Variant report

Variant	nsv1362
Chromosome Location	chr14:77853202-77898605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:401)
CpG islands
(count:549)
Chromatin interactive
region (count:73)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:77875080-77875949	K562	blood:	n/a	n/a
2	ARID3A	chr14:77856519-77856959	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:77872620-77873346	K562	blood:	n/a	n/a
4	ARID3A	chr14:77880772-77881236	K562	blood:	n/a	n/a
5	ATF1	chr14:77872623-77873983	K562	blood:	n/a	n/a
6	BACH1	chr14:77879426-77879456	K562	blood:	n/a	n/a
7	BACH1	chr14:77888285-77888336	K562	blood:	n/a	n/a
8	BACH1	chr14:77880246-77880411	K562	blood:	n/a	n/a
9	BACH1	chr14:77860429-77860506	K562	blood:	n/a	n/a
10	BHLHE40	chr14:77880720-77881066	K562	blood:	n/a	n/a
11	BHLHE40	chr14:77873639-77873841	K562	blood:	n/a	n/a
12	CBX3	chr14:77880702-77881084	K562	blood:	n/a	n/a
13	CBX3	chr14:77875481-77875974	K562	blood:	n/a	n/a
14	CCNT2	chr14:77873003-77873997	K562	blood:	n/a	n/a
15	CCNT2	chr14:77880764-77880991	K562	blood:	n/a	chr14:77880889-77880909
16	CEBPB	chr14:77856686-77856923	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:77892935-77893028	A549	lung:	n/a	n/a
18	CEBPB	chr14:77873146-77873844	K562	blood:	n/a	n/a
19	CEBPB	chr14:77856714-77856914	K562	blood:	n/a	n/a
20	CEBPB	chr14:77887596-77887887	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr14:77886893-77887090	K562	blood:	n/a	n/a
22	CEBPB	chr14:77881841-77882067	K562	blood:	n/a	n/a
23	CEBPB	chr14:77877149-77877345	K562	blood:	n/a	n/a
24	CEBPB	chr14:77866529-77867122	MCF-7	breast:	n/a	n/a
25	CEBPD	chr14:77882421-77882852	K562	blood:	n/a	n/a
26	CEBPD	chr14:77873568-77873958	K562	blood:	n/a	n/a
27	CEBPD	chr14:77873503-77873883	K562	blood:	n/a	n/a
28	CHD2	chr14:77875522-77875770	K562	blood:	n/a	n/a
29	CHD2	chr14:77875583-77875767	HepG2	liver:	n/a	n/a
30	CHD2	chr14:77880028-77880164	K562	blood:	n/a	n/a
31	CTCF	chr14:77875620-77875770	A549	lung:	n/a	n/a
32	CTCF	chr14:77875620-77875770	GM12866	blood:	n/a	n/a
33	CTCF	chr14:77875660-77875810	HRE	kidney:	n/a	n/a
34	CTCF	chr14:77875660-77875810	RPTEC	kidney:	n/a	n/a
35	CTCF	chr14:77875659-77875664	GM13976	blood:	n/a	n/a
36	CTCF	chr14:77875620-77875770	HVMF	connective:	n/a	n/a
37	CTCF	chr14:77875640-77875790	HMEC	breast:	n/a	n/a
38	CTCF	chr14:77875620-77875770	GM12872	blood:	n/a	n/a
39	CTCF	chr14:77875580-77875730	AG04450	lung:	n/a	n/a
40	CTCF	chr14:77875533-77875861	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr14:77875620-77875770	HRE	kidney:	n/a	n/a
42	CTCF	chr14:77875605-77875855	A549	lung:	n/a	n/a
43	CTCF	chr14:77875660-77875810	K562	blood:	n/a	n/a
44	CTCF	chr14:77875700-77875850	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr14:77875640-77875790	BE2_C	brain:	n/a	n/a
46	CTCF	chr14:77875580-77875730	HCT-116	colon:	n/a	n/a
47	CTCF	chr14:77875580-77875730	K562	blood:	n/a	n/a
48	CTCF	chr14:77875660-77875834	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr14:77875680-77875830	HEK293	kidney:	n/a	n/a
50	CTCF	chr14:77875627-77875798	T-47D	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:77893335-77893385	NHBE	bronchial:	n/a
2	chr14:77893335-77893385	RPTEC	kidney:	n/a
3	chr14:77890531-77890581	HL-60	blood:	n/a
4	chr14:77893335-77893385	HCPEpiC	choroid plexus:	n/a
5	chr14:77893335-77893385	K562	blood:	n/a
6	chr14:77890531-77890581	NHDF-neo	bronchial:	n/a
7	chr14:77889288-77889338	HAEpiC	amniotic membrane:	n/a
8	chr14:77889982-77890032	Hela-S3	cervix:	n/a
9	chr14:77860719-77860769	HL-60	blood:	n/a
10	chr14:77891531-77891581	HUVEC	blood vessel:	n/a
11	chr14:77889546-77889596	GM12891	blood:	n/a
12	chr14:77890519-77890569	SAEC	small airway:	n/a
13	chr14:77889288-77889338	MCF-7	breast:	n/a
14	chr14:77891531-77891581	Hepatocyte	liver:	n/a
15	chr14:77889546-77889596	NHDF-neo	bronchial:	n/a
16	chr14:77890519-77890569	ovcar-3	ovarian:	n/a
17	chr14:77889288-77889338	HCM	heart:	n/a
18	chr14:77890531-77890581	MCF10A-Er-Src	breast:	n/a
19	chr14:77891531-77891581	RPTEC	kidney:	n/a
20	chr14:77893335-77893385	ECC-1	luminal epithelium:	n/a
21	chr14:77891531-77891581	CMK	blood:	n/a
22	chr14:77889141-77889191	HEK293	kidney:	embryo
23	chr14:77889288-77889338	HepG2	liver:	n/a
24	chr14:77860719-77860769	U87	brain:	n/a
25	chr14:77890519-77890569	SK-N-MC	brain:	n/a
26	chr14:77889546-77889596	Caco-2	colon:	n/a
27	chr14:77889288-77889338	SK-N-SH	brain:	n/a
28	chr14:77889982-77890032	SKMC	muscle:	n/a
29	chr14:77889288-77889338	AG04450	lung:	fetal
30	chr14:77860719-77860769	NHDF-neo	bronchial:	n/a
31	chr14:77860719-77860769	PFSK-1	brain:	n/a
32	chr14:77889141-77889191	T-47D	breast:	n/a
33	chr14:77889141-77889191	LNCaP	prostate:	n/a
34	chr14:77889288-77889338	MCF10A-Er-Src	breast:	n/a
35	chr14:77889141-77889191	ovcar-3	ovarian:	n/a
36	chr14:77889546-77889596	AG09319	gingival:	n/a
37	chr14:77891531-77891581	BJ	skin:	n/a
38	chr14:77890519-77890569	HRCEpiC	kidney:	n/a
39	chr14:77889982-77890032	AG04450	lung:	fetal
40	chr14:77889141-77889191	HEEpiC	esophagus:	n/a
41	chr14:77889141-77889191	NH-A	brain:	n/a
42	chr14:77890519-77890569	NB4	blood:	n/a
43	chr14:77889288-77889338	SKMC	muscle:	n/a
44	chr14:77889288-77889338	AoSMC	blood vessel:	n/a
45	chr14:77889288-77889338	NHDF-neo	bronchial:	n/a
46	chr14:77890519-77890569	MCF10A-Er-Src	breast:	n/a
47	chr14:77889982-77890032	AG09309	skin:	n/a
48	chr14:77891531-77891581	BE2_C	brain:	n/a
49	chr14:77890531-77890581	GM12892	blood:	n/a
50	chr14:77890519-77890569	CMK	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:77855950..77857570-chr14:77862877..77864428,2	MCF-7	breast:
2	chr14:77868441..77870840-chr14:77872580..77875267,2	MCF-7	breast:
3	chr14:77784144..77784926-chr14:77866363..77867165,2	MCF-7	breast:
4	chr14:77867912..77869685-chr14:77872621..77875120,2	MCF-7	breast:
5	chr14:77610967..77611796-chr14:77866638..77867232,2	MCF-7	breast:
6	chr14:77852353..77854964-chr14:77856109..77858623,2	MCF-7	breast:
7	chr14:77855950..77857570-chr14:77862877..77864428,2	MCF-7	breast:
8	chr14:77859431..77861552-chr14:77871084..77872888,2	K562	blood:
9	chr14:77785202..77790958-chr14:77870163..77875663,11	MCF-7	breast:
10	chr14:77837819..77844743-chr14:77858917..77867107,14	MCF-7	breast:
11	chr14:77841179..77843934-chr14:77853805..77855515,2	K562	blood:
12	chr14:77786111..77789292-chr14:77879086..77881673,3	K562	blood:
13	chr14:77895563..77897867-chr14:77905169..77908165,2	K562	blood:
14	chr14:77872637..77877422-chr14:77877699..77881765,7	K562	blood:
15	chr14:77859416..77861552-chr14:77870946..77872888,2	K562	blood:
16	chr14:77390909..77391624-chr14:77866618..77867236,2	MCF-7	breast:
17	chr14:77840497..77841430-chr14:77866326..77867203,8	MCF-7	breast:
18	chr14:77845308..77847235-chr14:77862944..77864644,2	MCF-7	breast:
19	chr14:77788529..77790702-chr14:77876519..77879428,2	MCF-7	breast:
20	chr14:77767421..77771659-chr14:77864356..77866894,5	MCF-7	breast:
21	chr14:77886107..77889057-chr14:77889383..77893266,3	K562	blood:
22	chr14:77874131..77876982-chr14:77878794..77881765,4	K562	blood:
23	chr14:77858452..77860278-chr14:77863182..77865442,2	MCF-7	breast:
24	chr14:77781806..77790093-chr14:77860676..77869624,28	MCF-7	breast:
25	chr14:77785522..77790160-chr14:77881086..77890187,11	MCF-7	breast:
26	chr14:77535974..77536553-chr14:77866586..77867116,2	MCF-7	breast:
27	chr14:77852353..77854964-chr14:77856109..77858623,2	MCF-7	breast:
28	chr14:77859416..77861552-chr14:77870946..77872888,2	K562	blood:
29	chr14:77867128..77868672-chr14:77870898..77872420,2	MCF-7	breast:
30	chr14:77867128..77868672-chr14:77870898..77872420,2	MCF-7	breast:
31	chr14:77784077..77785080-chr14:77866328..77867222,8	MCF-7	breast:
32	chr14:77874085..77876680-chr14:77923987..77925697,2	K562	blood:
33	chr14:77840795..77844789-chr14:77870809..77874889,5	MCF-7	breast:
34	chr14:77866353..77867046-chr14:104159478..104160076,2	MCF-7	breast:
35	chr14:77607830..77608732-chr14:77866548..77867068,2	MCF-7	breast:
36	chr14:77784077..77785078-chr14:77866118..77867241,6	MCF-7	breast:
37	chr14:77851627..77854114-chr14:77860250..77862122,3	MCF-7	breast:
38	chr14:77611069..77611850-chr14:77866210..77867202,4	MCF-7	breast:
39	chr14:77851627..77854114-chr14:77860250..77862122,3	MCF-7	breast:
40	chr14:77859431..77861552-chr14:77871084..77872888,2	K562	blood:
41	chr14:77872257..77874007-chr14:78173034..78174621,2	MCF-7	breast:
42	chr14:77651269..77652877-chr14:77857403..77859042,2	MCF-7	breast:
43	chr14:77849630..77851345-chr14:77854420..77856161,2	K562	blood:
44	chr14:77867912..77869685-chr14:77872621..77875120,2	MCF-7	breast:
45	chr14:77886973..77888948-chr14:77891766..77893431,2	K562	blood:
46	chr14:77841243..77844321-chr14:77852412..77854032,3	MCF-7	breast:
47	chr14:77847001..77849955-chr14:77855644..77857264,2	MCF-7	breast:
48	chr14:77884155..77885856-chr14:77891489..77893112,2	K562	blood:
49	chr14:77785518..77787393-chr14:77882110..77884811,2	K562	blood:
50	chr14:77865069..77868017-chr14:77924592..77926353,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD15-2	chr14:77889598-77889861	NONHSAT037988
2	lnc-SAMD15-2	chr14:77890467-77890806	NONHSAT037988

No data

Variant related genes	Relation type
ENSG00000268156	TF binding region
NOXRED1	TF binding region
ENSG00000268156	CpG island
NOXRED1	CpG island
ENSG00000177108	chromatin interactions
ENSG00000100583	chromatin interactions
ENSG00000100591	chromatin interactions
ENSG00000151445	chromatin interactions
ENSG00000100580	chromatin interactions
ENSG00000119705	chromatin interactions
ENSG00000165555	chromatin interactions
ENSG00000100577	chromatin interactions
ENSG00000100601	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000259058	chromatin interactions

Extended variants
information (count: 1685 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183349263	chr14:77853210-77853211	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs535693006	chr14:77853278-77853279	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555370068	chr14:77853284-77853285	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs114696966	chr14:77853313-77853314	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs1012468	chr14:77853364-77853365	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368925172	chr14:77853405-77853406	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372595595	chr14:77853484-77853485	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554264088	chr14:77853525-77853526	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576893028	chr14:77853551-77853552	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545998230	chr14:77853555-77853556	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376811297	chr14:77853593-77853594	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs34336941	chr14:77853633-77853634	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150057011	chr14:77853756-77853757	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34904317	chr14:77853761-77853762	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147726181	chr14:77853765-77853766	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542553480	chr14:77853766-77853767	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550742739	chr14:77853785-77853786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs10133896	chr14:77853806-77853807	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs527313573	chr14:77853816-77853817	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188082058	chr14:77853854-77853855	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs115498354	chr14:77853868-77853869	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533016697	chr14:77853873-77853874	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200860275	chr14:77853876-77853877	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs569911739	chr14:77853938-77853939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142532897	chr14:77853993-77853994	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs146967806	chr14:77854050-77854051	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs112351134	chr14:77854194-77854195	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs75435183	chr14:77854229-77854230	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs61990323	chr14:77854231-77854232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12891485	chr14:77854266-77854267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs534213228	chr14:77854268-77854269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553708491	chr14:77854338-77854339	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs117303513	chr14:77854375-77854376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs192899072	chr14:77854377-77854378	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556227996	chr14:77854385-77854386	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114073646	chr14:77854406-77854407	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs17750993	chr14:77854415-77854416	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs562430003	chr14:77854506-77854507	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs572620171	chr14:77854516-77854517	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs17105746	chr14:77854543-77854544	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568022528	chr14:77854557-77854558	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs7155063	chr14:77854600-77854601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs532956030	chr14:77854645-77854646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs77312135	chr14:77854680-77854681	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554483316	chr14:77854685-77854686	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs201820980	chr14:77854724-77854725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376913427	chr14:77854726-77854727	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs77063228	chr14:77854803-77854804	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183799479	chr14:77854819-77854820	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149046840	chr14:77854839-77854840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77844400-77855600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr14:77844400-77862200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr14:77848000-77857200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:77850200-77854000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr14:77850200-77856400	Weak transcription	Fetal Intestine Small	intestine
6	chr14:77854000-77854800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr14:77854000-77855400	Enhancers	HepG2	liver
8	chr14:77855400-77855600	Enhancers	A549	lung
9	chr14:77855400-77856400	Weak transcription	HepG2	liver
10	chr14:77855600-77856600	Weak transcription	A549	lung
11	chr14:77856000-77857200	Enhancers	Fetal Intestine Large	intestine
12	chr14:77856200-77860800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr14:77856400-77857000	Enhancers	Fetal Intestine Small	intestine
14	chr14:77856400-77857200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:77856400-77858800	Enhancers	HepG2	liver
16	chr14:77856600-77857000	Flanking Active TSS	A549	lung
17	chr14:77857000-77857400	Enhancers	A549	lung
18	chr14:77857000-77860000	Weak transcription	Fetal Intestine Small	intestine
19	chr14:77857200-77857800	Weak transcription	Fetal Intestine Large	intestine
20	chr14:77857200-77858800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr14:77857800-77858000	Enhancers	Fetal Intestine Large	intestine
22	chr14:77858800-77860000	Weak transcription	HepG2	liver
23	chr14:77858800-77862000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:77859600-77886200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr14:77860000-77860400	Enhancers	HepG2	liver
26	chr14:77860000-77872400	Weak transcription	Brain Anterior Caudate	brain
27	chr14:77862000-77862200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr14:77862200-77862400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:77862200-77862600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
30	chr14:77862600-77872600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr14:77863800-77870800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr14:77867600-77875600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr14:77867800-77868200	Enhancers	Primary B cells from peripheral blood	blood
34	chr14:77867800-77868400	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr14:77867800-77868400	Weak transcription	Fetal Kidney	kidney
36	chr14:77868000-77868400	Enhancers	A549	lung
37	chr14:77868400-77869800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr14:77869800-77870000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr14:77870000-77870400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr14:77870200-77872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:77870400-77872400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr14:77870400-77872400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:77870800-77872600	Enhancers	Primary hematopoietic stem cells	blood
44	chr14:77872000-77872200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr14:77872200-77872800	Enhancers	K562	blood
46	chr14:77872200-77873200	Enhancers	Right Atrium	heart
47	chr14:77872200-77873200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr14:77872200-77873800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr14:77872200-77874200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:77872200-77874600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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