Variant report

Variant	nsv519266
Chromosome Location	chr9:110049477-110085255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:61)
Chromatin interactive
region (count:60)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:110059085-110059093	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:110079401-110079654	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:110084949-110085306	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:110058541-110058741	HepG2	liver:	n/a	n/a
5	BATF	chr9:110075922-110076187	GM12878	blood:	n/a	chr9:110076032-110076043
6	BATF	chr9:110075881-110076230	GM12878	blood:	n/a	chr9:110076032-110076043
7	BCL11A	chr9:110071618-110071906	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:110071566-110071861	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:110057094-110057418	K562	blood:	n/a	n/a
10	BRCA1	chr9:110051057-110051285	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:110049423-110049636	A549	lung:	n/a	chr9:110049539-110049552 chr9:110049539-110049550
12	CEBPB	chr9:110049417-110049658	HepG2	liver:	n/a	chr9:110049539-110049552 chr9:110049539-110049550
13	CEBPB	chr9:110050983-110051311	K562	blood:	n/a	n/a
14	CEBPB	chr9:110051039-110051340	K562	blood:	n/a	n/a
15	CEBPB	chr9:110049400-110049643	K562	blood:	n/a	chr9:110049539-110049552 chr9:110049539-110049550
16	CEBPB	chr9:110055120-110055331	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr9:110049457-110049561	H1-hESC	embryonic stem cell:	n/a	chr9:110049539-110049552 chr9:110049539-110049550
18	CEBPB	chr9:110051038-110051303	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:110051012-110051243	K562	blood:	n/a	n/a
20	CEBPB	chr9:110051004-110051347	Hela-S3	cervix:	n/a	n/a
21	CEBPZ	chr9:110049555-110049773	HepG2	liver:	n/a	n/a
22	CHD2	chr9:110055455-110055636	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr9:110061900-110062050	GM12878	blood:	n/a	n/a
24	CTCF	chr9:110061798-110062075	GM12878	blood:	n/a	n/a
25	CTCF	chr9:110061931-110061997	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr9:110061920-110062070	GM12869	blood:	n/a	n/a
27	CTCF	chr9:110061740-110061890	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:110061700-110061850	BE2_C	brain:	n/a	n/a
29	CTCF	chr9:110068709-110068763	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:110061820-110061970	GM12871	blood:	n/a	n/a
31	CTCF	chr9:110061900-110062050	AG09319	gingival:	n/a	n/a
32	CTCF	chr9:110066960-110067110	HMF	breast:	n/a	n/a
33	CTCF	chr9:110057100-110057250	HEK293	kidney:	n/a	n/a
34	CTCF	chr9:110061600-110061750	HFF	foreskin:	n/a	n/a
35	CTCF	chr9:110061840-110061990	HCFaa	heart:	n/a	n/a
36	CTCF	chr9:110061780-110061930	NHLF	lung:	n/a	n/a
37	CTCF	chr9:110061840-110061990	HMEC	breast:	n/a	n/a
38	CTCF	chr9:110061740-110061890	HCM	heart:	n/a	n/a
39	CTCF	chr9:110061860-110062010	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr9:110057120-110057270	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr9:110061800-110061950	AG09319	gingival:	n/a	n/a
42	CTCF	chr9:110061920-110062070	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:110067140-110067290	A549	lung:	n/a	n/a
44	CTCF	chr9:110061860-110062010	SAEC	small airway:	n/a	n/a
45	CTCF	chr9:110061880-110062030	GM12872	blood:	n/a	n/a
46	CTCF	chr9:110050758-110050840	ProgFib	skin:	n/a	n/a
47	CTCF	chr9:110061720-110061870	HRE	kidney:	n/a	n/a
48	CTCF	chr9:110075140-110075290	AG09309	skin:	n/a	n/a
49	CTCF	chr9:110050801-110050826	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:110068706-110068773	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:110056119-110056169	T-47D	breast:	n/a
2	chr9:110056119-110056169	Jurkat	blood:	n/a
3	chr9:110056119-110056169	BJ	skin:	n/a
4	chr9:110056119-110056169	Hepatocyte	liver:	n/a
5	chr9:110056119-110056169	ECC-1	luminal epithelium:	n/a
6	chr9:110056119-110056169	HAEpiC	amniotic membrane:	n/a
7	chr9:110056119-110056169	HUVEC	blood vessel:	n/a
8	chr9:110056119-110056169	HEK293	kidney:	embryo
9	chr9:110056119-110056169	AG09319	gingival:	n/a
10	chr9:110056119-110056169	HIPEpiC	eye:	n/a
11	chr9:110056119-110056169	HNPCEpiC	eye:	n/a
12	chr9:110056119-110056169	IMR90	lung:	fetal
13	chr9:110056119-110056169	HCF	heart:	n/a
14	chr9:110056119-110056169	SK-N-SH_RA	brain:	n/a
15	chr9:110056119-110056169	GM06990	blood:	n/a
16	chr9:110056119-110056169	AG04449	skin:	fetal
17	chr9:110056119-110056169	Caco-2	colon:	n/a
18	chr9:110056119-110056169	HRPEpiC	eye:	n/a
19	chr9:110056119-110056169	PFSK-1	brain:	n/a
20	chr9:110056119-110056169	RPTEC	kidney:	n/a
21	chr9:110056119-110056169	Hela-S3	cervix:	n/a
22	chr9:110056119-110056169	LNCaP	prostate:	n/a
23	chr9:110056119-110056169	SKMC	muscle:	n/a
24	chr9:110056119-110056169	HRE	kidney:	n/a
25	chr9:110056119-110056169	SK-N-MC	brain:	n/a
26	chr9:110056119-110056169	NHDF-neo	bronchial:	n/a
27	chr9:110056119-110056169	GM12892	blood:	n/a
28	chr9:110056119-110056169	NB4	blood:	n/a
29	chr9:110056119-110056169	GM19239	blood:	n/a
30	chr9:110056119-110056169	H1-hESC	embryonic stem cell:	embryo
31	chr9:110056119-110056169	HCM	heart:	n/a
32	chr9:110056119-110056169	K562	blood:	n/a
33	chr9:110056119-110056169	HMEC	breast:	n/a
34	chr9:110056119-110056169	A549	lung:	n/a
35	chr9:110056119-110056169	GM12878	blood:	n/a
36	chr9:110056119-110056169	ovcar-3	ovarian:	n/a
37	chr9:110056119-110056169	NH-A	brain:	n/a
38	chr9:110056119-110056169	HEEpiC	esophagus:	n/a
39	chr9:110056119-110056169	MCF-7	breast:	n/a
40	chr9:110056119-110056169	SAEC	small airway:	n/a
41	chr9:110056119-110056169	HCT-116	colon:	n/a
42	chr9:110056119-110056169	MCF10A-Er-Src	breast:	n/a
43	chr9:110056119-110056169	AG09309	skin:	n/a
44	chr9:110056119-110056169	NT2-D1	testis:	n/a
45	chr9:110056119-110056169	HL-60	blood:	n/a
46	chr9:110056119-110056169	AG10803	skin:	n/a
47	chr9:110056119-110056169	AG04450	lung:	fetal
48	chr9:110056119-110056169	AoSMC	blood vessel:	n/a
49	chr9:110056119-110056169	SK-N-SH	brain:	n/a
50	chr9:110056119-110056169	HPAEpiC	pulmonary alveolar:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:110001230..110003494-chr9:110052662..110055320,2	MCF-7	breast:
2	chr9:110044258..110048385-chr9:110059208..110064151,5	MCF-7	breast:
3	chr9:110070129..110072488-chr9:110081712..110083415,2	K562	blood:
4	chr9:110038034..110040721-chr9:110051893..110053905,2	MCF-7	breast:
5	chr9:110044750..110046904-chr9:110066196..110068105,2	K562	blood:
6	chr9:110052754..110054534-chr9:110055786..110058633,2	K562	blood:
7	chr9:110043401..110047935-chr9:110082393..110087962,7	K562	blood:
8	chr9:110001517..110002205-chr9:110061655..110062417,2	MCF-7	breast:
9	chr9:110054408..110057220-chr9:110063474..110066259,2	K562	blood:
10	chr9:110066546..110068820-chr9:110070099..110072888,2	K562	blood:
11	chr9:110054445..110058128-chr9:110059472..110062917,7	K562	blood:
12	chr9:110058012..110060076-chr9:110062055..110063823,2	MCF-7	breast:
13	chr9:110082760..110084728-chr9:110089883..110091772,2	MCF-7	breast:
14	chr9:110050203..110052215-chr9:110053888..110055858,2	K562	blood:
15	chr9:110070283..110073210-chr9:110082560..110084216,2	MCF-7	breast:
16	chr9:110058012..110060076-chr9:110062055..110063823,2	MCF-7	breast:
17	chr9:110062306..110064844-chr9:110068652..110070253,2	K562	blood:
18	chr9:110060491..110063428-chr9:110066349..110068184,2	MCF-7	breast:
19	chr9:110044605..110047075-chr9:110077754..110080578,5	MCF-7	breast:
20	chr9:110044399..110049612-chr9:110071012..110080286,12	K562	blood:
21	chr9:110045249..110048106-chr9:110077151..110079767,3	MCF-7	breast:
22	chr9:110069222..110072456-chr9:110073619..110076462,3	MCF-7	breast:
23	chr9:110044689..110046322-chr9:110067933..110070602,2	MCF-7	breast:
24	chr9:110054408..110057220-chr9:110063474..110066259,2	K562	blood:
25	chr9:110070283..110073210-chr9:110082560..110084216,2	MCF-7	breast:
26	chr9:110065252..110067384-chr9:110080833..110082892,2	K562	blood:
27	chr9:110049581..110051989-chr9:110070046..110072937,2	MCF-7	breast:
28	chr9:110079143..110082107-chr9:110082961..110085070,2	MCF-7	breast:
29	chr9:110044300..110048942-chr9:110067094..110074281,11	MCF-7	breast:
30	chr9:110056091..110058326-chr9:110068652..110070391,2	K562	blood:
31	chr9:110054445..110058128-chr9:110059472..110062917,7	K562	blood:
32	chr9:110043397..110048376-chr9:110058875..110065071,10	K562	blood:
33	chr9:110060441..110063203-chr9:110064051..110066274,3	MCF-7	breast:
34	chr9:110050203..110052215-chr9:110053888..110055858,2	K562	blood:
35	chr9:110070353..110073170-chr9:110078217..110082315,4	MCF-7	breast:
36	chr9:110060398..110063289-chr9:110066758..110069603,2	MCF-7	breast:
37	chr9:110060441..110063203-chr9:110064051..110066274,3	MCF-7	breast:
38	chr9:110079143..110082107-chr9:110082961..110085070,2	MCF-7	breast:
39	chr9:110069222..110072456-chr9:110073619..110076462,3	MCF-7	breast:
40	chr9:110049612..110053509-chr9:110059334..110062914,3	K562	blood:
41	chr9:110070129..110072488-chr9:110081712..110083415,2	K562	blood:
42	chr9:110052754..110054534-chr9:110055786..110058633,2	K562	blood:
43	chr9:110065252..110067384-chr9:110080833..110082892,2	K562	blood:
44	chr9:110070353..110073170-chr9:110078217..110082315,4	MCF-7	breast:
45	chr9:110049581..110051989-chr9:110070046..110072937,2	MCF-7	breast:
46	chr9:110081713..110085452-chr9:110093705..110096691,3	MCF-7	breast:
47	chr9:110042843..110044728-chr9:110074492..110076234,2	K562	blood:
48	chr9:110044896..110047317-chr9:110081780..110084455,3	MCF-7	breast:
49	chr9:110066546..110068820-chr9:110070099..110072888,2	K562	blood:
50	chr9:110056937..110059349-chr9:110068583..110071542,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF4-10	chr9:110054255-110054369	NONHSAT133865
2	lnc-KLF4-10	chr9:110056813-110056921	NONHSAT133865

No data

Variant related genes	Relation type
RAD23B	TF binding region
RAD23B	CpG island
ENSG00000119318	chromatin interactions

Extended variants
information (count: 1568 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1568 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7031906	chr9:110049477-110049478	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184472385	chr9:110049486-110049487	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115248785	chr9:110049497-110049498	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559607377	chr9:110049506-110049507	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs200119217	chr9:110049515-110049516	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200883347	chr9:110049516-110049517	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs398113776	chr9:110049524-110049525	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537534732	chr9:110049558-110049559	Active TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189138316	chr9:110049627-110049628	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs551207599	chr9:110049647-110049648	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs563020675	chr9:110049681-110049682	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs201701045	chr9:110049742-110049743	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs545601829	chr9:110049750-110049751	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553909248	chr9:110049762-110049763	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs530551614	chr9:110049793-110049794	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs7035611	chr9:110049828-110049829	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs76181849	chr9:110049847-110049848	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs10739236	chr9:110049848-110049849	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs546939127	chr9:110049870-110049871	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs558331013	chr9:110049881-110049882	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs554141915	chr9:110049886-110049887	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs113836469	chr9:110049889-110049890	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs7035725	chr9:110049914-110049915	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs557617897	chr9:110049932-110049933	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs181836228	chr9:110049942-110049943	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs534232490	chr9:110049977-110049978	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs558980208	chr9:110049979-110049980	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs71491275	chr9:110050001-110050002	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs71368008	chr9:110050006-110050007	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs140079074	chr9:110050008-110050009	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs184947210	chr9:110050029-110050030	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs145598387	chr9:110050069-110050070	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs377606120	chr9:110050115-110050116	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs56114094	chr9:110050116-110050117	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs562971064	chr9:110050124-110050125	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs12347496	chr9:110050132-110050133	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs12338320	chr9:110050133-110050134	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559383856	chr9:110050174-110050175	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577542348	chr9:110050229-110050230	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs544787339	chr9:110050245-110050246	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs371341131	chr9:110050252-110050253	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574951633	chr9:110050272-110050273	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200354979	chr9:110050274-110050275	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs73515722	chr9:110050311-110050312	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530638116	chr9:110050322-110050323	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs114592897	chr9:110050326-110050327	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs561051704	chr9:110050419-110050420	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs528066889	chr9:110050429-110050430	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs546623033	chr9:110050451-110050452	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs147300816	chr9:110050455-110050456	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110045000-110050600	Active TSS	NHLF	lung
2	chr9:110046800-110050800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:110046800-110050800	Weak transcription	Gastric	stomach
4	chr9:110046800-110050800	Weak transcription	Pancreas	Pancrea
5	chr9:110046800-110051000	Weak transcription	Spleen	Spleen
6	chr9:110047200-110049800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:110047200-110050600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr9:110047200-110050800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:110047200-110052400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:110047200-110052600	Enhancers	Primary B cells from peripheral blood	blood
11	chr9:110047200-110054600	Weak transcription	Lung	lung
12	chr9:110047600-110067200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:110047800-110049800	Enhancers	Primary B cells from cord blood	blood
14	chr9:110047800-110051800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr9:110047800-110054200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr9:110048000-110050200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr9:110048000-110051000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:110048000-110051200	Enhancers	Thymus	Thymus
19	chr9:110048000-110053200	Weak transcription	Fetal Thymus	thymus
20	chr9:110048000-110056000	Weak transcription	Aorta	Aorta
21	chr9:110048000-110058400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr9:110048200-110050200	Enhancers	Fetal Heart	heart
23	chr9:110048400-110051200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr9:110048400-110051400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:110048400-110051800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr9:110048400-110052800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr9:110048400-110058000	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr9:110048600-110049600	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr9:110048600-110049800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr9:110048600-110049800	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr9:110048600-110050000	Enhancers	Colon Smooth Muscle	Colon
32	chr9:110048600-110050000	Enhancers	Left Ventricle	heart
33	chr9:110048600-110050400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr9:110048600-110050400	Weak transcription	Small Intestine	intestine
35	chr9:110048600-110050600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:110048600-110050800	Weak transcription	Ovary	ovary
37	chr9:110048600-110050800	Weak transcription	Right Atrium	heart
38	chr9:110048600-110051400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr9:110048600-110051600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr9:110048600-110052000	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr9:110048600-110052000	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr9:110048600-110052000	Active TSS	GM12878-XiMat	blood
43	chr9:110048600-110052200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr9:110048600-110058000	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr9:110048800-110049800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr9:110048800-110049800	Weak transcription	Psoas Muscle	Psoas
47	chr9:110048800-110049800	Enhancers	Hela-S3	cervix
48	chr9:110048800-110050000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr9:110048800-110050200	Weak transcription	HUVEC	blood vessel
50	chr9:110048800-110050400	Weak transcription	Brain Cingulate Gyrus	brain

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