Variant report

Variant	nsv1037857
Chromosome Location	chr14:34943388-35007724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:867)
CpG islands
(count:366)
Chromatin interactive
region (count:87)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:34969548-34969921	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:34975027-34975388	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:34966063-34967571	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:34967988-34968420	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:34976759-34976917	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:34966093-34966592	K562	blood:	n/a	n/a
7	ATF1	chr14:34965963-34966707	K562	blood:	n/a	n/a
8	ATF3	chr14:34966038-34966443	K562	blood:	n/a	n/a
9	ATF3	chr14:34966016-34966535	HepG2	liver:	n/a	n/a
10	BACH1	chr14:34966388-34966391	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr14:34965668-34967101	A549	lung:	n/a	chr14:34966277-34966286 chr14:34966278-34966287
12	BCL3	chr14:34965672-34966667	A549	lung:	n/a	chr14:34966277-34966286 chr14:34966278-34966287
13	BHLHE40	chr14:34966762-34967159	HepG2	liver:	n/a	n/a
14	BHLHE40	chr14:34966072-34966515	HepG2	liver:	n/a	n/a
15	BHLHE40	chr14:34968137-34968262	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:34965905-34966483	K562	blood:	n/a	n/a
17	BHLHE40	chr14:34969615-34969812	HepG2	liver:	n/a	n/a
18	BHLHE40	chr14:34960561-34960835	HepG2	liver:	n/a	n/a
19	BRCA1	chr14:34965923-34966768	Hela-S3	cervix:	n/a	n/a
20	CCNT2	chr14:34965901-34966514	K562	blood:	n/a	n/a
21	CEBPB	chr14:34966050-34966477	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:34969707-34969961	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:34965945-34966490	K562	blood:	n/a	n/a
24	CEBPB	chr14:34951701-34951771	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:34969603-34970009	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:34969582-34970004	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:34983120-34983159	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr14:34973275-34973474	H1-hESC	embryonic stem cell:	n/a	chr14:34973418-34973429
29	CEBPB	chr14:34951600-34951872	MCF-7	breast:	n/a	n/a
30	CEBPB	chr14:34989112-34989177	A549	lung:	n/a	chr14:34989146-34989157
31	CEBPB	chr14:34969562-34970046	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:34983093-34983266	K562	blood:	n/a	n/a
33	CEBPB	chr14:34965556-34967123	A549	lung:	n/a	n/a
34	CEBPB	chr14:34962950-34963156	HepG2	liver:	n/a	chr14:34962987-34962998
35	CEBPB	chr14:34950009-34950542	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:34973271-34973511	HepG2	liver:	n/a	chr14:34973418-34973429
37	CEBPB	chr14:34965839-34966670	MCF-7	breast:	n/a	n/a
38	CEBPB	chr14:34960229-34960551	MCF-7	breast:	n/a	chr14:34960394-34960405 chr14:34960393-34960404 chr14:34960395-34960404
39	CEBPB	chr14:34960251-34960566	K562	blood:	n/a	chr14:34960394-34960405 chr14:34960393-34960404 chr14:34960395-34960404
40	CEBPB	chr14:34960253-34960552	Hela-S3	cervix:	n/a	chr14:34960394-34960405 chr14:34960393-34960404 chr14:34960395-34960404
41	CEBPB	chr14:34973268-34973473	K562	blood:	n/a	chr14:34973418-34973429
42	CEBPB	chr14:34965784-34967137	IMR90	lung:	n/a	n/a
43	CEBPB	chr14:34960258-34960574	HepG2	liver:	n/a	chr14:34960394-34960405 chr14:34960393-34960404 chr14:34960395-34960404
44	CEBPB	chr14:34960248-34960617	MCF-7	breast:	n/a	chr14:34960394-34960405 chr14:34960393-34960404 chr14:34960395-34960404
45	CEBPB	chr14:34965754-34967076	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr14:34966767-34967088	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:34950066-34950624	MCF-7	breast:	n/a	n/a
48	CEBPB	chr14:34966690-34967165	HepG2	liver:	n/a	n/a
49	CEBPB	chr14:34966122-34966432	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:34975538-34975797	HepG2	liver:	n/a	chr14:34975643-34975654

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:34966313-34966363	GM19239	blood:	n/a
2	chr14:34944819-34944869	IMR90	lung:	fetal
3	chr14:34966313-34966363	HEEpiC	esophagus:	n/a
4	chr14:34944819-34944869	NT2-D1	testis:	n/a
5	chr14:34944819-34944869	HCT-116	colon:	n/a
6	chr14:34944819-34944869	GM12878	blood:	n/a
7	chr14:34945225-34945275	NHDF-neo	bronchial:	n/a
8	chr14:34945225-34945275	AG09319	gingival:	n/a
9	chr14:34945225-34945275	K562	blood:	n/a
10	chr14:34966313-34966363	IMR90	lung:	fetal
11	chr14:34945475-34945525	HCM	heart:	n/a
12	chr14:34945475-34945525	HL-60	blood:	n/a
13	chr14:34945225-34945275	SAEC	small airway:	n/a
14	chr14:34971569-34971619	BE2_C	brain:	n/a
15	chr14:34945225-34945275	H1-hESC	embryonic stem cell:	embryo
16	chr14:34945225-34945275	T-47D	breast:	n/a
17	chr14:34945225-34945275	AG10803	skin:	n/a
18	chr14:34971569-34971619	ovcar-3	ovarian:	n/a
19	chr14:34944819-34944869	HepG2	liver:	n/a
20	chr14:35006074-35006124	U87	brain:	n/a
21	chr14:34971569-34971619	HEEpiC	esophagus:	n/a
22	chr14:34945475-34945525	PANC-1	pancreas:	n/a
23	chr14:35006074-35006124	AG04449	skin:	fetal
24	chr14:34966313-34966363	HNPCEpiC	eye:	n/a
25	chr14:34966313-34966363	H1-hESC	embryonic stem cell:	embryo
26	chr14:34971569-34971619	SKMC	muscle:	n/a
27	chr14:34966313-34966363	K562	blood:	n/a
28	chr14:34971569-34971619	RPTEC	kidney:	n/a
29	chr14:34944819-34944869	AG04449	skin:	fetal
30	chr14:35006074-35006124	ECC-1	luminal epithelium:	n/a
31	chr14:34945475-34945525	HRE	kidney:	n/a
32	chr14:35006074-35006124	AG04450	lung:	fetal
33	chr14:34945225-34945275	NH-A	brain:	n/a
34	chr14:34945225-34945275	GM19239	blood:	n/a
35	chr14:34944819-34944869	MCF10A-Er-Src	breast:	n/a
36	chr14:34944819-34944869	HEEpiC	esophagus:	n/a
37	chr14:34945225-34945275	GM12892	blood:	n/a
38	chr14:34944819-34944869	Hela-S3	cervix:	n/a
39	chr14:35006074-35006124	AoSMC	blood vessel:	n/a
40	chr14:35006074-35006124	NT2-D1	testis:	n/a
41	chr14:34945225-34945275	MCF-7	breast:	n/a
42	chr14:35006074-35006124	NHDF-neo	bronchial:	n/a
43	chr14:34945225-34945275	ovcar-3	ovarian:	n/a
44	chr14:34945225-34945275	HRCEpiC	kidney:	n/a
45	chr14:35006074-35006124	HRE	kidney:	n/a
46	chr14:34944819-34944869	HRCEpiC	kidney:	n/a
47	chr14:34945225-34945275	HCPEpiC	choroid plexus:	n/a
48	chr14:34971569-34971619	GM12878	blood:	n/a
49	chr14:34945225-34945275	SK-N-SH	brain:	n/a
50	chr14:34945475-34945525	NH-A	brain:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35000955..35003897-chr14:35015691..35017291,2	MCF-7	breast:
2	chr14:35005506..35011243-chr14:35020994..35025666,12	MCF-7	breast:
3	chr14:34930447..34933424-chr14:34957189..34958854,2	MCF-7	breast:
4	chr14:34957508..34960404-chr14:34964346..34966873,2	K562	blood:
5	chr14:34830829..34832701-chr14:34965153..34968151,2	MCF-7	breast:
6	chr14:34996976..35002931-chr14:35005430..35010920,7	MCF-7	breast:
7	chr14:34964955..34967907-chr14:34973617..34975342,2	MCF-7	breast:
8	chr14:34931775..34934321-chr14:34942958..34944462,2	K562	blood:
9	chr14:34930482..34933296-chr14:34952569..34954350,2	MCF-7	breast:
10	chr14:34997979..35000890-chr14:35004002..35008014,4	K562	blood:
11	chr14:34930993..34932561-chr14:34956860..34958975,2	MCF-7	breast:
12	chr14:34931690..34933656-chr14:35005412..35007221,2	K562	blood:
13	chr14:34955969..34958289-chr14:35024078..35025715,2	MCF-7	breast:
14	chr14:34918625..34921655-chr14:34965491..34967777,3	MCF-7	breast:
15	chr14:34935994..34938322-chr14:34940821..34943431,3	K562	blood:
16	chr14:34963976..34965714-chr14:35019570..35022197,2	MCF-7	breast:
17	chr14:34988212..34991745-chr14:34992465..34994604,3	MCF-7	breast:
18	chr14:34800393..34801534-chr14:34967736..34968695,6	MCF-7	breast:
19	chr14:34929449..34931749-chr14:34993451..34995469,2	MCF-7	breast:
20	chr14:34987498..34989819-chr14:35007397..35008989,2	MCF-7	breast:
21	chr14:34959614..34962811-chr14:34966236..34969041,3	K562	blood:
22	chr14:34990714..34993643-chr14:35006292..35008810,2	K562	blood:
23	chr14:34930215..34933464-chr14:34966414..34969338,4	MCF-7	breast:
24	chr14:34800908..34801526-chr14:34966566..34967258,2	MCF-7	breast:
25	chr14:34950779..34952315-chr14:34964739..34966921,2	MCF-7	breast:
26	chr14:34927994..34930347-chr14:34965334..34966847,2	K562	blood:
27	chr14:34929804..34932141-chr14:35000832..35004516,3	K562	blood:
28	chr14:35005104..35007114-chr14:35007414..35009874,3	K562	blood:
29	chr14:35003178..35006952-chr14:35007318..35009026,4	MCF-7	breast:
30	chr14:34992410..34994552-chr14:35006648..35008744,2	MCF-7	breast:
31	chr14:34990714..34993643-chr14:35006292..35008810,2	K562	blood:
32	chr14:34993830..34996289-chr14:35004002..35006048,2	K562	blood:
33	chr14:35004626..35011116-chr14:35015634..35020787,10	MCF-7	breast:
34	chr14:34928753..34932995-chr14:34963537..34968945,14	MCF-7	breast:
35	chr14:34938365..34940325-chr14:34941418..34943852,2	MCF-7	breast:
36	chr14:34834264..34835188-chr14:34967046..34968623,5	MCF-7	breast:
37	chr14:34997304..35000255-chr14:35008172..35010280,2	K562	blood:
38	chr14:34932436..34934680-chr14:34965867..34967830,2	K562	blood:
39	chr14:34800581..34801486-chr14:34967721..34968650,2	K562	blood:
40	chr14:35007630..35008465-chr16:73238858..73239382,2	MCF-7	breast:
41	chr14:34959614..34962811-chr14:34966236..34969041,3	K562	blood:
42	chr14:34957508..34960404-chr14:34964346..34966873,2	K562	blood:
43	chr14:34998512..35003069-chr14:35021669..35025917,5	MCF-7	breast:
44	chr14:34988212..34991745-chr14:34992465..34994604,3	MCF-7	breast:
45	chr14:34990134..34992154-chr14:35005229..35008582,3	MCF-7	breast:
46	chr14:34966374..34968147-chr14:35008912..35011090,2	MCF-7	breast:
47	chr14:35002309..35005186-chr14:35018776..35021150,2	MCF-7	breast:
48	chr14:34995358..34997093-chr14:35024116..35025822,2	K562	blood:
49	chr14:34950779..34952315-chr14:34964739..34966921,2	MCF-7	breast:
50	chr14:34929666..34933656-chr14:35005721..35010391,9	K562	blood:

No data

Variant related genes	Relation type
EAPP	TF binding region
ENSG00000237450	TF binding region
EAPP	CpG island
ENSG00000237450	CpG island
ENSG00000206588	chromatin interactions
ENSG00000129521	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000165389	chromatin interactions
ENSG00000206596	chromatin interactions
ENSG00000129518	chromatin interactions

Extended variants
information (count: 2713 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2713 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192119001	chr14:34943415-34943416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141042123	chr14:34943419-34943420	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114001809	chr14:34943585-34943586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565904403	chr14:34943619-34943620	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs183450659	chr14:34943666-34943667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187894062	chr14:34943667-34943668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568407084	chr14:34943673-34943674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536945570	chr14:34943719-34943720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557331153	chr14:34943749-34943750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570719147	chr14:34943823-34943824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs78835503	chr14:34943843-34943844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35955771	chr14:34943846-34943847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150679824	chr14:34943882-34943883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149825843	chr14:34943894-34943895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572983473	chr14:34943895-34943896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535690086	chr14:34943919-34943920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144924539	chr14:34943937-34943938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373126419	chr14:34944091-34944092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566276444	chr14:34944097-34944098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377733589	chr14:34944098-34944099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575535595	chr14:34944101-34944102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537032989	chr14:34944103-34944104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199590127	chr14:34944104-34944105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374897841	chr14:34944108-34944109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140917773	chr14:34944109-34944110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576736895	chr14:34944110-34944111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534866213	chr14:34944111-34944112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559526004	chr14:34944112-34944113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12884822	chr14:34944113-34944114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs76951948	chr14:34944116-34944117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs61981476	chr14:34944118-34944119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192784834	chr14:34944183-34944184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561820975	chr14:34944189-34944190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138516095	chr14:34944193-34944194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184171088	chr14:34944213-34944214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377508195	chr14:34944276-34944277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140257425	chr14:34944299-34944300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs386776366	chr14:34944307-34944308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546578419	chr14:34944378-34944379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76206126	chr14:34944442-34944443	Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535508677	chr14:34944455-34944456	Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555549617	chr14:34944482-34944483	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs367685753	chr14:34944497-34944498	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs10133741	chr14:34944501-34944502	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558195946	chr14:34944503-34944504	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs574996602	chr14:34944560-34944561	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs556227281	chr14:34944601-34944602	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs12587106	chr14:34944624-34944625	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs146679582	chr14:34944630-34944631	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs10133692	chr14:34944643-34944644	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:34932600-34944600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr14:34932600-34945000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:34942200-34945600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:34944400-34944600	Active TSS	HSMM	muscle
5	chr14:34944400-34944800	Bivalent/Poised TSS	GM12878-XiMat	blood
6	chr14:34944600-34944800	Enhancers	Primary hematopoietic stem cells	blood
7	chr14:34944600-34944800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr14:34944600-34944800	Flanking Active TSS	HSMM	muscle
9	chr14:34944600-34944800	Active TSS	NH-A	brain
10	chr14:34944600-34945600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr14:34945000-34945600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:34945600-34950400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:34945600-34952600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr14:34949000-34949400	Enhancers	HepG2	liver
15	chr14:34950000-34950200	Enhancers	Hela-S3	cervix
16	chr14:34950200-34950600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:34950200-34950600	Flanking Active TSS	Hela-S3	cervix
18	chr14:34950200-34950800	Enhancers	Placenta	Placenta
19	chr14:34950400-34950600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr14:34950600-34950800	Enhancers	Hela-S3	cervix
21	chr14:34950600-34966400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:34950800-34958200	Weak transcription	Placenta	Placenta
23	chr14:34951200-34952600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr14:34952000-34953400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:34952600-34952800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr14:34952600-34953400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr14:34952600-34953400	Bivalent Enhancer	HepG2	liver
28	chr14:34952800-34960200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr14:34957200-34957400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:34957400-34966000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr14:34958000-34959000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:34958000-34959000	Enhancers	Esophagus	oesophagus
33	chr14:34958000-34959000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr14:34958200-34958800	Enhancers	A549	lung
35	chr14:34958200-34959000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:34958200-34959000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:34958200-34959000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr14:34958200-34959000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr14:34958200-34959200	Enhancers	NHEK	skin
40	chr14:34958200-34960800	Enhancers	Placenta	Placenta
41	chr14:34958400-34959000	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr14:34958400-34959200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr14:34958600-34958800	Enhancers	HepG2	liver
44	chr14:34958600-34959000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr14:34958600-34959000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr14:34958800-34959000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:34958800-34959000	Enhancers	Hela-S3	cervix
48	chr14:34958800-34960400	Weak transcription	A549	lung
49	chr14:34959000-34959200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:34959000-34960200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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