Variant report

Variant	nsv1043916
Chromosome Location	chr14:97275088-97320354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:122)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97294291-97294540	K562	blood:	n/a	n/a
2	ARID3A	chr14:97297247-97298040	K562	blood:	n/a	chr14:97297827-97297843
3	ARID3A	chr14:97275339-97275687	K562	blood:	n/a	n/a
4	ARID3A	chr14:97300621-97300849	K562	blood:	n/a	chr14:97300643-97300659 chr14:97300646-97300662
5	ATF1	chr14:97275339-97275756	K562	blood:	n/a	n/a
6	ATF1	chr14:97297370-97297756	K562	blood:	n/a	n/a
7	BACH1	chr14:97303655-97303683	K562	blood:	n/a	n/a
8	BHLHE40	chr14:97284308-97284991	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:97293719-97293841	K562	blood:	n/a	n/a
10	BHLHE40	chr14:97282966-97283111	K562	blood:	n/a	n/a
11	BHLHE40	chr14:97299291-97299440	K562	blood:	n/a	n/a
12	BHLHE40	chr14:97275335-97275592	K562	blood:	n/a	n/a
13	CBX3	chr14:97296048-97296875	K562	blood:	n/a	n/a
14	CBX3	chr14:97304773-97305157	K562	blood:	n/a	n/a
15	CBX3	chr14:97296163-97296501	K562	blood:	n/a	n/a
16	CCNT2	chr14:97297264-97297625	K562	blood:	n/a	n/a
17	CEBPB	chr14:97274958-97275331	HepG2	liver:	n/a	chr14:97275143-97275154
18	CEBPB	chr14:97274988-97275348	ECC-1	luminal epithelium:	n/a	chr14:97275143-97275154
19	CEBPB	chr14:97274865-97275348	A549	lung:	n/a	chr14:97275143-97275154
20	CEBPB	chr14:97275013-97275314	K562	blood:	n/a	chr14:97275143-97275154
21	CEBPB	chr14:97308825-97309094	K562	blood:	n/a	n/a
22	CEBPB	chr14:97308924-97309057	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr14:97274864-97275284	MCF-7	breast:	n/a	chr14:97275143-97275154
24	CEBPB	chr14:97275003-97275328	HepG2	liver:	n/a	chr14:97275143-97275154
25	CEBPB	chr14:97274962-97275327	H1-hESC	embryonic stem cell:	n/a	chr14:97275143-97275154
26	CEBPB	chr14:97274966-97275330	MCF-7	breast:	n/a	chr14:97275143-97275154
27	CEBPB	chr14:97308815-97309130	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:97274807-97275620	K562	blood:	n/a	chr14:97275143-97275154
29	CEBPB	chr14:97274958-97275330	A549	lung:	n/a	chr14:97275143-97275154
30	CEBPB	chr14:97274953-97275289	ECC-1	luminal epithelium:	n/a	chr14:97275143-97275154
31	CEBPB	chr14:97274960-97275339	IMR90	lung:	n/a	chr14:97275143-97275154
32	CEBPB	chr14:97274920-97275346	A549	lung:	n/a	chr14:97275143-97275154
33	CEBPB	chr14:97315284-97315432	A549	lung:	n/a	n/a
34	CEBPB	chr14:97274911-97275643	K562	blood:	n/a	chr14:97275143-97275154
35	CEBPB	chr14:97274959-97275337	Hela-S3	cervix:	n/a	chr14:97275143-97275154
36	CEBPB	chr14:97308815-97309084	IMR90	lung:	n/a	n/a
37	CEBPD	chr14:97275006-97275799	K562	blood:	n/a	n/a
38	CTCF	chr14:97319280-97319430	GM06990	blood:	n/a	n/a
39	CTCF	chr14:97319300-97319450	GM12870	blood:	n/a	n/a
40	CTCF	chr14:97319300-97319450	AG09309	skin:	n/a	n/a
41	CTCF	chr14:97319600-97319750	GM12873	blood:	n/a	n/a
42	CTCF	chr14:97319340-97319490	HCT-116	colon:	n/a	n/a
43	CTCF	chr14:97319280-97319430	GM12872	blood:	n/a	n/a
44	CTCF	chr14:97319240-97319390	HepG2	liver:	n/a	n/a
45	CTCF	chr14:97319264-97319476	LNCaP	prostate:	n/a	n/a
46	CTCF	chr14:97319162-97319552	IMR90	lung:	n/a	n/a
47	CTCF	chr14:97319280-97319430	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr14:97319240-97319390	HMF	breast:	n/a	n/a
49	CTCF	chr14:97319220-97319370	GM12865	blood:	n/a	n/a
50	CTCF	chr14:97319279-97319473	Gliobla	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97286215-97286265	T-47D	breast:	n/a
2	chr14:97286215-97286265	SK-N-MC	brain:	n/a
3	chr14:97286215-97286265	RPTEC	kidney:	n/a
4	chr14:97282535-97282585	IMR90	lung:	fetal
5	chr14:97282535-97282585	BJ	skin:	n/a
6	chr14:97286215-97286265	HCT-116	colon:	n/a
7	chr14:97282535-97282585	AG04449	skin:	fetal
8	chr14:97282535-97282585	GM12892	blood:	n/a
9	chr14:97282535-97282585	PANC-1	pancreas:	n/a
10	chr14:97282535-97282585	SK-N-MC	brain:	n/a
11	chr14:97282535-97282585	PFSK-1	brain:	n/a
12	chr14:97282535-97282585	SKMC	muscle:	n/a
13	chr14:97282535-97282585	Hepatocyte	liver:	n/a
14	chr14:97282535-97282585	HCM	heart:	n/a
15	chr14:97282535-97282585	PrEC	prostate:	n/a
16	chr14:97282535-97282585	CMK	blood:	n/a
17	chr14:97282535-97282585	K562	blood:	n/a
18	chr14:97286215-97286265	NT2-D1	testis:	n/a
19	chr14:97282535-97282585	HCPEpiC	choroid plexus:	n/a
20	chr14:97286215-97286265	HCM	heart:	n/a
21	chr14:97282535-97282585	AG09309	skin:	n/a
22	chr14:97286215-97286265	HMEC	breast:	n/a
23	chr14:97282535-97282585	GM19239	blood:	n/a
24	chr14:97286215-97286265	H1-hESC	embryonic stem cell:	embryo
25	chr14:97282535-97282585	U87	brain:	n/a
26	chr14:97282535-97282585	HNPCEpiC	eye:	n/a
27	chr14:97286215-97286265	MCF-7	breast:	n/a
28	chr14:97282535-97282585	HCF	heart:	n/a
29	chr14:97282535-97282585	AG10803	skin:	n/a
30	chr14:97286215-97286265	NHBE	bronchial:	n/a
31	chr14:97282535-97282585	T-47D	breast:	n/a
32	chr14:97282535-97282585	NT2-D1	testis:	n/a
33	chr14:97282535-97282585	HRE	kidney:	n/a
34	chr14:97282535-97282585	HAEpiC	amniotic membrane:	n/a
35	chr14:97286215-97286265	HEEpiC	esophagus:	n/a
36	chr14:97286215-97286265	CMK	blood:	n/a
37	chr14:97282535-97282585	NHBE	bronchial:	n/a
38	chr14:97282535-97282585	HepG2	liver:	n/a
39	chr14:97286215-97286265	Hela-S3	cervix:	n/a
40	chr14:97286215-97286265	NB4	blood:	n/a
41	chr14:97282535-97282585	SK-N-SH	brain:	n/a
42	chr14:97286215-97286265	HCPEpiC	choroid plexus:	n/a
43	chr14:97286215-97286265	SK-N-SH	brain:	n/a
44	chr14:97282535-97282585	HUVEC	blood vessel:	n/a
45	chr14:97282535-97282585	NH-A	brain:	n/a
46	chr14:97282535-97282585	GM06990	blood:	n/a
47	chr14:97282535-97282585	A549	lung:	n/a
48	chr14:97286215-97286265	HRE	kidney:	n/a
49	chr14:97282535-97282585	GM12878	blood:	n/a
50	chr14:97286215-97286265	PrEC	prostate:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:97270252..97272755-chr14:97275339..97277575,4	K562	blood:
2	chr14:97274614..97276764-chr14:97277663..97279518,2	K562	blood:
3	chr14:97319882..97321804-chr14:97324094..97326598,3	K562	blood:
4	chr14:97293502..97295046-chr14:97299094..97301646,2	MCF-7	breast:
5	chr14:97291241..97293286-chr14:97295424..97297762,2	K562	blood:
6	chr14:97050419..97051179-chr14:97313148..97314310,4	MCF-7	breast:
7	chr14:97279153..97281602-chr14:97281672..97284139,2	MCF-7	breast:
8	chr14:97268802..97270728-chr14:97284735..97287343,2	MCF-7	breast:
9	chr14:97278908..97281500-chr14:97284326..97286978,2	MCF-7	breast:
10	chr14:97301856..97303907-chr14:97307668..97309196,2	MCF-7	breast:
11	chr14:97309879..97311402-chr14:97317013..97319777,2	K562	blood:
12	chr14:97265289..97269463-chr14:97278304..97281407,5	K562	blood:
13	chr14:97271567..97274016-chr14:97278732..97280457,2	K562	blood:
14	chr14:97301564..97304982-chr14:97305349..97308383,3	K562	blood:
15	chr14:97263560..97266144-chr14:97273752..97276345,2	MCF-7	breast:
16	chr14:97278908..97281500-chr14:97284326..97286978,2	MCF-7	breast:
17	chr14:97300473..97303064-chr14:97305409..97307983,2	K562	blood:
18	chr14:97285108..97286873-chr14:97288100..97291000,2	MCF-7	breast:
19	chr14:97295418..97297368-chr14:97301033..97303820,2	K562	blood:
20	chr14:97199537..97202098-chr14:97275666..97277302,2	K562	blood:
21	chr14:97293502..97295046-chr14:97299094..97301646,2	MCF-7	breast:
22	chr14:97301856..97303907-chr14:97307668..97309196,2	MCF-7	breast:
23	chr14:97274260..97276872-chr14:97281847..97286316,3	K562	blood:
24	chr14:97265880..97270207-chr14:97278911..97281407,6	K562	blood:
25	chr14:97308706..97311091-chr14:97311481..97313480,2	K562	blood:
26	chr14:97300473..97303064-chr14:97305409..97307983,2	K562	blood:
27	chr14:97301564..97304982-chr14:97305349..97308383,3	K562	blood:
28	chr14:97279153..97281602-chr14:97281672..97284139,2	MCF-7	breast:
29	chr14:97299339..97301771-chr14:97302252..97306278,3	MCF-7	breast:
30	chr14:97272734..97276764-chr14:97276840..97280627,4	K562	blood:
31	chr14:97308706..97311091-chr14:97311481..97313480,2	K562	blood:
32	chr14:97273377..97275528-chr14:97290757..97293307,2	K562	blood:
33	chr14:97306347..97308005-chr14:97316727..97319636,2	K562	blood:
34	chr14:97309902..97311886-chr14:97317929..97319777,2	K562	blood:
35	chr14:97263273..97266024-chr14:97282503..97285691,4	K562	blood:
36	chr14:97050550..97051166-chr14:97319962..97320604,2	MCF-7	breast:
37	chr14:97274260..97276872-chr14:97281847..97286316,3	K562	blood:
38	chr14:97261785..97264150-chr14:97280598..97283173,2	K562	blood:
39	chr14:97303558..97306091-chr14:97311531..97314081,2	K562	blood:
40	chr14:97295418..97297368-chr14:97301033..97303820,2	K562	blood:
41	chr14:97293055..97295755-chr14:97296835..97300397,4	MCF-7	breast:
42	chr14:97295429..97297910-chr14:97313409..97315091,2	K562	blood:
43	chr14:97274614..97276764-chr14:97277663..97279518,2	K562	blood:
44	chr14:97263901..97269146-chr14:97273376..97277295,5	K562	blood:
45	chr14:97263716..97268485-chr14:97284191..97287436,6	K562	blood:
46	chr14:97262876..97266959-chr14:97292166..97296485,5	K562	blood:
47	chr14:97264592..97266800-chr14:97290033..97292350,2	K562	blood:
48	chr14:97271958..97274868-chr14:97298626..97301164,2	MCF-7	breast:
49	chr14:97297616..97299303-chr14:97302743..97305605,2	K562	blood:
50	chr14:97263470..97265371-chr14:97287490..97290229,2	K562	blood:

No data

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

Extended variants
information (count: 1603 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571635667	chr14:97275111-97275112	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562325467	chr14:97275157-97275158	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528898073	chr14:97275163-97275164	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186672966	chr14:97275247-97275248	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12878184	chr14:97275256-97275257	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs533082121	chr14:97275297-97275298	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551167076	chr14:97275308-97275309	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542187305	chr14:97275336-97275337	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149406897	chr14:97275349-97275350	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144815896	chr14:97275355-97275356	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148584428	chr14:97275385-97275386	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569800215	chr14:97275424-97275425	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142995760	chr14:97275466-97275467	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147662627	chr14:97275567-97275568	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553718357	chr14:97275616-97275617	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192344101	chr14:97275632-97275633	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539954015	chr14:97275652-97275653	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183430985	chr14:97275718-97275719	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112528315	chr14:97275721-97275722	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144691817	chr14:97275769-97275770	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188566841	chr14:97275800-97275801	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74786634	chr14:97275871-97275872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541729356	chr14:97275875-97275876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201651717	chr14:97275885-97275886	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147261719	chr14:97275895-97275896	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58196233	chr14:97275905-97275906	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs28664086	chr14:97275906-97275907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566987608	chr14:97275907-97275908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376732211	chr14:97275908-97275909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199718311	chr14:97275911-97275912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559417906	chr14:97275914-97275915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs78357158	chr14:97275923-97275924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369752584	chr14:97275953-97275954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs55696631	chr14:97276005-97276006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs551230237	chr14:97276094-97276095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545129616	chr14:97276110-97276111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs75417496	chr14:97276124-97276125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563196535	chr14:97276150-97276151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550540544	chr14:97276161-97276162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192966793	chr14:97276171-97276172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76863466	chr14:97276287-97276288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546470103	chr14:97276293-97276294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201371728	chr14:97276390-97276391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185336539	chr14:97276427-97276428	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558233142	chr14:97276458-97276459	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376397413	chr14:97276476-97276477	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570022233	chr14:97276507-97276508	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537665836	chr14:97276549-97276550	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372731557	chr14:97276570-97276571	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574270350	chr14:97276604-97276605	ZNF genes & repeats Weak 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:860 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97264800-97278400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr14:97264800-97288000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr14:97264800-97321600	Weak transcription	Psoas Muscle	Psoas
4	chr14:97265000-97282000	Weak transcription	Fetal Thymus	thymus
5	chr14:97265200-97282200	Weak transcription	Primary T cells from cord blood	blood
6	chr14:97265200-97293200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr14:97265400-97277400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr14:97265400-97278600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr14:97265400-97282600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr14:97265600-97277600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr14:97265600-97282200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr14:97265600-97282400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr14:97265600-97291800	Weak transcription	A549	lung
14	chr14:97266200-97277600	Weak transcription	NHDF-Ad	bronchial
15	chr14:97266200-97277800	Weak transcription	HSMM	muscle
16	chr14:97266200-97282000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr14:97266200-97303200	Weak transcription	Hela-S3	cervix
18	chr14:97266800-97282200	Weak transcription	Thymus	Thymus
19	chr14:97270600-97278200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr14:97270800-97279000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr14:97271600-97284200	Weak transcription	NHLF	lung
22	chr14:97271600-97313800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr14:97271800-97277600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr14:97272000-97282200	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr14:97272200-97278400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:97272400-97293800	Weak transcription	Primary B cells from cord blood	blood
27	chr14:97272600-97275200	Enhancers	HepG2	liver
28	chr14:97272600-97275400	Weak transcription	Pancreas	Pancrea
29	chr14:97272600-97277200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr14:97272800-97277600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:97272800-97287200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr14:97273000-97287200	Weak transcription	HMEC	breast
33	chr14:97273400-97277600	Weak transcription	NHEK	skin
34	chr14:97273400-97284200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:97273600-97275400	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr14:97273600-97279400	Weak transcription	Dnd41	blood
37	chr14:97274400-97282200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr14:97274600-97276400	Enhancers	K562	blood
39	chr14:97275000-97275200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr14:97275000-97275800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr14:97275000-97280800	Weak transcription	Fetal Brain Male	brain
42	chr14:97275200-97275400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:97275400-97275600	Enhancers	Pancreas	Pancrea
44	chr14:97275400-97277400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:97275400-97281800	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr14:97275800-97276400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:97276400-97277000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:97276400-97280600	Weak transcription	K562	blood
49	chr14:97277000-97284200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr14:97277200-97277800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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