Variant report

Variant	nsv564349
Chromosome Location	chr14:37890433-38034434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:778)
CpG islands
(count:61)
Chromatin interactive
region (count:85)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37966619-37967091	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:37962806-37963218	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:38015300-38016974	HepG2	liver:	n/a	chr14:38015494-38015510
4	ARID3A	chr14:37916975-37917561	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:37935172-37936858	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:37937245-37937930	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:37996655-37996907	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:38014394-38014724	HepG2	liver:	n/a	chr14:38014521-38014537
9	ARID3A	chr14:38031258-38031519	HepG2	liver:	n/a	n/a
10	ATF3	chr14:38016010-38016388	A549	lung:	n/a	n/a
11	BACH1	chr14:38018020-38018181	K562	blood:	n/a	n/a
12	BCL3	chr14:38015991-38016548	A549	lung:	n/a	n/a
13	BCL3	chr14:38015925-38016570	A549	lung:	n/a	n/a
14	BHLHE40	chr14:37935661-37936300	HepG2	liver:	n/a	n/a
15	BHLHE40	chr14:38015947-38016344	HepG2	liver:	n/a	n/a
16	BHLHE40	chr14:38031008-38031043	K562	blood:	n/a	n/a
17	BHLHE40	chr14:38015971-38016568	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:37952866-37953238	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:37935615-37936171	HepG2	liver:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
20	CEBPB	chr14:37935591-37936194	HepG2	liver:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
21	CEBPB	chr14:37899136-37899190	HepG2	liver:	n/a	chr14:37899154-37899165
22	CEBPB	chr14:37894629-37894863	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:37952802-37953325	MCF-7	breast:	n/a	n/a
24	CEBPB	chr14:38015705-38016668	HepG2	liver:	n/a	chr14:38015725-38015738
25	CEBPB	chr14:37952839-37953270	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:37961531-37961805	IMR90	lung:	n/a	n/a
27	CEBPB	chr14:38014406-38014690	A549	lung:	n/a	chr14:38014510-38014519 chr14:38014508-38014521 chr14:38014508-38014521 chr14:38014508-38014519 chr14:38014510-38014521
28	CEBPB	chr14:38014375-38014691	IMR90	lung:	n/a	chr14:38014510-38014519 chr14:38014508-38014521 chr14:38014508-38014521 chr14:38014508-38014519 chr14:38014510-38014521
29	CEBPB	chr14:37937231-37937622	HepG2	liver:	n/a	chr14:37937449-37937460
30	CEBPB	chr14:37961519-37961800	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:37986758-37986770	K562	blood:	n/a	n/a
32	CEBPB	chr14:37935878-37935967	K562	blood:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
33	CEBPB	chr14:37961570-37961743	A549	lung:	n/a	n/a
34	CEBPB	chr14:38015623-38016763	MCF-7	breast:	n/a	chr14:38015725-38015738
35	CEBPB	chr14:37952947-37953208	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr14:37962814-37963236	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:37983530-37983823	HepG2	liver:	n/a	chr14:37983679-37983690 chr14:37983681-37983692 chr14:37983679-37983692
38	CEBPB	chr14:38031193-38031560	IMR90	lung:	n/a	chr14:38031354-38031365 chr14:38031355-38031366
39	CEBPB	chr14:37935577-37936272	HepG2	liver:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
40	CEBPB	chr14:37952857-37953222	K562	blood:	n/a	n/a
41	CEBPB	chr14:38014377-38014681	HepG2	liver:	n/a	chr14:38014510-38014519 chr14:38014508-38014521 chr14:38014508-38014521 chr14:38014508-38014519 chr14:38014510-38014521
42	CEBPB	chr14:37962189-37962375	HepG2	liver:	n/a	chr14:37962251-37962262 chr14:37962250-37962261
43	CEBPB	chr14:38003065-38003155	HepG2	liver:	n/a	chr14:38003068-38003079 chr14:38003067-38003078 chr14:38003067-38003080
44	CEBPB	chr14:38031198-38031546	HepG2	liver:	n/a	chr14:38031354-38031365 chr14:38031355-38031366
45	CEBPB	chr14:37952890-37953331	MCF-7	breast:	n/a	n/a
46	CEBPB	chr14:37977799-37978065	A549	lung:	n/a	n/a
47	CEBPB	chr14:37935729-37936138	A549	lung:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
48	CEBPB	chr14:37950035-37950380	HepG2	liver:	n/a	chr14:37950296-37950307
49	CEBPB	chr14:37977726-37978087	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:37935679-37936088	MCF-7	breast:	n/a	chr14:37935912-37935923 chr14:37935914-37935925

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38031240-38031290	HRCEpiC	kidney:	n/a
2	chr14:38031240-38031290	ovcar-3	ovarian:	n/a
3	chr14:38031240-38031290	GM12892	blood:	n/a
4	chr14:38031240-38031290	PrEC	prostate:	n/a
5	chr14:38031240-38031290	U87	brain:	n/a
6	chr14:38031240-38031290	MCF10A-Er-Src	breast:	n/a
7	chr14:38031240-38031290	GM19239	blood:	n/a
8	chr14:38031240-38031290	Jurkat	blood:	n/a
9	chr14:38031240-38031290	HCT-116	colon:	n/a
10	chr14:38031240-38031290	HNPCEpiC	eye:	n/a
11	chr14:38031240-38031290	RPTEC	kidney:	n/a
12	chr14:38031240-38031290	BJ	skin:	n/a
13	chr14:38031240-38031290	IMR90	lung:	fetal
14	chr14:38031240-38031290	MCF-7	breast:	n/a
15	chr14:38031240-38031290	K562	blood:	n/a
16	chr14:38031240-38031290	Hepatocyte	liver:	n/a
17	chr14:38031240-38031290	ECC-1	luminal epithelium:	n/a
18	chr14:38031240-38031290	AG09309	skin:	n/a
19	chr14:38031240-38031290	ProgFib	skin:	n/a
20	chr14:38031240-38031290	HL-60	blood:	n/a
21	chr14:38031240-38031290	AG09319	gingival:	n/a
22	chr14:38031240-38031290	NT2-D1	testis:	n/a
23	chr14:38031240-38031290	BE2_C	brain:	n/a
24	chr14:38031240-38031290	Hela-S3	cervix:	n/a
25	chr14:38031240-38031290	HCM	heart:	n/a
26	chr14:38031240-38031290	HMEC	breast:	n/a
27	chr14:38031240-38031290	HIPEpiC	eye:	n/a
28	chr14:38031240-38031290	GM06990	blood:	n/a
29	chr14:38031240-38031290	SK-N-SH_RA	brain:	n/a
30	chr14:38031240-38031290	LNCaP	prostate:	n/a
31	chr14:38031240-38031290	PANC-1	pancreas:	n/a
32	chr14:38031240-38031290	NHBE	bronchial:	n/a
33	chr14:38031240-38031290	PFSK-1	brain:	n/a
34	chr14:38031240-38031290	AoSMC	blood vessel:	n/a
35	chr14:38031240-38031290	GM12891	blood:	n/a
36	chr14:38031240-38031290	T-47D	breast:	n/a
37	chr14:38031240-38031290	HRPEpiC	eye:	n/a
38	chr14:38031240-38031290	AG10803	skin:	n/a
39	chr14:38031240-38031290	HepG2	liver:	n/a
40	chr14:38031240-38031290	HAEpiC	amniotic membrane:	n/a
41	chr14:38031240-38031290	NH-A	brain:	n/a
42	chr14:38031240-38031290	HCPEpiC	choroid plexus:	n/a
43	chr14:38031240-38031290	HUVEC	blood vessel:	n/a
44	chr14:38031240-38031290	SK-N-SH	brain:	n/a
45	chr14:38031240-38031290	AG04450	lung:	fetal
46	chr14:38031240-38031290	NB4	blood:	n/a
47	chr14:38031240-38031290	HEEpiC	esophagus:	n/a
48	chr14:38031240-38031290	GM12878	blood:	n/a
49	chr14:38031240-38031290	HEK293	kidney:	embryo
50	chr14:38031240-38031290	SAEC	small airway:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:38001638..38003802-chr14:38010426..38012246,2	MCF-7	breast:
2	chr14:37899686..37902705-chr14:38064003..38066607,3	MCF-7	breast:
3	chr14:37992987..37994554-chr14:37998762..38001417,2	K562	blood:
4	chr14:37914831..37917471-chr14:37919271..37922132,2	MCF-7	breast:
5	chr14:38014337..38017689-chr14:38019804..38021819,4	MCF-7	breast:
6	chr14:37966935..37969327-chr14:37979920..37982078,2	K562	blood:
7	chr14:37897535..37899895-chr14:38063797..38065302,2	MCF-7	breast:
8	chr14:38015701..38018409-chr14:38034493..38036492,3	MCF-7	breast:
9	chr14:38021477..38023434-chr14:38051873..38053665,2	MCF-7	breast:
10	chr14:38015801..38018885-chr14:38023439..38025861,3	MCF-7	breast:
11	chr14:37996088..37997734-chr14:38026387..38028218,2	MCF-7	breast:
12	chr14:37996356..38000397-chr14:38056446..38059493,3	MCF-7	breast:
13	chr14:37981930..37983702-chr14:37987537..37990336,2	MCF-7	breast:
14	chr14:37992113..37994949-chr14:37995785..37998678,3	MCF-7	breast:
15	chr14:38015790..38016628-chr14:38036265..38036824,2	MCF-7	breast:
16	chr14:38014337..38017689-chr14:38019804..38021819,4	MCF-7	breast:
17	chr14:38001707..38004632-chr14:38007880..38010262,2	MCF-7	breast:
18	chr14:38023383..38025089-chr14:38055151..38056886,2	MCF-7	breast:
19	chr14:38001707..38004632-chr14:38007880..38010262,2	MCF-7	breast:
20	chr14:37919150..37921478-chr14:38062353..38064686,2	MCF-7	breast:
21	chr14:38011441..38015766-chr14:38062652..38065926,9	MCF-7	breast:
22	chr14:37996620..37999759-chr14:38060620..38062986,3	MCF-7	breast:
23	chr14:37997035..38000891-chr14:38059791..38066021,6	MCF-7	breast:
24	chr14:38011817..38019831-chr14:38060493..38066722,23	MCF-7	breast:
25	chr14:37923519..37926055-chr14:37998366..38001362,2	MCF-7	breast:
26	chr14:38014910..38017892-chr14:38018379..38020104,3	MCF-7	breast:
27	chr14:37905530..37906254-chr14:38016253..38017008,2	MCF-7	breast:
28	chr14:37895105..37897353-chr14:37902428..37905218,2	MCF-7	breast:
29	chr14:37980983..37983518-chr14:37985566..37987146,2	MCF-7	breast:
30	chr14:37979957..37982463-chr14:37983099..37985878,2	MCF-7	breast:
31	chr14:38015801..38018885-chr14:38023439..38025861,3	MCF-7	breast:
32	chr14:37996088..37997734-chr14:38026387..38028218,2	MCF-7	breast:
33	chr14:38031576..38032423-chr14:38066583..38067091,2	MCF-7	breast:
34	chr14:37977669..37980526-chr14:38060967..38062630,2	MCF-7	breast:
35	chr14:38034290..38035240-chr14:38063014..38063525,2	MCF-7	breast:
36	chr14:37923519..37926055-chr14:37998366..38001362,2	MCF-7	breast:
37	chr14:37984075..37986407-chr14:37992639..37994265,2	MCF-7	breast:
38	chr14:37992987..37994554-chr14:37998762..38001417,2	K562	blood:
39	chr14:37979957..37982463-chr14:37983099..37985878,2	MCF-7	breast:
40	chr14:37966935..37969327-chr14:37979920..37982078,2	K562	blood:
41	chr14:38013794..38017816-chr14:38049871..38055560,6	MCF-7	breast:
42	chr14:37903287..37907312-chr14:38059908..38064571,5	MCF-7	breast:
43	chr14:38018016..38020323-chr14:38050834..38052652,3	MCF-7	breast:
44	chr14:37981930..37983702-chr14:37987537..37990336,2	MCF-7	breast:
45	chr14:38013523..38020726-chr14:38055776..38060374,10	MCF-7	breast:
46	chr14:38012929..38015442-chr14:38030781..38032707,2	MCF-7	breast:
47	chr14:38014910..38017892-chr14:38018379..38020104,3	MCF-7	breast:
48	chr14:37983365..37983885-chr6:24645754..24646643,2	Hela-S3	cervix:
49	chr14:38022120..38023729-chr14:38064020..38066950,2	MCF-7	breast:
50	chr14:37922172..37923880-chr14:37926758..37928419,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MIPOL1-1	chr14:38033434-38033567	XLOC_010804
2	lnc-MIPOL1-1	chr14:38033252-38033567	ENSG00000258414.1

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MIPOL1	hsa-miR-192-5p	chr14:38016587-38016594
2	MIPOL1	hsa-miR-215-5p	chr14:38016573-38016594
3	MIPOL1	hsa-miR-215-5p	chr14:38016587-38016594
4	MIPOL1	hsa-miR-192-5p	chr14:38016573-38016594

Variant related genes	Relation type
ENSG00000259087	TF binding region
RNU6-886P	TF binding region
ENSG00000258414	TF binding region
ENSG00000259087	CpG island
RNU6-886P	CpG island
ENSG00000258414	CpG island
ENSG00000258414	chromatin interactions
ENSG00000137261	chromatin interactions
ENSG00000207046	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000259087	chromatin interactions
ENSG00000139865	chromatin interactions

Extended variants
information (count: 4989 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4989 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1955949	chr14:37890433-37890434	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532479394	chr14:37890458-37890459	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371397186	chr14:37890501-37890502	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186777035	chr14:37890533-37890534	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs137979571	chr14:37890544-37890545	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527749649	chr14:37890549-37890550	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs149467796	chr14:37890573-37890574	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567810835	chr14:37890584-37890585	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs143017268	chr14:37890594-37890595	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550390323	chr14:37890599-37890600	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570248837	chr14:37890623-37890624	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190511347	chr14:37890644-37890645	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113291693	chr14:37890661-37890662	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548127253	chr14:37890688-37890689	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs566350598	chr14:37890818-37890819	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138960996	chr14:37890822-37890823	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181958681	chr14:37890865-37890866	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs376100259	chr14:37890897-37890898	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142919034	chr14:37890978-37890979	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543207523	chr14:37891058-37891059	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557168503	chr14:37891126-37891127	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147422758	chr14:37891131-37891132	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186536881	chr14:37891173-37891174	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189751974	chr14:37891176-37891177	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs35146931	chr14:37891212-37891213	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139675954	chr14:37891217-37891218	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370183773	chr14:37891243-37891244	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541496073	chr14:37891252-37891253	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs561358545	chr14:37891259-37891260	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570308038	chr14:37891392-37891393	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs565132251	chr14:37891415-37891416	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs111790776	chr14:37891444-37891445	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs550083471	chr14:37891463-37891464	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536676093	chr14:37891475-37891476	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs150653653	chr14:37891485-37891486	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs532662594	chr14:37891492-37891493	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554933597	chr14:37891497-37891498	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs139766888	chr14:37891505-37891506	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs149781118	chr14:37891536-37891537	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576501069	chr14:37891539-37891540	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs547824879	chr14:37891548-37891549	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs146793654	chr14:37891655-37891656	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs8022848	chr14:37891712-37891713	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556841483	chr14:37891749-37891750	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs576636152	chr14:37891758-37891759	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs182476025	chr14:37891806-37891807	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577444784	chr14:37891828-37891829	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373588060	chr14:37891891-37891892	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538934991	chr14:37891935-37891936	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531686126	chr14:37891937-37891938	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37867800-37898800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:37877800-37913200	Weak transcription	Ovary	ovary
3	chr14:37889800-37891800	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr14:37890000-37890600	Active TSS	A549	lung
5	chr14:37890000-37892400	Enhancers	HepG2	liver
6	chr14:37890200-37890600	Active TSS	Liver	Liver
7	chr14:37890600-37890800	Flanking Active TSS	Liver	Liver
8	chr14:37890600-37890800	Enhancers	A549	lung
9	chr14:37890800-37891600	Enhancers	Liver	Liver
10	chr14:37891600-37891800	Flanking Active TSS	Liver	Liver
11	chr14:37891600-37892200	Enhancers	Fetal Intestine Small	intestine
12	chr14:37891600-37895000	Weak transcription	Colon Smooth Muscle	Colon
13	chr14:37891800-37892000	Active TSS	Liver	Liver
14	chr14:37892000-37893000	Weak transcription	Liver	Liver
15	chr14:37892000-37894800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:37892200-37895000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr14:37892400-37916600	Weak transcription	HepG2	liver
18	chr14:37892600-37895200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:37893000-37893400	Enhancers	Liver	Liver
20	chr14:37893600-37896200	Weak transcription	HSMM	muscle
21	chr14:37894600-37923400	Weak transcription	Aorta	Aorta
22	chr14:37897600-37897800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:37898000-37898600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr14:37898000-37898800	Enhancers	NHEK	skin
25	chr14:37898000-37899400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:37898200-37899600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:37898600-37900000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr14:37898800-37899200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:37899000-37900200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr14:37899200-37908400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr14:37899600-37899800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr14:37899800-37900200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr14:37900000-37900400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr14:37900200-37906200	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr14:37905800-37906200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr14:37905800-37906200	Enhancers	A549	lung
37	chr14:37905800-37906400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr14:37905800-37906600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:37905800-37907200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr14:37905800-37907200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:37906000-37914600	Weak transcription	HUVEC	blood vessel
42	chr14:37906200-37906400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr14:37906200-37907200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr14:37906200-37909800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr14:37906400-37907400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr14:37906600-37907200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:37906600-37907200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr14:37907000-37907200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr14:37907200-37907600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr14:37907200-37907800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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