Variant report

Variant	nsv1043019
Chromosome Location	chr13:95924585-96152616
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3929)
CpG islands
(count:1527)
Chromatin interactive
region (count:59)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3929 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:96033005-96033202	K562	blood:	n/a	n/a
3	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
5	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
6	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:96090573-96090866	K562	blood:	n/a	n/a
8	ARID3A	chr13:96137375-96138176	K562	blood:	n/a	n/a
9	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
10	ARID3A	chr13:95937866-95938402	K562	blood:	n/a	n/a
11	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
12	ARID3A	chr13:95926468-95926904	K562	blood:	n/a	n/a
13	ARID3A	chr13:96129590-96129780	K562	blood:	n/a	n/a
14	ARID3A	chr13:95925793-95926072	K562	blood:	n/a	n/a
15	ARID3A	chr13:95931642-95931648	K562	blood:	n/a	n/a
16	ARID3A	chr13:96146340-96146763	HepG2	liver:	n/a	n/a
17	ARID3A	chr13:96130801-96131169	HepG2	liver:	n/a	n/a
18	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
19	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
20	ARID3A	chr13:96146399-96146694	K562	blood:	n/a	n/a
21	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
22	ATF1	chr13:95938012-95938442	K562	blood:	n/a	n/a
23	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
24	ATF2	chr13:96109477-96110062	GM12878	blood:	n/a	n/a
25	ATF2	chr13:96039455-96039980	GM12878	blood:	n/a	n/a
26	ATF2	chr13:95932871-95933559	GM12878	blood:	n/a	n/a
27	ATF2	chr13:95933714-95934499	GM12878	blood:	n/a	n/a
28	ATF2	chr13:96109557-96110047	GM12878	blood:	n/a	n/a
29	ATF2	chr13:95932888-95933441	GM12878	blood:	n/a	n/a
30	ATF2	chr13:96032895-96033280	GM12878	blood:	n/a	n/a
31	ATF2	chr13:96132243-96132785	GM12878	blood:	n/a	n/a
32	ATF3	chr13:95926553-95926854	K562	blood:	n/a	n/a
33	ATF3	chr13:95938112-95938426	K562	blood:	n/a	n/a
34	BACH1	chr13:96146450-96146650	K562	blood:	n/a	n/a
35	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr13:96038079-96038398	K562	blood:	n/a	n/a
37	BACH1	chr13:96056661-96056913	K562	blood:	n/a	n/a
38	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
40	BACH1	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr13:96089900-96090195	K562	blood:	n/a	chr13:96090032-96090046
42	BATF	chr13:96132378-96132759	GM12878	blood:	n/a	n/a
43	BATF	chr13:96124223-96124523	GM12878	blood:	n/a	n/a
44	BATF	chr13:96132237-96132726	GM12878	blood:	n/a	n/a
45	BATF	chr13:96038683-96038941	GM12878	blood:	n/a	n/a
46	BATF	chr13:96038573-96038973	GM12878	blood:	n/a	n/a
47	BATF	chr13:96109534-96109917	GM12878	blood:	n/a	n/a
48	BATF	chr13:96124220-96124534	GM12878	blood:	n/a	n/a
49	BCL11A	chr13:96109531-96109982	GM12878	blood:	n/a	n/a
50	BCL11A	chr13:96039640-96039821	GM12878	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95954080-95954130	MCF-7	breast:	n/a
2	chr13:95932467-95932517	PANC-1	pancreas:	n/a
3	chr13:95954080-95954130	MCF-7	breast:	n/a
4	chr13:95932467-95932517	PANC-1	pancreas:	n/a
5	chr13:96086098-96086148	PANC-1	pancreas:	n/a
6	chr13:96086023-96086073	SK-N-MC	brain:	n/a
7	chr13:95932467-95932517	HL-60	blood:	n/a
8	chr13:96086249-96086299	HMEC	breast:	n/a
9	chr13:95953574-95953624	IMR90	lung:	fetal
10	chr13:96085504-96085554	AG09309	skin:	n/a
11	chr13:95953505-95953555	HUVEC	blood vessel:	n/a
12	chr13:96008021-96008071	ECC-1	luminal epithelium:	n/a
13	chr13:96085969-96086019	ovcar-3	ovarian:	n/a
14	chr13:96087962-96088012	HRE	kidney:	n/a
15	chr13:95953574-95953624	AG09309	skin:	n/a
16	chr13:95953229-95953279	SKMC	muscle:	n/a
17	chr13:95954382-95954432	AG04449	skin:	fetal
18	chr13:95953574-95953624	PFSK-1	brain:	n/a
19	chr13:95952902-95952952	SKMC	muscle:	n/a
20	chr13:95953505-95953555	AoSMC	blood vessel:	n/a
21	chr13:95953574-95953624	GM06990	blood:	n/a
22	chr13:96056495-96056545	HEEpiC	esophagus:	n/a
23	chr13:96086023-96086073	ECC-1	luminal epithelium:	n/a
24	chr13:95932467-95932517	Hela-S3	cervix:	n/a
25	chr13:96086023-96086073	SKMC	muscle:	n/a
26	chr13:95954080-95954130	T-47D	breast:	n/a
27	chr13:95953482-95953532	ECC-1	luminal epithelium:	n/a
28	chr13:95953229-95953279	AG04450	lung:	fetal
29	chr13:96086275-96086325	Hela-S3	cervix:	n/a
30	chr13:95954534-95954584	HCT-116	colon:	n/a
31	chr13:96086023-96086073	GM12891	blood:	n/a
32	chr13:96008021-96008071	HCF	heart:	n/a
33	chr13:95953229-95953279	A549	lung:	n/a
34	chr13:95952937-95952987	HRPEpiC	eye:	n/a
35	chr13:96056495-96056545	U87	brain:	n/a
36	chr13:96085969-96086019	BE2_C	brain:	n/a
37	chr13:95933097-95933147	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:96008021-96008071	MCF10A-Er-Src	breast:	n/a
39	chr13:96089870-96089920	ovcar-3	ovarian:	n/a
40	chr13:95954534-95954584	SK-N-MC	brain:	n/a
41	chr13:96085969-96086019	HEEpiC	esophagus:	n/a
42	chr13:96085504-96085554	GM12878	blood:	n/a
43	chr13:96085969-96086019	PFSK-1	brain:	n/a
44	chr13:96056495-96056545	NHBE	bronchial:	n/a
45	chr13:95953941-95953991	U87	brain:	n/a
46	chr13:95953941-95953991	AG09319	gingival:	n/a
47	chr13:96008021-96008071	HepG2	liver:	n/a
48	chr13:95953941-95953991	NH-A	brain:	n/a
49	chr13:96087962-96088012	SK-N-SH	brain:	n/a
50	chr13:96086023-96086073	ProgFib	skin:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:95841327..95842256-chr13:96056178..96057119,5	MCF-7	breast:
2	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
3	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
4	chr13:95843651..95844564-chr13:96056296..96057006,3	MCF-7	breast:
5	chr13:96125206..96127161-chr13:96129356..96131300,2	K562	blood:
6	chr13:95841410..95841915-chr13:96130869..96131391,2	MCF-7	breast:
7	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
8	chr13:95843997..95844511-chr13:96130866..96131628,2	MCF-7	breast:
9	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
10	chr13:96148891..96151318-chr13:96153321..96155668,2	K562	blood:
11	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
12	chr13:95272285..95273035-chr13:96056279..96056904,2	K562	blood:
13	chr13:95924370..95928427-chr13:95951382..95954630,5	K562	blood:
14	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
15	chr13:95841276..95841834-chr13:96032679..96033583,3	K562	blood:
16	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
17	chr13:96146062..96146563-chr13:97619520..97620349,2	K562	blood:
18	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
19	chr13:95923828..95925504-chr13:95926180..95928122,2	K562	blood:
20	chr13:95873940..95876786-chr13:95925021..95926772,2	K562	blood:
21	chr13:96058665..96059376-chr13:96130506..96131218,2	MCF-7	breast:
22	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
23	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
24	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
25	chr13:95841692..95842231-chr13:96032699..96033435,2	MCF-7	breast:
26	chr13:95843758..95844705-chr13:96056220..96057135,5	MCF-7	breast:
27	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
28	chr13:96125206..96127161-chr13:96129356..96131300,2	K562	blood:
29	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
30	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
31	chr13:95841275..95842299-chr13:96056212..96057228,12	K562	blood:
32	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
33	chr13:96146074..96146987-chr13:96215991..96216972,6	MCF-7	breast:
34	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
35	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
36	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
37	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
38	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
39	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
40	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
41	chr13:96119619..96122365-chr13:96309013..96311626,2	MCF-7	breast:
42	chr13:95843500..95844639-chr13:96055881..96056848,6	K562	blood:
43	chr13:95923828..95925504-chr13:95926180..95928122,2	K562	blood:
44	chr13:95843719..95844609-chr13:96033049..96033649,3	MCF-7	breast:
45	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
46	chr13:96056383..96057194-chr13:96130599..96131185,2	MCF-7	breast:
47	chr13:96056383..96057194-chr13:96130599..96131185,2	MCF-7	breast:
48	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
49	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
50	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-1	chr13:95954705-95955669	XLOC_010696
2	lnc-ABCC4-1	chr13:95956351-95956401	XLOC_010696
3	lnc-DZIP1-2	chr13:96149313-96149381	NONHSAT034762
4	lnc-CLDN10-1	chr13:96056900-96057174	NONHSAT034760
5	lnc-CLDN10-6	chr13:95957471-95958654	NONHSAT034755
6	lnc-CLDN10-1	chr13:96056331-96056798	NONHSAT034760
7	lnc-DZIP1-2	chr13:96131698-96132216	NONHSAT034762
8	lnc-CLDN10-3	chr13:96046303-96046708	NONHSAT034759
9	lnc-ABCC4-2	chr13:96003796-96003967	NONHSAT034758
10	lnc-CLDN10-1	chr13:96056526-96056798	XLOC_010474
11	lnc-ABCC4-2	chr13:96056579-96056787	NONHSAT034758
12	lnc-CLDN10-1	chr13:96056900-96057258	XLOC_010474
13	lnc-DZIP1-2	chr13:96149313-96149379	ENSG00000223392
14	lnc-DZIP1-2	chr13:96131698-96132216	ENSG00000223392

No data

Variant related genes	Relation type
RNY4P27	TF binding region
CLDN10	TF binding region
ABCC4	TF binding region
MEMO1P5	TF binding region
RNY3P8	TF binding region
RNY4P27	CpG island
CLDN10	CpG island
ABCC4	CpG island
MEMO1P5	CpG island
RNY3P8	CpG island
ENSG00000125257	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000083544	chromatin interactions
SMAD4	miRNA target sites

Extended variants
information (count: 8742 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:8742 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114853878	chr13:95924594-95924595	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs150988051	chr13:95924637-95924638	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555774490	chr13:95924638-95924639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73548833	chr13:95924658-95924659	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540626700	chr13:95924667-95924668	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183347562	chr13:95924682-95924683	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577334560	chr13:95924752-95924753	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374702757	chr13:95924766-95924767	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188577095	chr13:95924814-95924815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529063432	chr13:95924825-95924826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541509246	chr13:95924837-95924838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs61972759	chr13:95924863-95924864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559386085	chr13:95924880-95924881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111749724	chr13:95924977-95924978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs7324503	chr13:95924983-95924984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs4773864	chr13:95925010-95925011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs533490923	chr13:95925011-95925012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549989381	chr13:95925027-95925028	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570268813	chr13:95925034-95925035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10607588	chr13:95925043-95925044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531591177	chr13:95925089-95925090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549507306	chr13:95925117-95925118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566041446	chr13:95925127-95925128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534951405	chr13:95925129-95925130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs202082095	chr13:95925140-95925141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534873717	chr13:95925142-95925143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs28647783	chr13:95925150-95925151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs28541531	chr13:95925156-95925157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs28704476	chr13:95925158-95925159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201187127	chr13:95925159-95925160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557353003	chr13:95925163-95925164	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10607589	chr13:95925174-95925175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369710555	chr13:95925175-95925176	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537185213	chr13:95925184-95925185	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112859374	chr13:95925228-95925229	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573829247	chr13:95925233-95925234	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7324355	chr13:95925235-95925236	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56891151	chr13:95925251-95925252	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs11839316	chr13:95925260-95925261	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs17268282	chr13:95925314-95925315	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs117989140	chr13:95925359-95925360	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533352317	chr13:95925364-95925365	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138943473	chr13:95925469-95925470	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532329407	chr13:95925497-95925498	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs59514866	chr13:95925507-95925508	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549326867	chr13:95925545-95925546	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565907515	chr13:95925566-95925567	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs115830162	chr13:95925610-95925611	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4148429	chr13:95925615-95925616	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142503725	chr13:95925620-95925621	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2425 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95897000-95927400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr13:95908000-95926600	Weak transcription	Gastric	stomach
3	chr13:95910200-95927400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr13:95913600-95932800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr13:95917000-95931400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr13:95919000-95925600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr13:95919000-95930000	Weak transcription	Esophagus	oesophagus
8	chr13:95919600-95924800	Enhancers	HUVEC	blood vessel
9	chr13:95919800-95924600	Enhancers	Rectal Smooth Muscle	rectum
10	chr13:95919800-95928000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr13:95920200-95928800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
13	chr13:95920400-95927400	Weak transcription	Hela-S3	cervix
14	chr13:95920600-95928200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr13:95920800-95925600	Weak transcription	Placenta	Placenta
16	chr13:95921200-95925600	Weak transcription	Lung	lung
17	chr13:95921400-95926200	Weak transcription	Right Atrium	heart
18	chr13:95921600-95924800	Enhancers	NHLF	lung
19	chr13:95921600-95927600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr13:95922200-95926200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr13:95922400-95926200	Weak transcription	Small Intestine	intestine
22	chr13:95922400-95927600	Weak transcription	Brain Anterior Caudate	brain
23	chr13:95922400-95927800	Weak transcription	NHEK	skin
24	chr13:95922800-95924600	Enhancers	Fetal Muscle Leg	muscle
25	chr13:95922800-95924800	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr13:95922800-95926400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:95922800-95928200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr13:95923000-95925400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr13:95923000-95925400	Weak transcription	Psoas Muscle	Psoas
30	chr13:95923000-95925600	Weak transcription	GM12878-XiMat	blood
31	chr13:95923000-95926400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr13:95923200-95924600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr13:95923200-95924800	Enhancers	Fetal Kidney	kidney
34	chr13:95923400-95924600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr13:95923600-95924600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:95923600-95924600	Enhancers	Primary hematopoietic stem cells	blood
37	chr13:95923600-95924600	Active TSS	A549	lung
38	chr13:95923600-95924800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr13:95923800-95924600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr13:95923800-95925600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr13:95923800-95925600	Weak transcription	Pancreas	Pancrea
42	chr13:95923800-95926000	Weak transcription	Ovary	ovary
43	chr13:95923800-95926200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr13:95923800-95941200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr13:95924000-95924600	Enhancers	Fetal Muscle Trunk	muscle
46	chr13:95924000-95924600	Enhancers	HSMM	muscle
47	chr13:95924000-95925400	Weak transcription	Brain Hippocampus Middle	brain
48	chr13:95924000-95925600	Weak transcription	Fetal Intestine Small	intestine
49	chr13:95924000-95926600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr13:95924000-95927400	Weak transcription	NHDF-Ad	bronchial

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