Variant report

Variant	nsv869952
Chromosome Location	chr3:46768163-46854438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:2015)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 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	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
2	ATF3	chr3:46792267-46792609	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	chr3:46773261-46773680	GM12878	blood:	n/a	n/a
6	BATF	chr3:46773278-46773701	GM12878	blood:	n/a	n/a
7	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:46773339-46773653	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
11	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
12	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
13	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
14	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
15	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
16	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
17	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
18	CEBPB	chr3:46780720-46780724	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:46780721-46781004	HepG2	liver:	n/a	n/a
21	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
22	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
23	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
24	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
25	CTCF	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
26	CTCF	chr3:46775179-46775181	GM10266	blood:	n/a	n/a
27	CTCF	chr3:46778040-46778165	MCF-7	breast:	n/a	chr3:46778094-46778115 chr3:46778092-46778110
28	CTCF	chr3:46775107-46775348	K562	blood:	n/a	n/a
29	CTCF	chr3:46775200-46775350	BJ	skin:	n/a	n/a
30	CTCF	chr3:46775182-46775279	Fibrobl	skin:	n/a	n/a
31	CTCF	chr3:46775156-46775293	GM12878	blood:	n/a	n/a
32	CTCF	chr3:46775160-46775310	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr3:46792287-46792555	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
34	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
35	CTCF	chr3:46775127-46775318	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:46775114-46775290	HepG2	liver:	n/a	n/a
37	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
38	CTCF	chr3:46775160-46775310	AG04449	skin:	n/a	n/a
39	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
40	CTCF	chr3:46775160-46775310	HAc	cerebellar:	n/a	n/a
41	CTCF	chr3:46775160-46775310	AG09309	skin:	n/a	n/a
42	CTCF	chr3:46775120-46775270	BJ	skin:	n/a	n/a
43	CTCF	chr3:46775118-46775327	GM12891	blood:	n/a	n/a
44	CTCF	chr3:46775160-46775310	HPF	lung:	n/a	n/a
45	CTCF	chr3:46775170-46775297	GM19239	blood:	n/a	n/a
46	CTCF	chr3:46775180-46775330	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr3:46775160-46775310	Caco-2	colon:	n/a	n/a
48	CTCF	chr3:46775132-46775332	IMR90	lung:	n/a	n/a
49	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr3:46798400-46798550	HVMF	connective:	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	chr3:46797928-46797978	IMR90	lung:	fetal
2	chr3:46854173-46854223	H1-hESC	embryonic stem cell:	embryo
3	chr3:46797928-46797978	IMR90	lung:	fetal
4	chr3:46854173-46854223	H1-hESC	embryonic stem cell:	embryo
5	chr3:46853850-46853900	NHBE	bronchial:	n/a
6	chr3:46854231-46854281	HCM	heart:	n/a
7	chr3:46853910-46853960	GM19239	blood:	n/a
8	chr3:46785957-46786007	H1-hESC	embryonic stem cell:	embryo
9	chr3:46786387-46786437	PFSK-1	brain:	n/a
10	chr3:46853910-46853960	SK-N-SH	brain:	n/a
11	chr3:46853850-46853900	ECC-1	luminal epithelium:	n/a
12	chr3:46794154-46794204	BE2_C	brain:	n/a
13	chr3:46789735-46789785	T-47D	breast:	n/a
14	chr3:46775899-46775949	HIPEpiC	eye:	n/a
15	chr3:46853631-46853681	IMR90	lung:	fetal
16	chr3:46792462-46792512	HepG2	liver:	n/a
17	chr3:46778871-46778921	AG10803	skin:	n/a
18	chr3:46787073-46787123	U87	brain:	n/a
19	chr3:46787073-46787123	HNPCEpiC	eye:	n/a
20	chr3:46854173-46854223	PANC-1	pancreas:	n/a
21	chr3:46776775-46776825	ovcar-3	ovarian:	n/a
22	chr3:46776775-46776825	HepG2	liver:	n/a
23	chr3:46794154-46794204	AG09309	skin:	n/a
24	chr3:46792192-46792242	NT2-D1	testis:	n/a
25	chr3:46794154-46794204	AG04449	skin:	fetal
26	chr3:46775569-46775619	PANC-1	pancreas:	n/a
27	chr3:46854231-46854281	HEK293	kidney:	embryo
28	chr3:46792462-46792512	NHBE	bronchial:	n/a
29	chr3:46790182-46790232	HCT-116	colon:	n/a
30	chr3:46798240-46798290	GM12892	blood:	n/a
31	chr3:46775544-46775594	A549	lung:	n/a
32	chr3:46796026-46796076	U87	brain:	n/a
33	chr3:46799010-46799060	NT2-D1	testis:	n/a
34	chr3:46787073-46787123	A549	lung:	n/a
35	chr3:46786238-46786288	HCM	heart:	n/a
36	chr3:46853986-46854036	HNPCEpiC	eye:	n/a
37	chr3:46789735-46789785	SK-N-MC	brain:	n/a
38	chr3:46775544-46775594	NHBE	bronchial:	n/a
39	chr3:46801208-46801258	PANC-1	pancreas:	n/a
40	chr3:46794154-46794204	AG09319	gingival:	n/a
41	chr3:46792357-46792407	Caco-2	colon:	n/a
42	chr3:46789735-46789785	ECC-1	luminal epithelium:	n/a
43	chr3:46778871-46778921	HEEpiC	esophagus:	n/a
44	chr3:46796026-46796076	T-47D	breast:	n/a
45	chr3:46785957-46786007	HL-60	blood:	n/a
46	chr3:46850588-46850638	U87	brain:	n/a
47	chr3:46775899-46775949	PFSK-1	brain:	n/a
48	chr3:46768322-46768372	U87	brain:	n/a
49	chr3:46850588-46850638	T-47D	breast:	n/a
50	chr3:46775899-46775949	NHBE	bronchial:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
2	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
3	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
4	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
5	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
6	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
7	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
8	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
9	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
10	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
11	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
12	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
13	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
14	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
15	chr3:46774953..46775682-chr3:46936746..46937314,2	K562	blood:
16	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
17	chr3:46783774..46785518-chr3:46915413..46918248,2	MCF-7	breast:
18	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
19	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
20	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
21	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
22	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
23	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
24	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
25	chr3:46770529..46772210-chr3:46784902..46786498,2	K562	blood:
26	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
27	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
28	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
29	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
30	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
31	chr3:46761792..46767256-chr3:46770894..46774909,6	K562	blood:
32	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
33	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
34	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
35	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
36	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
2	lnc-PRSS50-1	chr3:46853712-46854064	NONHSAT089457
3	lnc-PRSS50-1	chr3:46797532-46798119	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: 1819 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550547098	chr3:46768234-46768235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73063677	chr3:46768251-46768252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560290503	chr3:46768264-46768265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146130950	chr3:46768286-46768287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566446605	chr3:46768451-46768452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533797811	chr3:46768453-46768454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7626129	chr3:46768474-46768475	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs573828880	chr3:46768521-46768522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533763707	chr3:46768581-46768582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544300069	chr3:46768592-46768593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558326014	chr3:46768603-46768604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556441127	chr3:46768649-46768650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545510231	chr3:46768675-46768676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139856048	chr3:46768679-46768680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545352326	chr3:46768687-46768688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560443449	chr3:46768690-46768691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544134330	chr3:46768693-46768694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371490044	chr3:46768695-46768696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143321914	chr3:46768708-46768709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs55677826	chr3:46768721-46768722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531645016	chr3:46768894-46768895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550256263	chr3:46768926-46768927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77707116	chr3:46768956-46768957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182715885	chr3:46768962-46768963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9856479	chr3:46768964-46768965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60132352	chr3:46769004-46769005	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs566805855	chr3:46769005-46769006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116253267	chr3:46769020-46769021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541796364	chr3:46769086-46769087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187938284	chr3:46769094-46769095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548954033	chr3:46769107-46769108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567280061	chr3:46769119-46769120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371824431	chr3:46769154-46769155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561404549	chr3:46769182-46769183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556249341	chr3:46769197-46769198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578095986	chr3:46769202-46769203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192349976	chr3:46769250-46769251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73833610	chr3:46769366-46769367	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs76457642	chr3:46769397-46769398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183395870	chr3:46769460-46769461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530270948	chr3:46769498-46769499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146038969	chr3:46769541-46769542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371922758	chr3:46769552-46769553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533060130	chr3:46769561-46769562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560903874	chr3:46769563-46769564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528841390	chr3:46769600-46769601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537988087	chr3:46769622-46769623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150936766	chr3:46769628-46769629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs60643068	chr3:46769652-46769653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs527380114	chr3:46769673-46769674	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:525 , 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	chr3:46766200-46768400	Enhancers	Placenta Amnion	Placenta Amnion
3	chr3:46766600-46768200	Enhancers	HSMM	muscle
4	chr3:46767000-46768400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:46767200-46768400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:46767400-46769400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:46767600-46768400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:46767600-46769200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:46767800-46768400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:46767800-46769200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:46767800-46770800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr3:46768400-46768600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:46768400-46768800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr3:46768400-46768800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr3:46768400-46770600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr3:46768800-46769000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr3:46768800-46769600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:46769000-46792400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr3:46769200-46770600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr3:46769600-46770000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr3:46770000-46771000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr3:46770400-46770600	Weak transcription	Pancreas	Pancrea
23	chr3:46770600-46770800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:46770600-46770800	Enhancers	Pancreas	Pancrea
25	chr3:46770600-46771000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:46770800-46771000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:46770800-46776200	Weak transcription	Pancreas	Pancrea
28	chr3:46770800-46778000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:46772200-46773400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr3:46772400-46773600	Enhancers	GM12878-XiMat	blood
31	chr3:46773000-46773200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr3:46775400-46775600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr3:46775600-46775800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr3:46776200-46776600	Enhancers	Pancreas	Pancrea
35	chr3:46776600-46778800	Weak transcription	Pancreas	Pancrea
36	chr3:46777000-46779800	Enhancers	Thymus	Thymus
37	chr3:46778000-46778200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:46778000-46778200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr3:46778000-46780000	Enhancers	Fetal Thymus	thymus
40	chr3:46778200-46778400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr3:46778200-46778800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:46778400-46779200	Enhancers	Fetal Muscle Trunk	muscle
43	chr3:46778600-46779200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr3:46778600-46779200	Enhancers	Fetal Muscle Leg	muscle
45	chr3:46778800-46779000	Bivalent Enhancer	HSMM	muscle
46	chr3:46778800-46779200	Enhancers	Left Ventricle	heart
47	chr3:46778800-46779400	Enhancers	Pancreas	Pancrea
48	chr3:46779000-46779200	Enhancers	Spleen	Spleen
49	chr3:46779000-46779400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
50	chr3:46779200-46782000	Weak transcription	Left Ventricle	heart

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