Variant report

Variant	nsv564962
Chromosome Location	chr14:68795209-68837882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:610)
Chromatin interactive
region (count:65)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:68816387-68817027	HepG2	liver:	n/a	n/a
2	ATF2	chr14:68830858-68831544	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr14:68830671-68831505	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr14:68795135-68795607	GM12878	blood:	n/a	n/a
5	ATF2	chr14:68808250-68809007	GM12878	blood:	n/a	n/a
6	ATF2	chr14:68794929-68795747	GM12878	blood:	n/a	n/a
7	ATF2	chr14:68835505-68836644	GM12878	blood:	n/a	n/a
8	ATF2	chr14:68835033-68836738	GM12878	blood:	n/a	n/a
9	BACH1	chr14:68830803-68831362	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:68830332-68830593	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr14:68795182-68795653	GM12878	blood:	n/a	n/a
12	BATF	chr14:68836258-68836648	GM12878	blood:	n/a	chr14:68836492-68836501
13	BATF	chr14:68836129-68836656	GM12878	blood:	n/a	chr14:68836492-68836501
14	BATF	chr14:68835575-68835871	GM12878	blood:	n/a	n/a
15	BATF	chr14:68822171-68822361	GM12878	blood:	n/a	n/a
16	BATF	chr14:68795193-68795591	GM12878	blood:	n/a	n/a
17	BCL11A	chr14:68795134-68795647	GM12878	blood:	n/a	n/a
18	BCL3	chr14:68835457-68836596	GM12878	blood:	n/a	chr14:68835704-68835713
19	BCLAF1	chr14:68835415-68836691	GM12878	blood:	n/a	chr14:68835704-68835713 chr14:68836662-68836671
20	BCLAF1	chr14:68794955-68795631	GM12878	blood:	n/a	n/a
21	BCLAF1	chr14:68808441-68809041	GM12878	blood:	n/a	n/a
22	BCLAF1	chr14:68826082-68826462	GM12878	blood:	n/a	n/a
23	BCLAF1	chr14:68835341-68836622	GM12878	blood:	n/a	chr14:68835704-68835713
24	BHLHE40	chr14:68808730-68809251	K562	blood:	n/a	n/a
25	BHLHE40	chr14:68816581-68816934	HepG2	liver:	n/a	n/a
26	BHLHE40	chr14:68795270-68795560	GM12878	blood:	n/a	n/a
27	BHLHE40	chr14:68808510-68808999	GM12878	blood:	n/a	n/a
28	BHLHE40	chr14:68807005-68807119	GM12878	blood:	n/a	n/a
29	BRCA1	chr14:68826902-68827338	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr14:68830808-68830990	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr14:68831741-68832351	HCT-116	colon:	n/a	n/a
32	CBX3	chr14:68826730-68827449	HCT-116	colon:	n/a	n/a
33	CBX3	chr14:68805330-68805634	K562	blood:	n/a	n/a
34	CBX3	chr14:68826806-68827492	HCT-116	colon:	n/a	n/a
35	CCNT2	chr14:68809026-68809418	K562	blood:	n/a	n/a
36	CEBPB	chr14:68830225-68830343	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:68816603-68816993	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:68825083-68825193	IMR90	lung:	n/a	n/a
39	CEBPB	chr14:68807022-68807269	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:68816535-68817013	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:68835443-68837000	GM12878	blood:	n/a	n/a
42	CEBPB	chr14:68825177-68825181	K562	blood:	n/a	n/a
43	CEBPB	chr14:68812511-68812823	IMR90	lung:	n/a	chr14:68812685-68812696
44	CEBPB	chr14:68830643-68830766	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr14:68812672-68812719	HepG2	liver:	n/a	chr14:68812685-68812696
46	CEBPB	chr14:68812475-68812823	MCF-7	breast:	n/a	chr14:68812685-68812696
47	CEBPB	chr14:68816715-68816904	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:68824965-68825584	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr14:68794697-68795699	GM12878	blood:	n/a	n/a
50	CEBPB	chr14:68824922-68825549	ECC-1	luminal epithelium:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:68830813-68830863	BE2_C	brain:	n/a
2	chr14:68798365-68798415	PANC-1	pancreas:	n/a
3	chr14:68798365-68798415	SK-N-SH_RA	brain:	n/a
4	chr14:68809407-68809457	AG09319	gingival:	n/a
5	chr14:68816721-68816771	A549	lung:	n/a
6	chr14:68831210-68831260	PrEC	prostate:	n/a
7	chr14:68816721-68816771	HCM	heart:	n/a
8	chr14:68807524-68807574	HL-60	blood:	n/a
9	chr14:68798365-68798415	H1-hESC	embryonic stem cell:	embryo
10	chr14:68831098-68831148	HIPEpiC	eye:	n/a
11	chr14:68825875-68825925	Hela-S3	cervix:	n/a
12	chr14:68809407-68809457	PrEC	prostate:	n/a
13	chr14:68809407-68809457	AG09309	skin:	n/a
14	chr14:68816721-68816771	H1-hESC	embryonic stem cell:	embryo
15	chr14:68816721-68816771	NH-A	brain:	n/a
16	chr14:68816721-68816771	GM06990	blood:	n/a
17	chr14:68831210-68831260	U87	brain:	n/a
18	chr14:68830704-68830754	HIPEpiC	eye:	n/a
19	chr14:68798365-68798415	HNPCEpiC	eye:	n/a
20	chr14:68822877-68822927	PrEC	prostate:	n/a
21	chr14:68825875-68825925	HCF	heart:	n/a
22	chr14:68831210-68831260	GM19239	blood:	n/a
23	chr14:68809407-68809457	HUVEC	blood vessel:	n/a
24	chr14:68816721-68816771	NHBE	bronchial:	n/a
25	chr14:68830704-68830754	ovcar-3	ovarian:	n/a
26	chr14:68816721-68816771	NT2-D1	testis:	n/a
27	chr14:68798365-68798415	K562	blood:	n/a
28	chr14:68830704-68830754	GM19239	blood:	n/a
29	chr14:68798365-68798415	Hela-S3	cervix:	n/a
30	chr14:68798365-68798415	RPTEC	kidney:	n/a
31	chr14:68816721-68816771	PrEC	prostate:	n/a
32	chr14:68825875-68825925	NH-A	brain:	n/a
33	chr14:68807524-68807574	Jurkat	blood:	n/a
34	chr14:68830704-68830754	HCM	heart:	n/a
35	chr14:68825875-68825925	T-47D	breast:	n/a
36	chr14:68822877-68822927	HUVEC	blood vessel:	n/a
37	chr14:68831098-68831148	HRCEpiC	kidney:	n/a
38	chr14:68807524-68807574	CMK	blood:	n/a
39	chr14:68831098-68831148	HMEC	breast:	n/a
40	chr14:68831098-68831148	AG09319	gingival:	n/a
41	chr14:68807524-68807574	AG10803	skin:	n/a
42	chr14:68809407-68809457	Hela-S3	cervix:	n/a
43	chr14:68822877-68822927	HPAEpiC	pulmonary alveolar:	n/a
44	chr14:68822877-68822927	MCF-7	breast:	n/a
45	chr14:68830704-68830754	AG10803	skin:	n/a
46	chr14:68830704-68830754	BJ	skin:	n/a
47	chr14:68831210-68831260	NT2-D1	testis:	n/a
48	chr14:68831098-68831148	HEEpiC	esophagus:	n/a
49	chr14:68831098-68831148	NHDF-neo	bronchial:	n/a
50	chr14:68831098-68831148	BJ	skin:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:68828824..68831409-chr14:69259339..69261614,2	MCF-7	breast:
2	chr14:68819003..68821969-chr14:68824921..68827031,3	MCF-7	breast:
3	chr14:68834296..68836299-chr14:69281257..69283573,2	MCF-7	breast:
4	chr14:68815716..68817716-chr14:69259807..69261417,2	MCF-7	breast:
5	chr14:68798605..68800534-chr14:68804811..68807442,2	K562	blood:
6	chr14:68802480..68804741-chr14:68806549..68808439,2	MCF-7	breast:
7	chr14:68735494..68738369-chr14:68803513..68805085,2	K562	blood:
8	chr14:68827902..68830472-chr14:68830504..68833278,2	MCF-7	breast:
9	chr14:68823758..68825352-chr14:69246991..69249510,2	MCF-7	breast:
10	chr14:68834081..68836635-chr14:68840807..68842526,2	MCF-7	breast:
11	chr14:68830049..68833032-chr14:68833353..68836919,3	MCF-7	breast:
12	chr14:68831265..68833449-chr14:68839230..68840971,2	K562	blood:
13	chr14:68815687..68818492-chr14:68859330..68861722,2	MCF-7	breast:
14	chr14:68793230..68795249-chr14:68798426..68801112,3	MCF-7	breast:
15	chr14:68832613..68834269-chr14:69259859..69261484,2	MCF-7	breast:
16	chr14:68815378..68819225-chr14:68819272..68820880,3	MCF-7	breast:
17	chr14:68827902..68830472-chr14:68830504..68833278,2	MCF-7	breast:
18	chr14:68820537..68822571-chr14:68826087..68829022,2	MCF-7	breast:
19	chr14:68793230..68795249-chr14:68798426..68801112,3	MCF-7	breast:
20	chr14:68825872..68826457-chr3:128399962..128400924,2	Hela-S3	cervix:
21	chr14:68808236..68810684-chr14:68816764..68819058,2	K562	blood:
22	chr14:68816741..68820574-chr14:68865040..68867633,3	MCF-7	breast:
23	chr14:68818141..68819733-chr14:68823744..68826518,2	MCF-7	breast:
24	chr14:68605282..68608015-chr14:68828516..68831935,3	MCF-7	breast:
25	chr14:68715317..68717585-chr14:68825893..68828768,2	MCF-7	breast:
26	chr14:68806501..68808073-chr14:68812909..68815753,2	MCF-7	breast:
27	chr14:68830853..68833594-chr14:68845594..68847240,2	MCF-7	breast:
28	chr14:68815378..68819225-chr14:68819272..68820880,3	MCF-7	breast:
29	chr14:68833173..68835923-chr14:68849243..68851394,2	MCF-7	breast:
30	chr14:68797384..68800129-chr14:68809250..68811315,3	MCF-7	breast:
31	chr14:68829763..68832771-chr14:68932528..68934610,3	MCF-7	breast:
32	chr14:68815262..68818162-chr14:68930944..68932946,2	MCF-7	breast:
33	chr14:68410593..68411154-chr14:68830174..68830861,2	MCF-7	breast:
34	chr14:68716909..68718440-chr14:68825908..68828082,2	MCF-7	breast:
35	chr14:68825944..68827460-chr14:68863306..68865139,2	MCF-7	breast:
36	chr14:68813990..68815788-chr14:69260981..69262578,2	MCF-7	breast:
37	chr14:68834932..68837443-chr14:69252432..69254129,2	MCF-7	breast:
38	chr14:68819732..68821460-chr14:69260415..69262094,2	MCF-7	breast:
39	chr14:68806501..68808073-chr14:68812909..68815753,2	MCF-7	breast:
40	chr14:68827778..68831796-chr14:69251511..69256304,4	MCF-7	breast:
41	chr14:68773574..68776467-chr14:68830101..68831913,2	MCF-7	breast:
42	chr14:68833824..68836435-chr14:69255771..69258211,2	MCF-7	breast:
43	chr14:68821597..68823299-chr14:69259468..69262394,2	MCF-7	breast:
44	chr14:68715036..68715912-chr14:68829845..68830845,3	MCF-7	breast:
45	chr14:68829028..68831413-chr14:69258975..69262628,4	MCF-7	breast:
46	chr14:68778894..68781152-chr14:68792473..68795280,2	MCF-7	breast:
47	chr14:68819003..68821969-chr14:68824921..68827031,3	MCF-7	breast:
48	chr14:68762186..68763785-chr14:68835933..68838627,2	K562	blood:
49	chr14:68808236..68810684-chr14:68816764..68819058,2	K562	blood:
50	chr14:68741974..68743530-chr14:68829514..68831281,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000240210	TF binding region
ENSG00000240210	CpG island
ENSG00000240210	chromatin interactions
ENSG00000185650	chromatin interactions

Extended variants
information (count: 1571 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1571 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17755115	chr14:68795209-68795210	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551620437	chr14:68795237-68795238	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs4899238	chr14:68795239-68795240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs183805624	chr14:68795240-68795241	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540205965	chr14:68795247-68795248	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs530856904	chr14:68795267-68795268	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs564882912	chr14:68795323-68795324	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs144926852	chr14:68795398-68795399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs544492756	chr14:68795462-68795463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188579835	chr14:68795473-68795474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562545624	chr14:68795486-68795487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541305953	chr14:68795526-68795527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376172301	chr14:68795575-68795576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549285062	chr14:68795601-68795602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117050396	chr14:68795643-68795644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566599978	chr14:68795667-68795668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372958028	chr14:68795703-68795704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62635808	chr14:68795709-68795710	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs117747543	chr14:68795750-68795751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150920104	chr14:68795771-68795772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191850026	chr14:68795785-68795786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556766817	chr14:68795791-68795792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554683403	chr14:68795873-68795874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9989140	chr14:68795879-68795880	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs139456546	chr14:68795898-68795899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149677955	chr14:68795958-68795959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573002398	chr14:68795991-68795992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546628379	chr14:68796016-68796017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114667287	chr14:68796030-68796031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558316648	chr14:68796035-68796036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576725862	chr14:68796078-68796079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544189689	chr14:68796108-68796109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184317190	chr14:68796160-68796161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs9989152	chr14:68796175-68796176	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs9989153	chr14:68796192-68796193	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs557154369	chr14:68796206-68796207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190345283	chr14:68796207-68796208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181970557	chr14:68796325-68796326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185780676	chr14:68796420-68796421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564323040	chr14:68796421-68796422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145501138	chr14:68796434-68796435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12884901	chr14:68796465-68796466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs111490484	chr14:68796469-68796470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188987491	chr14:68796494-68796495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180913389	chr14:68796515-68796516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558100881	chr14:68796518-68796519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548052393	chr14:68796543-68796544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573412323	chr14:68796563-68796564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145415179	chr14:68796604-68796605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558581445	chr14:68796615-68796616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1169 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:68769000-68810000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:68785600-68812400	Weak transcription	Fetal Muscle Trunk	muscle
3	chr14:68786600-68799000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr14:68786800-68798800	Weak transcription	Brain Anterior Caudate	brain
5	chr14:68787400-68798400	Weak transcription	Fetal Stomach	stomach
6	chr14:68788200-68807000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr14:68788400-68796600	Weak transcription	Fetal Lung	lung
8	chr14:68789600-68810400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:68790200-68795600	Weak transcription	Psoas Muscle	Psoas
10	chr14:68790400-68795400	Enhancers	Primary B cells from peripheral blood	blood
11	chr14:68790800-68799200	Weak transcription	Fetal Muscle Leg	muscle
12	chr14:68792600-68798200	Weak transcription	Fetal Intestine Small	intestine
13	chr14:68793800-68798200	Weak transcription	Colon Smooth Muscle	Colon
14	chr14:68794400-68797400	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr14:68794400-68798000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr14:68795000-68795400	Flanking Active TSS	GM12878-XiMat	blood
17	chr14:68795000-68798200	Weak transcription	Primary B cells from cord blood	blood
18	chr14:68795200-68795400	Enhancers	Spleen	Spleen
19	chr14:68795200-68795600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr14:68795400-68796400	Enhancers	GM12878-XiMat	blood
21	chr14:68795400-68799200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr14:68796400-68798200	Weak transcription	GM12878-XiMat	blood
23	chr14:68796600-68799800	Enhancers	Fetal Lung	lung
24	chr14:68796800-68800200	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr14:68797400-68798400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr14:68798000-68798800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:68798000-68799400	Enhancers	Fetal Kidney	kidney
28	chr14:68798200-68798600	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr14:68798200-68798800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:68798200-68799200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr14:68798200-68799200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:68798200-68799200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:68798200-68799400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:68798200-68799400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr14:68798200-68799400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr14:68798200-68799600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr14:68798200-68799600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr14:68798200-68799600	Enhancers	GM12878-XiMat	blood
39	chr14:68798200-68799800	Enhancers	Fetal Intestine Small	intestine
40	chr14:68798200-68800000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr14:68798200-68800200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr14:68798200-68800200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr14:68798200-68800600	Enhancers	Colon Smooth Muscle	Colon
44	chr14:68798200-68802400	Enhancers	Primary B cells from cord blood	blood
45	chr14:68798400-68799000	Enhancers	HepG2	liver
46	chr14:68798400-68799400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr14:68798400-68799800	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr14:68798400-68800000	Enhancers	Fetal Stomach	stomach
49	chr14:68798600-68799400	Enhancers	Stomach Smooth Muscle	stomach
50	chr14:68798800-68799200	Enhancers	Fetal Intestine Large	intestine

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