Variant report

Variant	nsv1050258
Chromosome Location	chr14:69942127-69976694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:1098)
Chromatin interactive
region (count:34)
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	chr14:69970593-69970792	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:69941879-69942182	K562	blood:	n/a	n/a
3	ARID3A	chr14:69941910-69942131	HepG2	liver:	n/a	n/a
4	BACH1	chr14:69968018-69968246	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:69948920-69949253	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:69950648-69951056	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:69948935-69949141	K562	blood:	n/a	n/a
8	BCL3	chr14:69973295-69973474	GM12878	blood:	n/a	n/a
9	CEBPB	chr14:69959052-69959243	A549	lung:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
10	CEBPB	chr14:69957726-69958039	HepG2	liver:	n/a	chr14:69957884-69957895
11	CEBPB	chr14:69957851-69957951	K562	blood:	n/a	chr14:69957884-69957895
12	CEBPB	chr14:69950226-69950924	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr14:69959034-69959265	HepG2	liver:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
14	CHD2	chr14:69950982-69951100	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr14:69950474-69951751	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr14:69970620-69970770	HRE	kidney:	n/a	n/a
17	CTCF	chr14:69970578-69970756	MCF-7	breast:	n/a	n/a
18	CTCF	chr14:69970600-69970750	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr14:69970568-69970787	Gliobla	brain:	n/a	n/a
20	CTCF	chr14:69970463-69970894	HepG2	liver:	n/a	n/a
21	CTCF	chr14:69970980-69971130	GM12871	blood:	n/a	chr14:69970988-69971006
22	CTCF	chr14:69941980-69942130	HEEpiC	esophagus:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
23	CTCF	chr14:69970560-69970710	HepG2	liver:	n/a	n/a
24	CTCF	chr14:69942000-69942150	HBMEC	blood vessel:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
25	CTCF	chr14:69942020-69942170	GM12864	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
26	CTCF	chr14:69970620-69970770	HEK293	kidney:	n/a	n/a
27	CTCF	chr14:69941980-69942130	HA-sp	spinal cord:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
28	CTCF	chr14:69941980-69942130	AG04450	lung:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
29	CTCF	chr14:69970580-69970736	A549	lung:	n/a	n/a
30	CTCF	chr14:69970600-69970750	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr14:69942020-69942170	HFF-Myc	foreskin:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
32	CTCF	chr14:69941957-69942128	SK-N-SH_RA	brain:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
33	CTCF	chr14:69970640-69970790	GM06990	blood:	n/a	n/a
34	CTCF	chr14:69941942-69942204	A549	lung:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
35	CTCF	chr14:69951462-69951564	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr14:69951468-69951553	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:69942360-69942510	GM12868	blood:	n/a	n/a
38	CTCF	chr14:69970571-69970754	HepG2	liver:	n/a	n/a
39	CTCF	chr14:69942000-69942150	HPAF	blood vessel:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
40	CTCF	chr14:69942020-69942170	GM12868	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
41	CTCF	chr14:69941882-69942145	HepG2	liver:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
42	CTCF	chr14:69970920-69971070	NHDF-neo	bronchial:	n/a	chr14:69970988-69971006
43	CTCF	chr14:69943744-69943872	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:69941980-69942130	GM12870	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
45	CTCF	chr14:69970640-69970790	GM12864	blood:	n/a	n/a
46	CTCF	chr14:69942020-69942170	WI-38	lung:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
47	CTCF	chr14:69942360-69942510	HCFaa	heart:	n/a	n/a
48	CTCF	chr14:69942060-69942210	BJ	skin:	n/a	n/a
49	CTCF	chr14:69941981-69942211	MCF-7	breast:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
50	CTCF	chr14:69943495-69943965	HCT-116	colon:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69951422-69951472	HRE	kidney:	n/a
2	chr14:69950574-69950624	NB4	blood:	n/a
3	chr14:69950574-69950624	Jurkat	blood:	n/a
4	chr14:69951311-69951361	K562	blood:	n/a
5	chr14:69951211-69951261	AG09319	gingival:	n/a
6	chr14:69951495-69951545	PANC-1	pancreas:	n/a
7	chr14:69950116-69950166	K562	blood:	n/a
8	chr14:69951305-69951355	HMEC	breast:	n/a
9	chr14:69951372-69951422	AG09309	skin:	n/a
10	chr14:69951781-69951831	A549	lung:	n/a
11	chr14:69951781-69951831	HCT-116	colon:	n/a
12	chr14:69951720-69951770	NHBE	bronchial:	n/a
13	chr14:69951211-69951261	RPTEC	kidney:	n/a
14	chr14:69951211-69951261	Jurkat	blood:	n/a
15	chr14:69951839-69951889	SAEC	small airway:	n/a
16	chr14:69951211-69951261	K562	blood:	n/a
17	chr14:69952003-69952053	HRPEpiC	eye:	n/a
18	chr14:69950043-69950093	Caco-2	colon:	n/a
19	chr14:69951720-69951770	NHDF-neo	bronchial:	n/a
20	chr14:69951311-69951361	BE2_C	brain:	n/a
21	chr14:69951311-69951361	GM06990	blood:	n/a
22	chr14:69950043-69950093	BJ	skin:	n/a
23	chr14:69951839-69951889	ovcar-3	ovarian:	n/a
24	chr14:69951305-69951355	NH-A	brain:	n/a
25	chr14:69951211-69951261	NB4	blood:	n/a
26	chr14:69951211-69951261	BJ	skin:	n/a
27	chr14:69952003-69952053	H1-hESC	embryonic stem cell:	embryo
28	chr14:69951322-69951372	ProgFib	skin:	n/a
29	chr14:69947271-69947321	HNPCEpiC	eye:	n/a
30	chr14:69950574-69950624	CMK	blood:	n/a
31	chr14:69951839-69951889	AG09309	skin:	n/a
32	chr14:69968273-69968323	RPTEC	kidney:	n/a
33	chr14:69951305-69951355	NHDF-neo	bronchial:	n/a
34	chr14:69952003-69952053	GM12878	blood:	n/a
35	chr14:69950043-69950093	ovcar-3	ovarian:	n/a
36	chr14:69950116-69950166	SK-N-SH_RA	brain:	n/a
37	chr14:69951311-69951361	AoSMC	blood vessel:	n/a
38	chr14:69951720-69951770	AG09309	skin:	n/a
39	chr14:69952104-69952154	HCF	heart:	n/a
40	chr14:69951311-69951361	HMEC	breast:	n/a
41	chr14:69951495-69951545	AG04449	skin:	fetal
42	chr14:69954135-69954185	Hela-S3	cervix:	n/a
43	chr14:69951422-69951472	SK-N-SH_RA	brain:	n/a
44	chr14:69951305-69951355	HIPEpiC	eye:	n/a
45	chr14:69951211-69951261	HCF	heart:	n/a
46	chr14:69951322-69951372	U87	brain:	n/a
47	chr14:69951781-69951831	BE2_C	brain:	n/a
48	chr14:69951720-69951770	AoSMC	blood vessel:	n/a
49	chr14:69951372-69951422	LNCaP	prostate:	n/a
50	chr14:69951311-69951361	HCM	heart:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69970211..69971130-chr14:70193442..70194320,2	MCF-7	breast:
2	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
3	chr14:69940565..69944198-chr14:69948650..69951872,3	MCF-7	breast:
4	chr14:69863597..69866154-chr14:69965430..69966974,2	MCF-7	breast:
5	chr14:69877530..69878097-chr14:69941616..69942179,2	MCF-7	breast:
6	chr14:69862767..69865090-chr14:69948473..69950881,2	MCF-7	breast:
7	chr14:69970369..69971161-chr14:70041166..70042114,4	MCF-7	breast:
8	chr14:69863307..69865409-chr14:69940498..69943105,2	MCF-7	breast:
9	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
10	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
11	chr14:69864699..69866812-chr14:69943113..69945643,2	MCF-7	breast:
12	chr14:69949476..69951469-chr14:70232962..70234565,2	MCF-7	breast:
13	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
14	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
15	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
16	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
17	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
18	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
19	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
20	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
21	chr14:69951841..69953361-chr7:104652261..104653928,2	MCF-7	breast:
22	chr14:69951443..69953126-chr14:69953457..69956317,2	MCF-7	breast:
23	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:
24	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
25	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
26	chr14:69969961..69971754-chr14:70233921..70235579,2	K562	blood:
27	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
28	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
29	chr14:69952428..69953410-chr5:19316375..19317263,2	MCF-7	breast:
30	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
31	chr14:69970362..69971107-chr14:70041144..70041646,2	K562	blood:
32	chr14:69951860..69952360-chr7:104652907..104653592,2	Hela-S3	cervix:
33	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
34	chr14:69950456..69952040-chr14:70233397..70235258,2	MCF-7	breast:

No data

Variant related genes	Relation type
PLEKHD1	TF binding region
PLEKHD1	CpG island
ENSG00000267909	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000100632	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000175985	chromatin interactions
ENSG00000029364	chromatin interactions

Extended variants
information (count: 1093 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7156420	chr14:69942127-69942128	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531241275	chr14:69942189-69942190	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs571006324	chr14:69942192-69942193	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs117841589	chr14:69942193-69942194	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs544516436	chr14:69942301-69942302	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs568587910	chr14:69942345-69942346	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs73281409	chr14:69942346-69942347	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs554211888	chr14:69942409-69942410	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138498228	chr14:69942463-69942464	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs191524305	chr14:69942492-69942493	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs530738910	chr14:69942493-69942494	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs534085266	chr14:69942510-69942511	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs372014458	chr14:69942660-69942661	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs576939641	chr14:69942696-69942697	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs36070728	chr14:69942697-69942698	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs34218656	chr14:69942701-69942702	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7158020	chr14:69942713-69942714	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541568733	chr14:69942715-69942716	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs371521607	chr14:69942727-69942728	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs527319846	chr14:69942740-69942741	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs546452906	chr14:69942741-69942742	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564650205	chr14:69942752-69942753	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs531902019	chr14:69942756-69942757	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs550118504	chr14:69942772-69942773	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs142488009	chr14:69942773-69942774	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs143091553	chr14:69942782-69942783	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs547953812	chr14:69942795-69942796	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566064690	chr14:69942801-69942802	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs539478414	chr14:69942853-69942854	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs558781941	chr14:69942905-69942906	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs570664775	chr14:69942912-69942913	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs59116152	chr14:69942915-69942916	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532736897	chr14:69942930-69942931	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs561289170	chr14:69942933-69942934	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs35505104	chr14:69942974-69942975	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs74316475	chr14:69942978-69942979	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs555936269	chr14:69943011-69943012	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs117621534	chr14:69943034-69943035	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148235384	chr14:69943073-69943074	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs141259303	chr14:69943109-69943110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571976688	chr14:69943113-69943114	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs369762114	chr14:69943132-69943133	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs545500108	chr14:69943135-69943136	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs564763539	chr14:69943143-69943144	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs531917582	chr14:69943151-69943152	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs8004020	chr14:69943182-69943183	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs150796545	chr14:69943183-69943184	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs184001777	chr14:69943207-69943208	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs8003906	chr14:69943222-69943223	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs566193536	chr14:69943228-69943229	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hematopoietic stem cell	20738155	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69923600-69950400	Weak transcription	Gastric	stomach
2	chr14:69928600-69950600	Weak transcription	Aorta	Aorta
3	chr14:69942000-69942200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:69942000-69942200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
5	chr14:69942000-69942200	Enhancers	Spleen	Spleen
6	chr14:69942000-69942400	Enhancers	Stomach Mucosa	stomach
7	chr14:69942200-69942400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:69942400-69943400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:69943400-69943600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:69943600-69947800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:69946600-69946800	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr14:69947000-69947200	Enhancers	Esophagus	oesophagus
13	chr14:69948000-69948800	Enhancers	GM12878-XiMat	blood
14	chr14:69948000-69949400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
15	chr14:69948000-69950000	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr14:69948600-69949000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
17	chr14:69948600-69949000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr14:69948600-69949000	ZNF genes & repeats	Lung	lung
19	chr14:69948600-69949200	Enhancers	Primary B cells from peripheral blood	blood
20	chr14:69948600-69949400	Enhancers	Psoas Muscle	Psoas
21	chr14:69948600-69949400	Enhancers	K562	blood
22	chr14:69948600-69950000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:69948600-69950400	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr14:69948800-69949000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
25	chr14:69948800-69949000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
26	chr14:69948800-69949000	Enhancers	Esophagus	oesophagus
27	chr14:69948800-69949200	Flanking Active TSS	GM12878-XiMat	blood
28	chr14:69949000-69949200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
29	chr14:69949200-69949400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:69949200-69949400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
31	chr14:69949200-69949400	ZNF genes & repeats	Lung	lung
32	chr14:69949200-69949600	Enhancers	GM12878-XiMat	blood
33	chr14:69949200-69950600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr14:69949400-69950000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr14:69949400-69950400	Weak transcription	Lung	lung
36	chr14:69949400-69950400	Weak transcription	Psoas Muscle	Psoas
37	chr14:69949800-69952600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr14:69950000-69950400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr14:69950000-69950600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr14:69950000-69950600	Bivalent Enhancer	Brain Germinal Matrix	brain
41	chr14:69950000-69950600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr14:69950200-69950400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
43	chr14:69950200-69950400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
44	chr14:69950200-69950400	Bivalent/Poised TSS	Fetal Brain Female	brain
45	chr14:69950200-69950400	Enhancers	HSMM	muscle
46	chr14:69950200-69950800	Enhancers	Liver	Liver
47	chr14:69950400-69950600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
48	chr14:69950400-69950600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr14:69950400-69950600	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr14:69950400-69950600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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