Variant report

Variant	nsv1017488
Chromosome Location	chr5:152239716-152383640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:152250975-152251178	A549	lung:	n/a	chr5:152251072-152251083
2	CEBPB	chr5:152336825-152337124	A549	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
3	CEBPB	chr5:152336837-152337081	IMR90	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
4	CEBPB	chr5:152333400-152333656	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:152336825-152337119	Hela-S3	cervix:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
6	CEBPB	chr5:152332003-152332331	HepG2	liver:	n/a	chr5:152332151-152332162
7	CEBPB	chr5:152374246-152374450	HepG2	liver:	n/a	chr5:152374363-152374374
8	CEBPB	chr5:152364302-152364664	A549	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
9	CEBPB	chr5:152336869-152337086	K562	blood:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
10	CEBPB	chr5:152364398-152364644	K562	blood:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
11	CEBPB	chr5:152332064-152332264	H1-hESC	embryonic stem cell:	n/a	chr5:152332151-152332162
12	CEBPB	chr5:152364298-152364669	IMR90	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
13	CEBPB	chr5:152336818-152337158	HepG2	liver:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
14	CEBPB	chr5:152364298-152364651	HepG2	liver:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
15	CEBPB	chr5:152332017-152332290	A549	lung:	n/a	chr5:152332151-152332162
16	CEBPB	chr5:152250941-152251175	HepG2	liver:	n/a	chr5:152251072-152251083
17	CEBPB	chr5:152342360-152342457	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:152336872-152337072	MCF-7	breast:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
19	CEBPB	chr5:152332005-152332335	IMR90	lung:	n/a	chr5:152332151-152332162
20	CTCF	chr5:152285160-152285310	GM06990	blood:	n/a	n/a
21	CTCF	chr5:152345185-152345249	GM13976	blood:	n/a	n/a
22	CTCF	chr5:152315496-152315559	Lung_OC	lung:	n/a	n/a
23	CTCF	chr5:152287665-152287712	Kidney_OC	kidney:	n/a	chr5:152287696-152287704 chr5:152287680-152287696
24	CTCF	chr5:152383240-152383390	GM12869	blood:	n/a	n/a
25	CTCF	chr5:152283080-152283138	GM13976	blood:	n/a	n/a
26	CTCF	chr5:152265726-152265861	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr5:152309660-152309810	NHEK	skin:	n/a	n/a
28	CTCF	chr5:152352540-152352690	GM12873	blood:	n/a	n/a
29	CTCF	chr5:152302720-152302870	GM12869	blood:	n/a	n/a
30	E2F4	chr5:152341164-152341364	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr5:152333912-152334106	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr5:152370109-152370427	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr5:152336857-152337197	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr5:152247224-152247310	GM12878	blood:	n/a	chr5:152247273-152247284
35	EP300	chr5:152357319-152357360	K562	blood:	n/a	n/a
36	EP300	chr5:152292365-152292876	T-47D	breast:	n/a	n/a
37	EP300	chr5:152292457-152292982	T-47D	breast:	n/a	n/a
38	ESR1	chr5:152292402-152292907	T-47D	breast:	n/a	n/a
39	ESR1	chr5:152292437-152292764	T-47D	breast:	n/a	n/a
40	FOS	chr5:152373658-152373983	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr5:152370164-152370708	MCF10A-Er-Src	breast:	n/a	chr5:152370534-152370542 chr5:152370452-152370461 chr5:152370534-152370543 chr5:152370534-152370541 chr5:152370533-152370542
42	FOS	chr5:152370211-152370704	MCF10A-Er-Src	breast:	n/a	chr5:152370534-152370542 chr5:152370452-152370461 chr5:152370534-152370543 chr5:152370534-152370541 chr5:152370533-152370542
43	FOS	chr5:152336832-152337125	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr5:152370135-152370698	MCF10A-Er-Src	breast:	n/a	chr5:152370534-152370542 chr5:152370452-152370461 chr5:152370534-152370543 chr5:152370534-152370541 chr5:152370533-152370542
45	FOS	chr5:152373676-152373962	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr5:152336897-152337070	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr5:152336843-152337139	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr5:152373671-152373968	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr5:152373657-152373968	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr5:152370151-152370728	MCF10A-Er-Src	breast:	n/a	chr5:152370534-152370542 chr5:152370452-152370461 chr5:152370534-152370543 chr5:152370534-152370541 chr5:152370533-152370542

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:152374989-152375039	NT2-D1	testis:	n/a
2	chr5:152374989-152375039	NT2-D1	testis:	n/a
3	chr5:152309662-152309712	U87	brain:	n/a
4	chr5:152309662-152309712	AG09319	gingival:	n/a
5	chr5:152374989-152375039	HNPCEpiC	eye:	n/a
6	chr5:152309662-152309712	GM19239	blood:	n/a
7	chr5:152352468-152352518	HAEpiC	amniotic membrane:	n/a
8	chr5:152309662-152309712	ECC-1	luminal epithelium:	n/a
9	chr5:152352468-152352518	NHDF-neo	bronchial:	n/a
10	chr5:152376702-152376752	ovcar-3	ovarian:	n/a
11	chr5:152376702-152376752	HUVEC	blood vessel:	n/a
12	chr5:152309662-152309712	PFSK-1	brain:	n/a
13	chr5:152374989-152375039	HCPEpiC	choroid plexus:	n/a
14	chr5:152279040-152279090	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:152374989-152375039	GM19239	blood:	n/a
16	chr5:152376702-152376752	MCF-7	breast:	n/a
17	chr5:152374989-152375039	AG04449	skin:	fetal
18	chr5:152352468-152352518	NT2-D1	testis:	n/a
19	chr5:152352697-152352747	AG04449	skin:	fetal
20	chr5:152352468-152352518	GM12891	blood:	n/a
21	chr5:152309662-152309712	HIPEpiC	eye:	n/a
22	chr5:152374989-152375039	SK-N-SH_RA	brain:	n/a
23	chr5:152352468-152352518	HCPEpiC	choroid plexus:	n/a
24	chr5:152374989-152375039	AG10803	skin:	n/a
25	chr5:152279040-152279090	MCF10A-Er-Src	breast:	n/a
26	chr5:152279040-152279090	GM12892	blood:	n/a
27	chr5:152352468-152352518	PrEC	prostate:	n/a
28	chr5:152309662-152309712	SAEC	small airway:	n/a
29	chr5:152279040-152279090	Hela-S3	cervix:	n/a
30	chr5:152376702-152376752	HepG2	liver:	n/a
31	chr5:152352697-152352747	NB4	blood:	n/a
32	chr5:152279040-152279090	SK-N-SH_RA	brain:	n/a
33	chr5:152309662-152309712	PANC-1	pancreas:	n/a
34	chr5:152374989-152375039	RPTEC	kidney:	n/a
35	chr5:152376702-152376752	GM06990	blood:	n/a
36	chr5:152376702-152376752	GM12892	blood:	n/a
37	chr5:152352468-152352518	Caco-2	colon:	n/a
38	chr5:152376702-152376752	PFSK-1	brain:	n/a
39	chr5:152352697-152352747	AG10803	skin:	n/a
40	chr5:152352468-152352518	HUVEC	blood vessel:	n/a
41	chr5:152309662-152309712	HepG2	liver:	n/a
42	chr5:152374989-152375039	PANC-1	pancreas:	n/a
43	chr5:152352697-152352747	AG09309	skin:	n/a
44	chr5:152352468-152352518	RPTEC	kidney:	n/a
45	chr5:152279040-152279090	CMK	blood:	n/a
46	chr5:152279040-152279090	GM12891	blood:	n/a
47	chr5:152376702-152376752	PANC-1	pancreas:	n/a
48	chr5:152352697-152352747	Caco-2	colon:	n/a
49	chr5:152352697-152352747	IMR90	lung:	fetal
50	chr5:152374989-152375039	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
2	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
3	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
4	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMUR2-1	chr5:152318398-152318551	ENSG00000249484.4
2	lnc-NMUR2-1	chr5:152351574-152351793	ENSG00000249484.4
3	lnc-NMUR2-1	chr5:152351826-152351909	XLOC_005056
4	lnc-NMUR2-1	chr5:152351274-152351343	XLOC_005056
5	lnc-NMUR2-1	chr5:152345801-152345909	XLOC_005056
6	lnc-NMUR2-1	chr5:152351274-152351346	ENSG00000249484.4
7	lnc-NMUR2-1	chr5:152318398-152318551	XLOC_005056
8	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484.4
9	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
10	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484
11	lnc-NMUR2-1	chr5:152351826-152351909	ENSG00000249484
12	lnc-NMUR2-1	chr5:152351274-152351346	XLOC_005056
13	lnc-NMUR2-1	chr5:152352638-152352763	XLOC_005056
14	lnc-NMUR2-1	chr5:152351574-152351793	XLOC_005056
15	lnc-NMUR2-1	chr5:152264987-152265188	XLOC_005056
16	lnc-NMUR2-1	chr5:152346653-152346666	ENSG00000249484.4
17	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
18	lnc-NMUR2-1	chr5:152352638-152352763	ENSG00000249484.4

Variant related genes	Relation type
ENSG00000249484	TF binding region
ENSG00000249484	CpG island
DICER1	miRNA target sites
FAM122A	miRNA target sites

Extended variants
information (count: 1839 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1839 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117354673	chr5:152239723-152239724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149980800	chr5:152239800-152239801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570526620	chr5:152239848-152239849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537919796	chr5:152239849-152239850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569591810	chr5:152239850-152239851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556242111	chr5:152239896-152239897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145541287	chr5:152239921-152239922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199539551	chr5:152239935-152239936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554805693	chr5:152239957-152239958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535681550	chr5:152239981-152239982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553779407	chr5:152239984-152239985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146534909	chr5:152239987-152239988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141220815	chr5:152240005-152240006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564037870	chr5:152240018-152240019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576130202	chr5:152240022-152240023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143663261	chr5:152240038-152240039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146820550	chr5:152240070-152240071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4145744	chr5:152240081-152240082	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs193143430	chr5:152240087-152240088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148976553	chr5:152240115-152240116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143779868	chr5:152240143-152240144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72802874	chr5:152240163-152240164	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs552472566	chr5:152240212-152240213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570465836	chr5:152240225-152240226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182292306	chr5:152240236-152240237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549997435	chr5:152240325-152240326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186813150	chr5:152240398-152240399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535272460	chr5:152240406-152240407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553967616	chr5:152240417-152240418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572286816	chr5:152240420-152240421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539717820	chr5:152240423-152240424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558088816	chr5:152240450-152240451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191652648	chr5:152240471-152240472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17113732	chr5:152240474-152240475	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs151116189	chr5:152240475-152240476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573723241	chr5:152240517-152240518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528179055	chr5:152240613-152240614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540780550	chr5:152240630-152240631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530056542	chr5:152240678-152240679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4263546	chr5:152240716-152240717	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs560801763	chr5:152240890-152240891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527902911	chr5:152240936-152240937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546055377	chr5:152240943-152240944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528007131	chr5:152240959-152240960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35733576	chr5:152240990-152240991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184221080	chr5:152241000-152241001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552713891	chr5:152241031-152241032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141120707	chr5:152241049-152241050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6898262	chr5:152241059-152241060	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs568451362	chr5:152241060-152241061	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Deafness	19353646	CNVD
Developmental delay	19353646	CNVD
dysmorphism	19353646	CNVD
feeding difficulties	19353646	CNVD
strabismus	19353646	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152237400-152240400	Weak transcription	Stomach Mucosa	stomach
2	chr5:152240000-152240600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:152240200-152240800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr5:152240400-152241200	Enhancers	Stomach Mucosa	stomach
5	chr5:152241000-152241600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr5:152243200-152245200	Enhancers	HSMM	muscle
7	chr5:152246000-152247400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:152247200-152247400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr5:152247400-152247800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr5:152247400-152248400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr5:152248400-152248600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr5:152253400-152253600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:152253400-152253600	ZNF genes & repeats	Gastric	stomach
14	chr5:152261400-152262800	Enhancers	Fetal Brain Male	brain
15	chr5:152262000-152263200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr5:152262200-152264800	Enhancers	Brain Germinal Matrix	brain
17	chr5:152262400-152263200	Enhancers	Fetal Brain Female	brain
18	chr5:152279800-152280200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:152279800-152280600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:152279800-152280800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:152280000-152280600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:152280000-152280800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr5:152281200-152282200	Enhancers	Liver	Liver
24	chr5:152282200-152287000	Weak transcription	Liver	Liver
25	chr5:152287000-152287400	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr5:152287000-152287600	Active TSS	Liver	Liver
27	chr5:152287400-152287600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr5:152287600-152287800	Flanking Active TSS	Liver	Liver
29	chr5:152287800-152288000	Enhancers	Liver	Liver
30	chr5:152289600-152289800	Enhancers	Liver	Liver
31	chr5:152304600-152306000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:152305600-152305800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:152306400-152306800	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr5:152307600-152308000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:152308000-152309400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:152309400-152310000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:152312400-152313000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr5:152317000-152318600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:152317800-152318600	Enhancers	Liver	Liver
40	chr5:152318600-152318800	Flanking Active TSS	Liver	Liver
41	chr5:152318800-152319000	Active TSS	Liver	Liver
42	chr5:152328800-152329000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:152329000-152330800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:152329600-152330600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:152330000-152330600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:152330800-152331200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:152331200-152332400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:152333000-152333600	Enhancers	Liver	Liver
49	chr5:152333600-152334000	Flanking Active TSS	Liver	Liver
50	chr5:152334000-152334200	Enhancers	Liver	Liver

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