Variant report

Variant	esv2753514
Chromosome Location	chr13:63221699-63959299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1780)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1780 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:63740419-63740523	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:63818314-63818408	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:63630119-63630924	K562	blood:	n/a	n/a
4	ATF1	chr13:63618922-63619134	K562	blood:	n/a	n/a
5	ATF2	chr13:63758870-63759176	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:63295336-63295437	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:63805105-63805108	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:63582960-63583004	K562	blood:	n/a	n/a
9	BACH1	chr13:63666693-63666916	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr13:63615780-63616039	GM12878	blood:	n/a	n/a
11	BATF	chr13:63449339-63449575	GM12878	blood:	n/a	chr13:63449426-63449437
12	BCL3	chr13:63636565-63636764	K562	blood:	n/a	n/a
13	BCL3	chr13:63629979-63630226	K562	blood:	n/a	n/a
14	BDP1	chr13:63621761-63622431	Hela-S3	cervix:	n/a	n/a
15	BHLHE40	chr13:63621363-63621647	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:63269331-63269362	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:63646252-63646254	GM12878	blood:	n/a	n/a
18	BHLHE40	chr13:63321881-63322081	HepG2	liver:	n/a	n/a
19	BRCA1	chr13:63621532-63621757	GM12878	blood:	n/a	n/a
20	BRCA1	chr13:63645994-63646020	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr13:63631196-63631347	GM12878	blood:	n/a	n/a
22	BRCA1	chr13:63488576-63488593	GM12878	blood:	n/a	n/a
23	BRCA1	chr13:63646294-63646772	GM12878	blood:	n/a	n/a
24	BRCA1	chr13:63778099-63778105	GM12878	blood:	n/a	n/a
25	BRCA1	chr13:63636779-63637019	GM12878	blood:	n/a	n/a
26	BRCA1	chr13:63617055-63617144	GM12878	blood:	n/a	n/a
27	BRCA1	chr13:63662078-63662155	GM12878	blood:	n/a	n/a
28	CBX3	chr13:63280130-63280699	HCT-116	colon:	n/a	n/a
29	CCNT2	chr13:63623533-63624047	K562	blood:	n/a	n/a
30	CCNT2	chr13:63625757-63626259	K562	blood:	n/a	n/a
31	CCNT2	chr13:63636783-63637288	K562	blood:	n/a	n/a
32	CEBPB	chr13:63836547-63836805	HepG2	liver:	n/a	chr13:63836652-63836663
33	CEBPB	chr13:63776742-63776947	A549	lung:	n/a	n/a
34	CEBPB	chr13:63740269-63740585	HepG2	liver:	n/a	chr13:63740443-63740452 chr13:63740441-63740454 chr13:63740441-63740452
35	CEBPB	chr13:63378022-63378232	HepG2	liver:	n/a	chr13:63378135-63378148 chr13:63378136-63378147 chr13:63378134-63378151 chr13:63378135-63378148
36	CEBPB	chr13:63681234-63681693	IMR90	lung:	n/a	n/a
37	CEBPB	chr13:63345104-63345397	HepG2	liver:	n/a	chr13:63345274-63345285
38	CEBPB	chr13:63322255-63322610	IMR90	lung:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
39	CEBPB	chr13:63878639-63878883	Hela-S3	cervix:	n/a	chr13:63878814-63878825
40	CEBPB	chr13:63634182-63634519	K562	blood:	n/a	chr13:63634337-63634348 chr13:63634337-63634350
41	CEBPB	chr13:63432074-63432428	HepG2	liver:	n/a	chr13:63432246-63432257
42	CEBPB	chr13:63695754-63695954	K562	blood:	n/a	chr13:63695904-63695915
43	CEBPB	chr13:63632992-63633617	HepG2	liver:	n/a	chr13:63633575-63633588 chr13:63633467-63633478 chr13:63633463-63633480
44	CEBPB	chr13:63639251-63639536	K562	blood:	n/a	n/a
45	CEBPB	chr13:63733024-63733236	HepG2	liver:	n/a	chr13:63733111-63733122
46	CEBPB	chr13:63930231-63930544	IMR90	lung:	n/a	chr13:63930386-63930403 chr13:63930389-63930400
47	CEBPB	chr13:63227463-63227779	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:63773594-63773780	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:63412008-63412411	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:63839881-63840177	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:63264349-63264399	HepG2	liver:	n/a
2	chr13:63637003-63637053	HCM	heart:	n/a
3	chr13:63264349-63264399	HRPEpiC	eye:	n/a
4	chr13:63617080-63617130	AG09309	skin:	n/a
5	chr13:63617080-63617130	AoSMC	blood vessel:	n/a
6	chr13:63637003-63637053	PrEC	prostate:	n/a
7	chr13:63264349-63264399	HNPCEpiC	eye:	n/a
8	chr13:63264349-63264399	A549	lung:	n/a
9	chr13:63264349-63264399	SAEC	small airway:	n/a
10	chr13:63617080-63617130	H1-hESC	embryonic stem cell:	embryo
11	chr13:63264349-63264399	HMEC	breast:	n/a
12	chr13:63637003-63637053	ovcar-3	ovarian:	n/a
13	chr13:63637003-63637053	HMEC	breast:	n/a
14	chr13:63264349-63264399	HCF	heart:	n/a
15	chr13:63264349-63264399	Caco-2	colon:	n/a
16	chr13:63637003-63637053	GM12878	blood:	n/a
17	chr13:63617080-63617130	NB4	blood:	n/a
18	chr13:63637003-63637053	IMR90	lung:	fetal
19	chr13:63264349-63264399	PANC-1	pancreas:	n/a
20	chr13:63617080-63617130	HUVEC	blood vessel:	n/a
21	chr13:63637003-63637053	HUVEC	blood vessel:	n/a
22	chr13:63637003-63637053	RPTEC	kidney:	n/a
23	chr13:63617080-63617130	MCF10A-Er-Src	breast:	n/a
24	chr13:63637003-63637053	AG10803	skin:	n/a
25	chr13:63637003-63637053	HRPEpiC	eye:	n/a
26	chr13:63264349-63264399	Hepatocyte	liver:	n/a
27	chr13:63617080-63617130	ECC-1	luminal epithelium:	n/a
28	chr13:63264349-63264399	AG04449	skin:	fetal
29	chr13:63637003-63637053	NHBE	bronchial:	n/a
30	chr13:63617080-63617130	U87	brain:	n/a
31	chr13:63264349-63264399	HCM	heart:	n/a
32	chr13:63637003-63637053	Caco-2	colon:	n/a
33	chr13:63617080-63617130	AG04450	lung:	fetal
34	chr13:63617080-63617130	SKMC	muscle:	n/a
35	chr13:63637003-63637053	HEK293	kidney:	embryo
36	chr13:63617080-63617130	AG10803	skin:	n/a
37	chr13:63617080-63617130	Jurkat	blood:	n/a
38	chr13:63617080-63617130	IMR90	lung:	fetal
39	chr13:63617080-63617130	HIPEpiC	eye:	n/a
40	chr13:63264349-63264399	IMR90	lung:	fetal
41	chr13:63264349-63264399	MCF10A-Er-Src	breast:	n/a
42	chr13:63637003-63637053	GM06990	blood:	n/a
43	chr13:63637003-63637053	NHDF-neo	bronchial:	n/a
44	chr13:63637003-63637053	LNCaP	prostate:	n/a
45	chr13:63637003-63637053	HIPEpiC	eye:	n/a
46	chr13:63637003-63637053	SK-N-SH	brain:	n/a
47	chr13:63617080-63617130	GM06990	blood:	n/a
48	chr13:63264349-63264399	BJ	skin:	n/a
49	chr13:63637003-63637053	AG09309	skin:	n/a
50	chr13:63264349-63264399	NB4	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:63955263..63957196-chr13:63958888..63961483,2	MCF-7	breast:
2	chr13:63647679..63650483-chr20:26148365..26151073,2	K562	blood:
3	chr12:120076978..120077828-chr13:63812850..63813372,2	MCF-7	breast:
4	chr10:97173416..97174286-chr13:63349578..63350296,2	MCF-7	breast:
5	chr13:63647812..63648534-chr20:26148535..26149113,2	MCF-7	breast:
6	chr13:63619880..63624018-chr17:21665172..21668893,6	K562	blood:
7	chr13:63305859..63307828-chr13:63368512..63371200,2	K562	blood:
8	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:
9	chr13:63619768..63621405-chr17:21665172..21666856,2	MCF-7	breast:
10	chr13:63663754..63665958-chr13:63668093..63670026,2	K562	blood:
11	chr13:63663754..63665958-chr13:63668093..63670026,2	K562	blood:
12	chr13:63647686..63648379-chr3:64675736..64676331,2	MCF-7	breast:
13	chr13:63620345..63622864-chr17:21666900..21668712,2	K562	blood:
14	chr13:63637188..63639152-chr20:26145559..26148373,3	K562	blood:
15	chr13:63955263..63957196-chr13:63958888..63961483,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-3	chr13:63671473-63671829	XLOC_010410
2	lnc-AL445989.1-3	chr13:63609108-63609165	NONHSAT034157
3	lnc-PCDH20-18	chr13:63315448-63316259	ucscGeneNc_uc010aeh_1
4	lnc-PCDH20-20	chr13:63458505-63459173	NONHSAT034156
5	lnc-PCDH20-4	chr13:63370693-63370823	XLOC_010638
6	lnc-PCDH20-3	chr13:63260138-63260227	ENSG00000228669
7	lnc-PCDH20-18	chr13:63303588-63303986	NONHSAT034152
8	lnc-PCDH20-3	chr13:63305993-63306328	ENSG00000228669
9	lnc-PCDH20-6	chr13:63901377-63901488	XLOC_010640
10	lnc-PCDH20-4	chr13:63321740-63322054	XLOC_010638
11	lnc-PCDH20-5	chr13:63757234-63757461	XLOC_010639
12	lnc-PCDH20-20	chr13:63462230-63462334	NONHSAT034156
13	lnc-PCDH20-18	chr13:63311204-63311359	ucscGeneNc_uc010aeh_1
14	lnc-PCDH20-6	chr13:63902187-63902270	XLOC_010640
15	lnc-PCDH20-3	chr13:63306427-63306492	ENSG00000228669
16	lnc-AL445989.1-23	chr13:63222838-63223214	NONHSAT034150
17	lnc-PCDH20-20	chr13:63474519-63474543	NONHSAT034156
18	lnc-PCDH20-6	chr13:63901377-63901488	XLOC_010640
19	lnc-PCDH20-18	chr13:63311883-63313757	ucscGeneNc_uc010aeh_1
20	lnc-PCDH20-18	chr13:63300903-63301293	NONHSAT034152
21	lnc-PCDH20-20	chr13:63547376-63548145	NONHSAT034156
22	lnc-PCDH20-3	chr13:63306227-63306313	ENSG00000228669
23	lnc-PCDH20-4	chr13:63321841-63322054	NONHSAT034155
24	lnc-AL445989.1-3	chr13:63671472-63671829	NONHSAT034157
25	lnc-AL445989.1-3	chr13:63609109-63609165	XLOC_010410
26	lnc-PCDH20-20	chr13:63506481-63506671	NONHSAT034156
27	lnc-PCDH20-20	chr13:63475482-63475599	NONHSAT034156
28	lnc-PCDH20-6	chr13:63886242-63886263	XLOC_010640
29	lnc-PCDH20-3	chr13:63274749-63274830	ENSG00000228669
30	lnc-PCDH20-4	chr13:63368629-63368704	XLOC_010638
31	lnc-PCDH20-5	chr13:63768623-63768664	XLOC_010639
32	lnc-PCDH20-5	chr13:63801112-63801189	XLOC_010639
33	lnc-PCDH20-3	chr13:63246418-63246591	ENSG00000228669
34	lnc-PCDH20-18	chr13:63303588-63303661	ucscGeneNc_uc010aeh_1
35	lnc-PCDH20-6	chr13:63886242-63886263	XLOC_010640
36	lnc-PCDH20-6	chr13:63902193-63902270	XLOC_010640
37	lnc-PCDH20-18	chr13:63300981-63301286	ucscGeneNc_uc010aeh_1
38	lnc-PCDH20-4	chr13:63368629-63368706	NONHSAT034155

No data

Variant related genes	Relation type
LINC00376	TF binding region
LINC00448	TF binding region
LINC00376	CpG island
LINC00448	CpG island
ENSG00000095637	chromatin interactions
ENSG00000228669	chromatin interactions
PHF14	miRNA target sites
DNMT1	miRNA target sites

Extended variants
information (count: 10015 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:10015 , 50 per page) page: 1 2 3 4 5 6 7 ... 201

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61701243	chr13:63222850-63222851	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs60086429	chr13:63222890-63222891	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113623735	chr13:63222926-63222927	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs57871874	chr13:63222947-63222948	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534356020	chr13:63222990-63222991	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs558907221	chr13:63222997-63222998	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs576848116	chr13:63222998-63222999	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs193200186	chr13:63223037-63223038	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs529950451	chr13:63223047-63223048	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556112219	chr13:63223088-63223089	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs574139797	chr13:63223099-63223100	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs541424848	chr13:63223100-63223101	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs60989887	chr13:63223114-63223115	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs57450195	chr13:63223155-63223156	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs56342722	chr13:63223159-63223160	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564155390	chr13:63223199-63223200	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs183368292	chr13:63223200-63223201	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs967384	chr13:63223214-63223215	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs564441723	chr13:63231212-63231213	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531751395	chr13:63231267-63231268	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs60691111	chr13:63231326-63231327	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs76957377	chr13:63231349-63231350	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11619774	chr13:63231354-63231355	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs559723469	chr13:63231411-63231412	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs372524795	chr13:63231416-63231417	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs34526350	chr13:63231421-63231422	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547061887	chr13:63231449-63231450	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565709835	chr13:63231452-63231453	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs192410625	chr13:63231505-63231506	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs551606582	chr13:63231509-63231510	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs55930794	chr13:63231526-63231527	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542072841	chr13:63231539-63231540	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs537213787	chr13:63231572-63231573	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs555628480	chr13:63231581-63231582	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs571946919	chr13:63235473-63235474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539375512	chr13:63235501-63235502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142438927	chr13:63235560-63235561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569518371	chr13:63235603-63235604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192464582	chr13:63235648-63235649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146302850	chr13:63235658-63235659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147887642	chr13:63235667-63235668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557870806	chr13:63235683-63235684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533527642	chr13:63235694-63235695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558160606	chr13:63235704-63235705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74082743	chr13:63235746-63235747	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs117275546	chr13:63235760-63235761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114729606	chr13:63236093-63236094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528612727	chr13:63236159-63236160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540247623	chr13:63236161-63236162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565320296	chr13:63236169-63236170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	21346763	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:63231200-63231600	Active TSS	Spleen	Spleen
2	chr13:63235400-63235800	Enhancers	Fetal Heart	heart
3	chr13:63236000-63237400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:63236800-63238000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:63237200-63238000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr13:63237400-63237600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr13:63237600-63238600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr13:63239000-63239200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:63251800-63252600	Active TSS	A549	lung
10	chr13:63252200-63252600	Active TSS	Osteobl	bone
11	chr13:63252600-63252800	Flanking Active TSS	A549	lung
12	chr13:63263000-63265000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr13:63263200-63264400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr13:63263200-63266000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr13:63263400-63264000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr13:63263600-63264400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr13:63263600-63265200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr13:63264000-63264200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr13:63264000-63265800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr13:63264200-63264600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr13:63264200-63264600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr13:63264200-63264600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr13:63264200-63265200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr13:63264400-63264600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr13:63264600-63264800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr13:63264800-63265000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr13:63265000-63266000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr13:63266000-63266400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr13:63270800-63271000	Enhancers	Pancreas	Pancrea
30	chr13:63279000-63279200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:63279000-63280000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr13:63279800-63280000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr13:63280000-63284800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr13:63284600-63285200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr13:63284800-63285400	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr13:63289200-63290800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:63289800-63290200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:63296000-63296600	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr13:63304000-63304400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr13:63304000-63304400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr13:63321200-63321600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr13:63341800-63342000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr13:63341800-63342000	Enhancers	Gastric	stomach
44	chr13:63350200-63351000	Enhancers	Brain Hippocampus Middle	brain
45	chr13:63352800-63354200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr13:63353000-63354000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:63353000-63354200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr13:63353400-63354200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr13:63353400-63354400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr13:63362800-63363000	Enhancers	Adipose Nuclei	Adipose

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