Variant report

Variant	nsv876631
Chromosome Location	chr3:25185448-25231571
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	ATF2	chr3:25197041-25198078	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:25197045-25198071	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr3:25197196-25197507	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr3:25197656-25197929	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:25212335-25212578	A549	lung:	n/a	chr3:25212458-25212469
6	CEBPB	chr3:25197180-25197958	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr3:25212341-25212643	H1-hESC	embryonic stem cell:	n/a	chr3:25212458-25212469
8	CEBPB	chr3:25198190-25198515	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:25212333-25212577	HepG2	liver:	n/a	chr3:25212458-25212469
10	CEBPB	chr3:25190883-25191148	HepG2	liver:	n/a	chr3:25191030-25191041
11	CHD1	chr3:25198524-25198662	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr3:25197113-25198328	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr3:25197161-25198097	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr3:25197106-25197973	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr3:25215896-25215964	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:25219060-25219210	GM12878	blood:	n/a	n/a
17	CTCF	chr3:25191636-25191696	Lung_OC	lung:	n/a	n/a
18	CTCF	chr3:25215965-25215967	MCF-7	breast:	n/a	n/a
19	CTCF	chr3:25223904-25223960	GM13976	blood:	n/a	chr3:25223940-25223948
20	CTCF	chr3:25223896-25223899	GM13976	blood:	n/a	n/a
21	E2F4	chr3:25222675-25222850	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr3:25198307-25198506	MCF10A-Er-Src	breast:	n/a	n/a
23	ELK1	chr3:25193135-25193245	Hela-S3	cervix:	n/a	n/a
24	ELK1	chr3:25193084-25193106	GM12878	blood:	n/a	n/a
25	EP300	chr3:25197082-25197497	SK-N-SH_RA	brain:	n/a	chr3:25197174-25197183
26	EP300	chr3:25197025-25198012	H1-hESC	embryonic stem cell:	n/a	chr3:25197174-25197183
27	EP300	chr3:25197453-25198623	SK-N-SH	brain:	n/a	n/a
28	EP300	chr3:25212547-25213299	SK-N-SH_RA	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213136-25213150 chr3:25212704-25212714
29	EP300	chr3:25213543-25213823	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr3:25212226-25214085	SK-N-SH	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213452-25213462 chr3:25213136-25213150 chr3:25212704-25212714
31	EP300	chr3:25194737-25195080	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr3:25197194-25197539	H1-hESC	embryonic stem cell:	n/a	n/a
33	EP300	chr3:25197051-25197488	SK-N-SH_RA	brain:	n/a	chr3:25197174-25197183
34	EP300	chr3:25200974-25201312	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr3:25198224-25198547	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr3:25212538-25213287	SK-N-SH_RA	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213136-25213150 chr3:25212704-25212714
37	EP300	chr3:25213501-25213811	SK-N-SH_RA	brain:	n/a	n/a
38	FOS	chr3:25198285-25198512	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:25198183-25198567	MCF10A-Er-Src	breast:	n/a	chr3:25198504-25198513
40	FOS	chr3:25198208-25198523	MCF10A-Er-Src	breast:	n/a	chr3:25198504-25198513
41	FOS	chr3:25198191-25198491	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:25192689-25193476	HUVEC	blood vessel:	n/a	chr3:25193201-25193210
43	FOS	chr3:25198130-25198588	HUVEC	blood vessel:	n/a	chr3:25198504-25198513
44	FOSL2	chr3:25198062-25198596	SK-N-SH	brain:	n/a	chr3:25198504-25198513
45	GATA2	chr3:25212562-25213261	SH-SY5Y	brain:	n/a	n/a
46	GATA2	chr3:25194789-25195363	SH-SY5Y	brain:	n/a	n/a
47	GATA2	chr3:25192936-25193343	HUVEC	blood vessel:	n/a	n/a
48	GATA2	chr3:25206713-25207182	SH-SY5Y	brain:	n/a	n/a
49	GATA2	chr3:25222750-25223039	SH-SY5Y	brain:	n/a	chr3:25222852-25222868 chr3:25222854-25222866
50	GATA3	chr3:25206806-25207232	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:25197710-25197760	HRE	kidney:	n/a
2	chr3:25197710-25197760	AG09319	gingival:	n/a
3	chr3:25215914-25215964	HRPEpiC	eye:	n/a
4	chr3:25197710-25197760	HIPEpiC	eye:	n/a
5	chr3:25215914-25215964	ProgFib	skin:	n/a
6	chr3:25215914-25215964	Hela-S3	cervix:	n/a
7	chr3:25197710-25197760	Hela-S3	cervix:	n/a
8	chr3:25215914-25215964	HL-60	blood:	n/a
9	chr3:25215914-25215964	GM12891	blood:	n/a
10	chr3:25215914-25215964	MCF10A-Er-Src	breast:	n/a
11	chr3:25215914-25215964	Jurkat	blood:	n/a
12	chr3:25215914-25215964	U87	brain:	n/a
13	chr3:25215914-25215964	SK-N-SH	brain:	n/a
14	chr3:25215914-25215964	HRE	kidney:	n/a
15	chr3:25215914-25215964	HRCEpiC	kidney:	n/a
16	chr3:25197710-25197760	H1-hESC	embryonic stem cell:	embryo
17	chr3:25197710-25197760	NT2-D1	testis:	n/a
18	chr3:25197710-25197760	HEEpiC	esophagus:	n/a
19	chr3:25197710-25197760	NB4	blood:	n/a
20	chr3:25197710-25197760	SK-N-SH_RA	brain:	n/a
21	chr3:25197710-25197760	PrEC	prostate:	n/a
22	chr3:25197710-25197760	HUVEC	blood vessel:	n/a
23	chr3:25197710-25197760	Hepatocyte	liver:	n/a
24	chr3:25215914-25215964	SK-N-MC	brain:	n/a
25	chr3:25197710-25197760	HAEpiC	amniotic membrane:	n/a
26	chr3:25215914-25215964	ovcar-3	ovarian:	n/a
27	chr3:25197710-25197760	MCF10A-Er-Src	breast:	n/a
28	chr3:25197710-25197760	A549	lung:	n/a
29	chr3:25197710-25197760	IMR90	lung:	fetal
30	chr3:25197710-25197760	RPTEC	kidney:	n/a
31	chr3:25197710-25197760	AG04449	skin:	fetal
32	chr3:25197710-25197760	ECC-1	luminal epithelium:	n/a
33	chr3:25197710-25197760	T-47D	breast:	n/a
34	chr3:25197710-25197760	Jurkat	blood:	n/a
35	chr3:25215914-25215964	HMEC	breast:	n/a
36	chr3:25215914-25215964	ECC-1	luminal epithelium:	n/a
37	chr3:25215914-25215964	AG04450	lung:	fetal
38	chr3:25215914-25215964	NH-A	brain:	n/a
39	chr3:25197710-25197760	HMEC	breast:	n/a
40	chr3:25197710-25197760	HRPEpiC	eye:	n/a
41	chr3:25197710-25197760	HL-60	blood:	n/a
42	chr3:25215914-25215964	HCF	heart:	n/a
43	chr3:25215914-25215964	IMR90	lung:	fetal
44	chr3:25215914-25215964	A549	lung:	n/a
45	chr3:25197710-25197760	SK-N-SH	brain:	n/a
46	chr3:25215914-25215964	AG10803	skin:	n/a
47	chr3:25197710-25197760	HepG2	liver:	n/a
48	chr3:25215914-25215964	BE2_C	brain:	n/a
49	chr3:25197710-25197760	GM19239	blood:	n/a
50	chr3:25197710-25197760	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:25201532..25204868-chr3:25206067..25208834,3	K562	blood:
2	chr3:25224245..25226447-chr3:25227786..25229605,2	K562	blood:
3	chr3:25187342..25189876-chr3:25191897..25194177,2	MCF-7	breast:
4	chr3:25200008..25202995-chr3:25206457..25208830,2	MCF-7	breast:
5	chr3:25200008..25202995-chr3:25206457..25208830,2	MCF-7	breast:
6	chr3:25224245..25226447-chr3:25227786..25229605,2	K562	blood:
7	chr3:25173033..25175213-chr3:25183319..25185736,2	MCF-7	breast:
8	chr3:25201532..25204868-chr3:25206067..25208834,3	K562	blood:
9	chr3:25187342..25189876-chr3:25191897..25194177,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RARB-1	chr3:25215610-25215796	ENSG00000237838

Variant related genes	Relation type
RARB	TF binding region
RARB	CpG island

Extended variants
information (count: 2145 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2145 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9310772	chr3:25185448-25185449	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531041552	chr3:25185468-25185469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556347896	chr3:25185478-25185479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186335728	chr3:25185479-25185480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35183943	chr3:25185481-25185482	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs376598572	chr3:25185492-25185493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544431899	chr3:25185493-25185494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538619020	chr3:25185523-25185524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73048438	chr3:25185534-25185535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200274834	chr3:25185536-25185537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565681618	chr3:25185589-25185590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571785820	chr3:25185594-25185595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140158409	chr3:25185614-25185615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577692399	chr3:25185649-25185650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191339991	chr3:25185659-25185660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537290748	chr3:25185660-25185661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12495130	chr3:25185716-25185717	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs78837298	chr3:25185717-25185718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577025868	chr3:25185722-25185723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546083886	chr3:25185740-25185741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17015850	chr3:25185766-25185767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572916103	chr3:25185780-25185781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541904082	chr3:25185805-25185806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560175915	chr3:25185815-25185816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528908802	chr3:25185863-25185864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531004401	chr3:25185868-25185869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144872998	chr3:25185903-25185904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7620023	chr3:25186001-25186002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs78194912	chr3:25186051-25186052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531844548	chr3:25186055-25186056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547294013	chr3:25186120-25186121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373582930	chr3:25186163-25186164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551561716	chr3:25186209-25186210	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs182844383	chr3:25186210-25186211	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs571718753	chr3:25186225-25186226	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs187693261	chr3:25186250-25186251	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs9870811	chr3:25186287-25186288	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs116006783	chr3:25186293-25186294	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs537162485	chr3:25186297-25186298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556835029	chr3:25186315-25186316	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs547604468	chr3:25186402-25186403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558458103	chr3:25186408-25186409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192473198	chr3:25186434-25186435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370670960	chr3:25186440-25186441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183265919	chr3:25186456-25186457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187991099	chr3:25186487-25186488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561835514	chr3:25186528-25186529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575292999	chr3:25186596-25186597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544695376	chr3:25186608-25186609	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs73048442	chr3:25186624-25186625	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
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
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
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25184200-25186200	Enhancers	Fetal Lung	lung
2	chr3:25184600-25185600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr3:25184600-25187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:25185000-25186200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr3:25185200-25186000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr3:25185200-25186400	Weak transcription	Fetal Stomach	stomach
7	chr3:25185600-25192200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr3:25186000-25186800	Enhancers	Colon Smooth Muscle	Colon
9	chr3:25186200-25186400	Flanking Active TSS	Fetal Lung	lung
10	chr3:25186200-25186600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:25186200-25186800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:25186400-25186600	Enhancers	Fetal Lung	lung
13	chr3:25186600-25186800	Flanking Active TSS	Fetal Lung	lung
14	chr3:25186600-25191800	Weak transcription	Fetal Stomach	stomach
15	chr3:25186800-25187000	Enhancers	Fetal Lung	lung
16	chr3:25187400-25191000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:25190000-25190400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:25190000-25190600	Enhancers	Fetal Heart	heart
19	chr3:25190000-25191800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr3:25190400-25190600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:25190400-25190800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:25190600-25192000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr3:25190600-25194400	Weak transcription	Fetal Heart	heart
24	chr3:25190800-25191000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:25190800-25193000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:25191000-25191400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:25191000-25194400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:25191400-25194600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:25191400-25195200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr3:25191800-25192600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr3:25191800-25192800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr3:25191800-25192800	Enhancers	Right Atrium	heart
33	chr3:25191800-25193200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:25191800-25193200	Enhancers	Fetal Muscle Leg	muscle
35	chr3:25191800-25193400	Enhancers	Fetal Stomach	stomach
36	chr3:25192000-25192200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr3:25192000-25193800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr3:25192200-25192800	Enhancers	HUVEC	blood vessel
39	chr3:25192200-25193000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr3:25192200-25193400	Enhancers	Brain Germinal Matrix	brain
41	chr3:25192200-25193600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr3:25192400-25192600	Enhancers	Adipose Nuclei	Adipose
43	chr3:25192400-25194000	Active TSS	Aorta	Aorta
44	chr3:25192600-25192800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr3:25192600-25192800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr3:25192600-25192800	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr3:25192600-25192800	Enhancers	Brain Angular Gyrus	brain
48	chr3:25192600-25193400	Active TSS	Brain Anterior Caudate	brain
49	chr3:25192600-25193400	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr3:25192600-25193600	Active TSS	Colon Smooth Muscle	Colon

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