Variant report

Variant	nsv901639
Chromosome Location	chr14:37743583-38038468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1489)
CpG islands
(count:183)
Chromatin interactive
region (count:135)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:38014394-38014724	HepG2	liver:	n/a	chr14:38014521-38014537
2	ARID3A	chr14:37966619-37967091	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:37882908-37883266	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:37747860-37748994	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:38031258-38031519	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:37798163-37799893	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:37854210-37854747	HepG2	liver:	n/a	chr14:37854604-37854612
8	ARID3A	chr14:37962806-37963218	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:37937245-37937930	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:37916975-37917561	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:37996655-37996907	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:38015300-38016974	HepG2	liver:	n/a	chr14:38015494-38015510
13	ARID3A	chr14:38034684-38035216	HepG2	liver:	n/a	chr14:38034779-38034795
14	ARID3A	chr14:37935172-37936858	HepG2	liver:	n/a	n/a
15	ATF1	chr14:37868829-37869057	K562	blood:	n/a	n/a
16	ATF1	chr14:37886466-37886666	K562	blood:	n/a	n/a
17	ATF3	chr14:38016010-38016388	A549	lung:	n/a	n/a
18	ATF3	chr14:37868759-37869025	K562	blood:	n/a	n/a
19	BACH1	chr14:38018020-38018181	K562	blood:	n/a	n/a
20	BCL3	chr14:38015925-38016570	A549	lung:	n/a	n/a
21	BCL3	chr14:38036054-38036611	A549	lung:	n/a	n/a
22	BCL3	chr14:38036069-38036667	A549	lung:	n/a	n/a
23	BCL3	chr14:38015991-38016548	A549	lung:	n/a	n/a
24	BHLHE40	chr14:38031008-38031043	K562	blood:	n/a	n/a
25	BHLHE40	chr14:37854614-37854788	HepG2	liver:	n/a	n/a
26	BHLHE40	chr14:38015947-38016344	HepG2	liver:	n/a	n/a
27	BHLHE40	chr14:37935661-37936300	HepG2	liver:	n/a	n/a
28	BHLHE40	chr14:38015971-38016568	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:37960542-37960564	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:37752037-37752257	HepG2	liver:	n/a	chr14:37752149-37752160
31	CEBPB	chr14:37935591-37936194	HepG2	liver:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
32	CEBPB	chr14:37920948-37921143	K562	blood:	n/a	n/a
33	CEBPB	chr14:38036164-38036613	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:37867147-37867185	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:37880321-37880642	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr14:37950035-37950380	HepG2	liver:	n/a	chr14:37950296-37950307
37	CEBPB	chr14:38016090-38016420	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:37798396-37799173	HepG2	liver:	n/a	chr14:37799007-37799020
39	CEBPB	chr14:38014329-38014720	MCF-7	breast:	n/a	chr14:38014510-38014519 chr14:38014508-38014521 chr14:38014508-38014521 chr14:38014508-38014519 chr14:38014510-38014521
40	CEBPB	chr14:37961519-37961800	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:37866973-37867184	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr14:37952857-37953222	K562	blood:	n/a	n/a
43	CEBPB	chr14:37837419-37837687	HepG2	liver:	n/a	chr14:37837498-37837511 chr14:37837569-37837580 chr14:37837568-37837581
44	CEBPB	chr14:37952953-37953153	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr14:37875362-37875614	A549	lung:	n/a	chr14:37875492-37875505 chr14:37875492-37875503 chr14:37875494-37875505 chr14:37875492-37875505 chr14:37875397-37875408 chr14:37875494-37875505 chr14:37875492-37875505
46	CEBPB	chr14:37875340-37875664	Hela-S3	cervix:	n/a	chr14:37875492-37875505 chr14:37875492-37875503 chr14:37875494-37875505 chr14:37875492-37875505 chr14:37875397-37875408 chr14:37875494-37875505 chr14:37875492-37875505
47	CEBPB	chr14:37935679-37936088	MCF-7	breast:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
48	CEBPB	chr14:37950147-37950352	HepG2	liver:	n/a	chr14:37950296-37950307
49	CEBPB	chr14:37962886-37963121	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:37862046-37862226	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38031240-38031290	HEEpiC	esophagus:	n/a
2	chr14:37773865-37773915	HL-60	blood:	n/a
3	chr14:37825967-37826017	AG09319	gingival:	n/a
4	chr14:37773865-37773915	AG04450	lung:	fetal
5	chr14:37825967-37826017	HUVEC	blood vessel:	n/a
6	chr14:37773865-37773915	NHBE	bronchial:	n/a
7	chr14:37773865-37773915	GM06990	blood:	n/a
8	chr14:38031240-38031290	ProgFib	skin:	n/a
9	chr14:38031240-38031290	GM19239	blood:	n/a
10	chr14:37825967-37826017	AG04450	lung:	fetal
11	chr14:37825967-37826017	HCM	heart:	n/a
12	chr14:38031240-38031290	GM12892	blood:	n/a
13	chr14:38031240-38031290	HNPCEpiC	eye:	n/a
14	chr14:37825967-37826017	U87	brain:	n/a
15	chr14:37773865-37773915	CMK	blood:	n/a
16	chr14:37773865-37773915	GM19239	blood:	n/a
17	chr14:37773865-37773915	SK-N-MC	brain:	n/a
18	chr14:37825967-37826017	HEEpiC	esophagus:	n/a
19	chr14:37773865-37773915	BE2_C	brain:	n/a
20	chr14:37825967-37826017	GM12891	blood:	n/a
21	chr14:37825967-37826017	K562	blood:	n/a
22	chr14:38031240-38031290	AG04449	skin:	fetal
23	chr14:37825967-37826017	NHBE	bronchial:	n/a
24	chr14:37773865-37773915	HRPEpiC	eye:	n/a
25	chr14:37825967-37826017	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:37773865-37773915	PrEC	prostate:	n/a
27	chr14:37825967-37826017	Hela-S3	cervix:	n/a
28	chr14:38031240-38031290	HCM	heart:	n/a
29	chr14:37825967-37826017	A549	lung:	n/a
30	chr14:37773865-37773915	GM12878	blood:	n/a
31	chr14:37773865-37773915	H1-hESC	embryonic stem cell:	embryo
32	chr14:38031240-38031290	SK-N-SH_RA	brain:	n/a
33	chr14:37773865-37773915	HAEpiC	amniotic membrane:	n/a
34	chr14:37773865-37773915	K562	blood:	n/a
35	chr14:37825967-37826017	AG04449	skin:	fetal
36	chr14:37825967-37826017	SAEC	small airway:	n/a
37	chr14:37773865-37773915	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:37773865-37773915	RPTEC	kidney:	n/a
39	chr14:37825967-37826017	NT2-D1	testis:	n/a
40	chr14:37825967-37826017	PFSK-1	brain:	n/a
41	chr14:37773865-37773915	IMR90	lung:	fetal
42	chr14:37773865-37773915	ProgFib	skin:	n/a
43	chr14:37825967-37826017	HAEpiC	amniotic membrane:	n/a
44	chr14:37773865-37773915	NB4	blood:	n/a
45	chr14:37773865-37773915	HCPEpiC	choroid plexus:	n/a
46	chr14:37825967-37826017	HRPEpiC	eye:	n/a
47	chr14:37825967-37826017	PrEC	prostate:	n/a
48	chr14:38031240-38031290	H1-hESC	embryonic stem cell:	embryo
49	chr14:37773865-37773915	SK-N-SH	brain:	n/a
50	chr14:37773865-37773915	SK-N-SH_RA	brain:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:37897535..37899895-chr14:38063797..38065302,2	MCF-7	breast:
2	chr14:37749616..37751782-chr14:38055400..38058293,2	MCF-7	breast:
3	chr14:37881541..37884067-chr14:38063012..38064941,2	MCF-7	breast:
4	chr14:37868011..37870667-chr14:37877895..37880422,2	K562	blood:
5	chr14:38023383..38025089-chr14:38055151..38056886,2	MCF-7	breast:
6	chr14:37840146..37842839-chr14:37843811..37846339,2	K562	blood:
7	chr14:38015701..38018409-chr14:38034493..38036492,3	MCF-7	breast:
8	chr14:38011441..38015766-chr14:38062652..38065926,9	MCF-7	breast:
9	chr14:37793105..37794977-chr14:37796804..37798845,2	MCF-7	breast:
10	chr14:37923826..37925404-chr14:38041177..38044020,2	MCF-7	breast:
11	chr14:38014337..38017689-chr14:38019804..38021819,4	MCF-7	breast:
12	chr14:38035956..38036475-chr14:38064723..38065603,2	MCF-7	breast:
13	chr11:116508203..116508771-chr14:37786310..37786828,2	MCF-7	breast:
14	chr14:38037935..38040029-chr14:38060837..38063498,2	K562	blood:
15	chr14:37992113..37994949-chr14:37995785..37998678,3	MCF-7	breast:
16	chr14:37923519..37926055-chr14:37998366..38001362,2	MCF-7	breast:
17	chr14:38022120..38023729-chr14:38064020..38066950,2	MCF-7	breast:
18	chr14:37738574..37741001-chr14:37743646..37745651,2	MCF-7	breast:
19	chr14:38001638..38003802-chr14:38010426..38012246,2	MCF-7	breast:
20	chr14:37938461..37943364-chr14:38060246..38065845,4	MCF-7	breast:
21	chr14:38015801..38018885-chr14:38023439..38025861,3	MCF-7	breast:
22	chr14:38010426..38020494-chr14:38050537..38062032,33	MCF-7	breast:
23	chr14:37868487..37870431-chr14:37872042..37874988,2	K562	blood:
24	chr14:37744550..37746871-chr14:38059550..38062065,2	MCF-7	breast:
25	chr14:37789885..37792148-chr14:37882206..37884543,2	MCF-7	breast:
26	chr14:37984075..37986407-chr14:37992639..37994265,2	MCF-7	breast:
27	chr14:38012929..38015442-chr14:38030781..38032707,2	MCF-7	breast:
28	chr14:37743207..37745238-chr14:37747689..37750127,2	MCF-7	breast:
29	chr14:38033872..38034739-chr14:38064019..38064812,2	MCF-7	breast:
30	chr14:37981930..37983702-chr14:37987537..37990336,2	MCF-7	breast:
31	chr14:38015564..38017191-chr14:38035879..38037798,2	MCF-7	breast:
32	chr14:37979957..37982463-chr14:37983099..37985878,2	MCF-7	breast:
33	chr14:37992987..37994554-chr14:37998762..38001417,2	K562	blood:
34	chr14:37781292..37783643-chr14:37787358..37789012,2	MCF-7	breast:
35	chr14:38013523..38020726-chr14:38055776..38060374,10	MCF-7	breast:
36	chr14:38016427..38017937-chr14:38034115..38035659,2	MCF-7	breast:
37	chr14:38015765..38016748-chr14:38036033..38036608,3	MCF-7	breast:
38	chr14:37895105..37897353-chr14:37902428..37905218,2	MCF-7	breast:
39	chr14:38013794..38017816-chr14:38049871..38055560,6	MCF-7	breast:
40	chr14:37979957..37982463-chr14:37983099..37985878,2	MCF-7	breast:
41	chr14:38034290..38035240-chr14:38063014..38063525,2	MCF-7	breast:
42	chr14:37899686..37902705-chr14:38064003..38066607,3	MCF-7	breast:
43	chr14:38001707..38004632-chr14:38007880..38010262,2	MCF-7	breast:
44	chr14:38015801..38018885-chr14:38023439..38025861,3	MCF-7	breast:
45	chr14:38031576..38032423-chr14:38066583..38067091,2	MCF-7	breast:
46	chr14:38001707..38004632-chr14:38007880..38010262,2	MCF-7	breast:
47	chr14:38022489..38024339-chr14:38026702..38028833,2	MCF-7	breast:
48	chr14:37922172..37923880-chr14:37926758..37928419,2	MCF-7	breast:
49	chr14:37919150..37921478-chr14:38062353..38064686,2	MCF-7	breast:
50	chr14:37914831..37917471-chr14:37919271..37922132,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC6-2	chr14:37869005-37871105	NONHSAT036460
2	lnc-FOXA1-4	chr14:37853626-37855696	NONHSAT036459
3	lnc-MIPOL1-1	chr14:38033434-38033567	XLOC_010804
4	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	chr14:38016573-38016594
2	MIPOL1	hsa-miR-215-5p	chr14:38016573-38016594
3	MIPOL1	hsa-miR-192-5p	chr14:38016587-38016594
4	MIPOL1	hsa-miR-215-5p	chr14:38016587-38016594

Variant related genes	Relation type
ENSG00000259087	TF binding region
RNU6-886P	TF binding region
ENSG00000258414	TF binding region
MIPOL1	TF binding region
ENSG00000259087	CpG island
RNU6-886P	CpG island
ENSG00000258414	CpG island
MIPOL1	CpG island
ENSG00000129514	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000207046	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000258414	chromatin interactions
ENSG00000259087	chromatin interactions
ENSG00000137261	chromatin interactions

Extended variants
information (count: 10362 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:10362 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12886692	chr14:37743583-37743584	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529477166	chr14:37743604-37743605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185982136	chr14:37743614-37743615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190649938	chr14:37743621-37743622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570964671	chr14:37743706-37743707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534791498	chr14:37743742-37743743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs74047271	chr14:37743781-37743782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs538295682	chr14:37743790-37743791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536834401	chr14:37743792-37743793	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181800333	chr14:37743848-37743849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146134846	chr14:37743927-37743928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553208804	chr14:37743952-37743953	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138948383	chr14:37743970-37743971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149397097	chr14:37743975-37743976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117936633	chr14:37743990-37743991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575298540	chr14:37744000-37744001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543860566	chr14:37744030-37744031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563752619	chr14:37744035-37744036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577197902	chr14:37744037-37744038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111999799	chr14:37744105-37744106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540560932	chr14:37744121-37744122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200950349	chr14:37744186-37744187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143426625	chr14:37744191-37744192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560832710	chr14:37744210-37744211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12890929	chr14:37744215-37744216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186413723	chr14:37744269-37744270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17106544	chr14:37744293-37744294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs531859817	chr14:37744311-37744312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148627858	chr14:37744423-37744424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191220038	chr14:37744446-37744447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182491757	chr14:37744453-37744454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534168288	chr14:37744503-37744504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs8016268	chr14:37744582-37744583	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566753398	chr14:37744591-37744592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557678052	chr14:37744596-37744597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535340050	chr14:37744597-37744598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555544549	chr14:37744673-37744674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188011683	chr14:37744773-37744774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191053647	chr14:37744778-37744779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183367994	chr14:37744805-37744806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577262205	chr14:37744864-37744865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187222797	chr14:37744866-37744867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192042618	chr14:37744867-37744868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs8017263	chr14:37744882-37744883	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542918502	chr14:37744884-37744885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563120475	chr14:37744983-37744984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531917423	chr14:37744997-37744998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141152892	chr14:37745022-37745023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565369150	chr14:37745041-37745042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184491980	chr14:37745045-37745046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	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:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37694800-37756400	Weak transcription	Aorta	Aorta
2	chr14:37716000-37770600	Weak transcription	A549	lung
3	chr14:37733600-37758200	Weak transcription	Fetal Lung	lung
4	chr14:37736400-37744200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr14:37736800-37758400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr14:37737200-37744400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:37738000-37755000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr14:37738000-37756400	Weak transcription	Ovary	ovary
9	chr14:37738400-37757600	Weak transcription	Adipose Nuclei	Adipose
10	chr14:37740000-37762000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr14:37740200-37757800	Weak transcription	HUVEC	blood vessel
12	chr14:37740400-37760200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:37740600-37743600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:37743200-37745800	Weak transcription	Psoas Muscle	Psoas
15	chr14:37743600-37744000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:37744400-37745400	Enhancers	Liver	Liver
17	chr14:37744400-37745600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr14:37745400-37747400	Weak transcription	Liver	Liver
19	chr14:37747400-37748200	Enhancers	Liver	Liver
20	chr14:37747800-37749200	Enhancers	HepG2	liver
21	chr14:37748200-37749200	Flanking Active TSS	Liver	Liver
22	chr14:37748600-37758400	Weak transcription	Psoas Muscle	Psoas
23	chr14:37748800-37758600	Weak transcription	Fetal Stomach	stomach
24	chr14:37749200-37749400	Enhancers	Liver	Liver
25	chr14:37749200-37749600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:37749200-37761000	Weak transcription	Pancreas	Pancrea
27	chr14:37749200-37761800	Weak transcription	HepG2	liver
28	chr14:37749600-37761200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:37749800-37758600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr14:37750200-37758200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr14:37750600-37761400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr14:37750600-37761800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:37752400-37796200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr14:37753400-37758600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr14:37753400-37761600	Weak transcription	Fetal Intestine Large	intestine
36	chr14:37753600-37758800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr14:37754000-37760800	Weak transcription	Fetal Intestine Small	intestine
38	chr14:37754200-37762000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr14:37754200-37781400	Weak transcription	Colon Smooth Muscle	Colon
40	chr14:37754600-37758400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr14:37755000-37756800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr14:37755200-37755400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr14:37755200-37758800	Weak transcription	Left Ventricle	heart
44	chr14:37755200-37764800	Weak transcription	Right Ventricle	heart
45	chr14:37755400-37761800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:37756200-37758400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr14:37756400-37756600	Weak transcription	Lung	lung
48	chr14:37756400-37756800	Strong transcription	Ovary	ovary
49	chr14:37756400-37759000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr14:37756400-37759400	Strong transcription	Aorta	Aorta

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