Variant report

Variant	nsv834725
Chromosome Location	chr3:70199671-70395784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:578)
CpG islands
(count:366)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:70313397-70314038	HepG2	liver:	n/a	n/a
2	ATF3	chr3:70330643-70331286	A549	lung:	n/a	n/a
3	BACH1	chr3:70283052-70283329	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:70360134-70360158	K562	blood:	n/a	n/a
5	BCL3	chr3:70330602-70331311	A549	lung:	n/a	n/a
6	BCL3	chr3:70313284-70313962	A549	lung:	n/a	n/a
7	BCL3	chr3:70330686-70331249	A549	lung:	n/a	n/a
8	BCL3	chr3:70249451-70249729	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:70230966-70230996	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:70345132-70345162	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:70287413-70287437	A549	lung:	n/a	n/a
12	BHLHE40	chr3:70313367-70313809	HepG2	liver:	n/a	n/a
13	CBX3	chr3:70340237-70340430	K562	blood:	n/a	n/a
14	CEBPB	chr3:70298452-70299314	Hela-S3	cervix:	n/a	chr3:70299013-70299025 chr3:70299220-70299231 chr3:70298519-70298530
15	CEBPB	chr3:70330602-70331397	A549	lung:	n/a	n/a
16	CEBPB	chr3:70348297-70348536	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:70353517-70353712	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:70353466-70353709	A549	lung:	n/a	n/a
19	CEBPB	chr3:70386597-70386835	HepG2	liver:	n/a	chr3:70386718-70386729 chr3:70386717-70386728 chr3:70386743-70386754 chr3:70386717-70386730 chr3:70386717-70386728 chr3:70386717-70386730
20	CEBPB	chr3:70280494-70280726	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:70355088-70355214	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:70330850-70331283	A549	lung:	n/a	n/a
23	CEBPB	chr3:70288798-70289052	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:70386681-70386880	A549	lung:	n/a	chr3:70386718-70386729 chr3:70386717-70386728 chr3:70386743-70386754 chr3:70386717-70386730 chr3:70386717-70386728 chr3:70386717-70386730
25	CEBPB	chr3:70378111-70378296	K562	blood:	n/a	n/a
26	CEBPB	chr3:70291133-70291339	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:70330783-70331335	A549	lung:	n/a	n/a
28	CEBPB	chr3:70313188-70314071	A549	lung:	n/a	n/a
29	CEBPB	chr3:70218475-70218758	A549	lung:	n/a	chr3:70218618-70218629 chr3:70218620-70218629 chr3:70218620-70218629 chr3:70218620-70218629 chr3:70218620-70218629 chr3:70218619-70218630 chr3:70218617-70218634
30	CEBPB	chr3:70347482-70347867	Hela-S3	cervix:	n/a	chr3:70347639-70347652
31	CEBPB	chr3:70218505-70218742	HepG2	liver:	n/a	chr3:70218618-70218629 chr3:70218620-70218629 chr3:70218620-70218629 chr3:70218620-70218629 chr3:70218620-70218629 chr3:70218619-70218630 chr3:70218617-70218634
32	CEBPB	chr3:70291093-70291356	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:70313339-70313888	A549	lung:	n/a	n/a
34	CEBPB	chr3:70330700-70331346	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:70348318-70348533	A549	lung:	n/a	n/a
36	CEBPB	chr3:70245758-70245985	A549	lung:	n/a	n/a
37	CTCF	chr3:70228480-70228630	GM12864	blood:	n/a	n/a
38	CTCF	chr3:70358040-70358190	HAc	cerebellar:	n/a	n/a
39	CTCF	chr3:70358016-70358183	GM19239	blood:	n/a	n/a
40	CTCF	chr3:70357980-70358130	GM12871	blood:	n/a	n/a
41	CTCF	chr3:70358060-70358210	RPTEC	kidney:	n/a	n/a
42	CTCF	chr3:70358038-70358202	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr3:70357880-70358030	A549	lung:	n/a	n/a
44	CTCF	chr3:70357980-70358130	HFF	foreskin:	n/a	n/a
45	CTCF	chr3:70358060-70358210	AG10803	skin:	n/a	n/a
46	CTCF	chr3:70358060-70358210	AG04450	lung:	n/a	n/a
47	CTCF	chr3:70358000-70358150	AG04450	lung:	n/a	n/a
48	CTCF	chr3:70358020-70358170	GM12872	blood:	n/a	n/a
49	CTCF	chr3:70358000-70358150	GM12878	blood:	n/a	n/a
50	CTCF	chr3:70331020-70331170	A549	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:70374240-70374290	MCF10A-Er-Src	breast:	n/a
2	chr3:70339935-70339985	NHBE	bronchial:	n/a
3	chr3:70265622-70265672	HL-60	blood:	n/a
4	chr3:70265622-70265672	AG04450	lung:	fetal
5	chr3:70231495-70231545	NHDF-neo	bronchial:	n/a
6	chr3:70374240-70374290	MCF-7	breast:	n/a
7	chr3:70339935-70339985	HIPEpiC	eye:	n/a
8	chr3:70360572-70360622	AG04449	skin:	fetal
9	chr3:70339967-70340017	ovcar-3	ovarian:	n/a
10	chr3:70231495-70231545	GM19239	blood:	n/a
11	chr3:70374240-70374290	HIPEpiC	eye:	n/a
12	chr3:70339967-70340017	H1-hESC	embryonic stem cell:	embryo
13	chr3:70374240-70374290	Caco-2	colon:	n/a
14	chr3:70360572-70360622	MCF10A-Er-Src	breast:	n/a
15	chr3:70265622-70265672	MCF-7	breast:	n/a
16	chr3:70231495-70231545	IMR90	lung:	fetal
17	chr3:70339967-70340017	Caco-2	colon:	n/a
18	chr3:70231495-70231545	PrEC	prostate:	n/a
19	chr3:70265622-70265672	GM12891	blood:	n/a
20	chr3:70231495-70231545	SK-N-SH	brain:	n/a
21	chr3:70360572-70360622	HNPCEpiC	eye:	n/a
22	chr3:70360572-70360622	HIPEpiC	eye:	n/a
23	chr3:70339967-70340017	HL-60	blood:	n/a
24	chr3:70374240-70374290	H1-hESC	embryonic stem cell:	embryo
25	chr3:70231495-70231545	HUVEC	blood vessel:	n/a
26	chr3:70339967-70340017	NHBE	bronchial:	n/a
27	chr3:70339935-70339985	ECC-1	luminal epithelium:	n/a
28	chr3:70231495-70231545	HepG2	liver:	n/a
29	chr3:70339967-70340017	CMK	blood:	n/a
30	chr3:70231495-70231545	HRE	kidney:	n/a
31	chr3:70360572-70360622	NH-A	brain:	n/a
32	chr3:70374240-70374290	PANC-1	pancreas:	n/a
33	chr3:70265622-70265672	RPTEC	kidney:	n/a
34	chr3:70339967-70340017	HIPEpiC	eye:	n/a
35	chr3:70265622-70265672	CMK	blood:	n/a
36	chr3:70231495-70231545	T-47D	breast:	n/a
37	chr3:70339935-70339985	IMR90	lung:	fetal
38	chr3:70339935-70339985	CMK	blood:	n/a
39	chr3:70374240-70374290	AG04450	lung:	fetal
40	chr3:70231495-70231545	Hela-S3	cervix:	n/a
41	chr3:70339935-70339985	RPTEC	kidney:	n/a
42	chr3:70374240-70374290	HCM	heart:	n/a
43	chr3:70339935-70339985	NT2-D1	testis:	n/a
44	chr3:70265622-70265672	SK-N-SH_RA	brain:	n/a
45	chr3:70374240-70374290	GM06990	blood:	n/a
46	chr3:70374240-70374290	Hepatocyte	liver:	n/a
47	chr3:70360572-70360622	HRCEpiC	kidney:	n/a
48	chr3:70265622-70265672	GM19239	blood:	n/a
49	chr3:70360572-70360622	PANC-1	pancreas:	n/a
50	chr3:70339935-70339985	SKMC	muscle:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:70322866..70326501-chr3:70330007..70332995,3	MCF-7	breast:
2	chr3:70207198..70209047-chr3:70217090..70218982,2	K562	blood:
3	chr3:70207198..70209047-chr3:70217090..70218982,2	K562	blood:
4	chr3:70367804..70369875-chr3:70383298..70385013,2	K562	blood:
5	chr3:70339740..70342430-chr3:70343681..70346313,2	K562	blood:
6	chr3:70248598..70251037-chr3:70286556..70288471,2	K562	blood:
7	chr3:70242057..70244095-chr3:70247137..70248746,2	MCF-7	breast:
8	chr14:104497825..104500668-chr3:70209733..70212637,2	MCF-7	breast:
9	chr3:70248923..70251041-chr3:70253421..70256043,2	K562	blood:
10	chr3:70248598..70251037-chr3:70286556..70288471,2	K562	blood:
11	chr3:70201852..70203661-chr3:70215666..70218208,2	K562	blood:
12	chr3:70367804..70369875-chr3:70383298..70385013,2	K562	blood:
13	chr3:70261823..70265840-chr3:70267678..70269948,4	K562	blood:
14	chr3:70348474..70350327-chr3:70352138..70355044,2	K562	blood:
15	chr3:70246697..70248823-chr3:70250628..70252259,2	K562	blood:
16	chr11:95876540..95879060-chr3:70394191..70396704,2	MCF-7	breast:
17	chr3:70339740..70342430-chr3:70343681..70346313,2	K562	blood:
18	chr3:70251160..70253986-chr3:70255377..70257748,2	K562	blood:
19	chr3:70254171..70256260-chr3:70259844..70261403,2	K562	blood:
20	chr3:70322866..70326501-chr3:70330007..70332995,3	MCF-7	breast:
21	chr3:70242057..70244095-chr3:70247137..70248746,2	MCF-7	breast:
22	chr3:70246697..70248823-chr3:70250628..70252259,2	K562	blood:
23	chr3:70201852..70203661-chr3:70215666..70218208,2	K562	blood:
24	chr3:70261823..70265840-chr3:70267678..70269948,4	K562	blood:
25	chr3:70348474..70350327-chr3:70352138..70355044,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MITF-8	chr3:70304138-70304423	l_2385_chr3:70299646-70304423_testes
2	lnc-MITF-3	chr3:70216957-70217685	XLOC_002697
3	lnc-MITF-3	chr3:70221448-70221713	XLOC_002697
4	lnc-MITF-8	chr3:70299647-70300375	l_2385_chr3:70299646-70304423_testes

No data

Variant related genes	Relation type
ENSG00000242120	TF binding region
ENSG00000222615	TF binding region
ENSG00000242120	CpG island
ENSG00000222615	CpG island
ENSG00000242120	chromatin interactions

Extended variants
information (count: 3924 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3924 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561470978	chr3:70199680-70199681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530304985	chr3:70199704-70199705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540504475	chr3:70199728-70199729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560546889	chr3:70199730-70199731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532624268	chr3:70199754-70199755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75003725	chr3:70199764-70199765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528308956	chr3:70199776-70199777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192806985	chr3:70199780-70199781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373733283	chr3:70199815-70199816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184308434	chr3:70199819-70199820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11128165	chr3:70199824-70199825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370927174	chr3:70199906-70199907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72937582	chr3:70199907-70199908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572134094	chr3:70199975-70199976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547163653	chr3:70199986-70199987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372845484	chr3:70199987-70199988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190667017	chr3:70199990-70199991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539102951	chr3:70199997-70199998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540031105	chr3:70200022-70200023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs193004287	chr3:70200025-70200026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542878843	chr3:70200097-70200098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575627642	chr3:70200115-70200116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535146439	chr3:70200152-70200153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13319242	chr3:70200153-70200154	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs202082666	chr3:70200256-70200257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs66542432	chr3:70200257-70200258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71126482	chr3:70200259-70200260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200413824	chr3:70200260-70200261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6806567	chr3:70200275-70200276	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551482639	chr3:70200311-70200312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540943578	chr3:70200378-70200379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370002980	chr3:70200387-70200388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560627832	chr3:70200394-70200395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577516310	chr3:70200403-70200404	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7431658	chr3:70200450-70200451	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575898723	chr3:70200465-70200466	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35382188	chr3:70200520-70200521	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531714745	chr3:70200560-70200561	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78883357	chr3:70200583-70200584	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531996107	chr3:70201601-70201602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573451480	chr3:70201657-70201658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550543602	chr3:70201707-70201708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74797254	chr3:70201738-70201739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149770393	chr3:70201758-70201759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs6798250	chr3:70201770-70201771	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181058402	chr3:70201784-70201785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185795338	chr3:70201792-70201793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565800755	chr3:70202490-70202491	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs528070252	chr3:70202509-70202510	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551365571	chr3:70202570-70202571	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Mental retardation	17847001	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70198400-70200400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr3:70198800-70200000	Enhancers	Fetal Brain Female	brain
3	chr3:70199200-70200600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr3:70199800-70200000	Enhancers	Aorta	Aorta
5	chr3:70200400-70200600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
6	chr3:70201600-70201800	Enhancers	Fetal Lung	lung
7	chr3:70202400-70203200	Active TSS	A549	lung
8	chr3:70204400-70204800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:70220200-70220600	Enhancers	Fetal Brain Male	brain
10	chr3:70224400-70224600	Enhancers	Aorta	Aorta
11	chr3:70224600-70240000	Weak transcription	Aorta	Aorta
12	chr3:70226400-70227600	Weak transcription	Fetal Brain Male	brain
13	chr3:70227000-70227800	Enhancers	Colon Smooth Muscle	Colon
14	chr3:70227000-70230800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:70227200-70227600	Enhancers	Rectal Smooth Muscle	rectum
16	chr3:70227600-70227800	Enhancers	Fetal Brain Male	brain
17	chr3:70227600-70229200	Enhancers	Adipose Nuclei	Adipose
18	chr3:70227600-70230600	Enhancers	Primary B cells from peripheral blood	blood
19	chr3:70227600-70231000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr3:70227800-70228600	Weak transcription	Colon Smooth Muscle	Colon
21	chr3:70227800-70228600	Weak transcription	Fetal Brain Male	brain
22	chr3:70227800-70228800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr3:70227800-70229600	Enhancers	Primary B cells from cord blood	blood
24	chr3:70227800-70229800	Enhancers	GM12878-XiMat	blood
25	chr3:70228200-70229600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:70228400-70229000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr3:70228400-70229200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr3:70228400-70229200	Enhancers	HMEC	breast
29	chr3:70228600-70229000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr3:70228600-70229400	Enhancers	Colon Smooth Muscle	Colon
31	chr3:70228600-70233600	Enhancers	Fetal Brain Male	brain
32	chr3:70228800-70229000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr3:70229000-70229200	Enhancers	Fetal Brain Female	brain
34	chr3:70229200-70230200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr3:70229200-70230400	Weak transcription	Fetal Brain Female	brain
36	chr3:70229400-70231000	Weak transcription	Colon Smooth Muscle	Colon
37	chr3:70229800-70230400	Flanking Active TSS	GM12878-XiMat	blood
38	chr3:70229800-70232000	Enhancers	Fetal Stomach	stomach
39	chr3:70230000-70233000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr3:70230000-70233200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:70230200-70230400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr3:70230200-70230400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr3:70230200-70230400	Enhancers	Primary B cells from cord blood	blood
44	chr3:70230200-70230600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:70230200-70233200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr3:70230400-70230800	Enhancers	GM12878-XiMat	blood
47	chr3:70230400-70231400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr3:70230400-70231400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr3:70230400-70231400	Enhancers	Fetal Brain Female	brain
50	chr3:70230400-70233200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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