Variant report

Variant	nsv563128
Chromosome Location	chr13:111328765-111330368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:111328300-111329671	GM12878	blood:	n/a	n/a
2	ATF2	chr13:111328388-111328778	GM12878	blood:	n/a	n/a
3	BATF	chr13:111329690-111330085	GM12878	blood:	n/a	n/a
4	BATF	chr13:111328517-111328988	GM12878	blood:	n/a	n/a
5	BCL11A	chr13:111329451-111330173	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:111328428-111328936	GM12878	blood:	n/a	n/a
7	BCL3	chr13:111328387-111328879	GM12878	blood:	n/a	n/a
8	BCLAF1	chr13:111328295-111329322	GM12878	blood:	n/a	n/a
9	BCLAF1	chr13:111328372-111329520	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:111328344-111329778	GM12878	blood:	n/a	chr13:111328790-111328806 chr13:111328782-111328798
11	BRCA1	chr13:111328583-111329166	GM12878	blood:	n/a	n/a
12	CHD1	chr13:111328530-111329169	GM12878	blood:	n/a	n/a
13	CHD2	chr13:111328434-111329393	GM12878	blood:	n/a	n/a
14	CREB1	chr13:111328407-111329638	GM12878	blood:	n/a	n/a
15	CTCF	chr13:111328920-111329070	GM12873	blood:	n/a	n/a
16	CTCF	chr13:111328980-111329130	GM12873	blood:	n/a	n/a
17	CTCF	chr13:111328990-111329160	GM12878	blood:	n/a	n/a
18	CTCF	chr13:111328920-111329070	GM12872	blood:	n/a	n/a
19	CTCF	chr13:111328960-111329110	GM12870	blood:	n/a	n/a
20	CTCF	chr13:111330294-111330378	H1-hESC	embryonic stem cell:	n/a	chr13:111330308-111330326
21	CTCF	chr13:111328680-111328830	GM12878	blood:	n/a	n/a
22	CTCF	chr13:111328860-111329010	GM12873	blood:	n/a	n/a
23	CTCF	chr13:111328880-111329030	GM12869	blood:	n/a	n/a
24	CTCF	chr13:111329000-111329150	GM12866	blood:	n/a	n/a
25	CTCF	chr13:111328920-111329070	GM12865	blood:	n/a	n/a
26	CTCF	chr13:111328940-111329090	GM12869	blood:	n/a	n/a
27	CTCF	chr13:111328960-111329110	GM12865	blood:	n/a	n/a
28	CTCF	chr13:111329000-111329150	GM12872	blood:	n/a	n/a
29	CTCF	chr13:111328940-111329090	GM12864	blood:	n/a	n/a
30	CTCF	chr13:111328920-111329070	GM12868	blood:	n/a	n/a
31	CTCF	chr13:111329160-111329310	GM12870	blood:	n/a	chr13:111329271-111329280
32	CTCF	chr13:111328940-111329090	GM12874	blood:	n/a	n/a
33	CTCF	chr13:111329040-111329190	GM12875	blood:	n/a	n/a
34	CTCF	chr13:111328920-111329070	GM12875	blood:	n/a	n/a
35	CTCF	chr13:111330260-111330410	AG09309	skin:	n/a	chr13:111330308-111330326
36	CTCF	chr13:111328960-111329110	GM12868	blood:	n/a	n/a
37	CTCF	chr13:111328980-111329130	GM12878	blood:	n/a	n/a
38	CTCF	chr13:111328820-111328970	GM12867	blood:	n/a	n/a
39	CTCF	chr13:111330240-111330390	AG09309	skin:	n/a	chr13:111330308-111330326
40	CTCF	chr13:111328640-111328790	GM12872	blood:	n/a	n/a
41	CTCF	chr13:111328900-111329050	GM12864	blood:	n/a	n/a
42	CTCF	chr13:111328880-111329030	GM12872	blood:	n/a	n/a
43	CTCF	chr13:111328960-111329110	GM12878	blood:	n/a	n/a
44	CUX1	chr13:111328580-111329471	GM12878	blood:	n/a	n/a
45	EBF1	chr13:111328352-111329629	GM12878	blood:	n/a	chr13:111329363-111329374 chr13:111329386-111329397
46	EBF1	chr13:111328357-111329570	GM12878	blood:	n/a	chr13:111329363-111329374 chr13:111329386-111329397
47	EBF1	chr13:111329597-111330195	GM12878	blood:	n/a	n/a
48	EBF1	chr13:111328354-111329649	GM12878	blood:	n/a	chr13:111329363-111329374 chr13:111329386-111329397
49	EBF1	chr13:111329657-111330177	GM12878	blood:	n/a	n/a
50	EGR1	chr13:111328648-111328878	GM12878	blood:	n/a	chr13:111328774-111328788 chr13:111328776-111328786 chr13:111328773-111328786

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111329221-111329271	AG04449	skin:	fetal
2	chr13:111329221-111329271	AoSMC	blood vessel:	n/a
3	chr13:111328783-111328833	HepG2	liver:	n/a
4	chr13:111329221-111329271	HCM	heart:	n/a
5	chr13:111329221-111329271	ovcar-3	ovarian:	n/a
6	chr13:111328783-111328833	SK-N-SH_RA	brain:	n/a
7	chr13:111329221-111329271	MCF10A-Er-Src	breast:	n/a
8	chr13:111329221-111329271	GM12891	blood:	n/a
9	chr13:111328783-111328833	CMK	blood:	n/a
10	chr13:111328783-111328833	HRPEpiC	eye:	n/a
11	chr13:111328783-111328833	MCF10A-Er-Src	breast:	n/a
12	chr13:111329221-111329271	MCF-7	breast:	n/a
13	chr13:111329221-111329271	Hela-S3	cervix:	n/a
14	chr13:111329221-111329271	ECC-1	luminal epithelium:	n/a
15	chr13:111328783-111328833	Jurkat	blood:	n/a
16	chr13:111328783-111328833	ProgFib	skin:	n/a
17	chr13:111328783-111328833	PrEC	prostate:	n/a
18	chr13:111329221-111329271	LNCaP	prostate:	n/a
19	chr13:111329221-111329271	CMK	blood:	n/a
20	chr13:111328783-111328833	K562	blood:	n/a
21	chr13:111328783-111328833	SK-N-MC	brain:	n/a
22	chr13:111328783-111328833	GM12891	blood:	n/a
23	chr13:111329221-111329271	PrEC	prostate:	n/a
24	chr13:111329221-111329271	HEK293	kidney:	embryo
25	chr13:111329221-111329271	RPTEC	kidney:	n/a
26	chr13:111329221-111329271	GM19239	blood:	n/a
27	chr13:111328783-111328833	GM12892	blood:	n/a
28	chr13:111329221-111329271	HIPEpiC	eye:	n/a
29	chr13:111329221-111329271	NT2-D1	testis:	n/a
30	chr13:111328783-111328833	HCF	heart:	n/a
31	chr13:111329221-111329271	HCT-116	colon:	n/a
32	chr13:111328783-111328833	H1-hESC	embryonic stem cell:	embryo
33	chr13:111328783-111328833	HCM	heart:	n/a
34	chr13:111329221-111329271	AG04450	lung:	fetal
35	chr13:111328783-111328833	SAEC	small airway:	n/a
36	chr13:111329221-111329271	HL-60	blood:	n/a
37	chr13:111329221-111329271	HAEpiC	amniotic membrane:	n/a
38	chr13:111328783-111328833	ECC-1	luminal epithelium:	n/a
39	chr13:111329221-111329271	NHBE	bronchial:	n/a
40	chr13:111328783-111328833	T-47D	breast:	n/a
41	chr13:111328783-111328833	GM19239	blood:	n/a
42	chr13:111329221-111329271	Jurkat	blood:	n/a
43	chr13:111328783-111328833	PANC-1	pancreas:	n/a
44	chr13:111329221-111329271	HNPCEpiC	eye:	n/a
45	chr13:111329221-111329271	GM06990	blood:	n/a
46	chr13:111329221-111329271	ProgFib	skin:	n/a
47	chr13:111328783-111328833	A549	lung:	n/a
48	chr13:111328783-111328833	Hepatocyte	liver:	n/a
49	chr13:111328783-111328833	NB4	blood:	n/a
50	chr13:111329221-111329271	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:111328800..111330834-chr13:111364440..111366788,2	K562	blood:
2	chr13:111328800..111332502-chr13:111363272..111367932,6	K562	blood:

No data

Variant related genes	Relation type
CARS2	TF binding region
CARS2	CpG island
ENSG00000153487	chromatin interactions
ENSG00000134905	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2296654	chr13:111328765-111328766	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543403665	chr13:111328778-111328779	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs375198580	chr13:111328821-111328822	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs562244534	chr13:111328847-111328848	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147835903	chr13:111328878-111328879	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs541635768	chr13:111328927-111328928	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs552327634	chr13:111328954-111328955	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560478630	chr13:111328972-111328973	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559657986	chr13:111328979-111328980	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533679147	chr13:111328982-111328983	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568853593	chr13:111329004-111329005	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368265252	chr13:111329012-111329013	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369931168	chr13:111329027-111329028	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs193013297	chr13:111329039-111329040	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201825083	chr13:111329083-111329084	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531372127	chr13:111329088-111329089	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs73616053	chr13:111329090-111329091	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs74125030	chr13:111329099-111329100	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs59788073	chr13:111329119-111329120	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs139643538	chr13:111329161-111329162	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs3215828	chr13:111329200-111329201	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs74125031	chr13:111329214-111329215	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371196794	chr13:111329306-111329307	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374751888	chr13:111329325-111329326	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145315422	chr13:111329326-111329327	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369056410	chr13:111329344-111329345	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149601283	chr13:111329353-111329354	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs557671802	chr13:111329354-111329355	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs575915087	chr13:111329355-111329356	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs144283051	chr13:111329361-111329362	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs372177940	chr13:111329367-111329368	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs140056876	chr13:111329389-111329390	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs143818816	chr13:111329404-111329405	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537075451	chr13:111329422-111329423	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs199589765	chr13:111329435-111329436	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201064390	chr13:111329444-111329445	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs375938059	chr13:111329449-111329450	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs541127961	chr13:111329450-111329451	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs559902282	chr13:111329465-111329466	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs578236157	chr13:111329470-111329471	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369686025	chr13:111329471-111329472	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs545607309	chr13:111329475-111329476	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs200627513	chr13:111329486-111329487	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs562781182	chr13:111329504-111329505	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs185147145	chr13:111329514-111329515	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs189085438	chr13:111329529-111329530	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs113622654	chr13:111329579-111329580	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs74125032	chr13:111329589-111329590	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs56131494	chr13:111329596-111329597	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs76103038	chr13:111329610-111329611	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	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
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111297800-111336400	Weak transcription	Small Intestine	intestine
2	chr13:111302200-111351400	Weak transcription	Stomach Mucosa	stomach
3	chr13:111310800-111352200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr13:111311600-111352000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr13:111312800-111357400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr13:111316200-111330600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr13:111316600-111332800	Weak transcription	K562	blood
8	chr13:111319400-111337600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr13:111319800-111348400	Weak transcription	Fetal Brain Male	brain
10	chr13:111319800-111354600	Weak transcription	Fetal Heart	heart
11	chr13:111320200-111339200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr13:111321800-111328800	Weak transcription	Hela-S3	cervix
13	chr13:111321800-111332800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:111322000-111330000	Weak transcription	NHDF-Ad	bronchial
15	chr13:111322800-111333800	Weak transcription	Fetal Kidney	kidney
16	chr13:111322800-111349600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr13:111327600-111329600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr13:111327800-111329400	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr13:111327800-111331400	Strong transcription	Colonic Mucosa	Colon
20	chr13:111327800-111336000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr13:111327800-111344200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr13:111327800-111347400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr13:111327800-111355000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr13:111328000-111328800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:111328000-111328800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr13:111328000-111328800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr13:111328000-111328800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr13:111328000-111328800	ZNF genes & repeats	Esophagus	oesophagus
29	chr13:111328000-111328800	ZNF genes & repeats	Fetal Thymus	thymus
30	chr13:111328000-111329000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
31	chr13:111328000-111329000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr13:111328000-111329000	ZNF genes & repeats	Fetal Stomach	stomach
33	chr13:111328000-111329200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr13:111328000-111329200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr13:111328000-111329200	Strong transcription	Primary hematopoietic stem cells	blood
36	chr13:111328000-111329200	Strong transcription	Brain Angular Gyrus	brain
37	chr13:111328000-111329200	Strong transcription	Brain Hippocampus Middle	brain
38	chr13:111328000-111329200	Strong transcription	Colon Smooth Muscle	Colon
39	chr13:111328000-111329200	Strong transcription	A549	lung
40	chr13:111328000-111329200	Strong transcription	NH-A	brain
41	chr13:111328000-111329400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
42	chr13:111328000-111329400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr13:111328000-111329400	Flanking Active TSS	GM12878-XiMat	blood
44	chr13:111328000-111329400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr13:111328000-111329600	Strong transcription	Brain Anterior Caudate	brain
46	chr13:111328000-111330400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr13:111328000-111331000	Strong transcription	Fetal Lung	lung
48	chr13:111328000-111331200	Strong transcription	Fetal Muscle Trunk	muscle
49	chr13:111328000-111331600	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr13:111328000-111331800	Strong transcription	Brain Inferior Temporal Lobe	brain

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