Variant report

Variant	nsv964348
Chromosome Location	chr4:56782802-56815653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1016)
CpG islands
(count:794)
Chromatin interactive
region (count:27)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1016 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56814620-56815710	K562	blood:	n/a	chr4:56815625-56815641
2	ARID3A	chr4:56814236-56814399	K562	blood:	n/a	n/a
3	ARID3A	chr4:56815523-56816127	HepG2	liver:	n/a	chr4:56815625-56815641
4	ARID3A	chr4:56814765-56815291	HepG2	liver:	n/a	n/a
5	ATF2	chr4:56813391-56813954	GM12878	blood:	n/a	n/a
6	ATF2	chr4:56813229-56814436	GM12878	blood:	n/a	n/a
7	ATF2	chr4:56814710-56815130	GM12878	blood:	n/a	n/a
8	ATF2	chr4:56814601-56815380	GM12878	blood:	n/a	n/a
9	BACH1	chr4:56814557-56815281	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:56814755-56815080	GM12878	blood:	n/a	n/a
11	BATF	chr4:56814022-56814300	GM12878	blood:	n/a	n/a
12	BCLAF1	chr4:56813494-56814284	GM12878	blood:	n/a	n/a
13	BCLAF1	chr4:56814709-56815580	GM12878	blood:	n/a	chr4:56815020-56815033 chr4:56815289-56815302 chr4:56815251-56815264 chr4:56815101-56815110 chr4:56814922-56814935 chr4:56815325-56815338
14	BCLAF1	chr4:56814643-56815410	GM12878	blood:	n/a	chr4:56815020-56815033 chr4:56815289-56815302 chr4:56815251-56815264 chr4:56815101-56815110 chr4:56814922-56814935 chr4:56815325-56815338
15	BHLHE40	chr4:56814578-56815601	GM12878	blood:	n/a	chr4:56815246-56815262
16	BHLHE40	chr4:56814711-56815854	K562	blood:	n/a	chr4:56815246-56815262
17	BHLHE40	chr4:56814791-56815543	HepG2	liver:	n/a	chr4:56815246-56815262
18	BHLHE40	chr4:56813394-56814361	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:56814257-56814445	K562	blood:	n/a	n/a
20	BRCA1	chr4:56814762-56815264	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:56814648-56815007	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr4:56814809-56815005	HepG2	liver:	n/a	n/a
23	BRCA1	chr4:56814578-56815126	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr4:56815526-56815741	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr4:56814679-56815749	K562	blood:	n/a	n/a
26	CCNT2	chr4:56814694-56815509	K562	blood:	n/a	n/a
27	CEBPB	chr4:56797923-56798246	HepG2	liver:	n/a	chr4:56798073-56798084
28	CEBPB	chr4:56814253-56816046	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:56794635-56794833	K562	blood:	n/a	n/a
30	CEBPB	chr4:56783330-56783454	K562	blood:	n/a	n/a
31	CEBPB	chr4:56814808-56815253	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:56814725-56815095	K562	blood:	n/a	n/a
33	CEBPB	chr4:56815423-56815712	K562	blood:	n/a	n/a
34	CEBPB	chr4:56815404-56815658	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:56795484-56795573	HepG2	liver:	n/a	chr4:56795532-56795543
36	CEBPB	chr4:56815424-56815617	A549	lung:	n/a	n/a
37	CEBPB	chr4:56788897-56788904	K562	blood:	n/a	n/a
38	CEBPB	chr4:56814844-56815170	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:56813532-56813867	K562	blood:	n/a	n/a
40	CEBPB	chr4:56797909-56798383	IMR90	lung:	n/a	chr4:56798073-56798084
41	CEBPD	chr4:56815185-56815603	HepG2	liver:	n/a	n/a
42	CEBPD	chr4:56815023-56815519	K562	blood:	n/a	n/a
43	CHD1	chr4:56814803-56815294	H1-hESC	embryonic stem cell:	n/a	chr4:56814858-56814868
44	CHD1	chr4:56813363-56816295	GM12878	blood:	n/a	chr4:56815368-56815378 chr4:56814858-56814868
45	CHD2	chr4:56814752-56815508	Hela-S3	cervix:	n/a	chr4:56815368-56815378 chr4:56814858-56814868
46	CHD2	chr4:56814791-56815306	K562	blood:	n/a	chr4:56814858-56814868
47	CHD2	chr4:56814931-56815298	HepG2	liver:	n/a	n/a
48	CHD2	chr4:56813364-56815764	GM12878	blood:	n/a	chr4:56815368-56815378 chr4:56814858-56814868
49	CHD2	chr4:56815372-56815594	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:56814774-56815141	H1-hESC	embryonic stem cell:	n/a	chr4:56814858-56814868

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56814948-56814998	NHDF-neo	bronchial:	n/a
2	chr4:56814948-56814998	NHDF-neo	bronchial:	n/a
3	chr4:56815070-56815120	AG04450	lung:	fetal
4	chr4:56814925-56814975	HEEpiC	esophagus:	n/a
5	chr4:56813860-56813910	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:56814931-56814981	GM12878	blood:	n/a
7	chr4:56814934-56814984	ECC-1	luminal epithelium:	n/a
8	chr4:56815263-56815313	Caco-2	colon:	n/a
9	chr4:56815073-56815123	HNPCEpiC	eye:	n/a
10	chr4:56815263-56815313	SK-N-SH_RA	brain:	n/a
11	chr4:56815263-56815313	HUVEC	blood vessel:	n/a
12	chr4:56813898-56813948	A549	lung:	n/a
13	chr4:56815510-56815560	HepG2	liver:	n/a
14	chr4:56813860-56813910	PFSK-1	brain:	n/a
15	chr4:56815263-56815313	HepG2	liver:	n/a
16	chr4:56812321-56812371	PFSK-1	brain:	n/a
17	chr4:56813860-56813910	T-47D	breast:	n/a
18	chr4:56815606-56815656	HL-60	blood:	n/a
19	chr4:56813898-56813948	SKMC	muscle:	n/a
20	chr4:56813898-56813948	AG04449	skin:	fetal
21	chr4:56813898-56813948	HMEC	breast:	n/a
22	chr4:56814931-56814981	HAEpiC	amniotic membrane:	n/a
23	chr4:56814931-56814981	HepG2	liver:	n/a
24	chr4:56812321-56812371	GM12891	blood:	n/a
25	chr4:56815263-56815313	HNPCEpiC	eye:	n/a
26	chr4:56813860-56813910	HEK293	kidney:	embryo
27	chr4:56814925-56814975	HCF	heart:	n/a
28	chr4:56815510-56815560	PrEC	prostate:	n/a
29	chr4:56814934-56814984	PFSK-1	brain:	n/a
30	chr4:56814948-56814998	HMEC	breast:	n/a
31	chr4:56814925-56814975	HL-60	blood:	n/a
32	chr4:56814925-56814975	SK-N-MC	brain:	n/a
33	chr4:56815510-56815560	Caco-2	colon:	n/a
34	chr4:56815070-56815120	HepG2	liver:	n/a
35	chr4:56814934-56814984	NHBE	bronchial:	n/a
36	chr4:56815073-56815123	HAEpiC	amniotic membrane:	n/a
37	chr4:56814925-56814975	GM19239	blood:	n/a
38	chr4:56815070-56815120	HAEpiC	amniotic membrane:	n/a
39	chr4:56814931-56814981	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:56815073-56815123	RPTEC	kidney:	n/a
41	chr4:56815070-56815120	A549	lung:	n/a
42	chr4:56812321-56812371	HAEpiC	amniotic membrane:	n/a
43	chr4:56812321-56812371	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:56813898-56813948	ProgFib	skin:	n/a
45	chr4:56814925-56814975	PANC-1	pancreas:	n/a
46	chr4:56814948-56814998	HUVEC	blood vessel:	n/a
47	chr4:56814925-56814975	NT2-D1	testis:	n/a
48	chr4:56812321-56812371	Jurkat	blood:	n/a
49	chr4:56814925-56814975	SAEC	small airway:	n/a
50	chr4:56814948-56814998	PANC-1	pancreas:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:56720109..56722018-chr4:56797082..56799288,2	K562	blood:
2	chr4:56791515..56793046-chr4:56992694..56994388,2	K562	blood:
3	chr4:56718714..56721334-chr4:56789784..56792673,2	K562	blood:
4	chr4:56777785..56781071-chr4:56783446..56787071,3	K562	blood:
5	chr4:56814876..56815558-chr6:30584657..30585422,2	Hela-S3	cervix:
6	chr4:56782050..56785556-chr4:56813041..56815789,3	K562	blood:
7	chr4:56754886..56756394-chr4:56813463..56814975,2	MCF-7	breast:
8	chr4:56794068..56796669-chr4:56814956..56816613,2	K562	blood:
9	chr4:56804922..56810078-chr4:56811128..56817037,5	MCF-7	breast:
10	chr4:56246727..56248649-chr4:56813928..56816601,2	K562	blood:
11	chr4:56812961..56814619-chr4:57166848..57168708,2	K562	blood:
12	chr11:61582864..61583692-chr4:56814711..56815533,3	Hela-S3	cervix:
13	chr4:56814474..56815023-chr4:57666045..57666966,2	K562	blood:
14	chr4:56813951..56816639-chr4:57299941..57302593,2	K562	blood:
15	chr4:56812031..56813732-chr4:56817105..56819542,2	K562	blood:
16	chr4:56411182..56412770-chr4:56812130..56814893,2	K562	blood:
17	chr3:125313870..125314662-chr4:56814863..56815552,2	Hela-S3	cervix:
18	chr4:56815034..56815908-chr7:152373038..152373850,2	Hela-S3	cervix:
19	chr4:56807427..56809711-chr4:56812377..56814575,2	MCF-7	breast:
20	chr4:56794068..56796669-chr4:56814956..56816613,2	K562	blood:
21	chr4:56801770..56804535-chr4:56812941..56815208,2	K562	blood:
22	chr4:56815530..56818223-chr4:56910044..56912161,2	K562	blood:
23	chr19:10490704..10491561-chr4:56815133..56815686,2	NB4	blood:
24	chr4:56813904..56818311-chr4:57252529..57254894,5	K562	blood:
25	chr4:56797472..56800336-chr4:56814986..56817031,2	MCF-7	breast:
26	chr4:56807427..56809711-chr4:56812377..56814575,2	MCF-7	breast:
27	chr4:56411270..56413465-chr4:56811598..56813630,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMU-3	chr4:56804560-56804569	NONHSAT096484
2	lnc-NMU-3	chr4:56806683-56806798	NONHSAT096484
3	lnc-NMU-3	chr4:56804583-56805121	NONHSAT096484
4	lnc-NMU-3	chr4:56814006-56814177	NONHSAT096484
5	lnc-NMU-3	chr4:56814122-56815341	NONHSAT096485
6	lnc-CEP135-1	chr4:56794959-56795947	NONHSAT096482
7	lnc-CEP135-2	chr4:56792992-56793318	NONHSAT096481

No data

Variant related genes	Relation type
CEP135	TF binding region
ENSG00000222954	TF binding region
CEP135	CpG island
ENSG00000222954	CpG island
ENSG00000249700	chromatin interactions
ENSG00000222954	chromatin interactions
ENSG00000134852	chromatin interactions
ENSG00000269921	chromatin interactions
ENSG00000105397	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000144909	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000272969	chromatin interactions
ENSG00000128050	chromatin interactions
ENSG00000090989	chromatin interactions
ENSG00000174799	chromatin interactions
ENSG00000157426	chromatin interactions
ENSG00000196584	chromatin interactions
ENSG00000128059	chromatin interactions

Extended variants
information (count: 1065 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140448400	chr4:56782827-56782828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145556159	chr4:56782970-56782971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192393284	chr4:56782988-56782989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs114544561	chr4:56782990-56782991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529414473	chr4:56783055-56783056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542996649	chr4:56783074-56783075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141804411	chr4:56783078-56783079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559744263	chr4:56783104-56783105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528769728	chr4:56783123-56783124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184768068	chr4:56783172-56783173	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371028851	chr4:56783229-56783230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74356093	chr4:56783237-56783238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12501875	chr4:56783268-56783269	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550779838	chr4:56783294-56783295	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs144185915	chr4:56783353-56783354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148048300	chr4:56783482-56783483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189467933	chr4:56783530-56783531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552694353	chr4:56783534-56783535	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112589821	chr4:56783541-56783542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111355045	chr4:56783555-56783556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538542228	chr4:56783595-56783596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1838928	chr4:56783609-56783610	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34357056	chr4:56783679-56783680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575632844	chr4:56783694-56783695	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544379646	chr4:56783704-56783705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs5858358	chr4:56783705-56783706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554806815	chr4:56783706-56783707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs199658534	chr4:56783717-56783718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200073308	chr4:56783722-56783723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200160231	chr4:56783723-56783724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200681729	chr4:56783724-56783725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376366304	chr4:56783725-56783726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs58580140	chr4:56783726-56783727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371850856	chr4:56783727-56783728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376060559	chr4:56783736-56783737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371747190	chr4:56783738-56783739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371397470	chr4:56783761-56783762	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570748355	chr4:56783793-56783794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76195151	chr4:56783907-56783908	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76628966	chr4:56783908-56783909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150079166	chr4:56784012-56784013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564755373	chr4:56784121-56784122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545092911	chr4:56784146-56784147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374661096	chr4:56784168-56784169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531373140	chr4:56784180-56784181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116279454	chr4:56784182-56784183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550001947	chr4:56784188-56784189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550718387	chr4:56784239-56784240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567570717	chr4:56784243-56784244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568306363	chr4:56784251-56784252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56766800-56786800	Weak transcription	Ovary	ovary
2	chr4:56772000-56786600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr4:56772600-56784800	Weak transcription	Primary T cells from cord blood	blood
4	chr4:56772800-56793200	Weak transcription	Left Ventricle	heart
5	chr4:56773600-56788200	Weak transcription	Right Atrium	heart
6	chr4:56774000-56803200	Weak transcription	HUVEC	blood vessel
7	chr4:56774200-56786400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr4:56786400-56786600	Enhancers	HSMMtube	muscle
9	chr4:56786400-56787800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:56786400-56788000	Enhancers	Primary hematopoietic stem cells	blood
11	chr4:56786600-56786800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:56786600-56786800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr4:56786600-56787000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:56786600-56787000	Enhancers	Lung	lung
15	chr4:56786600-56787000	Flanking Active TSS	HSMMtube	muscle
16	chr4:56786600-56787200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:56786600-56787200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:56786600-56787200	Enhancers	Fetal Muscle Leg	muscle
19	chr4:56786600-56787200	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr4:56786600-56787200	Enhancers	NHLF	lung
21	chr4:56786600-56787800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:56786600-56787800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr4:56786600-56787800	Enhancers	NHDF-Ad	bronchial
24	chr4:56786600-56787800	Enhancers	Osteobl	bone
25	chr4:56786600-56788000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:56786800-56787000	Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr4:56786800-56787200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:56786800-56787200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:56786800-56787200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:56786800-56787200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr4:56786800-56787200	Enhancers	Ovary	ovary
32	chr4:56786800-56787200	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr4:56786800-56787400	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:56786800-56787400	Enhancers	Hela-S3	cervix
35	chr4:56786800-56787400	Enhancers	HSMM	muscle
36	chr4:56786800-56787800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:56787000-56787200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr4:56787000-56787200	Enhancers	HSMMtube	muscle
39	chr4:56787200-56789400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr4:56787200-56790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:56787200-56791400	Weak transcription	NHLF	lung
42	chr4:56787600-56787800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:56787800-56791000	Weak transcription	NHDF-Ad	bronchial
44	chr4:56787800-56791200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:56788400-56791000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:56789400-56789800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:56790000-56794200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr4:56791000-56791200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:56791000-56792800	Enhancers	NHDF-Ad	bronchial
50	chr4:56791200-56791800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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