Variant report

Variant	nsv1008289
Chromosome Location	chr3:46783247-46849577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
4	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
7	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
8	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
9	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
10	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
11	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
12	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
14	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
15	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a
16	CTCF	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
17	CTCF	chr3:46797989-46798564	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
18	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
19	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
20	CTCF	chr3:46798134-46798571	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
21	CTCF	chr3:46792209-46792538	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
22	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr3:46792360-46792510	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
24	CTCF	chr3:46798280-46798435	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
25	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
28	CTCF	chr3:46794180-46794330	GM12873	blood:	n/a	n/a
29	CTCF	chr3:46792287-46792555	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
30	CTCF	chr3:46798034-46798529	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
31	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
32	CTCF	chr3:46792356-46792487	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
33	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
34	CTCF	chr3:46794616-46794658	GM19240	blood:	n/a	n/a
35	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
36	CTCF	chr3:46794500-46794650	GM12866	blood:	n/a	n/a
37	CTCF	chr3:46794500-46794650	GM12873	blood:	n/a	n/a
38	CTCF	chr3:46798156-46798539	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
39	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
40	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr3:46798300-46798450	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
42	CTCF	chr3:46798359-46798450	LNCaP	prostate:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
43	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr3:46794360-46794510	GM12873	blood:	n/a	n/a
45	CTCF	chr3:46794460-46794610	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr3:46792152-46792625	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
47	CTCF	chr3:46798300-46798450	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
48	CTCF	chr3:46798136-46798509	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
49	CTCF	chr3:46794520-46794670	GM12864	blood:	n/a	n/a
50	CTCF	chr3:46794500-46794650	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46792364-46792414	NT2-D1	testis:	n/a
2	chr3:46792364-46792414	NT2-D1	testis:	n/a
3	chr3:46794154-46794204	HEEpiC	esophagus:	n/a
4	chr3:46785957-46786007	SAEC	small airway:	n/a
5	chr3:46797928-46797978	HCPEpiC	choroid plexus:	n/a
6	chr3:46791477-46791527	HEEpiC	esophagus:	n/a
7	chr3:46786238-46786288	HCT-116	colon:	n/a
8	chr3:46792364-46792414	U87	brain:	n/a
9	chr3:46792357-46792407	AG09319	gingival:	n/a
10	chr3:46796026-46796076	AG09309	skin:	n/a
11	chr3:46799010-46799060	U87	brain:	n/a
12	chr3:46786387-46786437	GM19239	blood:	n/a
13	chr3:46792462-46792512	A549	lung:	n/a
14	chr3:46792462-46792512	Hela-S3	cervix:	n/a
15	chr3:46797928-46797978	NT2-D1	testis:	n/a
16	chr3:46792023-46792073	SK-N-MC	brain:	n/a
17	chr3:46796026-46796076	HEEpiC	esophagus:	n/a
18	chr3:46799010-46799060	HEEpiC	esophagus:	n/a
19	chr3:46792462-46792512	AG04450	lung:	fetal
20	chr3:46796026-46796076	MCF-7	breast:	n/a
21	chr3:46789735-46789785	HRCEpiC	kidney:	n/a
22	chr3:46790182-46790232	LNCaP	prostate:	n/a
23	chr3:46797928-46797978	AG09319	gingival:	n/a
24	chr3:46792364-46792414	A549	lung:	n/a
25	chr3:46798240-46798290	SKMC	muscle:	n/a
26	chr3:46794154-46794204	A549	lung:	n/a
27	chr3:46792192-46792242	Caco-2	colon:	n/a
28	chr3:46799010-46799060	GM12891	blood:	n/a
29	chr3:46790182-46790232	HCM	heart:	n/a
30	chr3:46797928-46797978	SK-N-SH	brain:	n/a
31	chr3:46794154-46794204	HIPEpiC	eye:	n/a
32	chr3:46785957-46786007	GM19239	blood:	n/a
33	chr3:46796026-46796076	T-47D	breast:	n/a
34	chr3:46785957-46786007	LNCaP	prostate:	n/a
35	chr3:46786387-46786437	PrEC	prostate:	n/a
36	chr3:46801208-46801258	HEK293	kidney:	embryo
37	chr3:46794154-46794204	HL-60	blood:	n/a
38	chr3:46792357-46792407	SK-N-SH	brain:	n/a
39	chr3:46786387-46786437	H1-hESC	embryonic stem cell:	embryo
40	chr3:46796026-46796076	U87	brain:	n/a
41	chr3:46791477-46791527	K562	blood:	n/a
42	chr3:46792023-46792073	SK-N-SH	brain:	n/a
43	chr3:46786387-46786437	PANC-1	pancreas:	n/a
44	chr3:46799010-46799060	SAEC	small airway:	n/a
45	chr3:46786387-46786437	NT2-D1	testis:	n/a
46	chr3:46789735-46789785	Jurkat	blood:	n/a
47	chr3:46786387-46786437	Hepatocyte	liver:	n/a
48	chr3:46792192-46792242	U87	brain:	n/a
49	chr3:46792357-46792407	HRPEpiC	eye:	n/a
50	chr3:46789735-46789785	AG10803	skin:	n/a

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

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

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS45	TF binding region
ENSG00000238013	CpG island
PRSS45	CpG island
ENSG00000188086	chromatin interactions

Extended variants
information (count: 1065 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6805152	chr3:46783247-46783248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544467022	chr3:46783276-46783277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562677170	chr3:46783290-46783291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377503843	chr3:46783374-46783375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34229777	chr3:46783406-46783407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6810260	chr3:46783432-46783433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs182066517	chr3:46783538-46783539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4682827	chr3:46783548-46783549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4683270	chr3:46783549-46783550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60294661	chr3:46783556-46783557	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs549051292	chr3:46783602-46783603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59828146	chr3:46783629-46783630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs531306243	chr3:46783635-46783636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs59721087	chr3:46783637-46783638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs112576071	chr3:46783664-46783665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60394190	chr3:46783672-46783673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571520125	chr3:46783700-46783701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538915063	chr3:46783718-46783719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs57661142	chr3:46783757-46783758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs566052211	chr3:46783839-46783840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114352853	chr3:46783849-46783850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201730160	chr3:46783919-46783920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367859695	chr3:46783930-46783931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372095426	chr3:46783945-46783946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76238378	chr3:46783955-46783956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58830807	chr3:46783959-46783960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs542793284	chr3:46783962-46783963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200067285	chr3:46783964-46783965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112779825	chr3:46783969-46783970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201204047	chr3:46783972-46783973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200871872	chr3:46783973-46783974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs267599846	chr3:46783977-46783978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201868432	chr3:46783983-46783984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150250561	chr3:46783992-46783993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369619696	chr3:46783993-46783994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577935161	chr3:46783998-46783999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375965344	chr3:46784013-46784014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112874766	chr3:46784038-46784039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199904747	chr3:46784048-46784049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373445272	chr3:46784103-46784104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs58263848	chr3:46784133-46784134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs371210238	chr3:46784144-46784145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572797615	chr3:46784180-46784181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138709808	chr3:46784198-46784199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374454827	chr3:46784203-46784204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs59804016	chr3:46784221-46784222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs113825383	chr3:46784317-46784318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs60223148	chr3:46784318-46784319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs59859985	chr3:46784329-46784330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs61298367	chr3:46784352-46784353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:99 , 50 per page) page: 1 2

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	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
4	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
5	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
6	chr3:46780800-46785000	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:46784400-46785200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:46784400-46785200	Enhancers	Fetal Stomach	stomach
9	chr3:46784600-46785000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:46784600-46785000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:46784600-46785000	Enhancers	Placenta	Placenta
12	chr3:46784600-46785200	Enhancers	Fetal Lung	lung
13	chr3:46784600-46785200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr3:46784800-46785200	Enhancers	Fetal Intestine Small	intestine
15	chr3:46785000-46785200	Weak transcription	Placenta	Placenta
16	chr3:46785000-46785800	Strong transcription	Skeletal Muscle Male	skeletal muscle
17	chr3:46785000-46786200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:46785200-46785600	Enhancers	Placenta	Placenta
20	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
21	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
22	chr3:46785800-46786200	Enhancers	GM12878-XiMat	blood
23	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr3:46786200-46787800	Weak transcription	GM12878-XiMat	blood
25	chr3:46786400-46786600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr3:46787800-46789200	Enhancers	GM12878-XiMat	blood
27	chr3:46789200-46794200	Weak transcription	GM12878-XiMat	blood
28	chr3:46789600-46789800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:46789600-46790400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr3:46789600-46790400	Enhancers	Fetal Muscle Leg	muscle
31	chr3:46789800-46790000	Enhancers	Fetal Stomach	stomach
32	chr3:46789800-46790200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr3:46789800-46790400	Enhancers	Placenta	Placenta
34	chr3:46789800-46790600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr3:46790600-46791800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr3:46791800-46792400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:46792200-46792800	Flanking Bivalent TSS/Enh	K562	blood
38	chr3:46792400-46794200	Enhancers	Placenta Amnion	Placenta Amnion
39	chr3:46792400-46797800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:46792800-46795000	Enhancers	Thymus	Thymus
41	chr3:46793400-46795200	Enhancers	Fetal Thymus	thymus
42	chr3:46793400-46800000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:46793800-46794200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:46794200-46795000	Enhancers	GM12878-XiMat	blood
45	chr3:46795000-46796000	Weak transcription	Thymus	Thymus
46	chr3:46795200-46796200	Weak transcription	Fetal Thymus	thymus
47	chr3:46795600-46798000	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr3:46796000-46796800	Enhancers	Thymus	Thymus
49	chr3:46796400-46796600	Enhancers	Fetal Thymus	thymus
50	chr3:46797600-46797800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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