Variant report

Variant	nsv881369
Chromosome Location	chr5:12510848-12765292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1107)
CpG islands
(count:610)
Chromatin interactive
region (count:89)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:12605684-12605760	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:12573954-12574062	K562	blood:	n/a	n/a
3	ARID3A	chr5:12629284-12629314	K562	blood:	n/a	n/a
4	ARID3A	chr5:12611278-12611564	K562	blood:	n/a	n/a
5	ARID3A	chr5:12587530-12587610	K562	blood:	n/a	n/a
6	ARID3A	chr5:12625817-12626175	K562	blood:	n/a	n/a
7	ARID3A	chr5:12645737-12645937	K562	blood:	n/a	n/a
8	ARID3A	chr5:12615141-12616053	K562	blood:	n/a	n/a
9	ATF1	chr5:12636538-12636665	K562	blood:	n/a	n/a
10	ATF1	chr5:12625855-12626127	K562	blood:	n/a	n/a
11	ATF1	chr5:12615012-12615715	K562	blood:	n/a	n/a
12	ATF1	chr5:12599710-12599720	K562	blood:	n/a	n/a
13	ATF1	chr5:12611394-12611564	K562	blood:	n/a	n/a
14	ATF1	chr5:12612014-12612205	K562	blood:	n/a	n/a
15	ATF2	chr5:12668042-12668298	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:12662664-12663813	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:12658521-12660660	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:12660692-12662536	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:12657998-12658420	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:12662712-12663504	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:12623287-12624095	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:12667909-12668201	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:12648499-12649011	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr5:12627924-12628106	K562	blood:	n/a	n/a
25	BACH1	chr5:12615423-12615929	K562	blood:	n/a	n/a
26	BACH1	chr5:12627636-12627648	K562	blood:	n/a	n/a
27	BCLAF1	chr5:12615205-12615584	K562	blood:	n/a	n/a
28	BHLHE40	chr5:12616429-12616837	K562	blood:	n/a	n/a
29	BHLHE40	chr5:12574678-12575143	K562	blood:	n/a	n/a
30	BHLHE40	chr5:12614798-12616107	K562	blood:	n/a	n/a
31	CBX3	chr5:12662769-12663016	K562	blood:	n/a	n/a
32	CBX3	chr5:12615155-12615822	K562	blood:	n/a	n/a
33	CBX3	chr5:12574582-12575256	K562	blood:	n/a	n/a
34	CBX3	chr5:12578931-12579331	K562	blood:	n/a	n/a
35	CCNT2	chr5:12759535-12759728	K562	blood:	n/a	n/a
36	CCNT2	chr5:12574035-12574280	K562	blood:	n/a	n/a
37	CCNT2	chr5:12615096-12615905	K562	blood:	n/a	n/a
38	CCNT2	chr5:12574667-12575084	K562	blood:	n/a	n/a
39	CCNT2	chr5:12678478-12678604	K562	blood:	n/a	n/a
40	CEBPB	chr5:12637707-12637985	HepG2	liver:	n/a	chr5:12637809-12637820
41	CEBPB	chr5:12540762-12541082	HepG2	liver:	n/a	chr5:12540898-12540909
42	CEBPB	chr5:12642437-12642649	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr5:12592193-12592486	A549	lung:	n/a	chr5:12592345-12592356 chr5:12592343-12592356 chr5:12592343-12592354 chr5:12592345-12592354
44	CEBPB	chr5:12764527-12764819	A549	lung:	n/a	chr5:12764650-12764661 chr5:12764662-12764675
45	CEBPB	chr5:12592159-12592524	HepG2	liver:	n/a	chr5:12592345-12592356 chr5:12592343-12592356 chr5:12592343-12592354 chr5:12592345-12592354
46	CEBPB	chr5:12592174-12592498	K562	blood:	n/a	chr5:12592345-12592356 chr5:12592343-12592356 chr5:12592343-12592354 chr5:12592345-12592354
47	CEBPB	chr5:12566600-12566907	Hela-S3	cervix:	n/a	chr5:12566765-12566776
48	CEBPB	chr5:12642411-12642705	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr5:12605701-12606016	A549	lung:	n/a	chr5:12605883-12605894 chr5:12605840-12605851
50	CEBPB	chr5:12636335-12636855	A549	lung:	n/a	chr5:12636734-12636745

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:12615428-12615478	BE2_C	brain:	n/a
2	chr5:12660863-12660913	PFSK-1	brain:	n/a
3	chr5:12636281-12636331	HIPEpiC	eye:	n/a
4	chr5:12661875-12661925	CMK	blood:	n/a
5	chr5:12660863-12660913	GM19239	blood:	n/a
6	chr5:12636281-12636331	IMR90	lung:	fetal
7	chr5:12615428-12615478	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:12663018-12663068	NHBE	bronchial:	n/a
9	chr5:12636281-12636331	HUVEC	blood vessel:	n/a
10	chr5:12663018-12663068	IMR90	lung:	fetal
11	chr5:12669584-12669634	AG09309	skin:	n/a
12	chr5:12615428-12615478	A549	lung:	n/a
13	chr5:12663018-12663068	ProgFib	skin:	n/a
14	chr5:12669584-12669634	U87	brain:	n/a
15	chr5:12663018-12663068	Hepatocyte	liver:	n/a
16	chr5:12636281-12636331	PrEC	prostate:	n/a
17	chr5:12665869-12665919	BE2_C	brain:	n/a
18	chr5:12663018-12663068	HEEpiC	esophagus:	n/a
19	chr5:12669584-12669634	HMEC	breast:	n/a
20	chr5:12661875-12661925	HMEC	breast:	n/a
21	chr5:12615428-12615478	AG09319	gingival:	n/a
22	chr5:12669584-12669634	HRPEpiC	eye:	n/a
23	chr5:12623177-12623227	NH-A	brain:	n/a
24	chr5:12615428-12615478	T-47D	breast:	n/a
25	chr5:12615428-12615478	K562	blood:	n/a
26	chr5:12636281-12636331	SK-N-SH_RA	brain:	n/a
27	chr5:12665869-12665919	AG04450	lung:	fetal
28	chr5:12636281-12636331	HRPEpiC	eye:	n/a
29	chr5:12665869-12665919	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:12660863-12660913	IMR90	lung:	fetal
31	chr5:12574872-12574922	NH-A	brain:	n/a
32	chr5:12574872-12574922	Caco-2	colon:	n/a
33	chr5:12661875-12661925	IMR90	lung:	fetal
34	chr5:12574688-12574738	HIPEpiC	eye:	n/a
35	chr5:12661875-12661925	Hela-S3	cervix:	n/a
36	chr5:12574688-12574738	HepG2	liver:	n/a
37	chr5:12665869-12665919	H1-hESC	embryonic stem cell:	embryo
38	chr5:12636281-12636331	Caco-2	colon:	n/a
39	chr5:12636281-12636331	NH-A	brain:	n/a
40	chr5:12669584-12669634	AG04449	skin:	fetal
41	chr5:12574688-12574738	Hela-S3	cervix:	n/a
42	chr5:12660863-12660913	HEK293	kidney:	embryo
43	chr5:12661875-12661925	HCT-116	colon:	n/a
44	chr5:12661875-12661925	GM12878	blood:	n/a
45	chr5:12636281-12636331	Hepatocyte	liver:	n/a
46	chr5:12661875-12661925	LNCaP	prostate:	n/a
47	chr5:12665869-12665919	NHDF-neo	bronchial:	n/a
48	chr5:12660863-12660913	RPTEC	kidney:	n/a
49	chr5:12669584-12669634	GM06990	blood:	n/a
50	chr5:12574872-12574922	GM12891	blood:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:12743681..12745562-chr5:12760278..12762840,2	K562	blood:
2	chr5:12576814..12579689-chr5:12594654..12596559,2	K562	blood:
3	chr5:12608674..12611130-chr5:12636501..12638880,2	K562	blood:
4	chr5:12718842..12720474-chr5:12721962..12723532,2	K562	blood:
5	chr5:12637921..12640108-chr5:12640320..12642573,2	K562	blood:
6	chr5:12583560..12586029-chr5:12586598..12589035,2	K562	blood:
7	chr5:12757621..12760058-chr5:12760754..12763671,2	K562	blood:
8	chr5:12589520..12591629-chr5:12614668..12616853,2	K562	blood:
9	chr5:12702448..12704226-chr5:12718051..12720709,2	K562	blood:
10	chr1:153295251..153295999-chr5:12761269..12762010,2	MCF-7	breast:
11	chr5:12652956..12655094-chr5:12656361..12658712,2	MCF-7	breast:
12	chr5:12647069..12649041-chr5:12653810..12656965,3	K562	blood:
13	chr5:12702448..12704226-chr5:12718051..12720709,2	K562	blood:
14	chr5:12580769..12583015-chr5:13118744..13121010,2	K562	blood:
15	chr5:12743681..12745562-chr5:12760278..12762840,2	K562	blood:
16	chr5:12660866..12661403-chr5:12804029..12804604,2	MCF-7	breast:
17	chr5:12579389..12581538-chr5:12592252..12594102,2	K562	blood:
18	chr5:12588869..12590687-chr5:12605878..12607397,2	K562	blood:
19	chr5:12614374..12617488-chr5:12617619..12619777,3	K562	blood:
20	chr5:12573179..12575899-chr5:12592386..12594967,2	K562	blood:
21	chr5:12581974..12583485-chr5:12585485..12587761,2	K562	blood:
22	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:
23	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
24	chr5:12572185..12574233-chr5:12590584..12592577,2	K562	blood:
25	chr5:12583560..12586029-chr5:12586598..12589035,2	K562	blood:
26	chr5:12572879..12575641-chr5:12583464..12586142,3	K562	blood:
27	chr5:12588618..12591381-chr5:12596169..12597807,2	K562	blood:
28	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
29	chr5:12653349..12655490-chr5:12663314..12666064,2	K562	blood:
30	chr5:12569399..12571855-chr5:12571987..12574855,2	K562	blood:
31	chr5:12571887..12574871-chr5:12612831..12615771,3	K562	blood:
32	chr5:12537002..12539656-chr5:12586201..12588814,2	K562	blood:
33	chr5:12654971..12655664-chr8:60884734..60885526,2	MCF-7	breast:
34	chr5:12718842..12720474-chr5:12721962..12723532,2	K562	blood:
35	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
36	chr5:12579405..12581985-chr5:12616959..12619800,2	K562	blood:
37	chr5:12614374..12617488-chr5:12617619..12619777,3	K562	blood:
38	chr5:12576814..12579689-chr5:12594654..12596559,2	K562	blood:
39	chr5:12652370..12654399-chr5:12657778..12661483,4	K562	blood:
40	chr5:12652370..12654399-chr5:12657778..12661483,4	K562	blood:
41	chr5:12566855..12569678-chr5:12570834..12573967,4	MCF-7	breast:
42	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:
43	chr5:12710496..12712610-chr5:12713708..12716321,2	MCF-7	breast:
44	chr5:12579405..12581985-chr5:12616959..12619800,2	K562	blood:
45	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
46	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
47	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
48	chr5:12637921..12640108-chr5:12640320..12642573,2	K562	blood:
49	chr5:12760900..12763053-chr5:12763056..12765696,2	K562	blood:
50	chr5:12703528..12705046-chr5:12710595..12712392,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
2	lnc-CTNND2-3	chr5:12723669-12723939	NONHSAT100517
3	lnc-CTNND2-3	chr5:12737810-12737969	NONHSAT100517
4	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
5	lnc-TRIO-4	chr5:12574969-12575164	NONHSAT100511
6	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
7	lnc-TRIO-4	chr5:12711310-12711411	ENSG00000248131
8	lnc-CTNND2-3	chr5:12653170-12654688	NONHSAT100517
9	lnc-TRIO-4	chr5:12711310-12711411	NONHSAT100511
10	lnc-TRIO-9	chr5:12648871-12648890	l_2878_chr5:12648870-12708792_testes
11	lnc-CTNND2-3	chr5:12659546-12660157	NONHSAT100517
12	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
13	lnc-TRIO-4	chr5:12654759-12655799	ENSG00000248131
14	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
15	lnc-TRIO-4	chr5:12711310-12711411	ENSG00000248131
16	lnc-TRIO-9	chr5:12707759-12708641	l_2878_chr5:12648870-12708792_testes
17	lnc-CTNND2-3	chr5:12657511-12658227	NONHSAT100517
18	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
19	lnc-TRIO-9	chr5:12708650-12708792	l_2878_chr5:12648870-12708792_testes
20	lnc-TRIO-4	chr5:12574969-12575164	NONHSAT100514
21	lnc-TRIO-4	chr5:12711310-12711411	NONHSAT100514
22	lnc-CTNND2-3	chr5:12663441-12664022	NONHSAT100517
23	lnc-TRIO-4	chr5:12595809-12595890	NONHSAT100514
24	lnc-TRIO-4	chr5:12759471-12759760	ENSG00000248131

No data

Variant related genes	Relation type
ENSG00000248783	TF binding region
CT49	TF binding region
ENSG00000264921	TF binding region
ENSG00000248783	CpG island
CT49	CpG island
ENSG00000264921	CpG island
ENSG00000248131	chromatin interactions
ENSG00000231188	chromatin interactions
ENSG00000248783	chromatin interactions
ENSG00000099194	chromatin interactions
MLL2	miRNA target sites
PSMD7	miRNA target sites
CITED2	miRNA target sites
ARHGEF7	miRNA target sites
ABL2	miRNA target sites
PURA	miRNA target sites
BMPR2	miRNA target sites
NIN	miRNA target sites
FAM171A1	miRNA target sites
TRIM44	miRNA target sites

Extended variants
information (count: 7835 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:7835 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs32374	chr5:12510848-12510849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35830758	chr5:12510854-12510855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552601620	chr5:12510867-12510868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560222248	chr5:12510881-12510882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555082285	chr5:12510910-12510911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536203361	chr5:12510912-12510913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573358339	chr5:12510926-12510927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545935807	chr5:12510930-12510931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554510238	chr5:12510938-12510939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367894708	chr5:12510947-12510948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531821180	chr5:12510950-12510951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187134000	chr5:12511016-12511017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145591424	chr5:12511017-12511018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562222724	chr5:12511060-12511061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529397992	chr5:12511071-12511072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6554715	chr5:12511092-12511093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545498192	chr5:12511116-12511117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543903677	chr5:12511134-12511135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147029423	chr5:12511164-12511165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565760213	chr5:12511172-12511173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533209422	chr5:12511200-12511201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551471679	chr5:12511211-12511212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114218221	chr5:12511308-12511309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs32373	chr5:12511310-12511311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs577363987	chr5:12511320-12511321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556349422	chr5:12511322-12511323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568246709	chr5:12511327-12511328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535761679	chr5:12511328-12511329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553772865	chr5:12511332-12511333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572071796	chr5:12511344-12511345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545872786	chr5:12511353-12511354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192150760	chr5:12511415-12511416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377669459	chr5:12511429-12511430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370399144	chr5:12511453-12511454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367629325	chr5:12511469-12511470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs32372	chr5:12511473-12511474	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs386685572	chr5:12511481-12511482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114345267	chr5:12511482-12511483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182964849	chr5:12511484-12511485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185686270	chr5:12511548-12511549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564830866	chr5:12511549-12511550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115389420	chr5:12511553-12511554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71595876	chr5:12511556-12511557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143893877	chr5:12511557-12511558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369327505	chr5:12511559-12511560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543097422	chr5:12511561-12511562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539635603	chr5:12511568-12511569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557960577	chr5:12511569-12511570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549678037	chr5:12511620-12511621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370337337	chr5:12511625-12511626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:12507600-12522400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:12509800-12511800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr5:12532200-12532800	ZNF genes & repeats	Pancreas	Pancrea
4	chr5:12535400-12535600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:12535600-12535800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr5:12562600-12569200	Weak transcription	Placenta	Placenta
7	chr5:12565600-12570400	Weak transcription	K562	blood
8	chr5:12567600-12568200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:12569200-12570800	Strong transcription	Placenta	Placenta
10	chr5:12570400-12572400	Strong transcription	K562	blood
11	chr5:12570800-12573800	Weak transcription	Placenta	Placenta
12	chr5:12572400-12573000	Weak transcription	K562	blood
13	chr5:12573000-12576200	Active TSS	K562	blood
14	chr5:12573800-12575400	Active TSS	Placenta	Placenta
15	chr5:12576200-12577600	Weak transcription	K562	blood
16	chr5:12577800-12578000	ZNF genes & repeats	K562	blood
17	chr5:12578000-12581200	Weak transcription	K562	blood
18	chr5:12579800-12580800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:12579800-12581000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:12580200-12580800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:12580400-12580800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr5:12581200-12582000	Strong transcription	K562	blood
23	chr5:12582000-12596000	Weak transcription	K562	blood
24	chr5:12596000-12596400	Strong transcription	K562	blood
25	chr5:12596400-12597400	Weak transcription	K562	blood
26	chr5:12597400-12598400	Strong transcription	K562	blood
27	chr5:12598400-12610600	Weak transcription	K562	blood
28	chr5:12599000-12599200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr5:12602000-12612400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr5:12602400-12602800	Enhancers	Fetal Brain Male	brain
31	chr5:12610600-12610800	Enhancers	K562	blood
32	chr5:12610800-12612000	Active TSS	K562	blood
33	chr5:12612000-12612200	Flanking Active TSS	K562	blood
34	chr5:12612200-12614200	Enhancers	K562	blood
35	chr5:12612400-12612600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
36	chr5:12613400-12613600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:12613600-12617600	Enhancers	Dnd41	blood
38	chr5:12614200-12615000	Flanking Active TSS	K562	blood
39	chr5:12614600-12615200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:12614800-12616000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:12615000-12615200	Active TSS	K562	blood
42	chr5:12615200-12615400	Flanking Active TSS	K562	blood
43	chr5:12615200-12615600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr5:12615400-12615600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:12615400-12615600	Active TSS	K562	blood
46	chr5:12615600-12616200	Flanking Active TSS	K562	blood
47	chr5:12615600-12627200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr5:12616200-12616600	Enhancers	K562	blood
49	chr5:12616200-12622800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:12616600-12616800	Flanking Active TSS	K562	blood

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