Variant report

Variant	nsv892215
Chromosome Location	chr9:7799787-7889991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:663)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:7799673-7799970	K562	blood:	n/a	n/a
2	ATF3	chr9:7799628-7799981	HepG2	liver:	n/a	n/a
3	ATF3	chr9:7799547-7799974	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr9:7799559-7799954	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr9:7799216-7799916	GM12878	blood:	n/a	chr9:7799429-7799437
6	ATF3	chr9:7799704-7799917	GM12878	blood:	n/a	n/a
7	ATF3	chr9:7799647-7799949	K562	blood:	n/a	n/a
8	BATF	chr9:7799677-7799960	GM12878	blood:	n/a	n/a
9	BATF	chr9:7799872-7800146	GM12878	blood:	n/a	chr9:7800040-7800051
10	BATF	chr9:7799963-7800195	GM12878	blood:	n/a	chr9:7800040-7800051
11	BCLAF1	chr9:7799298-7799961	GM12878	blood:	n/a	n/a
12	BCLAF1	chr9:7799525-7800090	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:7799605-7799952	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:7800146-7800155	K562	blood:	n/a	n/a
15	BHLHE40	chr9:7799210-7800252	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:7799316-7799827	K562	blood:	n/a	n/a
17	BRCA1	chr9:7799429-7799943	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:7820000-7820344	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:7819955-7820368	A549	lung:	n/a	n/a
20	CEBPB	chr9:7819991-7820354	K562	blood:	n/a	n/a
21	CEBPB	chr9:7820026-7820292	A549	lung:	n/a	n/a
22	CEBPB	chr9:7844674-7844828	H1-hESC	embryonic stem cell:	n/a	chr9:7844743-7844756 chr9:7844743-7844756 chr9:7844743-7844754
23	CEBPB	chr9:7819997-7820319	A549	lung:	n/a	n/a
24	CEBPB	chr9:7821653-7821782	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:7820003-7820320	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:7802666-7802893	HepG2	liver:	n/a	n/a
27	CHD2	chr9:7799387-7799994	HepG2	liver:	n/a	n/a
28	CHD2	chr9:7879898-7880238	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr9:7799674-7799972	K562	blood:	n/a	n/a
30	CHD2	chr9:7799612-7800002	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:7799225-7800044	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr9:7799297-7799978	GM12878	blood:	n/a	n/a
33	CREB1	chr9:7799579-7800011	K562	blood:	n/a	n/a
34	CREB1	chr9:7799499-7799993	K562	blood:	n/a	n/a
35	CREB1	chr9:7799132-7800008	GM12878	blood:	n/a	n/a
36	CREB1	chr9:7799617-7799947	A549	lung:	n/a	n/a
37	CREB1	chr9:7799238-7800023	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr9:7799557-7799986	HepG2	liver:	n/a	n/a
39	CREB1	chr9:7799338-7800063	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr9:7799294-7800003	A549	lung:	n/a	n/a
41	CREB1	chr9:7799304-7800004	HepG2	liver:	n/a	n/a
42	CTCF	chr9:7844360-7844510	GM12869	blood:	n/a	n/a
43	CTCF	chr9:7844380-7844530	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr9:7844420-7844570	HL-60	blood:	n/a	n/a
45	CTCF	chr9:7799700-7799850	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr9:7844440-7844590	GM06990	blood:	n/a	n/a
47	CTCF	chr9:7844360-7844510	GM12801	blood:	n/a	n/a
48	CTCF	chr9:7844380-7844530	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:7844380-7844530	NHEK	skin:	n/a	n/a
50	CTCF	chr9:7844377-7844573	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:7800256-7800306	BJ	skin:	n/a
2	chr9:7799961-7800011	PANC-1	pancreas:	n/a
3	chr9:7799961-7800011	HUVEC	blood vessel:	n/a
4	chr9:7800256-7800306	H1-hESC	embryonic stem cell:	embryo
5	chr9:7800256-7800306	NT2-D1	testis:	n/a
6	chr9:7799961-7800011	GM19239	blood:	n/a
7	chr9:7800256-7800306	SK-N-SH_RA	brain:	n/a
8	chr9:7799961-7800011	HCT-116	colon:	n/a
9	chr9:7800256-7800306	AG10803	skin:	n/a
10	chr9:7799961-7800011	BJ	skin:	n/a
11	chr9:7799961-7800011	HRCEpiC	kidney:	n/a
12	chr9:7799961-7800011	H1-hESC	embryonic stem cell:	embryo
13	chr9:7800256-7800306	HCT-116	colon:	n/a
14	chr9:7800256-7800306	K562	blood:	n/a
15	chr9:7799961-7800011	MCF10A-Er-Src	breast:	n/a
16	chr9:7799961-7800011	HMEC	breast:	n/a
17	chr9:7799961-7800011	SK-N-MC	brain:	n/a
18	chr9:7799961-7800011	HNPCEpiC	eye:	n/a
19	chr9:7799961-7800011	BE2_C	brain:	n/a
20	chr9:7799961-7800011	HAEpiC	amniotic membrane:	n/a
21	chr9:7800256-7800306	Jurkat	blood:	n/a
22	chr9:7799961-7800011	T-47D	breast:	n/a
23	chr9:7799961-7800011	NHBE	bronchial:	n/a
24	chr9:7799961-7800011	SAEC	small airway:	n/a
25	chr9:7799961-7800011	Hepatocyte	liver:	n/a
26	chr9:7800256-7800306	PFSK-1	brain:	n/a
27	chr9:7800256-7800306	T-47D	breast:	n/a
28	chr9:7800256-7800306	U87	brain:	n/a
29	chr9:7799961-7800011	RPTEC	kidney:	n/a
30	chr9:7800256-7800306	GM12878	blood:	n/a
31	chr9:7799961-7800011	NT2-D1	testis:	n/a
32	chr9:7799961-7800011	HRPEpiC	eye:	n/a
33	chr9:7800256-7800306	ovcar-3	ovarian:	n/a
34	chr9:7800256-7800306	AG09319	gingival:	n/a
35	chr9:7800256-7800306	ECC-1	luminal epithelium:	n/a
36	chr9:7799961-7800011	Jurkat	blood:	n/a
37	chr9:7799961-7800011	GM06990	blood:	n/a
38	chr9:7800256-7800306	AG04449	skin:	fetal
39	chr9:7799961-7800011	GM12878	blood:	n/a
40	chr9:7800256-7800306	MCF10A-Er-Src	breast:	n/a
41	chr9:7800256-7800306	HCPEpiC	choroid plexus:	n/a
42	chr9:7800256-7800306	GM12891	blood:	n/a
43	chr9:7800256-7800306	BE2_C	brain:	n/a
44	chr9:7800256-7800306	Hepatocyte	liver:	n/a
45	chr9:7800256-7800306	PrEC	prostate:	n/a
46	chr9:7800256-7800306	Caco-2	colon:	n/a
47	chr9:7800256-7800306	HNPCEpiC	eye:	n/a
48	chr9:7799961-7800011	HepG2	liver:	n/a
49	chr9:7800256-7800306	HL-60	blood:	n/a
50	chr9:7800256-7800306	AG04450	lung:	fetal

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:7856837..7858769-chr9:7859331..7861674,2	K562	blood:
2	chr9:7799400..7802394-chr9:7804203..7806303,2	K562	blood:
3	chr17:56709050..56710030-chr9:7799215..7799951,2	NB4	blood:
4	chr9:7569899..7570770-chr9:7827280..7828131,4	MCF-7	breast:
5	chr9:7592716..7593255-chr9:7844122..7844707,2	MCF-7	breast:
6	chr9:7798904..7801575-chr9:7807644..7809978,3	K562	blood:
7	chr9:7870654..7872409-chr9:7873733..7876466,2	MCF-7	breast:
8	chr9:7870342..7873066-chr9:7873519..7876251,2	K562	blood:
9	chr9:7844225..7844973-chr9:8895548..8896327,4	MCF-7	breast:
10	chr15:59981502..59982267-chr9:7799535..7800195,2	NB4	blood:
11	chr9:7785236..7787094-chr9:7798343..7800559,2	K562	blood:
12	chr16:70408470..70409240-chr9:7799247..7799915,2	NB4	blood:
13	chr9:7785236..7788053-chr9:7798343..7800585,2	K562	blood:
14	chr9:7870342..7873066-chr9:7873519..7876251,2	K562	blood:
15	chr15:25414756..25415321-chr9:7799310..7799908,2	Hela-S3	cervix:
16	chr9:7592774..7593282-chr9:7827299..7827877,2	MCF-7	breast:
17	chr9:7764096..7766786-chr9:7797842..7799916,2	MCF-7	breast:
18	chr9:7799234..7801006-chr9:7803673..7806734,3	MCF-7	breast:
19	chr9:7870654..7872409-chr9:7873733..7876466,2	MCF-7	breast:
20	chr9:7856837..7858769-chr9:7859331..7861674,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-8	chr9:7888299-7888380	NONHSAT130179
2	lnc-PTPRD-8	chr9:7833925-7834006	NONHSAT130179
3	lnc-PTPRD-8	chr9:7800041-7800148	NONHSAT130178

No data

Variant related genes	Relation type
TMEM261	TF binding region
TMEM261	CpG island
ENSG00000140299	chromatin interactions
ENSG00000137038	chromatin interactions
ENSG00000270814	chromatin interactions
ENSG00000273056	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 2773 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2773 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2297554	chr9:7799787-7799788	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549336671	chr9:7799788-7799789	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs567829787	chr9:7799791-7799792	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs369193959	chr9:7799795-7799796	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs528988288	chr9:7799812-7799813	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547153933	chr9:7799814-7799815	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs565914019	chr9:7799830-7799831	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs539247669	chr9:7799841-7799842	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs558043080	chr9:7799860-7799861	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs569921107	chr9:7799870-7799871	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs538266820	chr9:7799897-7799898	Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs562960337	chr9:7799914-7799915	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs574873439	chr9:7799921-7799922	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs542386916	chr9:7799938-7799939	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs16926763	chr9:7799957-7799958	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572608451	chr9:7799962-7799963	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs183343814	chr9:7799980-7799981	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201187558	chr9:7799991-7799992	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs564822464	chr9:7800021-7800022	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531850571	chr9:7800043-7800044	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs543691371	chr9:7800064-7800065	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs138082452	chr9:7800083-7800084	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs149506816	chr9:7800093-7800094	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs547511698	chr9:7800095-7800096	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs534304409	chr9:7800111-7800112	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs565599174	chr9:7800119-7800120	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs115925066	chr9:7800129-7800130	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs374737763	chr9:7800135-7800136	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs186501848	chr9:7800143-7800144	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs72697241	chr9:7800190-7800191	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs537381100	chr9:7800217-7800218	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72697242	chr9:7800239-7800240	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs568505219	chr9:7800250-7800251	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs79956096	chr9:7800276-7800277	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554241574	chr9:7800280-7800281	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538041750	chr9:7800293-7800294	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs72697244	chr9:7800319-7800320	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540037696	chr9:7800347-7800348	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190029847	chr9:7800351-7800352	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs531897752	chr9:7800356-7800357	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543752871	chr9:7800357-7800358	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs72697245	chr9:7800383-7800384	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs144175226	chr9:7800401-7800402	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568714529	chr9:7800409-7800410	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540624633	chr9:7800417-7800418	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113280493	chr9:7800468-7800469	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532856227	chr9:7800511-7800512	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs551443870	chr9:7800526-7800527	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563505800	chr9:7800631-7800632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530711491	chr9:7800633-7800634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
Melanoma	18172304	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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Bipolar disorder	19114987	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7798200-7800400	Active TSS	K562	blood
2	chr9:7798400-7799800	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr9:7798400-7799800	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr9:7798400-7800000	Active TSS	Stomach Smooth Muscle	stomach
5	chr9:7798400-7800000	Active TSS	HSMMtube	muscle
6	chr9:7798400-7800200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr9:7798400-7800200	Active TSS	Psoas Muscle	Psoas
8	chr9:7798600-7799800	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr9:7798600-7799800	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr9:7798600-7800000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr9:7798600-7800000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr9:7798600-7800000	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr9:7798600-7800200	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr9:7798600-7800200	Active TSS	H1 Cell Line	embryonic stem cell
15	chr9:7798600-7800200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:7798600-7800200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr9:7798600-7800200	Active TSS	Fetal Kidney	kidney
18	chr9:7798600-7800200	Active TSS	NHLF	lung
19	chr9:7798600-7800400	Active TSS	Thymus	Thymus
20	chr9:7798800-7799800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr9:7798800-7799800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr9:7798800-7799800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr9:7798800-7799800	Active TSS	Esophagus	oesophagus
24	chr9:7798800-7799800	Active TSS	Placenta Amnion	Placenta Amnion
25	chr9:7798800-7800000	Active TSS	H9 Cell Line	embryonic stem cell
26	chr9:7798800-7800000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr9:7798800-7800000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr9:7798800-7800000	Active TSS	Colonic Mucosa	Colon
29	chr9:7798800-7800000	Active TSS	Lung	lung
30	chr9:7798800-7800000	Active TSS	Ovary	ovary
31	chr9:7798800-7800200	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr9:7798800-7800200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:7798800-7800200	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr9:7798800-7800200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:7798800-7800200	Active TSS	Aorta	Aorta
36	chr9:7798800-7800200	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr9:7798800-7800200	Active TSS	Fetal Muscle Trunk	muscle
38	chr9:7798800-7800200	Active TSS	Right Atrium	heart
39	chr9:7798800-7800200	Active TSS	Right Ventricle	heart
40	chr9:7799000-7799800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:7799000-7799800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr9:7799000-7799800	Active TSS	Fetal Brain Male	brain
43	chr9:7799000-7799800	Active TSS	Gastric	stomach
44	chr9:7799000-7800000	Active TSS	Muscle Satellite Cultured Cells	--
45	chr9:7799000-7800000	Active TSS	Fetal Intestine Large	intestine
46	chr9:7799000-7800000	Active TSS	Pancreas	Pancrea
47	chr9:7799000-7800000	Active TSS	Small Intestine	intestine
48	chr9:7799000-7800000	Active TSS	Hela-S3	cervix
49	chr9:7799000-7800000	Active TSS	HepG2	liver
50	chr9:7799000-7800200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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