Variant report

Variant	nsv876747
Chromosome Location	chr3:46785355-46867685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:1712)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 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	chr3:46792308-46792631	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	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
5	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
8	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
9	CBX3	chr3:46864817-46865093	K562	blood:	n/a	n/a
10	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
11	CBX3	chr3:46862333-46862734	K562	blood:	n/a	n/a
12	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
13	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
14	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
15	CBX3	chr3:46862397-46862721	K562	blood:	n/a	n/a
16	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
17	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
18	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
20	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
21	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
22	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
23	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
24	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
25	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
27	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	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	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
31	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
32	CTCF	chr3:46798136-46798509	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
33	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
34	CTCF	chr3:46792152-46792625	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
35	CTCF	chr3:46798156-46798539	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
36	CTCF	chr3:46798034-46798529	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
37	CTCF	chr3:46794520-46794670	GM12864	blood:	n/a	n/a
38	CTCF	chr3:46850120-46850270	GM12873	blood:	n/a	chr3:46850217-46850226
39	CTCF	chr3:46854876-46854950	GM20000	blood:	n/a	n/a
40	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
41	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:46794500-46794650	GM12872	blood:	n/a	n/a
43	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
44	CTCF	chr3:46794500-46794650	GM12873	blood:	n/a	n/a
45	CTCF	chr3:46798300-46798450	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
46	CTCF	chr3:46865442-46865496	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr3:46794360-46794510	GM12873	blood:	n/a	n/a
48	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
49	CTCF	chr3:46798300-46798450	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
50	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46787073-46787123	GM12878	blood:	n/a
2	chr3:46791477-46791527	MCF-7	breast:	n/a
3	chr3:46799010-46799060	AG04450	lung:	fetal
4	chr3:46792023-46792073	HMEC	breast:	n/a
5	chr3:46787073-46787123	GM12878	blood:	n/a
6	chr3:46791477-46791527	MCF-7	breast:	n/a
7	chr3:46799010-46799060	AG04450	lung:	fetal
8	chr3:46792023-46792073	HMEC	breast:	n/a
9	chr3:46853850-46853900	CMK	blood:	n/a
10	chr3:46853910-46853960	Hela-S3	cervix:	n/a
11	chr3:46792462-46792512	SKMC	muscle:	n/a
12	chr3:46854231-46854281	HMEC	breast:	n/a
13	chr3:46792192-46792242	GM19239	blood:	n/a
14	chr3:46789735-46789785	ovcar-3	ovarian:	n/a
15	chr3:46789735-46789785	BE2_C	brain:	n/a
16	chr3:46790182-46790232	PANC-1	pancreas:	n/a
17	chr3:46850588-46850638	HRCEpiC	kidney:	n/a
18	chr3:46792023-46792073	AG04449	skin:	fetal
19	chr3:46792462-46792512	AG09309	skin:	n/a
20	chr3:46786238-46786288	NH-A	brain:	n/a
21	chr3:46853850-46853900	AG04450	lung:	fetal
22	chr3:46798240-46798290	HRE	kidney:	n/a
23	chr3:46792462-46792512	PrEC	prostate:	n/a
24	chr3:46792462-46792512	LNCaP	prostate:	n/a
25	chr3:46792462-46792512	T-47D	breast:	n/a
26	chr3:46792357-46792407	SK-N-SH_RA	brain:	n/a
27	chr3:46792023-46792073	GM12892	blood:	n/a
28	chr3:46790182-46790232	GM19239	blood:	n/a
29	chr3:46794154-46794204	HCM	heart:	n/a
30	chr3:46853631-46853681	HEK293	kidney:	embryo
31	chr3:46853910-46853960	MCF10A-Er-Src	breast:	n/a
32	chr3:46853910-46853960	AG04449	skin:	fetal
33	chr3:46853910-46853960	AG09309	skin:	n/a
34	chr3:46787073-46787123	BJ	skin:	n/a
35	chr3:46799010-46799060	GM12891	blood:	n/a
36	chr3:46789735-46789785	GM19239	blood:	n/a
37	chr3:46792023-46792073	HL-60	blood:	n/a
38	chr3:46853631-46853681	AG09319	gingival:	n/a
39	chr3:46786238-46786288	HepG2	liver:	n/a
40	chr3:46801208-46801258	HMEC	breast:	n/a
41	chr3:46794154-46794204	LNCaP	prostate:	n/a
42	chr3:46789735-46789785	BJ	skin:	n/a
43	chr3:46854231-46854281	Jurkat	blood:	n/a
44	chr3:46799010-46799060	NT2-D1	testis:	n/a
45	chr3:46789735-46789785	AG04449	skin:	fetal
46	chr3:46799010-46799060	HepG2	liver:	n/a
47	chr3:46792192-46792242	BE2_C	brain:	n/a
48	chr3:46797928-46797978	BJ	skin:	n/a
49	chr3:46790182-46790232	BE2_C	brain:	n/a
50	chr3:46856803-46856853	HCPEpiC	choroid plexus:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
2	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
3	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
4	chr3:46783774..46785518-chr3:46915413..46918248,2	MCF-7	breast:
5	chr3:46864966..46867284-chr3:46873787..46876389,2	K562	blood:
6	chr3:46858188..46860125-chr3:46939783..46942119,2	K562	blood:
7	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
8	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
9	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
10	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
11	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
12	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
13	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
14	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
15	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:
16	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
17	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
18	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
19	chr3:46853522..46855564-chr3:46864841..46866780,2	K562	blood:
20	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
21	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
22	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
23	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
24	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
25	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
26	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
27	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
28	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
29	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
30	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
31	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS50	TF binding region
PRSS44	TF binding region
PRSS45	TF binding region
ENSG00000238013	CpG island
PRSS50	CpG island
PRSS44	CpG island
PRSS45	CpG island
ENSG00000178055	chromatin interactions
ENSG00000206549	chromatin interactions
ENSG00000188086	chromatin interactions

Extended variants
information (count: 1538 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1538 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4075012	chr3:46785355-46785356	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530967795	chr3:46785367-46785368	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199654171	chr3:46785415-46785416	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568521205	chr3:46785424-46785425	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375520921	chr3:46785432-46785433	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149457784	chr3:46785433-46785434	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372249018	chr3:46785453-46785454	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75143436	chr3:46785454-46785455	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369589811	chr3:46785466-46785467	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200583939	chr3:46785486-46785487	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371558672	chr3:46785494-46785495	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375359873	chr3:46785498-46785499	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144108838	chr3:46785502-46785503	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536132748	chr3:46785515-46785516	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190009780	chr3:46785517-46785518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202037937	chr3:46785518-46785519	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377008361	chr3:46785525-46785526	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201746980	chr3:46785536-46785537	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374553276	chr3:46785546-46785547	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201584451	chr3:46785547-46785548	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368138658	chr3:46785567-46785568	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79520135	chr3:46785582-46785583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376630125	chr3:46785642-46785643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370763199	chr3:46785643-46785644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373571824	chr3:46785645-46785646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554333195	chr3:46785756-46785757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576825482	chr3:46785865-46785866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148279437	chr3:46785882-46785883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141248149	chr3:46785899-46785900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530347234	chr3:46785946-46785947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542530401	chr3:46785950-46785951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564017328	chr3:46785965-46785966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531232937	chr3:46785991-46785992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552563190	chr3:46786039-46786040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182545637	chr3:46786060-46786061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34540907	chr3:46786132-46786133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs72899429	chr3:46786150-46786151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372133864	chr3:46786153-46786154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200785356	chr3:46786154-46786155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79958632	chr3:46786162-46786163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368296415	chr3:46786186-46786187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140073285	chr3:46786195-46786196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372045714	chr3:46786203-46786204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371708089	chr3:46786238-46786239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186615377	chr3:46786239-46786240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376116603	chr3:46786258-46786259	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs192802961	chr3:46786269-46786270	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs62246252	chr3:46786340-46786341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558097154	chr3:46786373-46786374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576795471	chr3:46786386-46786387	Weak transcription	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:503 , 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	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
4	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
5	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
6	chr3:46785000-46785800	Strong transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:46785000-46786200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:46785200-46785600	Enhancers	Placenta	Placenta
10	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
11	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
12	chr3:46785800-46786200	Enhancers	GM12878-XiMat	blood
13	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr3:46786200-46787800	Weak transcription	GM12878-XiMat	blood
15	chr3:46786400-46786600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr3:46787800-46789200	Enhancers	GM12878-XiMat	blood
17	chr3:46789200-46794200	Weak transcription	GM12878-XiMat	blood
18	chr3:46789600-46789800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr3:46789600-46790400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr3:46789600-46790400	Enhancers	Fetal Muscle Leg	muscle
21	chr3:46789800-46790000	Enhancers	Fetal Stomach	stomach
22	chr3:46789800-46790200	Enhancers	H9 Cell Line	embryonic stem cell
23	chr3:46789800-46790400	Enhancers	Placenta	Placenta
24	chr3:46789800-46790600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:46790600-46791800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:46791800-46792400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:46792200-46792800	Flanking Bivalent TSS/Enh	K562	blood
28	chr3:46792400-46794200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr3:46792400-46797800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr3:46792800-46795000	Enhancers	Thymus	Thymus
31	chr3:46793400-46795200	Enhancers	Fetal Thymus	thymus
32	chr3:46793400-46800000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:46793800-46794200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:46794200-46795000	Enhancers	GM12878-XiMat	blood
35	chr3:46795000-46796000	Weak transcription	Thymus	Thymus
36	chr3:46795200-46796200	Weak transcription	Fetal Thymus	thymus
37	chr3:46795600-46798000	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr3:46796000-46796800	Enhancers	Thymus	Thymus
39	chr3:46796400-46796600	Enhancers	Fetal Thymus	thymus
40	chr3:46797600-46797800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr3:46797600-46797800	Bivalent Enhancer	K562	blood
42	chr3:46797600-46798400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr3:46797800-46798400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:46798000-46798600	Enhancers	Placenta	Placenta
45	chr3:46798000-46798600	Active TSS	K562	blood
46	chr3:46798000-46801400	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr3:46798400-46801200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr3:46800600-46801400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:46801000-46801200	Enhancers	Fetal Stomach	stomach
50	chr3:46801000-46801400	Enhancers	Fetal Kidney	kidney

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