Variant report

Variant	nsv542180
Chromosome Location	chr14:97271794-97322583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:582)
CpG islands
(count:122)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97275339-97275687	K562	blood:	n/a	n/a
2	ARID3A	chr14:97300621-97300849	K562	blood:	n/a	chr14:97300643-97300659 chr14:97300646-97300662
3	ARID3A	chr14:97294291-97294540	K562	blood:	n/a	n/a
4	ARID3A	chr14:97297247-97298040	K562	blood:	n/a	chr14:97297827-97297843
5	ATF1	chr14:97275339-97275756	K562	blood:	n/a	n/a
6	ATF1	chr14:97273223-97273549	K562	blood:	n/a	n/a
7	ATF1	chr14:97297370-97297756	K562	blood:	n/a	n/a
8	ATF3	chr14:97273176-97273463	K562	blood:	n/a	n/a
9	BACH1	chr14:97303655-97303683	K562	blood:	n/a	n/a
10	BHLHE40	chr14:97284308-97284991	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:97282966-97283111	K562	blood:	n/a	n/a
12	BHLHE40	chr14:97293719-97293841	K562	blood:	n/a	n/a
13	BHLHE40	chr14:97299291-97299440	K562	blood:	n/a	n/a
14	BHLHE40	chr14:97275335-97275592	K562	blood:	n/a	n/a
15	CBX3	chr14:97296163-97296501	K562	blood:	n/a	n/a
16	CBX3	chr14:97304773-97305157	K562	blood:	n/a	n/a
17	CBX3	chr14:97296048-97296875	K562	blood:	n/a	n/a
18	CCNT2	chr14:97297264-97297625	K562	blood:	n/a	n/a
19	CEBPB	chr14:97274958-97275331	HepG2	liver:	n/a	chr14:97275143-97275154
20	CEBPB	chr14:97274911-97275643	K562	blood:	n/a	chr14:97275143-97275154
21	CEBPB	chr14:97273147-97273588	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:97273162-97273581	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:97273148-97273601	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:97273230-97273514	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:97274960-97275339	IMR90	lung:	n/a	chr14:97275143-97275154
26	CEBPB	chr14:97274966-97275330	MCF-7	breast:	n/a	chr14:97275143-97275154
27	CEBPB	chr14:97275003-97275328	HepG2	liver:	n/a	chr14:97275143-97275154
28	CEBPB	chr14:97274959-97275337	Hela-S3	cervix:	n/a	chr14:97275143-97275154
29	CEBPB	chr14:97308815-97309084	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:97273228-97273491	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:97308924-97309057	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:97274807-97275620	K562	blood:	n/a	chr14:97275143-97275154
33	CEBPB	chr14:97273162-97273536	A549	lung:	n/a	n/a
34	CEBPB	chr14:97273219-97273529	K562	blood:	n/a	n/a
35	CEBPB	chr14:97315284-97315432	A549	lung:	n/a	n/a
36	CEBPB	chr14:97275013-97275314	K562	blood:	n/a	chr14:97275143-97275154
37	CEBPB	chr14:97274864-97275284	MCF-7	breast:	n/a	chr14:97275143-97275154
38	CEBPB	chr14:97274953-97275289	ECC-1	luminal epithelium:	n/a	chr14:97275143-97275154
39	CEBPB	chr14:97274958-97275330	A549	lung:	n/a	chr14:97275143-97275154
40	CEBPB	chr14:97273152-97273507	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:97273177-97273523	IMR90	lung:	n/a	n/a
42	CEBPB	chr14:97274865-97275348	A549	lung:	n/a	chr14:97275143-97275154
43	CEBPB	chr14:97308825-97309094	K562	blood:	n/a	n/a
44	CEBPB	chr14:97274988-97275348	ECC-1	luminal epithelium:	n/a	chr14:97275143-97275154
45	CEBPB	chr14:97308815-97309130	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:97274962-97275327	H1-hESC	embryonic stem cell:	n/a	chr14:97275143-97275154
47	CEBPB	chr14:97274920-97275346	A549	lung:	n/a	chr14:97275143-97275154
48	CEBPB	chr14:97273233-97273567	K562	blood:	n/a	n/a
49	CEBPD	chr14:97273253-97273482	HepG2	liver:	n/a	n/a
50	CEBPD	chr14:97275006-97275799	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97282535-97282585	BJ	skin:	n/a
2	chr14:97282535-97282585	U87	brain:	n/a
3	chr14:97286215-97286265	HRPEpiC	eye:	n/a
4	chr14:97286215-97286265	PrEC	prostate:	n/a
5	chr14:97286215-97286265	HepG2	liver:	n/a
6	chr14:97282535-97282585	MCF-7	breast:	n/a
7	chr14:97282535-97282585	A549	lung:	n/a
8	chr14:97282535-97282585	GM12878	blood:	n/a
9	chr14:97282535-97282585	HEK293	kidney:	embryo
10	chr14:97282535-97282585	HNPCEpiC	eye:	n/a
11	chr14:97282535-97282585	GM12892	blood:	n/a
12	chr14:97286215-97286265	AG09319	gingival:	n/a
13	chr14:97282535-97282585	HAEpiC	amniotic membrane:	n/a
14	chr14:97286215-97286265	CMK	blood:	n/a
15	chr14:97286215-97286265	LNCaP	prostate:	n/a
16	chr14:97282535-97282585	HUVEC	blood vessel:	n/a
17	chr14:97286215-97286265	SKMC	muscle:	n/a
18	chr14:97282535-97282585	RPTEC	kidney:	n/a
19	chr14:97286215-97286265	SK-N-SH	brain:	n/a
20	chr14:97282535-97282585	NB4	blood:	n/a
21	chr14:97286215-97286265	SAEC	small airway:	n/a
22	chr14:97282535-97282585	Hela-S3	cervix:	n/a
23	chr14:97286215-97286265	AG09309	skin:	n/a
24	chr14:97286215-97286265	Hepatocyte	liver:	n/a
25	chr14:97286215-97286265	HCM	heart:	n/a
26	chr14:97286215-97286265	NHDF-neo	bronchial:	n/a
27	chr14:97286215-97286265	GM06990	blood:	n/a
28	chr14:97286215-97286265	U87	brain:	n/a
29	chr14:97286215-97286265	SK-N-MC	brain:	n/a
30	chr14:97282535-97282585	H1-hESC	embryonic stem cell:	embryo
31	chr14:97282535-97282585	SK-N-MC	brain:	n/a
32	chr14:97286215-97286265	ProgFib	skin:	n/a
33	chr14:97286215-97286265	H1-hESC	embryonic stem cell:	embryo
34	chr14:97286215-97286265	PFSK-1	brain:	n/a
35	chr14:97286215-97286265	NB4	blood:	n/a
36	chr14:97286215-97286265	ovcar-3	ovarian:	n/a
37	chr14:97282535-97282585	T-47D	breast:	n/a
38	chr14:97286215-97286265	GM12892	blood:	n/a
39	chr14:97286215-97286265	GM12878	blood:	n/a
40	chr14:97286215-97286265	GM12891	blood:	n/a
41	chr14:97282535-97282585	AG09309	skin:	n/a
42	chr14:97286215-97286265	HRCEpiC	kidney:	n/a
43	chr14:97282535-97282585	NH-A	brain:	n/a
44	chr14:97286215-97286265	NH-A	brain:	n/a
45	chr14:97286215-97286265	ECC-1	luminal epithelium:	n/a
46	chr14:97286215-97286265	HRE	kidney:	n/a
47	chr14:97286215-97286265	HAEpiC	amniotic membrane:	n/a
48	chr14:97282535-97282585	ovcar-3	ovarian:	n/a
49	chr14:97282535-97282585	AoSMC	blood vessel:	n/a
50	chr14:97286215-97286265	BJ	skin:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:97263901..97269146-chr14:97273376..97277295,5	K562	blood:
2	chr14:97265289..97269463-chr14:97278304..97281407,5	K562	blood:
3	chr14:97300473..97303064-chr14:97305409..97307983,2	K562	blood:
4	chr14:97293502..97295046-chr14:97299094..97301646,2	MCF-7	breast:
5	chr14:97285108..97286873-chr14:97288100..97291000,2	MCF-7	breast:
6	chr14:97279153..97281602-chr14:97281672..97284139,2	MCF-7	breast:
7	chr14:97295418..97297368-chr14:97301033..97303820,2	K562	blood:
8	chr14:97301856..97303907-chr14:97307668..97309196,2	MCF-7	breast:
9	chr14:97279153..97281602-chr14:97281672..97284139,2	MCF-7	breast:
10	chr14:97268802..97270728-chr14:97284735..97287343,2	MCF-7	breast:
11	chr14:97293502..97295046-chr14:97299094..97301646,2	MCF-7	breast:
12	chr14:97293055..97295755-chr14:97296835..97300397,4	MCF-7	breast:
13	chr14:97309879..97311402-chr14:97317013..97319777,2	K562	blood:
14	chr14:97274614..97276764-chr14:97277663..97279518,2	K562	blood:
15	chr14:97263273..97266024-chr14:97282503..97285691,4	K562	blood:
16	chr14:97272734..97276764-chr14:97276840..97280627,4	K562	blood:
17	chr14:97271567..97274016-chr14:97278732..97280457,2	K562	blood:
18	chr14:97270252..97272755-chr14:97275339..97277575,4	K562	blood:
19	chr14:97274260..97276872-chr14:97281847..97286316,3	K562	blood:
20	chr14:97295429..97297910-chr14:97313409..97315091,2	K562	blood:
21	chr14:97303558..97306091-chr14:97311531..97314081,2	K562	blood:
22	chr14:97262876..97266959-chr14:97292166..97296485,5	K562	blood:
23	chr14:97273377..97275528-chr14:97290757..97293307,2	K562	blood:
24	chr14:97265808..97269390-chr14:97269409..97272897,4	MCF-7	breast:
25	chr14:97293055..97295755-chr14:97296835..97300397,4	MCF-7	breast:
26	chr14:97261785..97264150-chr14:97280598..97283173,2	K562	blood:
27	chr14:97299339..97301771-chr14:97302252..97306278,3	MCF-7	breast:
28	chr14:97050550..97051166-chr14:97319962..97320604,2	MCF-7	breast:
29	chr14:97291241..97293286-chr14:97295424..97297762,2	K562	blood:
30	chr14:97278908..97281500-chr14:97284326..97286978,2	MCF-7	breast:
31	chr14:97303558..97306091-chr14:97311531..97314081,2	K562	blood:
32	chr14:97264592..97266800-chr14:97290033..97292350,2	K562	blood:
33	chr14:97308706..97311091-chr14:97311481..97313480,2	K562	blood:
34	chr14:97050419..97051179-chr14:97313148..97314310,4	MCF-7	breast:
35	chr14:97269964..97272713-chr14:97520420..97522820,2	K562	blood:
36	chr14:97278908..97281500-chr14:97284326..97286978,2	MCF-7	breast:
37	chr14:97263470..97265371-chr14:97287490..97290229,2	K562	blood:
38	chr14:97263560..97266144-chr14:97273752..97276345,2	MCF-7	breast:
39	chr14:97288589..97291273-chr14:97305528..97308304,2	K562	blood:
40	chr14:97306347..97308005-chr14:97316727..97319636,2	K562	blood:
41	chr14:97319882..97321804-chr14:97324094..97326598,3	K562	blood:
42	chr14:97301564..97304982-chr14:97305349..97308383,3	K562	blood:
43	chr14:97270310..97272481-chr14:97294425..97296809,2	K562	blood:
44	chr14:97299339..97301771-chr14:97302252..97306278,3	MCF-7	breast:
45	chr14:97295429..97297910-chr14:97313409..97315091,2	K562	blood:
46	chr14:97271958..97274868-chr14:97298626..97301164,2	MCF-7	breast:
47	chr14:97297616..97299303-chr14:97302743..97305605,2	K562	blood:
48	chr14:97297616..97299303-chr14:97302743..97305605,2	K562	blood:
49	chr14:97301856..97303907-chr14:97307668..97309196,2	MCF-7	breast:
50	chr14:97273377..97275528-chr14:97290757..97293307,2	K562	blood:

No data

Variant related genes	Relation type
VRK1	TF binding region
VRK1	CpG island
ENSG00000100749	chromatin interactions

Extended variants
information (count: 1838 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1838 , 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	rs76801838	chr14:97271814-97271815	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs542193309	chr14:97271851-97271852	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560463818	chr14:97271853-97271854	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192592655	chr14:97271887-97271888	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546972639	chr14:97271932-97271933	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550394375	chr14:97271965-97271966	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565402953	chr14:97271983-97271984	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77530135	chr14:97271988-97271989	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184180960	chr14:97272021-97272022	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569395403	chr14:97272112-97272113	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536841299	chr14:97272148-97272149	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548480500	chr14:97272176-97272177	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs374260571	chr14:97272181-97272182	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550828752	chr14:97272224-97272225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377516002	chr14:97272321-97272322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190030175	chr14:97272327-97272328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368273142	chr14:97272332-97272333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577652129	chr14:97272370-97272371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2224442	chr14:97272382-97272383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537571162	chr14:97272404-97272405	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556222347	chr14:97272428-97272429	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574586495	chr14:97272508-97272509	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34679642	chr14:97272519-97272520	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145218856	chr14:97272553-97272554	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78255406	chr14:97272564-97272565	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572346306	chr14:97272604-97272605	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs142420421	chr14:97272629-97272630	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146616411	chr14:97272631-97272632	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs368862083	chr14:97272660-97272661	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533991479	chr14:97272712-97272713	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs117846600	chr14:97272778-97272779	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192903753	chr14:97272814-97272815	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372272144	chr14:97272887-97272888	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs73355679	chr14:97272959-97272960	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs114883101	chr14:97272997-97272998	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368645641	chr14:97273070-97273071	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141356050	chr14:97273077-97273078	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184883267	chr14:97273092-97273093	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs552431387	chr14:97273116-97273117	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369812029	chr14:97273168-97273169	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570399319	chr14:97273171-97273172	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537839695	chr14:97273190-97273191	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555996590	chr14:97273250-97273251	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568102839	chr14:97273253-97273254	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377231943	chr14:97273301-97273302	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372580366	chr14:97273327-97273328	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375437338	chr14:97273366-97273367	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143584649	chr14:97273379-97273380	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189391322	chr14:97273403-97273404	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367781506	chr14:97273422-97273423	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	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
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
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97264600-97272400	Weak transcription	Spleen	Spleen
2	chr14:97264800-97272400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:97264800-97272400	Weak transcription	Gastric	stomach
4	chr14:97264800-97272400	Weak transcription	Pancreas	Pancrea
5	chr14:97264800-97278400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr14:97264800-97288000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:97264800-97321600	Weak transcription	Psoas Muscle	Psoas
8	chr14:97265000-97282000	Weak transcription	Fetal Thymus	thymus
9	chr14:97265200-97271800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr14:97265200-97282200	Weak transcription	Primary T cells from cord blood	blood
11	chr14:97265200-97293200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr14:97265400-97271800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr14:97265400-97274200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr14:97265400-97277400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:97265400-97278600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr14:97265400-97282600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr14:97265600-97271800	Weak transcription	Primary B cells from cord blood	blood
18	chr14:97265600-97272800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr14:97265600-97277600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr14:97265600-97282200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr14:97265600-97282400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr14:97265600-97291800	Weak transcription	A549	lung
23	chr14:97266200-97271800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:97266200-97272600	Weak transcription	NHEK	skin
25	chr14:97266200-97277600	Weak transcription	NHDF-Ad	bronchial
26	chr14:97266200-97277800	Weak transcription	HSMM	muscle
27	chr14:97266200-97282000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr14:97266200-97303200	Weak transcription	Hela-S3	cervix
29	chr14:97266600-97272400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr14:97266800-97282200	Weak transcription	Thymus	Thymus
31	chr14:97268000-97275000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:97269800-97272200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr14:97270000-97272000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr14:97270000-97272000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr14:97270000-97272800	Enhancers	Fetal Lung	lung
36	chr14:97270000-97273000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr14:97270200-97273200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr14:97270200-97274200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:97270400-97271800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr14:97270400-97272000	Enhancers	K562	blood
41	chr14:97270400-97275000	Enhancers	Fetal Brain Male	brain
42	chr14:97270600-97272400	Weak transcription	Dnd41	blood
43	chr14:97270600-97278200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr14:97270800-97279000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr14:97271000-97272600	Enhancers	Fetal Heart	heart
46	chr14:97271000-97272800	Enhancers	Adipose Nuclei	Adipose
47	chr14:97271200-97271800	Enhancers	GM12878-XiMat	blood
48	chr14:97271200-97271800	Enhancers	Osteobl	bone
49	chr14:97271200-97272000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr14:97271400-97271800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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