Variant report

Variant	nsv539896
Chromosome Location	chr9:471885-570097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1009)
CpG islands
(count:489)
Chromatin interactive
region (count:30)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1009 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:504390-504746	K562	blood:	n/a	n/a
2	ARID3A	chr9:489187-489524	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:495829-496174	HepG2	liver:	n/a	n/a
4	ATF1	chr9:491995-492195	K562	blood:	n/a	n/a
5	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
6	BACH1	chr9:503516-503574	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:505331-505595	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:503882-504954	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
12	BCL3	chr9:489067-489648	A549	lung:	n/a	n/a
13	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
14	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
15	BCL3	chr9:503842-504488	A549	lung:	n/a	chr9:504175-504184 chr9:504327-504340 chr9:504456-504469
16	BHLHE40	chr9:503924-504891	K562	blood:	n/a	chr9:504430-504446 chr9:504607-504623 chr9:504604-504620 chr9:504606-504622
17	BHLHE40	chr9:504376-504833	GM12878	blood:	n/a	chr9:504430-504446 chr9:504607-504623 chr9:504604-504620 chr9:504606-504622
18	BHLHE40	chr9:494860-495111	HepG2	liver:	n/a	n/a
19	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
20	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
21	BRCA1	chr9:504440-504580	HepG2	liver:	n/a	n/a
22	CCNT2	chr9:503997-505117	K562	blood:	n/a	chr9:504819-504828
23	CEBPB	chr9:561474-561777	MCF-7	breast:	n/a	n/a
24	CEBPB	chr9:495243-495543	A549	lung:	n/a	n/a
25	CEBPB	chr9:561371-561765	A549	lung:	n/a	n/a
26	CEBPB	chr9:530490-531138	HCT-116	colon:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
27	CEBPB	chr9:504299-504587	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:489177-489772	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:530652-530956	A549	lung:	n/a	n/a
30	CEBPB	chr9:489180-489720	MCF-7	breast:	n/a	n/a
31	CEBPB	chr9:563605-564145	A549	lung:	n/a	n/a
32	CEBPB	chr9:495311-495494	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:486108-486526	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr9:486083-486570	A549	lung:	n/a	n/a
35	CEBPB	chr9:530749-531005	A549	lung:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
36	CEBPB	chr9:561463-561714	A549	lung:	n/a	n/a
37	CEBPB	chr9:486090-486669	A549	lung:	n/a	n/a
38	CEBPB	chr9:489015-490295	A549	lung:	n/a	n/a
39	CEBPB	chr9:530695-530959	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:489357-489758	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr9:561219-561918	A549	lung:	n/a	n/a
42	CEBPB	chr9:495288-495533	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:489250-490182	A549	lung:	n/a	n/a
44	CEBPB	chr9:489122-489760	A549	lung:	n/a	n/a
45	CHD1	chr9:505142-505200	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr9:557966-558051	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr9:505550-505585	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr9:518207-518317	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr9:504693-504735	HepG2	liver:	n/a	n/a
50	CHD2	chr9:504228-504863	Hela-S3	cervix:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:503937-503987	AG04449	skin:	fetal
2	chr9:503937-503987	AG04449	skin:	fetal
3	chr9:505235-505285	HMEC	breast:	n/a
4	chr9:505721-505771	ProgFib	skin:	n/a
5	chr9:507411-507461	BE2_C	brain:	n/a
6	chr9:504774-504824	SK-N-SH	brain:	n/a
7	chr9:505235-505285	Hela-S3	cervix:	n/a
8	chr9:505571-505621	A549	lung:	n/a
9	chr9:472966-473016	BJ	skin:	n/a
10	chr9:505721-505771	CMK	blood:	n/a
11	chr9:505721-505771	HCPEpiC	choroid plexus:	n/a
12	chr9:505571-505621	HepG2	liver:	n/a
13	chr9:507411-507461	SK-N-SH_RA	brain:	n/a
14	chr9:472966-473016	Jurkat	blood:	n/a
15	chr9:507411-507461	PrEC	prostate:	n/a
16	chr9:507411-507461	U87	brain:	n/a
17	chr9:505571-505621	ovcar-3	ovarian:	n/a
18	chr9:471920-471970	LNCaP	prostate:	n/a
19	chr9:503937-503987	IMR90	lung:	fetal
20	chr9:472966-473016	AG09319	gingival:	n/a
21	chr9:505571-505621	CMK	blood:	n/a
22	chr9:505721-505771	T-47D	breast:	n/a
23	chr9:472966-473016	IMR90	lung:	fetal
24	chr9:503937-503987	HEK293	kidney:	embryo
25	chr9:504774-504824	PANC-1	pancreas:	n/a
26	chr9:472966-473016	H1-hESC	embryonic stem cell:	embryo
27	chr9:507411-507461	HCPEpiC	choroid plexus:	n/a
28	chr9:472966-473016	ECC-1	luminal epithelium:	n/a
29	chr9:505571-505621	HRCEpiC	kidney:	n/a
30	chr9:507411-507461	RPTEC	kidney:	n/a
31	chr9:507411-507461	GM19239	blood:	n/a
32	chr9:503937-503987	HRCEpiC	kidney:	n/a
33	chr9:505721-505771	GM19239	blood:	n/a
34	chr9:505721-505771	HCM	heart:	n/a
35	chr9:471920-471970	MCF10A-Er-Src	breast:	n/a
36	chr9:507411-507461	HRE	kidney:	n/a
37	chr9:471920-471970	PFSK-1	brain:	n/a
38	chr9:507411-507461	T-47D	breast:	n/a
39	chr9:472966-473016	PFSK-1	brain:	n/a
40	chr9:505571-505621	NH-A	brain:	n/a
41	chr9:503937-503987	Hepatocyte	liver:	n/a
42	chr9:505571-505621	K562	blood:	n/a
43	chr9:504774-504824	AG09309	skin:	n/a
44	chr9:503937-503987	H1-hESC	embryonic stem cell:	embryo
45	chr9:503937-503987	GM19239	blood:	n/a
46	chr9:471920-471970	HCT-116	colon:	n/a
47	chr9:505235-505285	PANC-1	pancreas:	n/a
48	chr9:472966-473016	MCF-7	breast:	n/a
49	chr9:504774-504824	ovcar-3	ovarian:	n/a
50	chr9:472966-473016	NH-A	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
2	chr9:469030..473266-chr9:476113..479118,4	MCF-7	breast:
3	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
4	chr9:469326..471004-chr9:547085..549851,2	MCF-7	breast:
5	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
6	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
7	chr9:385596..386468-chr9:546637..547164,2	MCF-7	breast:
8	chr9:494848..496689-chr9:501659..504144,2	MCF-7	breast:
9	chr9:470985..473419-chr9:489407..491415,2	MCF-7	breast:
10	chr9:490701..492635-chr9:494682..497058,2	K562	blood:
11	chr9:495605..498122-chr9:502386..505122,3	MCF-7	breast:
12	chr9:469974..471479-chr9:511045..512830,2	K562	blood:
13	chr9:469030..473266-chr9:476113..479118,4	MCF-7	breast:
14	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
15	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
16	chr9:468830..470676-chr9:503247..506779,4	MCF-7	breast:
17	chr9:468933..471416-chr9:484729..487754,3	MCF-7	breast:
18	chr9:494848..496689-chr9:501659..504144,2	MCF-7	breast:
19	chr9:487771..490019-chr9:514331..516293,2	MCF-7	breast:
20	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
21	chr9:500269..502662-chr9:502681..505040,2	MCF-7	breast:
22	chr9:504296..504898-chr9:21802481..21802992,2	HCT-116	colon:
23	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
24	chr9:468995..471572-chr9:503851..506185,2	MCF-7	breast:
25	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
26	chr9:490052..492255-chr9:502875..504712,2	MCF-7	breast:
27	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
28	chr9:490052..492255-chr9:502875..504712,2	MCF-7	breast:
29	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
30	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK8-2	chr9:547038-547341	NONHSAT129931
2	lnc-DOCK8-2	chr9:547317-547341	ENSG00000226403.1
3	lnc-DOCK8-5	chr9:473194-473273	NONHSAT129926
4	lnc-DOCK8-5	chr9:484282-484491	NONHSAT129926
5	lnc-DOCK8-1	chr9:487774-487803	ENSG00000228115.1
6	lnc-C9orf66-7	chr9:503057-504746	NONHSAT129929
7	lnc-DOCK8-2	chr9:549190-549531	ENSG00000226403.1
8	lnc-DOCK8-2	chr9:547318-547341	ENSG00000226403.1
9	lnc-DOCK8-1	chr9:495238-495610	ENSG00000228115.1
10	lnc-C9orf66-8	chr9:507258-507553	NONHSAT129930
11	lnc-DOCK8-5	chr9:473194-473273	NONHSAT129927
12	lnc-DOCK8-2	chr9:549107-549531	ENSG00000226403.1
13	lnc-DOCK8-5	chr9:476628-476769	NONHSAT129927
14	lnc-C9orf66-2	chr9:492084-492112	ENSG00000227155.3
15	lnc-C9orf66-2	chr9:488957-489066	ENSG00000227155.3
16	lnc-DOCK8-2	chr9:549107-549525	NONHSAT129931

No data

Variant related genes	Relation type
ENSG00000226403	TF binding region
RNU6-1327P	TF binding region
ENSG00000227155	TF binding region
RN7SL412P	TF binding region
KANK1	TF binding region
ENSG00000235330	TF binding region
ENSG00000228115	TF binding region
ENSG00000226403	CpG island
RNU6-1327P	CpG island
ENSG00000227155	CpG island
RN7SL412P	CpG island
KANK1	CpG island
ENSG00000235330	CpG island
ENSG00000228115	CpG island
ENSG00000107104	chromatin interactions
ENSG00000099810	chromatin interactions
ENSG00000235330	chromatin interactions
ENSG00000227155	chromatin interactions
ENSG00000264545	chromatin interactions
ENSG00000228115	chromatin interactions

Extended variants
information (count: 5307 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:5307 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182389322	chr9:471887-471888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs544603230	chr9:471911-471912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114192862	chr9:471915-471916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs578082643	chr9:471919-471920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540447665	chr9:471930-471931	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142791137	chr9:471933-471934	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529459595	chr9:471976-471977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs10974667	chr9:471982-471983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs562854382	chr9:471988-471989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs151073505	chr9:472005-472006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373589836	chr9:472024-472025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570432976	chr9:472028-472029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533084264	chr9:472059-472060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142413300	chr9:472061-472062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566644690	chr9:472062-472063	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534898895	chr9:472077-472078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558426788	chr9:472153-472154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs555659419	chr9:472157-472158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569214540	chr9:472162-472163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs116726076	chr9:472188-472189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145258913	chr9:472217-472218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114671226	chr9:472274-472275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371711018	chr9:472281-472282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186703720	chr9:472286-472287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540686767	chr9:472308-472309	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553867880	chr9:472329-472330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576988889	chr9:472409-472410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573846820	chr9:472416-472417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145416036	chr9:472442-472443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs57500851	chr9:472443-472444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147606742	chr9:472474-472475	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566926249	chr9:472480-472481	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562841544	chr9:472506-472507	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs142292822	chr9:472534-472535	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs10974690	chr9:472591-472592	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369092744	chr9:472598-472599	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556157784	chr9:472622-472623	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564075641	chr9:472645-472646	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138384292	chr9:472674-472675	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546628808	chr9:472680-472681	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11788982	chr9:472702-472703	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs112894317	chr9:472748-472749	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549244322	chr9:472749-472750	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs192613512	chr9:472762-472763	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs538172123	chr9:472769-472770	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs112826128	chr9:472775-472776	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs542638410	chr9:472807-472808	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184228270	chr9:472816-472817	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs137955931	chr9:472817-472818	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs80079439	chr9:472834-472835	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:2129 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:470800-472000	Enhancers	Stomach Mucosa	stomach
2	chr9:470800-472600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:470800-477400	Weak transcription	Aorta	Aorta
4	chr9:470800-477800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:471000-472000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:471000-472000	Enhancers	Left Ventricle	heart
7	chr9:471000-472400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:471000-472400	Enhancers	Esophagus	oesophagus
9	chr9:471000-472600	Enhancers	HepG2	liver
10	chr9:471000-472800	Enhancers	Placenta	Placenta
11	chr9:471000-473000	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr9:471000-473200	Enhancers	Fetal Thymus	thymus
13	chr9:471000-477600	Weak transcription	Fetal Stomach	stomach
14	chr9:471200-472600	Enhancers	Spleen	Spleen
15	chr9:471200-474400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:471200-476600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr9:471400-472200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:471400-472400	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr9:471400-472400	Weak transcription	Lung	lung
20	chr9:471400-472600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr9:471400-472600	Enhancers	Duodenum Mucosa	Duodenum
22	chr9:471400-473200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr9:471400-473200	Enhancers	Pancreas	Pancrea
24	chr9:471400-474200	Weak transcription	Primary T cells from cord blood	blood
25	chr9:471400-474400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr9:471400-474800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:471400-475200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr9:471400-475200	Weak transcription	Fetal Muscle Leg	muscle
29	chr9:471400-476200	Weak transcription	Gastric	stomach
30	chr9:471400-476400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr9:471400-476600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:471400-477800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:471400-480000	Weak transcription	Brain Substantia Nigra	brain
34	chr9:471600-472800	Weak transcription	Fetal Kidney	kidney
35	chr9:471600-475000	Weak transcription	Fetal Intestine Large	intestine
36	chr9:471600-475600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:471600-486000	Weak transcription	A549	lung
38	chr9:471800-472400	Weak transcription	Fetal Lung	lung
39	chr9:471800-474600	Weak transcription	Fetal Intestine Small	intestine
40	chr9:471800-475400	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr9:472000-474000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:472000-476600	Weak transcription	Stomach Mucosa	stomach
43	chr9:472200-472800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr9:472400-472600	Enhancers	Fetal Lung	lung
45	chr9:472400-472600	Enhancers	Lung	lung
46	chr9:472400-472800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr9:472400-473000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr9:472400-473200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr9:472400-479800	Weak transcription	Esophagus	oesophagus
50	chr9:472600-477600	Weak transcription	Duodenum Mucosa	Duodenum

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