Variant report

Variant	esv2752957
Chromosome Location	chr4:59655302-59923634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:42)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:59730625-59730656	K562	blood:	n/a	n/a
2	ATF2	chr4:59827047-59827354	GM12878	blood:	n/a	n/a
3	BATF	chr4:59828187-59828551	GM12878	blood:	n/a	chr4:59828359-59828370
4	BATF	chr4:59899806-59900046	GM12878	blood:	n/a	chr4:59899946-59899957
5	BATF	chr4:59827032-59827314	GM12878	blood:	n/a	n/a
6	BATF	chr4:59814508-59814738	GM12878	blood:	n/a	n/a
7	BATF	chr4:59828160-59828449	GM12878	blood:	n/a	chr4:59828359-59828370
8	BCL11A	chr4:59828266-59828482	GM12878	blood:	n/a	n/a
9	BCL3	chr4:59828214-59828425	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:59899851-59900022	GM12878	blood:	n/a	n/a
11	CEBPB	chr4:59923562-59923867	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:59676120-59676529	A549	lung:	n/a	n/a
13	CEBPB	chr4:59911007-59911142	H1-hESC	embryonic stem cell:	n/a	chr4:59911074-59911087
14	CEBPB	chr4:59674405-59674716	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:59655963-59656167	IMR90	lung:	n/a	chr4:59656116-59656127 chr4:59656117-59656128 chr4:59656116-59656129
16	CEBPB	chr4:59674430-59674925	IMR90	lung:	n/a	chr4:59674886-59674898
17	CEBPB	chr4:59674501-59674887	A549	lung:	n/a	n/a
18	CEBPB	chr4:59656015-59656160	A549	lung:	n/a	chr4:59656116-59656127 chr4:59656117-59656128 chr4:59656116-59656129
19	CEBPB	chr4:59655951-59656210	HepG2	liver:	n/a	chr4:59656116-59656127 chr4:59656117-59656128 chr4:59656116-59656129
20	CEBPB	chr4:59923445-59923978	MCF-7	breast:	n/a	n/a
21	CEBPB	chr4:59676013-59676638	A549	lung:	n/a	n/a
22	CEBPB	chr4:59923489-59923985	A549	lung:	n/a	n/a
23	CEBPB	chr4:59676094-59676436	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr4:59676096-59676447	A549	lung:	n/a	n/a
25	CEBPB	chr4:59674969-59675473	A549	lung:	n/a	chr4:59675028-59675041
26	CEBPB	chr4:59900090-59900198	A549	lung:	n/a	n/a
27	CEBPB	chr4:59923518-59923902	A549	lung:	n/a	n/a
28	CEBPB	chr4:59923602-59923884	MCF-7	breast:	n/a	n/a
29	CREB1	chr4:59828098-59828492	GM12878	blood:	n/a	n/a
30	CTCF	chr4:59701067-59701112	K562	blood:	n/a	n/a
31	CTCF	chr4:59922060-59922210	GM06990	blood:	n/a	n/a
32	CTCF	chr4:59834223-59834295	Medullo	brain:	n/a	n/a
33	CTCF	chr4:59803580-59803730	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr4:59828080-59828230	GM12864	blood:	n/a	n/a
35	CTCF	chr4:59813440-59813590	GM12871	blood:	n/a	n/a
36	CTCF	chr4:59684594-59684632	GM10248	blood:	n/a	n/a
37	CTCF	chr4:59879843-59879867	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:59738440-59738590	HL-60	blood:	n/a	n/a
39	CTCF	chr4:59702460-59702610	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:59705540-59705690	HCM	heart:	n/a	n/a
41	CUX1	chr4:59827102-59827107	GM12878	blood:	n/a	n/a
42	E2F4	chr4:59859708-59859988	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr4:59689849-59689859	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr4:59871829-59872052	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr4:59801535-59801571	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr4:59891505-59891664	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr4:59681946-59681987	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr4:59822235-59822507	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr4:59734067-59734333	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr4:59674596-59674651	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:59915929..59917798-chr4:59918941..59921861,2	MCF-7	breast:
2	chr4:59915929..59917798-chr4:59918941..59921861,2	MCF-7	breast:
3	chr4:59728253..59729166-chr6:123431104..123432018,2	MCF-7	breast:
4	chr4:59909700..59911681-chr4:59912339..59914598,2	MCF-7	breast:
5	chr4:59909700..59911681-chr4:59912339..59914598,2	MCF-7	breast:
6	chr4:59709166..59709865-chr8:124956173..124956896,2	MCF-7	breast:

(count:42 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IGFBP7-5	chr4:59726676-59726773	XLOC_003962
2	lnc-POLR2B-6	chr4:59912141-59912675	XLOC_003551
3	lnc-IGFBP7-5	chr4:59727050-59727134	XLOC_003962
4	lnc-IGFBP7-6	chr4:59913667-59913853	XLOC_003963
5	lnc-IGFBP7-5	chr4:59849724-59849820	XLOC_003962
6	lnc-IGFBP7-5	chr4:59849724-59849838	XLOC_003962
7	lnc-IGFBP7-5	chr4:59849724-59849859	XLOC_003962
8	lnc-IGFBP7-5	chr4:59713333-59713530	XLOC_003962
9	lnc-IGFBP7-5	chr4:59717135-59717370	ENSG00000251339
10	lnc-POLR2B-6	chr4:59850000-59850053	XLOC_003551
11	lnc-IGFBP7-5	chr4:59717359-59717370	XLOC_003962
12	lnc-IGFBP7-5	chr4:59849724-59849870	ENSG00000251339
13	lnc-IGFBP7-5	chr4:59842732-59842831	XLOC_003962
14	lnc-IGFBP7-5	chr4:59727050-59727134	XLOC_003962
15	lnc-IGFBP7-5	chr4:59727050-59727134	XLOC_003962
16	lnc-POLR2B-6	chr4:59906305-59906409	XLOC_003551
17	lnc-IGFBP7-5	chr4:59727050-59727134	NONHSAT096581
18	lnc-IGFBP7-5	chr4:59853534-59853607	XLOC_003962
19	lnc-IGFBP7-5	chr4:59727050-59727134	XLOC_003962
20	lnc-IGFBP7-5	chr4:59727050-59727134	XLOC_003962
21	lnc-IGFBP7-5	chr4:59853822-59853870	ENSG00000249382
22	lnc-IGFBP7-5	chr4:59853534-59853673	XLOC_003962
23	lnc-POLR2B-6	chr4:59879291-59879343	XLOC_003551
24	lnc-IGFBP7-6	chr4:59912738-59912778	ENSG00000250375
25	lnc-IGFBP7-5	chr4:59727050-59727134	ENSG00000251339
26	lnc-IGFBP7-5	chr4:59849724-59849848	XLOC_003962
27	lnc-IGFBP7-5	chr4:59842732-59842815	XLOC_003962
28	lnc-IGFBP7-6	chr4:59913667-59913853	ENSG00000250375
29	lnc-IGFBP7-6	chr4:59912738-59912778	XLOC_003963
30	lnc-IGFBP7-5	chr4:59853822-59853836	XLOC_003962
31	lnc-IGFBP7-5	chr4:59853822-59853878	XLOC_003962
32	lnc-IGFBP7-5	chr4:59727050-59727134	XLOC_003962
33	lnc-IGFBP7-5	chr4:59723790-59723913	XLOC_003962
34	lnc-IGFBP7-5	chr4:59853822-59853873	XLOC_003962
35	lnc-IGFBP7-5	chr4:59853534-59853607	XLOC_003962
36	lnc-IGFBP7-5	chr4:59853534-59853674	NONHSAT096581
37	lnc-IGFBP7-5	chr4:59853822-59853873	XLOC_003962
38	lnc-IGFBP7-5	chr4:59853534-59853673	XLOC_003962
39	lnc-IGFBP7-5	chr4:59853249-59853673	ENSG00000249382
40	lnc-IGFBP7-5	chr4:59853221-59853402	XLOC_003962
41	lnc-IGFBP7-5	chr4:59852905-59853402	XLOC_003962
42	lnc-POLR2B-6	chr4:59912141-59912677	XLOC_003551

No data

Variant related genes	Relation type
ENSG00000251266	TF binding region
ENSG00000249382	TF binding region
ENSG00000251339	TF binding region
PLP2	miRNA target sites
FLI1	miRNA target sites
KLF4	miRNA target sites
PLRG1	miRNA target sites
PDE12	miRNA target sites
BTBD3	miRNA target sites
FLNB	miRNA target sites
PDCD6IP	miRNA target sites
PLOD3	miRNA target sites

Extended variants
information (count: 1566 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1566 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571907500	chr4:59673409-59673410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552493386	chr4:59673423-59673424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564804468	chr4:59673431-59673432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35798062	chr4:59673433-59673434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13140955	chr4:59673434-59673435	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543352310	chr4:59673436-59673437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564733532	chr4:59673483-59673484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553368897	chr4:59673525-59673526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1449032	chr4:59673611-59673612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs545443937	chr4:59673634-59673635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1449031	chr4:59673650-59673651	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73200759	chr4:59673665-59673666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184377641	chr4:59673704-59673705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17218364	chr4:59673719-59673720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs1449030	chr4:59673724-59673725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs531222781	chr4:59673787-59673788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188913065	chr4:59673798-59673799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571009938	chr4:59673816-59673817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141909940	chr4:59673858-59673859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553557596	chr4:59673866-59673867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6850012	chr4:59673951-59673952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561160335	chr4:59673954-59673955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565745961	chr4:59673999-59674000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374110645	chr4:59674032-59674033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554539994	chr4:59674050-59674051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6850205	chr4:59674052-59674053	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs543264967	chr4:59674053-59674054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558435556	chr4:59674093-59674094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6853837	chr4:59674165-59674166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541245101	chr4:59674171-59674172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374723716	chr4:59674209-59674210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576398849	chr4:59674230-59674231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6831809	chr4:59674231-59674232	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145636973	chr4:59674239-59674240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77445088	chr4:59674253-59674254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369541147	chr4:59674259-59674260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530932212	chr4:59674290-59674291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552864403	chr4:59674314-59674315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74444428	chr4:59674346-59674347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs397731813	chr4:59674350-59674351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199957922	chr4:59674352-59674353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564787059	chr4:59674374-59674375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572177029	chr4:59674400-59674401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528822505	chr4:59674451-59674452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17051491	chr4:59674475-59674476	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs568601156	chr4:59674485-59674486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375333928	chr4:59674492-59674493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115862127	chr4:59674494-59674495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147727886	chr4:59674524-59674525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13149936	chr4:59674527-59674528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:59673400-59675400	Enhancers	A549	lung
2	chr4:59673600-59673800	Enhancers	Placenta	Placenta
3	chr4:59673800-59674600	Weak transcription	Placenta	Placenta
4	chr4:59674600-59676000	Enhancers	Placenta	Placenta
5	chr4:59674600-59676200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:59674600-59676200	Enhancers	Placenta Amnion	Placenta Amnion
7	chr4:59675200-59676200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:59675400-59676200	Flanking Active TSS	A549	lung
9	chr4:59675600-59676000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:59675600-59676200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:59675600-59676200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:59675600-59676200	Enhancers	Fetal Intestine Small	intestine
13	chr4:59676000-59676800	Weak transcription	Placenta	Placenta
14	chr4:59676200-59677600	Enhancers	A549	lung
15	chr4:59676200-59677800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:59676800-59677400	Enhancers	Placenta	Placenta
17	chr4:59677400-59682800	Weak transcription	Placenta	Placenta
18	chr4:59678000-59678200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:59682800-59683200	Enhancers	Placenta	Placenta
20	chr4:59683200-59684600	Weak transcription	Placenta	Placenta
21	chr4:59684600-59685200	Enhancers	Placenta	Placenta
22	chr4:59700600-59701000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:59707600-59708200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:59723000-59723200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr4:59737800-59738400	Enhancers	A549	lung
26	chr4:59801400-59801800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr4:59804600-59806400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:59804600-59806400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:59805600-59806400	Active TSS	A549	lung
30	chr4:59805800-59806000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:59806000-59806200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:59806200-59806400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:59813200-59813800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:59823000-59823600	Enhancers	Adipose Nuclei	Adipose
35	chr4:59843800-59844200	Active TSS	Aorta	Aorta
36	chr4:59849800-59850400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:59850000-59850400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:59859400-59859600	Enhancers	Fetal Heart	heart
39	chr4:59859600-59860600	Weak transcription	Fetal Heart	heart
40	chr4:59860600-59861200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:59860600-59861200	Enhancers	Fetal Heart	heart
42	chr4:59860800-59861600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr4:59861200-59867400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:59867400-59868400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:59891800-59892200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:59899400-59900200	Active TSS	A549	lung
47	chr4:59903600-59904000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr4:59903600-59904200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:59903600-59904400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:59910000-59910400	Enhancers	Fetal Kidney	kidney

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