Variant report

Variant	esv3375906
Chromosome Location	chr8:52810224-52812772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:644)
CpG islands
(count:549)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:52811680-52812095	GM12878	blood:	n/a	n/a
2	ATF2	chr8:52810669-52811095	GM12878	blood:	n/a	n/a
3	ATF2	chr8:52810776-52811229	GM12878	blood:	n/a	n/a
4	ATF2	chr8:52811380-52812241	GM12878	blood:	n/a	n/a
5	BACH1	chr8:52811342-52812397	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:52810415-52810596	K562	blood:	n/a	n/a
7	BATF	chr8:52810439-52810652	GM12878	blood:	n/a	n/a
8	BCL3	chr8:52811615-52812168	A549	lung:	n/a	chr8:52811769-52811778 chr8:52811648-52811661
9	BCLAF1	chr8:52811668-52812318	GM12878	blood:	n/a	chr8:52811769-52811778
10	BCLAF1	chr8:52810667-52811137	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:52810988-52811132	K562	blood:	n/a	n/a
12	BHLHE40	chr8:52811495-52812309	K562	blood:	n/a	chr8:52811532-52811548 chr8:52811540-52811556
13	BHLHE40	chr8:52810304-52811181	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:52811502-52812425	GM12878	blood:	n/a	chr8:52811532-52811548 chr8:52811540-52811556
15	BRCA1	chr8:52811530-52812087	GM12878	blood:	n/a	chr8:52811835-52811844
16	BRCA1	chr8:52811573-52812137	HepG2	liver:	n/a	chr8:52811835-52811844
17	BRCA1	chr8:52811581-52812830	Hela-S3	cervix:	n/a	chr8:52811835-52811844
18	BRCA1	chr8:52811602-52812208	H1-hESC	embryonic stem cell:	n/a	chr8:52811835-52811844
19	BRCA1	chr8:52809731-52811193	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr8:52811496-52812130	K562	blood:	n/a	n/a
21	CCNT2	chr8:52810916-52812365	K562	blood:	n/a	chr8:52811200-52811209 chr8:52811749-52811758
22	CCNT2	chr8:52810266-52810558	K562	blood:	n/a	n/a
23	CEBPB	chr8:52809770-52810861	K562	blood:	n/a	chr8:52810819-52810830 chr8:52810155-52810168 chr8:52810819-52810830
24	CEBPB	chr8:52809704-52810774	IMR90	lung:	n/a	chr8:52810155-52810168
25	CEBPB	chr8:52809687-52811166	Hela-S3	cervix:	n/a	chr8:52810819-52810830 chr8:52810155-52810168 chr8:52810819-52810830
26	CEBPB	chr8:52811442-52812736	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:52809826-52810355	A549	lung:	n/a	chr8:52810155-52810168
28	CEBPD	chr8:52811740-52812129	HepG2	liver:	n/a	n/a
29	CEBPD	chr8:52811426-52811662	HepG2	liver:	n/a	n/a
30	CEBPZ	chr8:52810413-52810423	HepG2	liver:	n/a	n/a
31	CHD1	chr8:52811946-52812148	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr8:52810051-52811169	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr8:52810391-52813306	GM12878	blood:	n/a	n/a
34	CHD2	chr8:52811337-52812345	HepG2	liver:	n/a	n/a
35	CHD2	chr8:52811494-52812417	K562	blood:	n/a	n/a
36	CHD2	chr8:52810364-52810958	K562	blood:	n/a	n/a
37	CHD2	chr8:52810215-52812751	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr8:52810402-52811165	GM12878	blood:	n/a	n/a
39	CHD2	chr8:52811445-52812394	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr8:52811367-52812395	GM12878	blood:	n/a	n/a
41	CREB1	chr8:52810767-52811195	A549	lung:	n/a	n/a
42	CREB1	chr8:52811378-52812100	A549	lung:	n/a	n/a
43	CTBP2	chr8:52810818-52812416	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:52811890-52811938	ProgFib	skin:	n/a	n/a
45	CTCF	chr8:52810809-52811021	GM12878	blood:	n/a	n/a
46	CTCF	chr8:52810860-52811010	GM12871	blood:	n/a	n/a
47	CTCF	chr8:52812200-52812350	BJ	skin:	n/a	n/a
48	CTCF	chr8:52811813-52811951	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:52812100-52812250	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr8:52811640-52811954	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:52811374-52811424	AG10803	skin:	n/a
2	chr8:52812092-52812142	K562	blood:	n/a
3	chr8:52811707-52811757	HMEC	breast:	n/a
4	chr8:52810866-52810916	PrEC	prostate:	n/a
5	chr8:52811374-52811424	ECC-1	luminal epithelium:	n/a
6	chr8:52810866-52810916	T-47D	breast:	n/a
7	chr8:52811707-52811757	AG09319	gingival:	n/a
8	chr8:52811768-52811818	K562	blood:	n/a
9	chr8:52810866-52810916	AG10803	skin:	n/a
10	chr8:52812171-52812221	HIPEpiC	eye:	n/a
11	chr8:52811711-52811761	HEK293	kidney:	embryo
12	chr8:52811707-52811757	AoSMC	blood vessel:	n/a
13	chr8:52811707-52811757	H1-hESC	embryonic stem cell:	embryo
14	chr8:52811768-52811818	HRE	kidney:	n/a
15	chr8:52812185-52812235	MCF-7	breast:	n/a
16	chr8:52812171-52812221	PrEC	prostate:	n/a
17	chr8:52812185-52812235	Caco-2	colon:	n/a
18	chr8:52812185-52812235	IMR90	lung:	fetal
19	chr8:52812311-52812361	MCF10A-Er-Src	breast:	n/a
20	chr8:52812311-52812361	SK-N-SH_RA	brain:	n/a
21	chr8:52812092-52812142	BJ	skin:	n/a
22	chr8:52811711-52811761	SAEC	small airway:	n/a
23	chr8:52811711-52811761	GM12878	blood:	n/a
24	chr8:52811711-52811761	BE2_C	brain:	n/a
25	chr8:52811768-52811818	HL-60	blood:	n/a
26	chr8:52811374-52811424	U87	brain:	n/a
27	chr8:52811374-52811424	HL-60	blood:	n/a
28	chr8:52810866-52810916	GM19239	blood:	n/a
29	chr8:52811711-52811761	HL-60	blood:	n/a
30	chr8:52811707-52811757	ECC-1	luminal epithelium:	n/a
31	chr8:52811768-52811818	MCF-7	breast:	n/a
32	chr8:52812092-52812142	SK-N-SH_RA	brain:	n/a
33	chr8:52810866-52810916	NHDF-neo	bronchial:	n/a
34	chr8:52812171-52812221	HepG2	liver:	n/a
35	chr8:52812171-52812221	NH-A	brain:	n/a
36	chr8:52812185-52812235	LNCaP	prostate:	n/a
37	chr8:52812171-52812221	Hela-S3	cervix:	n/a
38	chr8:52811711-52811761	SK-N-SH_RA	brain:	n/a
39	chr8:52811374-52811424	HCF	heart:	n/a
40	chr8:52810866-52810916	Hela-S3	cervix:	n/a
41	chr8:52811707-52811757	NHBE	bronchial:	n/a
42	chr8:52810866-52810916	SK-N-MC	brain:	n/a
43	chr8:52812171-52812221	PANC-1	pancreas:	n/a
44	chr8:52812171-52812221	IMR90	lung:	fetal
45	chr8:52812092-52812142	Jurkat	blood:	n/a
46	chr8:52812185-52812235	H1-hESC	embryonic stem cell:	embryo
47	chr8:52812171-52812221	GM12878	blood:	n/a
48	chr8:52812311-52812361	HCT-116	colon:	n/a
49	chr8:52812092-52812142	HIPEpiC	eye:	n/a
50	chr8:52812092-52812142	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:52812423..52815301-chr8:52851311..52852842,2	K562	blood:
2	chr8:52811334..52814143-chr8:52920449..52922864,2	MCF-7	breast:
3	chr8:52807403..52809441-chr8:52809988..52811800,2	MCF-7	breast:
4	chr8:52811900..52812447-chr8:52920564..52921322,2	MCF-7	breast:
5	chr16:2204828..2205571-chr8:52810604..52811800,3	Hela-S3	cervix:
6	chr8:52810955..52812797-chr8:53371753..53374505,2	MCF-7	breast:
7	chr10:70883013..70883710-chr8:52811371..52812277,2	NB4	blood:
8	chr15:72524142..72524977-chr8:52811199..52811704,2	Hela-S3	cervix:
9	chr8:52811463..52813634-chr8:52919548..52922718,3	MCF-7	breast:
10	chr15:91260067..91260698-chr8:52811501..52812214,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC090186.1-1	chr8:52812209-52812406	ENSG00000228801.4
2	lnc-AC090186.1-1	chr8:52812209-52812406	ENSG00000228801.4
3	lnc-AC090186.1-1	chr8:52811824-52812406	NONHSAT126539
4	lnc-AC090186.1-1	chr8:52812275-52812767	ENSG00000228801.4
5	lnc-AC090186.1-1	chr8:52812294-52812406	ENSG00000228801.4
6	lnc-AC090186.1-1	chr8:52811885-52812406	ENSG00000228801.4

No data

Variant related genes	Relation type
ENSG00000253475	TF binding region
ENSG00000228801	TF binding region
PCMTD1	TF binding region
ENSG00000253475	CpG island
ENSG00000228801	CpG island
PCMTD1	CpG island
ENSG00000253475	chromatin interactions
ENSG00000197299	chromatin interactions
ENSG00000259736	chromatin interactions
ENSG00000254136	chromatin interactions
ENSG00000260260	chromatin interactions
ENSG00000147488	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000122958	chromatin interactions
ENSG00000067225	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139172542	chr8:52810231-52810232	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs34961752	chr8:52810267-52810268	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560202892	chr8:52810270-52810271	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547122032	chr8:52810324-52810325	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7465225	chr8:52810332-52810333	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs149290316	chr8:52810345-52810346	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182137256	chr8:52810354-52810355	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149488520	chr8:52810362-52810363	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558007444	chr8:52810373-52810374	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs531599018	chr8:52810374-52810375	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs78754159	chr8:52810385-52810386	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532532919	chr8:52810410-52810411	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs1517306	chr8:52810423-52810424	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs535439843	chr8:52810427-52810428	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs553950748	chr8:52810456-52810457	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs571513307	chr8:52810501-52810502	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs565739933	chr8:52810511-52810512	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534133010	chr8:52810538-52810539	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367856813	chr8:52810540-52810541	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs7460311	chr8:52810543-52810544	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs368467198	chr8:52810548-52810549	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550708962	chr8:52810574-52810575	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs187155967	chr8:52810620-52810621	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs6473663	chr8:52810644-52810645	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554379783	chr8:52810668-52810669	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs574531528	chr8:52810685-52810686	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs541779339	chr8:52810704-52810705	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs146769996	chr8:52810725-52810726	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs370359314	chr8:52810729-52810730	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs3075021	chr8:52810733-52810734	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs79094024	chr8:52810734-52810735	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs191551310	chr8:52810768-52810769	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs527749049	chr8:52810790-52810791	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs545694440	chr8:52810815-52810816	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs535914925	chr8:52810818-52810819	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs185245003	chr8:52810862-52810863	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs550094842	chr8:52810918-52810919	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs386725341	chr8:52810919-52810920	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs143851803	chr8:52810921-52810922	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs148612053	chr8:52810926-52810927	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs528906530	chr8:52810992-52810993	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs13252580	chr8:52811025-52811026	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs71513562	chr8:52811035-52811036	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539488325	chr8:52811073-52811074	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs557555435	chr8:52811076-52811077	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs117568640	chr8:52811097-52811098	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs375179213	chr8:52811129-52811130	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs538054286	chr8:52811145-52811146	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs998709	chr8:52811213-52811214	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs142084927	chr8:52811216-52811217	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52771800-52810800	Weak transcription	Esophagus	oesophagus
2	chr8:52797400-52810800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:52798000-52810800	Weak transcription	Spleen	Spleen
4	chr8:52801800-52810800	Weak transcription	Gastric	stomach
5	chr8:52804200-52810400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:52804200-52810400	Weak transcription	Lung	lung
7	chr8:52807200-52810400	Weak transcription	Placenta	Placenta
8	chr8:52807600-52810400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr8:52808800-52812800	Active TSS	Fetal Brain Female	brain
10	chr8:52809000-52810400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr8:52809000-52810400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr8:52809000-52810600	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr8:52809000-52810600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:52809000-52813000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:52809000-52813200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:52809000-52813400	Active TSS	Ovary	ovary
17	chr8:52809000-52814000	Active TSS	GM12878-XiMat	blood
18	chr8:52809200-52810400	Flanking Active TSS	Dnd41	blood
19	chr8:52809200-52810600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr8:52809200-52811000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:52809200-52812800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:52809200-52812800	Active TSS	K562	blood
23	chr8:52809200-52813000	Active TSS	H1 Cell Line	embryonic stem cell
24	chr8:52809200-52813000	Active TSS	Stomach Smooth Muscle	stomach
25	chr8:52809200-52814000	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr8:52809400-52810600	Flanking Active TSS	Primary T cells from cord blood	blood
27	chr8:52809400-52810800	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr8:52809400-52811000	Active TSS	Fetal Brain Male	brain
29	chr8:52809400-52812800	Active TSS	NHLF	lung
30	chr8:52809400-52813000	Active TSS	Fetal Muscle Leg	muscle
31	chr8:52809400-52813000	Active TSS	Fetal Stomach	stomach
32	chr8:52809600-52810600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr8:52809600-52810600	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr8:52809600-52810600	Flanking Active TSS	Brain Anterior Caudate	brain
35	chr8:52809600-52810600	Flanking Active TSS	Brain Cingulate Gyrus	brain
36	chr8:52809600-52810600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr8:52809600-52810600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr8:52809600-52810800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
39	chr8:52809600-52812600	Active TSS	Fetal Thymus	thymus
40	chr8:52809600-52812800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr8:52809600-52813000	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr8:52809600-52813000	Active TSS	Fetal Intestine Large	intestine
43	chr8:52809600-52813000	Active TSS	Right Ventricle	heart
44	chr8:52809600-52813000	Active TSS	NHDF-Ad	bronchial
45	chr8:52809600-52813200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr8:52809600-52813200	Active TSS	Right Atrium	heart
47	chr8:52809600-52813400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr8:52809600-52813400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr8:52809600-52813400	Active TSS	HSMM	muscle
50	chr8:52809600-52813600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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