Variant report

Variant	nsv1010292
Chromosome Location	chr3:90057464-90192503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:90140843-90141039	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:90142224-90142549	HepG2	liver:	n/a	n/a
3	BATF	chr3:90057269-90057561	GM12878	blood:	n/a	chr3:90057406-90057415
4	BATF	chr3:90159937-90160210	GM12878	blood:	n/a	n/a
5	BATF	chr3:90084907-90085138	GM12878	blood:	n/a	n/a
6	BATF	chr3:90059634-90059882	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:90089745-90089993	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:90130173-90130430	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr3:90084913-90085168	GM12878	blood:	n/a	chr3:90085037-90085046
10	BCL11A	chr3:90089233-90089371	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:90089745-90089969	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:90059633-90059865	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:90084912-90085190	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:90065305-90065572	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:90101922-90101932	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:90105845-90105983	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:90089753-90089967	GM12878	blood:	n/a	n/a
18	CEBPB	chr3:90059170-90059853	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:90060754-90061499	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:90111939-90112367	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:90111852-90112330	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:90111880-90112340	MCF-7	breast:	n/a	n/a
23	CEBPB	chr3:90087777-90087892	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr3:90130910-90131157	IMR90	lung:	n/a	n/a
25	CEBPB	chr3:90060817-90061003	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:90130851-90131195	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr3:90089757-90089978	GM12878	blood:	n/a	n/a
28	CHD2	chr3:90084886-90085217	GM12878	blood:	n/a	n/a
29	CHD2	chr3:90105739-90105812	GM12878	blood:	n/a	n/a
30	CHD2	chr3:90060425-90060427	GM12878	blood:	n/a	n/a
31	CHD2	chr3:90106035-90106043	GM12878	blood:	n/a	n/a
32	CHD2	chr3:90101737-90101932	GM12878	blood:	n/a	n/a
33	CTCF	chr3:90142177-90142504	MCF-7	breast:	n/a	chr3:90142361-90142382
34	CTCF	chr3:90142275-90142457	GM13977	blood:	n/a	chr3:90142361-90142382
35	CTCF	chr3:90142272-90142480	SK-N-SH_RA	brain:	n/a	chr3:90142361-90142382
36	CTCF	chr3:90141880-90142030	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr3:90140856-90141054	LNCaP	prostate:	n/a	chr3:90140948-90140966
38	CTCF	chr3:90140826-90141017	SK-N-SH_RA	brain:	n/a	chr3:90140948-90140966
39	CTCF	chr3:90140795-90141021	HepG2	liver:	n/a	chr3:90140948-90140966
40	CTCF	chr3:90142280-90142430	AG04450	lung:	n/a	chr3:90142361-90142382
41	CTCF	chr3:90142280-90142430	HCFaa	heart:	n/a	chr3:90142361-90142382
42	CTCF	chr3:90142280-90142430	HEEpiC	esophagus:	n/a	chr3:90142361-90142382
43	CTCF	chr3:90140880-90141030	HA-sp	spinal cord:	n/a	chr3:90140948-90140966
44	CTCF	chr3:90140860-90141010	HRPEpiC	eye:	n/a	chr3:90140948-90140966
45	CTCF	chr3:90142300-90142450	GM12873	blood:	n/a	chr3:90142361-90142382
46	CTCF	chr3:90140460-90140610	HMEC	breast:	n/a	chr3:90140527-90140535
47	CTCF	chr3:90142200-90142350	RPTEC	kidney:	n/a	n/a
48	CTCF	chr3:90140880-90141030	HBMEC	blood vessel:	n/a	chr3:90140948-90140966
49	CTCF	chr3:90140860-90141010	NHEK	skin:	n/a	chr3:90140948-90140966
50	CTCF	chr3:90142000-90142150	GM12866	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:90086806-90086856	T-47D	breast:	n/a
2	chr3:90139296-90139346	K562	blood:	n/a
3	chr3:90139296-90139346	GM19239	blood:	n/a
4	chr3:90086806-90086856	HepG2	liver:	n/a
5	chr3:90086806-90086856	HCM	heart:	n/a
6	chr3:90139296-90139346	CMK	blood:	n/a
7	chr3:90139296-90139346	GM12892	blood:	n/a
8	chr3:90130850-90130900	NH-A	brain:	n/a
9	chr3:90130850-90130900	NT2-D1	testis:	n/a
10	chr3:90086806-90086856	AG09319	gingival:	n/a
11	chr3:90139296-90139346	BJ	skin:	n/a
12	chr3:90130850-90130900	HCPEpiC	choroid plexus:	n/a
13	chr3:90130850-90130900	U87	brain:	n/a
14	chr3:90130850-90130900	HepG2	liver:	n/a
15	chr3:90139296-90139346	U87	brain:	n/a
16	chr3:90086806-90086856	BE2_C	brain:	n/a
17	chr3:90130850-90130900	AoSMC	blood vessel:	n/a
18	chr3:90086806-90086856	IMR90	lung:	fetal
19	chr3:90086806-90086856	SK-N-SH_RA	brain:	n/a
20	chr3:90086806-90086856	GM12892	blood:	n/a
21	chr3:90086806-90086856	HNPCEpiC	eye:	n/a
22	chr3:90139296-90139346	AG04450	lung:	fetal
23	chr3:90086806-90086856	CMK	blood:	n/a
24	chr3:90139296-90139346	AoSMC	blood vessel:	n/a
25	chr3:90139296-90139346	NB4	blood:	n/a
26	chr3:90139296-90139346	AG04449	skin:	fetal
27	chr3:90086806-90086856	ECC-1	luminal epithelium:	n/a
28	chr3:90139296-90139346	IMR90	lung:	fetal
29	chr3:90139296-90139346	ECC-1	luminal epithelium:	n/a
30	chr3:90130850-90130900	HNPCEpiC	eye:	n/a
31	chr3:90139296-90139346	PFSK-1	brain:	n/a
32	chr3:90086806-90086856	MCF-7	breast:	n/a
33	chr3:90086806-90086856	NHBE	bronchial:	n/a
34	chr3:90139296-90139346	HEK293	kidney:	embryo
35	chr3:90086806-90086856	HEK293	kidney:	embryo
36	chr3:90086806-90086856	PrEC	prostate:	n/a
37	chr3:90139296-90139346	MCF-7	breast:	n/a
38	chr3:90086806-90086856	GM19239	blood:	n/a
39	chr3:90130850-90130900	BJ	skin:	n/a
40	chr3:90086806-90086856	PANC-1	pancreas:	n/a
41	chr3:90139296-90139346	HAEpiC	amniotic membrane:	n/a
42	chr3:90130850-90130900	Hela-S3	cervix:	n/a
43	chr3:90086806-90086856	NB4	blood:	n/a
44	chr3:90130850-90130900	SK-N-SH	brain:	n/a
45	chr3:90139296-90139346	Hepatocyte	liver:	n/a
46	chr3:90086806-90086856	HIPEpiC	eye:	n/a
47	chr3:90130850-90130900	IMR90	lung:	fetal
48	chr3:90130850-90130900	K562	blood:	n/a
49	chr3:90086806-90086856	GM12878	blood:	n/a
50	chr3:90130850-90130900	HL-60	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:90096383..90097903-chr8:137113417..137115130,2	MCF-7	breast:
2	chr3:90067745..90070170-chr3:90100154..90102360,2	MCF-7	breast:
3	chr3:89996606..89997218-chr3:90142348..90142978,2	MCF-7	breast:
4	chr3:90068937..90071174-chr3:90072001..90074074,2	MCF-7	breast:
5	chr3:89900833..89901811-chr3:90140473..90141334,4	MCF-7	breast:
6	chr3:89996325..89997175-chr3:90140367..90141418,4	MCF-7	breast:
7	chr3:90075388..90077133-chr3:90078504..90080483,2	MCF-7	breast:
8	chr3:90068937..90071174-chr3:90072001..90074074,2	MCF-7	breast:
9	chr3:89996596..89997810-chr3:90140377..90141392,6	MCF-7	breast:
10	chr3:90184075..90187070-chr3:90192628..90194644,2	MCF-7	breast:
11	chr3:90067745..90070170-chr3:90100154..90102360,2	MCF-7	breast:
12	chr3:90068533..90070645-chr3:90092564..90094236,2	MCF-7	breast:
13	chr3:89611242..89611987-chr3:90140381..90141293,2	MCF-7	breast:
14	chr3:90068533..90070645-chr3:90092564..90094236,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPHA3-1	chr3:90079434-90079644	NONHSAT090712

No data

Variant related genes	Relation type
ENSG00000212598	TF binding region
ENSG00000212598	CpG island
ENSG00000212598	chromatin interactions

Extended variants
information (count: 5114 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5114 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549922760	chr3:90057523-90057524	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs377022613	chr3:90057627-90057628	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs146567238	chr3:90057675-90057676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs35874514	chr3:90057709-90057710	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs140095374	chr3:90057710-90057711	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs190575966	chr3:90057727-90057728	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs149713276	chr3:90057821-90057822	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs181883731	chr3:90057849-90057850	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs145588878	chr3:90057887-90057888	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs570978684	chr3:90057890-90057891	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs148900085	chr3:90057892-90057893	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs186960862	chr3:90057909-90057910	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs143580664	chr3:90057914-90057915	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs575512463	chr3:90057946-90057947	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191188059	chr3:90057957-90057958	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553871170	chr3:90057960-90057961	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs572364043	chr3:90057978-90057979	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs182524920	chr3:90058025-90058026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185373436	chr3:90058052-90058053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76412514	chr3:90058089-90058090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543625030	chr3:90058097-90058098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370978109	chr3:90058162-90058163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561814700	chr3:90058165-90058166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11926877	chr3:90058181-90058182	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547430860	chr3:90058205-90058206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565544362	chr3:90058252-90058253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532913721	chr3:90058260-90058261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537206296	chr3:90058272-90058273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73153371	chr3:90058295-90058296	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571110062	chr3:90058309-90058310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538076340	chr3:90058343-90058344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189735203	chr3:90058385-90058386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182176389	chr3:90058391-90058392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188902711	chr3:90058419-90058420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374399339	chr3:90058506-90058507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs193242084	chr3:90058529-90058530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183622403	chr3:90058583-90058584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539783721	chr3:90058632-90058633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557799425	chr3:90058634-90058635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188507461	chr3:90058688-90058689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559195838	chr3:90058757-90058758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145806553	chr3:90058818-90058819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561877530	chr3:90058912-90058913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138711772	chr3:90058914-90058915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191756400	chr3:90058929-90058930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559365630	chr3:90058973-90058974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142778301	chr3:90058990-90058991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111452462	chr3:90059023-90059024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113564686	chr3:90059060-90059061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76413576	chr3:90059073-90059074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Soft tissue tumor	16732325	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Lung cancer	19547694	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:90056200-90058000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr3:90056200-90058000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:90056400-90057600	Enhancers	Fetal Brain Male	brain
4	chr3:90056400-90058000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr3:90056400-90058400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:90056600-90058000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:90056600-90058000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr3:90056800-90057600	Enhancers	NHDF-Ad	bronchial
9	chr3:90056800-90057800	Enhancers	Fetal Stomach	stomach
10	chr3:90056800-90058000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr3:90056800-90058200	Enhancers	Fetal Heart	heart
12	chr3:90057000-90057600	Enhancers	Stomach Mucosa	stomach
13	chr3:90057000-90057800	Enhancers	Fetal Brain Female	brain
14	chr3:90057000-90057800	Enhancers	Ovary	ovary
15	chr3:90057000-90058200	Enhancers	Colon Smooth Muscle	Colon
16	chr3:90057000-90058400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:90057200-90057600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr3:90057200-90057600	Flanking Active TSS	Fetal Lung	lung
19	chr3:90057200-90057600	Flanking Active TSS	HSMMtube	muscle
20	chr3:90057200-90059400	Weak transcription	Aorta	Aorta
21	chr3:90057400-90058800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr3:90057400-90058800	Enhancers	HSMM	muscle
23	chr3:90057400-90059200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:90057400-90059600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr3:90057400-90064400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr3:90057600-90057800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr3:90057600-90057800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:90057600-90058000	Enhancers	HSMMtube	muscle
29	chr3:90057600-90058400	Enhancers	Fetal Lung	lung
30	chr3:90057600-90060200	Weak transcription	NHDF-Ad	bronchial
31	chr3:90057800-90058000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:90057800-90058000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr3:90057800-90058000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr3:90057800-90059400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr3:90057800-90059600	Weak transcription	Ovary	ovary
36	chr3:90058000-90058400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:90058000-90058600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:90058000-90059000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr3:90058000-90059000	Weak transcription	HSMMtube	muscle
40	chr3:90058000-90059400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr3:90058000-90059600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:90058000-90060200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr3:90058000-90064600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr3:90058200-90058600	Weak transcription	Colon Smooth Muscle	Colon
45	chr3:90058200-90058600	Weak transcription	Fetal Heart	heart
46	chr3:90058400-90058800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:90058400-90059200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:90058400-90059400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr3:90058400-90059400	Weak transcription	Fetal Lung	lung
50	chr3:90058600-90059200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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