Variant report

Variant	nsv998699
Chromosome Location	chr3:46775383-46859820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:2015)
Chromatin interactive
region (count:35)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:46792267-46792609	K562	blood:	n/a	n/a
2	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
3	BACH1	chr3:46853993-46854163	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
5	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
8	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
9	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
10	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
11	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
12	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
13	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
14	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
15	CEBPB	chr3:46780721-46781004	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:46780720-46780724	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
19	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
20	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
21	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
22	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
23	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
24	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
25	CTCF	chr3:46798300-46798450	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
26	CTCF	chr3:46778138-46778154	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:46777949-46778273	H1-hESC	embryonic stem cell:	n/a	chr3:46778094-46778115 chr3:46778092-46778110
28	CTCF	chr3:46798134-46798571	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
29	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
30	CTCF	chr3:46778060-46778210	HepG2	liver:	n/a	chr3:46778094-46778115 chr3:46778092-46778110
31	CTCF	chr3:46776341-46776414	MCF-7	breast:	n/a	n/a
32	CTCF	chr3:46775066-46775390	K562	blood:	n/a	n/a
33	CTCF	chr3:46778040-46778165	MCF-7	breast:	n/a	chr3:46778094-46778115 chr3:46778092-46778110
34	CTCF	chr3:46798280-46798435	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
35	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:46794500-46794650	GM12872	blood:	n/a	n/a
37	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a
38	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr3:46776346-46776418	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
41	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
42	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
43	CTCF	chr3:46777895-46778249	H1-hESC	embryonic stem cell:	n/a	chr3:46778094-46778115 chr3:46778092-46778110
44	CTCF	chr3:46775070-46775401	K562	blood:	n/a	n/a
45	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr3:46794460-46794610	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
48	CTCF	chr3:46854876-46854950	GM20000	blood:	n/a	n/a
49	CTCF	chr3:46792360-46792510	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
50	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46786238-46786288	AG10803	skin:	n/a
2	chr3:46792192-46792242	NH-A	brain:	n/a
3	chr3:46786238-46786288	AG10803	skin:	n/a
4	chr3:46792192-46792242	NH-A	brain:	n/a
5	chr3:46799010-46799060	HL-60	blood:	n/a
6	chr3:46853910-46853960	HMEC	breast:	n/a
7	chr3:46799010-46799060	BJ	skin:	n/a
8	chr3:46792192-46792242	GM12878	blood:	n/a
9	chr3:46792357-46792407	GM19239	blood:	n/a
10	chr3:46854173-46854223	AG04450	lung:	fetal
11	chr3:46854231-46854281	GM19239	blood:	n/a
12	chr3:46786238-46786288	NHDF-neo	bronchial:	n/a
13	chr3:46853910-46853960	BE2_C	brain:	n/a
14	chr3:46792364-46792414	BE2_C	brain:	n/a
15	chr3:46791477-46791527	NHBE	bronchial:	n/a
16	chr3:46778871-46778921	NHDF-neo	bronchial:	n/a
17	chr3:46794154-46794204	GM06990	blood:	n/a
18	chr3:46796026-46796076	Hela-S3	cervix:	n/a
19	chr3:46792462-46792512	NT2-D1	testis:	n/a
20	chr3:46799010-46799060	NH-A	brain:	n/a
21	chr3:46775544-46775594	SK-N-SH_RA	brain:	n/a
22	chr3:46853910-46853960	AoSMC	blood vessel:	n/a
23	chr3:46853910-46853960	HCT-116	colon:	n/a
24	chr3:46775544-46775594	AoSMC	blood vessel:	n/a
25	chr3:46792364-46792414	K562	blood:	n/a
26	chr3:46786387-46786437	IMR90	lung:	fetal
27	chr3:46790182-46790232	NB4	blood:	n/a
28	chr3:46796026-46796076	AG09319	gingival:	n/a
29	chr3:46854311-46854361	HepG2	liver:	n/a
30	chr3:46856803-46856853	HRE	kidney:	n/a
31	chr3:46794154-46794204	SK-N-SH	brain:	n/a
32	chr3:46792364-46792414	AG10803	skin:	n/a
33	chr3:46792192-46792242	AoSMC	blood vessel:	n/a
34	chr3:46797928-46797978	Hepatocyte	liver:	n/a
35	chr3:46792192-46792242	CMK	blood:	n/a
36	chr3:46853986-46854036	SK-N-SH_RA	brain:	n/a
37	chr3:46799010-46799060	GM12892	blood:	n/a
38	chr3:46854231-46854281	NHBE	bronchial:	n/a
39	chr3:46790182-46790232	SK-N-MC	brain:	n/a
40	chr3:46786387-46786437	SAEC	small airway:	n/a
41	chr3:46786238-46786288	GM12892	blood:	n/a
42	chr3:46778871-46778921	HIPEpiC	eye:	n/a
43	chr3:46775899-46775949	HRPEpiC	eye:	n/a
44	chr3:46778871-46778921	AG09319	gingival:	n/a
45	chr3:46775544-46775594	SAEC	small airway:	n/a
46	chr3:46792357-46792407	AG04449	skin:	fetal
47	chr3:46853631-46853681	HCM	heart:	n/a
48	chr3:46786238-46786288	GM19239	blood:	n/a
49	chr3:46797928-46797978	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:46798240-46798290	HCF	heart:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
2	chr3:46858188..46860125-chr3:46939783..46942119,2	K562	blood:
3	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
4	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
5	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
6	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
7	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
8	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
9	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
10	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
11	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
12	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
13	chr3:46783774..46785518-chr3:46915413..46918248,2	MCF-7	breast:
14	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
15	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
16	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
17	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
18	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
19	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
20	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
21	chr3:46774953..46775682-chr3:46936746..46937314,2	K562	blood:
22	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
23	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
24	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
25	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
26	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
27	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
28	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
29	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
30	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
31	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
32	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
33	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
34	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:
35	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46853712-46854064	NONHSAT089457
2	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457
3	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
4	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS45	TF binding region
PRSS46	TF binding region
PRSS50	TF binding region
PRSS44	TF binding region
ENSG00000238013	CpG island
PRSS45	CpG island
PRSS46	CpG island
PRSS50	CpG island
PRSS44	CpG island
ENSG00000261603	chromatin interactions
ENSG00000188086	chromatin interactions

Extended variants
information (count: 1730 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1730 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12489663	chr3:46775383-46775384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12496832	chr3:46775410-46775411	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs531025615	chr3:46775414-46775415	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs556577962	chr3:46775415-46775416	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs72897492	chr3:46775425-46775426	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs545307879	chr3:46775426-46775427	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs549720883	chr3:46775449-46775450	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs560082983	chr3:46775498-46775499	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs148143145	chr3:46775504-46775505	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs374953427	chr3:46775509-46775510	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs115069364	chr3:46775532-46775533	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs568200456	chr3:46775559-46775560	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs535406552	chr3:46775569-46775570	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs73833619	chr3:46775583-46775584	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs561464871	chr3:46775589-46775590	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs547679707	chr3:46775591-46775592	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs529065522	chr3:46775598-46775599	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs550796731	chr3:46775606-46775607	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs68175547	chr3:46775608-46775609	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs533221358	chr3:46775641-46775642	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs111629792	chr3:46775642-46775643	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs139025660	chr3:46775701-46775702	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs566446763	chr3:46775712-46775713	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs527312483	chr3:46775759-46775760	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs56375912	chr3:46775766-46775767	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs567401668	chr3:46775768-46775769	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs375528297	chr3:46775781-46775782	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs537548934	chr3:46775803-46775804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188742146	chr3:46775834-46775835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571524507	chr3:46775900-46775901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56208931	chr3:46775948-46775949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs554073884	chr3:46776000-46776001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368980012	chr3:46776035-46776036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572089947	chr3:46776038-46776039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372674205	chr3:46776130-46776131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113877206	chr3:46776152-46776153	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs142116118	chr3:46776156-46776157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373588421	chr3:46776173-46776174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59790038	chr3:46776195-46776196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56232804	chr3:46776198-46776199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145827921	chr3:46776228-46776229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192539942	chr3:46776244-46776245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74498795	chr3:46776252-46776253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533183452	chr3:46776314-46776315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184926914	chr3:46776316-46776317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188116330	chr3:46776331-46776332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560475764	chr3:46776336-46776337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56752770	chr3:46776337-46776338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs555682327	chr3:46776357-46776358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548918114	chr3:46776374-46776375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46744000-46792200	Weak transcription	Right Atrium	heart
2	chr3:46769000-46792400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:46770800-46776200	Weak transcription	Pancreas	Pancrea
4	chr3:46770800-46778000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:46775400-46775600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
6	chr3:46775600-46775800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr3:46776200-46776600	Enhancers	Pancreas	Pancrea
8	chr3:46776600-46778800	Weak transcription	Pancreas	Pancrea
9	chr3:46777000-46779800	Enhancers	Thymus	Thymus
10	chr3:46778000-46778200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:46778000-46778200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
12	chr3:46778000-46780000	Enhancers	Fetal Thymus	thymus
13	chr3:46778200-46778400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr3:46778200-46778800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:46778400-46779200	Enhancers	Fetal Muscle Trunk	muscle
16	chr3:46778600-46779200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr3:46778600-46779200	Enhancers	Fetal Muscle Leg	muscle
18	chr3:46778800-46779000	Bivalent Enhancer	HSMM	muscle
19	chr3:46778800-46779200	Enhancers	Left Ventricle	heart
20	chr3:46778800-46779400	Enhancers	Pancreas	Pancrea
21	chr3:46779000-46779200	Enhancers	Spleen	Spleen
22	chr3:46779000-46779400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
23	chr3:46779200-46782000	Weak transcription	Left Ventricle	heart
24	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
25	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
26	chr3:46779600-46780400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
28	chr3:46780800-46785000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr3:46784400-46785200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr3:46784400-46785200	Enhancers	Fetal Stomach	stomach
31	chr3:46784600-46785000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:46784600-46785000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:46784600-46785000	Enhancers	Placenta	Placenta
34	chr3:46784600-46785200	Enhancers	Fetal Lung	lung
35	chr3:46784600-46785200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr3:46784800-46785200	Enhancers	Fetal Intestine Small	intestine
37	chr3:46785000-46785200	Weak transcription	Placenta	Placenta
38	chr3:46785000-46785800	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr3:46785000-46786200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:46785200-46785600	Enhancers	Placenta	Placenta
42	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
43	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
44	chr3:46785800-46786200	Enhancers	GM12878-XiMat	blood
45	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr3:46786200-46787800	Weak transcription	GM12878-XiMat	blood
47	chr3:46786400-46786600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr3:46787800-46789200	Enhancers	GM12878-XiMat	blood
49	chr3:46789200-46794200	Weak transcription	GM12878-XiMat	blood
50	chr3:46789600-46789800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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