Variant report

Variant	nsv6751
Chromosome Location	chr9:136967475-137007131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1000)
CpG islands
(count:550)
Chromatin interactive
region (count:39)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136988069-136988422	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:137001002-137001099	HepG2	liver:	n/a	n/a
3	ATF2	chr9:137000767-137001228	GM12878	blood:	n/a	n/a
4	ATF3	chr9:137000849-137001268	A549	lung:	n/a	chr9:137001158-137001167 chr9:137001053-137001062
5	BACH1	chr9:136996201-136996542	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr9:137000637-137001219	A549	lung:	n/a	chr9:137001205-137001214 chr9:137001206-137001219
7	BCL3	chr9:137000784-137001184	A549	lung:	n/a	n/a
8	BCL3	chr9:137001731-137002217	A549	lung:	n/a	n/a
9	BCLAF1	chr9:137000608-137001165	GM12878	blood:	n/a	chr9:137000613-137000626 chr9:137000612-137000625 chr9:137000616-137000629
10	BHLHE40	chr9:137000783-137001048	A549	lung:	n/a	n/a
11	BHLHE40	chr9:136988286-136988453	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:136979658-136979900	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:136999827-137000401	K562	blood:	n/a	n/a
14	BHLHE40	chr9:137006427-137006641	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:136988178-136988556	HepG2	liver:	n/a	n/a
16	BHLHE40	chr9:137000753-137001250	HepG2	liver:	n/a	chr9:137001217-137001233
17	BHLHE40	chr9:137001918-137002200	K562	blood:	n/a	n/a
18	BHLHE40	chr9:137000268-137001565	GM12878	blood:	n/a	chr9:137001217-137001233 chr9:137001329-137001345 chr9:137000615-137000631
19	BHLHE40	chr9:137000742-137001481	K562	blood:	n/a	chr9:137001217-137001233 chr9:137001329-137001345
20	BRCA1	chr9:137000807-137001129	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr9:136998075-136998140	GM12878	blood:	n/a	n/a
22	BRCA1	chr9:136996294-136996598	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr9:137000810-137001091	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr9:136996163-136996551	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr9:137000810-137001241	K562	blood:	n/a	n/a
26	CBX3	chr9:137000810-137001087	K562	blood:	n/a	n/a
27	CCNT2	chr9:137000345-137002103	K562	blood:	n/a	chr9:137001158-137001167 chr9:137001178-137001187
28	CEBPB	chr9:137000928-137001167	H1-hESC	embryonic stem cell:	n/a	chr9:137000930-137000942
29	CEBPB	chr9:136988055-136988425	IMR90	lung:	n/a	chr9:136988233-136988244
30	CEBPB	chr9:136987962-136988519	Hela-S3	cervix:	n/a	chr9:136988233-136988244
31	CEBPB	chr9:136988879-136989258	IMR90	lung:	n/a	chr9:136989065-136989076
32	CEBPB	chr9:136988925-136989222	K562	blood:	n/a	chr9:136989065-136989076
33	CEBPB	chr9:137004356-137004643	H1-hESC	embryonic stem cell:	n/a	chr9:137004481-137004492
34	CEBPB	chr9:137004215-137004596	MCF-7	breast:	n/a	chr9:137004481-137004492
35	CEBPB	chr9:136988052-136988424	A549	lung:	n/a	chr9:136988233-136988244
36	CEBPB	chr9:136988857-136989365	MCF-7	breast:	n/a	chr9:136989065-136989076
37	CEBPB	chr9:136988909-136989294	ECC-1	luminal epithelium:	n/a	chr9:136989065-136989076
38	CEBPB	chr9:136988885-136989265	A549	lung:	n/a	chr9:136989065-136989076
39	CEBPB	chr9:136988040-136988447	HepG2	liver:	n/a	chr9:136988233-136988244
40	CEBPB	chr9:137004309-137004683	K562	blood:	n/a	chr9:137004481-137004492
41	CEBPB	chr9:137000488-137001251	Hela-S3	cervix:	n/a	chr9:137000930-137000942
42	CEBPB	chr9:136988850-136989336	Hela-S3	cervix:	n/a	chr9:136989065-136989076
43	CEBPB	chr9:137004287-137004670	HepG2	liver:	n/a	chr9:137004481-137004492
44	CEBPB	chr9:136987994-136988435	K562	blood:	n/a	chr9:136988233-136988244
45	CEBPB	chr9:136988872-136989292	K562	blood:	n/a	chr9:136989065-136989076
46	CEBPB	chr9:137004174-137004781	A549	lung:	n/a	chr9:137004481-137004492
47	CEBPB	chr9:136988004-136988474	K562	blood:	n/a	chr9:136988233-136988244
48	CEBPB	chr9:136988876-136989262	HepG2	liver:	n/a	chr9:136989065-136989076
49	CEBPB	chr9:137002870-137003043	H1-hESC	embryonic stem cell:	n/a	chr9:137002931-137002942
50	CEBPB	chr9:137004341-137004621	K562	blood:	n/a	chr9:137004481-137004492

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:137005782-137005832	LNCaP	prostate:	n/a
2	chr9:137005782-137005832	LNCaP	prostate:	n/a
3	chr9:137001969-137002019	HRPEpiC	eye:	n/a
4	chr9:137001056-137001106	K562	blood:	n/a
5	chr9:137000014-137000064	RPTEC	kidney:	n/a
6	chr9:137000014-137000064	HCF	heart:	n/a
7	chr9:137001056-137001106	Hela-S3	cervix:	n/a
8	chr9:137001969-137002019	GM12891	blood:	n/a
9	chr9:137005782-137005832	BJ	skin:	n/a
10	chr9:137001737-137001787	HRE	kidney:	n/a
11	chr9:137005782-137005832	HRE	kidney:	n/a
12	chr9:137000014-137000064	ECC-1	luminal epithelium:	n/a
13	chr9:137001969-137002019	LNCaP	prostate:	n/a
14	chr9:137003752-137003802	BE2_C	brain:	n/a
15	chr9:137001027-137001077	HPAEpiC	pulmonary alveolar:	n/a
16	chr9:137005782-137005832	MCF10A-Er-Src	breast:	n/a
17	chr9:137001969-137002019	ProgFib	skin:	n/a
18	chr9:137000940-137000990	AG10803	skin:	n/a
19	chr9:137001969-137002019	HEEpiC	esophagus:	n/a
20	chr9:137003752-137003802	Caco-2	colon:	n/a
21	chr9:136997504-136997554	GM12878	blood:	n/a
22	chr9:137001027-137001077	MCF-7	breast:	n/a
23	chr9:137001737-137001787	SK-N-SH_RA	brain:	n/a
24	chr9:137001056-137001106	HCT-116	colon:	n/a
25	chr9:137003752-137003802	Hepatocyte	liver:	n/a
26	chr9:137001027-137001077	ovcar-3	ovarian:	n/a
27	chr9:137001056-137001106	MCF10A-Er-Src	breast:	n/a
28	chr9:137001737-137001787	BE2_C	brain:	n/a
29	chr9:137000940-137000990	GM12891	blood:	n/a
30	chr9:137001969-137002019	HRE	kidney:	n/a
31	chr9:137001056-137001106	HRE	kidney:	n/a
32	chr9:137001969-137002019	SKMC	muscle:	n/a
33	chr9:137001737-137001787	GM12891	blood:	n/a
34	chr9:137001969-137002019	SK-N-SH_RA	brain:	n/a
35	chr9:137001027-137001077	NT2-D1	testis:	n/a
36	chr9:137000940-137000990	AoSMC	blood vessel:	n/a
37	chr9:137000940-137000990	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:137001737-137001787	HepG2	liver:	n/a
39	chr9:137001737-137001787	MCF10A-Er-Src	breast:	n/a
40	chr9:137003752-137003802	AG04449	skin:	fetal
41	chr9:137001027-137001077	IMR90	lung:	fetal
42	chr9:137000014-137000064	GM12891	blood:	n/a
43	chr9:137001969-137002019	HL-60	blood:	n/a
44	chr9:136997504-136997554	Hepatocyte	liver:	n/a
45	chr9:136997504-136997554	Jurkat	blood:	n/a
46	chr9:137000014-137000064	HCT-116	colon:	n/a
47	chr9:136997504-136997554	HNPCEpiC	eye:	n/a
48	chr9:137000014-137000064	SKMC	muscle:	n/a
49	chr9:137001969-137002019	MCF-7	breast:	n/a
50	chr9:137001737-137001787	HEK293	kidney:	embryo

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:136934778..136936960-chr9:136965343..136968102,2	K562	blood:
2	chr9:137006870..137008925-chr9:137009202..137011699,2	K562	blood:
3	chr9:137001719..137003383-chr9:137240683..137243460,2	MCF-7	breast:
4	chr21:41236712..41238651-chr9:137001241..137003469,2	MCF-7	breast:
5	chr10:47680190..47680989-chr9:136998456..136999139,2	MCF-7	breast:
6	chr9:136932101..136934790-chr9:136997116..136999194,2	MCF-7	breast:
7	chr9:136931194..136934944-chr9:136998387..137002829,6	K562	blood:
8	chr9:136930118..136934023-chr9:136998387..137002829,10	K562	blood:
9	chr9:136282958..136284963-chr9:136998714..137001684,2	K562	blood:
10	chr9:136999035..137002778-chr9:137027888..137031331,5	K562	blood:
11	chr9:136856596..136858826-chr9:136986805..136989503,2	MCF-7	breast:
12	chr9:137003283..137007180-chr9:137027026..137030232,3	K562	blood:
13	chr9:136932690..136935080-chr9:137003441..137005032,2	MCF-7	breast:
14	chr9:136996126..136998065-chr9:137029177..137031559,2	MCF-7	breast:
15	chr9:136992413..136997235-chr9:136998349..137003411,7	K562	blood:
16	chr9:136931852..136933427-chr9:136988020..136990522,2	MCF-7	breast:
17	chr9:136928987..136935981-chr9:136998799..137005312,16	MCF-7	breast:
18	chr9:136999192..137001560-chr9:137216028..137218729,4	MCF-7	breast:
19	chr9:136924138..136926456-chr9:136992435..136994795,2	MCF-7	breast:
20	chr9:136999027..137003702-chr9:137026566..137032835,8	MCF-7	breast:
21	chr9:136987581..136991620-chr9:136999080..137002104,8	MCF-7	breast:
22	chr9:136889824..136891845-chr9:137000522..137002324,2	K562	blood:
23	chr9:136737938..136739664-chr9:136994862..136997731,2	MCF-7	breast:
24	chr9:137000635..137002837-chr9:137296498..137299052,2	MCF-7	breast:
25	chr9:136994448..136996074-chr9:136999589..137002197,2	K562	blood:
26	chr9:137000678..137001573-chr9:137029002..137029689,2	Hela-S3	cervix:
27	chr9:136919895..136922369-chr9:137000361..137002123,2	MCF-7	breast:
28	chr9:136888792..136891646-chr9:137000403..137003499,3	MCF-7	breast:
29	chr9:136967534..136969174-chr9:136971059..136973731,2	MCF-7	breast:
30	chr9:136967534..136969174-chr9:136971059..136973731,2	MCF-7	breast:
31	chr2:220091886..220094259-chr9:137000513..137003179,2	MCF-7	breast:
32	chr11:65194417..65195089-chr9:137001349..137002310,2	Hela-S3	cervix:
33	chr9:136997943..137000936-chr9:137029556..137031957,3	K562	blood:
34	chr9:136968920..136970584-chr9:136990772..136992877,2	MCF-7	breast:
35	chr9:136931362..136933512-chr9:137005797..137009467,3	MCF-7	breast:
36	chr9:137001564..137003951-chr9:137325246..137326831,2	MCF-7	breast:
37	chr9:136968920..136970584-chr9:136990772..136992877,2	MCF-7	breast:
38	chr16:401149..403748-chr9:137000262..137001904,2	MCF-7	breast:
39	chr9:136930108..136935337-chr9:136999374..137002737,14	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRD3-1	chr9:137000308-137001037	XLOC_007882
2	lnc-BRD3-1	chr9:136999207-137000046	XLOC_007882
3	lnc-BRD3-1	chr9:136999338-136999492	ENSG00000273249.1
4	lnc-WDR5-6	chr9:136974582-136974862	NONHSAT135374
5	lnc-WDR5-6	chr9:136968818-136968857	NONHSAT135374
6	lnc-BRD3-1	chr9:137000308-137000894	ENSG00000273249.1
7	lnc-BRD3-1	chr9:137000308-137000408	XLOC_007882
8	lnc-BRD3-1	chr9:136999157-136999458	XLOC_007882
9	lnc-BRD3-1	chr9:137000308-137000771	ENSG00000273249.1
10	lnc-WDR5-6	chr9:136973135-136973275	NONHSAT135374
11	lnc-BRD3-1	chr9:136997364-136997595	ENSG00000273249.1

No data

Variant related genes	Relation type
WDR5	TF binding region
ENSG00000273249	TF binding region
WDR5	CpG island
ENSG00000273249	CpG island
ENSG00000148300	chromatin interactions
ENSG00000235106	chromatin interactions
ENSG00000196363	chromatin interactions
ENSG00000103126	chromatin interactions
ENSG00000221676	chromatin interactions
ENSG00000198925	chromatin interactions
ENSG00000273249	chromatin interactions
ENSG00000186350	chromatin interactions
ENSG00000169925	chromatin interactions
ENSG00000160293	chromatin interactions

Extended variants
information (count: 1464 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531156947	chr9:136967509-136967510	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187322499	chr9:136967527-136967528	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73561316	chr9:136967540-136967541	Bivalent/Poised TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs528044736	chr9:136967594-136967595	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149842935	chr9:136967602-136967603	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546627686	chr9:136967606-136967607	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145721113	chr9:136967633-136967634	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139464279	chr9:136967640-136967641	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144304261	chr9:136967663-136967664	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568940632	chr9:136967664-136967665	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536079444	chr9:136967738-136967739	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554443531	chr9:136967767-136967768	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572806170	chr9:136967844-136967845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534660901	chr9:136967845-136967846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77607201	chr9:136967864-136967865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199538576	chr9:136967875-136967876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578026184	chr9:136967877-136967878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34668147	chr9:136967961-136967962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374919101	chr9:136967962-136967963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75105694	chr9:136967977-136967978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559254495	chr9:136967988-136967989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146574349	chr9:136967992-136967993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112350331	chr9:136968000-136968001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563839544	chr9:136968018-136968019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140366258	chr9:136968030-136968031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191958137	chr9:136968036-136968037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143537736	chr9:136968053-136968054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528808479	chr9:136968063-136968064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540195571	chr9:136968091-136968092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151018359	chr9:136968096-136968097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532165045	chr9:136968101-136968102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3123787	chr9:136968105-136968106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs201048690	chr9:136968109-136968110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150159031	chr9:136968121-136968122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138672608	chr9:136968146-136968147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566396543	chr9:136968153-136968154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142693517	chr9:136968155-136968156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185556702	chr9:136968157-136968158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533212945	chr9:136968171-136968172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539064897	chr9:136968183-136968184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557128977	chr9:136968184-136968185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575817636	chr9:136968185-136968186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563699508	chr9:136968199-136968200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146970460	chr9:136968205-136968206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137993075	chr9:136968214-136968215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573503143	chr9:136968226-136968227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540553504	chr9:136968245-136968246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188886434	chr9:136968253-136968254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116792379	chr9:136968254-136968255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10993934	chr9:136968269-136968270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136953400-136968400	Weak transcription	Gastric	stomach
2	chr9:136967200-136967800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:136968400-136968600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:136968400-136969200	ZNF genes & repeats	Gastric	stomach
5	chr9:136969200-136969400	Weak transcription	Gastric	stomach
6	chr9:136969400-136969600	Enhancers	Gastric	stomach
7	chr9:136974400-136974800	Enhancers	HepG2	liver
8	chr9:136974800-136979200	Weak transcription	HepG2	liver
9	chr9:136976400-136976800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:136979200-136979600	Enhancers	HepG2	liver
11	chr9:136986600-136987400	Enhancers	HepG2	liver
12	chr9:136986800-136987000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:136987000-136990400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:136987400-136987800	Weak transcription	HepG2	liver
15	chr9:136987600-136988200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr9:136987600-136989200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr9:136987800-136988000	Enhancers	HepG2	liver
18	chr9:136988000-136988200	Enhancers	Hela-S3	cervix
19	chr9:136988000-136988200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr9:136988000-136988600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr9:136988000-136988600	Flanking Active TSS	HepG2	liver
22	chr9:136988200-136988400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:136988200-136988600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr9:136988200-136988600	Enhancers	Placenta	Placenta
25	chr9:136988200-136988600	Flanking Active TSS	Hela-S3	cervix
26	chr9:136988200-136988600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr9:136988600-136988800	Enhancers	Hela-S3	cervix
28	chr9:136988600-136988800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr9:136988600-136989800	Enhancers	HepG2	liver
30	chr9:136988600-136990600	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr9:136988800-136989200	Flanking Active TSS	Hela-S3	cervix
32	chr9:136988800-136989200	Bivalent Enhancer	K562	blood
33	chr9:136988800-136989200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr9:136989200-136990000	Enhancers	Hela-S3	cervix
35	chr9:136989200-136990000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr9:136989800-136990600	Bivalent Enhancer	HepG2	liver
37	chr9:136990000-136994800	Weak transcription	Hela-S3	cervix
38	chr9:136990400-136990800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr9:136990400-136991200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:136990400-136994600	Enhancers	Spleen	Spleen
41	chr9:136990600-136991000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr9:136990600-136991000	Enhancers	HSMMtube	muscle
43	chr9:136990600-136991200	Flanking Bivalent TSS/Enh	HepG2	liver
44	chr9:136990800-136991000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr9:136990800-136991000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr9:136990800-136991000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr9:136990800-136991200	Enhancers	Pancreas	Pancrea
48	chr9:136990800-136996200	Enhancers	Fetal Muscle Leg	muscle
49	chr9:136991000-136991200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr9:136991000-136992400	Enhancers	Fetal Muscle Trunk	muscle

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