Variant report

Variant	nsv877615
Chromosome Location	chr3:145910430-145988231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:781)
CpG islands
(count:796)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:145936731-145937064	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:145939594-145940831	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:145941119-145941527	HepG2	liver:	n/a	n/a
4	ATF1	chr3:145959778-145959950	K562	blood:	n/a	n/a
5	BACH1	chr3:145968459-145969085	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:145936724-145936984	GM12878	blood:	n/a	chr3:145936966-145936975
7	BCL3	chr3:145939979-145940826	A549	lung:	n/a	n/a
8	BHLHE40	chr3:145968815-145968925	K562	blood:	n/a	n/a
9	BHLHE40	chr3:145940155-145940799	HepG2	liver:	n/a	n/a
10	BRCA1	chr3:145924542-145924588	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr3:145968563-145969088	K562	blood:	n/a	n/a
12	CEBPB	chr3:145933950-145934138	HepG2	liver:	n/a	chr3:145933968-145933979
13	CEBPB	chr3:145965734-145966053	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:145941324-145941541	A549	lung:	n/a	n/a
15	CEBPB	chr3:145928283-145928567	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:145975222-145975278	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:145946751-145947057	IMR90	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
18	CEBPB	chr3:145928233-145928556	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:145939105-145939296	A549	lung:	n/a	n/a
20	CEBPB	chr3:145982753-145983062	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:145936409-145936418	K562	blood:	n/a	n/a
22	CEBPB	chr3:145968610-145968627	K562	blood:	n/a	n/a
23	CEBPB	chr3:145940113-145940674	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:145933941-145934099	H1-hESC	embryonic stem cell:	n/a	chr3:145933968-145933979
25	CEBPB	chr3:145967604-145968179	Hela-S3	cervix:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
26	CEBPB	chr3:145943966-145944149	Hela-S3	cervix:	n/a	chr3:145944070-145944081
27	CEBPB	chr3:145968381-145969227	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr3:145946758-145947067	A549	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
29	CEBPB	chr3:145967627-145968119	IMR90	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
30	CEBPB	chr3:145946749-145947065	HepG2	liver:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
31	CEBPB	chr3:145943940-145944249	IMR90	lung:	n/a	chr3:145944070-145944081
32	CEBPB	chr3:145967646-145968183	A549	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
33	CEBPB	chr3:145943995-145944194	K562	blood:	n/a	chr3:145944070-145944081
34	CEBPB	chr3:145939060-145939389	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:145943941-145944226	HepG2	liver:	n/a	chr3:145944070-145944081
36	CEBPB	chr3:145928359-145928465	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr3:145967647-145967801	K562	blood:	n/a	n/a
38	CEBPZ	chr3:145940149-145940488	HepG2	liver:	n/a	n/a
39	CHD1	chr3:145983326-145983397	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr3:145940149-145940808	HepG2	liver:	n/a	n/a
41	CHD2	chr3:145968318-145969145	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr3:145968387-145969169	A549	lung:	n/a	n/a
43	CTBP2	chr3:145968207-145969151	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr3:145936760-145936910	NHEK	skin:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886
45	CTCF	chr3:145936780-145936930	GM12865	blood:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886
46	CTCF	chr3:145936504-145936621	GM12878	blood:	n/a	n/a
47	CTCF	chr3:145936727-145937013	ECC-1	luminal epithelium:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886
48	CTCF	chr3:145940600-145940750	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr3:145940660-145940810	Caco-2	colon:	n/a	n/a
50	CTCF	chr3:145936731-145936957	SK-N-SH_RA	brain:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145970385-145970435	RPTEC	kidney:	n/a
2	chr3:145968722-145968772	U87	brain:	n/a
3	chr3:145968726-145968776	K562	blood:	n/a
4	chr3:145970385-145970435	RPTEC	kidney:	n/a
5	chr3:145968722-145968772	U87	brain:	n/a
6	chr3:145968726-145968776	K562	blood:	n/a
7	chr3:145968242-145968292	GM19239	blood:	n/a
8	chr3:145968726-145968776	NH-A	brain:	n/a
9	chr3:145969625-145969675	Jurkat	blood:	n/a
10	chr3:145970385-145970435	HEK293	kidney:	embryo
11	chr3:145968620-145968670	HRPEpiC	eye:	n/a
12	chr3:145969007-145969057	SK-N-SH_RA	brain:	n/a
13	chr3:145969579-145969629	HAEpiC	amniotic membrane:	n/a
14	chr3:145970385-145970435	AoSMC	blood vessel:	n/a
15	chr3:145970385-145970435	NB4	blood:	n/a
16	chr3:145969718-145969768	PANC-1	pancreas:	n/a
17	chr3:145968242-145968292	K562	blood:	n/a
18	chr3:145969625-145969675	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:145969007-145969057	Caco-2	colon:	n/a
20	chr3:145968700-145968750	CMK	blood:	n/a
21	chr3:145968700-145968750	MCF10A-Er-Src	breast:	n/a
22	chr3:145968620-145968670	GM12878	blood:	n/a
23	chr3:145969718-145969768	BJ	skin:	n/a
24	chr3:145968700-145968750	HL-60	blood:	n/a
25	chr3:145968700-145968750	GM06990	blood:	n/a
26	chr3:145968242-145968292	GM12891	blood:	n/a
27	chr3:145969579-145969629	Hela-S3	cervix:	n/a
28	chr3:145968700-145968750	HRPEpiC	eye:	n/a
29	chr3:145968389-145968439	HMEC	breast:	n/a
30	chr3:145969625-145969675	HRCEpiC	kidney:	n/a
31	chr3:145968726-145968776	HIPEpiC	eye:	n/a
32	chr3:145968620-145968670	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:145970385-145970435	U87	brain:	n/a
34	chr3:145969625-145969675	ovcar-3	ovarian:	n/a
35	chr3:145968700-145968750	NH-A	brain:	n/a
36	chr3:145970385-145970435	ovcar-3	ovarian:	n/a
37	chr3:145969625-145969675	HRE	kidney:	n/a
38	chr3:145968389-145968439	SK-N-SH	brain:	n/a
39	chr3:145970385-145970435	A549	lung:	n/a
40	chr3:145969007-145969057	HMEC	breast:	n/a
41	chr3:145970385-145970435	NHDF-neo	bronchial:	n/a
42	chr3:145968722-145968772	HEK293	kidney:	embryo
43	chr3:145968696-145968746	HL-60	blood:	n/a
44	chr3:145969625-145969675	A549	lung:	n/a
45	chr3:145970385-145970435	GM06990	blood:	n/a
46	chr3:145968700-145968750	HMEC	breast:	n/a
47	chr3:145969625-145969675	H1-hESC	embryonic stem cell:	embryo
48	chr3:145969718-145969768	NT2-D1	testis:	n/a
49	chr3:145968620-145968670	HL-60	blood:	n/a
50	chr3:145969718-145969768	HEK293	kidney:	embryo

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:145936744..145937271-chr3:146358471..146359250,3	K562	blood:
2	chr3:145986622..145989134-chr3:145993598..145995580,2	MCF-7	breast:
3	chr3:145936710..145937294-chr3:146312292..146312926,2	K562	blood:
4	chr3:145936448..145937286-chr3:146358746..146359294,2	MCF-7	breast:
5	chr3:145883004..145884526-chr3:145908906..145911614,2	MCF-7	breast:
6	chr3:145938152..145938842-chr3:146358330..146358865,2	MCF-7	breast:
7	chr3:145979759..145981408-chr3:145991775..145993643,2	K562	blood:
8	chr3:145944002..145945741-chr3:145946348..145947988,2	K562	blood:
9	chr3:145940299..145941372-chr3:146044662..146045624,8	MCF-7	breast:
10	chr3:145936384..145937370-chr3:146044670..146045567,4	MCF-7	breast:
11	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
12	chr3:145938109..145938869-chr3:146044708..146045495,2	MCF-7	breast:
13	chr3:145936462..145937370-chr3:146044619..146045821,9	MCF-7	breast:
14	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
15	chr3:145938654..145939295-chr3:146044870..146045659,2	MCF-7	breast:
16	chr3:145937350..145938198-chr3:146044684..146045576,2	K562	blood:
17	chr3:145878599..145881384-chr3:145968449..145970595,2	MCF-7	breast:
18	chr3:145940254..145941134-chr3:146295120..146295978,3	MCF-7	breast:
19	chr3:145944002..145945741-chr3:145946348..145947988,2	K562	blood:
20	chr3:145936366..145937318-chr3:146295230..146296148,3	K562	blood:
21	chr3:145961600..145965107-chr3:145968575..145970473,3	K562	blood:

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PLSCR4	hsa-miR-15b-5p	chr3:145910629-145910622
2	PLSCR4	hsa-miR-15b-5p	chr3:145910793-145910815
3	PLSCR4	hsa-miR-16-5p	chr3:145910796-145910817
4	PLSCR4	hsa-miR-103a-3p	chr3:145910624-145910647
5	PLSCR4	hsa-miR-15b-5p	chr3:145910585-145910606
6	PLSCR4	hsa-miR-15b-5p	chr3:145910623-145910644
7	PLSCR4	hsa-miR-16-5p	chr3:145910585-145910607
8	PLSCR4	hsa-miR-16-5p	chr3:145910629-145910622
9	PLSCR4	hsa-miR-16-5p	chr3:145910623-145910644
10	PLSCR4	hsa-miR-124-3p	chr3:145910564-145910583

Variant related genes	Relation type
PLSCR4	TF binding region
PLSCR4	CpG island
ENSG00000114698	chromatin interactions
ENSG00000152952	chromatin interactions

Extended variants
information (count: 3209 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3209 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1059836	chr3:145910430-145910431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs55898074	chr3:145910446-145910447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143472690	chr3:145910447-145910448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540812689	chr3:145910510-145910511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537021642	chr3:145910540-145910541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73150819	chr3:145910543-145910544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554458210	chr3:145910549-145910550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371209269	chr3:145910555-145910556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572501304	chr3:145910567-145910568	Weak transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
10	rs76424208	chr3:145910600-145910601	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
11	rs148886956	chr3:145910601-145910602	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
12	rs539660697	chr3:145910603-145910604	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
13	rs12639098	chr3:145910607-145910608	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
14	rs3804658	chr3:145910608-145910609	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs76598265	chr3:145910618-145910619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376669109	chr3:145910640-145910641	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
17	rs78934870	chr3:145910713-145910714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573986776	chr3:145910805-145910806	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
19	rs540919295	chr3:145910826-145910827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3840207	chr3:145910839-145910840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs398082537	chr3:145910849-145910850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397805309	chr3:145910850-145910851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187644902	chr3:145910934-145910935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138858584	chr3:145910950-145910951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535339048	chr3:145911022-145911023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553595833	chr3:145911045-145911046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142069032	chr3:145911077-145911078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563352155	chr3:145911090-145911091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191762509	chr3:145911109-145911110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182493807	chr3:145911131-145911132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567111747	chr3:145911159-145911160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3749281	chr3:145911164-145911165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547739207	chr3:145911187-145911188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376273428	chr3:145911245-145911246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566065937	chr3:145911257-145911258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539621507	chr3:145911287-145911288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557974880	chr3:145911321-145911322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569803772	chr3:145911364-145911365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563999253	chr3:145911365-145911366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188311526	chr3:145911389-145911390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146294048	chr3:145911421-145911422	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541433566	chr3:145911432-145911433	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139533618	chr3:145911447-145911448	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141976573	chr3:145911464-145911465	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs998224	chr3:145911468-145911469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377109208	chr3:145911469-145911470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35859735	chr3:145911471-145911472	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150693427	chr3:145911475-145911476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192199239	chr3:145911513-145911514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184575685	chr3:145911650-145911651	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145880800-145914400	Weak transcription	Left Ventricle	heart
2	chr3:145883000-145913000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:145884800-145910800	Weak transcription	Liver	Liver
4	chr3:145895800-145918200	Weak transcription	NHDF-Ad	bronchial
5	chr3:145896000-145910600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:145896400-145910800	Weak transcription	Fetal Lung	lung
7	chr3:145896600-145911200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:145897000-145933600	Weak transcription	Fetal Stomach	stomach
9	chr3:145899600-145917400	Weak transcription	Pancreas	Pancrea
10	chr3:145901000-145923800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr3:145902000-145912000	Weak transcription	Fetal Intestine Large	intestine
12	chr3:145902800-145912400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr3:145902800-145923000	Weak transcription	Osteobl	bone
14	chr3:145902800-145923600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr3:145903000-145934800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr3:145903800-145911800	Weak transcription	Colon Smooth Muscle	Colon
17	chr3:145904000-145911800	Weak transcription	Fetal Heart	heart
18	chr3:145904800-145912600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr3:145905000-145933600	Weak transcription	NHLF	lung
20	chr3:145906400-145914600	Weak transcription	Fetal Brain Male	brain
21	chr3:145907000-145938600	Weak transcription	Fetal Intestine Small	intestine
22	chr3:145907400-145910800	Weak transcription	Stomach Smooth Muscle	stomach
23	chr3:145907400-145912000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:145907400-145913000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr3:145907400-145914400	Weak transcription	Psoas Muscle	Psoas
26	chr3:145907400-145918200	Weak transcription	HepG2	liver
27	chr3:145907600-145913200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr3:145907600-145915000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:145907600-145939200	Weak transcription	Brain Anterior Caudate	brain
30	chr3:145907800-145911400	Weak transcription	Fetal Kidney	kidney
31	chr3:145908200-145910800	Weak transcription	Adipose Nuclei	Adipose
32	chr3:145908200-145936400	Weak transcription	A549	lung
33	chr3:145908400-145917400	Weak transcription	Ovary	ovary
34	chr3:145908600-145914400	Weak transcription	Aorta	Aorta
35	chr3:145908800-145911400	Weak transcription	HUVEC	blood vessel
36	chr3:145909200-145910800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:145909200-145911800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr3:145909400-145912600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr3:145909600-145939200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr3:145909800-145912000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr3:145910400-145932400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:145910400-145940000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:145910600-145913000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr3:145910800-145913000	Strong transcription	Adipose Nuclei	Adipose
45	chr3:145910800-145913000	Strong transcription	Stomach Smooth Muscle	stomach
46	chr3:145910800-145913200	Strong transcription	Fetal Lung	lung
47	chr3:145910800-145913600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:145910800-145914800	Strong transcription	Liver	Liver
49	chr3:145911200-145914200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:145911400-145916200	Enhancers	HUVEC	blood vessel

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