Variant report

Variant	nsv1029046
Chromosome Location	chr8:62224341-62535277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2873)
CpG islands
(count:611)
Chromatin interactive
region (count:61)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2873 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:62475807-62476156	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:62475799-62476194	K562	blood:	n/a	n/a
3	ARID3A	chr8:62380218-62380318	K562	blood:	n/a	n/a
4	ARID3A	chr8:62335547-62335790	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:62381351-62381522	K562	blood:	n/a	n/a
6	ARID3A	chr8:62504019-62504386	K562	blood:	n/a	n/a
7	ARID3A	chr8:62288552-62288923	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:62224221-62224845	HepG2	liver:	n/a	n/a
9	ATF1	chr8:62475831-62476151	K562	blood:	n/a	n/a
10	ATF1	chr8:62282061-62282212	K562	blood:	n/a	n/a
11	ATF1	chr8:62504084-62504414	K562	blood:	n/a	n/a
12	ATF2	chr8:62278837-62279338	GM12878	blood:	n/a	n/a
13	ATF2	chr8:62278139-62278685	GM12878	blood:	n/a	n/a
14	ATF2	chr8:62278842-62279242	GM12878	blood:	n/a	n/a
15	ATF3	chr8:62400218-62400493	K562	blood:	n/a	chr8:62400416-62400430
16	ATF3	chr8:62504027-62504490	HCT-116	colon:	n/a	n/a
17	BACH1	chr8:62475746-62476168	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:62381474-62381507	K562	blood:	n/a	n/a
19	BACH1	chr8:62475830-62476186	K562	blood:	n/a	n/a
20	BACH1	chr8:62381408-62381690	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr8:62407456-62407819	GM12878	blood:	n/a	chr8:62407667-62407678
22	BATF	chr8:62278202-62278585	GM12878	blood:	n/a	n/a
23	BATF	chr8:62309685-62309904	GM12878	blood:	n/a	n/a
24	BATF	chr8:62278845-62279273	GM12878	blood:	n/a	chr8:62279057-62279068
25	BATF	chr8:62278861-62279305	GM12878	blood:	n/a	chr8:62279057-62279068
26	BCL11A	chr8:62278217-62278573	GM12878	blood:	n/a	chr8:62278490-62278499
27	BCL11A	chr8:62278912-62279308	GM12878	blood:	n/a	chr8:62279056-62279065 chr8:62279057-62279066
28	BCL11A	chr8:62278222-62278491	GM12878	blood:	n/a	n/a
29	BCL3	chr8:62270813-62271032	GM12878	blood:	n/a	n/a
30	BCL3	chr8:62527418-62528273	A549	lung:	n/a	n/a
31	BCL3	chr8:62531605-62534627	A549	lung:	n/a	chr8:62532186-62532195 chr8:62532579-62532588
32	BCL3	chr8:62528667-62529474	A549	lung:	n/a	n/a
33	BCL3	chr8:62519981-62520571	A549	lung:	n/a	n/a
34	BCL3	chr8:62423717-62424058	GM12878	blood:	n/a	n/a
35	BCL3	chr8:62530788-62536045	A549	lung:	n/a	chr8:62532186-62532195 chr8:62532579-62532588
36	BCL3	chr8:62534694-62535608	A549	lung:	n/a	n/a
37	BCL3	chr8:62303621-62303891	GM12878	blood:	n/a	n/a
38	BCL3	chr8:62526624-62529836	A549	lung:	n/a	chr8:62528363-62528372
39	BCLAF1	chr8:62381280-62381704	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:62381351-62381614	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:62380124-62380360	K562	blood:	n/a	n/a
42	BHLHE40	chr8:62224311-62224677	HepG2	liver:	n/a	n/a
43	BHLHE40	chr8:62408722-62408894	K562	blood:	n/a	n/a
44	BHLHE40	chr8:62278305-62278616	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:62477535-62477648	HepG2	liver:	n/a	n/a
46	BHLHE40	chr8:62504172-62504372	K562	blood:	n/a	n/a
47	BHLHE40	chr8:62381327-62381645	K562	blood:	n/a	n/a
48	BRCA1	chr8:62288838-62288843	HepG2	liver:	n/a	n/a
49	BRCA1	chr8:62248567-62248570	GM12878	blood:	n/a	n/a
50	BRCA1	chr8:62526885-62526976	Hela-S3	cervix:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:62415183-62415233	HMEC	breast:	n/a
2	chr8:62415183-62415233	HMEC	breast:	n/a
3	chr8:62520228-62520278	PANC-1	pancreas:	n/a
4	chr8:62529801-62529851	PFSK-1	brain:	n/a
5	chr8:62529801-62529851	NH-A	brain:	n/a
6	chr8:62505560-62505610	HL-60	blood:	n/a
7	chr8:62415183-62415233	PrEC	prostate:	n/a
8	chr8:62415183-62415233	Hela-S3	cervix:	n/a
9	chr8:62505560-62505610	BE2_C	brain:	n/a
10	chr8:62505560-62505610	ECC-1	luminal epithelium:	n/a
11	chr8:62442151-62442201	IMR90	lung:	fetal
12	chr8:62381505-62381555	GM06990	blood:	n/a
13	chr8:62520228-62520278	HUVEC	blood vessel:	n/a
14	chr8:62381505-62381555	HAEpiC	amniotic membrane:	n/a
15	chr8:62442151-62442201	HCM	heart:	n/a
16	chr8:62529801-62529851	HRPEpiC	eye:	n/a
17	chr8:62415183-62415233	SK-N-SH_RA	brain:	n/a
18	chr8:62415183-62415233	GM06990	blood:	n/a
19	chr8:62494502-62494552	HRCEpiC	kidney:	n/a
20	chr8:62442151-62442201	LNCaP	prostate:	n/a
21	chr8:62442151-62442201	GM12892	blood:	n/a
22	chr8:62534440-62534490	Hela-S3	cervix:	n/a
23	chr8:62381505-62381555	HCF	heart:	n/a
24	chr8:62520228-62520278	ProgFib	skin:	n/a
25	chr8:62381505-62381555	LNCaP	prostate:	n/a
26	chr8:62520228-62520278	HNPCEpiC	eye:	n/a
27	chr8:62415183-62415233	AG04449	skin:	fetal
28	chr8:62529801-62529851	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:62434052-62434102	HepG2	liver:	n/a
30	chr8:62494502-62494552	HMEC	breast:	n/a
31	chr8:62412760-62412810	NHBE	bronchial:	n/a
32	chr8:62442151-62442201	BJ	skin:	n/a
33	chr8:62520228-62520278	HepG2	liver:	n/a
34	chr8:62505560-62505610	HCT-116	colon:	n/a
35	chr8:62534440-62534490	BJ	skin:	n/a
36	chr8:62442151-62442201	NHBE	bronchial:	n/a
37	chr8:62415183-62415233	NHDF-neo	bronchial:	n/a
38	chr8:62494502-62494552	HepG2	liver:	n/a
39	chr8:62520228-62520278	MCF-7	breast:	n/a
40	chr8:62434052-62434102	HCF	heart:	n/a
41	chr8:62505560-62505610	NHBE	bronchial:	n/a
42	chr8:62381505-62381555	AoSMC	blood vessel:	n/a
43	chr8:62494502-62494552	SK-N-SH_RA	brain:	n/a
44	chr8:62434052-62434102	GM06990	blood:	n/a
45	chr8:62415183-62415233	SK-N-MC	brain:	n/a
46	chr8:62505560-62505610	LNCaP	prostate:	n/a
47	chr8:62434052-62434102	ovcar-3	ovarian:	n/a
48	chr8:62381505-62381555	PFSK-1	brain:	n/a
49	chr8:62381505-62381555	HCM	heart:	n/a
50	chr8:62529801-62529851	H1-hESC	embryonic stem cell:	embryo

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:62248452..62249208-chr8:62379820..62380370,2	MCF-7	breast:
2	chr8:62248249..62249123-chr8:62380724..62381961,7	MCF-7	breast:
3	chr8:62379782..62380618-chr8:62475892..62476541,2	K562	blood:
4	chr8:62225517..62227251-chr8:62230337..62232798,2	K562	blood:
5	chr8:62247832..62248787-chr8:62379922..62380668,2	MCF-7	breast:
6	chr8:62156345..62157248-chr8:62475582..62476441,2	MCF-7	breast:
7	chr8:62379524..62380909-chr8:62475525..62476519,9	MCF-7	breast:
8	chr8:62248558..62249344-chr8:62372696..62373675,2	MCF-7	breast:
9	chr8:62411280..62413596-chr8:62416283..62419042,2	K562	blood:
10	chr8:62411280..62413596-chr8:62416283..62419042,2	K562	blood:
11	chr8:62379715..62380732-chr8:62427877..62428562,3	MCF-7	breast:
12	chr8:62521782..62523437-chr8:62525104..62526707,2	K562	blood:
13	chr8:62156250..62157004-chr8:62428078..62428760,2	MCF-7	breast:
14	chr8:62502517..62504519-chr8:62506579..62509041,2	MCF-7	breast:
15	chr8:62156501..62157309-chr8:62475663..62476458,3	K562	blood:
16	chr8:62338693..62341513-chr8:62344299..62346129,2	K562	blood:
17	chr8:62225517..62227251-chr8:62230337..62232798,2	K562	blood:
18	chr8:62400838..62402510-chr8:62406453..62408446,2	K562	blood:
19	chr8:62278733..62281370-chr8:62291248..62293763,2	K562	blood:
20	chr8:62051677..62052206-chr8:62381213..62382143,4	K562	blood:
21	chr8:62379782..62380618-chr8:62475892..62476541,2	K562	blood:
22	chr8:62315268..62317052-chr8:62329952..62331844,2	K562	blood:
23	chr8:62381011..62381982-chr8:62475541..62476206,2	MCF-7	breast:
24	chr4:6690937..6691623-chr8:62425061..62425581,2	Hela-S3	cervix:
25	chr8:62338693..62341513-chr8:62344299..62346129,2	K562	blood:
26	chr8:61563491..61566283-chr8:62474677..62476882,2	MCF-7	breast:
27	chr8:62379524..62380909-chr8:62475525..62476519,9	MCF-7	breast:
28	chr8:62156342..62157143-chr8:62381140..62382022,5	K562	blood:
29	chr8:62248249..62249123-chr8:62380724..62381961,7	MCF-7	breast:
30	chr8:62156582..62157132-chr8:62381389..62382258,2	MCF-7	breast:
31	chr8:62248558..62249344-chr8:62372696..62373675,2	MCF-7	breast:
32	chr8:62408687..62410357-chr8:62411141..62412784,2	MCF-7	breast:
33	chr8:62437290..62439641-chr8:62440301..62441831,2	K562	blood:
34	chr8:62379715..62380732-chr8:62427877..62428562,3	MCF-7	breast:
35	chr8:62278733..62281370-chr8:62291248..62293763,2	K562	blood:
36	chr8:62488403..62489962-chr8:62494279..62497109,2	MCF-7	breast:
37	chr8:62529653..62532245-chr8:62535341..62537094,2	K562	blood:
38	chr8:62247832..62248787-chr8:62379922..62380668,2	MCF-7	breast:
39	chr8:62488403..62489962-chr8:62494279..62497109,2	MCF-7	breast:
40	chr8:62408687..62410357-chr8:62411141..62412784,2	MCF-7	breast:
41	chr8:62155417..62156246-chr8:62381440..62381973,2	MCF-7	breast:
42	chr8:62156342..62157195-chr8:62380225..62380826,2	MCF-7	breast:
43	chr8:62502517..62504519-chr8:62506579..62509041,2	MCF-7	breast:
44	chr8:62051294..62051870-chr8:62381197..62381952,2	MCF-7	breast:
45	chr8:62424036..62426266-chr8:62451007..62452674,2	MCF-7	breast:
46	chr8:62497711..62498456-chr8:62526163..62527120,2	MCF-7	breast:
47	chr8:62497711..62498456-chr8:62526163..62527120,2	MCF-7	breast:
48	chr8:62156269..62156884-chr8:62475900..62476409,2	MCF-7	breast:
49	chr8:62521782..62523437-chr8:62525104..62526707,2	K562	blood:
50	chr8:62400838..62402510-chr8:62406453..62408446,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA8-13	chr8:62495558-62496094	NONHSAT126868
2	lnc-CA8-13	chr8:62496503-62496588	NONHSAT126868
3	lnc-CA8-13	chr8:62531537-62531578	NONHSAT126868

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ASPH	hsa-miR-215-5p	chr8:62414484-62414503
2	ASPH	hsa-miR-155-5p	chr8:62415422-62415445
3	ASPH	hsa-miR-192-5p	chr8:62414484-62414503
4	ASPH	hsa-miR-155-5p	chr8:62414631-62414655

Variant related genes	Relation type
KRT8P3	TF binding region
CLVS1	TF binding region
ASPH	TF binding region
KRT8P3	CpG island
CLVS1	CpG island
ASPH	CpG island
ENSG00000254869	chromatin interactions
ENSG00000198363	chromatin interactions
ENSG00000255289	chromatin interactions

Extended variants
information (count: 11054 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:11054 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6985494	chr8:62224341-62224342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs59615571	chr8:62224354-62224355	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs553335215	chr8:62224360-62224361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73682219	chr8:62224361-62224362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs7817033	chr8:62224396-62224397	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182732064	chr8:62224404-62224405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77623697	chr8:62224488-62224489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541533440	chr8:62224508-62224509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149588707	chr8:62224522-62224523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116052867	chr8:62224591-62224592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549297415	chr8:62224606-62224607	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75239324	chr8:62224623-62224624	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79150778	chr8:62224661-62224662	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573215298	chr8:62224685-62224686	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138149496	chr8:62224702-62224703	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143628335	chr8:62224729-62224730	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538322888	chr8:62224745-62224746	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6471946	chr8:62224832-62224833	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs115300751	chr8:62224854-62224855	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs536494276	chr8:62224880-62224881	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186308620	chr8:62224883-62224884	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs76813524	chr8:62224884-62224885	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs376137110	chr8:62224891-62224892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs2931300	chr8:62224936-62224937	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs558650012	chr8:62224981-62224982	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147226835	chr8:62225007-62225008	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs79839066	chr8:62225057-62225058	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs191057034	chr8:62225079-62225080	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs572260406	chr8:62225102-62225103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs577143073	chr8:62225181-62225182	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs542804390	chr8:62225206-62225207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184047877	chr8:62225242-62225243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79259832	chr8:62225342-62225343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140597989	chr8:62225404-62225405	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs564712368	chr8:62225421-62225422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs532159149	chr8:62225443-62225444	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs142202401	chr8:62225446-62225447	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs565806558	chr8:62225459-62225460	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs187696878	chr8:62225545-62225546	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs150724735	chr8:62225591-62225592	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs111895683	chr8:62225625-62225626	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192670998	chr8:62225634-62225635	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149907521	chr8:62225638-62225639	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146452725	chr8:62225640-62225641	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535060178	chr8:62225646-62225647	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183070859	chr8:62225649-62225650	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574940628	chr8:62225655-62225656	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574395530	chr8:62225674-62225675	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542366905	chr8:62225698-62225699	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75661549	chr8:62225721-62225722	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Multiple myeloma	16461302	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
Salivary gland tumor	18059337	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:2701 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62221600-62226000	Enhancers	HepG2	liver
2	chr8:62221800-62226800	Enhancers	Fetal Intestine Small	intestine
3	chr8:62221800-62236200	Weak transcription	Brain Germinal Matrix	brain
4	chr8:62222600-62225000	Enhancers	Duodenum Mucosa	Duodenum
5	chr8:62222600-62225800	Weak transcription	Small Intestine	intestine
6	chr8:62222600-62226400	Enhancers	Fetal Intestine Large	intestine
7	chr8:62222800-62224600	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr8:62222800-62226800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr8:62223000-62225600	Weak transcription	Brain Anterior Caudate	brain
10	chr8:62223000-62226200	Enhancers	Stomach Mucosa	stomach
11	chr8:62224000-62224400	Weak transcription	Fetal Brain Female	brain
12	chr8:62224000-62224600	Enhancers	Pancreas	Pancrea
13	chr8:62224000-62224800	Enhancers	Colonic Mucosa	Colon
14	chr8:62224000-62224800	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr8:62224200-62224600	Enhancers	Liver	Liver
16	chr8:62224200-62225200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:62224400-62224600	Enhancers	Fetal Brain Female	brain
18	chr8:62224400-62225400	Weak transcription	Fetal Thymus	thymus
19	chr8:62224600-62224800	Flanking Active TSS	Liver	Liver
20	chr8:62224600-62225000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
21	chr8:62224600-62225600	Weak transcription	Fetal Brain Female	brain
22	chr8:62224800-62225400	Weak transcription	Colonic Mucosa	Colon
23	chr8:62224800-62225600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr8:62224800-62225800	Enhancers	Liver	Liver
25	chr8:62225000-62225200	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr8:62225000-62225400	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr8:62225200-62225800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:62225200-62226800	Enhancers	Duodenum Mucosa	Duodenum
29	chr8:62225400-62225600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr8:62225400-62226200	Enhancers	Colonic Mucosa	Colon
31	chr8:62225400-62226200	Enhancers	Fetal Thymus	thymus
32	chr8:62225600-62226200	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr8:62225600-62226400	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr8:62225600-62226800	Strong transcription	Fetal Brain Female	brain
35	chr8:62225800-62226400	Enhancers	Small Intestine	intestine
36	chr8:62225800-62228800	Weak transcription	Liver	Liver
37	chr8:62226400-62229000	Weak transcription	Fetal Intestine Large	intestine
38	chr8:62226800-62229000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr8:62226800-62235800	Weak transcription	Fetal Brain Female	brain
40	chr8:62228000-62228200	Enhancers	Fetal Thymus	thymus
41	chr8:62228800-62229400	Enhancers	Liver	Liver
42	chr8:62229000-62229400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr8:62229000-62229800	Enhancers	Fetal Intestine Large	intestine
44	chr8:62229200-62229800	Enhancers	Fetal Intestine Small	intestine
45	chr8:62233800-62234000	Enhancers	Fetal Brain Male	brain
46	chr8:62234200-62237400	Weak transcription	Fetal Brain Male	brain
47	chr8:62235800-62236000	Strong transcription	Fetal Brain Female	brain
48	chr8:62236000-62237400	ZNF genes & repeats	Fetal Brain Female	brain
49	chr8:62237400-62238000	ZNF genes & repeats	Fetal Brain Male	brain
50	chr8:62238000-62243400	Weak transcription	Fetal Brain Male	brain

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