Variant report

Variant	nsv1047409
Chromosome Location	chr14:37276300-37356945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:433)
CpG islands
(count:122)
Chromatin interactive
region (count:54)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:433 , 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	ATF2	chr14:37335935-37336504	GM12878	blood:	n/a	n/a
2	ATF3	chr14:37317462-37317744	K562	blood:	n/a	n/a
3	BCL11A	chr14:37327122-37327329	GM12878	blood:	n/a	chr14:37327310-37327319
4	BCL11A	chr14:37336084-37336424	GM12878	blood:	n/a	chr14:37336257-37336266
5	BHLHE40	chr14:37348927-37348928	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:37336138-37336380	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:37340086-37340286	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:37298765-37299131	K562	blood:	n/a	n/a
9	BHLHE40	chr14:37335399-37335519	GM12878	blood:	n/a	n/a
10	BRCA1	chr14:37295376-37295438	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:37297161-37297300	K562	blood:	n/a	chr14:37297176-37297189
12	CEBPB	chr14:37317480-37317746	K562	blood:	n/a	chr14:37317620-37317631
13	CEBPB	chr14:37351716-37351813	HepG2	liver:	n/a	chr14:37351744-37351755 chr14:37351743-37351756
14	CEBPB	chr14:37317482-37317775	A549	lung:	n/a	chr14:37317620-37317631
15	CEBPB	chr14:37325043-37326163	MCF-7	breast:	n/a	chr14:37325922-37325933
16	CEBPB	chr14:37317394-37317777	K562	blood:	n/a	chr14:37317620-37317631
17	CEBPB	chr14:37299081-37299210	HepG2	liver:	n/a	chr14:37299153-37299164
18	CEBPB	chr14:37350952-37351015	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:37322208-37322222	A549	lung:	n/a	n/a
20	CEBPB	chr14:37322667-37322857	H1-hESC	embryonic stem cell:	n/a	chr14:37322710-37322721
21	CEBPB	chr14:37317467-37317807	Hela-S3	cervix:	n/a	chr14:37317620-37317631
22	CEBPB	chr14:37297108-37297356	HepG2	liver:	n/a	chr14:37297297-37297310 chr14:37297176-37297189
23	CEBPB	chr14:37343712-37344408	MCF-7	breast:	n/a	n/a
24	CEBPB	chr14:37287931-37288274	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:37317494-37317782	HepG2	liver:	n/a	chr14:37317620-37317631
26	CEBPB	chr14:37317264-37317827	K562	blood:	n/a	chr14:37317620-37317631
27	CEBPB	chr14:37287998-37288471	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:37325805-37325996	HepG2	liver:	n/a	chr14:37325922-37325933
29	CEBPB	chr14:37322668-37322793	HepG2	liver:	n/a	chr14:37322710-37322721
30	CEBPB	chr14:37301933-37302166	HepG2	liver:	n/a	chr14:37302080-37302091
31	CEBPB	chr14:37286733-37286918	Hela-S3	cervix:	n/a	chr14:37286867-37286876 chr14:37286867-37286878 chr14:37286865-37286876 chr14:37286867-37286876 chr14:37286867-37286876 chr14:37286867-37286876
32	CEBPB	chr14:37292084-37292309	HepG2	liver:	n/a	chr14:37292160-37292173 chr14:37292161-37292172 chr14:37292247-37292260 chr14:37292188-37292199
33	CEBPB	chr14:37339105-37339322	HepG2	liver:	n/a	chr14:37339237-37339248
34	CEBPB	chr14:37317429-37317853	MCF-7	breast:	n/a	chr14:37317620-37317631
35	CEBPB	chr14:37286721-37287097	HepG2	liver:	n/a	chr14:37286867-37286876 chr14:37286867-37286878 chr14:37286865-37286876 chr14:37286867-37286876 chr14:37286867-37286876 chr14:37286867-37286876
36	CEBPB	chr14:37287961-37288260	A549	lung:	n/a	n/a
37	CEBPB	chr14:37322039-37322881	Hela-S3	cervix:	n/a	chr14:37322710-37322721
38	CEBPB	chr14:37328180-37328813	MCF-7	breast:	n/a	chr14:37328556-37328569 chr14:37328556-37328567 chr14:37328426-37328439
39	CEBPB	chr14:37286756-37287014	K562	blood:	n/a	chr14:37286867-37286876 chr14:37286867-37286878 chr14:37286865-37286876 chr14:37286867-37286876 chr14:37286867-37286876 chr14:37286867-37286876
40	CEBPB	chr14:37298988-37299290	K562	blood:	n/a	chr14:37299153-37299164
41	CEBPB	chr14:37286800-37287046	A549	lung:	n/a	chr14:37286867-37286876 chr14:37286867-37286878 chr14:37286865-37286876 chr14:37286867-37286876 chr14:37286867-37286876 chr14:37286867-37286876
42	CHD2	chr14:37327285-37327360	GM12878	blood:	n/a	n/a
43	CHD2	chr14:37335927-37335935	GM12878	blood:	n/a	n/a
44	CHD2	chr14:37322305-37322512	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr14:37332999-37333026	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:37332600-37332750	Caco-2	colon:	n/a	chr14:37332682-37332703 chr14:37332681-37332697
47	CTCF	chr14:37332660-37332810	HepG2	liver:	n/a	chr14:37332682-37332703 chr14:37332681-37332697
48	CTCF	chr14:37332540-37332690	WI-38	lung:	n/a	n/a
49	CTCF	chr14:37332560-37332710	HRPEpiC	eye:	n/a	chr14:37332682-37332703 chr14:37332681-37332697
50	CTCF	chr14:37332540-37332719	HepG2	liver:	n/a	chr14:37332682-37332703 chr14:37332681-37332697

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37295794-37295844	BE2_C	brain:	n/a
2	chr14:37326057-37326107	U87	brain:	n/a
3	chr14:37295794-37295844	ECC-1	luminal epithelium:	n/a
4	chr14:37295794-37295844	SKMC	muscle:	n/a
5	chr14:37326057-37326107	LNCaP	prostate:	n/a
6	chr14:37326057-37326107	MCF-7	breast:	n/a
7	chr14:37295794-37295844	HEEpiC	esophagus:	n/a
8	chr14:37326057-37326107	PrEC	prostate:	n/a
9	chr14:37326057-37326107	AG10803	skin:	n/a
10	chr14:37326057-37326107	RPTEC	kidney:	n/a
11	chr14:37295794-37295844	NHBE	bronchial:	n/a
12	chr14:37295794-37295844	PFSK-1	brain:	n/a
13	chr14:37295794-37295844	HCPEpiC	choroid plexus:	n/a
14	chr14:37326057-37326107	HRPEpiC	eye:	n/a
15	chr14:37295794-37295844	NH-A	brain:	n/a
16	chr14:37326057-37326107	SK-N-SH_RA	brain:	n/a
17	chr14:37295794-37295844	HRCEpiC	kidney:	n/a
18	chr14:37295794-37295844	U87	brain:	n/a
19	chr14:37326057-37326107	Hepatocyte	liver:	n/a
20	chr14:37295794-37295844	MCF10A-Er-Src	breast:	n/a
21	chr14:37326057-37326107	HCF	heart:	n/a
22	chr14:37295794-37295844	MCF-7	breast:	n/a
23	chr14:37326057-37326107	HIPEpiC	eye:	n/a
24	chr14:37295794-37295844	NHDF-neo	bronchial:	n/a
25	chr14:37326057-37326107	ovcar-3	ovarian:	n/a
26	chr14:37326057-37326107	AG04449	skin:	fetal
27	chr14:37295794-37295844	GM06990	blood:	n/a
28	chr14:37326057-37326107	HMEC	breast:	n/a
29	chr14:37295794-37295844	PrEC	prostate:	n/a
30	chr14:37326057-37326107	GM19239	blood:	n/a
31	chr14:37295794-37295844	Caco-2	colon:	n/a
32	chr14:37326057-37326107	BE2_C	brain:	n/a
33	chr14:37326057-37326107	AoSMC	blood vessel:	n/a
34	chr14:37326057-37326107	NH-A	brain:	n/a
35	chr14:37295794-37295844	H1-hESC	embryonic stem cell:	embryo
36	chr14:37295794-37295844	NT2-D1	testis:	n/a
37	chr14:37295794-37295844	Hela-S3	cervix:	n/a
38	chr14:37326057-37326107	AG04450	lung:	fetal
39	chr14:37295794-37295844	T-47D	breast:	n/a
40	chr14:37295794-37295844	Hepatocyte	liver:	n/a
41	chr14:37326057-37326107	HPAEpiC	pulmonary alveolar:	n/a
42	chr14:37326057-37326107	MCF10A-Er-Src	breast:	n/a
43	chr14:37326057-37326107	GM06990	blood:	n/a
44	chr14:37326057-37326107	HepG2	liver:	n/a
45	chr14:37326057-37326107	AG09309	skin:	n/a
46	chr14:37295794-37295844	HRPEpiC	eye:	n/a
47	chr14:37326057-37326107	ECC-1	luminal epithelium:	n/a
48	chr14:37326057-37326107	Hela-S3	cervix:	n/a
49	chr14:37326057-37326107	HCPEpiC	choroid plexus:	n/a
50	chr14:37295794-37295844	HUVEC	blood vessel:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:37304138..37305001-chr14:37328066..37328921,2	MCF-7	breast:
2	chr14:37286521..37289196-chr14:37301777..37303457,2	MCF-7	breast:
3	chr14:37130985..37132891-chr14:37324369..37327247,2	MCF-7	breast:
4	chr14:37317109..37319499-chr14:37322060..37324945,2	MCF-7	breast:
5	chr14:37296289..37298103-chr14:37306225..37308864,2	K562	blood:
6	chr14:37303736..37307044-chr14:37316621..37318859,4	K562	blood:
7	chr14:37228461..37230190-chr14:37276163..37278698,2	MCF-7	breast:
8	chr14:37304347..37306233-chr14:37307892..37310868,2	MCF-7	breast:
9	chr14:37284732..37287552-chr14:37297526..37299847,2	MCF-7	breast:
10	chr14:37311700..37315243-chr14:37317364..37319859,4	MCF-7	breast:
11	chr14:37323729..37326206-chr14:37335607..37338464,3	MCF-7	breast:
12	chr14:37296289..37298103-chr14:37306225..37308864,2	K562	blood:
13	chr14:37298955..37301197-chr14:37322240..37325212,2	MCF-7	breast:
14	chr14:37320896..37323806-chr14:37324538..37327389,3	MCF-7	breast:
15	chr14:37292414..37295157-chr14:37297735..37300581,3	K562	blood:
16	chr14:37280026..37283216-chr14:37286097..37288094,3	MCF-7	breast:
17	chr14:37334201..37336758-chr14:37341716..37343267,2	K562	blood:
18	chr14:37344813..37347006-chr14:37347146..37349594,2	MCF-7	breast:
19	chr14:37304138..37305001-chr14:37328066..37328921,2	MCF-7	breast:
20	chr14:37304347..37306233-chr14:37307892..37310868,2	MCF-7	breast:
21	chr14:37327092..37330029-chr14:37344946..37346865,2	MCF-7	breast:
22	chr14:37323565..37325232-chr14:37403567..37406309,2	MCF-7	breast:
23	chr14:37292414..37295157-chr14:37297735..37300581,3	K562	blood:
24	chr14:37317109..37318856-chr14:37319058..37321260,2	MCF-7	breast:
25	chr14:37327092..37330029-chr14:37344946..37346865,2	MCF-7	breast:
26	chr14:37326304..37329883-chr14:37330751..37333805,5	MCF-7	breast:
27	chr14:37305591..37310921-chr14:37313682..37319319,4	K562	blood:
28	chr14:37280026..37283216-chr14:37286097..37288094,3	MCF-7	breast:
29	chr14:37323729..37326206-chr14:37335607..37338464,3	MCF-7	breast:
30	chr14:37286811..37289259-chr14:37323877..37326404,2	MCF-7	breast:
31	chr14:37303736..37307044-chr14:37316621..37318859,4	K562	blood:
32	chr14:37334201..37336758-chr14:37341716..37343267,2	K562	blood:
33	chr14:37284732..37287552-chr14:37297526..37299847,2	MCF-7	breast:
34	chr14:37317109..37319499-chr14:37322060..37324945,2	MCF-7	breast:
35	chr14:37344813..37347006-chr14:37347146..37349594,2	MCF-7	breast:
36	chr14:37239954..37240721-chr14:37325375..37325944,2	MCF-7	breast:
37	chr14:37286521..37289196-chr14:37301777..37303457,2	MCF-7	breast:
38	chr14:37317109..37318856-chr14:37319058..37321260,2	MCF-7	breast:
39	chr14:37286811..37289259-chr14:37323877..37326404,2	MCF-7	breast:
40	chr14:37311700..37315243-chr14:37317364..37319859,4	MCF-7	breast:
41	chr14:37325745..37328673-chr14:37409950..37412663,2	MCF-7	breast:
42	chr14:37341569..37343794-chr14:37350326..37353286,2	K562	blood:
43	chr14:37348540..37350532-chr14:37354139..37356297,2	MCF-7	breast:
44	chr14:37307868..37310434-chr14:37313935..37316396,2	MCF-7	breast:
45	chr14:37317909..37319508-chr14:37322006..37324185,2	MCF-7	breast:
46	chr14:37298955..37301197-chr14:37322240..37325212,2	MCF-7	breast:
47	chr14:37341569..37343794-chr14:37350326..37353286,2	K562	blood:
48	chr14:37317909..37319508-chr14:37322006..37324185,2	MCF-7	breast:
49	chr14:37320896..37323806-chr14:37324538..37327389,3	MCF-7	breast:
50	chr14:37265327..37267473-chr14:37324922..37326801,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAX9-4	chr14:37297627-37297934	ENSG00000258601.1
2	lnc-PAX9-4	chr14:37278076-37278321	ENSG00000258601.1
3	lnc-PAX9-2	chr14:37276029-37276368	ENSG00000258690.1

No data

Variant related genes	Relation type
ENSG00000258601	TF binding region
ENSG00000258601	CpG island
ENSG00000198807	chromatin interactions
ENSG00000183032	chromatin interactions

Extended variants
information (count: 2755 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2755 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531306283	chr14:37276313-37276314	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs111293080	chr14:37276325-37276326	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs76141591	chr14:37276342-37276343	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs111368073	chr14:37276344-37276345	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs547803083	chr14:37276355-37276356	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs567844554	chr14:37276363-37276364	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs551438378	chr14:37276398-37276399	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184491120	chr14:37276400-37276401	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs550405640	chr14:37276404-37276405	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs189760926	chr14:37276407-37276408	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs7154494	chr14:37276436-37276437	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs848088	chr14:37276498-37276499	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs572380157	chr14:37276525-37276526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs17105392	chr14:37276539-37276540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs142201758	chr14:37276589-37276590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs111981931	chr14:37276637-37276638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146371081	chr14:37276656-37276657	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115229353	chr14:37276777-37276778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531811377	chr14:37276815-37276816	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139660929	chr14:37276851-37276852	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11628335	chr14:37276852-37276853	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs74045000	chr14:37276859-37276860	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs17105394	chr14:37276864-37276865	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs548059182	chr14:37276869-37276870	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561380546	chr14:37276896-37276897	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs11623729	chr14:37276956-37276957	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78351140	chr14:37276962-37276963	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550364744	chr14:37276977-37276978	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs17105396	chr14:37276980-37276981	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201537298	chr14:37277029-37277030	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543652430	chr14:37277042-37277043	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142934331	chr14:37277074-37277075	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs185933164	chr14:37277075-37277076	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs560280468	chr14:37277147-37277148	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566058277	chr14:37277160-37277161	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111928409	chr14:37277173-37277174	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534671655	chr14:37277179-37277180	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs146227376	chr14:37277229-37277230	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs189080800	chr14:37277236-37277237	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs139087443	chr14:37277244-37277245	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs1429845	chr14:37277315-37277316	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181746620	chr14:37277339-37277340	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544700540	chr14:37277390-37277391	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532697893	chr14:37277401-37277402	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558409859	chr14:37277439-37277440	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs572115540	chr14:37277537-37277538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540622480	chr14:37277543-37277544	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541384945	chr14:37277560-37277561	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs848087	chr14:37277643-37277644	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548429145	chr14:37277680-37277681	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37274600-37276800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:37274800-37278200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:37275000-37276400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr14:37275000-37276400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr14:37275000-37276600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr14:37276200-37277800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr14:37276400-37276800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr14:37276400-37277200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr14:37276600-37277600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr14:37276800-37277800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:37277800-37278800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:37278200-37278400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:37278800-37279000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:37283200-37285600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:37285200-37285800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr14:37285200-37286000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:37285200-37287800	Enhancers	NHEK	skin
18	chr14:37285400-37286200	Enhancers	HMEC	breast
19	chr14:37285400-37291800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:37285600-37292200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr14:37286000-37286800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:37286200-37286600	Weak transcription	HMEC	breast
23	chr14:37286400-37286800	Enhancers	Fetal Thymus	thymus
24	chr14:37286600-37286800	Enhancers	HMEC	breast
25	chr14:37286800-37287000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:37286800-37287000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:37286800-37289200	Weak transcription	HMEC	breast
28	chr14:37287000-37287600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr14:37287400-37290200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr14:37287600-37288400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:37287600-37288400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:37287600-37288800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:37287600-37289000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:37287800-37288200	Weak transcription	NHEK	skin
35	chr14:37287800-37289400	Enhancers	K562	blood
36	chr14:37287800-37289600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:37288000-37288200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr14:37288000-37288200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr14:37288000-37288400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr14:37288000-37288400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr14:37288200-37288400	Enhancers	NHEK	skin
42	chr14:37288200-37288600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr14:37288200-37288600	Bivalent Enhancer	Fetal Heart	heart
44	chr14:37288200-37289000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr14:37288200-37289400	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr14:37288200-37289600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr14:37288400-37289200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:37288400-37289200	Weak transcription	NHEK	skin
49	chr14:37288400-37289600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr14:37289000-37289600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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