Variant report

Variant	esv3407458
Chromosome Location	chr13:111357801-111360499
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:732)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111358502-111358688	HepG2	liver:	n/a	n/a
2	ATF2	chr13:111358404-111358906	GM12878	blood:	n/a	n/a
3	BACH1	chr13:111358564-111358921	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:111357933-111358316	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr13:111359273-111359700	GM12878	blood:	n/a	n/a
6	BCL3	chr13:111358321-111358947	GM12878	blood:	n/a	chr13:111358653-111358662
7	BCLAF1	chr13:111358471-111359475	GM12878	blood:	n/a	chr13:111358653-111358662
8	BCLAF1	chr13:111358123-111358873	GM12878	blood:	n/a	chr13:111358653-111358662
9	BHLHE40	chr13:111359523-111359649	K562	blood:	n/a	n/a
10	BHLHE40	chr13:111358088-111359042	K562	blood:	n/a	chr13:111358181-111358197
11	BHLHE40	chr13:111358350-111359050	HepG2	liver:	n/a	n/a
12	BHLHE40	chr13:111358083-111359001	GM12878	blood:	n/a	chr13:111358181-111358197
13	BRCA1	chr13:111357097-111357890	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr13:111358559-111358744	HepG2	liver:	n/a	n/a
15	BRCA1	chr13:111358426-111358827	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr13:111358407-111359006	K562	blood:	n/a	n/a
17	CCNT2	chr13:111358123-111358920	K562	blood:	n/a	n/a
18	CEBPB	chr13:111358060-111358836	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:111356593-111357855	Hela-S3	cervix:	n/a	chr13:111357227-111357238
20	CEBPB	chr13:111357102-111357884	HCT-116	colon:	n/a	chr13:111357227-111357238
21	CEBPB	chr13:111358752-111358816	K562	blood:	n/a	n/a
22	CEBPD	chr13:111358200-111358914	HepG2	liver:	n/a	n/a
23	CEBPD	chr13:111359305-111359625	HepG2	liver:	n/a	n/a
24	CHD1	chr13:111358187-111358261	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr13:111357649-111357949	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr13:111358740-111358941	GM12878	blood:	n/a	n/a
27	CHD2	chr13:111357831-111357840	GM12878	blood:	n/a	n/a
28	CHD2	chr13:111358070-111359069	GM12878	blood:	n/a	n/a
29	CHD2	chr13:111358256-111359009	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr13:111357161-111357837	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr13:111358575-111358963	HepG2	liver:	n/a	n/a
32	CHD2	chr13:111358156-111358874	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr13:111358651-111358913	K562	blood:	n/a	n/a
34	CREB1	chr13:111358236-111359102	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr13:111358182-111359028	A549	lung:	n/a	n/a
36	CREB1	chr13:111358195-111359143	GM12878	blood:	n/a	n/a
37	CREB1	chr13:111357982-111359292	HepG2	liver:	n/a	n/a
38	CTCF	chr13:111358500-111358650	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr13:111358120-111358270	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr13:111358500-111358650	GM12865	blood:	n/a	n/a
41	CTCF	chr13:111358120-111358270	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr13:111358100-111358250	AG09319	gingival:	n/a	n/a
43	CTCF	chr13:111358540-111358690	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr13:111358500-111358650	AG04449	skin:	n/a	n/a
45	CTCF	chr13:111358540-111358690	K562	blood:	n/a	n/a
46	CTCF	chr13:111358540-111358690	GM06990	blood:	n/a	n/a
47	CTCF	chr13:111358540-111358690	BJ	skin:	n/a	n/a
48	CTCF	chr13:111358542-111358637	K562	blood:	n/a	n/a
49	CTCF	chr13:111358500-111358650	GM12867	blood:	n/a	n/a
50	CTCF	chr13:111358100-111358250	HPF	lung:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111358291-111358341	RPTEC	kidney:	n/a
2	chr13:111358527-111358577	HMEC	breast:	n/a
3	chr13:111358522-111358572	HRE	kidney:	n/a
4	chr13:111358291-111358341	Jurkat	blood:	n/a
5	chr13:111358532-111358582	HEEpiC	esophagus:	n/a
6	chr13:111358291-111358341	K562	blood:	n/a
7	chr13:111358862-111358912	HMEC	breast:	n/a
8	chr13:111358552-111358602	HRPEpiC	eye:	n/a
9	chr13:111358803-111358853	T-47D	breast:	n/a
10	chr13:111358552-111358602	AG10803	skin:	n/a
11	chr13:111358291-111358341	SK-N-SH_RA	brain:	n/a
12	chr13:111358924-111358974	HEK293	kidney:	embryo
13	chr13:111358538-111358588	NHDF-neo	bronchial:	n/a
14	chr13:111358552-111358602	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:111358803-111358853	HepG2	liver:	n/a
16	chr13:111358538-111358588	HRPEpiC	eye:	n/a
17	chr13:111358522-111358572	SAEC	small airway:	n/a
18	chr13:111358522-111358572	AG09309	skin:	n/a
19	chr13:111358885-111358935	NB4	blood:	n/a
20	chr13:111357885-111357935	SK-N-MC	brain:	n/a
21	chr13:111358516-111358566	PrEC	prostate:	n/a
22	chr13:111357885-111357935	HCT-116	colon:	n/a
23	chr13:111358552-111358602	H1-hESC	embryonic stem cell:	embryo
24	chr13:111358538-111358588	SAEC	small airway:	n/a
25	chr13:111358291-111358341	SAEC	small airway:	n/a
26	chr13:111358862-111358912	GM12878	blood:	n/a
27	chr13:111358552-111358602	BE2_C	brain:	n/a
28	chr13:111358862-111358912	GM12891	blood:	n/a
29	chr13:111358291-111358341	HCT-116	colon:	n/a
30	chr13:111358522-111358572	NHBE	bronchial:	n/a
31	chr13:111358527-111358577	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:111358522-111358572	K562	blood:	n/a
33	chr13:111358516-111358566	HRPEpiC	eye:	n/a
34	chr13:111358803-111358853	Jurkat	blood:	n/a
35	chr13:111358803-111358853	HPAEpiC	pulmonary alveolar:	n/a
36	chr13:111358527-111358577	RPTEC	kidney:	n/a
37	chr13:111358885-111358935	Caco-2	colon:	n/a
38	chr13:111358552-111358602	SKMC	muscle:	n/a
39	chr13:111358803-111358853	MCF-7	breast:	n/a
40	chr13:111358532-111358582	GM19239	blood:	n/a
41	chr13:111358516-111358566	RPTEC	kidney:	n/a
42	chr13:111358532-111358582	BE2_C	brain:	n/a
43	chr13:111358532-111358582	HCPEpiC	choroid plexus:	n/a
44	chr13:111358803-111358853	K562	blood:	n/a
45	chr13:111358924-111358974	PFSK-1	brain:	n/a
46	chr13:111358538-111358588	HCF	heart:	n/a
47	chr13:111358885-111358935	HL-60	blood:	n/a
48	chr13:111358803-111358853	GM19239	blood:	n/a
49	chr13:111358552-111358602	NT2-D1	testis:	n/a
50	chr13:111358527-111358577	NB4	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:111357509..111359061-chr13:111566329..111568110,2	MCF-7	breast:
2	chr13:111266746..111269387-chr13:111357064..111359748,3	MCF-7	breast:
3	chr1:179718648..179719326-chr13:111357431..111357953,2	Hela-S3	cervix:
4	chr13:111357144..111360099-chr13:111360341..111362234,3	K562	blood:
5	chr12:52444794..52445706-chr13:111357930..111358458,2	Hela-S3	cervix:
6	chr13:111266587..111269692-chr13:111357018..111359356,4	K562	blood:
7	chr13:111358233..111358789-chr17:61904375..61905309,2	HCT-116	colon:

No data

Variant related genes	Relation type
CARS2	TF binding region
ING1	TF binding region
CARS2	CpG island
ING1	CpG island
ENSG00000134905	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000213995	chromatin interactions
ENSG00000087191	chromatin interactions
ENSG00000108592	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371386312	chr13:111357828-111357829	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs376640710	chr13:111357845-111357846	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369920147	chr13:111357849-111357850	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529804222	chr13:111357873-111357874	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553318183	chr13:111357885-111357886	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs201240343	chr13:111357888-111357889	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142620615	chr13:111357890-111357891	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs117788141	chr13:111357899-111357900	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372279480	chr13:111357915-111357916	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563580081	chr13:111357917-111357918	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs45518835	chr13:111357937-111357938	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs575585160	chr13:111357959-111357960	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs542789745	chr13:111357965-111357966	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs561412165	chr13:111357987-111357988	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs9521906	chr13:111358000-111358001	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546757676	chr13:111358018-111358019	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs565249603	chr13:111358071-111358072	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs532622061	chr13:111358074-111358075	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs374137047	chr13:111358174-111358175	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs367992898	chr13:111358193-111358194	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs200731397	chr13:111358198-111358199	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs569593326	chr13:111358207-111358208	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs199874662	chr13:111358263-111358264	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs548824493	chr13:111358272-111358273	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs371950209	chr13:111358319-111358320	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs567317952	chr13:111358340-111358341	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs534818713	chr13:111358377-111358378	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs553156729	chr13:111358468-111358469	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs3818496	chr13:111358488-111358489	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs373969900	chr13:111358518-111358519	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs28364706	chr13:111358521-111358522	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs112057163	chr13:111358527-111358528	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs557205099	chr13:111358537-111358538	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs116446024	chr13:111358583-111358584	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs542979511	chr13:111358588-111358589	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs193149161	chr13:111358637-111358638	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs572961489	chr13:111358642-111358643	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs113853514	chr13:111358690-111358691	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs115357804	chr13:111358701-111358702	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs3809344	chr13:111358705-111358706	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs377669041	chr13:111358773-111358774	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs563165512	chr13:111358774-111358775	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs530438737	chr13:111358792-111358793	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs184431642	chr13:111358826-111358827	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs567252251	chr13:111358838-111358839	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs75609837	chr13:111358863-111358864	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs547915121	chr13:111358914-111358915	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs150980899	chr13:111358949-111358950	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs3840808	chr13:111358969-111358970	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs67927137	chr13:111358971-111358972	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island 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:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111355600-111358000	Weak transcription	Small Intestine	intestine
2	chr13:111355800-111358000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:111355800-111358000	Weak transcription	Gastric	stomach
4	chr13:111356600-111358400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr13:111356600-111358800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr13:111356800-111358800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr13:111357000-111358000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr13:111357000-111358000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr13:111357000-111358200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr13:111357200-111358000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:111357200-111358000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr13:111357200-111358000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr13:111357200-111358000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr13:111357200-111358000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr13:111357200-111358000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr13:111357200-111358000	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr13:111357200-111358000	Enhancers	Placenta Amnion	Placenta Amnion
18	chr13:111357200-111358000	Flanking Active TSS	Dnd41	blood
19	chr13:111357200-111358000	Flanking Active TSS	HUVEC	blood vessel
20	chr13:111357200-111358000	Flanking Active TSS	NH-A	brain
21	chr13:111357200-111358000	Flanking Active TSS	Osteobl	bone
22	chr13:111357200-111358200	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr13:111357200-111358200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr13:111357200-111358200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr13:111357200-111358200	Flanking Active TSS	Fetal Brain Female	brain
26	chr13:111357200-111358800	Active TSS	H9 Cell Line	embryonic stem cell
27	chr13:111357200-111358800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:111357200-111358800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:111357200-111358800	Active TSS	NHDF-Ad	bronchial
30	chr13:111357200-111359000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:111357200-111359400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:111357400-111358000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr13:111357400-111358000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr13:111357400-111358000	Flanking Active TSS	Primary B cells from peripheral blood	blood
35	chr13:111357400-111358000	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr13:111357400-111358000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr13:111357400-111358000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr13:111357400-111358000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr13:111357400-111358000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr13:111357400-111358000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr13:111357400-111358000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr13:111357400-111358000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr13:111357400-111358000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr13:111357400-111358000	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr13:111357400-111358000	Flanking Active TSS	Brain Angular Gyrus	brain
46	chr13:111357400-111358000	Flanking Active TSS	Brain Anterior Caudate	brain
47	chr13:111357400-111358000	Flanking Active TSS	Brain Germinal Matrix	brain
48	chr13:111357400-111358000	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr13:111357400-111358000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr13:111357400-111358000	Flanking Active TSS	Fetal Heart	heart

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