Variant report

Variant	nsv902028
Chromosome Location	chr14:66980652-67059231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:66981162-66981258	GM12878	blood:	n/a	n/a
2	CEBPB	chr14:66981010-66981332	K562	blood:	n/a	n/a
3	CEBPB	chr14:66980960-66981344	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr14:67032442-67032536	HepG2	liver:	n/a	chr14:67032517-67032530 chr14:67032476-67032493 chr14:67032478-67032489 chr14:67032477-67032490
5	CEBPB	chr14:67008105-67008272	IMR90	lung:	n/a	chr14:67008160-67008171
6	CEBPB	chr14:66980997-66981296	IMR90	lung:	n/a	n/a
7	CEBPB	chr14:67022576-67022783	A549	lung:	n/a	n/a
8	CEBPB	chr14:66980983-66981296	A549	lung:	n/a	n/a
9	CEBPB	chr14:67009933-67010042	A549	lung:	n/a	n/a
10	CEBPB	chr14:66980971-66981309	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:67008036-67008341	HepG2	liver:	n/a	chr14:67008160-67008171
12	CTCF	chr14:66997445-66997540	MCF-7	breast:	n/a	n/a
13	CTCF	chr14:67016232-67016606	GM12878	blood:	n/a	n/a
14	CTCF	chr14:67016231-67016488	K562	blood:	n/a	n/a
15	CTCF	chr14:67016220-67016370	MCF-7	breast:	n/a	n/a
16	CTCF	chr14:67034950-67035316	MCF-7	breast:	n/a	chr14:67035128-67035149
17	CTCF	chr14:67050003-67050099	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr14:67016304-67016638	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:66991429-66991454	GM13977	blood:	n/a	n/a
20	CTCF	chr14:67016401-67016486	MCF-7	breast:	n/a	n/a
21	CTCF	chr14:67035105-67035220	LNCaP	prostate:	n/a	chr14:67035128-67035149
22	CTCF	chr14:67035108-67035135	Medullo	brain:	n/a	n/a
23	CTCF	chr14:67035040-67035222	HUVEC	blood vessel:	n/a	chr14:67035128-67035149
24	CTCF	chr14:67035056-67035192	Hela-S3	cervix:	n/a	chr14:67035128-67035149
25	CTCF	chr14:67016338-67016465	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr14:67035040-67035190	MCF-7	breast:	n/a	chr14:67035128-67035149
27	CTCF	chr14:67035063-67035165	MCF-7	breast:	n/a	chr14:67035128-67035149
28	CTCF	chr14:66981684-66981784	GM12878	blood:	n/a	n/a
29	CTCF	chr14:67016396-67016466	K562	blood:	n/a	n/a
30	CTCF	chr14:67035133-67035158	LNCaP	prostate:	n/a	n/a
31	CTCF	chr14:67016380-67016530	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr14:66997440-66997590	HepG2	liver:	n/a	n/a
33	CTCF	chr14:67035080-67035230	RPTEC	kidney:	n/a	chr14:67035128-67035149
34	CTCF	chr14:67014888-67014940	GM10248	blood:	n/a	n/a
35	CTCF	chr14:67049172-67049221	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr14:66997350-66997457	Fibrobl	skin:	n/a	n/a
37	CTCF	chr14:67022127-67022182	GM13976	blood:	n/a	n/a
38	CTCF	chr14:67035063-67035231	Spleen_OC	spleen:	n/a	chr14:67035128-67035149
39	CTCF	chr14:67016395-67016453	GM12878	blood:	n/a	n/a
40	CTCF	chr14:67035160-67035310	HMEC	breast:	n/a	n/a
41	CUX1	chr14:67046670-67046753	GM12878	blood:	n/a	n/a
42	E2F4	chr14:67017948-67018052	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr14:67024131-67024291	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr14:67003059-67003217	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr14:67015999-67016168	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr14:67043161-67043357	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr14:66980749-66981383	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr14:66985039-66985131	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr14:67034242-67034409	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr14:67034037-67034329	GM12878	blood:	n/a	chr14:67034180-67034189 chr14:67034178-67034189 chr14:67034179-67034189 chr14:67034178-67034191

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67012668-67012718	HMEC	breast:	n/a
2	chr14:67012668-67012718	GM06990	blood:	n/a
3	chr14:67012668-67012718	IMR90	lung:	fetal
4	chr14:67012668-67012718	AG04450	lung:	fetal
5	chr14:67012668-67012718	HCF	heart:	n/a
6	chr14:67012668-67012718	NB4	blood:	n/a
7	chr14:67012668-67012718	BE2_C	brain:	n/a
8	chr14:67012668-67012718	HNPCEpiC	eye:	n/a
9	chr14:67012668-67012718	T-47D	breast:	n/a
10	chr14:67012668-67012718	LNCaP	prostate:	n/a
11	chr14:67012668-67012718	ProgFib	skin:	n/a
12	chr14:67012668-67012718	GM12878	blood:	n/a
13	chr14:67012668-67012718	AG09319	gingival:	n/a
14	chr14:67012668-67012718	GM19239	blood:	n/a
15	chr14:67012668-67012718	NH-A	brain:	n/a
16	chr14:67012668-67012718	H1-hESC	embryonic stem cell:	embryo
17	chr14:67012668-67012718	SK-N-MC	brain:	n/a
18	chr14:67012668-67012718	SK-N-SH	brain:	n/a
19	chr14:67012668-67012718	MCF10A-Er-Src	breast:	n/a
20	chr14:67012668-67012718	PrEC	prostate:	n/a
21	chr14:67012668-67012718	GM12892	blood:	n/a
22	chr14:67012668-67012718	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:67012668-67012718	SK-N-SH_RA	brain:	n/a
24	chr14:67012668-67012718	K562	blood:	n/a
25	chr14:67012668-67012718	PFSK-1	brain:	n/a
26	chr14:67012668-67012718	SKMC	muscle:	n/a
27	chr14:67012668-67012718	ECC-1	luminal epithelium:	n/a
28	chr14:67012668-67012718	A549	lung:	n/a
29	chr14:67012668-67012718	Caco-2	colon:	n/a
30	chr14:67012668-67012718	MCF-7	breast:	n/a
31	chr14:67012668-67012718	Jurkat	blood:	n/a
32	chr14:67012668-67012718	HL-60	blood:	n/a
33	chr14:67012668-67012718	HUVEC	blood vessel:	n/a
34	chr14:67012668-67012718	HCT-116	colon:	n/a
35	chr14:67012668-67012718	GM12891	blood:	n/a
36	chr14:67012668-67012718	AG10803	skin:	n/a
37	chr14:67012668-67012718	SAEC	small airway:	n/a
38	chr14:67012668-67012718	Hela-S3	cervix:	n/a
39	chr14:67012668-67012718	NHBE	bronchial:	n/a
40	chr14:67012668-67012718	U87	brain:	n/a
41	chr14:67012668-67012718	Hepatocyte	liver:	n/a
42	chr14:67012668-67012718	BJ	skin:	n/a
43	chr14:67012668-67012718	AG04449	skin:	fetal
44	chr14:67012668-67012718	HRE	kidney:	n/a
45	chr14:67012668-67012718	HCPEpiC	choroid plexus:	n/a
46	chr14:67012668-67012718	HIPEpiC	eye:	n/a
47	chr14:67012668-67012718	HCM	heart:	n/a
48	chr14:67012668-67012718	NT2-D1	testis:	n/a
49	chr14:67012668-67012718	RPTEC	kidney:	n/a
50	chr14:67012668-67012718	PANC-1	pancreas:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:66972704..66976384-chr14:67000982..67004211,4	MCF-7	breast:
2	chr14:67013560..67014177-chr16:87123245..87123883,2	MCF-7	breast:
3	chr14:66973238..66976174-chr14:67016237..67019038,2	MCF-7	breast:
4	chr14:67044325..67045049-chr8:77423954..77424779,2	MCF-7	breast:
5	chr14:66972976..66974827-chr14:67023715..67025851,2	MCF-7	breast:
6	chr14:66998273..67000951-chr14:67001181..67003201,2	MCF-7	breast:
7	chr14:66979852..66981724-chr14:67004183..67006810,2	K562	blood:
8	chr14:66974580..66976543-chr14:66983199..66985930,3	MCF-7	breast:
9	chr14:66974208..66976195-chr14:67036443..67039003,2	MCF-7	breast:
10	chr14:66974018..66977412-chr14:66988835..66991120,3	MCF-7	breast:
11	chr14:66998273..67000951-chr14:67001181..67003201,2	MCF-7	breast:
12	chr14:66974791..66976543-chr14:66986687..66988455,2	MCF-7	breast:
13	chr14:66869840..66870579-chr14:67035035..67035552,2	MCF-7	breast:
14	chr14:66975009..66976777-chr14:67006452..67008690,2	MCF-7	breast:
15	chr14:67031416..67034033-chr14:67041598..67043348,2	MCF-7	breast:
16	chr14:66973828..66976621-chr14:66983168..66986678,3	MCF-7	breast:
17	chr14:66974103..66976751-chr14:66998338..67000349,2	MCF-7	breast:
18	chr14:67031416..67034033-chr14:67041598..67043348,2	MCF-7	breast:
19	chr14:67040072..67042253-chr14:67043564..67045326,2	MCF-7	breast:
20	chr14:66979852..66981724-chr14:67004183..67006810,2	K562	blood:
21	chr14:66961968..66962547-chr14:67034432..67035854,3	MCF-7	breast:
22	chr14:67040072..67042253-chr14:67043564..67045326,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2014B16.3.1-5	chr14:66983554-66984402	ucscGeneNc_uc001xji_1

No data

Variant related genes	Relation type
ENSG00000258561	TF binding region
ENSG00000258561	CpG island
ENSG00000171723	chromatin interactions
ENSG00000258561	chromatin interactions

Extended variants
information (count: 3335 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3335 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8004619	chr14:66980652-66980653	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536484475	chr14:66980670-66980671	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs182672308	chr14:66980743-66980744	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs367635758	chr14:66980799-66980800	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576251574	chr14:66980896-66980897	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs545073941	chr14:66980954-66980955	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113445957	chr14:66980981-66980982	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs571970644	chr14:66980983-66980984	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs540590068	chr14:66981033-66981034	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs112878896	chr14:66981043-66981044	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs560875817	chr14:66981066-66981067	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs116871228	chr14:66981069-66981070	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs529552312	chr14:66981190-66981191	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs35802045	chr14:66981203-66981204	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs117132215	chr14:66981212-66981213	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs562699401	chr14:66981227-66981228	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs531704515	chr14:66981239-66981240	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551430126	chr14:66981302-66981303	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs571575466	chr14:66981337-66981338	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs188815063	chr14:66981361-66981362	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs547457215	chr14:66981400-66981401	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs567589147	chr14:66981425-66981426	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs531377755	chr14:66981435-66981436	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs193209680	chr14:66981548-66981549	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs561313879	chr14:66981634-66981635	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556395824	chr14:66981640-66981641	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs199929257	chr14:66981740-66981741	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs548005033	chr14:66981794-66981795	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs148009556	chr14:66981800-66981801	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs538753316	chr14:66981827-66981828	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs546900492	chr14:66981860-66981861	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs558592215	chr14:66981864-66981865	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs572032277	chr14:66981920-66981921	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs541062302	chr14:66981922-66981923	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs11622637	chr14:66981923-66981924	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs571876524	chr14:66981925-66981926	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554265335	chr14:66981945-66981946	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs573997660	chr14:66981987-66981988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs542874836	chr14:66981988-66981989	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs74245900	chr14:66982025-66982026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368663925	chr14:66982069-66982070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141663262	chr14:66982127-66982128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376832174	chr14:66982159-66982160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570625539	chr14:66982211-66982212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28548143	chr14:66982217-66982218	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs79194468	chr14:66982314-66982315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546679554	chr14:66982405-66982406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527772523	chr14:66982421-66982422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547815250	chr14:66982468-66982469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76416301	chr14:66982507-66982508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
cataract	16735990	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66976600-66989800	Weak transcription	Aorta	Aorta
2	chr14:66976800-66983600	Weak transcription	Psoas Muscle	Psoas
3	chr14:66977000-66981000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr14:66977000-66981000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:66977600-66997200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr14:66978600-66982600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr14:66979200-66981000	Weak transcription	HepG2	liver
8	chr14:66979400-66981600	Weak transcription	Fetal Heart	heart
9	chr14:66979600-66981800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr14:66979600-66985400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:66980000-66981000	Weak transcription	Liver	Liver
12	chr14:66980400-66981600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr14:66980400-66981600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr14:66980400-66981800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr14:66980600-66980800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr14:66980600-66981600	Active TSS	GM12878-XiMat	blood
17	chr14:66980600-66982000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr14:66981000-66981200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr14:66981000-66981200	Enhancers	Liver	Liver
20	chr14:66981000-66981800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:66981000-66981800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr14:66981000-66981800	Enhancers	HepG2	liver
23	chr14:66981000-66982000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr14:66981200-66981600	Weak transcription	Liver	Liver
25	chr14:66981600-66981800	Enhancers	Liver	Liver
26	chr14:66981600-66982000	Enhancers	Fetal Heart	heart
27	chr14:66981600-66982000	Flanking Active TSS	GM12878-XiMat	blood
28	chr14:66981800-66982000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr14:66981800-66982000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:66981800-66982000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr14:66981800-66982400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr14:66981800-66989600	Weak transcription	Liver	Liver
33	chr14:66983600-66983800	Enhancers	Psoas Muscle	Psoas
34	chr14:66985400-66985600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr14:66989600-66990800	Enhancers	Liver	Liver
36	chr14:66990800-66993200	Weak transcription	Liver	Liver
37	chr14:66993200-66993800	Enhancers	Liver	Liver
38	chr14:66995400-66995600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr14:66995400-66996600	Weak transcription	Fetal Stomach	stomach
40	chr14:66995600-67003600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr14:66996400-66997400	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr14:66996400-66998000	Enhancers	Left Ventricle	heart
43	chr14:66996600-66997200	Strong transcription	Fetal Stomach	stomach
44	chr14:66996600-66997600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:66996800-66997600	Enhancers	Gastric	stomach
46	chr14:66996800-66997600	Enhancers	GM12878-XiMat	blood
47	chr14:66997000-66997400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:66997000-66997600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:66997000-66997600	Enhancers	Esophagus	oesophagus
50	chr14:66997000-66997600	Enhancers	Right Ventricle	heart

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