Variant report

Variant	nsv598313
Chromosome Location	chr5:60247815-60374912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1172)
CpG islands
(count:122)
Chromatin interactive
region (count:66)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60314308-60314387	K562	blood:	n/a	chr5:60314370-60314386
2	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
3	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
4	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
5	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
6	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
7	BATF	chr5:60347149-60347471	GM12878	blood:	n/a	chr5:60347322-60347333 chr5:60347323-60347333
8	BHLHE40	chr5:60273867-60274075	K562	blood:	n/a	n/a
9	BHLHE40	chr5:60274319-60275283	K562	blood:	n/a	n/a
10	BRCA1	chr5:60306630-60306773	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr5:60344262-60344845	HCT-116	colon:	n/a	n/a
12	CBX3	chr5:60277815-60278245	K562	blood:	n/a	n/a
13	CBX3	chr5:60348580-60349211	HCT-116	colon:	n/a	n/a
14	CBX3	chr5:60274711-60275276	K562	blood:	n/a	n/a
15	CBX3	chr5:60289241-60289660	HCT-116	colon:	n/a	n/a
16	CBX3	chr5:60289206-60289789	K562	blood:	n/a	n/a
17	CBX3	chr5:60344265-60344917	HCT-116	colon:	n/a	n/a
18	CBX3	chr5:60251024-60251519	HCT-116	colon:	n/a	n/a
19	CBX3	chr5:60289190-60289610	K562	blood:	n/a	n/a
20	CBX3	chr5:60274796-60275180	K562	blood:	n/a	n/a
21	CBX3	chr5:60351230-60351719	HCT-116	colon:	n/a	n/a
22	CBX3	chr5:60348517-60349283	HCT-116	colon:	n/a	n/a
23	CCNT2	chr5:60273908-60274052	K562	blood:	n/a	n/a
24	CCNT2	chr5:60274822-60275307	K562	blood:	n/a	n/a
25	CCNT2	chr5:60257762-60257798	K562	blood:	n/a	n/a
26	CCNT2	chr5:60336974-60337076	K562	blood:	n/a	n/a
27	CEBPB	chr5:60364086-60364309	HepG2	liver:	n/a	chr5:60364243-60364256
28	CEBPB	chr5:60257625-60257868	ECC-1	luminal epithelium:	n/a	chr5:60257738-60257749
29	CEBPB	chr5:60348698-60349132	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:60274785-60275239	K562	blood:	n/a	n/a
31	CEBPB	chr5:60257560-60257919	IMR90	lung:	n/a	chr5:60257738-60257749
32	CEBPB	chr5:60344184-60345032	HCT-116	colon:	n/a	chr5:60344922-60344933
33	CEBPB	chr5:60348499-60349238	HCT-116	colon:	n/a	n/a
34	CEBPB	chr5:60277826-60278023	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:60316342-60316622	A549	lung:	n/a	n/a
36	CEBPB	chr5:60346092-60346408	A549	lung:	n/a	n/a
37	CEBPB	chr5:60346083-60346428	K562	blood:	n/a	n/a
38	CEBPB	chr5:60316358-60316620	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:60362736-60363029	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:60346097-60346421	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:60316337-60316539	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:60346107-60346376	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr5:60316396-60316638	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:60257603-60257821	MCF-7	breast:	n/a	chr5:60257738-60257749
45	CEBPB	chr5:60257587-60257962	A549	lung:	n/a	chr5:60257738-60257749
46	CEBPB	chr5:60257618-60257870	K562	blood:	n/a	chr5:60257738-60257749
47	CEBPB	chr5:60257588-60257891	A549	lung:	n/a	chr5:60257738-60257749
48	CEBPB	chr5:60316315-60316656	MCF-7	breast:	n/a	n/a
49	CEBPB	chr5:60362769-60362975	A549	lung:	n/a	n/a
50	CEBPB	chr5:60257590-60257926	HepG2	liver:	n/a	chr5:60257738-60257749

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60346051-60346101	Jurkat	blood:	n/a
2	chr5:60346051-60346101	NHBE	bronchial:	n/a
3	chr5:60325493-60325543	HRPEpiC	eye:	n/a
4	chr5:60346051-60346101	MCF-7	breast:	n/a
5	chr5:60346051-60346101	NH-A	brain:	n/a
6	chr5:60325493-60325543	SKMC	muscle:	n/a
7	chr5:60346051-60346101	PANC-1	pancreas:	n/a
8	chr5:60346051-60346101	Hepatocyte	liver:	n/a
9	chr5:60325493-60325543	SK-N-SH	brain:	n/a
10	chr5:60346051-60346101	MCF10A-Er-Src	breast:	n/a
11	chr5:60346051-60346101	ECC-1	luminal epithelium:	n/a
12	chr5:60346051-60346101	BE2_C	brain:	n/a
13	chr5:60325493-60325543	GM06990	blood:	n/a
14	chr5:60346051-60346101	SAEC	small airway:	n/a
15	chr5:60346051-60346101	SK-N-MC	brain:	n/a
16	chr5:60325493-60325543	GM12891	blood:	n/a
17	chr5:60346051-60346101	T-47D	breast:	n/a
18	chr5:60325493-60325543	HCPEpiC	choroid plexus:	n/a
19	chr5:60325493-60325543	LNCaP	prostate:	n/a
20	chr5:60346051-60346101	HUVEC	blood vessel:	n/a
21	chr5:60346051-60346101	NT2-D1	testis:	n/a
22	chr5:60346051-60346101	AG04450	lung:	fetal
23	chr5:60325493-60325543	HCF	heart:	n/a
24	chr5:60325493-60325543	BJ	skin:	n/a
25	chr5:60346051-60346101	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:60346051-60346101	GM12892	blood:	n/a
27	chr5:60346051-60346101	HepG2	liver:	n/a
28	chr5:60346051-60346101	HAEpiC	amniotic membrane:	n/a
29	chr5:60325493-60325543	T-47D	breast:	n/a
30	chr5:60325493-60325543	Hepatocyte	liver:	n/a
31	chr5:60346051-60346101	AG04449	skin:	fetal
32	chr5:60346051-60346101	LNCaP	prostate:	n/a
33	chr5:60346051-60346101	CMK	blood:	n/a
34	chr5:60325493-60325543	AG04450	lung:	fetal
35	chr5:60325493-60325543	ProgFib	skin:	n/a
36	chr5:60325493-60325543	Hela-S3	cervix:	n/a
37	chr5:60325493-60325543	HAEpiC	amniotic membrane:	n/a
38	chr5:60325493-60325543	Caco-2	colon:	n/a
39	chr5:60346051-60346101	H1-hESC	embryonic stem cell:	embryo
40	chr5:60346051-60346101	HCPEpiC	choroid plexus:	n/a
41	chr5:60325493-60325543	AG09309	skin:	n/a
42	chr5:60346051-60346101	HIPEpiC	eye:	n/a
43	chr5:60325493-60325543	GM12892	blood:	n/a
44	chr5:60325493-60325543	PrEC	prostate:	n/a
45	chr5:60325493-60325543	AoSMC	blood vessel:	n/a
46	chr5:60325493-60325543	NH-A	brain:	n/a
47	chr5:60325493-60325543	Jurkat	blood:	n/a
48	chr5:60325493-60325543	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:60346051-60346101	HEK293	kidney:	embryo
50	chr5:60346051-60346101	PFSK-1	brain:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
2	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
3	chr5:60311498..60313138-chr5:60318136..60319841,2	K562	blood:
4	chr5:60351749..60354289-chr5:60357222..60359514,2	K562	blood:
5	chr5:60274623..60276264-chr5:60290570..60293305,2	K562	blood:
6	chr5:60321206..60323750-chr5:60323786..60326003,2	K562	blood:
7	chr5:60321206..60323750-chr5:60323786..60326003,2	K562	blood:
8	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
9	chr5:60261942..60265146-chr5:60457137..60459002,3	MCF-7	breast:
10	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
11	chr5:60318175..60320382-chr5:60629060..60630909,2	K562	blood:
12	chr5:60353410..60356120-chr5:60624338..60627119,3	MCF-7	breast:
13	chr5:60351342..60352964-chr5:60353710..60356675,2	K562	blood:
14	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
15	chr5:60351749..60354289-chr5:60357222..60359514,2	K562	blood:
16	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
17	chr5:60268329..60270384-chr5:60275561..60277405,2	K562	blood:
18	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
19	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
20	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
21	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
22	chr5:60350790..60351716-chr5:61229541..61230428,4	MCF-7	breast:
23	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
24	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
25	chr5:60238903..60241711-chr5:60255745..60258195,2	K562	blood:
26	chr5:60369695..60372434-chr5:60457768..60459538,2	K562	blood:
27	chr5:60365711..60368002-chr5:60369594..60371777,2	K562	blood:
28	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
29	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
30	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
31	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
32	chr5:60351204..60351892-chr5:60434644..60435198,2	MCF-7	breast:
33	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
34	chr5:60345949..60348661-chr5:60350845..60353374,3	K562	blood:
35	chr5:60239789..60242454-chr5:60245834..60249187,6	MCF-7	breast:
36	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
37	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
38	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
39	chr5:60334340..60336285-chr5:60341216..60344077,2	K562	blood:
40	chr5:60355839..60357550-chr5:60458247..60459791,2	MCF-7	breast:
41	chr5:60274623..60276264-chr5:60290570..60293305,2	K562	blood:
42	chr5:60254798..60255532-chr5:60954065..60954863,2	K562	blood:
43	chr5:60372533..60374046-chr5:60626026..60628135,2	MCF-7	breast:
44	chr5:60240835..60243505-chr5:60324746..60327313,2	MCF-7	breast:
45	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
46	chr5:59995891..59998683-chr5:60261062..60263658,2	K562	blood:
47	chr5:60320010..60322208-chr5:60331308..60333222,2	MCF-7	breast:
48	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
49	chr5:60330521..60333236-chr5:60333963..60336641,2	K562	blood:
50	chr5:60351160..60351880-chr5:60764388..60765010,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM6-4	chr5:60368953-60369018	NONHSAT101655

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
NDUFAF2	CpG island
ENSG00000164182	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000188725	chromatin interactions

Extended variants
information (count: 4246 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4246 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7722373	chr5:60247815-60247816	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115007869	chr5:60247849-60247850	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368029091	chr5:60247854-60247855	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532931917	chr5:60247963-60247964	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs193021417	chr5:60247964-60247965	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs565722801	chr5:60248010-60248011	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs559794214	chr5:60248028-60248029	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs528976382	chr5:60248031-60248032	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549128453	chr5:60248041-60248042	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs73759447	chr5:60248042-60248043	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs538107021	chr5:60248064-60248065	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs184218002	chr5:60248081-60248082	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571883122	chr5:60248097-60248098	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369062331	chr5:60248113-60248114	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534177364	chr5:60248139-60248140	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs188846744	chr5:60248203-60248204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181279061	chr5:60248209-60248210	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536753539	chr5:60248235-60248236	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs555554880	chr5:60248238-60248239	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557595009	chr5:60248264-60248265	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs62370483	chr5:60248314-60248315	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs544119900	chr5:60248328-60248329	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs139775013	chr5:60248383-60248384	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536997145	chr5:60248436-60248437	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs185423366	chr5:60248468-60248469	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs539812893	chr5:60248476-60248477	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs158913	chr5:60248552-60248553	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528911738	chr5:60248601-60248602	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs548669451	chr5:60248603-60248604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs189395766	chr5:60248616-60248617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs12519810	chr5:60248633-60248634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs144387128	chr5:60248637-60248638	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571884609	chr5:60248639-60248640	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534243591	chr5:60248700-60248701	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs172348	chr5:60248728-60248729	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs562146868	chr5:60248778-60248779	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147073370	chr5:60248785-60248786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6887938	chr5:60248790-60248791	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182187564	chr5:60248810-60248811	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556685636	chr5:60248823-60248824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187266676	chr5:60248848-60248849	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs191613559	chr5:60248851-60248852	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557688734	chr5:60248990-60248991	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577834499	chr5:60249006-60249007	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540143833	chr5:60249076-60249077	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559670467	chr5:60249083-60249084	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573297039	chr5:60249107-60249108	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs542252968	chr5:60249269-60249270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28582880	chr5:60249278-60249279	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs558706147	chr5:60249337-60249338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	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
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60242600-60249000	Weak transcription	K562	blood
2	chr5:60243000-60256200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr5:60243200-60248400	Weak transcription	HepG2	liver
4	chr5:60243200-60263000	Weak transcription	Hela-S3	cervix
5	chr5:60245200-60250400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:60248400-60248600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:60248400-60249200	Enhancers	HepG2	liver
8	chr5:60248600-60250000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr5:60250000-60250400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:60250000-60250400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr5:60250400-60251400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:60251400-60261800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:60253200-60255000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:60253400-60253800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:60253400-60253800	Enhancers	Psoas Muscle	Psoas
16	chr5:60253400-60254200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:60253400-60254800	Enhancers	NHDF-Ad	bronchial
18	chr5:60253600-60254000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr5:60253600-60254000	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr5:60253800-60254600	Enhancers	GM12878-XiMat	blood
21	chr5:60253800-60254800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:60254000-60254600	Enhancers	HSMM	muscle
23	chr5:60254000-60261600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr5:60254200-60288800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:60254400-60254800	Enhancers	Fetal Lung	lung
26	chr5:60254600-60255800	Weak transcription	GM12878-XiMat	blood
27	chr5:60254800-60256200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:60254800-60259800	Weak transcription	Fetal Lung	lung
29	chr5:60255000-60255400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:60255400-60256400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:60255800-60256200	Enhancers	GM12878-XiMat	blood
32	chr5:60256000-60256600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr5:60256200-60256400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:60256200-60256600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:60256200-60256600	Enhancers	Primary T cells from cord blood	blood
36	chr5:60256200-60256600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr5:60256200-60256600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr5:60256200-60256600	Enhancers	A549	lung
39	chr5:60256200-60256600	Flanking Active TSS	GM12878-XiMat	blood
40	chr5:60256200-60256800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr5:60256200-60256800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr5:60256200-60257000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr5:60256200-60257000	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr5:60256200-60257000	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr5:60256200-60258000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:60256400-60256600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:60256400-60256800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr5:60256400-60257000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:60256400-60257200	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr5:60256400-60257400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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