Variant report

Variant	nsv891408
Chromosome Location	chr8:117884270-117895239
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:790)
CpG islands
(count:978)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:117886984-117887416	K562	blood:	n/a	n/a
2	ARID3A	chr8:117887057-117887571	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:117889976-117890211	K562	blood:	n/a	n/a
4	ARID3A	chr8:117886484-117886598	K562	blood:	n/a	n/a
5	ARID3A	chr8:117885466-117885734	K562	blood:	n/a	n/a
6	ARID3A	chr8:117890462-117891664	K562	blood:	n/a	n/a
7	ATF1	chr8:117889902-117890175	K562	blood:	n/a	n/a
8	ATF1	chr8:117886944-117887373	K562	blood:	n/a	n/a
9	ATF1	chr8:117891279-117891548	K562	blood:	n/a	n/a
10	ATF2	chr8:117892283-117892985	GM12878	blood:	n/a	n/a
11	ATF2	chr8:117886779-117887536	GM12878	blood:	n/a	n/a
12	ATF3	chr8:117886848-117887480	A549	lung:	n/a	chr8:117887180-117887188
13	ATF3	chr8:117886980-117887238	K562	blood:	n/a	chr8:117887180-117887188
14	ATF3	chr8:117889880-117890281	K562	blood:	n/a	n/a
15	ATF3	chr8:117886900-117887354	A549	lung:	n/a	chr8:117887180-117887188
16	ATF3	chr8:117886937-117887317	K562	blood:	n/a	chr8:117887180-117887188
17	BACH1	chr8:117886697-117886711	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:117891238-117891493	K562	blood:	n/a	n/a
19	BACH1	chr8:117891281-117891302	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr8:117892417-117892635	GM12878	blood:	n/a	n/a
21	BCLAF1	chr8:117892247-117892772	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:117892372-117892708	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:117891392-117891417	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:117885777-117885899	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:117885748-117885946	K562	blood:	n/a	n/a
26	BHLHE40	chr8:117886425-117886732	K562	blood:	n/a	chr8:117886710-117886726
27	BHLHE40	chr8:117886420-117887510	GM12878	blood:	n/a	chr8:117886710-117886726 chr8:117886963-117886979 chr8:117886957-117886973
28	BHLHE40	chr8:117891238-117891591	K562	blood:	n/a	n/a
29	BHLHE40	chr8:117886962-117887378	K562	blood:	n/a	chr8:117886963-117886979
30	BRCA1	chr8:117886435-117886633	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr8:117886924-117887475	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr8:117894371-117894395	GM12878	blood:	n/a	n/a
33	BRCA1	chr8:117884921-117885939	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr8:117886509-117886524	GM12878	blood:	n/a	n/a
35	BRCA1	chr8:117886982-117887162	HepG2	liver:	n/a	n/a
36	CBX3	chr8:117886858-117887488	K562	blood:	n/a	n/a
37	CCNT2	chr8:117891172-117891642	K562	blood:	n/a	n/a
38	CCNT2	chr8:117886333-117887286	K562	blood:	n/a	chr8:117887126-117887135
39	CEBPB	chr8:117887018-117887437	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:117887079-117887443	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:117885248-117885756	K562	blood:	n/a	n/a
42	CEBPB	chr8:117889856-117890219	H1-hESC	embryonic stem cell:	n/a	chr8:117890039-117890050
43	CEBPB	chr8:117889857-117890210	IMR90	lung:	n/a	chr8:117890039-117890050
44	CEBPB	chr8:117887061-117887515	K562	blood:	n/a	n/a
45	CEBPB	chr8:117889845-117890305	Hela-S3	cervix:	n/a	chr8:117890039-117890050
46	CEBPB	chr8:117887035-117887463	K562	blood:	n/a	n/a
47	CEBPB	chr8:117889884-117890093	K562	blood:	n/a	chr8:117890039-117890050
48	CEBPB	chr8:117894090-117894258	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:117887065-117887443	A549	lung:	n/a	n/a
50	CEBPB	chr8:117887144-117887358	HepG2	liver:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:117887286-117887336	HCPEpiC	choroid plexus:	n/a
2	chr8:117886537-117886587	HAEpiC	amniotic membrane:	n/a
3	chr8:117887286-117887336	HCPEpiC	choroid plexus:	n/a
4	chr8:117886537-117886587	HAEpiC	amniotic membrane:	n/a
5	chr8:117887022-117887072	GM12878	blood:	n/a
6	chr8:117887256-117887306	GM06990	blood:	n/a
7	chr8:117886418-117886468	HCF	heart:	n/a
8	chr8:117887184-117887234	NHDF-neo	bronchial:	n/a
9	chr8:117887318-117887368	K562	blood:	n/a
10	chr8:117887282-117887332	GM12891	blood:	n/a
11	chr8:117887184-117887234	K562	blood:	n/a
12	chr8:117885438-117885488	HCPEpiC	choroid plexus:	n/a
13	chr8:117887081-117887131	Caco-2	colon:	n/a
14	chr8:117887288-117887338	BE2_C	brain:	n/a
15	chr8:117887305-117887355	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:117886418-117886468	IMR90	lung:	fetal
17	chr8:117887282-117887332	MCF10A-Er-Src	breast:	n/a
18	chr8:117887184-117887234	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:117886537-117886587	AG09319	gingival:	n/a
20	chr8:117886618-117886668	AG04450	lung:	fetal
21	chr8:117887282-117887332	AoSMC	blood vessel:	n/a
22	chr8:117886887-117886937	GM12891	blood:	n/a
23	chr8:117886418-117886468	GM06990	blood:	n/a
24	chr8:117887288-117887338	HL-60	blood:	n/a
25	chr8:117886618-117886668	SK-N-SH_RA	brain:	n/a
26	chr8:117887282-117887332	SK-N-SH	brain:	n/a
27	chr8:117887022-117887072	T-47D	breast:	n/a
28	chr8:117886602-117886652	SK-N-SH	brain:	n/a
29	chr8:117887256-117887306	GM19239	blood:	n/a
30	chr8:117887022-117887072	HRPEpiC	eye:	n/a
31	chr8:117887288-117887338	SK-N-SH_RA	brain:	n/a
32	chr8:117886887-117886937	Hela-S3	cervix:	n/a
33	chr8:117887256-117887306	PrEC	prostate:	n/a
34	chr8:117886602-117886652	HEEpiC	esophagus:	n/a
35	chr8:117887022-117887072	AG10803	skin:	n/a
36	chr8:117887218-117887268	PFSK-1	brain:	n/a
37	chr8:117887286-117887336	LNCaP	prostate:	n/a
38	chr8:117886602-117886652	HRCEpiC	kidney:	n/a
39	chr8:117887218-117887268	A549	lung:	n/a
40	chr8:117887305-117887355	AG09309	skin:	n/a
41	chr8:117886602-117886652	AG09319	gingival:	n/a
42	chr8:117887022-117887072	Jurkat	blood:	n/a
43	chr8:117887318-117887368	CMK	blood:	n/a
44	chr8:117886537-117886587	PrEC	prostate:	n/a
45	chr8:117887282-117887332	BE2_C	brain:	n/a
46	chr8:117886602-117886652	U87	brain:	n/a
47	chr8:117887288-117887338	AG04450	lung:	fetal
48	chr8:117887022-117887072	HNPCEpiC	eye:	n/a
49	chr8:117887022-117887072	GM12892	blood:	n/a
50	chr8:117886537-117886587	NT2-D1	testis:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:7475777..7476285-chr8:117886539..117887113,2	Hela-S3	cervix:
2	chr8:117776578..117778707-chr8:117885688..117887716,2	MCF-7	breast:
3	chr8:117889283..117892255-chr8:117894837..117897119,2	MCF-7	breast:
4	chr19:531051..531863-chr8:117886115..117886910,2	Hela-S3	cervix:
5	chr10:3827279..3828214-chr8:117886115..117887011,2	Hela-S3	cervix:
6	chr8:117860936..117862672-chr8:117885542..117887768,2	MCF-7	breast:
7	chr8:117882042..117883991-chr8:117888629..117890364,2	K562	blood:
8	chr5:108745137..108745914-chr8:117885074..117885909,2	Hela-S3	cervix:
9	chr8:117888535..117891194-chr8:117894187..117898380,4	K562	blood:
10	chr16:70285325..70286015-chr8:117886552..117887078,2	HCT-116	colon:
11	chr8:117778445..117780504-chr8:117889619..117892569,2	K562	blood:
12	chr8:117777450..117780279-chr8:117883824..117887176,3	MCF-7	breast:
13	chr8:117775214..117779057-chr8:117886515..117888588,5	K562	blood:
14	chr8:117783766..117785704-chr8:117889249..117891473,2	K562	blood:
15	chr8:117886361..117888320-chr8:117890566..117894266,3	MCF-7	breast:
16	chr8:117889283..117892255-chr8:117894837..117897119,2	MCF-7	breast:
17	chr8:117863976..117865833-chr8:117886990..117888804,2	MCF-7	breast:
18	chr8:117766167..117768500-chr8:117885619..117887391,2	K562	blood:
19	chr8:117884616..117888716-chr8:117892437..117896963,6	MCF-7	breast:
20	chr8:117886286..117887284-chr9:131790245..131790850,2	Hela-S3	cervix:
21	chr2:86850708..86851436-chr8:117885912..117886540,2	Hela-S3	cervix:
22	chr8:117888535..117891194-chr8:117894187..117898380,4	K562	blood:
23	chr8:117777051..117780452-chr8:117884154..117888588,6	K562	blood:
24	chr8:117885681..117888687-chr8:117888823..117892545,5	K562	blood:
25	chr12:120517214..120519596-chr8:117884799..117887415,2	MCF-7	breast:
26	chr17:57182556..57185500-chr8:117885243..117887257,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAD21-AS1-1	chr8:117887660-117889107	ENSG00000253327.2
2	lnc-RAD21-AS1-1	chr8:117886663-117887224	ENSG00000253327.2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3610	chr8:117886979-117886998	MIMAT0017987

No data

Variant related genes	Relation type
RAD21	TF binding region
RAD21-AS1	TF binding region
MIR3610	TF binding region
RAD21	CpG island
RAD21-AS1	CpG island
MIR3610	CpG island
ENSG00000147679	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000224738	chromatin interactions
ENSG00000164754	chromatin interactions
ENSG00000135127	chromatin interactions
ENSG00000099804	chromatin interactions
ENSG00000067082	chromatin interactions
ENSG00000108395	chromatin interactions
ENSG00000147677	chromatin interactions
ENSG00000264875	chromatin interactions
ENSG00000239305	chromatin interactions
ENSG00000198961	chromatin interactions
ENSG00000148341	chromatin interactions
ENSG00000161960	chromatin interactions

Extended variants
information (count: 412 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11786746	chr8:117884270-117884271	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539314702	chr8:117884271-117884272	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs78875948	chr8:117884300-117884301	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs200844619	chr8:117884305-117884306	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs572583493	chr8:117884312-117884313	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs185051166	chr8:117884314-117884315	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs151191212	chr8:117884354-117884355	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs191082602	chr8:117884391-117884392	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs558750979	chr8:117884394-117884395	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs528871133	chr8:117884398-117884399	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs16889153	chr8:117884416-117884417	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs577210462	chr8:117884425-117884426	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs545274725	chr8:117884437-117884438	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs534869893	chr8:117884455-117884456	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs3020131	chr8:117884498-117884499	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs527456534	chr8:117884507-117884508	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs144147094	chr8:117884520-117884521	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs560925972	chr8:117884533-117884534	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs531437444	chr8:117884552-117884553	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs1374298	chr8:117884571-117884572	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs571211761	chr8:117884608-117884609	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs201458035	chr8:117884634-117884635	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs200884104	chr8:117884635-117884636	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183800757	chr8:117884663-117884664	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs1374297	chr8:117884696-117884697	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573228200	chr8:117884736-117884737	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs576079216	chr8:117884759-117884760	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs16889160	chr8:117884762-117884763	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs374501642	chr8:117884772-117884773	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs112528947	chr8:117884774-117884775	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs376577569	chr8:117884778-117884779	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs199781596	chr8:117884779-117884780	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs16889164	chr8:117884796-117884797	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs397835159	chr8:117884800-117884801	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs35111358	chr8:117884802-117884803	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs373042389	chr8:117884804-117884805	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs56759325	chr8:117884805-117884806	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs541091086	chr8:117884806-117884807	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs547055336	chr8:117884839-117884840	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs16889172	chr8:117884944-117884945	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs140465540	chr8:117884948-117884949	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs561059244	chr8:117884949-117884950	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs78153792	chr8:117884961-117884962	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs188912095	chr8:117884987-117884988	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs144308509	chr8:117885061-117885062	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs535382119	chr8:117885090-117885091	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs532102738	chr8:117885100-117885101	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs547092197	chr8:117885123-117885124	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs16889177	chr8:117885167-117885168	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79066013	chr8:117885181-117885182	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:132)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17268525	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	19204574	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:117860400-117885800	Weak transcription	Esophagus	oesophagus
2	chr8:117864400-117885800	Weak transcription	Gastric	stomach
3	chr8:117865200-117885800	Weak transcription	Pancreas	Pancrea
4	chr8:117865600-117885800	Weak transcription	Spleen	Spleen
5	chr8:117867000-117885200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:117867000-117885600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:117870000-117884400	Weak transcription	Colonic Mucosa	Colon
8	chr8:117870200-117884800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr8:117872600-117884400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:117876000-117884600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr8:117877400-117885000	Enhancers	Fetal Heart	heart
12	chr8:117877800-117884400	Weak transcription	Fetal Intestine Small	intestine
13	chr8:117877800-117884600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:117878200-117884400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:117878400-117884600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr8:117878400-117884800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr8:117878600-117884800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr8:117878800-117885800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr8:117879000-117884400	Enhancers	A549	lung
20	chr8:117879000-117884600	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr8:117879000-117884600	Weak transcription	Brain Substantia Nigra	brain
22	chr8:117879600-117884600	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr8:117879600-117885000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr8:117879800-117884600	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr8:117880000-117884800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr8:117880200-117884800	Weak transcription	Brain Angular Gyrus	brain
27	chr8:117880800-117884400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr8:117881000-117884400	Enhancers	Thymus	Thymus
29	chr8:117881200-117884400	Enhancers	HepG2	liver
30	chr8:117881200-117884600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:117881200-117884800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:117881200-117887800	Active TSS	GM12878-XiMat	blood
33	chr8:117881400-117884400	Enhancers	HMEC	breast
34	chr8:117881400-117884400	Enhancers	NHDF-Ad	bronchial
35	chr8:117881400-117884400	Enhancers	NHEK	skin
36	chr8:117881600-117884400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr8:117881600-117884800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr8:117881600-117885200	Enhancers	Colon Smooth Muscle	Colon
39	chr8:117881600-117885200	Enhancers	Small Intestine	intestine
40	chr8:117881800-117884600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:117881800-117884800	Enhancers	Adipose Nuclei	Adipose
42	chr8:117881800-117884800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr8:117881800-117885600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:117881800-117885800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:117882200-117884800	Enhancers	Primary hematopoietic stem cells	blood
46	chr8:117882200-117885000	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr8:117882400-117884400	Enhancers	HUVEC	blood vessel
48	chr8:117882400-117884600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr8:117882400-117885200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr8:117882400-117885600	Enhancers	Primary B cells from peripheral blood	blood

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