Variant report

Variant	nsv1022434
Chromosome Location	chr8:10866242-10916523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1024)
CpG islands
(count:1651)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:10901534-10901559	K562	blood:	n/a	n/a
2	ATF1	chr8:10873976-10874327	K562	blood:	n/a	n/a
3	ATF2	chr8:10873806-10874116	GM12878	blood:	n/a	n/a
4	ATF2	chr8:10873647-10874313	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:10873723-10874238	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:10889516-10889660	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:10872506-10873262	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:10873577-10874254	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:10883862-10884157	GM12878	blood:	n/a	n/a
10	BATF	chr8:10868286-10868515	GM12878	blood:	n/a	n/a
11	BCLAF1	chr8:10873793-10874275	GM12878	blood:	n/a	chr8:10873813-10873826
12	BHLHE40	chr8:10873848-10874279	K562	blood:	n/a	n/a
13	BHLHE40	chr8:10873644-10874487	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:10873202-10873388	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:10872416-10872832	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:10873874-10874286	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr8:10872763-10872964	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr8:10873813-10874278	K562	blood:	n/a	n/a
19	CCNT2	chr8:10873332-10874389	K562	blood:	n/a	chr8:10873949-10873958 chr8:10874252-10874261
20	CEBPB	chr8:10883535-10883715	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:10880085-10880313	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:10878321-10878611	IMR90	lung:	n/a	chr8:10878490-10878501 chr8:10878489-10878502
23	CEBPB	chr8:10880060-10880393	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:10878327-10878626	K562	blood:	n/a	chr8:10878490-10878501 chr8:10878489-10878502
25	CEBPB	chr8:10907525-10907527	K562	blood:	n/a	n/a
26	CEBPB	chr8:10880111-10880341	A549	lung:	n/a	n/a
27	CEBPB	chr8:10882490-10882800	A549	lung:	n/a	chr8:10882636-10882647
28	CEBPB	chr8:10878351-10878632	A549	lung:	n/a	chr8:10878490-10878501 chr8:10878489-10878502
29	CEBPB	chr8:10905082-10905328	IMR90	lung:	n/a	chr8:10905215-10905226
30	CEBPB	chr8:10905125-10905281	A549	lung:	n/a	chr8:10905215-10905226
31	CEBPB	chr8:10874740-10874952	K562	blood:	n/a	n/a
32	CEBPB	chr8:10905148-10905348	K562	blood:	n/a	chr8:10905215-10905226
33	CEBPB	chr8:10878340-10878646	HepG2	liver:	n/a	chr8:10878490-10878501 chr8:10878489-10878502
34	CEBPB	chr8:10871788-10872189	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:10882503-10882815	HepG2	liver:	n/a	chr8:10882636-10882647
36	CEBPB	chr8:10905066-10905339	HepG2	liver:	n/a	chr8:10905215-10905226
37	CEBPB	chr8:10878349-10878650	H1-hESC	embryonic stem cell:	n/a	chr8:10878490-10878501 chr8:10878489-10878502
38	CEBPB	chr8:10880154-10880314	K562	blood:	n/a	n/a
39	CEBPB	chr8:10883498-10883736	A549	lung:	n/a	n/a
40	CEBPB	chr8:10873871-10874213	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPD	chr8:10873911-10874805	K562	blood:	n/a	n/a
42	CEBPD	chr8:10873966-10874878	K562	blood:	n/a	n/a
43	CHD1	chr8:10872397-10872982	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr8:10873779-10874073	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr8:10873756-10874238	GM12878	blood:	n/a	n/a
46	CHD2	chr8:10872923-10873107	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr8:10872893-10873059	GM12878	blood:	n/a	n/a
48	CHD2	chr8:10873791-10874217	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:10873924-10874224	K562	blood:	n/a	n/a
50	CHD2	chr8:10873342-10874261	GM12878	blood:	n/a	n/a

(count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10872819-10872869	NH-A	brain:	n/a
2	chr8:10874215-10874265	SK-N-SH_RA	brain:	n/a
3	chr8:10874215-10874265	HNPCEpiC	eye:	n/a
4	chr8:10874016-10874066	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:10872819-10872869	NH-A	brain:	n/a
6	chr8:10874215-10874265	SK-N-SH_RA	brain:	n/a
7	chr8:10874215-10874265	HNPCEpiC	eye:	n/a
8	chr8:10874016-10874066	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:10893965-10894015	HRPEpiC	eye:	n/a
10	chr8:10897405-10897455	HCM	heart:	n/a
11	chr8:10878898-10878948	PANC-1	pancreas:	n/a
12	chr8:10873155-10873205	GM06990	blood:	n/a
13	chr8:10877312-10877362	HCF	heart:	n/a
14	chr8:10871371-10871421	HIPEpiC	eye:	n/a
15	chr8:10871191-10871241	NHDF-neo	bronchial:	n/a
16	chr8:10873155-10873205	SK-N-SH	brain:	n/a
17	chr8:10872626-10872676	HMEC	breast:	n/a
18	chr8:10874215-10874265	PANC-1	pancreas:	n/a
19	chr8:10915402-10915452	HRCEpiC	kidney:	n/a
20	chr8:10897293-10897343	HMEC	breast:	n/a
21	chr8:10915402-10915452	HCM	heart:	n/a
22	chr8:10907750-10907800	HEEpiC	esophagus:	n/a
23	chr8:10873155-10873205	LNCaP	prostate:	n/a
24	chr8:10872626-10872676	H1-hESC	embryonic stem cell:	embryo
25	chr8:10878898-10878948	IMR90	lung:	fetal
26	chr8:10893100-10893150	NHBE	bronchial:	n/a
27	chr8:10915402-10915452	MCF-7	breast:	n/a
28	chr8:10873619-10873669	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:10875246-10875296	K562	blood:	n/a
30	chr8:10897405-10897455	HEEpiC	esophagus:	n/a
31	chr8:10907788-10907838	HRE	kidney:	n/a
32	chr8:10875534-10875584	HCPEpiC	choroid plexus:	n/a
33	chr8:10872648-10872698	HEK293	kidney:	embryo
34	chr8:10907718-10907768	U87	brain:	n/a
35	chr8:10871191-10871241	H1-hESC	embryonic stem cell:	embryo
36	chr8:10893965-10894015	U87	brain:	n/a
37	chr8:10892823-10892873	HepG2	liver:	n/a
38	chr8:10906938-10906988	RPTEC	kidney:	n/a
39	chr8:10873619-10873669	BE2_C	brain:	n/a
40	chr8:10871191-10871241	HRCEpiC	kidney:	n/a
41	chr8:10875534-10875584	MCF-7	breast:	n/a
42	chr8:10907718-10907768	SK-N-MC	brain:	n/a
43	chr8:10872626-10872676	K562	blood:	n/a
44	chr8:10915402-10915452	Hela-S3	cervix:	n/a
45	chr8:10871371-10871421	SAEC	small airway:	n/a
46	chr8:10907788-10907838	MCF10A-Er-Src	breast:	n/a
47	chr8:10893965-10894015	ovcar-3	ovarian:	n/a
48	chr8:10897293-10897343	HNPCEpiC	eye:	n/a
49	chr8:10873155-10873205	HNPCEpiC	eye:	n/a
50	chr8:10871371-10871421	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:10887222..10889685-chr8:10905766..10908616,2	K562	blood:
2	chr8:10785284..10786125-chr8:10873662..10874301,2	K562	blood:
3	chr8:10786051..10786569-chr8:10873648..10874515,2	MCF-7	breast:
4	chr8:10883944..10886637-chr8:10888412..10890996,2	K562	blood:
5	chr8:10911187..10913100-chr8:10924744..10926931,2	MCF-7	breast:
6	chr8:10869029..10871589-chr8:10873580..10875933,2	MCF-7	breast:
7	chr8:10883944..10886637-chr8:10888412..10890996,2	K562	blood:
8	chr8:10772740..10774724-chr8:10885497..10887029,2	K562	blood:
9	chr8:10861649..10864572-chr8:10871901..10875246,3	K562	blood:
10	chr8:10905368..10906915-chr8:10917694..10919634,2	K562	blood:
11	chr8:10785690..10786544-chr8:10913111..10914143,3	MCF-7	breast:
12	chr8:10865711..10867297-chr8:10870824..10872479,2	K562	blood:
13	chr8:10867872..10870530-chr8:10872109..10874885,2	K562	blood:
14	chr8:10886694..10889685-chr8:10905766..10907458,2	K562	blood:
15	chr8:10864237..10865901-chr8:10868526..10870693,2	MCF-7	breast:
16	chr8:10869029..10871589-chr8:10873580..10875933,2	MCF-7	breast:
17	chr8:10867872..10870530-chr8:10872109..10874885,2	K562	blood:
18	chr8:10887222..10889685-chr8:10905766..10908616,2	K562	blood:
19	chr8:10865711..10867297-chr8:10870824..10872479,2	K562	blood:
20	chr8:10886694..10889685-chr8:10905766..10907458,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF131215.6.1-2	chr8:10880370-10880644	NONHSAT125029
2	lnc-AF131215.6.1-2	chr8:10881285-10881816	NONHSAT125029

miRNA name	Chromosome Location	mirBase accession
hsa-miR-598-5p	chr8:10892767-10892789	MIMAT0026620
hsa-miR-598-3p	chr8:10892731-10892752	MIMAT0003266

No data

Variant related genes	Relation type
MIR598	TF binding region
MIR598	CpG island
SPIN1	Mature miRNA region
HIVEP2	Mature miRNA region
PTMA	Mature miRNA region
NPM1	Mature miRNA region
URI1	Mature miRNA region
FAM21A	Mature miRNA region
CASP8AP2	Mature miRNA region
CALM1	Mature miRNA region
NCL	Mature miRNA region
TNPO2	Mature miRNA region
HIST4H4	Mature miRNA region
BCOR	Mature miRNA region
GTF3C1	Mature miRNA region
CCT7	Mature miRNA region
C1orf174	Mature miRNA region

Extended variants
information (count: 2604 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2604 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11988372	chr8:10866242-10866243	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540818397	chr8:10866249-10866250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568056013	chr8:10866262-10866263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188014467	chr8:10866280-10866281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556973657	chr8:10866281-10866282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575266094	chr8:10866291-10866292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117292948	chr8:10866300-10866301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557514956	chr8:10866307-10866308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373793886	chr8:10866327-10866328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192820289	chr8:10866346-10866347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139711133	chr8:10866347-10866348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149776388	chr8:10866371-10866372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573657444	chr8:10866409-10866410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145747555	chr8:10866424-10866425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562969289	chr8:10866448-10866449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112880882	chr8:10866454-10866455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533279813	chr8:10866487-10866488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551883574	chr8:10866502-10866503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139983604	chr8:10866510-10866511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570361597	chr8:10866522-10866523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182271811	chr8:10866534-10866535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549659925	chr8:10866567-10866568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567965387	chr8:10866587-10866588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61427182	chr8:10866603-10866604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs550322257	chr8:10866618-10866619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568869184	chr8:10866634-10866635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539140506	chr8:10866683-10866684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531211378	chr8:10866698-10866699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558946688	chr8:10866700-10866701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528044160	chr8:10866702-10866703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368726267	chr8:10866709-10866710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145513927	chr8:10866710-10866711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147730634	chr8:10866711-10866712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572690927	chr8:10866741-10866742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186520222	chr8:10866743-10866744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191210618	chr8:10866750-10866751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142638737	chr8:10866824-10866825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544558171	chr8:10866830-10866831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34329552	chr8:10866851-10866852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539457761	chr8:10866894-10866895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556341374	chr8:10866932-10866933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577990819	chr8:10866935-10866936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545511425	chr8:10866944-10866945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571200365	chr8:10866954-10866955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560580152	chr8:10866969-10866970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs57240497	chr8:10866989-10866990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184792809	chr8:10867001-10867002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530280888	chr8:10867003-10867004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28446808	chr8:10867012-10867013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369719987	chr8:10867038-10867039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10859400-10872200	Weak transcription	Brain Angular Gyrus	brain
2	chr8:10865000-10866400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:10865200-10870400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:10865400-10870400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr8:10865400-10870600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr8:10865800-10870600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr8:10866000-10870400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:10866400-10870600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:10870400-10870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:10870400-10870600	Enhancers	Pancreas	Pancrea
11	chr8:10870400-10870600	Active TSS	Spleen	Spleen
12	chr8:10870400-10871200	Enhancers	H9 Cell Line	embryonic stem cell
13	chr8:10870400-10871400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr8:10870400-10872400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:10870600-10871200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:10870600-10871200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr8:10870600-10871400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr8:10870600-10871400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr8:10870600-10871400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:10870600-10871600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:10870600-10872000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:10870600-10872400	Weak transcription	Spleen	Spleen
23	chr8:10870800-10871400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
24	chr8:10870800-10871400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr8:10870800-10872400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:10870800-10872400	Weak transcription	Pancreas	Pancrea
27	chr8:10871000-10872400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr8:10871200-10871400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:10871200-10871800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr8:10871200-10871800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr8:10871200-10872600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr8:10871200-10872600	Bivalent Enhancer	NHEK	skin
33	chr8:10871400-10871600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:10871400-10871600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
35	chr8:10871400-10871600	Enhancers	HMEC	breast
36	chr8:10871400-10871800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
37	chr8:10871400-10871800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr8:10871400-10872400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr8:10871400-10872400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:10871400-10872600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
41	chr8:10871400-10872600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:10871400-10872800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:10871400-10873000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:10871400-10874200	Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr8:10871400-10874400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr8:10871600-10872000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
47	chr8:10871600-10872200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:10871600-10872200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:10871600-10872400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr8:10871600-10872400	Weak transcription	HMEC	breast

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