Variant report

Variant	nsv1034776
Chromosome Location	chr5:12502153-12748961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1077)
CpG islands
(count:610)
Chromatin interactive
region (count:81)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:12629284-12629314	K562	blood:	n/a	n/a
2	ARID3A	chr5:12611278-12611564	K562	blood:	n/a	n/a
3	ARID3A	chr5:12625817-12626175	K562	blood:	n/a	n/a
4	ARID3A	chr5:12605684-12605760	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:12615141-12616053	K562	blood:	n/a	n/a
6	ARID3A	chr5:12587530-12587610	K562	blood:	n/a	n/a
7	ARID3A	chr5:12645737-12645937	K562	blood:	n/a	n/a
8	ARID3A	chr5:12573954-12574062	K562	blood:	n/a	n/a
9	ATF1	chr5:12599710-12599720	K562	blood:	n/a	n/a
10	ATF1	chr5:12625855-12626127	K562	blood:	n/a	n/a
11	ATF1	chr5:12636538-12636665	K562	blood:	n/a	n/a
12	ATF1	chr5:12611394-12611564	K562	blood:	n/a	n/a
13	ATF1	chr5:12612014-12612205	K562	blood:	n/a	n/a
14	ATF1	chr5:12615012-12615715	K562	blood:	n/a	n/a
15	ATF2	chr5:12623287-12624095	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:12667909-12668201	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:12668042-12668298	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:12662664-12663813	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:12660692-12662536	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:12657998-12658420	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:12648499-12649011	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:12658521-12660660	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:12662712-12663504	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr5:12627636-12627648	K562	blood:	n/a	n/a
25	BACH1	chr5:12615423-12615929	K562	blood:	n/a	n/a
26	BACH1	chr5:12627924-12628106	K562	blood:	n/a	n/a
27	BCL11A	chr5:12505213-12505415	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCLAF1	chr5:12615205-12615584	K562	blood:	n/a	n/a
29	BHLHE40	chr5:12614798-12616107	K562	blood:	n/a	n/a
30	BHLHE40	chr5:12574678-12575143	K562	blood:	n/a	n/a
31	BHLHE40	chr5:12616429-12616837	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	CBX3	chr5:12662769-12663016	K562	blood:	n/a	n/a
36	CCNT2	chr5:12574035-12574280	K562	blood:	n/a	n/a
37	CCNT2	chr5:12678478-12678604	K562	blood:	n/a	n/a
38	CCNT2	chr5:12615096-12615905	K562	blood:	n/a	n/a
39	CCNT2	chr5:12574667-12575084	K562	blood:	n/a	n/a
40	CEBPB	chr5:12592192-12592505	IMR90	lung:	n/a	chr5:12592345-12592356 chr5:12592343-12592356 chr5:12592343-12592354 chr5:12592345-12592354
41	CEBPB	chr5:12611333-12611629	K562	blood:	n/a	n/a
42	CEBPB	chr5:12636566-12636843	K562	blood:	n/a	chr5:12636734-12636745
43	CEBPB	chr5:12540762-12541082	HepG2	liver:	n/a	chr5:12540898-12540909
44	CEBPB	chr5:12635898-12635980	HepG2	liver:	n/a	chr5:12635944-12635955 chr5:12635924-12635935
45	CEBPB	chr5:12726389-12726675	HepG2	liver:	n/a	chr5:12726541-12726552
46	CEBPB	chr5:12605701-12606007	Hela-S3	cervix:	n/a	chr5:12605883-12605894 chr5:12605840-12605851
47	CEBPB	chr5:12503100-12503364	A549	lung:	n/a	chr5:12503277-12503288
48	CEBPB	chr5:12743804-12744042	MCF-7	breast:	n/a	n/a
49	CEBPB	chr5:12635759-12636051	K562	blood:	n/a	chr5:12635944-12635955 chr5:12635924-12635935
50	CEBPB	chr5:12605701-12606016	A549	lung:	n/a	chr5:12605883-12605894 chr5:12605840-12605851

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:12660863-12660913	HRE	kidney:	n/a
2	chr5:12660863-12660913	HCF	heart:	n/a
3	chr5:12636281-12636331	K562	blood:	n/a
4	chr5:12615428-12615478	HCF	heart:	n/a
5	chr5:12574872-12574922	Caco-2	colon:	n/a
6	chr5:12574688-12574738	HL-60	blood:	n/a
7	chr5:12636281-12636331	HCM	heart:	n/a
8	chr5:12661875-12661925	NHDF-neo	bronchial:	n/a
9	chr5:12615428-12615478	RPTEC	kidney:	n/a
10	chr5:12574688-12574738	H1-hESC	embryonic stem cell:	embryo
11	chr5:12574872-12574922	ProgFib	skin:	n/a
12	chr5:12615428-12615478	LNCaP	prostate:	n/a
13	chr5:12615428-12615478	Jurkat	blood:	n/a
14	chr5:12665869-12665919	GM12892	blood:	n/a
15	chr5:12574688-12574738	A549	lung:	n/a
16	chr5:12574688-12574738	ovcar-3	ovarian:	n/a
17	chr5:12669584-12669634	ProgFib	skin:	n/a
18	chr5:12574688-12574738	HRCEpiC	kidney:	n/a
19	chr5:12661875-12661925	HEK293	kidney:	embryo
20	chr5:12574872-12574922	H1-hESC	embryonic stem cell:	embryo
21	chr5:12623177-12623227	SK-N-MC	brain:	n/a
22	chr5:12660863-12660913	HAEpiC	amniotic membrane:	n/a
23	chr5:12615428-12615478	AG09309	skin:	n/a
24	chr5:12660863-12660913	SK-N-MC	brain:	n/a
25	chr5:12663018-12663068	HNPCEpiC	eye:	n/a
26	chr5:12665869-12665919	MCF10A-Er-Src	breast:	n/a
27	chr5:12623177-12623227	IMR90	lung:	fetal
28	chr5:12574872-12574922	HL-60	blood:	n/a
29	chr5:12636281-12636331	ProgFib	skin:	n/a
30	chr5:12574872-12574922	HAEpiC	amniotic membrane:	n/a
31	chr5:12660863-12660913	HCT-116	colon:	n/a
32	chr5:12615428-12615478	NT2-D1	testis:	n/a
33	chr5:12623177-12623227	ProgFib	skin:	n/a
34	chr5:12660863-12660913	HUVEC	blood vessel:	n/a
35	chr5:12574872-12574922	HIPEpiC	eye:	n/a
36	chr5:12665869-12665919	HRPEpiC	eye:	n/a
37	chr5:12623177-12623227	A549	lung:	n/a
38	chr5:12661875-12661925	IMR90	lung:	fetal
39	chr5:12623177-12623227	PFSK-1	brain:	n/a
40	chr5:12636281-12636331	GM06990	blood:	n/a
41	chr5:12661875-12661925	HAEpiC	amniotic membrane:	n/a
42	chr5:12660863-12660913	BE2_C	brain:	n/a
43	chr5:12623177-12623227	HIPEpiC	eye:	n/a
44	chr5:12660863-12660913	HRPEpiC	eye:	n/a
45	chr5:12661875-12661925	AG04450	lung:	fetal
46	chr5:12665869-12665919	HNPCEpiC	eye:	n/a
47	chr5:12665869-12665919	BJ	skin:	n/a
48	chr5:12636281-12636331	T-47D	breast:	n/a
49	chr5:12574872-12574922	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:12669584-12669634	HNPCEpiC	eye:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:12576814..12579689-chr5:12594654..12596559,2	K562	blood:
2	chr5:12588869..12590687-chr5:12605878..12607397,2	K562	blood:
3	chr5:12572879..12575641-chr5:12583464..12586142,3	K562	blood:
4	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
5	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
6	chr5:12573778..12576984-chr5:12577746..12580874,3	K562	blood:
7	chr5:12652956..12655094-chr5:12656361..12658712,2	MCF-7	breast:
8	chr5:12571887..12574871-chr5:12612831..12615771,3	K562	blood:
9	chr5:12743681..12745562-chr5:12760278..12762840,2	K562	blood:
10	chr5:12579405..12581985-chr5:12616959..12619800,2	K562	blood:
11	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
12	chr5:12608674..12611130-chr5:12636501..12638880,2	K562	blood:
13	chr5:12554220..12555829-chr5:12556078..12558191,2	MCF-7	breast:
14	chr5:12579389..12581538-chr5:12592252..12594102,2	K562	blood:
15	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:
16	chr5:12572185..12574233-chr5:12590584..12592577,2	K562	blood:
17	chr5:12537002..12539656-chr5:12586201..12588814,2	K562	blood:
18	chr5:12647069..12649041-chr5:12653810..12656965,3	K562	blood:
19	chr5:12652370..12654399-chr5:12657778..12661483,4	K562	blood:
20	chr5:12560874..12562617-chr5:12573988..12576942,2	K562	blood:
21	chr5:12608674..12611130-chr5:12636501..12638880,2	K562	blood:
22	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
23	chr5:12588618..12591381-chr5:12596169..12597807,2	K562	blood:
24	chr5:12542323..12544151-chr5:12547320..12550095,2	K562	blood:
25	chr5:12576312..12579149-chr5:12776108..12778231,2	K562	blood:
26	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
27	chr5:12652370..12654399-chr5:12657778..12661483,4	K562	blood:
28	chr5:12579463..12582015-chr5:12766907..12769227,3	K562	blood:
29	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
30	chr5:12583560..12586029-chr5:12586598..12589035,2	K562	blood:
31	chr5:12579405..12581985-chr5:12616959..12619800,2	K562	blood:
32	chr5:12652956..12655094-chr5:12656361..12658712,2	MCF-7	breast:
33	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
34	chr5:12653349..12655490-chr5:12663314..12666064,2	K562	blood:
35	chr5:12637921..12640108-chr5:12640320..12642573,2	K562	blood:
36	chr5:12710496..12712610-chr5:12713708..12716321,2	MCF-7	breast:
37	chr5:12537002..12539656-chr5:12586201..12588814,2	K562	blood:
38	chr5:12637921..12640108-chr5:12640320..12642573,2	K562	blood:
39	chr5:12660866..12661403-chr5:12804029..12804604,2	MCF-7	breast:
40	chr5:12703528..12705046-chr5:12710595..12712392,2	K562	blood:
41	chr5:12583560..12586029-chr5:12586598..12589035,2	K562	blood:
42	chr5:12292464..12293235-chr5:12598697..12599332,3	MCF-7	breast:
43	chr5:12647069..12649041-chr5:12653810..12656965,3	K562	blood:
44	chr5:12702448..12704226-chr5:12718051..12720709,2	K562	blood:
45	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:
46	chr5:12577735..12580318-chr5:12581576..12583762,3	K562	blood:
47	chr5:12554220..12555829-chr5:12556078..12558191,2	MCF-7	breast:
48	chr5:12573179..12575899-chr5:12592386..12594967,2	K562	blood:
49	chr5:12696352..12698473-chr5:12701723..12704711,2	MCF-7	breast:
50	chr5:12577735..12580318-chr5:12581576..12583762,3	K562	blood:

(count:23 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 8154 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:8154 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80254115	chr5:12502195-12502196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536382178	chr5:12502241-12502242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537139374	chr5:12502245-12502246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377041381	chr5:12502357-12502358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554830918	chr5:12502362-12502363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558661665	chr5:12502405-12502406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2052522	chr5:12502417-12502418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576608742	chr5:12502421-12502422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193072387	chr5:12502422-12502423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550151069	chr5:12502430-12502431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114688548	chr5:12502469-12502470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544612209	chr5:12502504-12502505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189924394	chr5:12502555-12502556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542107271	chr5:12502571-12502572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75428458	chr5:12502584-12502585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192533510	chr5:12502609-12502610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560890955	chr5:12502611-12502612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528292191	chr5:12502665-12502666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546536336	chr5:12502666-12502667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112389633	chr5:12502696-12502697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376488777	chr5:12502715-12502716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78930772	chr5:12502777-12502778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73744904	chr5:12502782-12502783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568528720	chr5:12502784-12502785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369046355	chr5:12502801-12502802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535941674	chr5:12502809-12502810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148475119	chr5:12502830-12502831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188116075	chr5:12502844-12502845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76713641	chr5:12502845-12502846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559239478	chr5:12502871-12502872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577589404	chr5:12502909-12502910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538569664	chr5:12503104-12503105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377352745	chr5:12503188-12503189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78381873	chr5:12503190-12503191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76949875	chr5:12503191-12503192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574798228	chr5:12503197-12503198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142520426	chr5:12503228-12503229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563268604	chr5:12503229-12503230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182029416	chr5:12503289-12503290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368736332	chr5:12503315-12503316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113295451	chr5:12503343-12503344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370438135	chr5:12503386-12503387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532240974	chr5:12503403-12503404	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184624910	chr5:12503419-12503420	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562100332	chr5:12503421-12503422	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529704714	chr5:12503439-12503440	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538182093	chr5:12503456-12503457	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547918790	chr5:12503491-12503492	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189072543	chr5:12503492-12503493	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150919897	chr5:12503559-12503560	ZNF genes & repeats 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:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:12501600-12505600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:12503400-12504600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
3	chr5:12504000-12505000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr5:12504200-12505000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:12504200-12507000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:12504400-12506200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:12504600-12505000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:12504600-12507400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:12505000-12505200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr5:12505000-12505200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr5:12505000-12506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:12505200-12505400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:12505200-12505400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:12505400-12505600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr5:12505400-12505800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr5:12505600-12505800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr5:12505600-12506400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:12505800-12506000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr5:12505800-12506400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr5:12507200-12507400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr5:12507600-12522400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:12509800-12511800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:12532200-12532800	ZNF genes & repeats	Pancreas	Pancrea
24	chr5:12535400-12535600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr5:12535600-12535800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:12562600-12569200	Weak transcription	Placenta	Placenta
27	chr5:12565600-12570400	Weak transcription	K562	blood
28	chr5:12567600-12568200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:12569200-12570800	Strong transcription	Placenta	Placenta
30	chr5:12570400-12572400	Strong transcription	K562	blood
31	chr5:12570800-12573800	Weak transcription	Placenta	Placenta
32	chr5:12572400-12573000	Weak transcription	K562	blood
33	chr5:12573000-12576200	Active TSS	K562	blood
34	chr5:12573800-12575400	Active TSS	Placenta	Placenta
35	chr5:12576200-12577600	Weak transcription	K562	blood
36	chr5:12577800-12578000	ZNF genes & repeats	K562	blood
37	chr5:12578000-12581200	Weak transcription	K562	blood
38	chr5:12579800-12580800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr5:12579800-12581000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:12580200-12580800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr5:12580400-12580800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:12581200-12582000	Strong transcription	K562	blood
43	chr5:12582000-12596000	Weak transcription	K562	blood
44	chr5:12596000-12596400	Strong transcription	K562	blood
45	chr5:12596400-12597400	Weak transcription	K562	blood
46	chr5:12597400-12598400	Strong transcription	K562	blood
47	chr5:12598400-12610600	Weak transcription	K562	blood
48	chr5:12599000-12599200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr5:12602000-12612400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr5:12602400-12602800	Enhancers	Fetal Brain Male	brain

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