Variant report

Variant	nsv1015485
Chromosome Location	chr8:4127704-4272847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:4130358-4130684	H1-hESC	embryonic stem cell:	n/a	chr8:4130518-4130529
2	CEBPB	chr8:4227126-4227302	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:4150042-4150242	HepG2	liver:	n/a	chr8:4150160-4150171
4	CEBPB	chr8:4130359-4130708	IMR90	lung:	n/a	chr8:4130518-4130529
5	CEBPB	chr8:4167594-4167820	K562	blood:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
6	CEBPB	chr8:4130382-4130659	K562	blood:	n/a	chr8:4130518-4130529
7	CEBPB	chr8:4227032-4227320	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:4167514-4167871	H1-hESC	embryonic stem cell:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
9	CEBPB	chr8:4130370-4130681	HepG2	liver:	n/a	chr8:4130518-4130529
10	CEBPB	chr8:4193140-4193359	HepG2	liver:	n/a	chr8:4193194-4193205 chr8:4193194-4193207
11	CEBPB	chr8:4242430-4242568	A549	lung:	n/a	n/a
12	CEBPB	chr8:4167533-4167842	IMR90	lung:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
13	CEBPB	chr8:4167517-4167869	HepG2	liver:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
14	CEBPB	chr8:4250895-4251106	HepG2	liver:	n/a	chr8:4250917-4250928
15	CEBPB	chr8:4214721-4214989	HepG2	liver:	n/a	chr8:4214850-4214859 chr8:4214850-4214859 chr8:4214850-4214859
16	CEBPB	chr8:4130385-4130669	A549	lung:	n/a	chr8:4130518-4130529
17	CTCF	chr8:4257280-4257430	A549	lung:	n/a	n/a
18	CTCF	chr8:4138586-4138732	Medullo	brain:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
19	CTCF	chr8:4257441-4257652	Pancreas_OC	pancreas:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
20	CTCF	chr8:4138514-4138766	H1-hESC	embryonic stem cell:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
21	CTCF	chr8:4138531-4138750	LNCaP	prostate:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
22	CTCF	chr8:4138537-4138751	A549	lung:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
23	CTCF	chr8:4138560-4138710	WERI-Rb-1	eye:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
24	CTCF	chr8:4257467-4257635	Lung_OC	lung:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
25	CTCF	chr8:4138560-4138710	K562	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
26	CTCF	chr8:4138580-4138730	SK-N-SH_RA	brain:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
27	CTCF	chr8:4138536-4138751	MCF-7	breast:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
28	CTCF	chr8:4138560-4138710	GM12870	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
29	CTCF	chr8:4257440-4257590	RPTEC	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
30	CTCF	chr8:4257479-4257619	Hela-S3	cervix:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
31	CTCF	chr8:4138460-4138750	A549	lung:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
32	CTCF	chr8:4138580-4138730	GM12874	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
33	CTCF	chr8:4257440-4257590	NHEK	skin:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
34	CTCF	chr8:4257388-4257676	HepG2	liver:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
35	CTCF	chr8:4167620-4167770	HL-60	blood:	n/a	chr8:4167714-4167735 chr8:4167724-4167732
36	CTCF	chr8:4138560-4138710	GM12867	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
37	CTCF	chr8:4138571-4138737	K562	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
38	CTCF	chr8:4257440-4257590	HAc	cerebellar:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
39	CTCF	chr8:4257460-4257610	HepG2	liver:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
40	CTCF	chr8:4138560-4138710	GM12875	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
41	CTCF	chr8:4257420-4257570	SK-N-SH_RA	brain:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
42	CTCF	chr8:4138578-4138729	GM12878	blood:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
43	CTCF	chr8:4220160-4220310	HCFaa	heart:	n/a	n/a
44	CTCF	chr8:4257485-4257570	MCF-7	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
45	CTCF	chr8:4257472-4257613	Medullo	brain:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
46	CTCF	chr8:4138620-4138770	RPTEC	kidney:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
47	CTCF	chr8:4257464-4257602	HepG2	liver:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
48	CTCF	chr8:4138500-4138650	GM12873	blood:	n/a	chr8:4138628-4138641
49	CTCF	chr8:4138508-4138804	H1-hESC	embryonic stem cell:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
50	CTCF	chr8:4257460-4257610	HRE	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4238976-4239026	GM12878	blood:	n/a
2	chr8:4238976-4239026	GM12878	blood:	n/a
3	chr8:4188646-4188696	A549	lung:	n/a
4	chr8:4183726-4183776	NHDF-neo	bronchial:	n/a
5	chr8:4238976-4239026	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:4183880-4183930	PrEC	prostate:	n/a
7	chr8:4183880-4183930	HRCEpiC	kidney:	n/a
8	chr8:4238976-4239026	PrEC	prostate:	n/a
9	chr8:4238976-4239026	ProgFib	skin:	n/a
10	chr8:4183642-4183692	HL-60	blood:	n/a
11	chr8:4183880-4183930	U87	brain:	n/a
12	chr8:4183726-4183776	PrEC	prostate:	n/a
13	chr8:4183880-4183930	AG09319	gingival:	n/a
14	chr8:4183726-4183776	AG04450	lung:	fetal
15	chr8:4183726-4183776	ECC-1	luminal epithelium:	n/a
16	chr8:4188646-4188696	BE2_C	brain:	n/a
17	chr8:4188646-4188696	PANC-1	pancreas:	n/a
18	chr8:4188646-4188696	RPTEC	kidney:	n/a
19	chr8:4183642-4183692	AG04450	lung:	fetal
20	chr8:4188646-4188696	AG10803	skin:	n/a
21	chr8:4183726-4183776	NH-A	brain:	n/a
22	chr8:4183880-4183930	HepG2	liver:	n/a
23	chr8:4183726-4183776	PFSK-1	brain:	n/a
24	chr8:4183880-4183930	A549	lung:	n/a
25	chr8:4183642-4183692	ProgFib	skin:	n/a
26	chr8:4238976-4239026	NT2-D1	testis:	n/a
27	chr8:4238976-4239026	GM06990	blood:	n/a
28	chr8:4188646-4188696	SAEC	small airway:	n/a
29	chr8:4183726-4183776	LNCaP	prostate:	n/a
30	chr8:4188646-4188696	LNCaP	prostate:	n/a
31	chr8:4183880-4183930	HCM	heart:	n/a
32	chr8:4183642-4183692	HUVEC	blood vessel:	n/a
33	chr8:4183642-4183692	K562	blood:	n/a
34	chr8:4188646-4188696	GM12891	blood:	n/a
35	chr8:4238976-4239026	NH-A	brain:	n/a
36	chr8:4183880-4183930	AG09309	skin:	n/a
37	chr8:4183642-4183692	HMEC	breast:	n/a
38	chr8:4188646-4188696	HCM	heart:	n/a
39	chr8:4238976-4239026	Caco-2	colon:	n/a
40	chr8:4238976-4239026	SAEC	small airway:	n/a
41	chr8:4183642-4183692	LNCaP	prostate:	n/a
42	chr8:4188646-4188696	H1-hESC	embryonic stem cell:	embryo
43	chr8:4183642-4183692	PANC-1	pancreas:	n/a
44	chr8:4188646-4188696	ovcar-3	ovarian:	n/a
45	chr8:4183726-4183776	ovcar-3	ovarian:	n/a
46	chr8:4188646-4188696	Caco-2	colon:	n/a
47	chr8:4183880-4183930	HCT-116	colon:	n/a
48	chr8:4183642-4183692	HCT-116	colon:	n/a
49	chr8:4188646-4188696	SK-N-SH_RA	brain:	n/a
50	chr8:4183880-4183930	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:4092133..4092721-chr8:4257157..4257997,2	MCF-7	breast:
2	chr1:103323089..103325462-chr8:4135925..4138695,2	MCF-7	breast:
3	chr8:4138578..4139163-chr8:4399169..4399679,2	MCF-7	breast:
4	chr8:3141838..3142362-chr8:4257194..4257921,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-8	chr8:4250344-4250612	NONHSAT124750

Variant related genes	Relation type
RN7SL872P	TF binding region
RN7SL872P	CpG island
ENSG00000183117	chromatin interactions

Extended variants
information (count: 7164 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:7164 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542221480	chr8:4128008-4128009	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560330041	chr8:4128012-4128013	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528378217	chr8:4128030-4128031	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546589398	chr8:4128039-4128040	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571374486	chr8:4128064-4128065	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371518415	chr8:4128083-4128084	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548119552	chr8:4128109-4128110	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190464289	chr8:4128129-4128130	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs710256	chr8:4128143-4128144	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs138541904	chr8:4128146-4128147	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141556920	chr8:4128150-4128151	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568383596	chr8:4128160-4128161	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554548412	chr8:4128166-4128167	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369174154	chr8:4128170-4128171	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181841740	chr8:4128176-4128177	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146203183	chr8:4128183-4128184	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111376283	chr8:4128194-4128195	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544803997	chr8:4128195-4128196	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186046387	chr8:4128202-4128203	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574981470	chr8:4128212-4128213	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188848233	chr8:4128224-4128225	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560499277	chr8:4128234-4128235	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555643977	chr8:4128246-4128247	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572354095	chr8:4128248-4128249	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540493625	chr8:4128251-4128252	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550876572	chr8:4128254-4128255	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575814632	chr8:4128256-4128257	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532309729	chr8:4128271-4128272	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550341932	chr8:4128277-4128278	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs137941531	chr8:4128288-4128289	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529733586	chr8:4128296-4128297	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547981886	chr8:4128309-4128310	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78686130	chr8:4128311-4128312	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533565418	chr8:4128325-4128326	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552182441	chr8:4128329-4128330	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571137887	chr8:4128337-4128338	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538585718	chr8:4128338-4128339	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556785431	chr8:4128339-4128340	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62481985	chr8:4128340-4128341	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149391371	chr8:4128347-4128348	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35901734	chr8:4128350-4128351	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553997240	chr8:4128377-4128378	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181307864	chr8:4128388-4128389	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186364019	chr8:4128397-4128398	Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372861279	chr8:4128405-4128406	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs144811956	chr8:4128415-4128416	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs576726307	chr8:4128426-4128427	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs73660721	chr8:4128435-4128436	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs62481986	chr8:4128437-4128438	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs190796841	chr8:4128448-4128449	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Schizophrenia	21346763	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	22315472	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4128000-4128400	Active TSS	Duodenum Mucosa	Duodenum
2	chr8:4128000-4128400	Enhancers	Fetal Intestine Small	intestine
3	chr8:4128000-4128400	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr8:4128000-4132600	Bivalent Enhancer	Fetal Heart	heart
5	chr8:4139400-4140000	Enhancers	Fetal Brain Female	brain
6	chr8:4145600-4146000	Enhancers	Dnd41	blood
7	chr8:4146800-4148000	Enhancers	Fetal Brain Male	brain
8	chr8:4147400-4148200	Enhancers	Fetal Brain Female	brain
9	chr8:4148000-4149000	Weak transcription	Fetal Brain Male	brain
10	chr8:4149000-4149200	Enhancers	Fetal Brain Male	brain
11	chr8:4150600-4150800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:4170400-4171200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:4170600-4171000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:4170800-4171000	Enhancers	Pancreas	Pancrea
15	chr8:4171000-4172400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:4171000-4188800	Weak transcription	Pancreas	Pancrea
17	chr8:4172400-4172600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:4175000-4175400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
19	chr8:4180800-4182400	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr8:4181200-4183000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr8:4181400-4181800	Enhancers	Stomach Mucosa	stomach
22	chr8:4181800-4182000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:4181800-4182200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr8:4182000-4183200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:4182600-4182800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:4182600-4183200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr8:4182600-4183800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr8:4182800-4183400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:4183000-4183400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:4187800-4189800	Enhancers	Fetal Intestine Large	intestine
31	chr8:4188200-4188800	Enhancers	Liver	Liver
32	chr8:4188200-4190000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:4188200-4190000	Enhancers	Brain Germinal Matrix	brain
34	chr8:4188400-4190000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:4188400-4190000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:4188400-4190000	Enhancers	Stomach Mucosa	stomach
37	chr8:4188600-4188800	Enhancers	Duodenum Mucosa	Duodenum
38	chr8:4188600-4189000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr8:4188600-4189800	Enhancers	Dnd41	blood
40	chr8:4188600-4190000	Enhancers	Brain Anterior Caudate	brain
41	chr8:4188800-4189000	Flanking Active TSS	Liver	Liver
42	chr8:4188800-4189200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr8:4188800-4189400	Enhancers	Fetal Intestine Small	intestine
44	chr8:4188800-4189600	Weak transcription	Duodenum Mucosa	Duodenum
45	chr8:4188800-4189800	Enhancers	Brain Hippocampus Middle	brain
46	chr8:4188800-4189800	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr8:4188800-4190000	Enhancers	Brain Angular Gyrus	brain
48	chr8:4188800-4190000	Enhancers	Brain Cingulate Gyrus	brain
49	chr8:4188800-4190200	Enhancers	Pancreas	Pancrea
50	chr8:4189000-4189200	Enhancers	Liver	Liver

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