Variant report

Variant	nsv1037720
Chromosome Location	chr10:92063438-92259359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:959)
CpG islands
(count:305)
Chromatin interactive
region (count:18)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:92079277-92079707	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr10:92180364-92180842	GM12878	blood:	n/a	n/a
3	ATF2	chr10:92079033-92079660	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr10:92079146-92079685	HCT-116	colon:	n/a	n/a
5	ATF3	chr10:92079201-92079608	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr10:92073505-92074222	HCT-116	colon:	n/a	n/a
7	ATF3	chr10:92079291-92079622	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:92184912-92184933	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:92076070-92076080	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:92079099-92079716	H1-hESC	embryonic stem cell:	n/a	chr10:92079432-92079446
11	BATF	chr10:92180389-92180682	GM12878	blood:	n/a	n/a
12	BATF	chr10:92180437-92180697	GM12878	blood:	n/a	n/a
13	BATF	chr10:92079259-92079651	GM12878	blood:	n/a	chr10:92079435-92079446 chr10:92079436-92079446
14	BATF	chr10:92079240-92079608	GM12878	blood:	n/a	chr10:92079435-92079446 chr10:92079436-92079446
15	BCL11A	chr10:92123906-92124192	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr10:92079360-92079636	H1-hESC	embryonic stem cell:	n/a	chr10:92079445-92079454 chr10:92079435-92079444 chr10:92079434-92079443
17	BCL11A	chr10:92079310-92079648	H1-hESC	embryonic stem cell:	n/a	chr10:92079445-92079454 chr10:92079435-92079444 chr10:92079434-92079443
18	BCL11A	chr10:92079217-92079614	GM12878	blood:	n/a	chr10:92079445-92079454 chr10:92079435-92079444 chr10:92079434-92079443
19	BCL11A	chr10:92180396-92180743	GM12878	blood:	n/a	n/a
20	BCL11A	chr10:92180394-92180720	GM12878	blood:	n/a	n/a
21	BCL3	chr10:92079236-92079578	GM12878	blood:	n/a	chr10:92079445-92079454 chr10:92079435-92079444 chr10:92079434-92079443
22	BCL3	chr10:92140213-92140457	GM12878	blood:	n/a	n/a
23	BHLHE40	chr10:92112120-92112285	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:92197207-92197414	GM12878	blood:	n/a	n/a
25	BRCA1	chr10:92066345-92066351	GM12878	blood:	n/a	n/a
26	CBX3	chr10:92210988-92211708	HCT-116	colon:	n/a	n/a
27	CBX3	chr10:92078836-92079769	HCT-116	colon:	n/a	n/a
28	CBX3	chr10:92078377-92079843	HCT-116	colon:	n/a	n/a
29	CBX3	chr10:92166724-92167371	HCT-116	colon:	n/a	n/a
30	CBX3	chr10:92073552-92074239	HCT-116	colon:	n/a	n/a
31	CBX3	chr10:92073318-92074921	HCT-116	colon:	n/a	n/a
32	CEBPB	chr10:92195503-92195785	IMR90	lung:	n/a	chr10:92195629-92195640
33	CEBPB	chr10:92176649-92177551	IMR90	lung:	n/a	chr10:92176960-92176971
34	CEBPB	chr10:92073634-92074170	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr10:92123565-92124095	H1-hESC	embryonic stem cell:	n/a	chr10:92123748-92123759
36	CEBPB	chr10:92166813-92167244	MCF-7	breast:	n/a	n/a
37	CEBPB	chr10:92218923-92219095	A549	lung:	n/a	n/a
38	CEBPB	chr10:92081166-92081600	ECC-1	luminal epithelium:	n/a	chr10:92081409-92081422 chr10:92081410-92081421 chr10:92081409-92081420
39	CEBPB	chr10:92222493-92222842	IMR90	lung:	n/a	chr10:92222653-92222664
40	CEBPB	chr10:92123619-92123868	HepG2	liver:	n/a	chr10:92123748-92123759
41	CEBPB	chr10:92078780-92079923	HCT-116	colon:	n/a	n/a
42	CEBPB	chr10:92172474-92172671	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:92222567-92222801	Hela-S3	cervix:	n/a	chr10:92222653-92222664
44	CEBPB	chr10:92166878-92167401	MCF-7	breast:	n/a	n/a
45	CEBPB	chr10:92176813-92177155	HepG2	liver:	n/a	chr10:92176960-92176971
46	CEBPB	chr10:92079351-92079766	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr10:92079194-92079780	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr10:92179011-92179592	HepG2	liver:	n/a	chr10:92179492-92179503
49	CEBPB	chr10:92071301-92071461	HepG2	liver:	n/a	n/a
50	CEBPB	chr10:92176747-92177351	MCF-7	breast:	n/a	chr10:92176960-92176971

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:92213389-92213439	BJ	skin:	n/a
2	chr10:92213236-92213286	ECC-1	luminal epithelium:	n/a
3	chr10:92079600-92079650	SKMC	muscle:	n/a
4	chr10:92123669-92123719	GM12878	blood:	n/a
5	chr10:92213389-92213439	ECC-1	luminal epithelium:	n/a
6	chr10:92213389-92213439	Hela-S3	cervix:	n/a
7	chr10:92123669-92123719	SK-N-MC	brain:	n/a
8	chr10:92079600-92079650	BJ	skin:	n/a
9	chr10:92123669-92123719	MCF-7	breast:	n/a
10	chr10:92079600-92079650	CMK	blood:	n/a
11	chr10:92123669-92123719	NHBE	bronchial:	n/a
12	chr10:92213389-92213439	CMK	blood:	n/a
13	chr10:92213236-92213286	NT2-D1	testis:	n/a
14	chr10:92079600-92079650	HEEpiC	esophagus:	n/a
15	chr10:92153495-92153545	BJ	skin:	n/a
16	chr10:92213389-92213439	HIPEpiC	eye:	n/a
17	chr10:92079600-92079650	H1-hESC	embryonic stem cell:	embryo
18	chr10:92079600-92079650	RPTEC	kidney:	n/a
19	chr10:92153495-92153545	HCT-116	colon:	n/a
20	chr10:92153495-92153545	ProgFib	skin:	n/a
21	chr10:92213236-92213286	HNPCEpiC	eye:	n/a
22	chr10:92079600-92079650	LNCaP	prostate:	n/a
23	chr10:92153495-92153545	H1-hESC	embryonic stem cell:	embryo
24	chr10:92213236-92213286	HepG2	liver:	n/a
25	chr10:92213236-92213286	H1-hESC	embryonic stem cell:	embryo
26	chr10:92213389-92213439	U87	brain:	n/a
27	chr10:92213236-92213286	HRPEpiC	eye:	n/a
28	chr10:92213236-92213286	Jurkat	blood:	n/a
29	chr10:92123669-92123719	PANC-1	pancreas:	n/a
30	chr10:92123669-92123719	HRCEpiC	kidney:	n/a
31	chr10:92123669-92123719	AoSMC	blood vessel:	n/a
32	chr10:92213236-92213286	HRE	kidney:	n/a
33	chr10:92153495-92153545	SK-N-MC	brain:	n/a
34	chr10:92213389-92213439	PFSK-1	brain:	n/a
35	chr10:92153495-92153545	NHDF-neo	bronchial:	n/a
36	chr10:92213236-92213286	HPAEpiC	pulmonary alveolar:	n/a
37	chr10:92213236-92213286	HCM	heart:	n/a
38	chr10:92213236-92213286	ProgFib	skin:	n/a
39	chr10:92123669-92123719	IMR90	lung:	fetal
40	chr10:92123669-92123719	HEK293	kidney:	embryo
41	chr10:92153495-92153545	K562	blood:	n/a
42	chr10:92213236-92213286	GM12878	blood:	n/a
43	chr10:92213236-92213286	U87	brain:	n/a
44	chr10:92079600-92079650	AG09319	gingival:	n/a
45	chr10:92079600-92079650	ProgFib	skin:	n/a
46	chr10:92123669-92123719	NB4	blood:	n/a
47	chr10:92123669-92123719	HPAEpiC	pulmonary alveolar:	n/a
48	chr10:92213389-92213439	HEK293	kidney:	embryo
49	chr10:92079600-92079650	U87	brain:	n/a
50	chr10:92079600-92079650	HRE	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:92248193..92249705-chr10:92254263..92256644,2	MCF-7	breast:
2	chr10:92184835..92186685-chr10:92187388..92189622,2	MCF-7	breast:
3	chr10:92079088..92081474-chr10:92085377..92088671,3	MCF-7	breast:
4	chr10:91585659..91588157-chr10:92199771..92201481,2	MCF-7	breast:
5	chr10:92177056..92178628-chr10:92179037..92181377,2	MCF-7	breast:
6	chr10:92184835..92186685-chr10:92187388..92189622,2	MCF-7	breast:
7	chr10:92254197..92256394-chr10:92257440..92260010,2	MCF-7	breast:
8	chr10:92079088..92081474-chr10:92085377..92088671,3	MCF-7	breast:
9	chr10:92255876..92258347-chr10:92261128..92263614,2	MCF-7	breast:
10	chr10:92064760..92066679-chr10:92166883..92168806,2	MCF-7	breast:
11	chr10:92196966..92197656-chr10:92339492..92340259,2	MCF-7	breast:
12	chr10:92047473..92050346-chr10:92165247..92168101,3	MCF-7	breast:
13	chr10:92248193..92249705-chr10:92254263..92256644,2	MCF-7	breast:
14	chr10:92177056..92178628-chr10:92179037..92181377,2	MCF-7	breast:
15	chr10:92051318..92054074-chr10:92099394..92101764,2	MCF-7	breast:
16	chr10:92064760..92066679-chr10:92166883..92168806,2	MCF-7	breast:
17	chr10:92197334..92197860-chr10:92338992..92339734,2	MCF-7	breast:
18	chr10:92254197..92256394-chr10:92257440..92260010,2	MCF-7	breast:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPP30-6	chr10:92213927-92214072	ENSG00000224750
2	lnc-HTR7-2	chr10:92201417-92201570	NONHSAT015585
3	lnc-HTR7-1	chr10:92162711-92162796	XLOC_008901
4	lnc-RPP30-6	chr10:92213926-92214072	XLOC_008556
5	lnc-RPP30-10	chr10:92235756-92235809	NONHSAT015587
6	lnc-RPP30-9	chr10:92215653-92215725	NONHSAT015591
7	lnc-HTR7-2	chr10:92156187-92156332	NONHSAT015585
8	lnc-RPP30-10	chr10:92249010-92249108	NONHSAT015590
9	lnc-RPP30-6	chr10:92259030-92261197	ENSG00000224750
10	lnc-RPP30-6	chr10:92245776-92245829	XLOC_008556
11	lnc-RPP30-6	chr10:92245776-92245829	XLOC_008556
12	lnc-RPP30-10	chr10:92204417-92204560	NONHSAT015588
13	lnc-RPP30-6	chr10:92259030-92259128	XLOC_008556
14	lnc-HTR7-1	chr10:92163745-92163811	XLOC_008901
15	lnc-HTR7-2	chr10:92152258-92152545	NONHSAT015585
16	lnc-RPP30-9	chr10:92212454-92213123	NONHSAT015591
17	lnc-RPP30-10	chr10:92249010-92251177	NONHSAT015587
18	lnc-RPP30-6	chr10:92214437-92214580	XLOC_008556
19	lnc-RPP30-10	chr10:92235756-92235809	NONHSAT015589
20	lnc-RPP30-10	chr10:92203906-92204052	ucscGeneNc_uc001kgy_2
21	lnc-RPP30-6	chr10:92245776-92245829	ENSG00000224750
22	lnc-HTR7-1	chr10:92162278-92162565	XLOC_008901
23	lnc-RPP30-5	chr10:92222474-92223143	XLOC_008557
24	lnc-RPP30-6	chr10:92220529-92221258	XLOC_008556
25	lnc-RPP30-10	chr10:92249010-92251172	ucscGeneNc_uc001kgy_2
26	lnc-RPP30-6	chr10:92214455-92214580	XLOC_008556
27	lnc-RPP30-6	chr10:92214455-92214580	XLOC_008556
28	lnc-RPP30-10	chr10:92204435-92204560	NONHSAT015589
29	lnc-RPP30-10	chr10:92204435-92204560	NONHSAT015590
30	lnc-RPP30-5	chr10:92227622-92227709	XLOC_008557
31	lnc-RPP30-6	chr10:92259030-92261192	XLOC_008556
32	lnc-RPP30-10	chr10:92203907-92204052	NONHSAT015587
33	lnc-RPP30-5	chr10:92225673-92225745	XLOC_008557
34	lnc-HTR7-1	chr10:92166207-92166352	XLOC_008901
35	lnc-RPP30-6	chr10:92245776-92245829	XLOC_008556
36	lnc-RPP30-10	chr10:92235756-92235809	ucscGeneNc_uc001kgy_2
37	lnc-RPP30-10	chr10:92249010-92249108	NONHSAT015589
38	lnc-HTR7-2	chr10:92152691-92152776	NONHSAT015585
39	lnc-HTR7-1	chr10:92211437-92211590	XLOC_008901
40	lnc-RPP30-6	chr10:92259030-92259128	XLOC_008556
41	lnc-RPP30-9	chr10:92217602-92217689	NONHSAT015591
42	lnc-RPP30-10	chr10:92252523-92252705	NONHSAT015589
43	lnc-HTR7-2	chr10:92153725-92153791	NONHSAT015585
44	lnc-RPP30-10	chr10:92235756-92235809	NONHSAT015590
45	lnc-RPP30-10	chr10:92210509-92211238	NONHSAT015588

No data

Variant related genes	Relation type
ENSG00000238291	TF binding region
ENSG00000224750	TF binding region
ENSG00000238291	CpG island
ENSG00000224750	CpG island
MLL2	miRNA target sites
BCL11B	miRNA target sites

Extended variants
information (count: 6748 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:6748 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559598835	chr10:92063471-92063472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184689561	chr10:92063485-92063486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189057476	chr10:92063555-92063556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145499124	chr10:92063596-92063597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550126636	chr10:92063614-92063615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148825216	chr10:92063623-92063624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181279561	chr10:92063632-92063633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570900998	chr10:92063633-92063634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11186114	chr10:92063696-92063697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570195314	chr10:92063697-92063698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533253018	chr10:92063712-92063713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546647759	chr10:92063754-92063755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186326185	chr10:92063873-92063874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535607273	chr10:92063896-92063897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145286573	chr10:92063928-92063929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189225731	chr10:92064042-92064043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201974058	chr10:92064061-92064062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144446944	chr10:92064062-92064063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561824518	chr10:92064082-92064083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555814942	chr10:92064194-92064195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10881780	chr10:92064234-92064235	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs536693282	chr10:92064280-92064281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556918053	chr10:92064304-92064305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs957646	chr10:92064322-92064323	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs539553191	chr10:92064336-92064337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553073305	chr10:92064338-92064339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558145877	chr10:92064343-92064344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573100536	chr10:92064376-92064377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368068756	chr10:92064452-92064453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561877988	chr10:92064466-92064467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs137880986	chr10:92064476-92064477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368397357	chr10:92064487-92064488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544134020	chr10:92064499-92064500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201508435	chr10:92064502-92064503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1409300	chr10:92064506-92064507	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs375855916	chr10:92064514-92064515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141140799	chr10:92064593-92064594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567021093	chr10:92064655-92064656	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs562559192	chr10:92064656-92064657	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs372313309	chr10:92064659-92064660	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs546711410	chr10:92064672-92064673	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs560193256	chr10:92064674-92064675	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs201165971	chr10:92064676-92064677	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs76017685	chr10:92064684-92064685	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs369435493	chr10:92064688-92064689	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs1409299	chr10:92064689-92064690	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138686759	chr10:92064691-92064692	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs78143249	chr10:92064700-92064701	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs78728220	chr10:92064701-92064702	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs200203342	chr10:92064705-92064706	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92060800-92064600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:92061400-92077800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:92061600-92065400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr10:92061800-92064000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr10:92061800-92065200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr10:92062200-92063600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr10:92062200-92065600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr10:92062800-92064200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:92062800-92066200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:92063000-92063800	Enhancers	Fetal Stomach	stomach
11	chr10:92063000-92064200	Weak transcription	Fetal Lung	lung
12	chr10:92063000-92065000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr10:92063200-92063600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr10:92063200-92068800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr10:92063400-92066200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr10:92063600-92063800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr10:92063600-92063800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr10:92063600-92063800	Enhancers	Fetal Kidney	kidney
19	chr10:92063600-92067200	Enhancers	NHLF	lung
20	chr10:92063800-92066200	Weak transcription	Fetal Stomach	stomach
21	chr10:92063800-92074200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr10:92064000-92065000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr10:92064200-92064400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr10:92064200-92065400	Enhancers	Fetal Lung	lung
25	chr10:92064400-92065000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr10:92064600-92064800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:92064800-92065000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr10:92065000-92065200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr10:92065000-92065200	Enhancers	Fetal Kidney	kidney
30	chr10:92065000-92065400	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr10:92065000-92065400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr10:92065000-92065800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr10:92065200-92065400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
34	chr10:92065200-92065400	Bivalent Enhancer	NH-A	brain
35	chr10:92065200-92066600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr10:92065200-92066600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:92065200-92066600	Enhancers	Osteobl	bone
38	chr10:92065200-92068800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr10:92065400-92065600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr10:92065400-92065600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:92065400-92066200	Weak transcription	Fetal Lung	lung
42	chr10:92065400-92066200	Enhancers	NH-A	brain
43	chr10:92065400-92066600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr10:92065400-92066800	Enhancers	HUVEC	blood vessel
45	chr10:92065600-92066600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:92065600-92074200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr10:92065800-92066600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:92066000-92066200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr10:92066200-92066400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr10:92066200-92066400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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