Variant report

Variant	nsv1001316
Chromosome Location	chr3:84773522-85071342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:85055673-85057144	HepG2	liver:	n/a	chr3:85056293-85056309 chr3:85056322-85056338 chr3:85056292-85056308
2	ATF2	chr3:84886062-84886466	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr3:85014321-85014662	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr3:85056278-85056714	A549	lung:	n/a	n/a
5	ATF3	chr3:85014281-85014577	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:85053329-85053616	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:85011727-85011885	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr3:85007700-85007990	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:85008844-85009156	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr3:85056259-85056743	A549	lung:	n/a	n/a
11	BCL3	chr3:85056181-85056857	A549	lung:	n/a	n/a
12	BHLHE40	chr3:84954233-84954576	HepG2	liver:	n/a	n/a
13	BHLHE40	chr3:85056422-85056714	HepG2	liver:	n/a	n/a
14	BRCA1	chr3:85007545-85007619	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr3:84774057-84774336	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:84930983-84931198	A549	lung:	n/a	n/a
17	CEBPB	chr3:84958863-84959065	A549	lung:	n/a	chr3:84958954-84958965
18	CEBPB	chr3:85055910-85057107	HepG2	liver:	n/a	chr3:85056514-85056525 chr3:85056945-85056956 chr3:85056478-85056489
19	CEBPB	chr3:85010675-85010724	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:85044482-85044772	A549	lung:	n/a	chr3:85044516-85044527 chr3:85044606-85044615 chr3:85044594-85044605
21	CEBPB	chr3:85066421-85066723	A549	lung:	n/a	n/a
22	CEBPB	chr3:84874694-84874997	HepG2	liver:	n/a	chr3:84874822-84874833 chr3:84874824-84874833
23	CEBPB	chr3:85052603-85053081	A549	lung:	n/a	chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052823-85052832 chr3:85052822-85052833 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052821-85052832
24	CEBPB	chr3:85044478-85044775	HepG2	liver:	n/a	chr3:85044516-85044527 chr3:85044606-85044615 chr3:85044594-85044605
25	CEBPB	chr3:85036362-85036987	A549	lung:	n/a	chr3:85036822-85036833 chr3:85036502-85036513 chr3:85036822-85036835 chr3:85036503-85036512 chr3:85036501-85036512
26	CEBPB	chr3:85014267-85014637	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:84886005-84886347	MCF-7	breast:	n/a	n/a
28	CEBPB	chr3:85052663-85053009	A549	lung:	n/a	chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052823-85052832 chr3:85052822-85052833 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052821-85052832
29	CEBPB	chr3:85036414-85036614	IMR90	lung:	n/a	chr3:85036502-85036513 chr3:85036503-85036512 chr3:85036501-85036512
30	CEBPB	chr3:84804907-84805204	HepG2	liver:	n/a	chr3:84805028-84805039
31	CEBPB	chr3:85042549-85042764	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr3:84886070-84886388	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:85055972-85056094	A549	lung:	n/a	n/a
34	CEBPB	chr3:85056360-85056728	HepG2	liver:	n/a	chr3:85056514-85056525 chr3:85056478-85056489
35	CEBPB	chr3:85056309-85056780	A549	lung:	n/a	chr3:85056514-85056525 chr3:85056478-85056489
36	CEBPB	chr3:85056316-85056704	Hela-S3	cervix:	n/a	chr3:85056514-85056525 chr3:85056478-85056489
37	CEBPB	chr3:85052636-85053009	HepG2	liver:	n/a	chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052823-85052832 chr3:85052822-85052833 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052821-85052832
38	CEBPB	chr3:85056337-85056780	HepG2	liver:	n/a	chr3:85056514-85056525 chr3:85056478-85056489
39	CEBPB	chr3:85052638-85052987	A549	lung:	n/a	chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052823-85052832 chr3:85052822-85052833 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052823-85052832 chr3:85052821-85052834 chr3:85052821-85052832
40	CEBPB	chr3:84958813-84959139	HepG2	liver:	n/a	chr3:84958954-84958965
41	CEBPB	chr3:84858168-84858322	H1-hESC	embryonic stem cell:	n/a	chr3:84858283-84858294
42	CEBPB	chr3:84804939-84805174	A549	lung:	n/a	chr3:84805028-84805039
43	CEBPB	chr3:85040390-85040687	HepG2	liver:	n/a	chr3:85040521-85040532 chr3:85040472-85040483 chr3:85040470-85040483 chr3:85040470-85040481 chr3:85040470-85040483
44	CEBPB	chr3:84858191-84858414	HepG2	liver:	n/a	chr3:84858283-84858294
45	CEBPB	chr3:84992560-84992803	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:85016899-85017319	Hela-S3	cervix:	n/a	chr3:85017262-85017273
47	CEBPB	chr3:84781948-84782264	A549	lung:	n/a	n/a
48	CEBPB	chr3:84886127-84886390	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr3:85036358-85036562	HepG2	liver:	n/a	chr3:85036502-85036513 chr3:85036503-85036512 chr3:85036501-85036512
50	CEBPB	chr3:85056201-85057105	A549	lung:	n/a	chr3:85056514-85056525 chr3:85056945-85056956 chr3:85056478-85056489

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85054782-85054832	K562	blood:	n/a
2	chr3:85054782-85054832	K562	blood:	n/a
3	chr3:85054782-85054832	ECC-1	luminal epithelium:	n/a
4	chr3:85008105-85008155	ProgFib	skin:	n/a
5	chr3:85042454-85042504	HCF	heart:	n/a
6	chr3:85017543-85017593	ovcar-3	ovarian:	n/a
7	chr3:85008587-85008637	HRPEpiC	eye:	n/a
8	chr3:85007817-85007867	ProgFib	skin:	n/a
9	chr3:85007894-85007944	H1-hESC	embryonic stem cell:	embryo
10	chr3:85007992-85008042	AG09309	skin:	n/a
11	chr3:85005177-85005227	GM12878	blood:	n/a
12	chr3:85007959-85008009	ProgFib	skin:	n/a
13	chr3:85017543-85017593	GM12891	blood:	n/a
14	chr3:84909261-84909311	CMK	blood:	n/a
15	chr3:84884069-84884119	ECC-1	luminal epithelium:	n/a
16	chr3:85042454-85042504	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:85007817-85007867	AG09319	gingival:	n/a
18	chr3:85008587-85008637	MCF-7	breast:	n/a
19	chr3:85007732-85007782	GM12878	blood:	n/a
20	chr3:84919438-84919488	ProgFib	skin:	n/a
21	chr3:85007992-85008042	Jurkat	blood:	n/a
22	chr3:85010677-85010727	Caco-2	colon:	n/a
23	chr3:85017543-85017593	GM12892	blood:	n/a
24	chr3:85005177-85005227	RPTEC	kidney:	n/a
25	chr3:85008105-85008155	NH-A	brain:	n/a
26	chr3:85008991-85009041	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:85008587-85008637	AG09309	skin:	n/a
28	chr3:85006115-85006165	BJ	skin:	n/a
29	chr3:85008678-85008728	HCPEpiC	choroid plexus:	n/a
30	chr3:85008828-85008878	A549	lung:	n/a
31	chr3:85054782-85054832	SK-N-SH	brain:	n/a
32	chr3:85008156-85008206	HUVEC	blood vessel:	n/a
33	chr3:85008061-85008111	Hela-S3	cervix:	n/a
34	chr3:85008587-85008637	AG04450	lung:	fetal
35	chr3:84885990-84886040	RPTEC	kidney:	n/a
36	chr3:84885990-84886040	NH-A	brain:	n/a
37	chr3:85007992-85008042	HAEpiC	amniotic membrane:	n/a
38	chr3:85008786-85008836	HCF	heart:	n/a
39	chr3:85017543-85017593	HCF	heart:	n/a
40	chr3:84919226-84919276	AG04450	lung:	fetal
41	chr3:84851738-84851788	LNCaP	prostate:	n/a
42	chr3:84919226-84919276	AG09319	gingival:	n/a
43	chr3:85054782-85054832	NHBE	bronchial:	n/a
44	chr3:85007992-85008042	MCF-7	breast:	n/a
45	chr3:85010606-85010656	NH-A	brain:	n/a
46	chr3:85006115-85006165	AG09309	skin:	n/a
47	chr3:84884069-84884119	SK-N-SH_RA	brain:	n/a
48	chr3:85010606-85010656	MCF-7	breast:	n/a
49	chr3:85042454-85042504	ovcar-3	ovarian:	n/a
50	chr3:85007959-85008009	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:84967378..84970376-chr6:74219853..74222987,3	MCF-7	breast:
2	chr3:85029590..85031359-chr3:85035312..85037118,2	K562	blood:
3	chr3:85038561..85040690-chr3:85042508..85045093,2	MCF-7	breast:
4	chr3:84994697..84996927-chr3:85551100..85552839,2	K562	blood:
5	chr3:85038561..85040690-chr3:85042508..85045093,2	MCF-7	breast:
6	chr3:85011548..85014009-chr3:85014905..85018347,3	MCF-7	breast:
7	chr3:85029590..85031359-chr3:85035312..85037118,2	K562	blood:
8	chr3:83995499..83996096-chr3:84821714..84822693,2	MCF-7	breast:
9	chr3:84992684..84993232-chr3:85391799..85392321,2	MCF-7	breast:
10	chr3:85023240..85023756-chr3:85409642..85410352,2	MCF-7	breast:
11	chr3:84968846..84970373-chr6:74221820..74224403,2	K562	blood:
12	chr3:85011548..85014009-chr3:85014905..85018347,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL3-6	chr3:84841319-84841442	ENSG00000242641.1
2	lnc-VGLL3-6	chr3:84918054-84918175	NONHSAT090649
3	lnc-VGLL3-6	chr3:84912387-84912587	NONHSAT090652
4	lnc-VGLL3-6	chr3:84838789-84838923	ENSG00000242641.1
5	lnc-VGLL3-9	chr3:84798241-84801697	ucscGeneNc_uc003dqi_2
6	lnc-VGLL3-9	chr3:84776054-84776127	ucscGeneNc_uc003dqi_2
7	lnc-VGLL3-9	chr3:84985783-84985856	ucscGeneNc_uc003dqi_2
8	lnc-VGLL3-9	chr3:84827999-84828182	ucscGeneNc_uc003dqi_2
9	lnc-VGLL3-9	chr3:84803425-84803544	ucscGeneNc_uc003dqi_2
10	lnc-VGLL3-6	chr3:84917749-84917819	NONHSAT090649
11	lnc-VGLL3-6	chr3:84903093-84903166	NONHSAT090649
12	lnc-CADM2-1	chr3:84942393-84942530	XLOC_002723
13	lnc-VGLL3-6	chr3:84918742-84918779	ENSG00000242641.1
14	lnc-VGLL3-6	chr3:84795196-84795488	NONHSAT090649
15	lnc-VGLL3-6	chr3:84903093-84903166	ENSG00000242641.1
16	lnc-VGLL3-6	chr3:84918429-84918637	NONHSAT090652
17	lnc-VGLL3-9	chr3:84924009-84924132	ucscGeneNc_uc003dqi_2
18	lnc-VGLL3-6	chr3:84838789-84838923	NONHSAT090649
19	lnc-CADM2-1	chr3:84942392-84942530	NONHSAT090654
20	lnc-CHMP2B-6	chr3:85008140-85008643	NONHSAT090657
21	lnc-VGLL3-6	chr3:84917749-84917819	NONHSAT090652
22	lnc-VGLL3-6	chr3:84918054-84918175	ENSG00000242641.1
23	lnc-VGLL3-9	chr3:85000439-85000509	ucscGeneNc_uc003dqi_2
24	lnc-VGLL3-6	chr3:84918054-84918175	NONHSAT090652
25	lnc-VGLL3-9	chr3:84804462-84804746	ucscGeneNc_uc003dqi_2
26	lnc-VGLL3-9	chr3:84995547-84995846	ucscGeneNc_uc003dqi_2
27	lnc-VGLL3-9	chr3:85001119-85001416	ucscGeneNc_uc003dqi_2
28	lnc-VGLL3-6	chr3:84918429-84918726	NONHSAT090649
29	lnc-VGLL3-9	chr3:84995057-84995277	ucscGeneNc_uc003dqi_2
30	lnc-VGLL3-6	chr3:84912857-84913156	NONHSAT090649
31	lnc-VGLL3-6	chr3:84912367-84912587	NONHSAT090649
32	lnc-VGLL3-9	chr3:84827206-84827356	ucscGeneNc_uc003dqi_2
33	lnc-VGLL3-9	chr3:85000744-85000865	ucscGeneNc_uc003dqi_2
34	lnc-VGLL3-9	chr3:84815450-84815519	ucscGeneNc_uc003dqi_2
35	lnc-VGLL3-6	chr3:84841319-84841442	NONHSAT090649
36	lnc-VGLL3-9	chr3:84994564-84994662	ucscGeneNc_uc003dqi_2
37	lnc-CHMP2B-6	chr3:85009248-85009589	NONHSAT090658
38	lnc-VGLL3-9	chr3:84921479-84921613	ucscGeneNc_uc003dqi_2
39	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
40	lnc-VGLL3-6	chr3:84908966-84909074	ENSG00000242641.1
41	lnc-CHMP2B-6	chr3:85008156-85008819	NONHSAT090658
42	lnc-VGLL3-6	chr3:84917933-84917994	ENSG00000242641.1
43	lnc-VGLL3-6	chr3:84912367-84912587	ENSG00000242641.1
44	lnc-CHMP2B-6	chr3:85008741-85008787	NONHSAT090657
45	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
46	lnc-CADM2-1	chr3:84934087-84934274	XLOC_002723
47	lnc-VGLL3-9	chr3:84991656-84991764	ucscGeneNc_uc003dqi_2
48	lnc-VGLL3-6	chr3:84851600-84851903	ENSG00000242641.1
49	lnc-VGLL3-6	chr3:84930640-84930830	ENSG00000242641.1
50	lnc-VGLL3-9	chr3:84877886-84878178	ucscGeneNc_uc003dqi_2

Variant related genes	Relation type
ENSG00000266025	TF binding region
CADM2	TF binding region
ENSG00000242339	TF binding region
LINC00971	TF binding region
ENSG00000266025	CpG island
CADM2	CpG island
ENSG00000242339	CpG island
LINC00971	CpG island
THAP6	miRNA target sites
TCEAL1	miRNA target sites
YES1	miRNA target sites

Extended variants
information (count: 5146 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5146 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566515604	chr3:84773823-84773824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142369027	chr3:84773835-84773836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558781163	chr3:84773910-84773911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564932313	chr3:84773925-84773926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538402695	chr3:84773938-84773939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556504384	chr3:84773939-84773940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs151278648	chr3:84773976-84773977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542343680	chr3:84773980-84773981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182350166	chr3:84773998-84773999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561079798	chr3:84774002-84774003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530393870	chr3:84774024-84774025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6795469	chr3:84774030-84774031	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs111752305	chr3:84774079-84774080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532469898	chr3:84774115-84774116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544521736	chr3:84774132-84774133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79940559	chr3:84774235-84774236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529938612	chr3:84774255-84774256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150404809	chr3:84774268-84774269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566626184	chr3:84774283-84774284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72909339	chr3:84774300-84774301	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs200659150	chr3:84774306-84774307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184987845	chr3:84774340-84774341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190171197	chr3:84774438-84774439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527805646	chr3:84774448-84774449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556852277	chr3:84774478-84774479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182434866	chr3:84774486-84774487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77547468	chr3:84774504-84774505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188390230	chr3:84774508-84774509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554659685	chr3:84774579-84774580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35308526	chr3:84774606-84774607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111303043	chr3:84774649-84774650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146632877	chr3:84774650-84774651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558563971	chr3:84774739-84774740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193029739	chr3:84774753-84774754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112746626	chr3:84774830-84774831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544167454	chr3:84774840-84774841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62255511	chr3:84774861-84774862	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs368088990	chr3:84774922-84774923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183407856	chr3:84774930-84774931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189254877	chr3:84775020-84775021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560182538	chr3:84775067-84775068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527803715	chr3:84775087-84775088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548343461	chr3:84775098-84775099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552265591	chr3:84775158-84775159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72909341	chr3:84775234-84775235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs386663056	chr3:84775255-84775256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192459389	chr3:84775273-84775274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141475444	chr3:84775280-84775281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563494133	chr3:84775281-84775282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183925438	chr3:84775282-84775283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Medulloblastoma	16783165	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Schizophrenia	23813976	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84773800-84775000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr3:84774200-84774800	Enhancers	HSMM	muscle
3	chr3:84774800-84776200	Weak transcription	HSMM	muscle
4	chr3:84775000-84776400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr3:84776200-84776600	Enhancers	HSMM	muscle
6	chr3:84776400-84777200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr3:84777800-84778200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr3:84786400-84787200	Enhancers	Fetal Brain Female	brain
9	chr3:84786800-84787800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr3:84787000-84787400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:84787000-84787400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:84787200-84791600	Weak transcription	Fetal Brain Female	brain
13	chr3:84787400-84787800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:84787800-84788600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr3:84788600-84788800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr3:84791600-84793200	Enhancers	Fetal Brain Female	brain
17	chr3:84792000-84793200	Enhancers	Fetal Brain Male	brain
18	chr3:84792800-84793200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr3:84793200-84794600	Weak transcription	Fetal Brain Female	brain
20	chr3:84794800-84795000	Enhancers	Fetal Brain Female	brain
21	chr3:84805200-84805400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:84805400-84806000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr3:84806000-84806200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:84806200-84806400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr3:84806400-84806600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:84806400-84808800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr3:84806600-84808400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:84808400-84809200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:84808400-84809400	Enhancers	Pancreas	Pancrea
30	chr3:84808800-84809000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr3:84809400-84809800	Weak transcription	Pancreas	Pancrea
32	chr3:84809800-84810200	Enhancers	Pancreas	Pancrea
33	chr3:84837800-84839400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr3:84838200-84839400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:84842400-84843200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:84845200-84856400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:84850800-84851400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr3:84850800-84851400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:84850800-84851800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr3:84850800-84851800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:84850800-84851800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr3:84851000-84851400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:84851000-84851400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr3:84851000-84851600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr3:84856400-84856600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr3:84856600-84856800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:84864600-84865000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
48	chr3:84864600-84865000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr3:84877600-84880000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr3:84882000-84884800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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