Variant report

Variant	nsv880414
Chromosome Location	chr5:29194872-29495564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:790)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:790 , 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	ATF1	chr5:29425986-29425989	K562	blood:	n/a	n/a
2	ATF1	chr5:29300805-29300808	K562	blood:	n/a	n/a
3	ATF1	chr5:29479289-29479312	K562	blood:	n/a	n/a
4	ATF1	chr5:29211158-29211220	K562	blood:	n/a	n/a
5	ATF1	chr5:29431656-29431817	K562	blood:	n/a	n/a
6	ATF1	chr5:29425063-29425178	K562	blood:	n/a	n/a
7	ATF1	chr5:29261746-29261789	K562	blood:	n/a	n/a
8	BACH1	chr5:29433080-29433172	K562	blood:	n/a	n/a
9	BCL3	chr5:29262604-29263216	A549	lung:	n/a	n/a
10	BRCA1	chr5:29247231-29248089	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr5:29307600-29307906	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr5:29197449-29199081	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr5:29239726-29241168	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr5:29262408-29263657	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr5:29263899-29264484	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr5:29256507-29256622	K562	blood:	n/a	n/a
17	CCNT2	chr5:29203655-29203807	K562	blood:	n/a	n/a
18	CEBPB	chr5:29390959-29391192	HepG2	liver:	n/a	chr5:29391028-29391039
19	CEBPB	chr5:29424874-29425236	HepG2	liver:	n/a	chr5:29425044-29425055
20	CEBPB	chr5:29433374-29433733	IMR90	lung:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
21	CEBPB	chr5:29478255-29478405	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:29293313-29293632	IMR90	lung:	n/a	chr5:29293483-29293494
23	CEBPB	chr5:29433473-29433683	K562	blood:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
24	CEBPB	chr5:29262929-29262971	K562	blood:	n/a	n/a
25	CEBPB	chr5:29459773-29459805	K562	blood:	n/a	n/a
26	CEBPB	chr5:29390980-29391087	K562	blood:	n/a	chr5:29391028-29391039
27	CEBPB	chr5:29276960-29277157	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:29386189-29386287	HepG2	liver:	n/a	chr5:29386206-29386217
29	CEBPB	chr5:29293399-29293591	H1-hESC	embryonic stem cell:	n/a	chr5:29293483-29293494
30	CEBPB	chr5:29351314-29351662	HepG2	liver:	n/a	chr5:29351485-29351496
31	CEBPB	chr5:29414090-29414343	K562	blood:	n/a	n/a
32	CEBPB	chr5:29262798-29263210	A549	lung:	n/a	chr5:29262923-29262940
33	CEBPB	chr5:29293316-29293607	Hela-S3	cervix:	n/a	chr5:29293483-29293494
34	CEBPB	chr5:29237950-29238255	HepG2	liver:	n/a	chr5:29238102-29238113 chr5:29238073-29238086 chr5:29238074-29238085 chr5:29238102-29238115 chr5:29238020-29238032
35	CEBPB	chr5:29262193-29263529	Hela-S3	cervix:	n/a	chr5:29262923-29262940 chr5:29263293-29263306
36	CEBPB	chr5:29239174-29239457	Hela-S3	cervix:	n/a	chr5:29239301-29239312 chr5:29239301-29239314 chr5:29239303-29239312 chr5:29239303-29239314
37	CEBPB	chr5:29491915-29492166	A549	lung:	n/a	n/a
38	CEBPB	chr5:29337230-29337430	HepG2	liver:	n/a	chr5:29337327-29337338 chr5:29337343-29337354
39	CEBPB	chr5:29478222-29478505	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:29282563-29282822	HepG2	liver:	n/a	chr5:29282672-29282683 chr5:29282673-29282684
41	CEBPB	chr5:29478214-29478508	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:29282526-29282798	Hela-S3	cervix:	n/a	chr5:29282672-29282683 chr5:29282673-29282684
43	CEBPB	chr5:29239700-29240109	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:29391032-29391067	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr5:29387050-29387411	IMR90	lung:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
46	CEBPB	chr5:29261308-29261971	Hela-S3	cervix:	n/a	chr5:29261494-29261505 chr5:29261494-29261507
47	CEBPB	chr5:29337963-29338183	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:29387041-29387392	A549	lung:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
49	CEBPB	chr5:29307586-29307932	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:29478220-29478499	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:29238187-29238237	HRE	kidney:	n/a
2	chr5:29238187-29238237	HL-60	blood:	n/a
3	chr5:29238187-29238237	GM19239	blood:	n/a
4	chr5:29238187-29238237	PANC-1	pancreas:	n/a
5	chr5:29238187-29238237	GM12891	blood:	n/a
6	chr5:29238187-29238237	K562	blood:	n/a
7	chr5:29238187-29238237	AG04449	skin:	fetal
8	chr5:29238187-29238237	ProgFib	skin:	n/a
9	chr5:29238187-29238237	GM06990	blood:	n/a
10	chr5:29238187-29238237	U87	brain:	n/a
11	chr5:29238187-29238237	A549	lung:	n/a
12	chr5:29238187-29238237	CMK	blood:	n/a
13	chr5:29238187-29238237	RPTEC	kidney:	n/a
14	chr5:29238187-29238237	BJ	skin:	n/a
15	chr5:29238187-29238237	H1-hESC	embryonic stem cell:	embryo
16	chr5:29238187-29238237	GM12892	blood:	n/a
17	chr5:29238187-29238237	MCF10A-Er-Src	breast:	n/a
18	chr5:29238187-29238237	NT2-D1	testis:	n/a
19	chr5:29238187-29238237	MCF-7	breast:	n/a
20	chr5:29238187-29238237	BE2_C	brain:	n/a
21	chr5:29238187-29238237	HEEpiC	esophagus:	n/a
22	chr5:29238187-29238237	HepG2	liver:	n/a
23	chr5:29238187-29238237	AG09319	gingival:	n/a
24	chr5:29238187-29238237	Jurkat	blood:	n/a
25	chr5:29238187-29238237	HCF	heart:	n/a
26	chr5:29238187-29238237	NH-A	brain:	n/a
27	chr5:29238187-29238237	AG04450	lung:	fetal
28	chr5:29238187-29238237	HIPEpiC	eye:	n/a
29	chr5:29238187-29238237	GM12878	blood:	n/a
30	chr5:29238187-29238237	Hela-S3	cervix:	n/a
31	chr5:29238187-29238237	SK-N-MC	brain:	n/a
32	chr5:29238187-29238237	HCM	heart:	n/a
33	chr5:29238187-29238237	HRCEpiC	kidney:	n/a
34	chr5:29238187-29238237	HRPEpiC	eye:	n/a
35	chr5:29238187-29238237	T-47D	breast:	n/a
36	chr5:29238187-29238237	HMEC	breast:	n/a
37	chr5:29238187-29238237	Caco-2	colon:	n/a
38	chr5:29238187-29238237	ovcar-3	ovarian:	n/a
39	chr5:29238187-29238237	SK-N-SH	brain:	n/a
40	chr5:29238187-29238237	HUVEC	blood vessel:	n/a
41	chr5:29238187-29238237	HEK293	kidney:	embryo
42	chr5:29238187-29238237	LNCaP	prostate:	n/a
43	chr5:29238187-29238237	AoSMC	blood vessel:	n/a
44	chr5:29238187-29238237	SK-N-SH_RA	brain:	n/a
45	chr5:29238187-29238237	PrEC	prostate:	n/a
46	chr5:29238187-29238237	IMR90	lung:	fetal
47	chr5:29238187-29238237	AG10803	skin:	n/a
48	chr5:29238187-29238237	AG09309	skin:	n/a
49	chr5:29238187-29238237	HCPEpiC	choroid plexus:	n/a
50	chr5:29238187-29238237	NB4	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:29199626..29201396-chr5:29206824..29209711,2	K562	blood:
2	chr5:29231388..29233462-chr5:29237084..29239691,2	K562	blood:
3	chr5:28809387..28811298-chr5:29193650..29195834,2	K562	blood:
4	chr5:29005255..29006082-chr5:29217591..29218623,4	MCF-7	breast:
5	chr5:29367229..29368191-chr5:29697633..29698544,4	MCF-7	breast:
6	chr5:29374107..29376875-chr5:29377791..29380634,2	K562	blood:
7	chr5:29005476..29006055-chr5:29218041..29218711,2	MCF-7	breast:
8	chr5:29231388..29233462-chr5:29237084..29239691,2	K562	blood:
9	chr5:29367557..29368187-chr5:29811640..29812581,2	MCF-7	breast:
10	chr5:29199626..29201396-chr5:29206824..29209711,2	K562	blood:
11	chr5:29213344..29216134-chr5:29219975..29221826,2	K562	blood:
12	chr5:29374107..29376875-chr5:29377791..29380634,2	K562	blood:
13	chr5:29195975..29198561-chr5:29201740..29203808,2	MCF-7	breast:
14	chr5:29192802..29195589-chr5:29735604..29737359,2	K562	blood:
15	chr5:28932533..28934760-chr5:29193358..29195088,2	K562	blood:
16	chr5:29367148..29368248-chr5:29697562..29698574,8	MCF-7	breast:
17	chr5:29161582..29162331-chr5:29218131..29218799,3	MCF-7	breast:
18	chr5:29191166..29194055-chr5:29197511..29200144,2	MCF-7	breast:
19	chr5:29367263..29368784-chr5:29811787..29812627,6	MCF-7	breast:
20	chr5:29394432..29396496-chr5:29400311..29402057,2	MCF-7	breast:
21	chr15:65588158..65588726-chr5:29225549..29226510,2	MCF-7	breast:
22	chr5:29213344..29216134-chr5:29219975..29221826,2	K562	blood:
23	chr4:37677151..37677824-chr5:29224902..29225727,2	MCF-7	breast:
24	chr5:29195975..29198561-chr5:29201740..29203808,2	MCF-7	breast:

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DROSHA-12	chr5:29415951-29416189	l_2897_chr5:29390052-29431912_testes
2	lnc-DROSHA-12	chr5:29390053-29390256	l_2897_chr5:29390052-29431912_testes
3	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
4	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
5	lnc-CDH6-10	chr5:29200794-29200910	ucscGeneNc_uc003jhb_1
6	lnc-DROSHA-7	chr5:29380373-29380432	XLOC_004765
7	lnc-CDH6-9	chr5:29228922-29228979	l_2896_chr5:29228921-29247267_testes
8	lnc-DROSHA-7	chr5:29380403-29380432	XLOC_004765
9	lnc-CDH6-10	chr5:29198280-29198453	ucscGeneNc_uc003jhb_1
10	lnc-DROSHA-12	chr5:29425675-29425803	l_2897_chr5:29390052-29431912_testes
11	lnc-DROSHA-12	chr5:29391719-29391826	l_2897_chr5:29390052-29431912_testes
12	lnc-DROSHA-7	chr5:29384404-29384499	XLOC_004765
13	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
14	lnc-DROSHA-7	chr5:29380196-29380432	NR_104628
15	lnc-DROSHA-12	chr5:29420161-29420256	l_2897_chr5:29390052-29431912_testes
16	lnc-DROSHA-7	chr5:29384404-29384499	XLOC_004765
17	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
18	lnc-DROSHA-12	chr5:29431718-29431912	l_2897_chr5:29390052-29431912_testes
19	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
20	lnc-CDH6-10	chr5:29207907-29208222	ucscGeneNc_uc003jhb_1
21	lnc-CDH6-9	chr5:29244724-29244803	l_2896_chr5:29228921-29247267_testes
22	lnc-DROSHA-12	chr5:29417717-29417826	l_2897_chr5:29390052-29431912_testes
23	lnc-CDH6-10	chr5:29205424-29205450	ucscGeneNc_uc003jhb_1
24	lnc-DROSHA-7	chr5:29355912-29356069	XLOC_004765
25	lnc-DROSHA-7	chr5:29395961-29396088	XLOC_004765
26	lnc-CDH6-9	chr5:29247176-29247267	l_2896_chr5:29228921-29247267_testes
27	lnc-DROSHA-12	chr5:29399178-29399246	l_2897_chr5:29390052-29431912_testes
28	lnc-DROSHA-7	chr5:29381960-29382069	NR_104628
29	lnc-DROSHA-7	chr5:29389918-29390046	NR_104628
30	lnc-DROSHA-7	chr5:29389918-29390046	XLOC_004765
31	lnc-DROSHA-7	chr5:29383211-29383410	XLOC_004765
32	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
33	lnc-CDH6-10	chr5:29200281-29200378	ucscGeneNc_uc003jhb_1
34	lnc-DROSHA-7	chr5:29384427-29384499	NR_104628
35	lnc-DROSHA-7	chr5:29389918-29390047	XLOC_004765
36	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
37	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
38	lnc-DROSHA-7	chr5:29363459-29363489	XLOC_004765
39	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
40	lnc-DROSHA-7	chr5:29395961-29396083	NR_104628

No data

Variant related genes	Relation type
ENSG00000248391	TF binding region
ENSG00000248391	CpG island
ENSG00000199568	chromatin interactions
ENSG00000248391	chromatin interactions
FMNL2	miRNA target sites
DGKA	miRNA target sites
AGPAT3	miRNA target sites
AHCTF1	miRNA target sites
SGMS1	miRNA target sites
AGK	miRNA target sites
AGL	miRNA target sites
AGXT2L1	miRNA target sites
SERPINB2	miRNA target sites

Extended variants
information (count: 3600 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3600 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10051008	chr5:29194872-29194873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184839299	chr5:29194875-29194876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145621248	chr5:29194894-29194895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529838144	chr5:29194899-29194900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549855413	chr5:29194947-29194948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141417814	chr5:29195083-29195084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569941822	chr5:29195088-29195089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530554296	chr5:29195093-29195094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369251989	chr5:29195154-29195155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9292306	chr5:29195198-29195199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534728523	chr5:29195203-29195204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569519999	chr5:29195219-29195220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566312096	chr5:29195282-29195283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536427687	chr5:29195294-29195295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554878858	chr5:29195295-29195296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187605028	chr5:29195309-29195310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10472676	chr5:29195400-29195401	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571434735	chr5:29195401-29195402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192036996	chr5:29195412-29195413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10472150	chr5:29195482-29195483	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs541553607	chr5:29195487-29195488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138340031	chr5:29195489-29195490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149628097	chr5:29195493-29195494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371620873	chr5:29195531-29195532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184216542	chr5:29195574-29195575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530846587	chr5:29195619-29195620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376164902	chr5:29195685-29195686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369490827	chr5:29195703-29195704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536832041	chr5:29195742-29195743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570470778	chr5:29195751-29195752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528073052	chr5:29195786-29195787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144341934	chr5:29195797-29195798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568048497	chr5:29195825-29195826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148767870	chr5:29195901-29195902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553814644	chr5:29195910-29195911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574979252	chr5:29195953-29195954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4507498	chr5:29195987-29195988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs554764574	chr5:29196069-29196070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536598733	chr5:29196096-29196097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569869128	chr5:29196112-29196113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537358142	chr5:29196117-29196118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189392267	chr5:29196374-29196375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1154773	chr5:29196378-29196379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs192911760	chr5:29196399-29196400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532572542	chr5:29196432-29196433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555420970	chr5:29196442-29196443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559797033	chr5:29196444-29196445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184523941	chr5:29196483-29196484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10039707	chr5:29196517-29196518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs542311730	chr5:29196559-29196560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD

Chromatin state (count:134 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29194200-29197800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:29194400-29197400	Weak transcription	Hela-S3	cervix
3	chr5:29197400-29198200	Enhancers	Hela-S3	cervix
4	chr5:29197600-29198600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:29197800-29198000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr5:29197800-29198200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:29198000-29198800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:29198200-29198600	Flanking Active TSS	Hela-S3	cervix
9	chr5:29198200-29198800	Enhancers	A549	lung
10	chr5:29198600-29199800	Enhancers	Hela-S3	cervix
11	chr5:29201200-29202000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr5:29202000-29202200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:29202200-29211000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr5:29208000-29208800	Enhancers	Hela-S3	cervix
15	chr5:29208200-29208600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:29208200-29208600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr5:29208200-29208600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:29208200-29208600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr5:29208400-29208600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:29208600-29211200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr5:29208600-29213800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr5:29208800-29209200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:29209200-29211200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:29210600-29214200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:29211000-29211200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:29211200-29211800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:29211200-29212000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:29211200-29214200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr5:29211200-29214200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr5:29211400-29211600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr5:29211600-29212800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr5:29212000-29212400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr5:29212400-29212600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr5:29212400-29213200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr5:29212600-29212800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:29212600-29213800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr5:29212800-29213000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:29213000-29213800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr5:29213200-29213600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr5:29213400-29213600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr5:29213600-29214000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:29213800-29214000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr5:29213800-29214000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:29213800-29214200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:29213800-29214200	Enhancers	Liver	Liver
46	chr5:29213800-29214200	Enhancers	Stomach Mucosa	stomach
47	chr5:29225800-29226000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:29227600-29227800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:29227800-29229400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:29229400-29230200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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