Variant report

Variant	nsv526084
Chromosome Location	chr5:75410511-75530494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:613)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:75476928-75477230	K562	blood:	n/a	n/a
2	ATF1	chr5:75458345-75458529	K562	blood:	n/a	n/a
3	ATF1	chr5:75442283-75442385	K562	blood:	n/a	n/a
4	ATF1	chr5:75517243-75517452	K562	blood:	n/a	n/a
5	ATF1	chr5:75471623-75472170	K562	blood:	n/a	n/a
6	ATF1	chr5:75515637-75515837	K562	blood:	n/a	n/a
7	ATF2	chr5:75483142-75483633	GM12878	blood:	n/a	n/a
8	ATF2	chr5:75476912-75477609	GM12878	blood:	n/a	n/a
9	ATF2	chr5:75474597-75475178	GM12878	blood:	n/a	n/a
10	ATF2	chr5:75476882-75477667	GM12878	blood:	n/a	n/a
11	ATF2	chr5:75474650-75475133	GM12878	blood:	n/a	n/a
12	ATF2	chr5:75471452-75472442	GM12878	blood:	n/a	n/a
13	ATF2	chr5:75471604-75472348	GM12878	blood:	n/a	n/a
14	ATF3	chr5:75471599-75472016	K562	blood:	n/a	n/a
15	BATF	chr5:75474748-75475148	GM12878	blood:	n/a	n/a
16	BATF	chr5:75471890-75472287	GM12878	blood:	n/a	n/a
17	BATF	chr5:75476907-75477562	GM12878	blood:	n/a	n/a
18	BATF	chr5:75476903-75477253	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:75474738-75475112	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:75476940-75477332	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:75440843-75440979	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr5:75473860-75474199	GM12878	blood:	n/a	n/a
23	BCL3	chr5:75471555-75472304	GM12878	blood:	n/a	n/a
24	BCL3	chr5:75474685-75475133	GM12878	blood:	n/a	n/a
25	BCL3	chr5:75476943-75477631	GM12878	blood:	n/a	n/a
26	BCLAF1	chr5:75476931-75477519	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:75470838-75471335	GM12878	blood:	n/a	n/a
28	BCLAF1	chr5:75471604-75472393	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:75471619-75472026	K562	blood:	n/a	n/a
30	BHLHE40	chr5:75441876-75442076	K562	blood:	n/a	n/a
31	BHLHE40	chr5:75470933-75471235	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:75471965-75472226	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:75515244-75515285	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:75476870-75477240	K562	blood:	n/a	n/a
35	CBX3	chr5:75471552-75472056	K562	blood:	n/a	n/a
36	CBX3	chr5:75476823-75477541	K562	blood:	n/a	n/a
37	CBX3	chr5:75505170-75505419	K562	blood:	n/a	n/a
38	CCNT2	chr5:75471729-75471951	K562	blood:	n/a	chr5:75471940-75471949
39	CCNT2	chr5:75476951-75477181	K562	blood:	n/a	n/a
40	CEBPB	chr5:75439719-75440089	IMR90	lung:	n/a	chr5:75439901-75439912
41	CEBPB	chr5:75500597-75501069	MCF-7	breast:	n/a	chr5:75500852-75500863
42	CEBPB	chr5:75439743-75440041	K562	blood:	n/a	chr5:75439901-75439912
43	CEBPB	chr5:75471561-75471990	K562	blood:	n/a	n/a
44	CEBPB	chr5:75476703-75477146	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:75444208-75444493	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:75439723-75440097	H1-hESC	embryonic stem cell:	n/a	chr5:75439901-75439912
47	CEBPB	chr5:75439766-75440023	ECC-1	luminal epithelium:	n/a	chr5:75439901-75439912
48	CEBPB	chr5:75439722-75440030	MCF-7	breast:	n/a	chr5:75439901-75439912
49	CEBPB	chr5:75439724-75440079	A549	lung:	n/a	chr5:75439901-75439912
50	CEBPB	chr5:75476639-75476847	HepG2	liver:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75471166-75471216	HMEC	breast:	n/a
2	chr5:75473201-75473251	NB4	blood:	n/a
3	chr5:75472143-75472193	GM12878	blood:	n/a
4	chr5:75471166-75471216	HMEC	breast:	n/a
5	chr5:75473201-75473251	NB4	blood:	n/a
6	chr5:75472143-75472193	GM12878	blood:	n/a
7	chr5:75524056-75524106	HCM	heart:	n/a
8	chr5:75469969-75470019	NT2-D1	testis:	n/a
9	chr5:75473201-75473251	MCF10A-Er-Src	breast:	n/a
10	chr5:75470039-75470089	SK-N-MC	brain:	n/a
11	chr5:75524056-75524106	ECC-1	luminal epithelium:	n/a
12	chr5:75472143-75472193	NHBE	bronchial:	n/a
13	chr5:75472143-75472193	HIPEpiC	eye:	n/a
14	chr5:75524056-75524106	Hepatocyte	liver:	n/a
15	chr5:75464408-75464458	SK-N-SH	brain:	n/a
16	chr5:75469969-75470019	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:75464408-75464458	MCF-7	breast:	n/a
18	chr5:75471166-75471216	PrEC	prostate:	n/a
19	chr5:75464408-75464458	NH-A	brain:	n/a
20	chr5:75470039-75470089	HRCEpiC	kidney:	n/a
21	chr5:75469826-75469876	GM12891	blood:	n/a
22	chr5:75465603-75465653	PANC-1	pancreas:	n/a
23	chr5:75473201-75473251	T-47D	breast:	n/a
24	chr5:75469969-75470019	K562	blood:	n/a
25	chr5:75469826-75469876	BE2_C	brain:	n/a
26	chr5:75471166-75471216	SK-N-SH_RA	brain:	n/a
27	chr5:75464408-75464458	NHDF-neo	bronchial:	n/a
28	chr5:75469904-75469954	AG09319	gingival:	n/a
29	chr5:75470039-75470089	LNCaP	prostate:	n/a
30	chr5:75472143-75472193	HUVEC	blood vessel:	n/a
31	chr5:75469826-75469876	U87	brain:	n/a
32	chr5:75472143-75472193	HRE	kidney:	n/a
33	chr5:75464408-75464458	CMK	blood:	n/a
34	chr5:75473201-75473251	H1-hESC	embryonic stem cell:	embryo
35	chr5:75471166-75471216	NH-A	brain:	n/a
36	chr5:75469826-75469876	Jurkat	blood:	n/a
37	chr5:75472143-75472193	Jurkat	blood:	n/a
38	chr5:75469969-75470019	HRE	kidney:	n/a
39	chr5:75464408-75464458	MCF10A-Er-Src	breast:	n/a
40	chr5:75469826-75469876	BJ	skin:	n/a
41	chr5:75465603-75465653	SAEC	small airway:	n/a
42	chr5:75472143-75472193	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:75464408-75464458	PFSK-1	brain:	n/a
44	chr5:75465603-75465653	HIPEpiC	eye:	n/a
45	chr5:75469969-75470019	RPTEC	kidney:	n/a
46	chr5:75469826-75469876	HRCEpiC	kidney:	n/a
47	chr5:75470039-75470089	SK-N-SH	brain:	n/a
48	chr5:75469904-75469954	HCT-116	colon:	n/a
49	chr5:75469969-75470019	GM12892	blood:	n/a
50	chr5:75469904-75469954	HCM	heart:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75369710..75371593-chr5:75472300..75473889,2	K562	blood:
2	chr5:75470625..75471456-chr5:75551799..75552684,5	MCF-7	breast:
3	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
4	chr5:75520569..75523367-chr5:75540398..75542001,2	K562	blood:
5	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
6	chr5:75370258..75370917-chr5:75470691..75471438,2	MCF-7	breast:
7	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
8	chr2:175960283..175962736-chr5:75428852..75431360,2	MCF-7	breast:
9	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
10	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
11	chr2:77243462..77244011-chr5:75510913..75511675,2	MCF-7	breast:
12	chr5:75370002..75370997-chr5:75470399..75471572,8	MCF-7	breast:
13	chr5:75031130..75031721-chr5:75470748..75471418,2	MCF-7	breast:
14	chr5:75441859..75445534-chr5:75469171..75472141,3	K562	blood:
15	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
16	chr5:75182130..75182669-chr5:75470688..75471450,3	MCF-7	breast:
17	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
18	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
19	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
20	chr5:75469938..75472744-chr5:75476639..75478302,2	K562	blood:
21	chr5:75011937..75013471-chr5:75474552..75477211,2	MCF-7	breast:
22	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
23	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
24	chr5:75030911..75031730-chr5:75470555..75471416,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000251668	TF binding region
ENSG00000254893	TF binding region
ENSG00000251668	CpG island
ENSG00000254893	CpG island
ENSG00000249777	chromatin interactions
ENSG00000254893	chromatin interactions
ENSG00000152359	chromatin interactions

Extended variants
information (count: 2926 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2926 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10054931	chr5:75410511-75410512	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs111785672	chr5:75410515-75410516	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569281280	chr5:75410542-75410543	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs535370778	chr5:75410593-75410594	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143593284	chr5:75410599-75410600	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs565635235	chr5:75410609-75410610	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs534545776	chr5:75410621-75410622	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs183766	chr5:75410631-75410632	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs113470488	chr5:75410711-75410712	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs543873172	chr5:75410716-75410717	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs530895510	chr5:75410762-75410763	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs375049411	chr5:75410763-75410764	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs12659929	chr5:75410898-75410899	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs78547236	chr5:75410922-75410923	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs16873213	chr5:75410996-75410997	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs73764474	chr5:75411020-75411021	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs528758893	chr5:75411030-75411031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184047078	chr5:75411064-75411065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113192885	chr5:75411090-75411091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150479589	chr5:75411098-75411099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549172925	chr5:75411139-75411140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145376734	chr5:75411170-75411171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188737443	chr5:75411171-75411172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528331409	chr5:75411192-75411193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549192617	chr5:75411206-75411207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181493027	chr5:75411231-75411232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373228435	chr5:75411266-75411267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142524337	chr5:75411341-75411342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548550100	chr5:75411394-75411395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79305426	chr5:75411435-75411436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534886942	chr5:75411526-75411527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186969040	chr5:75411563-75411564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76230792	chr5:75411581-75411582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371379459	chr5:75411644-75411645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374473303	chr5:75411662-75411663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576063401	chr5:75411727-75411728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557528505	chr5:75411728-75411729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565800139	chr5:75411741-75411742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537403448	chr5:75411764-75411765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10043369	chr5:75411804-75411805	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553389287	chr5:75411850-75411851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567582520	chr5:75411868-75411869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536569042	chr5:75411892-75411893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545655189	chr5:75411924-75411925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565341185	chr5:75411929-75411930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575835140	chr5:75411974-75411975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561340673	chr5:75412049-75412050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116662155	chr5:75412072-75412073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563071172	chr5:75412080-75412081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528938250	chr5:75412121-75412122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75408200-75410600	Enhancers	Gastric	stomach
2	chr5:75409400-75411400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr5:75409400-75412200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:75409600-75410600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:75409600-75410600	Enhancers	Duodenum Mucosa	Duodenum
6	chr5:75409800-75410600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:75409800-75410600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:75409800-75410600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:75409800-75410600	Enhancers	Left Ventricle	heart
10	chr5:75409800-75410600	Enhancers	Lung	lung
11	chr5:75409800-75410600	Enhancers	HUVEC	blood vessel
12	chr5:75409800-75411000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:75409800-75411000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:75410000-75412800	Enhancers	Stomach Mucosa	stomach
15	chr5:75410200-75410600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:75410200-75410600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr5:75410200-75410600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr5:75410200-75411000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
19	chr5:75410200-75411200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:75410400-75410600	Enhancers	Brain Anterior Caudate	brain
21	chr5:75410400-75410600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
22	chr5:75410400-75410600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
23	chr5:75410400-75410800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:75410600-75411000	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr5:75410600-75411600	Weak transcription	Lung	lung
26	chr5:75410600-75412000	Weak transcription	Gastric	stomach
27	chr5:75410600-75412000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr5:75410600-75412400	Weak transcription	Brain Anterior Caudate	brain
29	chr5:75411000-75411200	Enhancers	Brain Hippocampus Middle	brain
30	chr5:75411200-75412600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:75411600-75411800	Enhancers	Lung	lung
32	chr5:75412000-75412200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr5:75412200-75412400	Enhancers	Gastric	stomach
34	chr5:75412400-75412600	Enhancers	Brain Anterior Caudate	brain
35	chr5:75419600-75419800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr5:75419800-75420000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr5:75420000-75421800	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr5:75421800-75422600	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr5:75422200-75422400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr5:75422200-75422600	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr5:75428000-75428200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr5:75428000-75428200	Enhancers	Pancreas	Pancrea
43	chr5:75430800-75431600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:75433600-75434200	Enhancers	Placenta	Placenta
45	chr5:75438000-75440400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:75439200-75439400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:75439400-75439600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr5:75439600-75441400	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr5:75439800-75442400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:75440000-75440200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell

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