Variant report

Variant	nsv902026
Chromosome Location	chr14:66061020-66171541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:244)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:571 , 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	chr14:66060978-66061178	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:66071728-66072103	K562	blood:	n/a	n/a
3	ATF2	chr14:66104327-66104964	GM12878	blood:	n/a	n/a
4	ATF2	chr14:66104367-66104999	GM12878	blood:	n/a	n/a
5	ATF3	chr14:66067517-66067789	HepG2	liver:	n/a	n/a
6	BACH1	chr14:66170506-66170838	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:66148425-66148528	K562	blood:	n/a	n/a
8	BATF	chr14:66104430-66104869	GM12878	blood:	n/a	n/a
9	BATF	chr14:66104377-66104890	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:66104363-66104972	GM12878	blood:	n/a	n/a
11	BCL11A	chr14:66104468-66104896	GM12878	blood:	n/a	n/a
12	BCL3	chr14:66143700-66143997	GM12878	blood:	n/a	n/a
13	BCL3	chr14:66143757-66143941	GM12878	blood:	n/a	n/a
14	BCL3	chr14:66104394-66104855	GM12878	blood:	n/a	n/a
15	BCLAF1	chr14:66104342-66104906	GM12878	blood:	n/a	n/a
16	BCLAF1	chr14:66104385-66104951	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:66104506-66104910	GM12878	blood:	n/a	n/a
18	BHLHE40	chr14:66143428-66143628	HepG2	liver:	n/a	n/a
19	BRCA1	chr14:66153584-66153881	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr14:66060970-66061362	HepG2	liver:	n/a	chr14:66061151-66061162
21	CEBPB	chr14:66067487-66067850	HepG2	liver:	n/a	chr14:66067654-66067665
22	CEBPB	chr14:66165073-66165298	A549	lung:	n/a	chr14:66165180-66165191 chr14:66165180-66165193 chr14:66165181-66165192
23	CEBPB	chr14:66067526-66067805	H1-hESC	embryonic stem cell:	n/a	chr14:66067654-66067665
24	CEBPB	chr14:66060755-66061346	MCF-7	breast:	n/a	chr14:66061151-66061162
25	CEBPB	chr14:66060931-66061240	A549	lung:	n/a	chr14:66061151-66061162
26	CEBPB	chr14:66060913-66061337	HepG2	liver:	n/a	chr14:66061151-66061162
27	CEBPB	chr14:66060969-66061321	A549	lung:	n/a	chr14:66061151-66061162
28	CEBPB	chr14:66061091-66061269	K562	blood:	n/a	chr14:66061151-66061162
29	CEBPB	chr14:66104302-66105025	GM12878	blood:	n/a	n/a
30	CEBPB	chr14:66170548-66171476	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:66168049-66168340	IMR90	lung:	n/a	n/a
32	CEBPB	chr14:66087079-66087441	HepG2	liver:	n/a	chr14:66087262-66087273
33	CEBPB	chr14:66067545-66067691	HepG2	liver:	n/a	chr14:66067654-66067665
34	CEBPB	chr14:66067436-66067881	MCF-7	breast:	n/a	chr14:66067654-66067665
35	CEBPB	chr14:66168074-66168298	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr14:66067492-66067826	K562	blood:	n/a	chr14:66067654-66067665
37	CEBPB	chr14:66067466-66067797	MCF-7	breast:	n/a	chr14:66067654-66067665
38	CEBPB	chr14:66168065-66168272	A549	lung:	n/a	n/a
39	CEBPB	chr14:66168018-66168324	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:66067425-66067911	A549	lung:	n/a	chr14:66067654-66067665
41	CEBPB	chr14:66060853-66061435	A549	lung:	n/a	chr14:66061151-66061162
42	CEBPB	chr14:66061074-66061208	HepG2	liver:	n/a	chr14:66061151-66061162
43	CEBPB	chr14:66087102-66087390	K562	blood:	n/a	chr14:66087262-66087273
44	CEBPB	chr14:66067498-66067809	A549	lung:	n/a	chr14:66067654-66067665
45	CEBPB	chr14:66060951-66061282	HepG2	liver:	n/a	chr14:66061151-66061162
46	CEBPB	chr14:66104887-66105109	HepG2	liver:	n/a	chr14:66105026-66105037
47	CEBPB	chr14:66067499-66067819	IMR90	lung:	n/a	chr14:66067654-66067665
48	CEBPB	chr14:66060989-66061307	IMR90	lung:	n/a	chr14:66061151-66061162
49	CEBPB	chr14:66060868-66061724	H1-hESC	embryonic stem cell:	n/a	chr14:66061151-66061162
50	CEBPB	chr14:66165020-66165324	HepG2	liver:	n/a	chr14:66165180-66165191 chr14:66165180-66165193 chr14:66165181-66165192

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:66171222-66171272	BE2_C	brain:	n/a
2	chr14:66135379-66135429	NB4	blood:	n/a
3	chr14:66135379-66135429	LNCaP	prostate:	n/a
4	chr14:66100719-66100769	GM12891	blood:	n/a
5	chr14:66100719-66100769	HNPCEpiC	eye:	n/a
6	chr14:66100719-66100769	HAEpiC	amniotic membrane:	n/a
7	chr14:66100719-66100769	BJ	skin:	n/a
8	chr14:66100719-66100769	HCF	heart:	n/a
9	chr14:66136078-66136128	MCF10A-Er-Src	breast:	n/a
10	chr14:66100719-66100769	AG10803	skin:	n/a
11	chr14:66171222-66171272	HUVEC	blood vessel:	n/a
12	chr14:66171222-66171272	ECC-1	luminal epithelium:	n/a
13	chr14:66100719-66100769	ECC-1	luminal epithelium:	n/a
14	chr14:66100719-66100769	PFSK-1	brain:	n/a
15	chr14:66136078-66136128	ProgFib	skin:	n/a
16	chr14:66136078-66136128	ovcar-3	ovarian:	n/a
17	chr14:66136078-66136128	HIPEpiC	eye:	n/a
18	chr14:66136078-66136128	SK-N-SH_RA	brain:	n/a
19	chr14:66171222-66171272	K562	blood:	n/a
20	chr14:66171222-66171272	PFSK-1	brain:	n/a
21	chr14:66171222-66171272	NH-A	brain:	n/a
22	chr14:66136078-66136128	PFSK-1	brain:	n/a
23	chr14:66136078-66136128	BJ	skin:	n/a
24	chr14:66100719-66100769	HepG2	liver:	n/a
25	chr14:66135379-66135429	HRE	kidney:	n/a
26	chr14:66171222-66171272	HRCEpiC	kidney:	n/a
27	chr14:66135379-66135429	PFSK-1	brain:	n/a
28	chr14:66171222-66171272	GM12891	blood:	n/a
29	chr14:66171222-66171272	AG09319	gingival:	n/a
30	chr14:66135379-66135429	SK-N-SH_RA	brain:	n/a
31	chr14:66171222-66171272	PANC-1	pancreas:	n/a
32	chr14:66135379-66135429	Jurkat	blood:	n/a
33	chr14:66135379-66135429	AG09309	skin:	n/a
34	chr14:66171222-66171272	HCPEpiC	choroid plexus:	n/a
35	chr14:66136078-66136128	HRPEpiC	eye:	n/a
36	chr14:66135379-66135429	T-47D	breast:	n/a
37	chr14:66100719-66100769	CMK	blood:	n/a
38	chr14:66135379-66135429	AG04449	skin:	fetal
39	chr14:66171222-66171272	BJ	skin:	n/a
40	chr14:66171222-66171272	Jurkat	blood:	n/a
41	chr14:66136078-66136128	HRCEpiC	kidney:	n/a
42	chr14:66135379-66135429	H1-hESC	embryonic stem cell:	embryo
43	chr14:66135379-66135429	SK-N-SH	brain:	n/a
44	chr14:66136078-66136128	CMK	blood:	n/a
45	chr14:66135379-66135429	SK-N-MC	brain:	n/a
46	chr14:66135379-66135429	SKMC	muscle:	n/a
47	chr14:66171222-66171272	Hepatocyte	liver:	n/a
48	chr14:66135379-66135429	ECC-1	luminal epithelium:	n/a
49	chr14:66171222-66171272	NT2-D1	testis:	n/a
50	chr14:66136078-66136128	A549	lung:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:66125185..66127124-chr14:66130505..66132106,2	MCF-7	breast:
2	chr14:65878891..65881500-chr14:66106027..66108177,2	MCF-7	breast:
3	chr14:66082417..66084676-chr14:66092751..66094403,2	MCF-7	breast:
4	chr14:66107011..66108860-chr3:124216151..124218690,2	MCF-7	breast:
5	chr14:66049169..66051440-chr14:66059588..66062985,3	MCF-7	breast:
6	chr14:66078999..66081088-chr14:66082459..66085029,2	MCF-7	breast:
7	chr14:65877765..65881174-chr14:66059720..66062565,3	MCF-7	breast:
8	chr14:66114802..66117268-chr14:66124084..66126827,2	MCF-7	breast:
9	chr14:66072945..66075543-chr14:66078088..66081039,2	MCF-7	breast:
10	chr14:66066064..66069081-chr14:66080288..66082777,3	MCF-7	breast:
11	chr14:66066064..66069081-chr14:66080288..66082777,3	MCF-7	breast:
12	chr14:66136933..66139072-chr14:66142582..66145379,2	MCF-7	breast:
13	chr14:66145656..66147261-chr14:66154036..66156276,2	MCF-7	breast:
14	chr14:66082417..66084676-chr14:66092751..66094403,2	MCF-7	breast:
15	chr14:66055552..66057835-chr14:66062107..66064874,2	MCF-7	breast:
16	chr14:66145656..66147261-chr14:66154036..66156276,2	MCF-7	breast:
17	chr14:66114802..66117268-chr14:66124084..66126827,2	MCF-7	breast:
18	chr14:66062925..66064543-chr14:66085225..66086774,2	MCF-7	breast:
19	chr14:65878369..65881220-chr14:66065484..66068700,4	MCF-7	breast:
20	chr14:66169539..66172058-chr14:66175074..66177504,2	K562	blood:
21	chr14:66111572..66114792-chr14:66115017..66117759,3	MCF-7	breast:
22	chr14:66071591..66073659-chr14:66076243..66079071,2	MCF-7	breast:
23	chr14:66066380..66068212-chr14:66091661..66094526,2	MCF-7	breast:
24	chr14:66060976..66063420-chr14:66066312..66068203,2	MCF-7	breast:
25	chr14:66082764..66084424-chr14:66084646..66087072,2	K562	blood:
26	chr14:66082764..66084424-chr14:66084646..66087072,2	K562	blood:
27	chr14:66136933..66139072-chr14:66142582..66145379,2	MCF-7	breast:
28	chr14:66111572..66114792-chr14:66115017..66117759,3	MCF-7	breast:
29	chr14:66125185..66127124-chr14:66130505..66132106,2	MCF-7	breast:
30	chr14:66071591..66073659-chr14:66076243..66079071,2	MCF-7	breast:
31	chr14:66066380..66068212-chr14:66091661..66094526,2	MCF-7	breast:
32	chr14:66078999..66081088-chr14:66082459..66085029,2	MCF-7	breast:
33	chr14:66062925..66064543-chr14:66085225..66086774,2	MCF-7	breast:
34	chr14:66072945..66075543-chr14:66078088..66081039,2	MCF-7	breast:
35	chr14:66109125..66110872-chr14:66135151..66136835,2	MCF-7	breast:
36	chr14:66060976..66063420-chr14:66066312..66068203,2	MCF-7	breast:

No data

Variant related genes	Relation type
FUT8	TF binding region
FUT8	CpG island
ENSG00000033170	chromatin interactions

Extended variants
information (count: 4090 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4090 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1952605	chr14:66061020-66061021	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376514058	chr14:66061021-66061022	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143971176	chr14:66061031-66061032	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544074500	chr14:66061047-66061048	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148628990	chr14:66061124-66061125	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191393333	chr14:66061135-66061136	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111643214	chr14:66061138-66061139	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs74926673	chr14:66061150-66061151	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536244636	chr14:66061200-66061201	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563766055	chr14:66061210-66061211	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535116275	chr14:66061231-66061232	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs202142808	chr14:66061245-66061246	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554911330	chr14:66061250-66061251	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568611537	chr14:66061272-66061273	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537904934	chr14:66061276-66061277	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142072567	chr14:66061292-66061293	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577412250	chr14:66061324-66061325	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546057901	chr14:66061348-66061349	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553736156	chr14:66061349-66061350	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111947190	chr14:66061350-66061351	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182153785	chr14:66061389-66061390	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542266497	chr14:66061390-66061391	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189120383	chr14:66061420-66061421	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201193274	chr14:66061425-66061426	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544733985	chr14:66061431-66061432	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564422874	chr14:66061441-66061442	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533183008	chr14:66061468-66061469	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532720783	chr14:66061475-66061476	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74058526	chr14:66061511-66061512	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs147339928	chr14:66061512-66061513	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6573619	chr14:66061560-66061561	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548575717	chr14:66061561-66061562	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568551403	chr14:66061580-66061581	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537438430	chr14:66061581-66061582	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557862081	chr14:66061597-66061598	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571237371	chr14:66061601-66061602	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs117540798	chr14:66061612-66061613	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553577246	chr14:66061648-66061649	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573581113	chr14:66061658-66061659	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536117075	chr14:66061661-66061662	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370528470	chr14:66061662-66061663	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575642592	chr14:66061691-66061692	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544260894	chr14:66061711-66061712	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73286148	chr14:66061720-66061721	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141030440	chr14:66061728-66061729	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540038946	chr14:66061810-66061811	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528103735	chr14:66061895-66061896	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559872159	chr14:66061904-66061905	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529042439	chr14:66061909-66061910	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548911478	chr14:66061911-66061912	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	23393157	CNVD
Schizophrenia	23393157	CNVD
Seizures	23393157	CNVD
Schizophrenia	23813976	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD

Chromatin state (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66039800-66061200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr14:66058200-66079000	Weak transcription	Primary T cells from cord blood	blood
3	chr14:66058600-66070600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr14:66059200-66062800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr14:66059200-66082600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr14:66060800-66061200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:66060800-66061200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:66060800-66061200	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr14:66060800-66061200	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr14:66060800-66061400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr14:66060800-66061400	Flanking Active TSS	H9 Cell Line	embryonic stem cell
12	chr14:66060800-66061400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr14:66060800-66061400	Enhancers	Duodenum Mucosa	Duodenum
14	chr14:66060800-66061400	Enhancers	Left Ventricle	heart
15	chr14:66060800-66061400	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr14:66060800-66061400	ZNF genes & repeats	Thymus	Thymus
17	chr14:66060800-66061400	Flanking Active TSS	A549	lung
18	chr14:66060800-66061400	Flanking Active TSS	HepG2	liver
19	chr14:66060800-66061600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:66060800-66061600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr14:66060800-66061600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr14:66060800-66061600	Enhancers	Liver	Liver
23	chr14:66060800-66061600	Enhancers	Brain Substantia Nigra	brain
24	chr14:66060800-66061600	Enhancers	Right Ventricle	heart
25	chr14:66060800-66061800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:66060800-66061800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
27	chr14:66060800-66061800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr14:66060800-66061800	Enhancers	Adipose Nuclei	Adipose
29	chr14:66060800-66061800	Enhancers	Pancreas	Pancrea
30	chr14:66060800-66061800	ZNF genes & repeats	Dnd41	blood
31	chr14:66060800-66061800	ZNF genes & repeats	GM12878-XiMat	blood
32	chr14:66060800-66062000	Strong transcription	Primary B cells from cord blood	blood
33	chr14:66061000-66061200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
34	chr14:66061000-66061200	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr14:66061000-66061400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr14:66061000-66061400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr14:66061000-66061400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:66061000-66061400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:66061000-66061400	Enhancers	Primary T cells fromperipheralblood	blood
40	chr14:66061000-66061400	Enhancers	Brain Hippocampus Middle	brain
41	chr14:66061000-66061400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr14:66061000-66061400	Enhancers	Colonic Mucosa	Colon
43	chr14:66061000-66061600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:66061000-66061600	Enhancers	Esophagus	oesophagus
45	chr14:66061000-66061600	Enhancers	Gastric	stomach
46	chr14:66061000-66061600	Enhancers	Lung	lung
47	chr14:66061000-66061600	Enhancers	Right Atrium	heart
48	chr14:66061000-66061600	Enhancers	Stomach Mucosa	stomach
49	chr14:66061000-66061800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:66061000-66061800	ZNF genes & repeats	Fetal Intestine Small	intestine

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