Variant report

Variant	nsv877107
Chromosome Location	chr3:85814620-86037162
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	ARID3A	chr3:85851137-85851447	HepG2	liver:	n/a	n/a
2	BACH1	chr3:85939421-85939743	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr3:85955029-85955316	HepG2	liver:	n/a	chr3:85955169-85955180
4	CEBPB	chr3:85896067-85896437	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr3:85886427-85886774	IMR90	lung:	n/a	chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886587-85886598 chr3:85886586-85886599
6	CEBPB	chr3:85886482-85886818	A549	lung:	n/a	chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886587-85886598 chr3:85886586-85886599
7	CEBPB	chr3:85971548-85971855	ECC-1	luminal epithelium:	n/a	chr3:85971702-85971713
8	CEBPB	chr3:85971492-85971930	ECC-1	luminal epithelium:	n/a	chr3:85971702-85971713
9	CEBPB	chr3:85998031-85998303	HepG2	liver:	n/a	chr3:85998184-85998195
10	CEBPB	chr3:85917602-85917801	A549	lung:	n/a	n/a
11	CEBPB	chr3:86032225-86032466	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:85971551-85971913	A549	lung:	n/a	chr3:85971702-85971713
13	CEBPB	chr3:86004855-86004999	A549	lung:	n/a	chr3:86004898-86004915 chr3:86004899-86004912 chr3:86004899-86004910 chr3:86004901-86004910 chr3:86004900-86004911
14	CEBPB	chr3:86025508-86025712	HepG2	liver:	n/a	chr3:86025645-86025656 chr3:86025645-86025658
15	CEBPB	chr3:85886417-85886774	H1-hESC	embryonic stem cell:	n/a	chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886587-85886598 chr3:85886586-85886599
16	CEBPB	chr3:86032275-86032495	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:85845113-85845881	Hela-S3	cervix:	n/a	chr3:85845353-85845364 chr3:85845328-85845341 chr3:85845351-85845364
18	CEBPB	chr3:85971340-85971904	Hela-S3	cervix:	n/a	chr3:85971702-85971713
19	CEBPB	chr3:85975553-85975807	HepG2	liver:	n/a	chr3:85975699-85975712 chr3:85975700-85975711
20	CEBPB	chr3:85971522-85971906	K562	blood:	n/a	chr3:85971702-85971713
21	CEBPB	chr3:85886457-85886778	A549	lung:	n/a	chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886587-85886598 chr3:85886586-85886599
22	CEBPB	chr3:86025494-86025771	IMR90	lung:	n/a	chr3:86025645-86025656 chr3:86025645-86025658
23	CEBPB	chr3:86032257-86032539	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr3:86032927-86033161	H1-hESC	embryonic stem cell:	n/a	chr3:86033086-86033099 chr3:86033088-86033097 chr3:86033088-86033097 chr3:86033088-86033097
25	CEBPB	chr3:85975640-85975771	K562	blood:	n/a	chr3:85975699-85975712 chr3:85975700-85975711
26	CEBPB	chr3:85827947-85828147	HepG2	liver:	n/a	chr3:85828058-85828067 chr3:85828057-85828068
27	CEBPB	chr3:86032921-86033173	IMR90	lung:	n/a	chr3:86033086-86033099 chr3:86033088-86033097 chr3:86033088-86033097 chr3:86033088-86033097
28	CEBPB	chr3:85976766-85976926	HepG2	liver:	n/a	chr3:85976836-85976847 chr3:85976836-85976849 chr3:85976836-85976849 chr3:85976837-85976848
29	CEBPB	chr3:85841949-85842088	A549	lung:	n/a	n/a
30	CEBPB	chr3:85971533-85971920	A549	lung:	n/a	chr3:85971702-85971713
31	CEBPB	chr3:85955009-85955361	Hela-S3	cervix:	n/a	chr3:85955169-85955180
32	CEBPB	chr3:86004741-86005020	HepG2	liver:	n/a	chr3:86004898-86004915 chr3:86004899-86004912 chr3:86004899-86004910 chr3:86004901-86004910 chr3:86004900-86004911
33	CEBPB	chr3:85955056-85955294	A549	lung:	n/a	chr3:85955169-85955180
34	CEBPB	chr3:85998052-85998329	Hela-S3	cervix:	n/a	chr3:85998184-85998195
35	CEBPB	chr3:85971501-85971955	A549	lung:	n/a	chr3:85971702-85971713
36	CEBPB	chr3:85955002-85955272	H1-hESC	embryonic stem cell:	n/a	chr3:85955169-85955180
37	CEBPB	chr3:85856028-85856064	A549	lung:	n/a	n/a
38	CEBPB	chr3:85971544-85971896	MCF-7	breast:	n/a	chr3:85971702-85971713
39	CEBPB	chr3:85971519-85971896	H1-hESC	embryonic stem cell:	n/a	chr3:85971702-85971713
40	CEBPB	chr3:85886417-85886772	Hela-S3	cervix:	n/a	chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886587-85886598 chr3:85886586-85886599
41	CEBPB	chr3:85851819-85852119	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:86032226-86032480	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:86033039-86033132	A549	lung:	n/a	chr3:86033086-86033099 chr3:86033088-86033097 chr3:86033088-86033097 chr3:86033088-86033097
44	CEBPB	chr3:86032276-86032492	A549	lung:	n/a	n/a
45	CEBPB	chr3:85971520-85971896	IMR90	lung:	n/a	chr3:85971702-85971713
46	CEBPB	chr3:86032262-86032516	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:85971538-85971894	HepG2	liver:	n/a	chr3:85971702-85971713
48	CEBPB	chr3:85976716-85976963	Hela-S3	cervix:	n/a	chr3:85976836-85976847 chr3:85976836-85976849 chr3:85976836-85976849 chr3:85976837-85976848
49	CEBPB	chr3:85834934-85835244	Hela-S3	cervix:	n/a	chr3:85834998-85835011 chr3:85834998-85835009 chr3:85834998-85835011
50	CEBPB	chr3:85886451-85886767	HepG2	liver:	n/a	chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886588-85886597 chr3:85886587-85886598 chr3:85886586-85886599

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85938637-85938687	AoSMC	blood vessel:	n/a
2	chr3:85938637-85938687	AG10803	skin:	n/a
3	chr3:85938637-85938687	A549	lung:	n/a
4	chr3:85938637-85938687	NB4	blood:	n/a
5	chr3:85938637-85938687	Hela-S3	cervix:	n/a
6	chr3:85938637-85938687	NT2-D1	testis:	n/a
7	chr3:85938637-85938687	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:85938637-85938687	HL-60	blood:	n/a
9	chr3:85938637-85938687	AG09309	skin:	n/a
10	chr3:85938637-85938687	AG09319	gingival:	n/a
11	chr3:85938637-85938687	HCM	heart:	n/a
12	chr3:85938637-85938687	HEEpiC	esophagus:	n/a
13	chr3:85938637-85938687	Hepatocyte	liver:	n/a
14	chr3:85938637-85938687	HRPEpiC	eye:	n/a
15	chr3:85938637-85938687	K562	blood:	n/a
16	chr3:85938637-85938687	MCF10A-Er-Src	breast:	n/a
17	chr3:85938637-85938687	AG04449	skin:	fetal
18	chr3:85938637-85938687	U87	brain:	n/a
19	chr3:85938637-85938687	GM19239	blood:	n/a
20	chr3:85938637-85938687	ProgFib	skin:	n/a
21	chr3:85938637-85938687	MCF-7	breast:	n/a
22	chr3:85938637-85938687	GM12892	blood:	n/a
23	chr3:85938637-85938687	RPTEC	kidney:	n/a
24	chr3:85938637-85938687	AG04450	lung:	fetal
25	chr3:85938637-85938687	HNPCEpiC	eye:	n/a
26	chr3:85938637-85938687	CMK	blood:	n/a
27	chr3:85938637-85938687	Caco-2	colon:	n/a
28	chr3:85938637-85938687	BJ	skin:	n/a
29	chr3:85938637-85938687	HRE	kidney:	n/a
30	chr3:85938637-85938687	HRCEpiC	kidney:	n/a
31	chr3:85938637-85938687	T-47D	breast:	n/a
32	chr3:85938637-85938687	HUVEC	blood vessel:	n/a
33	chr3:85938637-85938687	GM06990	blood:	n/a
34	chr3:85938637-85938687	LNCaP	prostate:	n/a
35	chr3:85938637-85938687	NHBE	bronchial:	n/a
36	chr3:85938637-85938687	NHDF-neo	bronchial:	n/a
37	chr3:85938637-85938687	HCPEpiC	choroid plexus:	n/a
38	chr3:85938637-85938687	SAEC	small airway:	n/a
39	chr3:85938637-85938687	H1-hESC	embryonic stem cell:	embryo
40	chr3:85938637-85938687	ovcar-3	ovarian:	n/a
41	chr3:85938637-85938687	HAEpiC	amniotic membrane:	n/a
42	chr3:85938637-85938687	SK-N-MC	brain:	n/a
43	chr3:85938637-85938687	IMR90	lung:	fetal
44	chr3:85938637-85938687	SK-N-SH_RA	brain:	n/a
45	chr3:85938637-85938687	NH-A	brain:	n/a
46	chr3:85938637-85938687	HepG2	liver:	n/a
47	chr3:85938637-85938687	PrEC	prostate:	n/a
48	chr3:85938637-85938687	GM12878	blood:	n/a
49	chr3:85938637-85938687	SK-N-SH	brain:	n/a
50	chr3:85938637-85938687	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:85877448..85879251-chr3:85882149..85884941,2	K562	blood:
2	chr3:85979706..85982115-chr3:85984634..85986729,2	K562	blood:
3	chr3:85877448..85879251-chr3:85882149..85884941,2	K562	blood:
4	chr3:85870032..85871016-chr3:86611753..86613106,6	MCF-7	breast:
5	chr3:85865485..85867730-chr3:85868016..85870182,2	K562	blood:
6	chr3:86010163..86013071-chr3:86015856..86017969,2	K562	blood:
7	chr3:85979706..85982115-chr3:85984634..85986729,2	K562	blood:
8	chr3:85865485..85867730-chr3:85868016..85870182,2	K562	blood:
9	chr3:85869951..85870538-chr3:86612290..86613009,2	MCF-7	breast:
10	chr3:85963263..85965350-chr3:85981290..85983775,2	MCF-7	breast:
11	chr3:86010163..86013071-chr3:86015856..86017969,2	K562	blood:
12	chr3:85870003..85870955-chr3:86294230..86295150,6	MCF-7	breast:
13	chr3:85963263..85965350-chr3:85981290..85983775,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL3-5	chr3:85849137-85849573	ENSG00000241648.1
2	lnc-VGLL3-5	chr3:85854604-85854735	ENSG00000241648.1
3	lnc-VGLL3-5	chr3:85849953-85850101	ENSG00000241648.1
4	lnc-VGLL3-5	chr3:85877151-85877200	ENSG00000241648.1

Variant related genes	Relation type
CADM2-AS2	TF binding region
CADM2-AS2	CpG island

Extended variants
information (count: 4309 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4309 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17023295	chr3:85814620-85814621	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535517392	chr3:85814659-85814660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553940449	chr3:85814685-85814686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73845647	chr3:85814692-85814693	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs9881886	chr3:85814733-85814734	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs558332021	chr3:85814737-85814738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576618172	chr3:85814838-85814839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544110230	chr3:85814941-85814942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190495293	chr3:85815011-85815012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574013424	chr3:85815062-85815063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563981170	chr3:85815108-85815109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559468006	chr3:85815158-85815159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563069391	chr3:85815187-85815188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145197560	chr3:85815205-85815206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs180867315	chr3:85815208-85815209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6792733	chr3:85815228-85815229	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184880437	chr3:85815241-85815242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188720397	chr3:85815313-85815314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528939256	chr3:85815315-85815316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547514391	chr3:85815401-85815402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532060754	chr3:85815459-85815460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565735099	chr3:85815525-85815526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539549834	chr3:85815529-85815530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138006924	chr3:85828003-85828004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577528020	chr3:85828004-85828005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539768765	chr3:85828013-85828014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72906501	chr3:85828054-85828055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs538721738	chr3:85828069-85828070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569750519	chr3:85828075-85828076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115268847	chr3:85828086-85828087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555489634	chr3:85828090-85828091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376852097	chr3:85828098-85828099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142003510	chr3:85828134-85828135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148800786	chr3:85830012-85830013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555425249	chr3:85830030-85830031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567556908	chr3:85830099-85830100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181932364	chr3:85830104-85830105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552953154	chr3:85830175-85830176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575261276	chr3:85830180-85830181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142434235	chr3:85830197-85830198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544735275	chr3:85830224-85830225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536521621	chr3:85830228-85830229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73845663	chr3:85830302-85830303	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73845664	chr3:85830364-85830365	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs151300639	chr3:85830419-85830420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186743295	chr3:85830561-85830562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77121077	chr3:85830572-85830573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77025486	chr3:85830581-85830582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140130824	chr3:85830605-85830606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145546821	chr3:85830612-85830613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Prostate cancer	21307934	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85801200-85815000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:85814000-85815000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:85814000-85815200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:85814400-85814800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:85814400-85815000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr3:85814600-85815200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:85814800-85815400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:85815000-85815200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:85815000-85815200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr3:85815000-85815200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:85815000-85815600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:85815200-85815400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:85828000-85828200	Enhancers	Brain Cingulate Gyrus	brain
14	chr3:85830000-85832800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:85830200-85832600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr3:85830200-85832800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:85830400-85832200	Enhancers	Fetal Lung	lung
18	chr3:85830800-85831400	Enhancers	Colon Smooth Muscle	Colon
19	chr3:85831400-85832400	Weak transcription	Colon Smooth Muscle	Colon
20	chr3:85831600-85832800	Enhancers	Primary hematopoietic stem cells	blood
21	chr3:85832200-85833000	Weak transcription	Fetal Lung	lung
22	chr3:85832400-85832600	Enhancers	Colon Smooth Muscle	Colon
23	chr3:85832400-85832800	Enhancers	Adipose Nuclei	Adipose
24	chr3:85832400-85833000	Enhancers	HUVEC	blood vessel
25	chr3:85832600-85832800	Enhancers	Brain Substantia Nigra	brain
26	chr3:85832800-85833800	Weak transcription	Adipose Nuclei	Adipose
27	chr3:85832800-85839400	Weak transcription	Brain Substantia Nigra	brain
28	chr3:85833000-85833400	Enhancers	Fetal Brain Male	brain
29	chr3:85833000-85833400	Enhancers	Fetal Lung	lung
30	chr3:85833000-85834600	Weak transcription	HUVEC	blood vessel
31	chr3:85833800-85834000	Enhancers	Adipose Nuclei	Adipose
32	chr3:85834000-85834400	Weak transcription	Adipose Nuclei	Adipose
33	chr3:85834400-85834800	Enhancers	Adipose Nuclei	Adipose
34	chr3:85834600-85835000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr3:85834600-85835200	Enhancers	HUVEC	blood vessel
36	chr3:85834600-85835800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:85835800-85837000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:85836800-85837200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr3:85837000-85837200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:85837000-85837400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:85839400-85840000	Enhancers	Brain Anterior Caudate	brain
42	chr3:85839400-85840000	Enhancers	Brain Cingulate Gyrus	brain
43	chr3:85839400-85840000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr3:85839400-85840200	Enhancers	Brain Hippocampus Middle	brain
45	chr3:85839400-85840200	Enhancers	Brain Substantia Nigra	brain
46	chr3:85839600-85840000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:85839800-85840200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr3:85839800-85840200	Enhancers	Aorta	Aorta
49	chr3:85839800-85840200	Enhancers	Brain Angular Gyrus	brain
50	chr3:85839800-85840600	Enhancers	Brain Inferior Temporal Lobe	brain

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