Variant report

Variant	nsv1019625
Chromosome Location	chr7:104429371-104461487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:94)
CpG islands
(count:367)
Chromatin interactive
region (count:17)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:94 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:104448236-104448258	K562	blood:	n/a	n/a
2	CEBPB	chr7:104433532-104433845	IMR90	lung:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
3	CEBPB	chr7:104433576-104433893	A549	lung:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
4	CEBPB	chr7:104433614-104433830	A549	lung:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
5	CEBPB	chr7:104433540-104433841	HepG2	liver:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
6	CEBPB	chr7:104433473-104433846	MCF-7	breast:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
7	CEBPB	chr7:104433566-104433846	K562	blood:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
8	CTCF	chr7:104434868-104434889	Lung_OC	lung:	n/a	n/a
9	CTCF	chr7:104453040-104453190	GM12864	blood:	n/a	n/a
10	FOS	chr7:104430909-104431190	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr7:104433660-104433802	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr7:104430863-104431965	HUVEC	blood vessel:	n/a	n/a
13	FOS	chr7:104434724-104434847	MCF10A-Er-Src	breast:	n/a	chr7:104434775-104434783
14	FOS	chr7:104431490-104431910	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr7:104431597-104431801	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr7:104435708-104436416	HUVEC	blood vessel:	n/a	chr7:104436250-104436261
17	FOS	chr7:104431503-104431877	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr7:104436200-104436300	MCF10A-Er-Src	breast:	n/a	chr7:104436250-104436261
19	FOS	chr7:104436182-104436326	MCF10A-Er-Src	breast:	n/a	chr7:104436250-104436261
20	FOS	chr7:104434647-104434952	MCF10A-Er-Src	breast:	n/a	chr7:104434775-104434783
21	FOS	chr7:104434627-104434962	MCF10A-Er-Src	breast:	n/a	chr7:104434775-104434783
22	FOS	chr7:104433608-104433860	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr7:104430927-104431193	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr7:104434647-104434895	MCF10A-Er-Src	breast:	n/a	chr7:104434775-104434783
25	FOXA2	chr7:104431414-104431815	A549	lung:	n/a	chr7:104431692-104431704
26	FOXA2	chr7:104431559-104431948	A549	lung:	n/a	chr7:104431692-104431704
27	GATA2	chr7:104432949-104433434	HUVEC	blood vessel:	n/a	chr7:104433202-104433211
28	GATA3	chr7:104459454-104459598	SH-SY5Y	brain:	n/a	n/a
29	MAFF	chr7:104430341-104430546	HepG2	liver:	n/a	n/a
30	MAFK	chr7:104430298-104430553	IMR90	lung:	n/a	n/a
31	MAFK	chr7:104430280-104430574	HepG2	liver:	n/a	n/a
32	MAFK	chr7:104430252-104430603	HepG2	liver:	n/a	n/a
33	MAX	chr7:104460608-104460615	NB4	blood:	n/a	n/a
34	MAX	chr7:104444630-104444774	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAZ	chr7:104431852-104431977	HepG2	liver:	n/a	n/a
36	MYC	chr7:104431537-104431602	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr7:104430924-104431124	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr7:104431553-104431814	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr7:104434647-104434847	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr7:104434648-104434995	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr7:104433609-104433759	MCF10A-Er-Src	breast:	n/a	n/a
42	NR2F2	chr7:104431524-104432007	MCF-7	breast:	n/a	n/a
43	POLR2A	chr7:104452364-104453460	K562	blood:	n/a	n/a
44	POLR2A	chr7:104442676-104443078	K562	blood:	n/a	n/a
45	POLR2A	chr7:104453957-104454119	MCF-7	breast:	n/a	n/a
46	POLR2A	chr7:104431829-104432253	K562	blood:	n/a	n/a
47	POLR2A	chr7:104448937-104449297	K562	blood:	n/a	n/a
48	POLR2A	chr7:104436285-104436299	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr7:104440016-104442130	K562	blood:	n/a	n/a
50	POLR2A	chr7:104445832-104445860	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:104459130-104459180	HAEpiC	amniotic membrane:	n/a
2	chr7:104459130-104459180	HAEpiC	amniotic membrane:	n/a
3	chr7:104445585-104445635	RPTEC	kidney:	n/a
4	chr7:104445585-104445635	AG10803	skin:	n/a
5	chr7:104445402-104445452	AG09319	gingival:	n/a
6	chr7:104445402-104445452	SAEC	small airway:	n/a
7	chr7:104444707-104444757	CMK	blood:	n/a
8	chr7:104444707-104444757	AG09319	gingival:	n/a
9	chr7:104445402-104445452	RPTEC	kidney:	n/a
10	chr7:104445402-104445452	K562	blood:	n/a
11	chr7:104460407-104460457	GM12878	blood:	n/a
12	chr7:104445402-104445452	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:104460407-104460457	AG04449	skin:	fetal
14	chr7:104445402-104445452	Jurkat	blood:	n/a
15	chr7:104445585-104445635	HRPEpiC	eye:	n/a
16	chr7:104445585-104445635	GM19239	blood:	n/a
17	chr7:104445402-104445452	GM12891	blood:	n/a
18	chr7:104445402-104445452	GM12892	blood:	n/a
19	chr7:104459130-104459180	Hepatocyte	liver:	n/a
20	chr7:104444687-104444737	SAEC	small airway:	n/a
21	chr7:104444687-104444737	T-47D	breast:	n/a
22	chr7:104444687-104444737	LNCaP	prostate:	n/a
23	chr7:104445402-104445452	HL-60	blood:	n/a
24	chr7:104444687-104444737	HL-60	blood:	n/a
25	chr7:104459130-104459180	Caco-2	colon:	n/a
26	chr7:104445585-104445635	HRE	kidney:	n/a
27	chr7:104445585-104445635	T-47D	breast:	n/a
28	chr7:104445402-104445452	CMK	blood:	n/a
29	chr7:104460407-104460457	Jurkat	blood:	n/a
30	chr7:104459130-104459180	A549	lung:	n/a
31	chr7:104445585-104445635	GM12892	blood:	n/a
32	chr7:104460407-104460457	HEEpiC	esophagus:	n/a
33	chr7:104445585-104445635	HCT-116	colon:	n/a
34	chr7:104459130-104459180	MCF10A-Er-Src	breast:	n/a
35	chr7:104445585-104445635	AG04449	skin:	fetal
36	chr7:104444687-104444737	NH-A	brain:	n/a
37	chr7:104445585-104445635	NT2-D1	testis:	n/a
38	chr7:104444707-104444757	HCT-116	colon:	n/a
39	chr7:104444707-104444757	NT2-D1	testis:	n/a
40	chr7:104459130-104459180	RPTEC	kidney:	n/a
41	chr7:104445402-104445452	HAEpiC	amniotic membrane:	n/a
42	chr7:104444707-104444757	SKMC	muscle:	n/a
43	chr7:104445402-104445452	HNPCEpiC	eye:	n/a
44	chr7:104444687-104444737	BE2_C	brain:	n/a
45	chr7:104460407-104460457	CMK	blood:	n/a
46	chr7:104460407-104460457	HCT-116	colon:	n/a
47	chr7:104445585-104445635	A549	lung:	n/a
48	chr7:104459130-104459180	GM06990	blood:	n/a
49	chr7:104445402-104445452	HRCEpiC	kidney:	n/a
50	chr7:104445402-104445452	PFSK-1	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:104453530..104456071-chr7:104485897..104488742,2	K562	blood:
2	chr7:104415740..104417803-chr7:104432798..104435671,2	K562	blood:
3	chr7:104435065..104437773-chr7:104442766..104444672,2	K562	blood:
4	chr7:103848353..103851254-chr7:104459006..104460903,2	K562	blood:
5	chr7:104189213..104191693-chr7:104438258..104440897,2	K562	blood:
6	chr7:104451035..104453878-chr7:104454466..104456364,2	K562	blood:
7	chr7:104427635..104430340-chr7:104433804..104436120,2	K562	blood:
8	chr7:104458052..104460838-chr7:104463968..104465824,2	K562	blood:
9	chr7:104455637..104457503-chr7:104461736..104463277,2	K562	blood:
10	chr7:104427635..104430340-chr7:104433804..104436120,2	K562	blood:
11	chr7:104443017..104446705-chr7:104447012..104450843,4	K562	blood:
12	chr7:104302642..104305367-chr7:104448713..104450769,2	K562	blood:
13	chr7:104438743..104441735-chr7:104443965..104445982,2	K562	blood:
14	chr7:104432454..104433087-chrX:39058476..39059438,2	MCF-7	breast:
15	chr7:104423057..104424601-chr7:104428990..104431789,2	MCF-7	breast:
16	chr7:104451035..104453878-chr7:104454466..104456364,2	K562	blood:
17	chr7:104435065..104439363-chr7:104442614..104444965,4	K562	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-4	chr7:104444403-104444554	ENSG00000226869.2
2	lnc-MLL5-10	chr7:104442608-104443160	expReg_chr7_7212_+
3	lnc-SRPK2-4	chr7:104438784-104438854	ENSG00000226869.2
4	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
5	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
6	lnc-SRPK2-4	chr7:104440265-104440516	NONHSAT122568
7	lnc-SRPK2-4	chr7:104443286-104443410	NONHSAT122568
8	lnc-SRPK2-4	chr7:104444403-104444531	ENSG00000226869.2
9	lnc-SRPK2-4	chr7:104438784-104438854	ENSG00000226869.2
10	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
11	lnc-SRPK2-4	chr7:104444403-104444554	ENSG00000226869.2
12	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
13	lnc-SRPK2-4	chr7:104444403-104444533	ENSG00000226869.2
14	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
15	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
16	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
17	lnc-SRPK2-4	chr7:104439840-104440516	ENSG00000226869.2
18	lnc-SRPK2-4	chr7:104436954-104437396	NONHSAT122568
19	lnc-MLL5-9	chr7:104443904-104444763	expReg_chr7_7219_+
20	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
21	lnc-SRPK2-4	chr7:104444403-104444539	NONHSAT122570
22	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
23	lnc-SRPK2-4	chr7:104439447-104440516	NONHSAT122570
24	lnc-SRPK2-4	chr7:104444403-104444535	ENSG00000226869.2
25	lnc-MLL5-8	chr7:104456917-104457497	expReg_chr7_7241_+
26	lnc-SRPK2-4	chr7:104438225-104441824	l_3463_NR_024586
27	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
28	lnc-SRPK2-4	chr7:104443899-104443986	ENSG00000226869.2
29	lnc-SRPK2-4	chr7:104444403-104444539	NONHSAT122568
30	lnc-SRPK2-4	chr7:104436953-104437396	ENSG00000226869.2
31	lnc-SRPK2-4	chr7:104436963-104437396	ENSG00000226869.2
32	lnc-SRPK2-4	chr7:104443286-104443410	NONHSAT122570
33	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2

No data

Variant related genes	Relation type
LHFPL3-AS1	TF binding region
LHFPL3-AS1	CpG island
ENSG00000164815	chromatin interactions
ENSG00000226869	chromatin interactions

Extended variants
information (count: 1112 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188292849	chr7:104429374-104429375	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192140388	chr7:104429393-104429394	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533022574	chr7:104429411-104429412	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546472246	chr7:104429413-104429414	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184658333	chr7:104429488-104429489	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141892317	chr7:104429493-104429494	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549118659	chr7:104429542-104429543	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375812739	chr7:104429562-104429563	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569755639	chr7:104429594-104429595	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549408974	chr7:104429612-104429613	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368986934	chr7:104429647-104429648	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555371628	chr7:104429678-104429679	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531736305	chr7:104429692-104429693	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551918252	chr7:104429698-104429699	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369076547	chr7:104429744-104429745	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571855688	chr7:104429761-104429762	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577823433	chr7:104429763-104429764	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375967518	chr7:104429764-104429765	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534425104	chr7:104429765-104429766	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554505913	chr7:104429812-104429813	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568011529	chr7:104429817-104429818	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568002250	chr7:104429818-104429819	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs56214042	chr7:104429840-104429841	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs555068234	chr7:104429854-104429855	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117066538	chr7:104429881-104429882	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188728240	chr7:104429901-104429902	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534865264	chr7:104429904-104429905	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377581124	chr7:104429920-104429921	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543986320	chr7:104429923-104429924	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557756456	chr7:104429983-104429984	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4730048	chr7:104429993-104429994	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs577393707	chr7:104430004-104430005	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4730049	chr7:104430056-104430057	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs74742986	chr7:104430081-104430082	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529153979	chr7:104430086-104430087	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542979539	chr7:104430114-104430115	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538715483	chr7:104430156-104430157	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377635201	chr7:104430162-104430163	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562757520	chr7:104430207-104430208	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73714126	chr7:104430293-104430294	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557028462	chr7:104430407-104430408	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531767240	chr7:104430432-104430433	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138311356	chr7:104430452-104430453	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80212447	chr7:104430453-104430454	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13238018	chr7:104430466-104430467	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548016539	chr7:104430472-104430473	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567908536	chr7:104430473-104430474	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34031396	chr7:104430540-104430541	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2470967	chr7:104430564-104430565	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs573001379	chr7:104430603-104430604	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104423800-104430800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:104428200-104430800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:104430400-104432000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:104430600-104432000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:104430600-104432400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:104430600-104432400	Enhancers	HMEC	breast
7	chr7:104430600-104432800	Enhancers	HUVEC	blood vessel
8	chr7:104430800-104433400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:104430800-104436800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:104431000-104431400	Enhancers	Brain Anterior Caudate	brain
11	chr7:104431000-104432000	Enhancers	Osteobl	bone
12	chr7:104431200-104431800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr7:104431200-104431800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:104431200-104432000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:104431200-104432000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:104431400-104431800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr7:104431400-104432000	Enhancers	NH-A	brain
18	chr7:104431400-104432400	Enhancers	Brain Germinal Matrix	brain
19	chr7:104431400-104433000	Enhancers	Brain Cingulate Gyrus	brain
20	chr7:104431600-104431800	Enhancers	Brain Substantia Nigra	brain
21	chr7:104431600-104432400	Enhancers	Brain Hippocampus Middle	brain
22	chr7:104431800-104432000	Enhancers	Brain Angular Gyrus	brain
23	chr7:104431800-104434200	Weak transcription	Brain Substantia Nigra	brain
24	chr7:104431800-104434800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:104431800-104436000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:104432000-104433800	Weak transcription	Osteobl	bone
27	chr7:104432000-104434000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:104432000-104434000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:104432000-104434600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr7:104432400-104433800	Weak transcription	HMEC	breast
31	chr7:104432400-104434600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:104432800-104433200	Weak transcription	HUVEC	blood vessel
33	chr7:104433000-104434600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr7:104433200-104433400	Enhancers	HUVEC	blood vessel
35	chr7:104433400-104434600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:104433400-104435200	Weak transcription	HUVEC	blood vessel
37	chr7:104433400-104439600	Weak transcription	Fetal Intestine Small	intestine
38	chr7:104433800-104434000	Enhancers	Osteobl	bone
39	chr7:104433800-104435000	Enhancers	HMEC	breast
40	chr7:104434000-104434400	Weak transcription	Osteobl	bone
41	chr7:104434000-104436800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:104434000-104436800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:104434200-104437000	Enhancers	Brain Substantia Nigra	brain
44	chr7:104434200-104441200	Weak transcription	Fetal Intestine Large	intestine
45	chr7:104434400-104436200	Enhancers	Osteobl	bone
46	chr7:104434400-104437000	Enhancers	Brain Hippocampus Middle	brain
47	chr7:104434600-104435000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:104434600-104435200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr7:104434600-104436800	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:104434600-104437200	Enhancers	Cortex derived primary cultured neurospheres	brain

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