805512	Medullo	brain:	n/a	n/a
45	CTCF	chr4:165805320-165805470	HepG2	liver:	n/a	n/a
46	CTCF	chr4:165805286-165805627	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:165834680-165834830	GM12866	blood:	n/a	n/a
48	CTCF	chr4:165834720-165834870	GM12872	blood:	n/a	n/a
49	CTCF	chr4:165805340-165805490	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:165805347-165805532	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165798316-165798366	H1-hESC	embryonic stem cell:	embryo
2	chr4:165798316-165798366	HRCEpiC	kidney:	n/a
3	chr4:165798316-165798366	HepG2	liver:	n/a
4	chr4:165798316-165798366	PANC-1	pancreas:	n/a
5	chr4:165798316-165798366	Hela-S3	cervix:	n/a
6	chr4:165798316-165798366	AoSMC	blood vessel:	n/a
7	chr4:165798316-165798366	HEEpiC	esophagus:	n/a
8	chr4:165798316-165798366	AG09309	skin:	n/a
9	chr4:165798316-165798366	ECC-1	luminal epithelium:	n/a
10	chr4:165798316-165798366	SK-N-MC	brain:	n/a
11	chr4:165798316-165798366	GM19239	blood:	n/a
12	chr4:165798316-165798366	BJ	skin:	n/a
13	chr4:165798316-165798366	HUVEC	blood vessel:	n/a
14	chr4:165798316-165798366	GM06990	blood:	n/a
15	chr4:165798316-165798366	HNPCEpiC	eye:	n/a
16	chr4:165798316-165798366	MCF-7	breast:	n/a
17	chr4:165798316-165798366	MCF10A-Er-Src	breast:	n/a
18	chr4:165798316-165798366	PrEC	prostate:	n/a
19	chr4:165798316-165798366	NH-A	brain:	n/a
20	chr4:165798316-165798366	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:165798316-165798366	PFSK-1	brain:	n/a
22	chr4:165798316-165798366	AG10803	skin:	n/a
23	chr4:165798316-165798366	AG04449	skin:	fetal
24	chr4:165798316-165798366	HMEC	breast:	n/a
25	chr4:165798316-165798366	A549	lung:	n/a
26	chr4:165798316-165798366	HCPEpiC	choroid plexus:	n/a
27	chr4:165798316-165798366	Caco-2	colon:	n/a
28	chr4:165798316-165798366	ProgFib	skin:	n/a
29	chr4:165798316-165798366	IMR90	lung:	fetal
30	chr4:165798316-165798366	ovcar-3	ovarian:	n/a
31	chr4:165798316-165798366	BE2_C	brain:	n/a
32	chr4:165798316-165798366	NHBE	bronchial:	n/a
33	chr4:165798316-165798366	HCF	heart:	n/a
34	chr4:165798316-165798366	GM12891	blood:	n/a
35	chr4:165798316-165798366	GM12878	blood:	n/a
36	chr4:165798316-165798366	HEK293	kidney:	embryo
37	chr4:165798316-165798366	SK-N-SH	brain:	n/a
38	chr4:165798316-165798366	T-47D	breast:	n/a
39	chr4:165798316-165798366	GM12892	blood:	n/a
40	chr4:165798316-165798366	CMK	blood:	n/a
41	chr4:165798316-165798366	RPTEC	kidney:	n/a
42	chr4:165798316-165798366	AG04450	lung:	fetal
43	chr4:165798316-165798366	HRE	kidney:	n/a
44	chr4:165798316-165798366	HAEpiC	amniotic membrane:	n/a
45	chr4:165798316-165798366	Hepatocyte	liver:	n/a
46	chr4:165798316-165798366	HIPEpiC	eye:	n/a
47	chr4:165798316-165798366	HRPEpiC	eye:	n/a
48	chr4:165798316-165798366	LNCaP	prostate:	n/a
49	chr4:165798316-165798366	Jurkat	blood:	n/a
50	chr4:165798316-165798366	NHDF-neo	bronchial:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 2439 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2439 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10028712	chr4:165777000-165777001	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs557015284	chr4:165777019-165777020	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs72998131	chr4:165777020-165777021	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs553073124	chr4:165777022-165777023	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs149626562	chr4:165777026-165777027	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs144332745	chr4:165777031-165777032	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs551146424	chr4:165777032-165777033	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs74342048	chr4:165777036-165777037	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs556980314	chr4:165777045-165777046	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs569386156	chr4:165777109-165777110	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs575492830	chr4:165777133-165777134	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs146793970	chr4:165777168-165777169	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs564491754	chr4:165777171-165777172	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs6536871	chr4:165777179-165777180	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs187265603	chr4:165777216-165777217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561804803	chr4:165777219-165777220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529448175	chr4:165777247-165777248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75184310	chr4:165777250-165777251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113729476	chr4:165777306-165777307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563078338	chr4:165777321-165777322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368914691	chr4:165777324-165777325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370394738	chr4:165777370-165777371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527985313	chr4:165777375-165777376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533659720	chr4:165777444-165777445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551911620	chr4:165777445-165777446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144195130	chr4:165777460-165777461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528061567	chr4:165777504-165777505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4588417	chr4:165777512-165777513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs71618422	chr4:165777530-165777531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568117554	chr4:165777533-165777534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374402953	chr4:165777550-165777551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535338012	chr4:165777569-165777570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529050933	chr4:165777609-165777610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs6850057	chr4:165777616-165777617	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs539698264	chr4:165777617-165777618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191762730	chr4:165777620-165777621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs151071214	chr4:165777657-165777658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183930245	chr4:165777686-165777687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140989692	chr4:165777689-165777690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150361454	chr4:165777774-165777775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144974740	chr4:165777784-165777785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114289165	chr4:165777873-165777874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533334549	chr4:165777877-165777878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565600729	chr4:165777929-165777930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545696075	chr4:165777934-165777935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560729599	chr4:165777978-165777979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72695868	chr4:165777992-165777993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139837551	chr4:165778035-165778036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374013228	chr4:165778072-165778073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568204645	chr4:165778123-165778124	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:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165777000-165777200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:165777000-165777200	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:165777200-165780800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:165777600-165778000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:165782200-165787000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr4:165786000-165786200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:165786200-165787000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:165786400-165786600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr4:165786400-165786600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:165786600-165787800	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:165786600-165787800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:165786600-165788400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:165786600-165789400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:165786600-165796000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr4:165786800-165787800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:165787000-165787800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:165787000-165788800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:165787000-165789000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:165787000-165789000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:165787200-165789400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:165787400-165789000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:165787600-165789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:165787800-165788200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr4:165787800-165788200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr4:165787800-165788200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr4:165787800-165788800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:165787800-165789000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr4:165788200-165788600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:165788200-165788600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:165788200-165788800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr4:165788200-165789400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:165788400-165788800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:165788600-165788800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr4:165788600-165788800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr4:165788800-165789000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr4:165788800-165789800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:165789000-165796000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr4:165789000-165796000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr4:165789000-165796000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:165789400-165795600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr4:165792600-165793000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:165792600-165793200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:165792800-165793000	Enhancers	Gastric	stomach
44	chr4:165793000-165798200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:165793200-165796000	Weak transcription	Gastric	stomach
46	chr4:165795000-165797600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr4:165795600-165796200	Enhancers	Fetal Intestine Large	intestine
48	chr4:165795600-165796400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr4:165795600-165797200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:165795600-165797400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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