Variant report

Variant	nsv1026981
Chromosome Location	chr9:21748202-21811697
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1170)
CpG islands
(count:123)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:21803118-21803488	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:21802071-21802841	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:21789478-21789800	HepG2	liver:	n/a	n/a
4	ATF2	chr9:21801686-21802601	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:21801897-21802754	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:21809644-21810268	GM12878	blood:	n/a	n/a
7	ATF2	chr9:21761267-21761735	GM12878	blood:	n/a	n/a
8	ATF2	chr9:21761271-21761724	GM12878	blood:	n/a	n/a
9	ATF2	chr9:21809791-21810234	GM12878	blood:	n/a	n/a
10	ATF2	chr9:21803035-21803552	GM12878	blood:	n/a	n/a
11	ATF2	chr9:21751899-21752360	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr9:21802148-21802961	GM12878	blood:	n/a	n/a
13	BACH1	chr9:21803191-21803447	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:21801873-21802989	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr9:21809783-21810274	GM12878	blood:	n/a	n/a
16	BATF	chr9:21761251-21761742	GM12878	blood:	n/a	n/a
17	BATF	chr9:21809849-21810198	GM12878	blood:	n/a	n/a
18	BATF	chr9:21761304-21761682	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:21761371-21761656	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:21761331-21761649	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:21809820-21810259	GM12878	blood:	n/a	n/a
22	BCL3	chr9:21809834-21810198	GM12878	blood:	n/a	n/a
23	BCL3	chr9:21801929-21802620	A549	lung:	n/a	n/a
24	BCLAF1	chr9:21802276-21803522	GM12878	blood:	n/a	chr9:21803052-21803065
25	BCLAF1	chr9:21761256-21761703	GM12878	blood:	n/a	n/a
26	BCLAF1	chr9:21802237-21803665	GM12878	blood:	n/a	chr9:21803052-21803065
27	BHLHE40	chr9:21802333-21803403	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:21802429-21803636	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:21789495-21789922	GM12878	blood:	n/a	n/a
30	BRCA1	chr9:21802666-21802686	HepG2	liver:	n/a	n/a
31	BRCA1	chr9:21801990-21802795	Hela-S3	cervix:	n/a	chr9:21802251-21802260
32	BRCA1	chr9:21781752-21782557	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr9:21803114-21803364	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr9:21802102-21802325	HepG2	liver:	n/a	chr9:21802251-21802260
35	BRCA1	chr9:21802131-21802402	GM12878	blood:	n/a	chr9:21802251-21802260
36	BRCA1	chr9:21789505-21790056	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr9:21801824-21802695	H1-hESC	embryonic stem cell:	n/a	chr9:21802251-21802260
38	CBX3	chr9:21754761-21755206	HCT-116	colon:	n/a	n/a
39	CBX3	chr9:21754643-21755240	HCT-116	colon:	n/a	n/a
40	CEBPB	chr9:21778205-21778555	HepG2	liver:	n/a	chr9:21778531-21778543 chr9:21778363-21778374
41	CEBPB	chr9:21779968-21780273	HepG2	liver:	n/a	chr9:21780122-21780133
42	CEBPB	chr9:21751940-21752386	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:21801775-21802753	H1-hESC	embryonic stem cell:	n/a	chr9:21801943-21801956 chr9:21801943-21801954 chr9:21801943-21801956
44	CEBPB	chr9:21801903-21802217	HepG2	liver:	n/a	chr9:21801943-21801956 chr9:21801943-21801954 chr9:21801943-21801956
45	CEBPB	chr9:21764205-21764405	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr9:21809891-21810217	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:21777477-21779098	HCT-116	colon:	n/a	chr9:21778531-21778543 chr9:21778363-21778374
48	CEBPB	chr9:21769460-21769564	A549	lung:	n/a	n/a
49	CEBPB	chr9:21782159-21782560	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr9:21758585-21758632	Hela-S3	cervix:	n/a	chr9:21758605-21758616 chr9:21758603-21758616

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21802598-21802648	HEEpiC	esophagus:	n/a
2	chr9:21802598-21802648	HEEpiC	esophagus:	n/a
3	chr9:21802598-21802648	H1-hESC	embryonic stem cell:	embryo
4	chr9:21802598-21802648	HIPEpiC	eye:	n/a
5	chr9:21801897-21801947	HEK293	kidney:	embryo
6	chr9:21802598-21802648	HRPEpiC	eye:	n/a
7	chr9:21801897-21801947	ovcar-3	ovarian:	n/a
8	chr9:21802598-21802648	Hepatocyte	liver:	n/a
9	chr9:21801897-21801947	K562	blood:	n/a
10	chr9:21801897-21801947	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:21802598-21802648	NT2-D1	testis:	n/a
12	chr9:21801897-21801947	AG04449	skin:	fetal
13	chr9:21801897-21801947	NT2-D1	testis:	n/a
14	chr9:21802598-21802648	HEK293	kidney:	embryo
15	chr9:21801897-21801947	MCF-7	breast:	n/a
16	chr9:21801897-21801947	SK-N-SH	brain:	n/a
17	chr9:21802598-21802648	U87	brain:	n/a
18	chr9:21802598-21802648	LNCaP	prostate:	n/a
19	chr9:21801897-21801947	A549	lung:	n/a
20	chr9:21802598-21802648	HUVEC	blood vessel:	n/a
21	chr9:21802598-21802648	A549	lung:	n/a
22	chr9:21801897-21801947	HMEC	breast:	n/a
23	chr9:21801897-21801947	PrEC	prostate:	n/a
24	chr9:21801897-21801947	Hela-S3	cervix:	n/a
25	chr9:21801897-21801947	T-47D	breast:	n/a
26	chr9:21802598-21802648	SK-N-SH	brain:	n/a
27	chr9:21801897-21801947	CMK	blood:	n/a
28	chr9:21802598-21802648	HRE	kidney:	n/a
29	chr9:21802598-21802648	CMK	blood:	n/a
30	chr9:21801897-21801947	GM06990	blood:	n/a
31	chr9:21801897-21801947	HCF	heart:	n/a
32	chr9:21802598-21802648	AG09309	skin:	n/a
33	chr9:21801897-21801947	U87	brain:	n/a
34	chr9:21801897-21801947	HRPEpiC	eye:	n/a
35	chr9:21801897-21801947	HAEpiC	amniotic membrane:	n/a
36	chr9:21801897-21801947	SAEC	small airway:	n/a
37	chr9:21801897-21801947	ProgFib	skin:	n/a
38	chr9:21802598-21802648	GM12891	blood:	n/a
39	chr9:21802598-21802648	AG10803	skin:	n/a
40	chr9:21802598-21802648	PFSK-1	brain:	n/a
41	chr9:21801897-21801947	GM19239	blood:	n/a
42	chr9:21801897-21801947	HL-60	blood:	n/a
43	chr9:21802598-21802648	HNPCEpiC	eye:	n/a
44	chr9:21801897-21801947	ECC-1	luminal epithelium:	n/a
45	chr9:21802598-21802648	Hela-S3	cervix:	n/a
46	chr9:21802598-21802648	AG04449	skin:	fetal
47	chr9:21802598-21802648	Caco-2	colon:	n/a
48	chr9:21801897-21801947	HCM	heart:	n/a
49	chr9:21801897-21801947	MCF10A-Er-Src	breast:	n/a
50	chr9:21801897-21801947	HUVEC	blood vessel:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8215310..8215810-chr9:21789446..21790131,2	MCF-7	breast:
2	chr9:21334810..21337205-chr9:21800546..21802816,2	MCF-7	breast:
3	chr22:44319656..44320398-chr9:21801855..21802795,2	Hela-S3	cervix:
4	chr9:21804218..21806075-chr9:22088261..22090402,2	MCF-7	breast:
5	chr9:21465639..21466595-chr9:21789434..21790168,4	MCF-7	breast:
6	chr9:21747038..21749658-chr9:21801876..21803848,2	MCF-7	breast:
7	chr9:21796497..21798731-chr9:21800652..21802433,2	MCF-7	breast:
8	chr6:74230283..74230812-chr9:21802552..21803080,2	Hela-S3	cervix:
9	chr9:21586208..21586976-chr9:21789155..21790210,3	MCF-7	breast:
10	chr9:21802179..21803949-chr9:21994356..21995893,2	MCF-7	breast:
11	chr9:21318068..21318780-chr9:21789413..21789937,2	MCF-7	breast:
12	chr9:21709315..21710109-chr9:21789136..21789898,2	MCF-7	breast:
13	chr9:21709125..21709738-chr9:21789173..21789997,3	MCF-7	breast:
14	chr9:21805334..21807056-chr9:22107638..22109490,2	MCF-7	breast:
15	chr9:21465480..21466871-chr9:21788898..21790282,6	MCF-7	breast:
16	chr17:47268713..47269635-chr9:21781541..21782153,2	Hela-S3	cervix:
17	chr9:21491433..21492444-chr9:21789127..21790263,7	MCF-7	breast:
18	chr9:21803351..21805632-chr9:22007857..22009751,2	MCF-7	breast:
19	chr10:65280669..65281593-chr9:21802930..21803555,2	HCT-116	colon:
20	chr9:21811237..21820561-chr9:21988636..21997115,18	MCF-7	breast:
21	chr9:21464451..21467378-chr9:21800569..21802345,2	MCF-7	breast:
22	chr6:32939770..32940649-chr9:21802247..21802836,2	HCT-116	colon:
23	chr1:149858070..149858646-chr9:21802522..21803492,2	Hela-S3	cervix:
24	chr9:21796497..21798731-chr9:21800652..21802433,2	MCF-7	breast:
25	chr9:21586444..21586977-chr9:21789496..21790440,2	MCF-7	breast:
26	chr9:21788671..21790825-chr9:21801157..21804087,2	MCF-7	breast:
27	chr9:21492643..21493283-chr9:21789425..21789929,2	MCF-7	breast:
28	chr9:504296..504898-chr9:21802481..21802992,2	HCT-116	colon:
29	chr9:21800247..21802715-chr9:22007122..22010872,3	MCF-7	breast:
30	chr9:21801607..21803714-chr9:21992951..21995865,2	MCF-7	breast:
31	chr9:21811532..21820564-chr9:21988281..21997291,17	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000264545	TF binding region
ENSG00000266732	TF binding region
MTAP	TF binding region
ENSG00000264545	CpG island
ENSG00000266732	CpG island
MTAP	CpG island
ENSG00000266446	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000264545	chromatin interactions
ENSG00000147889	chromatin interactions
ENSG00000099810	chromatin interactions
ENSG00000107104	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000147883	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000263756	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000100344	chromatin interactions
ENSG00000240498	chromatin interactions
ENSG00000165476	chromatin interactions
ENSG00000198642	chromatin interactions

Extended variants
information (count: 3058 )
Associated
traits (count: 167 )

Variant overlapped rSNPs/rCNVs (count:3058 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1414242	chr9:21748239-21748240	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143748900	chr9:21748246-21748247	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371942755	chr9:21748289-21748290	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571808281	chr9:21748296-21748297	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs17833407	chr9:21748320-21748321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs73649976	chr9:21748323-21748324	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs4375086	chr9:21748332-21748333	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs370552148	chr9:21748397-21748398	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs60456483	chr9:21748398-21748399	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs187924815	chr9:21748418-21748419	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs1414243	chr9:21748433-21748434	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs537495039	chr9:21748466-21748467	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs1335505	chr9:21748484-21748485	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577702309	chr9:21748489-21748490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557889292	chr9:21748491-21748492	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539932772	chr9:21748521-21748522	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs1414244	chr9:21748532-21748533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4543632	chr9:21748618-21748619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs566969871	chr9:21748782-21748783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs563221357	chr9:21748797-21748798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576798187	chr9:21748819-21748820	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545450129	chr9:21748850-21748851	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374160504	chr9:21748915-21748916	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565108900	chr9:21748959-21748960	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs114459709	chr9:21748960-21748961	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs2165409	chr9:21748962-21748963	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs543906090	chr9:21749099-21749100	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs560304146	chr9:21749132-21749133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146841102	chr9:21749134-21749135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs548765006	chr9:21749161-21749162	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs568854240	chr9:21749199-21749200	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs191555390	chr9:21749200-21749201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377296731	chr9:21749214-21749215	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs184832751	chr9:21749217-21749218	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189640544	chr9:21749284-21749285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs553549256	chr9:21749318-21749319	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574182079	chr9:21749340-21749341	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs536886176	chr9:21749362-21749363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs192122813	chr9:21749375-21749376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111397104	chr9:21749438-21749439	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs72689398	chr9:21749459-21749460	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs544810157	chr9:21749483-21749484	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144418378	chr9:21749490-21749491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs151109103	chr9:21749493-21749494	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs375479433	chr9:21749511-21749512	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561273536	chr9:21749515-21749516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530125299	chr9:21749526-21749527	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372784181	chr9:21749549-21749550	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185322508	chr9:21749578-21749579	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189396174	chr9:21749588-21749589	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:167)

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
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Oral cancer	22144094	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Barrett''s syndrome	19417022	CNVD
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Chordoma	21215367	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung adenocarcinoma	17982442	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21743200-21750000	Weak transcription	NH-A	brain
2	chr9:21743400-21750000	Weak transcription	Osteobl	bone
3	chr9:21744200-21752200	Enhancers	HMEC	breast
4	chr9:21745000-21748800	Enhancers	NHEK	skin
5	chr9:21746600-21748600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:21746600-21748800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:21746600-21751200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:21746800-21748400	Enhancers	Hela-S3	cervix
9	chr9:21747000-21750000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:21747200-21752000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr9:21747600-21750000	Weak transcription	NHDF-Ad	bronchial
12	chr9:21747800-21749800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:21747800-21751800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:21748400-21754400	Weak transcription	Hela-S3	cervix
15	chr9:21748600-21754400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:21748800-21750000	Weak transcription	NHEK	skin
17	chr9:21748800-21754400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:21749600-21751400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr9:21749800-21750400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:21749800-21750600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:21750000-21750400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr9:21750000-21750400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:21750000-21750400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr9:21750000-21750400	Enhancers	Osteobl	bone
25	chr9:21750000-21751200	Enhancers	NHEK	skin
26	chr9:21750200-21750400	Enhancers	NHDF-Ad	bronchial
27	chr9:21750400-21752000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr9:21751000-21754000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:21751200-21753600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:21751200-21753600	Weak transcription	NHEK	skin
31	chr9:21751200-21754000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:21751800-21752200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:21751800-21752600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
34	chr9:21751800-21752600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
35	chr9:21751800-21752800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
36	chr9:21751800-21752800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
37	chr9:21751800-21752800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
38	chr9:21752000-21752200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
39	chr9:21752000-21752200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:21752000-21752200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:21752000-21752400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:21752000-21752400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr9:21752000-21752400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:21752200-21753600	Weak transcription	HMEC	breast
45	chr9:21752400-21752600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr9:21752800-21753000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
47	chr9:21753600-21753800	Enhancers	NHEK	skin
48	chr9:21753600-21754800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:21753600-21755400	Enhancers	HMEC	breast
50	chr9:21753800-21754200	Weak transcription	NHEK	skin

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