Variant report

Variant	esv2756433
Chromosome Location	chr13:91841599-91968099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:820)
CpG islands
(count:61)
Chromatin interactive
region (count:153)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:91900207-91900334	K562	blood:	n/a	n/a
2	ATF1	chr13:91929555-91929564	K562	blood:	n/a	n/a
3	ATF2	chr13:91954330-91954722	GM12878	blood:	n/a	n/a
4	ATF2	chr13:91954290-91954805	GM12878	blood:	n/a	n/a
5	BATF	chr13:91890352-91890701	GM12878	blood:	n/a	n/a
6	BATF	chr13:91890320-91890633	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:91954430-91954628	GM12878	blood:	n/a	chr13:91954472-91954481
8	BCL11A	chr13:91869613-91869841	H1-hESC	embryonic stem cell:	n/a	chr13:91869699-91869706
9	BCLAF1	chr13:91965316-91965766	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:91925293-91925297	K562	blood:	n/a	n/a
11	BHLHE40	chr13:91886326-91886518	K562	blood:	n/a	n/a
12	BHLHE40	chr13:91965465-91965726	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:91890402-91890691	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:91854367-91854514	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr13:91967797-91967955	K562	blood:	n/a	n/a
16	CEBPB	chr13:91852138-91852489	K562	blood:	n/a	chr13:91852311-91852322
17	CEBPB	chr13:91863298-91863581	HepG2	liver:	n/a	chr13:91863426-91863437
18	CEBPB	chr13:91852154-91852459	IMR90	lung:	n/a	chr13:91852311-91852322
19	CEBPB	chr13:91916763-91917039	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:91925958-91926325	HepG2	liver:	n/a	chr13:91926151-91926162
21	CEBPB	chr13:91863404-91863470	K562	blood:	n/a	chr13:91863426-91863437
22	CEBPB	chr13:91852162-91852463	HepG2	liver:	n/a	chr13:91852311-91852322
23	CEBPB	chr13:91929941-91930163	A549	lung:	n/a	n/a
24	CEBPB	chr13:91926960-91927121	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr13:91929898-91930178	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:91855896-91856134	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:91854574-91854612	HepG2	liver:	n/a	n/a
28	CEBPB	chr13:91848241-91848578	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:91945390-91945396	K562	blood:	n/a	n/a
30	CEBPB	chr13:91863303-91863551	A549	lung:	n/a	chr13:91863426-91863437
31	CEBPB	chr13:91941747-91941802	K562	blood:	n/a	n/a
32	CEBPB	chr13:91852277-91852405	H1-hESC	embryonic stem cell:	n/a	chr13:91852311-91852322
33	CEBPB	chr13:91908190-91908228	HepG2	liver:	n/a	chr13:91908194-91908211
34	CEBPB	chr13:91916887-91916954	A549	lung:	n/a	n/a
35	CHD1	chr13:91965413-91965663	GM12878	blood:	n/a	n/a
36	CHD2	chr13:91955553-91955594	K562	blood:	n/a	n/a
37	CHD2	chr13:91869564-91869907	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr13:91954274-91954799	GM12878	blood:	n/a	n/a
39	CTCF	chr13:91965460-91965610	GM12878	blood:	n/a	chr13:91965509-91965530 chr13:91965510-91965519 chr13:91965507-91965525
40	CTCF	chr13:91965380-91965530	GM12867	blood:	n/a	chr13:91965509-91965530 chr13:91965510-91965519 chr13:91965507-91965525
41	CTCF	chr13:91960580-91960730	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr13:91960700-91960850	GM12878	blood:	n/a	n/a
43	CTCF	chr13:91937400-91937550	GM12869	blood:	n/a	n/a
44	CTCF	chr13:91900160-91900310	GM12873	blood:	n/a	chr13:91900222-91900243 chr13:91900228-91900244 chr13:91900227-91900245
45	CTCF	chr13:91960660-91960810	HCT-116	colon:	n/a	n/a
46	CTCF	chr13:91960640-91960790	GM12864	blood:	n/a	n/a
47	CTCF	chr13:91943526-91943566	MCF-7	breast:	n/a	n/a
48	CTCF	chr13:91960680-91960830	GM12867	blood:	n/a	n/a
49	CTCF	chr13:91900080-91900295	HepG2	liver:	n/a	chr13:91900222-91900243 chr13:91900228-91900244 chr13:91900227-91900245
50	CTCF	chr13:91900160-91900310	HRE	kidney:	n/a	chr13:91900222-91900243 chr13:91900228-91900244 chr13:91900227-91900245

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:91855918-91855968	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:91855918-91855968	ProgFib	skin:	n/a
3	chr13:91855918-91855968	GM12891	blood:	n/a
4	chr13:91855918-91855968	RPTEC	kidney:	n/a
5	chr13:91855918-91855968	GM12892	blood:	n/a
6	chr13:91855918-91855968	HRPEpiC	eye:	n/a
7	chr13:91855918-91855968	SKMC	muscle:	n/a
8	chr13:91855918-91855968	HRE	kidney:	n/a
9	chr13:91855918-91855968	AG04449	skin:	fetal
10	chr13:91855918-91855968	Jurkat	blood:	n/a
11	chr13:91855918-91855968	HMEC	breast:	n/a
12	chr13:91855918-91855968	HNPCEpiC	eye:	n/a
13	chr13:91855918-91855968	NHDF-neo	bronchial:	n/a
14	chr13:91855918-91855968	CMK	blood:	n/a
15	chr13:91855918-91855968	Hela-S3	cervix:	n/a
16	chr13:91855918-91855968	SAEC	small airway:	n/a
17	chr13:91855918-91855968	Hepatocyte	liver:	n/a
18	chr13:91855918-91855968	HAEpiC	amniotic membrane:	n/a
19	chr13:91855918-91855968	HEEpiC	esophagus:	n/a
20	chr13:91855918-91855968	AG09309	skin:	n/a
21	chr13:91855918-91855968	HCF	heart:	n/a
22	chr13:91855918-91855968	PANC-1	pancreas:	n/a
23	chr13:91855918-91855968	AoSMC	blood vessel:	n/a
24	chr13:91855918-91855968	GM06990	blood:	n/a
25	chr13:91855918-91855968	MCF-7	breast:	n/a
26	chr13:91855918-91855968	NT2-D1	testis:	n/a
27	chr13:91855918-91855968	Caco-2	colon:	n/a
28	chr13:91855918-91855968	ECC-1	luminal epithelium:	n/a
29	chr13:91855918-91855968	SK-N-MC	brain:	n/a
30	chr13:91855918-91855968	MCF10A-Er-Src	breast:	n/a
31	chr13:91855918-91855968	IMR90	lung:	fetal
32	chr13:91855918-91855968	HL-60	blood:	n/a
33	chr13:91855918-91855968	PFSK-1	brain:	n/a
34	chr13:91855918-91855968	HUVEC	blood vessel:	n/a
35	chr13:91855918-91855968	HepG2	liver:	n/a
36	chr13:91855918-91855968	GM19239	blood:	n/a
37	chr13:91855918-91855968	PrEC	prostate:	n/a
38	chr13:91855918-91855968	SK-N-SH_RA	brain:	n/a
39	chr13:91855918-91855968	HCM	heart:	n/a
40	chr13:91855918-91855968	HIPEpiC	eye:	n/a
41	chr13:91855918-91855968	GM12878	blood:	n/a
42	chr13:91855918-91855968	ovcar-3	ovarian:	n/a
43	chr13:91855918-91855968	LNCaP	prostate:	n/a
44	chr13:91855918-91855968	T-47D	breast:	n/a
45	chr13:91855918-91855968	BJ	skin:	n/a
46	chr13:91855918-91855968	BE2_C	brain:	n/a
47	chr13:91855918-91855968	HRCEpiC	kidney:	n/a
48	chr13:91855918-91855968	HEK293	kidney:	embryo
49	chr13:91855918-91855968	AG10803	skin:	n/a
50	chr13:91855918-91855968	NH-A	brain:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr13:91958716..91961650-chr13:91963120..91965633,4	K562	blood:
2	chr13:91917368..91919651-chr13:91919738..91922189,2	K562	blood:
3	chr13:91869159..91872300-chr13:91997996..92002623,4	K562	blood:
4	chr13:91887562..91890351-chr13:91903749..91906128,3	K562	blood:
5	chr13:91894505..91897383-chr13:91999710..92001323,3	K562	blood:
6	chr13:91887562..91890351-chr13:91903749..91905859,2	K562	blood:
7	chr13:91934968..91937600-chr13:91939155..91942130,2	K562	blood:
8	chr13:91891188..91893020-chr13:91913377..91915649,2	K562	blood:
9	chr13:91967595..91969691-chr13:91969721..91972624,2	MCF-7	breast:
10	chr13:91903377..91907424-chr13:91999812..92002571,4	K562	blood:
11	chr13:91954347..91956053-chr13:91969045..91970728,2	K562	blood:
12	chr13:91955114..91958656-chr13:91998727..92001292,4	MCF-7	breast:
13	chr13:91887387..91891925-chr13:91893469..91896614,5	K562	blood:
14	chr13:91893680..91897355-chr13:92007107..92011169,4	K562	blood:
15	chr13:91959172..91961374-chr13:91999584..92001899,2	MCF-7	breast:
16	chr13:91965062..91965969-chr13:92058596..92059538,2	K562	blood:
17	chr13:91857551..91859591-chr13:91862399..91864537,2	K562	blood:
18	chr1:162473001..162475319-chr13:91889993..91891513,2	K562	blood:
19	chr13:91860520..91862440-chr13:92006561..92009210,2	K562	blood:
20	chr13:91925284..91927675-chr13:92003883..92005533,2	K562	blood:
21	chr13:91893680..91896156-chr13:92009275..92010984,2	K562	blood:
22	chr13:91958716..91961650-chr13:91963120..91965633,4	K562	blood:
23	chr13:91906437..91909303-chr13:91916493..91918143,2	K562	blood:
24	chr13:91887329..91890707-chr13:91908939..91913306,4	K562	blood:
25	chr13:91834823..91837428-chr13:91840778..91842501,2	K562	blood:
26	chr13:91943369..91945474-chr13:91945727..91947965,2	K562	blood:
27	chr13:91847806..91850062-chr13:91858588..91860776,2	K562	blood:
28	chr13:91906437..91909303-chr13:91916493..91918143,2	K562	blood:
29	chr13:91934968..91937600-chr13:91939155..91942130,2	K562	blood:
30	chr13:91910219..91913312-chr13:92006561..92009211,3	K562	blood:
31	chr13:91847806..91850062-chr13:91858588..91860776,2	K562	blood:
32	chr13:91813911..91816549-chr13:91910671..91913045,2	K562	blood:
33	chr13:91922956..91924872-chr13:91999191..92001609,2	K562	blood:
34	chr13:91951723..91953848-chr13:91956197..91958040,2	K562	blood:
35	chr13:91876019..91881518-chr13:91996097..92003192,7	K562	blood:
36	chr13:91865105..91867880-chr13:91873303..91875140,2	K562	blood:
37	chr13:91906077..91908122-chr13:92005714..92008494,2	K562	blood:
38	chr13:91883488..91886150-chr13:92002562..92005490,3	K562	blood:
39	chr13:91920712..91923592-chr13:92007874..92010601,2	K562	blood:
40	chr13:91917284..91919036-chr13:91998164..92000188,2	K562	blood:
41	chr13:91931913..91934676-chr13:91949979..91951646,2	K562	blood:
42	chr13:91786654..91787507-chr13:91899493..91900284,2	K562	blood:
43	chr13:91852326..91855280-chr13:92009520..92011626,2	K562	blood:
44	chr11:2326274..2326822-chr13:91904534..91905054,2	MCF-7	breast:
45	chr13:91857551..91859591-chr13:91862399..91864537,2	K562	blood:
46	chr13:91920179..91922847-chr13:92012969..92015159,3	K562	blood:
47	chr13:91901797..91903631-chr13:91908143..91910086,2	K562	blood:
48	chr13:91951723..91953848-chr13:91956197..91958040,2	K562	blood:
49	chr13:91782767..91785374-chr13:91956665..91959107,2	K562	blood:
50	chr13:91851245..91855773-chr13:92007361..92011020,5	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCT-17	chr13:91924335-91924831	NONHSAT034664
2	lnc-GPC5-5	chr13:91903888-91903985	NONHSAT034663
3	lnc-GPC5-5	chr13:91895754-91895794	NONHSAT034663
4	lnc-DCT-6	chr13:91863884-91863952	NONHSAT034661
5	lnc-GPC5-5	chr13:91905839-91906176	NONHSAT034663
6	lnc-DCT-6	chr13:91846268-91846334	NONHSAT034661

No data

Variant related genes	Relation type
PPIAP23	TF binding region
PPIAP23	CpG island
ENSG00000229557	chromatin interactions
ENSG00000234625	chromatin interactions
ENSG00000215417	chromatin interactions
ENSG00000214178	chromatin interactions

Extended variants
information (count: 4451 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4451 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9583893	chr13:91841608-91841609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575981790	chr13:91841648-91841649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564956326	chr13:91841650-91841651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115060790	chr13:91841651-91841652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114100285	chr13:91841689-91841690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115750958	chr13:91841693-91841694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371954772	chr13:91841716-91841717	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs28479243	chr13:91841748-91841749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549617982	chr13:91841780-91841781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567785802	chr13:91841793-91841794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190427378	chr13:91841804-91841805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144473058	chr13:91841829-91841830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114044387	chr13:91841840-91841841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs146672929	chr13:91841845-91841846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374094132	chr13:91841867-91841868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs193010325	chr13:91841869-91841870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs71720353	chr13:91841871-91841872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs75313663	chr13:91841889-91841890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561550685	chr13:91841892-91841893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542080352	chr13:91841912-91841913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144064358	chr13:91841941-91841942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs536174032	chr13:91841948-91841949	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554824331	chr13:91841969-91841970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146452268	chr13:91842035-91842036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540418503	chr13:91842059-91842060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558730622	chr13:91842072-91842073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547194193	chr13:91842079-91842080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577015405	chr13:91842102-91842103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563988309	chr13:91842138-91842139	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371141219	chr13:91842166-91842167	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9301711	chr13:91842186-91842187	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs287530	chr13:91842203-91842204	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs143122205	chr13:91842258-91842259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542979971	chr13:91842259-91842260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561612734	chr13:91842264-91842265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs151186348	chr13:91842297-91842298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185727130	chr13:91842298-91842299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368645589	chr13:91842329-91842330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571463463	chr13:91842348-91842349	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550038271	chr13:91842436-91842437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189036454	chr13:91842469-91842470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140404331	chr13:91842489-91842490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569183458	chr13:91842497-91842498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180948846	chr13:91842549-91842550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554606555	chr13:91842553-91842554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs185421702	chr13:91842617-91842618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575046667	chr13:91842629-91842630	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148005840	chr13:91842667-91842668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534031739	chr13:91842735-91842736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533880644	chr13:91842766-91842767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:91836800-91845000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:91840200-91847000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr13:91840400-91841600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr13:91841600-91842000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr13:91842000-91847000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:91845000-91846000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:91845800-91846000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
8	chr13:91846000-91846400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:91846000-91847800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr13:91846400-91846600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:91846600-91848400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr13:91847000-91848800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr13:91847000-91848800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr13:91847800-91848800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr13:91848000-91848800	Enhancers	Primary hematopoietic stem cells	blood
16	chr13:91848400-91848800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr13:91848800-91856000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr13:91852600-91854000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:91853000-91853400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr13:91853000-91853800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr13:91853800-91854200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr13:91854000-91855400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:91854200-91854400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr13:91854400-91854600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:91854400-91855600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr13:91854600-91854800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:91854600-91855600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr13:91854800-91855400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr13:91855000-91856400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr13:91855000-91856400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr13:91855400-91855600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr13:91855400-91856400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:91855400-91856400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr13:91855400-91856400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr13:91855400-91856600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:91855400-91856600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:91855400-91856800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr13:91855600-91855800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr13:91855600-91856200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr13:91855600-91856400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr13:91855600-91856400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr13:91855600-91856400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr13:91855600-91856400	Enhancers	HepG2	liver
44	chr13:91855600-91856600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr13:91855600-91856600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr13:91855800-91856000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr13:91855800-91859200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr13:91856000-91856200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr13:91856000-91856400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr13:91856000-91857000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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