Variant report

Variant	nsv1025917
Chromosome Location	chr9:588657-742803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2016)
CpG islands
(count:306)
Chromatin interactive
region (count:56)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
2	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
15	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:652937-653241	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
21	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
22	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
23	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
24	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
27	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
28	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr9:647176-647333	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:709961-710330	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:682561-683227	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:618520-618739	HepG2	liver:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
33	CEBPB	chr9:687423-687597	HepG2	liver:	n/a	chr9:687549-687562
34	CEBPB	chr9:602928-603376	MCF-7	breast:	n/a	n/a
35	CEBPB	chr9:674165-674905	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:652997-653155	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr9:673657-674592	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:706971-707283	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:710023-710247	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:709974-710470	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:682501-683161	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:720255-720473	HepG2	liver:	n/a	chr9:720400-720411
43	CEBPB	chr9:599907-600250	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
44	CEBPB	chr9:602628-603112	MCF-7	breast:	n/a	n/a
45	CEBPB	chr9:599889-600308	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
46	CEBPB	chr9:618469-618742	A549	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
47	CEBPB	chr9:599921-600405	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
48	CEBPB	chr9:683680-684078	H1-hESC	embryonic stem cell:	n/a	chr9:683965-683978 chr9:683771-683782 chr9:684035-684047
49	CEBPB	chr9:710003-710250	A549	lung:	n/a	n/a
50	CEBPB	chr9:650454-650746	H1-hESC	embryonic stem cell:	n/a	chr9:650606-650617

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:705143-705193	AoSMC	blood vessel:	n/a
2	chr9:705143-705193	AoSMC	blood vessel:	n/a
3	chr9:714269-714319	GM12892	blood:	n/a
4	chr9:707387-707437	HMEC	breast:	n/a
5	chr9:707410-707460	Hela-S3	cervix:	n/a
6	chr9:705143-705193	Hepatocyte	liver:	n/a
7	chr9:707410-707460	U87	brain:	n/a
8	chr9:705143-705193	BJ	skin:	n/a
9	chr9:714269-714319	GM19239	blood:	n/a
10	chr9:707166-707216	SK-N-SH	brain:	n/a
11	chr9:707410-707460	T-47D	breast:	n/a
12	chr9:707410-707460	HIPEpiC	eye:	n/a
13	chr9:707410-707460	Jurkat	blood:	n/a
14	chr9:705143-705193	IMR90	lung:	fetal
15	chr9:714269-714319	HEK293	kidney:	embryo
16	chr9:707410-707460	A549	lung:	n/a
17	chr9:707410-707460	GM12892	blood:	n/a
18	chr9:705143-705193	MCF10A-Er-Src	breast:	n/a
19	chr9:707166-707216	LNCaP	prostate:	n/a
20	chr9:707166-707216	HL-60	blood:	n/a
21	chr9:707166-707216	HRPEpiC	eye:	n/a
22	chr9:707410-707460	HUVEC	blood vessel:	n/a
23	chr9:714269-714319	SKMC	muscle:	n/a
24	chr9:707166-707216	MCF10A-Er-Src	breast:	n/a
25	chr9:707387-707437	LNCaP	prostate:	n/a
26	chr9:705143-705193	NHBE	bronchial:	n/a
27	chr9:707166-707216	NB4	blood:	n/a
28	chr9:707166-707216	GM12892	blood:	n/a
29	chr9:707410-707460	ECC-1	luminal epithelium:	n/a
30	chr9:707387-707437	NT2-D1	testis:	n/a
31	chr9:707166-707216	HAEpiC	amniotic membrane:	n/a
32	chr9:714269-714319	HCF	heart:	n/a
33	chr9:707166-707216	Caco-2	colon:	n/a
34	chr9:705143-705193	NHDF-neo	bronchial:	n/a
35	chr9:714269-714319	K562	blood:	n/a
36	chr9:707387-707437	HCPEpiC	choroid plexus:	n/a
37	chr9:707166-707216	PFSK-1	brain:	n/a
38	chr9:707387-707437	GM19239	blood:	n/a
39	chr9:707387-707437	HAEpiC	amniotic membrane:	n/a
40	chr9:705143-705193	HCM	heart:	n/a
41	chr9:714269-714319	SK-N-SH	brain:	n/a
42	chr9:707166-707216	GM19239	blood:	n/a
43	chr9:707166-707216	NHDF-neo	bronchial:	n/a
44	chr9:707166-707216	HCM	heart:	n/a
45	chr9:707166-707216	SAEC	small airway:	n/a
46	chr9:714269-714319	BE2_C	brain:	n/a
47	chr9:705143-705193	HCF	heart:	n/a
48	chr9:707166-707216	AG09319	gingival:	n/a
49	chr9:705143-705193	SK-N-SH	brain:	n/a
50	chr9:705143-705193	HNPCEpiC	eye:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
2	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
3	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
4	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
5	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
6	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
7	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
8	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
9	chr9:704209..707068-chr9:719899..721523,2	MCF-7	breast:
10	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
11	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
12	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
13	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
14	chr9:730043..732840-chr9:737557..739917,2	MCF-7	breast:
15	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
16	chr9:385789..386423-chr9:612104..612846,2	K562	blood:
17	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
18	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
19	chr17:17584235..17586582-chr9:741151..743803,2	MCF-7	breast:
20	chr9:697287..699295-chr9:705065..707332,2	K562	blood:
21	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
22	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
23	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
24	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
25	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
26	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
27	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
28	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
29	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
30	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
31	chr9:706307..708254-chr9:737100..740465,4	MCF-7	breast:
32	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
33	chr9:682966..685572-chr9:709711..712587,2	MCF-7	breast:
34	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
35	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
36	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
37	chr16:1239384..1239884-chr9:736833..737597,2	MCF-7	breast:
38	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
39	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
40	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
41	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
42	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
43	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
44	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
45	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
46	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
47	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
48	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
49	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
50	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-3	chr9:673817-674379	ENSG00000227914.1
2	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.3
3	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.3
4	lnc-C9orf66-3	chr9:673478-674379	ENSG00000227914.3
5	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.1
6	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.1
7	lnc-C9orf66-3	chr9:674124-674379	ENSG00000227914.3
8	lnc-C9orf66-3	chr9:677542-677628	ENSG00000227914.3
9	lnc-DMRT1-3	chr9:659986-660326	NONHSAT129934

No data

Variant related genes	Relation type
ENSG00000227914	TF binding region
KANK1	TF binding region
ENSG00000229875	TF binding region
ENSG00000227914	CpG island
KANK1	CpG island
ENSG00000229875	CpG island
ENSG00000108557	chromatin interactions
ENSG00000107104	chromatin interactions
ENSG00000227914	chromatin interactions

Extended variants
information (count: 9408 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:9408 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375878057	chr9:588705-588706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568181050	chr9:588737-588738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537257220	chr9:588738-588739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183191060	chr9:588739-588740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570956191	chr9:588742-588743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540168730	chr9:588745-588746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116354706	chr9:588757-588758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571345661	chr9:588764-588765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534570760	chr9:588794-588795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554717252	chr9:588796-588797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574544188	chr9:588826-588827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142030423	chr9:588829-588830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563544868	chr9:588847-588848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576954065	chr9:588867-588868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35992203	chr9:588882-588883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186039033	chr9:588889-588890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559358688	chr9:588921-588922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191305070	chr9:588927-588928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548138386	chr9:588940-588941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150691964	chr9:588955-588956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115736128	chr9:589019-589020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147265081	chr9:589033-589034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550653073	chr9:589042-589043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140037962	chr9:589051-589052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72689653	chr9:589070-589071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547292187	chr9:589106-589107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567016563	chr9:589113-589114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146820552	chr9:589147-589148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554557338	chr9:589149-589150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367866898	chr9:589153-589154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139589243	chr9:589181-589182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371041175	chr9:589189-589190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537183343	chr9:589199-589200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35308063	chr9:589210-589211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183367785	chr9:589211-589212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149719238	chr9:589234-589235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12341500	chr9:589252-589253	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12338563	chr9:589271-589272	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs372399679	chr9:589310-589311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559607539	chr9:589312-589313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572754944	chr9:589323-589324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541720450	chr9:589348-589349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113928207	chr9:589356-589357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187857853	chr9:589378-589379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559533892	chr9:589385-589386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147637670	chr9:589413-589414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141977994	chr9:589427-589428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75768907	chr9:589467-589468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534293565	chr9:589468-589469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192734699	chr9:589483-589484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	21272361	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:5449 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:549800-593800	Weak transcription	Lung	lung
2	chr9:572000-589400	Weak transcription	Aorta	Aorta
3	chr9:572200-589800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr9:574400-589000	Weak transcription	Brain Substantia Nigra	brain
5	chr9:574600-589400	Weak transcription	HMEC	breast
6	chr9:575200-589200	Weak transcription	Right Ventricle	heart
7	chr9:579800-589200	Weak transcription	Brain Anterior Caudate	brain
8	chr9:581400-588800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:581400-589600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr9:581400-591400	Weak transcription	Fetal Intestine Large	intestine
11	chr9:582000-589000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:582000-589400	Weak transcription	Esophagus	oesophagus
13	chr9:582000-591400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:582200-589200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr9:582200-589200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:582400-589000	Weak transcription	Right Atrium	heart
17	chr9:582400-589400	Weak transcription	A549	lung
18	chr9:582600-589200	Weak transcription	Pancreas	Pancrea
19	chr9:582600-591400	Weak transcription	Gastric	stomach
20	chr9:583000-594400	Weak transcription	Fetal Kidney	kidney
21	chr9:584400-589600	Weak transcription	Stomach Mucosa	stomach
22	chr9:585200-589800	Enhancers	Fetal Heart	heart
23	chr9:585400-589200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:586800-589200	Weak transcription	Ovary	ovary
25	chr9:587000-589200	Weak transcription	Left Ventricle	heart
26	chr9:587400-588800	Weak transcription	Brain Hippocampus Middle	brain
27	chr9:587800-589200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr9:588200-588800	Enhancers	Fetal Intestine Small	intestine
29	chr9:588200-590600	Enhancers	Duodenum Mucosa	Duodenum
30	chr9:588600-588800	Enhancers	Small Intestine	intestine
31	chr9:588600-589200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr9:588600-589200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr9:588600-589600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:588800-589400	Weak transcription	Small Intestine	intestine
35	chr9:588800-589600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:588800-590200	Enhancers	Brain Hippocampus Middle	brain
37	chr9:588800-591000	Weak transcription	Fetal Intestine Small	intestine
38	chr9:588800-591400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:589000-589600	Enhancers	NHEK	skin
40	chr9:589000-589800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr9:589000-590000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:589000-590200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr9:589000-590200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:589000-590400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr9:589000-590400	Enhancers	Brain Substantia Nigra	brain
46	chr9:589000-590400	Enhancers	Right Atrium	heart
47	chr9:589000-591600	Enhancers	Brain Cingulate Gyrus	brain
48	chr9:589000-592000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:589200-589400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:589200-589600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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