Variant report

Variant	nsv892736
Chromosome Location	chr9:21327141-21391698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:683 , 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	ARID3A	chr9:21335140-21335629	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:21382111-21382396	HepG2	liver:	n/a	n/a
3	ATF2	chr9:21381554-21382273	GM12878	blood:	n/a	n/a
4	ATF2	chr9:21357382-21358261	GM12878	blood:	n/a	n/a
5	ATF2	chr9:21357496-21358239	GM12878	blood:	n/a	n/a
6	ATF2	chr9:21381480-21382315	GM12878	blood:	n/a	n/a
7	BATF	chr9:21357454-21358119	GM12878	blood:	n/a	chr9:21357570-21357578
8	BATF	chr9:21367253-21367565	GM12878	blood:	n/a	chr9:21367396-21367407
9	BATF	chr9:21381702-21382092	GM12878	blood:	n/a	n/a
10	BATF	chr9:21357677-21358125	GM12878	blood:	n/a	n/a
11	BATF	chr9:21367292-21367542	GM12878	blood:	n/a	chr9:21367396-21367407
12	BATF	chr9:21381625-21382187	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:21381619-21382272	GM12878	blood:	n/a	chr9:21381986-21381995
14	BCL11A	chr9:21367236-21367595	GM12878	blood:	n/a	chr9:21367349-21367358
15	BCL11A	chr9:21357729-21358161	GM12878	blood:	n/a	chr9:21357946-21357955
16	BCL11A	chr9:21381656-21382167	GM12878	blood:	n/a	chr9:21381986-21381995
17	BCL3	chr9:21381640-21382241	GM12878	blood:	n/a	chr9:21381986-21381995
18	BCLAF1	chr9:21357669-21358158	GM12878	blood:	n/a	chr9:21357946-21357955
19	BCLAF1	chr9:21357598-21358237	GM12878	blood:	n/a	chr9:21357946-21357955
20	BCLAF1	chr9:21334546-21335763	GM12878	blood:	n/a	chr9:21335213-21335226
21	BCLAF1	chr9:21381612-21382254	GM12878	blood:	n/a	chr9:21381986-21381995
22	BCLAF1	chr9:21381621-21382291	GM12878	blood:	n/a	chr9:21381986-21381995
23	BCLAF1	chr9:21334845-21335704	GM12878	blood:	n/a	chr9:21335213-21335226
24	BCLAF1	chr9:21332001-21332441	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:21357676-21358145	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:21381496-21382354	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:21382053-21382377	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:21372342-21372396	A549	lung:	n/a	n/a
29	CEBPB	chr9:21333555-21333914	HepG2	liver:	n/a	chr9:21333705-21333716
30	CEBPB	chr9:21338859-21339115	HepG2	liver:	n/a	chr9:21338965-21338976
31	CEBPB	chr9:21338931-21339096	A549	lung:	n/a	chr9:21338965-21338976
32	CEBPB	chr9:21335042-21335396	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr9:21335201-21335584	HepG2	liver:	n/a	n/a
34	CHD1	chr9:21334968-21334969	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr9:21334246-21335759	GM12878	blood:	n/a	n/a
36	CHD2	chr9:21334958-21335658	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr9:21335126-21335643	HepG2	liver:	n/a	n/a
38	CHD2	chr9:21381529-21382364	GM12878	blood:	n/a	n/a
39	CHD2	chr9:21334869-21335741	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr9:21357523-21358277	GM12878	blood:	n/a	n/a
41	CHD2	chr9:21334619-21335711	GM12878	blood:	n/a	n/a
42	CREB1	chr9:21381528-21382321	GM12878	blood:	n/a	n/a
43	CREB1	chr9:21357597-21358171	GM12878	blood:	n/a	n/a
44	CREB1	chr9:21381605-21382275	GM12878	blood:	n/a	n/a
45	CREB1	chr9:21335023-21335646	A549	lung:	n/a	n/a
46	CTCF	chr9:21335100-21335250	GM12867	blood:	n/a	n/a
47	CTCF	chr9:21335227-21335351	Lung_OC	lung:	n/a	n/a
48	CTCF	chr9:21350760-21350910	HEK293	kidney:	n/a	n/a
49	CTCF	chr9:21336560-21336710	HepG2	liver:	n/a	n/a
50	CTCF	chr9:21363650-21363739	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21368292-21368342	GM12878	blood:	n/a
2	chr9:21335551-21335601	SK-N-SH	brain:	n/a
3	chr9:21335126-21335176	BJ	skin:	n/a
4	chr9:21335126-21335176	CMK	blood:	n/a
5	chr9:21335551-21335601	NT2-D1	testis:	n/a
6	chr9:21335551-21335601	GM06990	blood:	n/a
7	chr9:21335126-21335176	RPTEC	kidney:	n/a
8	chr9:21335126-21335176	NH-A	brain:	n/a
9	chr9:21335126-21335176	NT2-D1	testis:	n/a
10	chr9:21335551-21335601	GM12878	blood:	n/a
11	chr9:21335551-21335601	PANC-1	pancreas:	n/a
12	chr9:21368292-21368342	U87	brain:	n/a
13	chr9:21335126-21335176	AG10803	skin:	n/a
14	chr9:21335126-21335176	Hela-S3	cervix:	n/a
15	chr9:21335551-21335601	HL-60	blood:	n/a
16	chr9:21335551-21335601	GM12891	blood:	n/a
17	chr9:21368292-21368342	AG10803	skin:	n/a
18	chr9:21335551-21335601	AG04449	skin:	fetal
19	chr9:21335551-21335601	PrEC	prostate:	n/a
20	chr9:21335126-21335176	AG09309	skin:	n/a
21	chr9:21368292-21368342	GM12891	blood:	n/a
22	chr9:21335126-21335176	HEEpiC	esophagus:	n/a
23	chr9:21335126-21335176	MCF10A-Er-Src	breast:	n/a
24	chr9:21368292-21368342	SAEC	small airway:	n/a
25	chr9:21335551-21335601	Caco-2	colon:	n/a
26	chr9:21335126-21335176	SAEC	small airway:	n/a
27	chr9:21335551-21335601	HMEC	breast:	n/a
28	chr9:21335126-21335176	HRE	kidney:	n/a
29	chr9:21335551-21335601	U87	brain:	n/a
30	chr9:21335551-21335601	HRCEpiC	kidney:	n/a
31	chr9:21368292-21368342	HEEpiC	esophagus:	n/a
32	chr9:21368292-21368342	H1-hESC	embryonic stem cell:	embryo
33	chr9:21368292-21368342	HAEpiC	amniotic membrane:	n/a
34	chr9:21368292-21368342	HRCEpiC	kidney:	n/a
35	chr9:21368292-21368342	CMK	blood:	n/a
36	chr9:21368292-21368342	SKMC	muscle:	n/a
37	chr9:21368292-21368342	HUVEC	blood vessel:	n/a
38	chr9:21335126-21335176	ProgFib	skin:	n/a
39	chr9:21335551-21335601	BE2_C	brain:	n/a
40	chr9:21335126-21335176	HCT-116	colon:	n/a
41	chr9:21335551-21335601	IMR90	lung:	fetal
42	chr9:21335551-21335601	NHBE	bronchial:	n/a
43	chr9:21335551-21335601	H1-hESC	embryonic stem cell:	embryo
44	chr9:21335551-21335601	AG10803	skin:	n/a
45	chr9:21368292-21368342	AG04449	skin:	fetal
46	chr9:21368292-21368342	SK-N-SH_RA	brain:	n/a
47	chr9:21368292-21368342	GM12892	blood:	n/a
48	chr9:21335126-21335176	NB4	blood:	n/a
49	chr9:21335126-21335176	K562	blood:	n/a
50	chr9:21335126-21335176	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:21326292..21327207-chr9:21395450..21396631,5	MCF-7	breast:
2	chr9:21334810..21337205-chr9:21800546..21802816,2	MCF-7	breast:
3	chr9:21326879..21332228-chr9:21332519..21336640,9	MCF-7	breast:
4	chr9:21336962..21338707-chr9:21339878..21341386,2	MCF-7	breast:
5	chr9:21336544..21337265-chr9:21395858..21396561,2	MCF-7	breast:
6	chr9:21325580..21327702-chr9:21329735..21331651,2	MCF-7	breast:
7	chr1:174969137..174969741-chr9:21335404..21336059,2	NB4	blood:
8	chr5:138629198..138630197-chr9:21335314..21335966,2	NB4	blood:
9	chr9:21336962..21338707-chr9:21339878..21341386,2	MCF-7	breast:
10	chr9:21333378..21336066-chr9:21351386..21353061,2	MCF-7	breast:
11	chr9:21328009..21333190-chr9:21333474..21336678,6	MCF-7	breast:
12	chr12:10875091..10875955-chr9:21334907..21335831,2	NB4	blood:
13	chr9:21334599..21336705-chr9:21337057..21341673,5	MCF-7	breast:
14	chr9:21334662..21337253-chr9:21343810..21346609,2	MCF-7	breast:
15	chr9:21348973..21351463-chr9:21362839..21365132,2	MCF-7	breast:
16	chr9:21325580..21327702-chr9:21329735..21331651,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL9-1	chr9:21335096-21335352	NONHSAT130380
2	lnc-KLHL9-1	chr9:21329330-21329418	NONHSAT130380
3	lnc-KLHL9-1	chr9:21330797-21330912	NONHSAT130380

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLHL9	hsa-miR-330-5p	chr9:21332257-21332278

Variant related genes	Relation type
IFNA13	TF binding region
IFNA6	TF binding region
KLHL9	TF binding region
IFNA2	TF binding region
IFNA13	CpG island
IFNA6	CpG island
KLHL9	CpG island
IFNA2	CpG island
ENSG00000261696	chromatin interactions
ENSG00000060138	chromatin interactions
ENSG00000264545	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000099810	chromatin interactions
ENSG00000120725	chromatin interactions
ENSG00000015479	chromatin interactions
ENSG00000198642	chromatin interactions
ENSG00000120235	chromatin interactions

Extended variants
information (count: 2092 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:2092 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs913931	chr9:21327141-21327142	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570231780	chr9:21327167-21327168	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs190585518	chr9:21327186-21327187	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs149610173	chr9:21327230-21327231	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs73649580	chr9:21327245-21327246	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs59069805	chr9:21327264-21327265	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375546913	chr9:21327337-21327338	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533792784	chr9:21327338-21327339	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553782700	chr9:21327348-21327349	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527817577	chr9:21327363-21327364	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369873666	chr9:21327466-21327467	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185608674	chr9:21327512-21327513	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147309162	chr9:21327537-21327538	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs62559019	chr9:21327553-21327554	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375748074	chr9:21327606-21327607	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs576188280	chr9:21327669-21327670	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544834830	chr9:21327704-21327705	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565393320	chr9:21327706-21327707	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372086560	chr9:21327710-21327711	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7852588	chr9:21327723-21327724	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564052853	chr9:21327738-21327739	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191256009	chr9:21327742-21327743	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182711127	chr9:21327783-21327784	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531110392	chr9:21327805-21327806	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs72697305	chr9:21327811-21327812	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374425824	chr9:21327812-21327813	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11285347	chr9:21327817-21327818	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550455673	chr9:21327829-21327830	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs75455814	chr9:21327878-21327879	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539238438	chr9:21327901-21327902	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs192133509	chr9:21327924-21327925	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571394663	chr9:21327933-21327934	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533858299	chr9:21327971-21327972	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs368919566	chr9:21327984-21327985	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs570919289	chr9:21327998-21327999	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553844343	chr9:21328010-21328011	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371679078	chr9:21328046-21328047	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs58264638	chr9:21328050-21328051	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573676474	chr9:21328096-21328097	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147812102	chr9:21328118-21328119	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368414602	chr9:21328121-21328122	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183207214	chr9:21328137-21328138	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs57371737	chr9:21328138-21328139	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76455110	chr9:21328146-21328147	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs566917369	chr9:21328147-21328148	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs576222476	chr9:21328158-21328159	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545207552	chr9:21328168-21328169	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187942441	chr9:21328170-21328171	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141016120	chr9:21328183-21328184	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565413656	chr9:21328186-21328187	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
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
Oral cancer	21386901	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
Breast cancer	21858162	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
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	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
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:1067 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21316600-21330600	Weak transcription	Small Intestine	intestine
2	chr9:21317200-21331600	Weak transcription	Esophagus	oesophagus
3	chr9:21317200-21331600	Weak transcription	Gastric	stomach
4	chr9:21318200-21330000	Weak transcription	Brain Anterior Caudate	brain
5	chr9:21318200-21330400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:21318800-21330600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr9:21318800-21331000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:21318800-21331200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:21318800-21331800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr9:21318800-21332600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr9:21318800-21332800	Weak transcription	Fetal Kidney	kidney
12	chr9:21319000-21332200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr9:21319000-21333200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:21319400-21329400	Weak transcription	Fetal Heart	heart
15	chr9:21319600-21333200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:21320600-21331600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:21321400-21331600	Weak transcription	Spleen	Spleen
18	chr9:21321600-21333400	Weak transcription	Colonic Mucosa	Colon
19	chr9:21322000-21331600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr9:21322000-21331600	Weak transcription	HepG2	liver
21	chr9:21322200-21333600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr9:21322400-21330400	Weak transcription	Psoas Muscle	Psoas
23	chr9:21322800-21330000	Weak transcription	Stomach Mucosa	stomach
24	chr9:21323400-21331800	Weak transcription	Aorta	Aorta
25	chr9:21323400-21333800	Weak transcription	Lung	lung
26	chr9:21323600-21330800	Weak transcription	Pancreas	Pancrea
27	chr9:21323600-21331600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr9:21323800-21331800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr9:21324000-21331400	Weak transcription	Right Ventricle	heart
30	chr9:21324000-21333000	Weak transcription	Placenta	Placenta
31	chr9:21324200-21330400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr9:21324200-21331600	Weak transcription	Fetal Thymus	thymus
33	chr9:21324200-21331600	Weak transcription	A549	lung
34	chr9:21324400-21329200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr9:21324400-21330000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:21324400-21330000	Weak transcription	Liver	Liver
37	chr9:21324400-21330200	Weak transcription	Brain Hippocampus Middle	brain
38	chr9:21324400-21330200	Weak transcription	Left Ventricle	heart
39	chr9:21324400-21330200	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr9:21324400-21330400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr9:21324400-21330800	Weak transcription	Ovary	ovary
42	chr9:21324400-21331600	Weak transcription	Thymus	Thymus
43	chr9:21324400-21333200	Weak transcription	Primary B cells from cord blood	blood
44	chr9:21324400-21333200	Weak transcription	Fetal Stomach	stomach
45	chr9:21324400-21333400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:21324600-21328400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:21324600-21330400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:21324800-21328200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr9:21324800-21328200	Weak transcription	Brain Germinal Matrix	brain
50	chr9:21324800-21328400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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