Variant report

Variant	nsv456335
Chromosome Location	chr14:69928307-69971598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:761)
CpG islands
(count:1159)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:69941910-69942131	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:69941879-69942182	K562	blood:	n/a	n/a
3	ARID3A	chr14:69970593-69970792	HepG2	liver:	n/a	n/a
4	BACH1	chr14:69948920-69949253	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:69968018-69968246	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	BATF	chr14:69938611-69938940	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
9	BATF	chr14:69938610-69938873	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
10	BHLHE40	chr14:69938666-69938985	GM12878	blood:	n/a	n/a
11	CEBPB	chr14:69959034-69959265	HepG2	liver:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
12	CEBPB	chr14:69957851-69957951	K562	blood:	n/a	chr14:69957884-69957895
13	CEBPB	chr14:69940288-69940504	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr14:69950226-69950924	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr14:69935812-69935918	IMR90	lung:	n/a	n/a
16	CEBPB	chr14:69957726-69958039	HepG2	liver:	n/a	chr14:69957884-69957895
17	CEBPB	chr14:69959052-69959243	A549	lung:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
18	CHD2	chr14:69950982-69951100	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr14:69950474-69951751	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr14:69943739-69943832	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr14:69970620-69970770	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr14:69941960-69942110	HRE	kidney:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
23	CTCF	chr14:69941940-69942090	GM12872	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
24	CTCF	chr14:69970980-69971130	GM12871	blood:	n/a	chr14:69970988-69971006
25	CTCF	chr14:69970600-69970750	HMEC	breast:	n/a	n/a
26	CTCF	chr14:69943771-69943863	Gliobla	brain:	n/a	n/a
27	CTCF	chr14:69941980-69942130	GM12870	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
28	CTCF	chr14:69942000-69942150	GM12866	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
29	CTCF	chr14:69942020-69942170	SK-N-SH_RA	brain:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
30	CTCF	chr14:69943600-69943750	NHEK	skin:	n/a	n/a
31	CTCF	chr14:69941980-69942130	AG09309	skin:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
32	CTCF	chr14:69941740-69941890	GM12868	blood:	n/a	n/a
33	CTCF	chr14:69943671-69943796	HepG2	liver:	n/a	n/a
34	CTCF	chr14:69970620-69970770	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr14:69970600-69970750	GM12871	blood:	n/a	n/a
36	CTCF	chr14:69941937-69942203	GM13977	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
37	CTCF	chr14:69941952-69942136	LNCaP	prostate:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
38	CTCF	chr14:69943620-69943770	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:69970968-69971009	H1-hESC	embryonic stem cell:	n/a	chr14:69970988-69971006
40	CTCF	chr14:69943620-69943770	HMF	breast:	n/a	n/a
41	CTCF	chr14:69970860-69971010	AoAF	blood vessel:	n/a	chr14:69970988-69971006
42	CTCF	chr14:69970620-69970770	GM12872	blood:	n/a	n/a
43	CTCF	chr14:69970640-69970790	GM06990	blood:	n/a	n/a
44	CTCF	chr14:69970484-69970860	GM12878	blood:	n/a	n/a
45	CTCF	chr14:69941980-69942130	Caco-2	colon:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
46	CTCF	chr14:69970600-69970750	A549	lung:	n/a	n/a
47	CTCF	chr14:69943741-69943879	GM12891	blood:	n/a	n/a
48	CTCF	chr14:69943800-69943950	BJ	skin:	n/a	n/a
49	CTCF	chr14:69941946-69942245	H1-hESC	embryonic stem cell:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
50	CTCF	chr14:69951456-69951545	MCF-7	breast:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69952003-69952053	AG04450	lung:	fetal
2	chr14:69954135-69954185	NH-A	brain:	n/a
3	chr14:69950116-69950166	BJ	skin:	n/a
4	chr14:69951720-69951770	AG09319	gingival:	n/a
5	chr14:69950043-69950093	SAEC	small airway:	n/a
6	chr14:69968273-69968323	HIPEpiC	eye:	n/a
7	chr14:69951305-69951355	HPAEpiC	pulmonary alveolar:	n/a
8	chr14:69947271-69947321	Caco-2	colon:	n/a
9	chr14:69951372-69951422	PrEC	prostate:	n/a
10	chr14:69952003-69952053	NHBE	bronchial:	n/a
11	chr14:69951422-69951472	AG10803	skin:	n/a
12	chr14:69951311-69951361	Hepatocyte	liver:	n/a
13	chr14:69951781-69951831	Jurkat	blood:	n/a
14	chr14:69950574-69950624	ProgFib	skin:	n/a
15	chr14:69951839-69951889	Caco-2	colon:	n/a
16	chr14:69951372-69951422	NHBE	bronchial:	n/a
17	chr14:69950043-69950093	SK-N-MC	brain:	n/a
18	chr14:69952104-69952154	AG04449	skin:	fetal
19	chr14:69951839-69951889	GM06990	blood:	n/a
20	chr14:69951781-69951831	HNPCEpiC	eye:	n/a
21	chr14:69951211-69951261	Hepatocyte	liver:	n/a
22	chr14:69954135-69954185	AG04450	lung:	fetal
23	chr14:69951422-69951472	HL-60	blood:	n/a
24	chr14:69951322-69951372	SKMC	muscle:	n/a
25	chr14:69952104-69952154	MCF10A-Er-Src	breast:	n/a
26	chr14:69951372-69951422	AoSMC	blood vessel:	n/a
27	chr14:69931877-69931927	AG10803	skin:	n/a
28	chr14:69951422-69951472	HMEC	breast:	n/a
29	chr14:69951372-69951422	AG04449	skin:	fetal
30	chr14:69950043-69950093	AoSMC	blood vessel:	n/a
31	chr14:69950574-69950624	PrEC	prostate:	n/a
32	chr14:69951322-69951372	HRE	kidney:	n/a
33	chr14:69950116-69950166	T-47D	breast:	n/a
34	chr14:69951839-69951889	U87	brain:	n/a
35	chr14:69951720-69951770	ovcar-3	ovarian:	n/a
36	chr14:69950116-69950166	NH-A	brain:	n/a
37	chr14:69954135-69954185	HUVEC	blood vessel:	n/a
38	chr14:69951781-69951831	GM06990	blood:	n/a
39	chr14:69950574-69950624	A549	lung:	n/a
40	chr14:69951495-69951545	HEEpiC	esophagus:	n/a
41	chr14:69947271-69947321	GM12892	blood:	n/a
42	chr14:69951495-69951545	RPTEC	kidney:	n/a
43	chr14:69931877-69931927	HPAEpiC	pulmonary alveolar:	n/a
44	chr14:69950116-69950166	NHDF-neo	bronchial:	n/a
45	chr14:69968273-69968323	NB4	blood:	n/a
46	chr14:69951311-69951361	ovcar-3	ovarian:	n/a
47	chr14:69950043-69950093	Caco-2	colon:	n/a
48	chr14:69951322-69951372	PFSK-1	brain:	n/a
49	chr14:69951720-69951770	HNPCEpiC	eye:	n/a
50	chr14:69950574-69950624	Jurkat	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
2	chr14:69951443..69953126-chr14:69953457..69956317,2	MCF-7	breast:
3	chr14:69949476..69951469-chr14:70232962..70234565,2	MCF-7	breast:
4	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
5	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
6	chr14:69970362..69971107-chr14:70041144..70041646,2	K562	blood:
7	chr14:69969961..69971754-chr14:70233921..70235579,2	K562	blood:
8	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
9	chr14:69708308..69710896-chr14:69926995..69929013,2	MCF-7	breast:
10	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
11	chr14:69877530..69878097-chr14:69941616..69942179,2	MCF-7	breast:
12	chr14:69950456..69952040-chr14:70233397..70235258,2	MCF-7	breast:
13	chr14:69940565..69944198-chr14:69948650..69951872,3	MCF-7	breast:
14	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
15	chr14:69864699..69866812-chr14:69943113..69945643,2	MCF-7	breast:
16	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
17	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
18	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
19	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
20	chr14:69951860..69952360-chr7:104652907..104653592,2	Hela-S3	cervix:
21	chr14:69952428..69953410-chr5:19316375..19317263,2	MCF-7	breast:
22	chr14:69829365..69831341-chr14:69925811..69928602,2	MCF-7	breast:
23	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
24	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
25	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
26	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
27	chr14:69932792..69935168-chr14:70232400..70234408,2	K562	blood:
28	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
29	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
30	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:
31	chr14:69863597..69866154-chr14:69965430..69966974,2	MCF-7	breast:
32	chr14:69970369..69971161-chr14:70041166..70042114,4	MCF-7	breast:
33	chr14:69863461..69868593-chr14:69924955..69929429,6	MCF-7	breast:
34	chr14:69878685..69880394-chr14:69926350..69928996,2	K562	blood:
35	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
36	chr14:69862767..69865090-chr14:69948473..69950881,2	MCF-7	breast:
37	chr14:69863307..69865409-chr14:69940498..69943105,2	MCF-7	breast:
38	chr14:69970211..69971130-chr14:70193442..70194320,2	MCF-7	breast:
39	chr14:69951841..69953361-chr7:104652261..104653928,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1524 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1045301	chr14:69928307-69928308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376608039	chr14:69928312-69928313	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369963478	chr14:69928313-69928314	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186428485	chr14:69928357-69928358	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs149457691	chr14:69928392-69928393	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568548794	chr14:69928404-69928405	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs111495442	chr14:69928413-69928414	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189660282	chr14:69928443-69928444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs537771501	chr14:69928497-69928498	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553952254	chr14:69928499-69928500	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs148648575	chr14:69928545-69928546	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35662607	chr14:69928551-69928552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs117254841	chr14:69928637-69928638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558192662	chr14:69928659-69928660	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576553506	chr14:69928746-69928747	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544509869	chr14:69928804-69928805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs182292760	chr14:69928834-69928835	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529828475	chr14:69928839-69928840	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542031704	chr14:69928841-69928842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186043624	chr14:69928850-69928851	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs142157402	chr14:69928862-69928863	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7276	chr14:69928943-69928944	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs1045534	chr14:69929040-69929041	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554756051	chr14:69929062-69929063	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368825923	chr14:69929155-69929156	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576944871	chr14:69929222-69929223	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565276734	chr14:69929252-69929253	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550043379	chr14:69929270-69929271	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs568760965	chr14:69929362-69929363	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs116002167	chr14:69929374-69929375	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554360241	chr14:69929385-69929386	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372754188	chr14:69929422-69929423	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs61982404	chr14:69929433-69929434	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs547824118	chr14:69929450-69929451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115753093	chr14:69929508-69929509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191298531	chr14:69929509-69929510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576490176	chr14:69929515-69929516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543865683	chr14:69929526-69929527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183053089	chr14:69929540-69929541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574694644	chr14:69929555-69929556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369604734	chr14:69929574-69929575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146250981	chr14:69929610-69929611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530232469	chr14:69929611-69929612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560300312	chr14:69929733-69929734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572191319	chr14:69929765-69929766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545482314	chr14:69929784-69929785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530002776	chr14:69929788-69929789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371830506	chr14:69929802-69929803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114183845	chr14:69929804-69929805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549387145	chr14:69929810-69929811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69892200-69931400	Weak transcription	K562	blood
2	chr14:69903600-69937800	Weak transcription	Psoas Muscle	Psoas
3	chr14:69909000-69933200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:69915800-69932600	Weak transcription	Fetal Heart	heart
5	chr14:69918400-69929200	Strong transcription	Primary T cells from cord blood	blood
6	chr14:69919200-69929600	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr14:69919600-69929000	Strong transcription	Primary B cells from peripheral blood	blood
8	chr14:69919800-69928600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr14:69919800-69929000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:69919800-69929000	Strong transcription	Dnd41	blood
11	chr14:69919800-69929400	Strong transcription	Fetal Intestine Large	intestine
12	chr14:69919800-69929600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr14:69919800-69929800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr14:69920000-69928600	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr14:69920000-69928800	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr14:69920000-69929000	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr14:69920000-69929000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr14:69920000-69929000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr14:69920000-69929400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:69920000-69929400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr14:69920000-69930400	Weak transcription	Right Ventricle	heart
22	chr14:69920200-69929200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr14:69920400-69929000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:69920600-69929000	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr14:69921000-69930400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr14:69922000-69929400	Strong transcription	Fetal Muscle Leg	muscle
27	chr14:69922200-69931600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr14:69922400-69929000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr14:69922400-69929400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr14:69922400-69929400	Strong transcription	Fetal Muscle Trunk	muscle
31	chr14:69922600-69929400	Strong transcription	Fetal Lung	lung
32	chr14:69923000-69928800	Strong transcription	Thymus	Thymus
33	chr14:69923400-69931000	Weak transcription	Stomach Mucosa	stomach
34	chr14:69923600-69930400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:69923600-69950400	Weak transcription	Gastric	stomach
36	chr14:69923800-69930400	Weak transcription	HMEC	breast
37	chr14:69923800-69930800	Weak transcription	HepG2	liver
38	chr14:69923800-69931200	Weak transcription	NHDF-Ad	bronchial
39	chr14:69924200-69931400	Weak transcription	Small Intestine	intestine
40	chr14:69924800-69928600	Strong transcription	GM12878-XiMat	blood
41	chr14:69925400-69931200	Weak transcription	Lung	lung
42	chr14:69925400-69931400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr14:69925400-69939600	Weak transcription	Pancreas	Pancrea
44	chr14:69925400-69942000	Weak transcription	Spleen	Spleen
45	chr14:69925600-69929800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr14:69925600-69930000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr14:69925600-69930400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:69925600-69940000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr14:69925600-69940000	Weak transcription	Hela-S3	cervix
50	chr14:69925800-69930000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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