Variant report

Variant	nsv1004881
Chromosome Location	chr3:50900793-51032918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:717)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:51008874-51009194	HepG2	liver:	n/a	n/a
2	BACH1	chr3:50964582-50964613	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:50938610-50938847	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:51008904-51009174	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:50961992-50962449	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:50911188-50911474	GM12878	blood:	n/a	n/a
7	BATF	chr3:50911234-50911452	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:50928457-50928733	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr3:50911182-50911482	GM12878	blood:	n/a	n/a
10	BRCA1	chr3:50929896-50930024	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr3:50984019-50984209	GM12878	blood:	n/a	n/a
12	CCNT2	chr3:50998968-50999090	K562	blood:	n/a	n/a
13	CEBPB	chr3:51021021-51021169	A549	lung:	n/a	chr3:51021089-51021100
14	CEBPB	chr3:50991325-50991608	ECC-1	luminal epithelium:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
15	CEBPB	chr3:51016807-51017083	HepG2	liver:	n/a	chr3:51016952-51016963
16	CEBPB	chr3:50991122-50991607	H1-hESC	embryonic stem cell:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
17	CEBPB	chr3:50952273-50952485	A549	lung:	n/a	chr3:50952408-50952419
18	CEBPB	chr3:51016788-51017127	H1-hESC	embryonic stem cell:	n/a	chr3:51016952-51016963
19	CEBPB	chr3:50928341-50928402	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:50991292-50991588	HepG2	liver:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
21	CEBPB	chr3:51016846-51017053	MCF-7	breast:	n/a	chr3:51016952-51016963
22	CEBPB	chr3:50991276-50991626	Hela-S3	cervix:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
23	CEBPB	chr3:50922998-50923208	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr3:50914612-50914830	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:51016794-51017138	K562	blood:	n/a	chr3:51016952-51016963
26	CEBPB	chr3:50991272-50991633	K562	blood:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
27	CEBPB	chr3:51020974-51021229	HepG2	liver:	n/a	chr3:51021089-51021100
28	CEBPB	chr3:50952252-50952492	HepG2	liver:	n/a	chr3:50952408-50952419
29	CEBPB	chr3:50991287-50991610	A549	lung:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
30	CEBPB	chr3:50991273-50991623	HepG2	liver:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
31	CEBPB	chr3:51032020-51032220	A549	lung:	n/a	chr3:51032142-51032153
32	CEBPB	chr3:50991323-50991509	HepG2	liver:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
33	CEBPB	chr3:50991279-50991598	IMR90	lung:	n/a	chr3:50991453-50991464 chr3:50991433-50991444
34	CEBPB	chr3:50914631-50914895	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:50953710-50953822	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:51032009-51032300	HepG2	liver:	n/a	chr3:51032142-51032153
37	CHD1	chr3:51016768-51017003	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr3:50965815-50965817	GM12878	blood:	n/a	n/a
39	CHD1	chr3:50964640-50964682	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr3:50911265-50911516	GM12878	blood:	n/a	n/a
41	CTCF	chr3:50923054-50923211	HepG2	liver:	n/a	n/a
42	CTCF	chr3:51016900-51017050	HCT-116	colon:	n/a	n/a
43	CTCF	chr3:51008795-51009250	HepG2	liver:	n/a	n/a
44	CTCF	chr3:51016897-51017051	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:51016900-51017050	HMEC	breast:	n/a	n/a
46	CTCF	chr3:51008980-51009130	RPTEC	kidney:	n/a	n/a
47	CTCF	chr3:51008960-51009110	GM12866	blood:	n/a	n/a
48	CTCF	chr3:50923040-50923190	HMEC	breast:	n/a	n/a
49	CTCF	chr3:51008928-51009186	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr3:50923012-50923279	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51016232-51016282	SK-N-MC	brain:	n/a
2	chr3:51016232-51016282	SK-N-SH_RA	brain:	n/a
3	chr3:51016232-51016282	AG04450	lung:	fetal
4	chr3:51016232-51016282	HepG2	liver:	n/a
5	chr3:51016232-51016282	SK-N-SH	brain:	n/a
6	chr3:50962133-50962183	GM19239	blood:	n/a
7	chr3:50962133-50962183	HRPEpiC	eye:	n/a
8	chr3:51016232-51016282	LNCaP	prostate:	n/a
9	chr3:50962133-50962183	AG09309	skin:	n/a
10	chr3:50962133-50962183	HRE	kidney:	n/a
11	chr3:50962133-50962183	HEEpiC	esophagus:	n/a
12	chr3:51016232-51016282	NH-A	brain:	n/a
13	chr3:50962133-50962183	A549	lung:	n/a
14	chr3:50962133-50962183	NH-A	brain:	n/a
15	chr3:51016232-51016282	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:50962133-50962183	LNCaP	prostate:	n/a
17	chr3:50962133-50962183	Jurkat	blood:	n/a
18	chr3:50962133-50962183	IMR90	lung:	fetal
19	chr3:50962133-50962183	H1-hESC	embryonic stem cell:	embryo
20	chr3:50962133-50962183	ECC-1	luminal epithelium:	n/a
21	chr3:51016232-51016282	MCF10A-Er-Src	breast:	n/a
22	chr3:51016232-51016282	GM12878	blood:	n/a
23	chr3:50962133-50962183	Caco-2	colon:	n/a
24	chr3:51016232-51016282	AG04449	skin:	fetal
25	chr3:51016232-51016282	T-47D	breast:	n/a
26	chr3:51016232-51016282	ovcar-3	ovarian:	n/a
27	chr3:51016232-51016282	ECC-1	luminal epithelium:	n/a
28	chr3:50962133-50962183	U87	brain:	n/a
29	chr3:50962133-50962183	NHBE	bronchial:	n/a
30	chr3:51016232-51016282	PFSK-1	brain:	n/a
31	chr3:51016232-51016282	GM06990	blood:	n/a
32	chr3:51016232-51016282	GM12891	blood:	n/a
33	chr3:50962133-50962183	HMEC	breast:	n/a
34	chr3:51016232-51016282	HUVEC	blood vessel:	n/a
35	chr3:51016232-51016282	NHDF-neo	bronchial:	n/a
36	chr3:51016232-51016282	H1-hESC	embryonic stem cell:	embryo
37	chr3:51016232-51016282	HCPEpiC	choroid plexus:	n/a
38	chr3:50962133-50962183	BE2_C	brain:	n/a
39	chr3:50962133-50962183	HL-60	blood:	n/a
40	chr3:51016232-51016282	HRE	kidney:	n/a
41	chr3:50962133-50962183	SK-N-SH	brain:	n/a
42	chr3:50962133-50962183	AG09319	gingival:	n/a
43	chr3:50962133-50962183	HCF	heart:	n/a
44	chr3:51016232-51016282	NHBE	bronchial:	n/a
45	chr3:50962133-50962183	PrEC	prostate:	n/a
46	chr3:50962133-50962183	HNPCEpiC	eye:	n/a
47	chr3:51016232-51016282	GM19239	blood:	n/a
48	chr3:50962133-50962183	SK-N-MC	brain:	n/a
49	chr3:51016232-51016282	Jurkat	blood:	n/a
50	chr3:51016232-51016282	A549	lung:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51008625..51009202-chr3:51425877..51426490,2	MCF-7	breast:
2	chr3:50979915..50982588-chr3:50988969..50990913,2	K562	blood:
3	chr3:50712677..50713421-chr3:50922505..50923533,3	MCF-7	breast:
4	chr3:51008595..51009448-chr3:51119304..51120395,7	MCF-7	breast:
5	chr3:51008918..51009575-chr3:51137618..51138247,3	MCF-7	breast:
6	chr3:50965494..50967505-chr3:50968785..50971501,2	K562	blood:
7	chr3:51008103..51009082-chr3:51409134..51409784,2	K562	blood:
8	chr3:50653145..50653910-chr3:51008876..51009480,2	MCF-7	breast:
9	chr3:51008779..51009534-chr3:51409019..51409634,2	MCF-7	breast:
10	chr3:50979915..50982588-chr3:50988969..50990913,2	K562	blood:
11	chr3:51004752..51006712-chr3:51007570..51009531,2	K562	blood:
12	chr3:51008595..51009447-chr3:51137461..51138173,2	MCF-7	breast:
13	chr3:50965494..50967505-chr3:50968785..50971501,2	K562	blood:
14	chr3:50979924..50980442-chr8:43092410..43092931,4	MCF-7	breast:
15	chr3:50968160..50970692-chr3:50972135..50973895,2	K562	blood:
16	chr3:51008599..51009587-chr3:51348291..51349166,3	MCF-7	breast:
17	chr3:50712592..50713370-chr3:51008912..51009511,3	MCF-7	breast:
18	chr3:51004752..51006712-chr3:51007570..51009531,2	K562	blood:
19	chr3:50899740..50900296-chr3:51008634..51009161,2	MCF-7	breast:
20	chr1:228327981..228328815-chr3:50994545..50995455,2	MCF-7	breast:
21	chr3:50968160..50970692-chr3:50972135..50973895,2	K562	blood:
22	chr3:50665167..50665869-chr3:50923042..50923583,2	MCF-7	breast:
23	chr3:50978925..50980444-chr8:43095229..43096751,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CISH-4	chr3:50914500-50915088	NONHSAT089857
2	lnc-CISH-4	chr3:50914143-50914287	NONHSAT089857

No data

Variant related genes	Relation type
ST13P14	TF binding region
ST13P14	CpG island
ENSG00000143774	chromatin interactions
ENSG00000088538	chromatin interactions

Extended variants
information (count: 3709 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3709 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375475596	chr3:50900808-50900809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369707515	chr3:50900813-50900814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116544419	chr3:50900815-50900816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376210323	chr3:50900824-50900825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369402845	chr3:50900825-50900826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577064935	chr3:50900863-50900864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373305996	chr3:50900865-50900866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541339225	chr3:50900876-50900877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559351107	chr3:50900881-50900882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376261171	chr3:50900889-50900890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370473323	chr3:50900900-50900901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374715124	chr3:50900902-50900903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547902310	chr3:50900903-50900904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192898630	chr3:50900908-50900909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2675826	chr3:50900969-50900970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2675825	chr3:50900974-50900975	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571530470	chr3:50900978-50900979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2609027	chr3:50901030-50901031	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547957123	chr3:50901049-50901050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13314257	chr3:50901057-50901058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs146549556	chr3:50901061-50901062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563029642	chr3:50901127-50901128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2675824	chr3:50901188-50901189	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs112260011	chr3:50901253-50901254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570026257	chr3:50901324-50901325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537543999	chr3:50901334-50901335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2609028	chr3:50901345-50901346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184185968	chr3:50901367-50901368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540902925	chr3:50901375-50901376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553108319	chr3:50901379-50901380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79286255	chr3:50901419-50901420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188589245	chr3:50901485-50901486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562951924	chr3:50901592-50901593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2609029	chr3:50901593-50901594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs527665543	chr3:50901596-50901597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545510958	chr3:50901651-50901652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183708212	chr3:50901736-50901737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2125368	chr3:50901817-50901818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs2675823	chr3:50901856-50901857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs573658857	chr3:50901910-50901911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140958184	chr3:50901934-50901935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548854391	chr3:50901998-50901999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189075086	chr3:50902060-50902061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537407031	chr3:50902079-50902080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113675353	chr3:50902082-50902083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149797332	chr3:50902093-50902094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145775349	chr3:50902144-50902145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77031559	chr3:50902213-50902214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577264549	chr3:50902233-50902234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182512375	chr3:50902252-50902253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	20164919	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50897400-50910000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:50898400-50910200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:50899600-50900800	Enhancers	Brain Hippocampus Middle	brain
4	chr3:50900000-50900800	Enhancers	Left Ventricle	heart
5	chr3:50905200-50910200	Weak transcription	Brain Substantia Nigra	brain
6	chr3:50909800-50910600	ZNF genes & repeats	Esophagus	oesophagus
7	chr3:50909800-50910800	Enhancers	GM12878-XiMat	blood
8	chr3:50910000-50911400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:50910200-50911200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:50910200-50911400	Enhancers	Brain Substantia Nigra	brain
11	chr3:50910200-50911400	Enhancers	Left Ventricle	heart
12	chr3:50910200-50911600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr3:50910400-50911000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:50910400-50911400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr3:50910400-50911400	Enhancers	Right Ventricle	heart
16	chr3:50910600-50911200	Enhancers	Brain Hippocampus Middle	brain
17	chr3:50910600-50911400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:50910600-50911600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr3:50910600-50912800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:50910800-50911000	Enhancers	Esophagus	oesophagus
21	chr3:50910800-50911200	Enhancers	Brain Anterior Caudate	brain
22	chr3:50910800-50911200	Enhancers	Brain Cingulate Gyrus	brain
23	chr3:50910800-50911400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr3:50910800-50911400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:50910800-50911400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr3:50910800-50911400	Flanking Active TSS	GM12878-XiMat	blood
27	chr3:50910800-50911600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr3:50910800-50911600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr3:50911000-50912000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr3:50911200-50914400	Weak transcription	Brain Hippocampus Middle	brain
31	chr3:50911400-50911800	Enhancers	GM12878-XiMat	blood
32	chr3:50911400-50912400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr3:50911400-50912400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr3:50911400-50912400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:50911400-50912600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:50911600-50912000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr3:50911600-50912000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:50911600-50912000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr3:50912000-50913000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr3:50912000-50913200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:50912000-50913200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr3:50912200-50912800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr3:50912200-50913400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr3:50912400-50912600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr3:50912400-50912800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:50912400-50913000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr3:50912600-50912800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:50912600-50912800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:50914000-50915000	Enhancers	Rectal Smooth Muscle	rectum
50	chr3:50914000-50915000	Enhancers	Stomach Smooth Muscle	stomach

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