Variant report

Variant	nsv892866
Chromosome Location	chr9:27274370-27332818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:27276433-27276779	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:27276480-27276766	K562	blood:	n/a	n/a
3	ATF3	chr9:27303237-27303477	K562	blood:	n/a	n/a
4	BACH1	chr9:27303314-27303568	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:27303260-27303653	K562	blood:	n/a	n/a
6	BACH1	chr9:27308693-27309302	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr9:27303181-27303595	K562	blood:	n/a	n/a
8	BHLHE40	chr9:27281155-27281334	K562	blood:	n/a	n/a
9	CBX3	chr9:27303220-27303571	K562	blood:	n/a	n/a
10	CEBPB	chr9:27316982-27317252	Hela-S3	cervix:	n/a	chr9:27317119-27317130
11	CEBPB	chr9:27303105-27303500	K562	blood:	n/a	n/a
12	CEBPB	chr9:27316969-27317234	HepG2	liver:	n/a	chr9:27317119-27317130
13	CTCF	chr9:27276560-27276710	HCM	heart:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
14	CTCF	chr9:27276520-27276670	GM12872	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
15	CTCF	chr9:27276580-27276730	SAEC	small airway:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
16	CTCF	chr9:27277193-27277248	GM20000	blood:	n/a	n/a
17	CTCF	chr9:27276520-27276670	AG04449	skin:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
18	CTCF	chr9:27276540-27276690	HPAF	blood vessel:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
19	CTCF	chr9:27324812-27324959	Fibrobl	skin:	n/a	n/a
20	CTCF	chr9:27276480-27276753	GM12878	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
21	CTCF	chr9:27321621-27321700	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr9:27276540-27276690	HepG2	liver:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
23	CTCF	chr9:27276540-27276690	HCPEpiC	choroid plexus:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
24	CTCF	chr9:27276523-27276721	GM20000	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
25	CTCF	chr9:27276560-27276710	HRE	kidney:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
26	CTCF	chr9:27276540-27276690	GM12868	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
27	CTCF	chr9:27276492-27276767	HUVEC	blood vessel:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
28	CTCF	chr9:27276501-27276757	Pancreas_OC	pancreas:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
29	CTCF	chr9:27276940-27277090	AG04449	skin:	n/a	n/a
30	CTCF	chr9:27276523-27276725	GM13976	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
31	CTCF	chr9:27276520-27276670	GM12873	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
32	CTCF	chr9:27276520-27276670	AG09309	skin:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
33	CTCF	chr9:27276500-27276650	MCF-7	breast:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
34	CTCF	chr9:27276509-27276683	GM19238	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
35	CTCF	chr9:27328580-27328730	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr9:27276414-27276800	K562	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
37	CTCF	chr9:27276540-27276690	K562	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
38	CTCF	chr9:27276560-27276710	A549	lung:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
39	CTCF	chr9:27276514-27276680	GM19240	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
40	CTCF	chr9:27276280-27276430	GM12873	blood:	n/a	n/a
41	CTCF	chr9:27276540-27276690	GM06990	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
42	CTCF	chr9:27320407-27320459	GM13976	blood:	n/a	n/a
43	CTCF	chr9:27276340-27276490	GM12878	blood:	n/a	n/a
44	CTCF	chr9:27276494-27276673	SK-N-SH_RA	brain:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
45	CTCF	chr9:27276300-27276450	A549	lung:	n/a	n/a
46	CTCF	chr9:27276550-27276626	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:27276540-27276690	Hela-S3	cervix:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
48	CTCF	chr9:27276560-27276710	NHDF-neo	bronchial:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
49	CTCF	chr9:27276240-27276390	GM12874	blood:	n/a	n/a
50	CTCF	chr9:27276524-27276705	A549	lung:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:27327953-27328003	PFSK-1	brain:	n/a
2	chr9:27327953-27328003	PFSK-1	brain:	n/a
3	chr9:27282580-27282630	PANC-1	pancreas:	n/a
4	chr9:27282580-27282630	HEEpiC	esophagus:	n/a
5	chr9:27292606-27292656	BE2_C	brain:	n/a
6	chr9:27282580-27282630	NH-A	brain:	n/a
7	chr9:27297089-27297139	CMK	blood:	n/a
8	chr9:27282580-27282630	CMK	blood:	n/a
9	chr9:27297335-27297385	GM12878	blood:	n/a
10	chr9:27282776-27282826	HRCEpiC	kidney:	n/a
11	chr9:27297335-27297385	Hepatocyte	liver:	n/a
12	chr9:27282776-27282826	H1-hESC	embryonic stem cell:	embryo
13	chr9:27282580-27282630	SK-N-SH	brain:	n/a
14	chr9:27292606-27292656	SAEC	small airway:	n/a
15	chr9:27297335-27297385	K562	blood:	n/a
16	chr9:27327953-27328003	Jurkat	blood:	n/a
17	chr9:27292606-27292656	GM19239	blood:	n/a
18	chr9:27292606-27292656	LNCaP	prostate:	n/a
19	chr9:27297089-27297139	AG10803	skin:	n/a
20	chr9:27282580-27282630	NHBE	bronchial:	n/a
21	chr9:27297335-27297385	IMR90	lung:	fetal
22	chr9:27292606-27292656	ECC-1	luminal epithelium:	n/a
23	chr9:27327953-27328003	Hela-S3	cervix:	n/a
24	chr9:27292606-27292656	HAEpiC	amniotic membrane:	n/a
25	chr9:27327953-27328003	SK-N-MC	brain:	n/a
26	chr9:27282776-27282826	SK-N-MC	brain:	n/a
27	chr9:27297335-27297385	HCF	heart:	n/a
28	chr9:27297089-27297139	HL-60	blood:	n/a
29	chr9:27297089-27297139	HIPEpiC	eye:	n/a
30	chr9:27292606-27292656	H1-hESC	embryonic stem cell:	embryo
31	chr9:27282580-27282630	AG10803	skin:	n/a
32	chr9:27282776-27282826	AG09319	gingival:	n/a
33	chr9:27282776-27282826	HCM	heart:	n/a
34	chr9:27297335-27297385	GM12892	blood:	n/a
35	chr9:27292606-27292656	A549	lung:	n/a
36	chr9:27292606-27292656	PrEC	prostate:	n/a
37	chr9:27282580-27282630	NHDF-neo	bronchial:	n/a
38	chr9:27282580-27282630	PrEC	prostate:	n/a
39	chr9:27297335-27297385	RPTEC	kidney:	n/a
40	chr9:27282776-27282826	PrEC	prostate:	n/a
41	chr9:27282776-27282826	HepG2	liver:	n/a
42	chr9:27297089-27297139	HRPEpiC	eye:	n/a
43	chr9:27282776-27282826	HUVEC	blood vessel:	n/a
44	chr9:27282776-27282826	Hepatocyte	liver:	n/a
45	chr9:27282580-27282630	SAEC	small airway:	n/a
46	chr9:27327953-27328003	HL-60	blood:	n/a
47	chr9:27282776-27282826	Jurkat	blood:	n/a
48	chr9:27282776-27282826	HIPEpiC	eye:	n/a
49	chr9:27292606-27292656	AG10803	skin:	n/a
50	chr9:27327953-27328003	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:27328991..27331118-chr9:27335749..27338717,2	K562	blood:
2	chr9:27300012..27302683-chr9:27305254..27307396,2	K562	blood:
3	chr9:27280860..27282970-chr9:27289180..27290823,2	K562	blood:
4	chr9:27033540..27034483-chr9:27275947..27276717,3	MCF-7	breast:
5	chr9:27247423..27248703-chr9:27275999..27276820,3	MCF-7	breast:
6	chr9:27033503..27034503-chr9:27276144..27277065,4	K562	blood:
7	chr9:27300012..27302683-chr9:27305254..27307396,2	K562	blood:
8	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
9	chr9:27328788..27330536-chr9:27524466..27526577,2	K562	blood:
10	chr9:27329438..27331174-chr9:27537261..27539824,2	K562	blood:
11	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOB3B-1	chr9:27292411-27292485	NONHSAT130613
2	lnc-MOB3B-1	chr9:27294314-27294493	NONHSAT130613
3	lnc-MOB3B-1	chr9:27296611-27296738	NONHSAT130613

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

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

Extended variants
information (count: 2106 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:2106 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10967844	chr9:27274370-27274371	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185762782	chr9:27274373-27274374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568024290	chr9:27274386-27274387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138758382	chr9:27274418-27274419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs386733905	chr9:27274423-27274424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10967846	chr9:27274424-27274425	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs13288748	chr9:27274428-27274429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs141977081	chr9:27274436-27274437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567561018	chr9:27274439-27274440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146291998	chr9:27274488-27274489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369172487	chr9:27274493-27274494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186269999	chr9:27274524-27274525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10967847	chr9:27274602-27274603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556041364	chr9:27274637-27274638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373833923	chr9:27274649-27274650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557108215	chr9:27274660-27274661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191795397	chr9:27274661-27274662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184033100	chr9:27274678-27274679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111684888	chr9:27274705-27274706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536844257	chr9:27274714-27274715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559253242	chr9:27274724-27274725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554826656	chr9:27274741-27274742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143092677	chr9:27274773-27274774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112469210	chr9:27274796-27274797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144388558	chr9:27274821-27274822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576839286	chr9:27274835-27274836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187273085	chr9:27274836-27274837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544170300	chr9:27274846-27274847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201553802	chr9:27274864-27274865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114461379	chr9:27274866-27274867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541910560	chr9:27274889-27274890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190856414	chr9:27274943-27274944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148781565	chr9:27274945-27274946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182081537	chr9:27274967-27274968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187033397	chr9:27275036-27275037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370268316	chr9:27275042-27275043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76587836	chr9:27275089-27275090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142383379	chr9:27275093-27275094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561387381	chr9:27275103-27275104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386414730	chr9:27275104-27275105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs58215573	chr9:27275121-27275122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568985490	chr9:27275131-27275132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569828613	chr9:27275178-27275179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150537792	chr9:27275306-27275307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140372971	chr9:27275325-27275326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566985492	chr9:27275337-27275338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534365879	chr9:27275360-27275361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530571673	chr9:27275391-27275392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13295463	chr9:27275421-27275422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76832908	chr9:27275453-27275454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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

Chromatin state (count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27272600-27274600	Enhancers	Fetal Intestine Small	intestine
2	chr9:27273000-27276000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:27273000-27278200	Weak transcription	Fetal Intestine Large	intestine
4	chr9:27273600-27276200	Weak transcription	Stomach Mucosa	stomach
5	chr9:27274600-27276000	Weak transcription	Fetal Intestine Small	intestine
6	chr9:27276000-27276200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:27276000-27276200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr9:27276000-27276200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr9:27276000-27276200	Enhancers	Adipose Nuclei	Adipose
10	chr9:27276000-27276200	Enhancers	Liver	Liver
11	chr9:27276000-27276200	Enhancers	Brain Germinal Matrix	brain
12	chr9:27276000-27276200	Enhancers	Colon Smooth Muscle	Colon
13	chr9:27276000-27276200	Enhancers	Fetal Intestine Small	intestine
14	chr9:27276000-27276400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:27276000-27276400	Enhancers	HSMMtube	muscle
16	chr9:27276000-27276600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr9:27276000-27276600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:27276000-27276600	Active TSS	Brain Angular Gyrus	brain
19	chr9:27276000-27276600	Enhancers	Psoas Muscle	Psoas
20	chr9:27276000-27276600	Enhancers	HMEC	breast
21	chr9:27276000-27276600	Enhancers	HUVEC	blood vessel
22	chr9:27276000-27276600	Enhancers	NHLF	lung
23	chr9:27276200-27276400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:27276200-27276400	Active TSS	Brain Hippocampus Middle	brain
25	chr9:27276200-27276400	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr9:27276200-27276400	Active TSS	Fetal Brain Male	brain
27	chr9:27276200-27276400	Enhancers	Gastric	stomach
28	chr9:27276200-27276600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr9:27276200-27276600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:27276200-27276600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr9:27276200-27276600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr9:27276200-27276600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:27276200-27276600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:27276200-27276600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:27276200-27276600	Active TSS	Primary hematopoietic stem cells	blood
36	chr9:27276200-27276600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr9:27276200-27276600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:27276200-27276600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr9:27276200-27276600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr9:27276200-27276600	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr9:27276200-27276600	Active TSS	Aorta	Aorta
42	chr9:27276200-27276600	Flanking Active TSS	Liver	Liver
43	chr9:27276200-27276600	Active TSS	Brain Anterior Caudate	brain
44	chr9:27276200-27276600	Active TSS	Brain Cingulate Gyrus	brain
45	chr9:27276200-27276600	Active TSS	Brain Germinal Matrix	brain
46	chr9:27276200-27276600	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr9:27276200-27276600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr9:27276200-27276600	Enhancers	Brain Substantia Nigra	brain
49	chr9:27276200-27276600	Flanking Active TSS	Colon Smooth Muscle	Colon
50	chr9:27276200-27276600	Enhancers	Duodenum Mucosa	Duodenum

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