Variant report

Variant	nsv561615
Chromosome Location	chr13:50042983-50086266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:1099)
Chromatin interactive
region (count:38)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:50069823-50070213	GM12878	blood:	n/a	n/a
2	ATF2	chr13:50069871-50070277	GM12878	blood:	n/a	n/a
3	BACH1	chr13:50070386-50070773	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr13:50069852-50070221	GM12878	blood:	n/a	n/a
5	BATF	chr13:50069835-50070194	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:50069845-50070179	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:50069906-50070213	GM12878	blood:	n/a	n/a
8	BCLAF1	chr13:50069804-50070564	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:50070022-50070675	HepG2	liver:	n/a	n/a
10	BHLHE40	chr13:50070011-50070578	K562	blood:	n/a	n/a
11	BHLHE40	chr13:50069894-50070748	GM12878	blood:	n/a	n/a
12	CCNT2	chr13:50069986-50070520	K562	blood:	n/a	n/a
13	CEBPB	chr13:50074043-50074625	IMR90	lung:	n/a	chr13:50074316-50074329
14	CEBPB	chr13:50070496-50070680	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr13:50059755-50060081	HepG2	liver:	n/a	chr13:50059911-50059922
16	CEBPB	chr13:50056604-50056893	IMR90	lung:	n/a	n/a
17	CEBPB	chr13:50069968-50070142	Hela-S3	cervix:	n/a	n/a
18	CEBPD	chr13:50069958-50070195	HepG2	liver:	n/a	n/a
19	CHD1	chr13:50069576-50069595	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr13:50070457-50070735	GM12878	blood:	n/a	n/a
21	CHD1	chr13:50071204-50071404	GM12878	blood:	n/a	n/a
22	CHD1	chr13:50069847-50070200	GM12878	blood:	n/a	n/a
23	CHD2	chr13:50069978-50070737	GM12878	blood:	n/a	n/a
24	CHD2	chr13:50070351-50070617	K562	blood:	n/a	n/a
25	CHD2	chr13:50069999-50070579	HepG2	liver:	n/a	n/a
26	CHD2	chr13:50070029-50070575	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr13:50070489-50070513	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr13:50071071-50071524	GM12878	blood:	n/a	n/a
29	CREB1	chr13:50071136-50071497	GM12878	blood:	n/a	n/a
30	CREB1	chr13:50069994-50070225	A549	lung:	n/a	n/a
31	CTCF	chr13:50070099-50070540	MCF-7	breast:	n/a	n/a
32	CTCF	chr13:50070315-50070722	GM12892	blood:	n/a	n/a
33	CTCF	chr13:50070220-50070370	AG09309	skin:	n/a	n/a
34	CTCF	chr13:50068820-50068970	GM12872	blood:	n/a	n/a
35	CTCF	chr13:50070113-50070509	K562	blood:	n/a	n/a
36	CTCF	chr13:50068854-50068994	MCF-7	breast:	n/a	n/a
37	CTCF	chr13:50068840-50068990	GM12873	blood:	n/a	n/a
38	CTCF	chr13:50068820-50068970	HL-60	blood:	n/a	n/a
39	CTCF	chr13:50070240-50070390	GM12870	blood:	n/a	n/a
40	CTCF	chr13:50070300-50070450	AG04450	lung:	n/a	n/a
41	CTCF	chr13:50070320-50070470	SAEC	small airway:	n/a	n/a
42	CTCF	chr13:50071525-50071610	Lung_OC	lung:	n/a	n/a
43	CTCF	chr13:50070180-50070330	GM12865	blood:	n/a	n/a
44	CTCF	chr13:50070300-50070450	HMEC	breast:	n/a	n/a
45	CTCF	chr13:50068720-50068990	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr13:50070300-50070450	AG09319	gingival:	n/a	n/a
47	CTCF	chr13:50070280-50070430	GM12866	blood:	n/a	n/a
48	CTCF	chr13:50068760-50068910	HFF	foreskin:	n/a	n/a
49	CTCF	chr13:50070307-50070706	GM19239	blood:	n/a	n/a
50	CTCF	chr13:50045125-50045216	Fibrobl	skin:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50070718-50070768	HCF	heart:	n/a
2	chr13:50070718-50070768	HCF	heart:	n/a
3	chr13:50062611-50062661	GM12892	blood:	n/a
4	chr13:50069705-50069755	MCF10A-Er-Src	breast:	n/a
5	chr13:50056284-50056334	SKMC	muscle:	n/a
6	chr13:50070045-50070095	MCF-7	breast:	n/a
7	chr13:50070499-50070549	GM12891	blood:	n/a
8	chr13:50070550-50070600	HIPEpiC	eye:	n/a
9	chr13:50070504-50070554	GM12878	blood:	n/a
10	chr13:50056284-50056334	RPTEC	kidney:	n/a
11	chr13:50070499-50070549	HCPEpiC	choroid plexus:	n/a
12	chr13:50062611-50062661	Hela-S3	cervix:	n/a
13	chr13:50074189-50074239	PANC-1	pancreas:	n/a
14	chr13:50070102-50070152	RPTEC	kidney:	n/a
15	chr13:50070718-50070768	HRE	kidney:	n/a
16	chr13:50070436-50070486	NHBE	bronchial:	n/a
17	chr13:50069722-50069772	Caco-2	colon:	n/a
18	chr13:50069705-50069755	AG04449	skin:	fetal
19	chr13:50070436-50070486	CMK	blood:	n/a
20	chr13:50070520-50070570	ovcar-3	ovarian:	n/a
21	chr13:50074189-50074239	NB4	blood:	n/a
22	chr13:50070482-50070532	AG09319	gingival:	n/a
23	chr13:50070766-50070816	BE2_C	brain:	n/a
24	chr13:50070102-50070152	Jurkat	blood:	n/a
25	chr13:50070504-50070554	ProgFib	skin:	n/a
26	chr13:50070550-50070600	HCPEpiC	choroid plexus:	n/a
27	chr13:50070482-50070532	U87	brain:	n/a
28	chr13:50056284-50056334	NHDF-neo	bronchial:	n/a
29	chr13:50070550-50070600	AG09309	skin:	n/a
30	chr13:50069722-50069772	PrEC	prostate:	n/a
31	chr13:50068486-50068536	BJ	skin:	n/a
32	chr13:50068486-50068536	GM12891	blood:	n/a
33	chr13:50070499-50070549	NHBE	bronchial:	n/a
34	chr13:50062611-50062661	AG09309	skin:	n/a
35	chr13:50056284-50056334	HEEpiC	esophagus:	n/a
36	chr13:50062611-50062661	ECC-1	luminal epithelium:	n/a
37	chr13:50070550-50070600	Hepatocyte	liver:	n/a
38	chr13:50068486-50068536	NT2-D1	testis:	n/a
39	chr13:50069705-50069755	SKMC	muscle:	n/a
40	chr13:50070718-50070768	ECC-1	luminal epithelium:	n/a
41	chr13:50070550-50070600	BE2_C	brain:	n/a
42	chr13:50069705-50069755	RPTEC	kidney:	n/a
43	chr13:50070504-50070554	GM19239	blood:	n/a
44	chr13:50056284-50056334	GM12892	blood:	n/a
45	chr13:50070520-50070570	HL-60	blood:	n/a
46	chr13:50070766-50070816	HRPEpiC	eye:	n/a
47	chr13:50070436-50070486	GM19239	blood:	n/a
48	chr13:50070550-50070600	H1-hESC	embryonic stem cell:	embryo
49	chr13:50069509-50069559	NB4	blood:	n/a
50	chr13:50070102-50070152	HMEC	breast:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
2	chr13:50068906..50071236-chr13:50159028..50161203,3	MCF-7	breast:
3	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
4	chr13:50072641..50077099-chr13:50079863..50082927,4	MCF-7	breast:
5	chr13:50068795..50071828-chr13:50072712..50075254,3	K562	blood:
6	chr13:50060291..50062533-chr13:50067429..50069545,2	K562	blood:
7	chr13:50085860..50087945-chr13:50089850..50091816,2	MCF-7	breast:
8	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
9	chr13:50072605..50075983-chr13:50085931..50088388,3	MCF-7	breast:
10	chr13:50016481..50018378-chr13:50070335..50072171,3	K562	blood:
11	chr13:50016483..50020444-chr13:50068529..50072853,4	MCF-7	breast:
12	chr13:50019424..50021164-chr13:50065782..50068488,2	MCF-7	breast:
13	chr13:50038863..50040866-chr13:50041548..50043299,2	K562	blood:
14	chr13:50045650..50047733-chr13:50190939..50192914,2	MCF-7	breast:
15	chr13:50061049..50067624-chr13:50068104..50073631,8	MCF-7	breast:
16	chr13:50064832..50068654-chr13:50068754..50072882,4	K562	blood:
17	chr13:50069004..50071273-chr13:50075738..50077658,2	MCF-7	breast:
18	chr13:50068733..50070336-chr13:50083872..50086385,2	MCF-7	breast:
19	chr13:50071845..50075663-chr13:50092471..50095842,3	K562	blood:
20	chr13:50033311..50035354-chr13:50074002..50076664,2	MCF-7	breast:
21	chr13:50063834..50065648-chr13:50067086..50070077,2	MCF-7	breast:
22	chr13:50060291..50062533-chr13:50067429..50069545,2	K562	blood:
23	chr13:50086064..50088335-chr13:50090580..50092913,2	K562	blood:
24	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
25	chr13:50068064..50069672-chr13:50174689..50176260,2	MCF-7	breast:
26	chr13:50072641..50077099-chr13:50079863..50082927,4	MCF-7	breast:
27	chr13:50068725..50070861-chr13:50073455..50076048,3	MCF-7	breast:
28	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
29	chr13:50068795..50071791-chr13:50072712..50074851,3	K562	blood:
30	chr13:50064483..50067847-chr13:50070204..50072747,3	K562	blood:
31	chr13:50061049..50067624-chr13:50068104..50073631,8	MCF-7	breast:
32	chr13:50068585..50069355-chr13:50091395..50092213,3	MCF-7	breast:
33	chr13:50070028..50071869-chr13:50072608..50075376,5	MCF-7	breast:
34	chr13:50071647..50073472-chr13:50180377..50183221,3	MCF-7	breast:
35	chr13:50072605..50075983-chr13:50085931..50088388,3	MCF-7	breast:
36	chr13:50020071..50022197-chr13:50067941..50070115,2	K562	blood:
37	chr13:50068457..50070652-chr13:50081260..50083175,3	MCF-7	breast:
38	chr13:49993633..49996417-chr13:50068251..50070383,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF11-1	chr13:50063383-50063500	NONHSAT033745
2	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033747
3	lnc-SETDB2-1	chr13:50070120-50070231	NONHSAT033746
4	lnc-SETDB2-1	chr13:50070372-50070584	NONHSAT033747
5	lnc-SETDB2-1	chr13:50080771-50080892	NONHSAT033746
6	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033746
7	lnc-PHF11-1	chr13:50063106-50063206	NONHSAT033745

No data

Variant related genes	Relation type
PHF11	TF binding region
SNRPGP14	TF binding region
PHF11	CpG island
SNRPGP14	CpG island
ENSG00000136144	chromatin interactions
ENSG00000102547	chromatin interactions
ENSG00000236577	chromatin interactions
ENSG00000136147	chromatin interactions
ENSG00000136169	chromatin interactions
ENSG00000215462	chromatin interactions

Extended variants
information (count: 1537 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:1537 , 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	rs9568215	chr13:50042983-50042984	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565661715	chr13:50043062-50043063	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535825307	chr13:50043101-50043102	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9596111	chr13:50043226-50043227	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs192687215	chr13:50043279-50043280	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145401146	chr13:50043292-50043293	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184303198	chr13:50043319-50043320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578083582	chr13:50043373-50043374	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188950510	chr13:50043396-50043397	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9568216	chr13:50043414-50043415	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs572809494	chr13:50043436-50043437	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573123541	chr13:50043475-50043476	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145100278	chr13:50043480-50043481	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561313605	chr13:50043530-50043531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531735395	chr13:50043565-50043566	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181637671	chr13:50043636-50043637	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373329031	chr13:50043671-50043672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559289771	chr13:50043711-50043712	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532182626	chr13:50043746-50043747	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2407692	chr13:50043820-50043821	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs532195170	chr13:50043840-50043841	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575492963	chr13:50043850-50043851	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565625367	chr13:50043854-50043855	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184746776	chr13:50043878-50043879	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377147027	chr13:50044007-50044008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548081088	chr13:50044010-50044011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149102742	chr13:50044074-50044075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544221839	chr13:50044119-50044120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537063914	chr13:50044186-50044187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558340998	chr13:50044218-50044219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371088337	chr13:50044236-50044237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374200645	chr13:50044253-50044254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376694520	chr13:50044255-50044256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189470725	chr13:50044269-50044270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554446590	chr13:50044317-50044318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182587174	chr13:50044345-50044346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185911984	chr13:50044349-50044350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555252776	chr13:50044350-50044351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576323849	chr13:50044418-50044419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543823243	chr13:50044451-50044452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565215184	chr13:50044457-50044458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532675928	chr13:50044556-50044557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7995283	chr13:50044585-50044586	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs530123314	chr13:50044590-50044591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146477545	chr13:50044659-50044660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6561525	chr13:50044675-50044676	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs191163091	chr13:50044676-50044677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7994115	chr13:50044710-50044711	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs563619243	chr13:50044715-50044716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530403153	chr13:50044754-50044755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD

Chromatin state (count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50020200-50068400	Weak transcription	HMEC	breast
2	chr13:50022000-50069000	Weak transcription	Fetal Brain Male	brain
3	chr13:50023000-50068000	Weak transcription	Hela-S3	cervix
4	chr13:50031800-50068800	Weak transcription	Psoas Muscle	Psoas
5	chr13:50034400-50050800	Weak transcription	NHEK	skin
6	chr13:50034400-50052200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:50034400-50068800	Weak transcription	NH-A	brain
8	chr13:50036400-50068600	Weak transcription	Stomach Mucosa	stomach
9	chr13:50036600-50068000	Weak transcription	K562	blood
10	chr13:50037000-50045600	Weak transcription	Fetal Heart	heart
11	chr13:50037800-50050200	Weak transcription	Osteobl	bone
12	chr13:50037800-50050600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr13:50037800-50050800	Weak transcription	Brain Angular Gyrus	brain
14	chr13:50037800-50051000	Weak transcription	Spleen	Spleen
15	chr13:50037800-50064000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr13:50037800-50068400	Weak transcription	HUVEC	blood vessel
17	chr13:50037800-50069000	Weak transcription	Colonic Mucosa	Colon
18	chr13:50038000-50043400	Weak transcription	Placenta	Placenta
19	chr13:50038000-50044600	Weak transcription	Fetal Stomach	stomach
20	chr13:50038000-50044600	Weak transcription	Lung	lung
21	chr13:50038000-50049000	Weak transcription	Gastric	stomach
22	chr13:50038000-50050200	Weak transcription	Esophagus	oesophagus
23	chr13:50038000-50050200	Weak transcription	HSMMtube	muscle
24	chr13:50038000-50050200	Weak transcription	NHLF	lung
25	chr13:50038000-50050800	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr13:50038000-50051200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr13:50038000-50062800	Strong transcription	Primary B cells from peripheral blood	blood
28	chr13:50038000-50063400	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr13:50038000-50063600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr13:50038000-50063800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr13:50038000-50068800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr13:50038200-50046600	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr13:50038200-50050800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr13:50038200-50051000	Weak transcription	Aorta	Aorta
35	chr13:50038200-50054200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr13:50038200-50062400	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr13:50038200-50063400	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr13:50038400-50043400	Weak transcription	NHDF-Ad	bronchial
39	chr13:50038400-50044400	Weak transcription	Dnd41	blood
40	chr13:50038400-50044400	Weak transcription	GM12878-XiMat	blood
41	chr13:50038400-50045600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:50038400-50048400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr13:50038400-50048800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr13:50038400-50048800	Weak transcription	Right Ventricle	heart
45	chr13:50038400-50049200	Weak transcription	Brain Cingulate Gyrus	brain
46	chr13:50038400-50049400	Weak transcription	Brain Substantia Nigra	brain
47	chr13:50038400-50050200	Weak transcription	Fetal Brain Female	brain
48	chr13:50038400-50050200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr13:50038400-50050600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr13:50038400-50050800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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