Variant report

Variant	nsv564902
Chromosome Location	chr14:64230089-64280206
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	chr14:64236943-64237235	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:64276060-64276100	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:64266422-64266582	K562	blood:	n/a	n/a
4	ARID3A	chr14:64250330-64250801	HepG2	liver:	n/a	n/a
5	BATF	chr14:64262299-64262591	GM12878	blood:	n/a	chr14:64262436-64262447
6	BATF	chr14:64262240-64262563	GM12878	blood:	n/a	chr14:64262436-64262447
7	BHLHE40	chr14:64230913-64231276	HepG2	liver:	n/a	n/a
8	BHLHE40	chr14:64266527-64266668	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:64278436-64278680	HepG2	liver:	n/a	n/a
10	BRCA1	chr14:64236919-64237251	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr14:64278719-64278999	K562	blood:	n/a	n/a
12	CEBPB	chr14:64272115-64272315	HepG2	liver:	n/a	chr14:64272160-64272171
13	CEBPB	chr14:64276720-64277041	HepG2	liver:	n/a	chr14:64276892-64276903
14	CEBPB	chr14:64265798-64265989	Hela-S3	cervix:	n/a	chr14:64265852-64265863
15	CEBPB	chr14:64272108-64272191	H1-hESC	embryonic stem cell:	n/a	chr14:64272160-64272171
16	CEBPB	chr14:64255832-64255953	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:64276736-64276998	Hela-S3	cervix:	n/a	chr14:64276892-64276903
18	CEBPB	chr14:64268325-64268362	HepG2	liver:	n/a	chr14:64268342-64268353
19	CEBPB	chr14:64276736-64277026	A549	lung:	n/a	chr14:64276892-64276903
20	CEBPB	chr14:64243809-64244085	IMR90	lung:	n/a	n/a
21	CEBPB	chr14:64265785-64266007	HepG2	liver:	n/a	chr14:64265852-64265863
22	CEBPB	chr14:64231461-64231854	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:64276036-64276292	HepG2	liver:	n/a	chr14:64276151-64276162
24	CEBPB	chr14:64243767-64244142	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:64272079-64272323	K562	blood:	n/a	chr14:64272160-64272171
26	CEBPB	chr14:64255817-64256000	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:64248099-64248719	Hela-S3	cervix:	n/a	chr14:64248258-64248269
28	CEBPB	chr14:64248131-64248314	HepG2	liver:	n/a	chr14:64248258-64248269
29	CEBPB	chr14:64276737-64277013	IMR90	lung:	n/a	chr14:64276892-64276903
30	CEBPB	chr14:64268139-64268450	MCF-7	breast:	n/a	chr14:64268342-64268353
31	CHD2	chr14:64244843-64244994	HepG2	liver:	n/a	n/a
32	CHD2	chr14:64249717-64250102	K562	blood:	n/a	n/a
33	CHD2	chr14:64244774-64245019	K562	blood:	n/a	n/a
34	CTCF	chr14:64237000-64237150	WERI-Rb-1	eye:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
35	CTCF	chr14:64266420-64266570	HMEC	breast:	n/a	chr14:64266499-64266517 chr14:64266501-64266522
36	CTCF	chr14:64237500-64237650	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr14:64237040-64237190	HMEC	breast:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
38	CTCF	chr14:64237040-64237190	GM12868	blood:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
39	CTCF	chr14:64266411-64266672	H1-hESC	embryonic stem cell:	n/a	chr14:64266499-64266517 chr14:64266501-64266522
40	CTCF	chr14:64237387-64237395	Gliobla	brain:	n/a	n/a
41	CTCF	chr14:64266420-64266570	AG10803	skin:	n/a	chr14:64266499-64266517 chr14:64266501-64266522
42	CTCF	chr14:64266460-64266610	HRPEpiC	eye:	n/a	chr14:64266499-64266517 chr14:64266501-64266522
43	CTCF	chr14:64237060-64237210	GM12864	blood:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
44	CTCF	chr14:64237000-64237150	GM12864	blood:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
45	CTCF	chr14:64237060-64237210	HFF-Myc	foreskin:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
46	CTCF	chr14:64266340-64266722	IMR90	lung:	n/a	chr14:64266499-64266517 chr14:64266501-64266522
47	CTCF	chr14:64266400-64266550	NHDF-neo	bronchial:	n/a	chr14:64266499-64266517 chr14:64266501-64266522
48	CTCF	chr14:64237040-64237190	BJ	skin:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
49	CTCF	chr14:64237019-64237224	GM10248	blood:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111
50	CTCF	chr14:64236985-64237261	Pancreas_OC	pancreas:	n/a	chr14:64237096-64237114 chr14:64237097-64237113 chr14:64237091-64237112 chr14:64237102-64237111 chr14:64237098-64237111

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:64270264-64270314	U87	brain:	n/a
2	chr14:64270264-64270314	PANC-1	pancreas:	n/a
3	chr14:64270264-64270314	SK-N-SH_RA	brain:	n/a
4	chr14:64270264-64270314	HEK293	kidney:	embryo
5	chr14:64270264-64270314	IMR90	lung:	fetal
6	chr14:64270264-64270314	BE2_C	brain:	n/a
7	chr14:64270264-64270314	AG09309	skin:	n/a
8	chr14:64270264-64270314	HUVEC	blood vessel:	n/a
9	chr14:64270264-64270314	CMK	blood:	n/a
10	chr14:64270264-64270314	GM19239	blood:	n/a
11	chr14:64270264-64270314	HNPCEpiC	eye:	n/a
12	chr14:64270264-64270314	HRCEpiC	kidney:	n/a
13	chr14:64270264-64270314	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:64270264-64270314	AG04449	skin:	fetal
15	chr14:64270264-64270314	GM12892	blood:	n/a
16	chr14:64270264-64270314	HEEpiC	esophagus:	n/a
17	chr14:64270264-64270314	NB4	blood:	n/a
18	chr14:64270264-64270314	AG09319	gingival:	n/a
19	chr14:64270264-64270314	PrEC	prostate:	n/a
20	chr14:64270264-64270314	PFSK-1	brain:	n/a
21	chr14:64270264-64270314	Hepatocyte	liver:	n/a
22	chr14:64270264-64270314	HepG2	liver:	n/a
23	chr14:64270264-64270314	MCF10A-Er-Src	breast:	n/a
24	chr14:64270264-64270314	HL-60	blood:	n/a
25	chr14:64270264-64270314	HCPEpiC	choroid plexus:	n/a
26	chr14:64270264-64270314	K562	blood:	n/a
27	chr14:64270264-64270314	HRE	kidney:	n/a
28	chr14:64270264-64270314	GM12878	blood:	n/a
29	chr14:64270264-64270314	A549	lung:	n/a
30	chr14:64270264-64270314	Jurkat	blood:	n/a
31	chr14:64270264-64270314	ProgFib	skin:	n/a
32	chr14:64270264-64270314	SKMC	muscle:	n/a
33	chr14:64270264-64270314	RPTEC	kidney:	n/a
34	chr14:64270264-64270314	AG10803	skin:	n/a
35	chr14:64270264-64270314	H1-hESC	embryonic stem cell:	embryo
36	chr14:64270264-64270314	ovcar-3	ovarian:	n/a
37	chr14:64270264-64270314	AG04450	lung:	fetal
38	chr14:64270264-64270314	HCF	heart:	n/a
39	chr14:64270264-64270314	NH-A	brain:	n/a
40	chr14:64270264-64270314	GM06990	blood:	n/a
41	chr14:64270264-64270314	AoSMC	blood vessel:	n/a
42	chr14:64270264-64270314	NT2-D1	testis:	n/a
43	chr14:64270264-64270314	NHDF-neo	bronchial:	n/a
44	chr14:64270264-64270314	Caco-2	colon:	n/a
45	chr14:64270264-64270314	SAEC	small airway:	n/a
46	chr14:64270264-64270314	HIPEpiC	eye:	n/a
47	chr14:64270264-64270314	HCT-116	colon:	n/a
48	chr14:64270264-64270314	HMEC	breast:	n/a
49	chr14:64270264-64270314	GM12891	blood:	n/a
50	chr14:64270264-64270314	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:64258294..64260685-chr14:64264198..64267177,2	K562	blood:
2	chr14:64107765..64108416-chr14:64237040..64237554,2	K562	blood:
3	chr14:64258294..64260685-chr14:64264198..64267177,2	K562	blood:
4	chr14:64265985..64266560-chr14:64769846..64770485,2	MCF-7	breast:
5	chr14:64265952..64266822-chr14:64460521..64461407,3	MCF-7	breast:
6	chr14:64194851..64195663-chr14:64236638..64237222,3	MCF-7	breast:
7	chr14:64099391..64099947-chr14:64236858..64237506,2	MCF-7	breast:
8	chr14:64194707..64195311-chr14:64236987..64237506,2	MCF-7	breast:
9	chr14:64253240..64254789-chr14:64255821..64258714,2	MCF-7	breast:
10	chr14:64099760..64100293-chr14:64236657..64237382,3	MCF-7	breast:
11	chr14:64253240..64254789-chr14:64255821..64258714,2	MCF-7	breast:

Variant related genes	Relation type
RPS28P1	TF binding region
RPS28P1	CpG island
ENSG00000126821	chromatin interactions
ENSG00000140006	chromatin interactions

Extended variants
information (count: 1808 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1808 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4902242	chr14:64230089-64230090	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572097648	chr14:64230119-64230120	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs142125311	chr14:64230175-64230176	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs11622195	chr14:64230195-64230196	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs111332176	chr14:64230339-64230340	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187085502	chr14:64230377-64230378	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563546785	chr14:64230394-64230395	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549643145	chr14:64230401-64230402	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192367540	chr14:64230497-64230498	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs78537886	chr14:64230525-64230526	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527783819	chr14:64230530-64230531	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145983404	chr14:64230552-64230553	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567435129	chr14:64230604-64230605	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538300863	chr14:64230681-64230682	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536417528	chr14:64230686-64230687	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370030476	chr14:64230709-64230710	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533482506	chr14:64230716-64230717	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183260219	chr14:64230841-64230842	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569998544	chr14:64230919-64230920	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75415278	chr14:64230947-64230948	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558520751	chr14:64231010-64231011	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370060237	chr14:64231030-64231031	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541031522	chr14:64231060-64231061	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138859227	chr14:64231061-64231062	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12890867	chr14:64231125-64231126	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528664966	chr14:64231146-64231147	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550281609	chr14:64231159-64231160	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374309932	chr14:64231185-64231186	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377399221	chr14:64231228-64231229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370175807	chr14:64231235-64231236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373653994	chr14:64231254-64231255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529355939	chr14:64231274-64231275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201471755	chr14:64231275-64231276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34093002	chr14:64231290-64231291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370163032	chr14:64231291-64231292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569893208	chr14:64231307-64231308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547407632	chr14:64231413-64231414	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377226433	chr14:64231504-64231505	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535637630	chr14:64231535-64231536	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370504043	chr14:64231581-64231582	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530165096	chr14:64231621-64231622	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149267692	chr14:64231635-64231636	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190233167	chr14:64231636-64231637	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375353356	chr14:64231661-64231662	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182818812	chr14:64231739-64231740	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144517766	chr14:64231765-64231766	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528493751	chr14:64231768-64231769	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534296777	chr14:64231778-64231779	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147981347	chr14:64231783-64231784	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186703189	chr14:64231789-64231790	Genic enhancers Weak transcription Flanking Active TSS 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
Malignant peripheral nerve sheath tumor	18522746	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
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64216400-64230200	Weak transcription	HepG2	liver
2	chr14:64220000-64243400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:64226600-64234800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr14:64228200-64230800	Active TSS	Primary B cells from cord blood	blood
5	chr14:64229000-64231400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:64230000-64230400	Flanking Active TSS	Placenta	Placenta
7	chr14:64230000-64231200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr14:64230200-64232000	Enhancers	HepG2	liver
9	chr14:64230400-64230800	Enhancers	Fetal Stomach	stomach
10	chr14:64230400-64234400	Enhancers	Placenta	Placenta
11	chr14:64230800-64231000	Enhancers	NHLF	lung
12	chr14:64231200-64231400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr14:64231400-64231800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr14:64231400-64231800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr14:64231800-64232000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr14:64231800-64232000	Enhancers	NHLF	lung
17	chr14:64231800-64254400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:64232000-64233000	Weak transcription	HepG2	liver
19	chr14:64232000-64233400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
20	chr14:64233000-64233400	Enhancers	HepG2	liver
21	chr14:64233200-64233600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:64233200-64233600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr14:64233200-64233600	Enhancers	GM12878-XiMat	blood
24	chr14:64233400-64234600	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr14:64233400-64234600	Weak transcription	HepG2	liver
26	chr14:64233600-64235600	Weak transcription	GM12878-XiMat	blood
27	chr14:64234400-64235400	Weak transcription	Placenta	Placenta
28	chr14:64234600-64235800	Enhancers	HepG2	liver
29	chr14:64234600-64236400	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr14:64234800-64235000	Enhancers	Duodenum Mucosa	Duodenum
31	chr14:64235000-64235800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr14:64235400-64237400	Enhancers	Primary B cells from peripheral blood	blood
33	chr14:64235400-64237400	Enhancers	Placenta	Placenta
34	chr14:64235600-64236200	Enhancers	GM12878-XiMat	blood
35	chr14:64235800-64236200	Enhancers	Duodenum Mucosa	Duodenum
36	chr14:64236200-64240000	Weak transcription	GM12878-XiMat	blood
37	chr14:64236400-64236800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr14:64236800-64237200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr14:64236800-64237400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr14:64236800-64237600	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr14:64237200-64237400	Enhancers	Brain Angular Gyrus	brain
42	chr14:64237400-64254200	Weak transcription	Placenta	Placenta
43	chr14:64237600-64254000	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr14:64240000-64240600	Enhancers	A549	lung
45	chr14:64240000-64240800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr14:64240000-64240800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:64240000-64240800	Enhancers	GM12878-XiMat	blood
48	chr14:64240000-64240800	Enhancers	HMEC	breast
49	chr14:64240000-64241000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:64240000-64241000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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