Variant report

Variant	esv35077
Chromosome Location	chr5:40875843-41000671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:888)
CpG islands
(count:550)
Chromatin interactive
region (count:44)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:888 , 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	chr5:40877967-40878007	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:40879566-40879848	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:40904018-40905206	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:40909857-40910242	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:40879437-40879846	K562	blood:	n/a	n/a
6	ARID3A	chr5:40991223-40991942	HepG2	liver:	n/a	n/a
7	ATF1	chr5:40985762-40985851	K562	blood:	n/a	n/a
8	BACH1	chr5:40876221-40876385	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:40957286-40957375	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:40915947-40915993	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr5:40877820-40878038	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:40904889-40905059	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:40904775-40905170	K562	blood:	n/a	n/a
14	CBX3	chr5:40877462-40877985	K562	blood:	n/a	n/a
15	CBX3	chr5:40877683-40878085	HCT-116	colon:	n/a	n/a
16	CBX3	chr5:40877491-40877821	K562	blood:	n/a	n/a
17	CEBPB	chr5:40991337-40991938	HepG2	liver:	n/a	chr5:40991525-40991536 chr5:40991767-40991780 chr5:40991524-40991537
18	CEBPB	chr5:40991274-40991795	HepG2	liver:	n/a	chr5:40991525-40991536 chr5:40991767-40991780 chr5:40991524-40991537
19	CEBPB	chr5:40915141-40915454	HepG2	liver:	n/a	chr5:40915435-40915446
20	CEBPB	chr5:40914987-40915468	Hela-S3	cervix:	n/a	chr5:40915435-40915446
21	CEBPB	chr5:40876134-40876329	HepG2	liver:	n/a	chr5:40876252-40876263
22	CEBPB	chr5:40956045-40956290	HepG2	liver:	n/a	chr5:40956174-40956185
23	CEBPB	chr5:40974072-40974407	IMR90	lung:	n/a	chr5:40974236-40974247
24	CEBPB	chr5:40938639-40938901	HepG2	liver:	n/a	chr5:40938772-40938783
25	CEBPB	chr5:40995719-40995933	A549	lung:	n/a	chr5:40995835-40995846
26	CEBPB	chr5:40973622-40973787	A549	lung:	n/a	n/a
27	CEBPB	chr5:40991414-40991648	HepG2	liver:	n/a	chr5:40991525-40991536 chr5:40991524-40991537
28	CEBPB	chr5:40903563-40903664	HepG2	liver:	n/a	chr5:40903636-40903645 chr5:40903634-40903647 chr5:40903636-40903647 chr5:40903634-40903645
29	CEBPB	chr5:40991326-40991871	MCF-7	breast:	n/a	chr5:40991525-40991536 chr5:40991767-40991780 chr5:40991524-40991537
30	CEBPB	chr5:40915069-40915821	H1-hESC	embryonic stem cell:	n/a	chr5:40915435-40915446
31	CEBPB	chr5:40903583-40903783	K562	blood:	n/a	chr5:40903636-40903645 chr5:40903634-40903647 chr5:40903636-40903647 chr5:40903634-40903645
32	CEBPB	chr5:40991426-40991834	MCF-7	breast:	n/a	chr5:40991525-40991536 chr5:40991767-40991780 chr5:40991524-40991537
33	CEBPB	chr5:40991361-40991926	IMR90	lung:	n/a	chr5:40991525-40991536 chr5:40991767-40991780 chr5:40991524-40991537
34	CEBPB	chr5:40995724-40995915	K562	blood:	n/a	chr5:40995835-40995846
35	CEBPB	chr5:40974085-40974421	K562	blood:	n/a	chr5:40974236-40974247
36	CEBPB	chr5:40965401-40965585	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:40936932-40937135	HepG2	liver:	n/a	chr5:40936998-40937015
38	CEBPB	chr5:40995669-40996006	HepG2	liver:	n/a	chr5:40995835-40995846
39	CEBPB	chr5:40914942-40915531	IMR90	lung:	n/a	chr5:40915435-40915446
40	CEBPB	chr5:40883320-40883335	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:40876221-40876315	H1-hESC	embryonic stem cell:	n/a	chr5:40876252-40876263
42	CEBPB	chr5:40991296-40991882	HepG2	liver:	n/a	chr5:40991525-40991536 chr5:40991767-40991780 chr5:40991524-40991537
43	CEBPB	chr5:40876194-40876288	HepG2	liver:	n/a	chr5:40876252-40876263
44	CEBPB	chr5:40896250-40896349	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:40974125-40974378	HepG2	liver:	n/a	chr5:40974236-40974247
46	CEBPD	chr5:40991391-40991678	HepG2	liver:	n/a	chr5:40991525-40991536
47	CHD1	chr5:40904767-40905697	IMR90	lung:	n/a	n/a
48	CHD2	chr5:40904825-40905098	HepG2	liver:	n/a	n/a
49	CHD2	chr5:40972729-40972811	HepG2	liver:	n/a	n/a
50	CHD2	chr5:40895937-40895951	H1-hESC	embryonic stem cell:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:40908778-40908828	NHBE	bronchial:	n/a
2	chr5:40908778-40908828	NHBE	bronchial:	n/a
3	chr5:40984654-40984704	AG10803	skin:	n/a
4	chr5:40908780-40908830	NH-A	brain:	n/a
5	chr5:40908395-40908445	GM12891	blood:	n/a
6	chr5:40982092-40982142	ECC-1	luminal epithelium:	n/a
7	chr5:40933444-40933494	PrEC	prostate:	n/a
8	chr5:40908395-40908445	U87	brain:	n/a
9	chr5:40908778-40908828	NT2-D1	testis:	n/a
10	chr5:40905255-40905305	SKMC	muscle:	n/a
11	chr5:40905255-40905305	HRCEpiC	kidney:	n/a
12	chr5:40982092-40982142	Hepatocyte	liver:	n/a
13	chr5:40982092-40982142	HNPCEpiC	eye:	n/a
14	chr5:40908395-40908445	HEK293	kidney:	embryo
15	chr5:40908228-40908278	NHDF-neo	bronchial:	n/a
16	chr5:40984654-40984704	HAEpiC	amniotic membrane:	n/a
17	chr5:40909532-40909582	NB4	blood:	n/a
18	chr5:40908780-40908830	HNPCEpiC	eye:	n/a
19	chr5:40908228-40908278	LNCaP	prostate:	n/a
20	chr5:40908395-40908445	ECC-1	luminal epithelium:	n/a
21	chr5:40909532-40909582	HEEpiC	esophagus:	n/a
22	chr5:40909532-40909582	GM06990	blood:	n/a
23	chr5:40908780-40908830	BJ	skin:	n/a
24	chr5:40905255-40905305	HL-60	blood:	n/a
25	chr5:40905255-40905305	GM12891	blood:	n/a
26	chr5:40982092-40982142	AG10803	skin:	n/a
27	chr5:40933444-40933494	HNPCEpiC	eye:	n/a
28	chr5:40909532-40909582	RPTEC	kidney:	n/a
29	chr5:40933444-40933494	HCM	heart:	n/a
30	chr5:40908228-40908278	PrEC	prostate:	n/a
31	chr5:40905255-40905305	HEEpiC	esophagus:	n/a
32	chr5:40982092-40982142	GM12891	blood:	n/a
33	chr5:40909532-40909582	PFSK-1	brain:	n/a
34	chr5:40905255-40905305	H1-hESC	embryonic stem cell:	embryo
35	chr5:40908778-40908828	PFSK-1	brain:	n/a
36	chr5:40909532-40909582	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:40908395-40908445	GM12892	blood:	n/a
38	chr5:40933444-40933494	AG09319	gingival:	n/a
39	chr5:40905255-40905305	GM19239	blood:	n/a
40	chr5:40905255-40905305	IMR90	lung:	fetal
41	chr5:40933444-40933494	GM12892	blood:	n/a
42	chr5:40982092-40982142	AG09309	skin:	n/a
43	chr5:40908780-40908830	NB4	blood:	n/a
44	chr5:40905255-40905305	HRPEpiC	eye:	n/a
45	chr5:40905255-40905305	HMEC	breast:	n/a
46	chr5:40908778-40908828	AoSMC	blood vessel:	n/a
47	chr5:40909532-40909582	AG04449	skin:	fetal
48	chr5:40984654-40984704	HMEC	breast:	n/a
49	chr5:40908395-40908445	AoSMC	blood vessel:	n/a
50	chr5:40908778-40908828	HL-60	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:40953904..40955665-chr5:40958137..40961291,3	K562	blood:
2	chr5:40904832..40905544-chr5:41118009..41119184,4	MCF-7	breast:
3	chr5:40839617..40842545-chr5:40884343..40886931,2	K562	blood:
4	chr5:40857647..40860536-chr5:40876647..40878892,2	K562	blood:
5	chr5:40906764..40908944-chr5:40910686..40913310,2	K562	blood:
6	chr5:40976435..40978654-chr5:40981165..40983348,2	MCF-7	breast:
7	chr5:40832193..40835504-chr5:40894325..40897011,3	MCF-7	breast:
8	chr5:40755051..40755677-chr5:40904503..40905135,2	MCF-7	breast:
9	chr5:40833805..40835893-chr5:40886432..40888322,2	MCF-7	breast:
10	chr5:40956867..40959314-chr5:40961623..40964279,2	K562	blood:
11	chr5:40904836..40905424-chr5:41118089..41118768,2	MCF-7	breast:
12	chr5:40834243..40835904-chr5:40876719..40878395,2	K562	blood:
13	chr5:40862902..40865200-chr5:40878368..40881036,2	K562	blood:
14	chr5:40904833..40905459-chr5:41270472..41271168,3	MCF-7	breast:
15	chr5:40754832..40756166-chr5:40878991..40879947,5	MCF-7	breast:
16	chr5:40987621..40990606-chr5:40992275..40995928,3	K562	blood:
17	chr5:40877064..40878620-chr5:40889249..40891456,2	MCF-7	breast:
18	chr5:40877064..40878620-chr5:40889249..40891456,2	MCF-7	breast:
19	chr5:40887409..40889987-chr5:40893974..40896767,2	MCF-7	breast:
20	chr5:40956867..40959314-chr5:40961623..40964279,2	K562	blood:
21	chr5:40989247..40991997-chr5:41008432..41010660,2	MCF-7	breast:
22	chr5:40825327..40827684-chr5:40878879..40880894,2	K562	blood:
23	chr5:40887409..40889987-chr5:40893974..40896767,2	MCF-7	breast:
24	chr5:40753879..40756719-chr5:40886752..40889953,3	K562	blood:
25	chr5:40904256..40905017-chr5:41641481..41642261,2	MCF-7	breast:
26	chr5:40754836..40755851-chr5:40878943..40880145,7	K562	blood:
27	chr5:40797441..40799812-chr5:40889313..40890816,2	MCF-7	breast:
28	chr5:40904937..40905544-chr5:41641443..41642188,2	K562	blood:
29	chr5:40953904..40955665-chr5:40958137..40961291,3	K562	blood:
30	chr5:40942973..40944757-chr5:40947112..40948755,2	K562	blood:
31	chr5:40904493..40905461-chr5:40962028..40963060,5	MCF-7	breast:
32	chr5:40774463..40775388-chr5:40879209..40879987,4	MCF-7	breast:
33	chr5:40966521..40968978-chr5:40972964..40975614,2	K562	blood:
34	chr5:40982776..40984808-chr5:40985903..40987745,2	MCF-7	breast:
35	chr5:40904493..40905461-chr5:40962028..40963060,5	MCF-7	breast:
36	chr5:40973576..40975248-chr5:40975301..40976808,2	K562	blood:
37	chr5:40904574..40905604-chr5:41346513..41347365,3	MCF-7	breast:
38	chr5:40825063..40827594-chr5:40875913..40878688,2	K562	blood:
39	chr5:40982776..40984808-chr5:40985903..40987745,2	MCF-7	breast:
40	chr5:40942973..40944757-chr5:40947112..40948755,2	K562	blood:
41	chr5:40879793..40882550-chr5:40882872..40884630,2	K562	blood:
42	chr5:40987621..40990606-chr5:40992275..40995928,3	K562	blood:
43	chr5:40832872..40835658-chr5:40893806..40896562,2	MCF-7	breast:
44	chr5:40879793..40882550-chr5:40882872..40884630,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HEATR7B2-2	chr5:40967607-40967865	NONHSAT101165

No data

Variant related genes	Relation type
RNU7-161P	TF binding region
ENSG00000248120	TF binding region
MROH2B	TF binding region
C7	TF binding region
RNU7-161P	CpG island
ENSG00000248120	CpG island
MROH2B	CpG island
C7	CpG island
ENSG00000132356	chromatin interactions
ENSG00000113638	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000212296	chromatin interactions
ENSG00000253098	chromatin interactions
ENSG00000132357	chromatin interactions
ENSG00000248120	chromatin interactions
ENSG00000112936	chromatin interactions

Extended variants
information (count: 5129 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5129 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574820362	chr5:40875855-40875856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs404223	chr5:40875879-40875880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs560344774	chr5:40875888-40875889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114898582	chr5:40875902-40875903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7702096	chr5:40875933-40875934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs567165	chr5:40875994-40875995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536403190	chr5:40876019-40876020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532384808	chr5:40876020-40876021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550593543	chr5:40876074-40876075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184726368	chr5:40876084-40876085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530471932	chr5:40876118-40876119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555334054	chr5:40876155-40876156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112690199	chr5:40876178-40876179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374537516	chr5:40876181-40876182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556262561	chr5:40876186-40876187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140032666	chr5:40876215-40876216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189652159	chr5:40876226-40876227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143667237	chr5:40876236-40876237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565260414	chr5:40876322-40876323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10035621	chr5:40876335-40876336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs371232955	chr5:40876336-40876337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76438535	chr5:40876341-40876342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180879192	chr5:40876362-40876363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115107847	chr5:40876451-40876452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574784386	chr5:40876455-40876456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544371603	chr5:40876514-40876515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542150188	chr5:40876515-40876516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370227974	chr5:40876518-40876519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10041257	chr5:40876523-40876524	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs572211158	chr5:40876524-40876525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144736225	chr5:40876566-40876567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183481305	chr5:40876567-40876568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532495468	chr5:40876584-40876585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189376451	chr5:40876818-40876819	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs56204127	chr5:40876868-40876869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546810822	chr5:40876879-40876880	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570540722	chr5:40876936-40876937	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185965173	chr5:40876940-40876941	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs151102869	chr5:40876977-40876978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529934878	chr5:40877036-40877037	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78238607	chr5:40877051-40877052	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73088503	chr5:40877062-40877063	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs142614221	chr5:40877064-40877065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs71623867	chr5:40877066-40877067	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78408051	chr5:40877071-40877072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554047771	chr5:40877081-40877082	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs59608477	chr5:40877091-40877092	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112266711	chr5:40877092-40877093	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs144959011	chr5:40877101-40877102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545568309	chr5:40877152-40877153	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Bladder cancer	21909424	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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:40872000-40876600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:40879400-40879600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:40879400-40879600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:40879400-40879600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:40879400-40879600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:40879400-40879600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr5:40879400-40879600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr5:40879400-40879600	Enhancers	Fetal Lung	lung
9	chr5:40879400-40879600	Enhancers	A549	lung
10	chr5:40879400-40879600	Enhancers	K562	blood
11	chr5:40879400-40879600	Enhancers	NHDF-Ad	bronchial
12	chr5:40879400-40879600	Enhancers	NHLF	lung
13	chr5:40879400-40879600	Enhancers	Osteobl	bone
14	chr5:40879400-40879800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr5:40879400-40880000	Enhancers	Liver	Liver
16	chr5:40879400-40880000	Enhancers	Hela-S3	cervix
17	chr5:40882400-40884800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:40883000-40883400	Enhancers	Fetal Intestine Large	intestine
19	chr5:40883000-40883400	Enhancers	Fetal Intestine Small	intestine
20	chr5:40883000-40883600	Active TSS	Duodenum Mucosa	Duodenum
21	chr5:40883200-40883600	Enhancers	HepG2	liver
22	chr5:40883400-40883800	Active TSS	Fetal Intestine Small	intestine
23	chr5:40883600-40885200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:40885000-40885200	Enhancers	Fetal Brain Male	brain
25	chr5:40885200-40895400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:40889800-40890200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
27	chr5:40893800-40894400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:40893800-40894600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr5:40893800-40894800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr5:40893800-40895200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr5:40894000-40894200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr5:40894000-40894200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:40894000-40894600	Enhancers	H9 Cell Line	embryonic stem cell
34	chr5:40894200-40895400	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr5:40894400-40894800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr5:40894400-40895600	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr5:40894600-40895000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr5:40894600-40895200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:40894800-40895200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr5:40894800-40895200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr5:40895000-40895200	Enhancers	HepG2	liver
42	chr5:40895000-40895600	Enhancers	H9 Cell Line	embryonic stem cell
43	chr5:40895200-40895400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr5:40895200-40895600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:40895200-40895600	Flanking Active TSS	HepG2	liver
46	chr5:40895200-40895800	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr5:40895200-40895800	Enhancers	H1 Cell Line	embryonic stem cell
48	chr5:40895200-40895800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr5:40895200-40895800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr5:40895400-40895600	Active TSS	iPS-20b Cell Line	embryonic stem cell

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