Variant report

Variant	nsv466337
Chromosome Location	chr9:27250868-27353460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:815)
CpG islands
(count:489)
Chromatin interactive
region (count:18)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:27276480-27276766	K562	blood:	n/a	n/a
2	ARID3A	chr9:27261532-27261892	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:27276433-27276779	HepG2	liver:	n/a	n/a
4	ATF2	chr9:27352454-27352815	GM12878	blood:	n/a	n/a
5	ATF2	chr9:27352330-27352860	GM12878	blood:	n/a	n/a
6	ATF2	chr9:27353339-27353693	GM12878	blood:	n/a	n/a
7	ATF2	chr9:27353230-27353657	GM12878	blood:	n/a	n/a
8	ATF3	chr9:27303237-27303477	K562	blood:	n/a	n/a
9	BACH1	chr9:27308693-27309302	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:27303260-27303653	K562	blood:	n/a	n/a
11	BACH1	chr9:27303314-27303568	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:27352461-27352773	GM12878	blood:	n/a	n/a
13	BATF	chr9:27353336-27353679	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:27353306-27353704	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:27352443-27352727	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
16	BCL11A	chr9:27353335-27353638	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:27352393-27352840	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
18	BCLAF1	chr9:27352397-27352746	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
19	BCLAF1	chr9:27353329-27353747	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:27352426-27352853	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
21	BHLHE40	chr9:27352412-27353761	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:27281155-27281334	K562	blood:	n/a	n/a
23	BHLHE40	chr9:27303181-27303595	K562	blood:	n/a	n/a
24	BHLHE40	chr9:27261364-27261936	HepG2	liver:	n/a	n/a
25	BHLHE40	chr9:27333307-27333503	K562	blood:	n/a	n/a
26	BRCA1	chr9:27333193-27333639	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr9:27261881-27262104	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr9:27303220-27303571	K562	blood:	n/a	n/a
29	CEBPB	chr9:27333228-27333580	H1-hESC	embryonic stem cell:	n/a	chr9:27333339-27333347
30	CEBPB	chr9:27272984-27273198	A549	lung:	n/a	chr9:27273158-27273171
31	CEBPB	chr9:27333147-27333559	A549	lung:	n/a	chr9:27333339-27333347
32	CEBPB	chr9:27341228-27341562	H1-hESC	embryonic stem cell:	n/a	chr9:27341393-27341406
33	CEBPB	chr9:27333282-27333519	K562	blood:	n/a	chr9:27333339-27333347
34	CEBPB	chr9:27333222-27333556	HepG2	liver:	n/a	chr9:27333339-27333347
35	CEBPB	chr9:27261315-27261855	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:27261286-27261670	MCF-7	breast:	n/a	n/a
37	CEBPB	chr9:27258776-27259077	A549	lung:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
38	CEBPB	chr9:27261315-27262115	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr9:27316982-27317252	Hela-S3	cervix:	n/a	chr9:27317119-27317130
40	CEBPB	chr9:27316969-27317234	HepG2	liver:	n/a	chr9:27317119-27317130
41	CEBPB	chr9:27333188-27333603	Hela-S3	cervix:	n/a	chr9:27333339-27333347
42	CEBPB	chr9:27258775-27259094	HepG2	liver:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
43	CEBPB	chr9:27303105-27303500	K562	blood:	n/a	n/a
44	CEBPB	chr9:27258771-27259071	K562	blood:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
45	CHD1	chr9:27333921-27334049	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr9:27351436-27351439	GM12878	blood:	n/a	n/a
47	CTCF	chr9:27260580-27260730	AG04450	lung:	n/a	n/a
48	CTCF	chr9:27333222-27333476	K562	blood:	n/a	chr9:27333328-27333341 chr9:27333325-27333343
49	CTCF	chr9:27292800-27292950	NHLF	lung:	n/a	n/a
50	CTCF	chr9:27276520-27276670	HCT-116	colon:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:27333402-27333452	LNCaP	prostate:	n/a
2	chr9:27333402-27333452	LNCaP	prostate:	n/a
3	chr9:27342183-27342233	IMR90	lung:	fetal
4	chr9:27342183-27342233	ovcar-3	ovarian:	n/a
5	chr9:27342183-27342233	GM12892	blood:	n/a
6	chr9:27342183-27342233	MCF10A-Er-Src	breast:	n/a
7	chr9:27333402-27333452	HRE	kidney:	n/a
8	chr9:27297089-27297139	CMK	blood:	n/a
9	chr9:27292606-27292656	GM06990	blood:	n/a
10	chr9:27297089-27297139	IMR90	lung:	fetal
11	chr9:27292606-27292656	AG10803	skin:	n/a
12	chr9:27282580-27282630	NT2-D1	testis:	n/a
13	chr9:27327953-27328003	AoSMC	blood vessel:	n/a
14	chr9:27297089-27297139	LNCaP	prostate:	n/a
15	chr9:27297335-27297385	AG10803	skin:	n/a
16	chr9:27297335-27297385	Hepatocyte	liver:	n/a
17	chr9:27292606-27292656	NB4	blood:	n/a
18	chr9:27282580-27282630	HCPEpiC	choroid plexus:	n/a
19	chr9:27297335-27297385	AG09309	skin:	n/a
20	chr9:27292606-27292656	AG04449	skin:	fetal
21	chr9:27282580-27282630	A549	lung:	n/a
22	chr9:27297335-27297385	NH-A	brain:	n/a
23	chr9:27342183-27342233	SKMC	muscle:	n/a
24	chr9:27327953-27328003	IMR90	lung:	fetal
25	chr9:27292606-27292656	T-47D	breast:	n/a
26	chr9:27342183-27342233	NHBE	bronchial:	n/a
27	chr9:27333402-27333452	K562	blood:	n/a
28	chr9:27282776-27282826	AG04449	skin:	fetal
29	chr9:27282580-27282630	GM12892	blood:	n/a
30	chr9:27282776-27282826	GM06990	blood:	n/a
31	chr9:27282776-27282826	K562	blood:	n/a
32	chr9:27282580-27282630	MCF-7	breast:	n/a
33	chr9:27342183-27342233	AG09309	skin:	n/a
34	chr9:27333402-27333452	GM06990	blood:	n/a
35	chr9:27297089-27297139	HCPEpiC	choroid plexus:	n/a
36	chr9:27342183-27342233	A549	lung:	n/a
37	chr9:27297089-27297139	GM12878	blood:	n/a
38	chr9:27282776-27282826	HCM	heart:	n/a
39	chr9:27297335-27297385	GM12891	blood:	n/a
40	chr9:27333402-27333452	GM12878	blood:	n/a
41	chr9:27292606-27292656	ProgFib	skin:	n/a
42	chr9:27282580-27282630	AG04450	lung:	fetal
43	chr9:27327953-27328003	GM19239	blood:	n/a
44	chr9:27282776-27282826	SAEC	small airway:	n/a
45	chr9:27297335-27297385	HCPEpiC	choroid plexus:	n/a
46	chr9:27282776-27282826	CMK	blood:	n/a
47	chr9:27292606-27292656	Jurkat	blood:	n/a
48	chr9:27342183-27342233	SK-N-MC	brain:	n/a
49	chr9:27342183-27342233	H1-hESC	embryonic stem cell:	embryo
50	chr9:27342183-27342233	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:27332939..27333807-chr9:27547988..27549046,3	K562	blood:
2	chr9:27300012..27302683-chr9:27305254..27307396,2	K562	blood:
3	chr9:27033503..27034503-chr9:27276144..27277065,4	K562	blood:
4	chr9:27329438..27331174-chr9:27537261..27539824,2	K562	blood:
5	chr9:27247423..27248703-chr9:27275999..27276820,3	MCF-7	breast:
6	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
7	chr9:27300012..27302683-chr9:27305254..27307396,2	K562	blood:
8	chr9:27332980..27333834-chr9:27547941..27548663,3	MCF-7	breast:
9	chr1:146644212..146644715-chr9:27340015..27340515,2	MCF-7	breast:
10	chr9:27332966..27333852-chr9:27535507..27536468,2	K562	blood:
11	chr9:27033540..27034483-chr9:27275947..27276717,3	MCF-7	breast:
12	chr9:27280860..27282970-chr9:27289180..27290823,2	K562	blood:
13	chr9:27328991..27331118-chr9:27335749..27338717,2	K562	blood:
14	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
15	chr9:27333009..27333876-chr9:27535565..27536408,4	MCF-7	breast:
16	chr9:27328991..27331118-chr9:27335749..27338717,2	K562	blood:
17	chr9:27332963..27333812-chr9:27529343..27530314,6	MCF-7	breast:
18	chr9:27328788..27330536-chr9:27524466..27526577,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf11-1	chr9:27270426-27270613	l_3745_NR_026687
2	lnc-C9orf11-1	chr9:27251828-27252034	NONHSAT130610
3	lnc-C9orf11-1	chr9:27268359-27268726	NONHSAT130610
4	lnc-C9orf11-1	chr9:27267549-27267774	l_3745_NR_026687
5	lnc-C9orf11-1	chr9:27251828-27252034	l_3745_NR_026687
6	lnc-C9orf11-1	chr9:27268359-27268726	l_3745_NR_026687
7	lnc-C9orf11-1	chr9:27267549-27267774	NONHSAT130610
8	lnc-C9orf11-1	chr9:27265780-27265948	NONHSAT130610
9	lnc-C9orf11-1	chr9:27252710-27252801	l_3745_NR_026687
10	lnc-C9orf11-1	chr9:27272328-27272791	l_3745_NR_026687
11	lnc-C9orf11-1	chr9:27270766-27270922	NONHSAT130610
12	lnc-C9orf11-1	chr9:27264088-27264284	NONHSAT130610
13	lnc-C9orf11-1	chr9:27253207-27253263	l_3745_NR_026687
14	lnc-C9orf11-1	chr9:27261925-27262086	NONHSAT130610
15	lnc-MOB3B-1	chr9:27296611-27296738	NONHSAT130613
16	lnc-MOB3B-1	chr9:27294314-27294493	NONHSAT130613
17	lnc-C9orf11-1	chr9:27253207-27253263	NONHSAT130610
18	lnc-C9orf11-1	chr9:27265780-27265948	l_3745_NR_026687
19	lnc-C9orf11-1	chr9:27258419-27258515	l_3745_NR_026687
20	lnc-C9orf11-1	chr9:27252710-27252801	NONHSAT130610
21	lnc-C9orf11-1	chr9:27270426-27270613	NONHSAT130610
22	lnc-C9orf11-1	chr9:27272328-27272791	NONHSAT130610
23	lnc-MOB3B-1	chr9:27292411-27292485	NONHSAT130613
24	lnc-C9orf11-1	chr9:27258419-27258515	NONHSAT130610
25	lnc-C9orf11-1	chr9:27264088-27264284	l_3745_NR_026687
26	lnc-C9orf11-1	chr9:27266962-27267108	NONHSAT130610
27	lnc-C9orf11-1	chr9:27266962-27267108	l_3745_NR_026687
28	lnc-C9orf11-1	chr9:27261925-27262086	l_3745_NR_026687
29	lnc-C9orf11-1	chr9:27270766-27270922	l_3745_NR_026687

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MOBKL2B	hsa-miR-98-5p	chr9:27328932-27328925
2	MOBKL2B	hsa-miR-181a-5p	chr9:27329179-27329173

Variant related genes	Relation type
LINC00032	TF binding region
EQTN	TF binding region
LINC00032	CpG island
EQTN	CpG island
ENSG00000231459	chromatin interactions
ENSG00000120162	chromatin interactions
ENSG00000237188	chromatin interactions

Extended variants
information (count: 3526 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:3526 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538803987	chr9:27251858-27251859	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs181108860	chr9:27251859-27251860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs554252129	chr9:27251883-27251884	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs186613596	chr9:27251890-27251891	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs564652491	chr9:27251895-27251896	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs12236801	chr9:27251903-27251904	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549930116	chr9:27251904-27251905	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs568067496	chr9:27251925-27251926	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs373172028	chr9:27251926-27251927	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs535563352	chr9:27251929-27251930	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs143380384	chr9:27251968-27251969	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs34085219	chr9:27251969-27251970	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs397797813	chr9:27251971-27251972	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs11787553	chr9:27252019-27252020	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs111489171	chr9:27252759-27252760	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs187128541	chr9:27252768-27252769	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs548989582	chr9:27252779-27252780	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs568358349	chr9:27252780-27252781	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs10967811	chr9:27252785-27252786	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs191046256	chr9:27252800-27252801	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs535712087	chr9:27253213-27253214	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs10120973	chr9:27253229-27253230	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs115207202	chr9:27258452-27258453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs540039659	chr9:27258462-27258463	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs557902692	chr9:27258472-27258473	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs59374465	chr9:27258478-27258479	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146914930	chr9:27259405-27259406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567968568	chr9:27259416-27259417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534957169	chr9:27259417-27259418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553339404	chr9:27259477-27259478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546948585	chr9:27259494-27259495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139306617	chr9:27259525-27259526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557518108	chr9:27259555-27259556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575793050	chr9:27259556-27259557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190804207	chr9:27259591-27259592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561684677	chr9:27259597-27259598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536125954	chr9:27259600-27259601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567350347	chr9:27260211-27260212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs137909651	chr9:27260230-27260231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547154442	chr9:27260235-27260236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183889294	chr9:27260249-27260250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376470833	chr9:27260276-27260277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187715462	chr9:27260277-27260278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142343816	chr9:27260290-27260291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536648571	chr9:27260292-27260293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554794419	chr9:27260294-27260295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74546483	chr9:27260296-27260297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146030949	chr9:27260314-27260315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534343929	chr9:27260331-27260332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553106530	chr9:27260395-27260396	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Epilepsy	22083797	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27259400-27259600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:27260200-27260600	Enhancers	Lung	lung
3	chr9:27260600-27262200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr9:27260800-27262400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr9:27261000-27262000	Enhancers	HepG2	liver
6	chr9:27261000-27262200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr9:27261000-27262200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr9:27261200-27261400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:27261200-27261400	Enhancers	Placenta	Placenta
10	chr9:27261200-27261800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr9:27261200-27262200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr9:27261200-27262200	Enhancers	Hela-S3	cervix
13	chr9:27261400-27261800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:27261400-27262200	Enhancers	Gastric	stomach
15	chr9:27261600-27261800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:27261600-27261800	Enhancers	Stomach Mucosa	stomach
17	chr9:27261600-27262000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr9:27261600-27262200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr9:27261800-27262200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:27261800-27262200	Enhancers	NHEK	skin
21	chr9:27262000-27262200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:27262000-27262200	Enhancers	Placenta	Placenta
23	chr9:27262200-27262400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr9:27266800-27267000	Enhancers	Pancreas	Pancrea
25	chr9:27269600-27270400	Enhancers	Stomach Mucosa	stomach
26	chr9:27270000-27270400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:27270400-27272800	Weak transcription	Stomach Mucosa	stomach
28	chr9:27272600-27273000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr9:27272600-27273000	Enhancers	Fetal Intestine Large	intestine
30	chr9:27272600-27274600	Enhancers	Fetal Intestine Small	intestine
31	chr9:27272800-27273600	Enhancers	Stomach Mucosa	stomach
32	chr9:27273000-27276000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr9:27273000-27278200	Weak transcription	Fetal Intestine Large	intestine
34	chr9:27273600-27276200	Weak transcription	Stomach Mucosa	stomach
35	chr9:27274600-27276000	Weak transcription	Fetal Intestine Small	intestine
36	chr9:27276000-27276200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:27276000-27276200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr9:27276000-27276200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr9:27276000-27276200	Enhancers	Adipose Nuclei	Adipose
40	chr9:27276000-27276200	Enhancers	Liver	Liver
41	chr9:27276000-27276200	Enhancers	Brain Germinal Matrix	brain
42	chr9:27276000-27276200	Enhancers	Colon Smooth Muscle	Colon
43	chr9:27276000-27276200	Enhancers	Fetal Intestine Small	intestine
44	chr9:27276000-27276400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr9:27276000-27276400	Enhancers	HSMMtube	muscle
46	chr9:27276000-27276600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr9:27276000-27276600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:27276000-27276600	Active TSS	Brain Angular Gyrus	brain
49	chr9:27276000-27276600	Enhancers	Psoas Muscle	Psoas
50	chr9:27276000-27276600	Enhancers	HMEC	breast

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