Variant report

Variant	esv3433497
Chromosome Location	chr13:29786122-29917797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:427)
Chromatin interactive
region (count:15)
LncRNA
region (count:52)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:29869040-29869359	K562	blood:	n/a	n/a
2	BACH1	chr13:29869093-29869336	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr13:29875197-29875418	H1-hESC	embryonic stem cell:	n/a	chr13:29875277-29875286
4	CEBPB	chr13:29853177-29853484	HepG2	liver:	n/a	chr13:29853320-29853331
5	CEBPB	chr13:29876299-29876537	HepG2	liver:	n/a	chr13:29876434-29876445
6	CEBPB	chr13:29825553-29825702	IMR90	lung:	n/a	chr13:29825627-29825638
7	CEBPB	chr13:29801819-29802072	Hela-S3	cervix:	n/a	chr13:29801920-29801933 chr13:29801920-29801933
8	CEBPB	chr13:29825486-29825750	HepG2	liver:	n/a	chr13:29825627-29825638
9	CEBPB	chr13:29853279-29853480	K562	blood:	n/a	chr13:29853320-29853331
10	CEBPB	chr13:29876276-29876558	H1-hESC	embryonic stem cell:	n/a	chr13:29876434-29876445
11	CEBPB	chr13:29891975-29892179	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:29853176-29853424	IMR90	lung:	n/a	chr13:29853320-29853331
13	CEBPB	chr13:29840324-29840517	K562	blood:	n/a	n/a
14	CEBPB	chr13:29824577-29824694	A549	lung:	n/a	n/a
15	CHD2	chr13:29875276-29875541	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr13:29875174-29875584	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr13:29916807-29916836	LNCaP	prostate:	n/a	n/a
18	CTCF	chr13:29789898-29789997	K562	blood:	n/a	n/a
19	CTCF	chr13:29840592-29840623	Medullo	brain:	n/a	n/a
20	CTCF	chr13:29834080-29834230	Caco-2	colon:	n/a	n/a
21	CTCF	chr13:29840520-29840670	HRE	kidney:	n/a	n/a
22	CTCF	chr13:29834982-29835093	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr13:29858834-29859250	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:29858980-29859130	NHEK	skin:	n/a	n/a
25	CTCF	chr13:29834920-29835070	GM12866	blood:	n/a	n/a
26	CTCF	chr13:29858858-29859178	MCF-7	breast:	n/a	n/a
27	CTCF	chr13:29834960-29835110	AG04449	skin:	n/a	n/a
28	CTCF	chr13:29840581-29840623	GM10266	blood:	n/a	n/a
29	CTCF	chr13:29859014-29859113	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr13:29834856-29835104	GM12878	blood:	n/a	n/a
31	CTCF	chr13:29911135-29911161	GM13977	blood:	n/a	n/a
32	CTCF	chr13:29858990-29859118	LNCaP	prostate:	n/a	n/a
33	CTCF	chr13:29789877-29790003	MCF-7	breast:	n/a	n/a
34	CTCF	chr13:29834949-29835116	ProgFib	skin:	n/a	n/a
35	CTCF	chr13:29858940-29859090	HCT-116	colon:	n/a	n/a
36	CTCF	chr13:29880282-29880338	LNCaP	prostate:	n/a	n/a
37	CTCF	chr13:29893745-29893868	Fibrobl	skin:	n/a	n/a
38	CTCF	chr13:29834940-29835090	RPTEC	kidney:	n/a	n/a
39	CTCF	chr13:29858945-29859171	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:29840600-29840750	BE2_C	brain:	n/a	n/a
41	CTCF	chr13:29893672-29893910	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr13:29835000-29835150	GM12864	blood:	n/a	n/a
43	CTCF	chr13:29834844-29835202	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr13:29834920-29835070	GM12871	blood:	n/a	n/a
45	CTCF	chr13:29893760-29893910	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr13:29840607-29840629	HepG2	liver:	n/a	n/a
47	CTCF	chr13:29834931-29835130	MCF-7	breast:	n/a	n/a
48	CTCF	chr13:29858960-29859110	BE2_C	brain:	n/a	n/a
49	CTCF	chr13:29834900-29835050	GM12875	blood:	n/a	n/a
50	CTCF	chr13:29790106-29790165	Lung_OC	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:29914097-29914147	HAEpiC	amniotic membrane:	n/a
2	chr13:29913347-29913397	Hela-S3	cervix:	n/a
3	chr13:29910801-29910851	HMEC	breast:	n/a
4	chr13:29910801-29910851	SAEC	small airway:	n/a
5	chr13:29916117-29916167	ovcar-3	ovarian:	n/a
6	chr13:29914097-29914147	AG04450	lung:	fetal
7	chr13:29914097-29914147	HUVEC	blood vessel:	n/a
8	chr13:29913347-29913397	PrEC	prostate:	n/a
9	chr13:29910801-29910851	AG10803	skin:	n/a
10	chr13:29875027-29875077	HIPEpiC	eye:	n/a
11	chr13:29914200-29914250	PANC-1	pancreas:	n/a
12	chr13:29914200-29914250	GM06990	blood:	n/a
13	chr13:29875027-29875077	NHDF-neo	bronchial:	n/a
14	chr13:29913347-29913397	PFSK-1	brain:	n/a
15	chr13:29916117-29916167	PrEC	prostate:	n/a
16	chr13:29914097-29914147	HIPEpiC	eye:	n/a
17	chr13:29913347-29913397	HepG2	liver:	n/a
18	chr13:29913935-29913985	HAEpiC	amniotic membrane:	n/a
19	chr13:29910801-29910851	RPTEC	kidney:	n/a
20	chr13:29916117-29916167	SKMC	muscle:	n/a
21	chr13:29875027-29875077	AG09309	skin:	n/a
22	chr13:29875027-29875077	SAEC	small airway:	n/a
23	chr13:29913347-29913397	MCF10A-Er-Src	breast:	n/a
24	chr13:29914097-29914147	NB4	blood:	n/a
25	chr13:29914097-29914147	Hela-S3	cervix:	n/a
26	chr13:29914200-29914250	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:29913347-29913397	HL-60	blood:	n/a
28	chr13:29914097-29914147	K562	blood:	n/a
29	chr13:29916117-29916167	AG09309	skin:	n/a
30	chr13:29916117-29916167	Hela-S3	cervix:	n/a
31	chr13:29910801-29910851	PrEC	prostate:	n/a
32	chr13:29913935-29913985	IMR90	lung:	fetal
33	chr13:29916117-29916167	BE2_C	brain:	n/a
34	chr13:29916117-29916167	HIPEpiC	eye:	n/a
35	chr13:29913347-29913397	BE2_C	brain:	n/a
36	chr13:29875027-29875077	GM12891	blood:	n/a
37	chr13:29913347-29913397	NT2-D1	testis:	n/a
38	chr13:29916117-29916167	HNPCEpiC	eye:	n/a
39	chr13:29913347-29913397	Hepatocyte	liver:	n/a
40	chr13:29875027-29875077	PFSK-1	brain:	n/a
41	chr13:29875027-29875077	SKMC	muscle:	n/a
42	chr13:29914097-29914147	MCF10A-Er-Src	breast:	n/a
43	chr13:29913347-29913397	NH-A	brain:	n/a
44	chr13:29875027-29875077	AG10803	skin:	n/a
45	chr13:29913347-29913397	NB4	blood:	n/a
46	chr13:29913935-29913985	GM12878	blood:	n/a
47	chr13:29913347-29913397	Jurkat	blood:	n/a
48	chr13:29914200-29914250	MCF-7	breast:	n/a
49	chr13:29914097-29914147	Hepatocyte	liver:	n/a
50	chr13:29914097-29914147	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:29754593..29756935-chr13:29798508..29800857,2	K562	blood:
2	chr13:29890625..29892336-chr13:29895861..29897875,2	K562	blood:
3	chr13:29858534..29859475-chr13:29937067..29937809,7	MCF-7	breast:
4	chr13:29798482..29800939-chr13:29808529..29811047,2	MCF-7	breast:
5	chr13:29888475..29891043-chr13:29899150..29901551,2	MCF-7	breast:
6	chr13:29858426..29859109-chr13:29936606..29937542,4	MCF-7	breast:
7	chr13:29858379..29859549-chr13:29943302..29943872,3	MCF-7	breast:
8	chr13:29379087..29379680-chr13:29834729..29835443,3	MCF-7	breast:
9	chr13:29834619..29835251-chr3:64307275..64308025,2	MCF-7	breast:
10	chr13:29785961..29788916-chr13:29921659..29923397,2	MCF-7	breast:
11	chr13:29888475..29891043-chr13:29899150..29901551,2	MCF-7	breast:
12	chr13:29798482..29800939-chr13:29808529..29811047,2	MCF-7	breast:
13	chr13:29890625..29892336-chr13:29895861..29897875,2	K562	blood:
14	chr13:29844261..29845821-chr9:131938747..131941105,2	MCF-7	breast:
15	chr13:29654983..29655766-chr13:29834963..29835491,2	MCF-7	breast:

(count:52 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC7A1-2	chr13:29842609-29842662	NONHSAT032728
2	lnc-SLC7A1-2	chr13:29835313-29835363	NONHSAT032727
3	lnc-SLC7A1-2	chr13:29844422-29844511	NONHSAT032719
4	lnc-SLC7A1-2	chr13:29812407-29813605	NONHSAT032719
5	lnc-SLC7A1-2	chr13:29812418-29813605	ucscGeneNc_uc001usu_1
6	lnc-SLC7A1-2	chr13:29814597-29815023	NONHSAT032724
7	lnc-SLC7A1-2	chr13:29835298-29835363	NONHSAT032724
8	lnc-SLC7A1-2	chr13:29844422-29844511	NONHSAT032726
9	lnc-SLC7A1-2	chr13:29835298-29835363	NONHSAT032725
10	lnc-SLC7A1-2	chr13:29830391-29830513	NONHSAT032725
11	lnc-SLC7A1-2	chr13:29844422-29844511	NONHSAT032727
12	lnc-SLC7A1-2	chr13:29824552-29824691	ENSG00000236758.1
13	lnc-SLC7A1-2	chr13:29835298-29835363	NONHSAT032719
14	lnc-SLC7A1-2	chr13:29839738-29839854	ucscGeneNc_uc001usu_1
15	lnc-SLC7A1-2	chr13:29836206-29836333	NONHSAT032725
16	lnc-SLC7A1-2	chr13:29848964-29849282	NONHSAT032726
17	lnc-SLC7A1-8	chr13:29788497-29788771	NONHSAT032717
18	lnc-SLC7A1-2	chr13:29829879-29830026	NONHSAT032726
19	lnc-SLC7A1-2	chr13:29846140-29846230	NONHSAT032729
20	lnc-SLC7A1-6	chr13:29894354-29894374	NONHSAT032730
21	lnc-SLC7A1-2	chr13:29824552-29824691	ENSG00000236758.1
22	lnc-SLC7A1-2	chr13:29830391-29830513	NONHSAT032726
23	lnc-SLC7A1-2	chr13:29847604-29847913	NONHSAT032729
24	lnc-SLC7A1-2	chr13:29813760-29814095	ENSG00000236758.1
25	lnc-SLC7A1-2	chr13:29813516-29814095	ENSG00000236758.1
26	lnc-SLC7A1-2	chr13:29816666-29816835	ENSG00000236758.1
27	lnc-SLC7A1-2	chr13:29844959-29845169	NONHSAT032727
28	lnc-SLC7A1-2	chr13:29847604-29847913	NONHSAT032726
29	lnc-SLC7A1-2	chr13:29848964-29849101	NONHSAT032729
30	lnc-SLC7A1-2	chr13:29813924-29814264	ENSG00000236758.1
31	lnc-SLC7A1-6	chr13:29891656-29892082	NONHSAT032730
32	lnc-SLC7A1-2	chr13:29816666-29816835	ENSG00000236758.1
33	lnc-SLC7A1-2	chr13:29830391-29830513	NONHSAT032724
34	lnc-SLC7A1-2	chr13:29844422-29844511	ucscGeneNc_uc001usu_1
35	lnc-SLC7A1-2	chr13:29845920-29846051	NONHSAT032728
36	lnc-SLC7A1-2	chr13:29835298-29835363	NONHSAT032726
37	lnc-SLC7A1-2	chr13:29836206-29836342	NONHSAT032720
38	lnc-SLC7A1-2	chr13:29839738-29839804	NONHSAT032720
39	lnc-SLC7A1-2	chr13:29845920-29846036	ucscGeneNc_uc001usu_1
40	lnc-SLC7A1-2	chr13:29839738-29839854	NONHSAT032719
41	lnc-SLC7A1-2	chr13:29844422-29844511	NONHSAT032728
42	lnc-SLC7A1-8	chr13:29791886-29792040	NONHSAT032717
43	lnc-SLC7A1-2	chr13:29845920-29846036	NONHSAT032719
44	lnc-SLC7A1-2	chr13:29829402-29829529	NONHSAT032725
45	lnc-SLC7A1-2	chr13:29835298-29835363	NONHSAT032720
46	lnc-SLC7A1-2	chr13:29837607-29837898	NONHSAT032724
47	lnc-SLC7A1-2	chr13:29836206-29836342	NONHSAT032724
48	lnc-SLC7A1-2	chr13:29829879-29830026	NONHSAT032725
49	lnc-SLC7A1-2	chr13:29813496-29813733	NONHSAT032720
50	lnc-SLC7A1-2	chr13:29839738-29839854	NONHSAT032727

No data

Variant related genes	Relation type
ENSG00000270680	TF binding region
GAPDHP69	TF binding region
MTUS2-AS2	TF binding region
ENSG00000221670	TF binding region
ENSG00000270680	CpG island
GAPDHP69	CpG island
MTUS2-AS2	CpG island
ENSG00000221670	CpG island
ENSG00000204055	chromatin interactions
ENSG00000188483	chromatin interactions

Extended variants
information (count: 4815 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4815 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549477393	chr13:29786123-29786124	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs181129785	chr13:29786128-29786129	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551886598	chr13:29786138-29786139	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs914261	chr13:29786142-29786143	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs551762911	chr13:29786143-29786144	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs571941608	chr13:29786191-29786192	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs185715412	chr13:29786192-29786193	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs190627648	chr13:29786260-29786261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9551624	chr13:29786270-29786271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9314940	chr13:29786291-29786292	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs574085268	chr13:29786313-29786314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576386934	chr13:29786377-29786378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571660138	chr13:29786426-29786427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148432103	chr13:29786457-29786458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536704557	chr13:29786477-29786478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9550450	chr13:29786486-29786487	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs201848991	chr13:29786499-29786500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200385126	chr13:29786503-29786504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146685780	chr13:29786520-29786521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545223537	chr13:29786542-29786543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376086367	chr13:29786613-29786614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7995580	chr13:29786615-29786616	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572353598	chr13:29786629-29786630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540932338	chr13:29786634-29786635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369189211	chr13:29786643-29786644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111341440	chr13:29786696-29786697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377294666	chr13:29786704-29786705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142789543	chr13:29786733-29786734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569859783	chr13:29786754-29786755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563422921	chr13:29786762-29786763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531793589	chr13:29786783-29786784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117575661	chr13:29786807-29786808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116968196	chr13:29786813-29786814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551989789	chr13:29786834-29786835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571842164	chr13:29786858-29786859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7997357	chr13:29786888-29786889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548117122	chr13:29786915-29786916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147408904	chr13:29786927-29786928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140773236	chr13:29786929-29786930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs74463745	chr13:29786941-29786942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150863090	chr13:29786965-29786966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6490370	chr13:29786977-29786978	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538454235	chr13:29786993-29786994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558672369	chr13:29786999-29787000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7339092	chr13:29787017-29787018	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs540895555	chr13:29787024-29787025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11619729	chr13:29787033-29787034	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569678006	chr13:29787046-29787047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371239121	chr13:29787083-29787084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7337727	chr13:29787121-29787122	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29785800-29786200	Flanking Active TSS	Dnd41	blood
2	chr13:29786200-29787600	Enhancers	Dnd41	blood
3	chr13:29794600-29794800	Enhancers	Aorta	Aorta
4	chr13:29794800-29797400	Weak transcription	Aorta	Aorta
5	chr13:29795000-29795600	Enhancers	Fetal Heart	heart
6	chr13:29795600-29797600	Weak transcription	Fetal Heart	heart
7	chr13:29796600-29797000	Enhancers	Fetal Muscle Trunk	muscle
8	chr13:29796600-29798200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:29796600-29798400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:29796800-29798400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr13:29796800-29798400	ZNF genes & repeats	Dnd41	blood
12	chr13:29797000-29797200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr13:29797000-29797800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
14	chr13:29797000-29798400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
15	chr13:29797200-29798200	ZNF genes & repeats	Liver	Liver
16	chr13:29797200-29798200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
17	chr13:29797400-29798200	ZNF genes & repeats	Brain Anterior Caudate	brain
18	chr13:29797400-29798400	ZNF genes & repeats	Aorta	Aorta
19	chr13:29797600-29798000	Active TSS	Colon Smooth Muscle	Colon
20	chr13:29797600-29798200	ZNF genes & repeats	Fetal Heart	heart
21	chr13:29797600-29798200	ZNF genes & repeats	Fetal Stomach	stomach
22	chr13:29798000-29798200	Flanking Active TSS	Colon Smooth Muscle	Colon
23	chr13:29798000-29799400	Enhancers	Rectal Smooth Muscle	rectum
24	chr13:29798000-29799400	Enhancers	Stomach Smooth Muscle	stomach
25	chr13:29798200-29799000	Enhancers	Colon Smooth Muscle	Colon
26	chr13:29798200-29799000	Weak transcription	Fetal Heart	heart
27	chr13:29798200-29799000	Weak transcription	Fetal Muscle Trunk	muscle
28	chr13:29798200-29801000	Weak transcription	Fetal Stomach	stomach
29	chr13:29798400-29799000	Weak transcription	Aorta	Aorta
30	chr13:29798400-29806800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr13:29799000-29799200	Enhancers	Aorta	Aorta
32	chr13:29799000-29799200	Flanking Active TSS	Colon Smooth Muscle	Colon
33	chr13:29799000-29799200	Enhancers	Fetal Heart	heart
34	chr13:29799000-29799400	Enhancers	Fetal Muscle Trunk	muscle
35	chr13:29799200-29799400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr13:29799200-29799400	Genic enhancers	Aorta	Aorta
37	chr13:29799200-29799400	Enhancers	Colon Smooth Muscle	Colon
38	chr13:29799200-29799600	Weak transcription	Fetal Heart	heart
39	chr13:29799400-29800000	Weak transcription	Fetal Muscle Trunk	muscle
40	chr13:29799400-29801000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr13:29799400-29801400	Weak transcription	Colon Smooth Muscle	Colon
42	chr13:29799400-29801600	Weak transcription	Stomach Smooth Muscle	stomach
43	chr13:29799400-29807400	Weak transcription	Aorta	Aorta
44	chr13:29799600-29800400	Enhancers	Fetal Heart	heart
45	chr13:29800400-29800800	Weak transcription	Fetal Heart	heart
46	chr13:29800800-29803200	Enhancers	Fetal Heart	heart
47	chr13:29801000-29801200	Enhancers	Fetal Muscle Trunk	muscle
48	chr13:29801000-29801800	Enhancers	Fetal Muscle Leg	muscle
49	chr13:29801000-29802400	Enhancers	Fetal Stomach	stomach
50	chr13:29801000-29802600	Enhancers	Rectal Smooth Muscle	rectum

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