Variant report

Variant	nsv437576
Chromosome Location	chr7:140182985-140217670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:730)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140192901-140193239	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:140207814-140208178	K562	blood:	n/a	n/a
3	ARID3A	chr7:140192828-140193232	K562	blood:	n/a	n/a
4	ARID3A	chr7:140188071-140188442	K562	blood:	n/a	n/a
5	ARID3A	chr7:140185697-140185852	K562	blood:	n/a	n/a
6	ATF1	chr7:140207761-140208095	K562	blood:	n/a	n/a
7	ATF1	chr7:140188073-140188434	K562	blood:	n/a	n/a
8	ATF2	chr7:140217634-140218254	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:140217665-140218267	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:140188143-140188310	K562	blood:	n/a	n/a
11	BACH1	chr7:140207714-140208142	K562	blood:	n/a	n/a
12	BACH1	chr7:140185767-140185904	K562	blood:	n/a	n/a
13	BACH1	chr7:140185073-140185560	K562	blood:	n/a	n/a
14	BACH1	chr7:140185264-140185985	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr7:140186510-140186778	GM12878	blood:	n/a	chr7:140186679-140186690
16	BCL3	chr7:140217664-140218205	A549	lung:	n/a	chr7:140217948-140217956
17	BHLHE40	chr7:140188071-140188558	K562	blood:	n/a	n/a
18	BHLHE40	chr7:140195509-140195736	K562	blood:	n/a	n/a
19	BHLHE40	chr7:140192782-140192808	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:140198127-140198217	K562	blood:	n/a	n/a
21	BHLHE40	chr7:140184833-140184843	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:140206633-140207127	K562	blood:	n/a	n/a
23	BHLHE40	chr7:140212464-140212677	K562	blood:	n/a	n/a
24	BHLHE40	chr7:140194624-140195010	HepG2	liver:	n/a	n/a
25	BHLHE40	chr7:140207742-140208120	K562	blood:	n/a	n/a
26	BHLHE40	chr7:140185293-140185448	K562	blood:	n/a	n/a
27	BHLHE40	chr7:140192882-140193142	K562	blood:	n/a	n/a
28	BRCA1	chr7:140217649-140217958	HepG2	liver:	n/a	n/a
29	BRCA1	chr7:140212524-140212674	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr7:140217649-140218199	K562	blood:	n/a	n/a
31	CBX3	chr7:140187741-140188634	K562	blood:	n/a	n/a
32	CBX3	chr7:140206525-140207232	K562	blood:	n/a	n/a
33	CBX3	chr7:140207578-140208382	K562	blood:	n/a	n/a
34	CBX3	chr7:140207731-140208126	K562	blood:	n/a	n/a
35	CBX3	chr7:140212377-140212774	K562	blood:	n/a	n/a
36	CBX3	chr7:140188694-140189191	K562	blood:	n/a	n/a
37	CCNT2	chr7:140207745-140208073	K562	blood:	n/a	n/a
38	CCNT2	chr7:140195518-140195761	K562	blood:	n/a	n/a
39	CCNT2	chr7:140188070-140188497	K562	blood:	n/a	n/a
40	CEBPB	chr7:140207730-140208052	K562	blood:	n/a	n/a
41	CEBPB	chr7:140185435-140185689	A549	lung:	n/a	n/a
42	CEBPB	chr7:140199136-140199337	K562	blood:	n/a	n/a
43	CEBPB	chr7:140184951-140185817	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:140194680-140194780	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:140207703-140208241	K562	blood:	n/a	n/a
46	CEBPB	chr7:140194652-140194899	HepG2	liver:	n/a	chr7:140194842-140194854
47	CEBPB	chr7:140199179-140199299	A549	lung:	n/a	n/a
48	CEBPB	chr7:140217615-140217643	K562	blood:	n/a	n/a
49	CEBPB	chr7:140194612-140194798	K562	blood:	n/a	n/a
50	CEBPB	chr7:140200938-140200952	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140206867-140206917	U87	brain:	n/a
2	chr7:140206867-140206917	NB4	blood:	n/a
3	chr7:140206867-140206917	A549	lung:	n/a
4	chr7:140206867-140206917	GM06990	blood:	n/a
5	chr7:140206867-140206917	NT2-D1	testis:	n/a
6	chr7:140206867-140206917	PANC-1	pancreas:	n/a
7	chr7:140206867-140206917	HRPEpiC	eye:	n/a
8	chr7:140206867-140206917	PFSK-1	brain:	n/a
9	chr7:140206867-140206917	HCPEpiC	choroid plexus:	n/a
10	chr7:140206867-140206917	MCF10A-Er-Src	breast:	n/a
11	chr7:140206867-140206917	HEEpiC	esophagus:	n/a
12	chr7:140206867-140206917	Jurkat	blood:	n/a
13	chr7:140206867-140206917	HRE	kidney:	n/a
14	chr7:140206867-140206917	T-47D	breast:	n/a
15	chr7:140206867-140206917	ProgFib	skin:	n/a
16	chr7:140206867-140206917	GM12892	blood:	n/a
17	chr7:140206867-140206917	Caco-2	colon:	n/a
18	chr7:140206867-140206917	HAEpiC	amniotic membrane:	n/a
19	chr7:140206867-140206917	SK-N-SH_RA	brain:	n/a
20	chr7:140206867-140206917	SK-N-MC	brain:	n/a
21	chr7:140206867-140206917	AoSMC	blood vessel:	n/a
22	chr7:140206867-140206917	HCF	heart:	n/a
23	chr7:140206867-140206917	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:140206867-140206917	SAEC	small airway:	n/a
25	chr7:140206867-140206917	NHBE	bronchial:	n/a
26	chr7:140206867-140206917	ovcar-3	ovarian:	n/a
27	chr7:140206867-140206917	GM12878	blood:	n/a
28	chr7:140206867-140206917	Hela-S3	cervix:	n/a
29	chr7:140206867-140206917	AG04450	lung:	fetal
30	chr7:140206867-140206917	HCT-116	colon:	n/a
31	chr7:140206867-140206917	HIPEpiC	eye:	n/a
32	chr7:140206867-140206917	GM12891	blood:	n/a
33	chr7:140206867-140206917	HMEC	breast:	n/a
34	chr7:140206867-140206917	H1-hESC	embryonic stem cell:	embryo
35	chr7:140206867-140206917	GM19239	blood:	n/a
36	chr7:140206867-140206917	HEK293	kidney:	embryo
37	chr7:140206867-140206917	BE2_C	brain:	n/a
38	chr7:140206867-140206917	HNPCEpiC	eye:	n/a
39	chr7:140206867-140206917	BJ	skin:	n/a
40	chr7:140206867-140206917	HL-60	blood:	n/a
41	chr7:140206867-140206917	SKMC	muscle:	n/a
42	chr7:140206867-140206917	HCM	heart:	n/a
43	chr7:140206867-140206917	HepG2	liver:	n/a
44	chr7:140206867-140206917	AG04449	skin:	fetal
45	chr7:140206867-140206917	HRCEpiC	kidney:	n/a
46	chr7:140206867-140206917	AG09309	skin:	n/a
47	chr7:140206867-140206917	AG10803	skin:	n/a
48	chr7:140206867-140206917	Hepatocyte	liver:	n/a
49	chr7:140206867-140206917	LNCaP	prostate:	n/a
50	chr7:140206867-140206917	K562	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:140217454..140218853-chr7:140346568..140347735,7	MCF-7	breast:
2	chr7:140175661..140178823-chr7:140215593..140219447,3	K562	blood:
3	chr7:140177326..140179506-chr7:140211313..140213860,2	MCF-7	breast:
4	chr7:140199121..140201459-chr7:140204634..140207029,2	K562	blood:
5	chr7:140199959..140203037-chr7:140204634..140207948,3	K562	blood:
6	chr7:140177918..140179517-chr7:140199453..140201506,2	MCF-7	breast:
7	chr7:140217452..140219514-chr7:140224086..140226868,2	K562	blood:
8	chr7:140203425..140205241-chr7:140714133..140716127,2	K562	blood:
9	chr7:140175927..140181758-chr7:140182392..140187030,7	K562	blood:
10	chr7:140217150..140218325-chr7:140711569..140712510,4	K562	blood:
11	chr7:140177025..140179254-chr7:140191554..140194261,2	K562	blood:
12	chr7:140177655..140180336-chr7:140200057..140202817,2	MCF-7	breast:
13	chr7:140217094..140218389-chr7:140352924..140354007,12	K562	blood:
14	chr7:140178521..140180888-chr7:140189014..140190989,2	K562	blood:
15	chr7:140188257..140190605-chr7:140190654..140192972,3	K562	blood:
16	chr7:140217465..140218703-chr7:140352465..140353922,9	MCF-7	breast:
17	chr7:140217421..140218389-chr7:140683292..140684296,3	K562	blood:
18	chr7:140182169..140184861-chr7:140185042..140187424,2	K562	blood:
19	chr7:140177890..140180491-chr7:140207898..140209465,2	K562	blood:
20	chr7:139875628..139877580-chr7:140184540..140187021,2	K562	blood:
21	chr7:140177800..140180943-chr7:140182386..140186052,5	MCF-7	breast:
22	chr7:140178138..140180332-chr7:140181621..140183452,2	MCF-7	breast:
23	chr7:140217530..140218341-chr7:140338101..140338802,2	MCF-7	breast:
24	chr7:140207803..140209523-chr7:140395462..140398526,3	K562	blood:
25	chr7:140182169..140184861-chr7:140185042..140187424,2	K562	blood:
26	chr7:140175647..140176450-chr7:140217181..140217731,2	K562	blood:
27	chr7:140177440..140179360-chr7:140192962..140194522,2	MCF-7	breast:
28	chr7:140175277..140176182-chr7:140192249..140193505,5	MCF-7	breast:
29	chr7:140211069..140212654-chr7:140215627..140217284,2	MCF-7	breast:
30	chr7:140216375..140219201-chr7:140345522..140347108,2	MCF-7	breast:
31	chr7:140176571..140180021-chr7:140187634..140190989,3	K562	blood:
32	chr7:140217266..140218508-chr7:140352702..140354109,29	MCF-7	breast:
33	chr7:140216273..140216881-chr7:140352919..140353865,2	K562	blood:
34	chr7:140177891..140180376-chr7:140211143..140213801,3	MCF-7	breast:
35	chr7:140217592..140218317-chr7:140346880..140347484,2	MCF-7	breast:
36	chr7:140174812..140177161-chr7:140216236..140218009,2	K562	blood:
37	chr7:140211069..140212654-chr7:140215627..140217284,2	MCF-7	breast:
38	chr7:140199959..140203037-chr7:140204634..140207948,3	K562	blood:
39	chr7:140177802..140179914-chr7:140192649..140195054,2	MCF-7	breast:
40	chr7:140175249..140176269-chr7:140192550..140193514,8	K562	blood:
41	chr7:140199121..140201459-chr7:140204634..140207029,2	K562	blood:
42	chr7:140188257..140190605-chr7:140190654..140192972,3	K562	blood:
43	chr7:140216203..140218694-chr7:140353097..140355919,3	MCF-7	breast:

No data

Variant related genes	Relation type
MKRN1	TF binding region
MKRN1	CpG island
ENSG00000240889	chromatin interactions
ENSG00000006459	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000240173	chromatin interactions
ENSG00000133606	chromatin interactions
ENSG00000090263	chromatin interactions
ENSG00000260231	chromatin interactions

Extended variants
information (count: 1530 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6971596	chr7:140182985-140182986	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140569384	chr7:140183017-140183018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112424242	chr7:140183018-140183019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77172386	chr7:140183021-140183022	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11972850	chr7:140183022-140183023	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529093026	chr7:140183049-140183050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150281981	chr7:140183052-140183053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550453492	chr7:140183112-140183113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562819826	chr7:140183131-140183132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10227027	chr7:140183146-140183147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs187756752	chr7:140183191-140183192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553132930	chr7:140183269-140183270	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192672436	chr7:140183285-140183286	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184417449	chr7:140183324-140183325	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551681373	chr7:140183348-140183349	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545537692	chr7:140183404-140183405	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189290542	chr7:140183413-140183414	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530958362	chr7:140183528-140183529	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543329030	chr7:140183540-140183541	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs9648842	chr7:140183545-140183546	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114396382	chr7:140183546-140183547	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9648843	chr7:140183607-140183608	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs144891594	chr7:140183608-140183609	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149040646	chr7:140183617-140183618	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143072221	chr7:140183672-140183673	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs62490453	chr7:140183703-140183704	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs569293075	chr7:140183719-140183720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538453933	chr7:140183735-140183736	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536687811	chr7:140183790-140183791	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138705485	chr7:140183828-140183829	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567399165	chr7:140183833-140183834	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558244004	chr7:140183862-140183863	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142764436	chr7:140183866-140183867	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4726825	chr7:140183878-140183879	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192761377	chr7:140183882-140183883	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540679834	chr7:140183901-140183902	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545499040	chr7:140183971-140183972	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538974550	chr7:140183978-140183979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575702036	chr7:140183983-140183984	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542702030	chr7:140184018-140184019	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184614121	chr7:140184022-140184023	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188716833	chr7:140184069-140184070	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555789861	chr7:140184104-140184105	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181447372	chr7:140184168-140184169	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186252026	chr7:140184169-140184170	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189402353	chr7:140184174-140184175	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11974767	chr7:140184208-140184209	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554038788	chr7:140184230-140184231	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532601813	chr7:140184231-140184232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs574312824	chr7:140184257-140184258	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19826477	CNVD
Melanoma	19509136	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140179800-140183000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:140179800-140183400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:140179800-140183400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:140179800-140184400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr7:140179800-140184600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr7:140179800-140184800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:140179800-140185200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:140179800-140187800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:140179800-140198000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:140180000-140183200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:140180000-140183200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:140180000-140183200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:140180000-140183400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr7:140180000-140184400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:140180000-140184400	Weak transcription	Fetal Intestine Large	intestine
16	chr7:140180000-140184400	Weak transcription	Fetal Intestine Small	intestine
17	chr7:140180000-140184400	Weak transcription	Hela-S3	cervix
18	chr7:140180000-140184400	Weak transcription	K562	blood
19	chr7:140180000-140184600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:140180000-140184600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:140180000-140184600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:140180000-140184800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:140180000-140184800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:140180000-140184800	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr7:140180000-140185200	Weak transcription	NHEK	skin
26	chr7:140180000-140188200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr7:140181400-140183200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr7:140181600-140183200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr7:140181600-140183200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:140181600-140183200	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr7:140182200-140184600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:140183000-140185800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:140183200-140183600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:140183200-140183800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr7:140183200-140184600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:140183200-140184600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:140183200-140184600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:140183200-140185200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr7:140183200-140185200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr7:140183400-140184600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:140183400-140185200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:140183400-140185800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr7:140183600-140184400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:140183800-140184200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:140184200-140184600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:140184400-140185000	Enhancers	Duodenum Mucosa	Duodenum
47	chr7:140184400-140185200	Enhancers	Hela-S3	cervix
48	chr7:140184400-140185400	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr7:140184400-140185600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:140184400-140185600	Enhancers	Fetal Intestine Large	intestine

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