Variant report

Variant	nsv8365
Chromosome Location	chr8:91014360-91019600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:198)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:198 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:91014756-91014930	HepG2	liver:	n/a	n/a
2	ATF2	chr8:91017903-91018335	GM12878	blood:	n/a	n/a
3	BACH1	chr8:91014866-91014897	K562	blood:	n/a	n/a
4	BCL11A	chr8:91018008-91018229	GM12878	blood:	n/a	n/a
5	BCL11A	chr8:91017973-91018347	GM12878	blood:	n/a	n/a
6	BCL3	chr8:91017910-91018365	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:91018064-91018295	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:91017670-91017690	GM12878	blood:	n/a	n/a
9	CEBPB	chr8:91018144-91018280	K562	blood:	n/a	n/a
10	CHD1	chr8:91018220-91018608	GM12878	blood:	n/a	n/a
11	CHD2	chr8:91018025-91018319	GM12878	blood:	n/a	n/a
12	CHD2	chr8:91012997-91014682	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr8:91014540-91014690	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr8:91014560-91014710	HCFaa	heart:	n/a	n/a
15	CTCF	chr8:91018127-91018241	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr8:91014520-91014670	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr8:91014440-91014590	HCM	heart:	n/a	n/a
18	CTCF	chr8:91014580-91014730	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr8:91018100-91018250	GM12864	blood:	n/a	n/a
20	CTCF	chr8:91018220-91018370	GM12873	blood:	n/a	n/a
21	CTCF	chr8:91018160-91018310	GM12873	blood:	n/a	n/a
22	CTCF	chr8:91014520-91014670	AG04449	skin:	n/a	n/a
23	CTCF	chr8:91018160-91018310	GM12872	blood:	n/a	n/a
24	CTCF	chr8:91018160-91018310	GM12874	blood:	n/a	n/a
25	CTCF	chr8:91014580-91014730	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr8:91018220-91018370	NHEK	skin:	n/a	n/a
27	CTCF	chr8:91014240-91014390	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr8:91014520-91014670	HPAF	blood vessel:	n/a	n/a
29	EBF1	chr8:91018045-91018343	GM12878	blood:	n/a	n/a
30	EBF1	chr8:91014585-91014687	GM12878	blood:	n/a	n/a
31	EBF1	chr8:91017978-91018407	GM12878	blood:	n/a	n/a
32	EBF1	chr8:91017924-91018398	GM12878	blood:	n/a	n/a
33	EGR1	chr8:91017950-91018220	GM12878	blood:	n/a	chr8:91018106-91018120
34	EGR1	chr8:91017633-91018279	K562	blood:	n/a	chr8:91018106-91018120
35	EGR1	chr8:91017981-91018297	GM12878	blood:	n/a	chr8:91018106-91018120
36	EGR1	chr8:91017955-91018288	K562	blood:	n/a	chr8:91018106-91018120
37	ELF1	chr8:91012856-91014728	MCF-7	breast:	n/a	n/a
38	ELF1	chr8:91012770-91014426	MCF-7	breast:	n/a	n/a
39	ELF1	chr8:91017966-91018235	GM12878	blood:	n/a	chr8:91018131-91018144
40	ELF1	chr8:91012901-91014404	GM12878	blood:	n/a	n/a
41	ELF1	chr8:91017871-91018359	GM12878	blood:	n/a	chr8:91018131-91018144
42	ELF1	chr8:91017920-91018332	K562	blood:	n/a	chr8:91018131-91018144
43	ELK1	chr8:91018025-91018205	GM12878	blood:	n/a	n/a
44	EP300	chr8:91015328-91015353	K562	blood:	n/a	n/a
45	EP300	chr8:91017749-91017836	K562	blood:	n/a	n/a
46	EP300	chr8:91014205-91014832	GM12878	blood:	n/a	chr8:91014704-91014718 chr8:91014412-91014425 chr8:91014698-91014712
47	EP300	chr8:91018020-91018474	GM12878	blood:	n/a	n/a
48	EP300	chr8:91018045-91018227	GM12878	blood:	n/a	n/a
49	EP300	chr8:91018040-91018247	GM12878	blood:	n/a	n/a
50	FOS	chr8:91016982-91017287	MCF10A-Er-Src	breast:	n/a	chr8:91017143-91017153 chr8:91017143-91017153 chr8:91017143-91017153 chr8:91017142-91017154 chr8:91017143-91017153 chr8:91017144-91017153

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:91014327-91014377	GM06990	blood:	n/a
2	chr8:91014327-91014377	U87	brain:	n/a
3	chr8:91014327-91014377	HAEpiC	amniotic membrane:	n/a
4	chr8:91014327-91014377	MCF-7	breast:	n/a
5	chr8:91014327-91014377	H1-hESC	embryonic stem cell:	embryo
6	chr8:91014327-91014377	PrEC	prostate:	n/a
7	chr8:91014327-91014377	AoSMC	blood vessel:	n/a
8	chr8:91014327-91014377	NT2-D1	testis:	n/a
9	chr8:91017761-91017811	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:91017761-91017811	GM12878	blood:	n/a
11	chr8:91017761-91017811	BJ	skin:	n/a
12	chr8:91014327-91014377	PFSK-1	brain:	n/a
13	chr8:91014327-91014377	HRCEpiC	kidney:	n/a
14	chr8:91017761-91017811	HRCEpiC	kidney:	n/a
15	chr8:91017761-91017811	HNPCEpiC	eye:	n/a
16	chr8:91014327-91014377	K562	blood:	n/a
17	chr8:91017761-91017811	HUVEC	blood vessel:	n/a
18	chr8:91014327-91014377	Hepatocyte	liver:	n/a
19	chr8:91017761-91017811	RPTEC	kidney:	n/a
20	chr8:91017761-91017811	HCF	heart:	n/a
21	chr8:91014327-91014377	MCF10A-Er-Src	breast:	n/a
22	chr8:91017761-91017811	HCPEpiC	choroid plexus:	n/a
23	chr8:91017761-91017811	Caco-2	colon:	n/a
24	chr8:91014327-91014377	T-47D	breast:	n/a
25	chr8:91014327-91014377	CMK	blood:	n/a
26	chr8:91014327-91014377	HRPEpiC	eye:	n/a
27	chr8:91017761-91017811	HRE	kidney:	n/a
28	chr8:91017761-91017811	Hela-S3	cervix:	n/a
29	chr8:91017761-91017811	T-47D	breast:	n/a
30	chr8:91017761-91017811	NHBE	bronchial:	n/a
31	chr8:91017761-91017811	LNCaP	prostate:	n/a
32	chr8:91014327-91014377	HEEpiC	esophagus:	n/a
33	chr8:91017761-91017811	GM19239	blood:	n/a
34	chr8:91014327-91014377	NB4	blood:	n/a
35	chr8:91017761-91017811	ProgFib	skin:	n/a
36	chr8:91014327-91014377	BJ	skin:	n/a
37	chr8:91014327-91014377	HMEC	breast:	n/a
38	chr8:91017761-91017811	HMEC	breast:	n/a
39	chr8:91014327-91014377	GM19239	blood:	n/a
40	chr8:91017761-91017811	HAEpiC	amniotic membrane:	n/a
41	chr8:91014327-91014377	Hela-S3	cervix:	n/a
42	chr8:91017761-91017811	CMK	blood:	n/a
43	chr8:91017761-91017811	SAEC	small airway:	n/a
44	chr8:91014327-91014377	AG04450	lung:	fetal
45	chr8:91017761-91017811	MCF10A-Er-Src	breast:	n/a
46	chr8:91017761-91017811	HEK293	kidney:	embryo
47	chr8:91014327-91014377	SK-N-MC	brain:	n/a
48	chr8:91014327-91014377	ovcar-3	ovarian:	n/a
49	chr8:91014327-91014377	HepG2	liver:	n/a
50	chr8:91017761-91017811	A549	lung:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:91012528..91015432-chr8:91026705..91029174,2	MCF-7	breast:
2	chr8:91017521..91019447-chr8:91254781..91258818,3	MCF-7	breast:
3	chr8:91009932..91012698-chr8:91017026..91019725,2	K562	blood:
4	chr8:91018959..91021069-chr8:91131778..91133318,2	K562	blood:
5	chr8:91016481..91019330-chr8:91020288..91024587,4	MCF-7	breast:
6	chr8:90995093..90997814-chr8:91010770..91014611,5	MCF-7	breast:
7	chr19:19729717..19731294-chr8:91013062..91014796,2	MCF-7	breast:
8	chr8:90738912..90741485-chr8:91017416..91019883,2	K562	blood:
9	chr8:90913245..90914861-chr8:91017042..91018822,2	K562	blood:
10	chr8:90996289..90998136-chr8:91010778..91015164,5	K562	blood:
11	chr8:91012176..91015175-chr8:91997197..91999133,2	K562	blood:
12	chr8:90993651..90998172-chr8:91012740..91014695,4	MCF-7	breast:
13	chr8:91012916..91015532-chr8:91016976..91019163,4	K562	blood:
14	chr8:91010711..91015173-chr8:91016537..91023019,10	MCF-7	breast:
15	chr8:91019182..91020697-chr8:91041408..91042988,2	K562	blood:
16	chr8:91017661..91019638-chr8:91023682..91026247,2	K562	blood:
17	chr8:90769284..90770792-chr8:91016368..91018006,2	MCF-7	breast:
18	chr8:91011918..91015233-chr8:91657389..91660471,3	K562	blood:
19	chr8:91015944..91018143-chr8:91550446..91553140,2	K562	blood:
20	chr8:91012457..91016466-chr8:91233540..91237741,4	K562	blood:

No data

Variant related genes	Relation type
NBN	TF binding region
NBN	CpG island
ENSG00000253394	chromatin interactions
ENSG00000253250	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000246792	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000180694	chromatin interactions
ENSG00000105717	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000164823	chromatin interactions

Extended variants
information (count: 164 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:164 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7828767	chr8:91014407-91014408	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs7832531	chr8:91014513-91014514	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs7828932	chr8:91014522-91014523	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs547978786	chr8:91014547-91014548	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs7845562	chr8:91014571-91014572	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs544446625	chr8:91014601-91014602	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs546913440	chr8:91014602-91014603	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs562718725	chr8:91014624-91014625	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs568365292	chr8:91014627-91014628	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs7832805	chr8:91014673-91014674	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs557345483	chr8:91014720-91014721	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs369731091	chr8:91014722-91014723	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs386727651	chr8:91014725-91014726	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs202194896	chr8:91014732-91014733	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs200249159	chr8:91014734-91014735	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs533036502	chr8:91014775-91014776	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs189254946	chr8:91014832-91014833	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs3026277	chr8:91014907-91014908	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs545290894	chr8:91014988-91014989	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs564318698	chr8:91014997-91014998	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs368696972	chr8:91015000-91015001	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs180734687	chr8:91015042-91015043	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs568239867	chr8:91015045-91015046	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs1805851	chr8:91015051-91015052	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1805852	chr8:91015057-91015058	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs185513647	chr8:91015083-91015084	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs539700632	chr8:91015100-91015101	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs73696853	chr8:91015129-91015130	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs142819801	chr8:91015152-91015153	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs117157713	chr8:91015164-91015165	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs550817124	chr8:91015217-91015218	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs188369014	chr8:91015252-91015253	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570744070	chr8:91015256-91015257	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573743727	chr8:91015318-91015319	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534568563	chr8:91015412-91015413	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1805805	chr8:91015502-91015503	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs74656551	chr8:91015517-91015518	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs1805853	chr8:91015541-91015542	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs78816944	chr8:91015543-91015544	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557521903	chr8:91015572-91015573	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs148486292	chr8:91015611-91015612	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs543731647	chr8:91015612-91015613	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs528443948	chr8:91015617-91015618	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561544554	chr8:91015671-91015672	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138465605	chr8:91015676-91015677	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539504092	chr8:91015684-91015685	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs540204053	chr8:91015720-91015721	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs561765628	chr8:91015770-91015771	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181190500	chr8:91015843-91015844	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529010698	chr8:91015853-91015854	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91012800-91014400	Active TSS	Fetal Brain Female	brain
2	chr8:91012800-91014600	Active TSS	Monocytes-CD14+_RO01746	blood
3	chr8:91012800-91014800	Active TSS	Fetal Brain Male	brain
4	chr8:91012800-91015000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:91012800-91015200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:91012800-91015200	Active TSS	Thymus	Thymus
7	chr8:91013000-91014400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr8:91013000-91014400	Active TSS	Primary T helper naive cells from peripheral blood	blood
9	chr8:91013000-91014400	Active TSS	Brain Germinal Matrix	brain
10	chr8:91013000-91014400	Active TSS	Fetal Kidney	kidney
11	chr8:91013000-91014600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr8:91013000-91014600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:91013000-91014600	Active TSS	Brain Cingulate Gyrus	brain
14	chr8:91013000-91014600	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr8:91013000-91014600	Active TSS	Hela-S3	cervix
16	chr8:91013000-91014800	Active TSS	H1 Cell Line	embryonic stem cell
17	chr8:91013000-91014800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr8:91013000-91014800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr8:91013000-91014800	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr8:91013000-91014800	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr8:91013000-91014800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:91013000-91014800	Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr8:91013000-91014800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:91013000-91014800	Active TSS	Brain Substantia Nigra	brain
25	chr8:91013000-91014800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr8:91013000-91014800	Active TSS	Fetal Muscle Trunk	muscle
27	chr8:91013000-91014800	Active TSS	Stomach Mucosa	stomach
28	chr8:91013000-91015000	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr8:91013000-91015000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:91013000-91015000	Active TSS	Primary monocytes fromperipheralblood	blood
31	chr8:91013000-91015000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:91013000-91015000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:91013000-91015000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:91013000-91015000	Active TSS	Brain Angular Gyrus	brain
35	chr8:91013000-91015000	Active TSS	Colon Smooth Muscle	Colon
36	chr8:91013000-91015000	Active TSS	Fetal Muscle Leg	muscle
37	chr8:91013000-91015000	Active TSS	Right Ventricle	heart
38	chr8:91013000-91015000	Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr8:91013000-91015200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr8:91013000-91015200	Active TSS	Fetal Intestine Small	intestine
41	chr8:91013000-91015200	Active TSS	Stomach Smooth Muscle	stomach
42	chr8:91013200-91014400	Active TSS	Primary B cells from peripheral blood	blood
43	chr8:91013200-91014400	Active TSS	Primary T cells from cord blood	blood
44	chr8:91013200-91014400	Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr8:91013200-91014400	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
46	chr8:91013200-91014600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:91013200-91014600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:91013200-91014600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:91013200-91014600	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr8:91013200-91014600	Active TSS	iPS-18 Cell Line	embryonic stem cell

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