Variant report

Variant	nsv1032488
Chromosome Location	chr8:4072826-4328057
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	BACH1	chr8:4101087-4101507	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:4299608-4299681	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:4107408-4107727	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr8:4092217-4092221	GM12878	blood:	n/a	n/a
5	BRCA1	chr8:4080738-4080739	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr8:4214721-4214989	HepG2	liver:	n/a	chr8:4214850-4214859 chr8:4214850-4214859 chr8:4214850-4214859
7	CEBPB	chr8:4081697-4082078	HepG2	liver:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
8	CEBPB	chr8:4102669-4102952	H1-hESC	embryonic stem cell:	n/a	chr8:4102773-4102784
9	CEBPB	chr8:4081771-4082062	ECC-1	luminal epithelium:	n/a	chr8:4081879-4081890
10	CEBPB	chr8:4306031-4306222	H1-hESC	embryonic stem cell:	n/a	chr8:4306101-4306110 chr8:4306099-4306110 chr8:4306100-4306111 chr8:4306101-4306110 chr8:4306101-4306110 chr8:4306099-4306112 chr8:4306099-4306112 chr8:4306101-4306110
11	CEBPB	chr8:4300811-4301138	A549	lung:	n/a	chr8:4300971-4300982
12	CEBPB	chr8:4102603-4102944	A549	lung:	n/a	chr8:4102773-4102784
13	CEBPB	chr8:4127206-4127570	HepG2	liver:	n/a	chr8:4127386-4127399 chr8:4127386-4127397
14	CEBPB	chr8:4311207-4311343	HepG2	liver:	n/a	chr8:4311320-4311329 chr8:4311318-4311331 chr8:4311320-4311329 chr8:4311318-4311331 chr8:4311320-4311329 chr8:4311320-4311329
15	CEBPB	chr8:4242430-4242568	A549	lung:	n/a	n/a
16	CEBPB	chr8:4102599-4102930	HepG2	liver:	n/a	chr8:4102773-4102784
17	CEBPB	chr8:4167533-4167842	IMR90	lung:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
18	CEBPB	chr8:4227126-4227302	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:4081702-4082079	H1-hESC	embryonic stem cell:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
20	CEBPB	chr8:4130358-4130684	H1-hESC	embryonic stem cell:	n/a	chr8:4130518-4130529
21	CEBPB	chr8:4250895-4251106	HepG2	liver:	n/a	chr8:4250917-4250928
22	CEBPB	chr8:4300804-4301145	HepG2	liver:	n/a	chr8:4300971-4300982
23	CEBPB	chr8:4130385-4130669	A549	lung:	n/a	chr8:4130518-4130529
24	CEBPB	chr8:4081697-4082074	IMR90	lung:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
25	CEBPB	chr8:4081771-4081978	A549	lung:	n/a	chr8:4081879-4081890
26	CEBPB	chr8:4130370-4130681	HepG2	liver:	n/a	chr8:4130518-4130529
27	CEBPB	chr8:4167514-4167871	H1-hESC	embryonic stem cell:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
28	CEBPB	chr8:4305929-4306248	HepG2	liver:	n/a	chr8:4306101-4306110 chr8:4306099-4306110 chr8:4306100-4306111 chr8:4306101-4306110 chr8:4306101-4306110 chr8:4306099-4306112 chr8:4306099-4306112 chr8:4306101-4306110
29	CEBPB	chr8:4300789-4301140	IMR90	lung:	n/a	chr8:4300971-4300982
30	CEBPB	chr8:4127238-4127649	A549	lung:	n/a	chr8:4127386-4127399 chr8:4127386-4127397
31	CEBPB	chr8:4193140-4193359	HepG2	liver:	n/a	chr8:4193194-4193205 chr8:4193194-4193207
32	CEBPB	chr8:4081798-4082075	ECC-1	luminal epithelium:	n/a	chr8:4081879-4081890
33	CEBPB	chr8:4167594-4167820	K562	blood:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
34	CEBPB	chr8:4102595-4102967	IMR90	lung:	n/a	chr8:4102773-4102784
35	CEBPB	chr8:4130382-4130659	K562	blood:	n/a	chr8:4130518-4130529
36	CEBPB	chr8:4150042-4150242	HepG2	liver:	n/a	chr8:4150160-4150171
37	CEBPB	chr8:4081701-4082072	K562	blood:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
38	CEBPB	chr8:4081708-4082060	A549	lung:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
39	CEBPB	chr8:4127347-4127403	H1-hESC	embryonic stem cell:	n/a	chr8:4127386-4127399 chr8:4127386-4127397
40	CEBPB	chr8:4127248-4127571	IMR90	lung:	n/a	chr8:4127386-4127399 chr8:4127386-4127397
41	CEBPB	chr8:4081643-4082076	A549	lung:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
42	CEBPB	chr8:4167517-4167869	HepG2	liver:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
43	CEBPB	chr8:4081706-4082064	Hela-S3	cervix:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
44	CEBPB	chr8:4227032-4227320	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:4300849-4301101	K562	blood:	n/a	chr8:4300971-4300982
46	CEBPB	chr8:4130359-4130708	IMR90	lung:	n/a	chr8:4130518-4130529
47	CHD2	chr8:4080831-4080853	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:4210715-4210728	Lung_OC	lung:	n/a	n/a
49	CTCF	chr8:4138580-4138730	RPTEC	kidney:	n/a	chr8:4138628-4138641 chr8:4138641-4138662 chr8:4138639-4138657
50	CTCF	chr8:4092134-4092136	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4183642-4183692	NHBE	bronchial:	n/a
2	chr8:4183642-4183692	NHBE	bronchial:	n/a
3	chr8:4238976-4239026	MCF10A-Er-Src	breast:	n/a
4	chr8:4188646-4188696	K562	blood:	n/a
5	chr8:4183642-4183692	PFSK-1	brain:	n/a
6	chr8:4188646-4188696	HEEpiC	esophagus:	n/a
7	chr8:4183726-4183776	HRPEpiC	eye:	n/a
8	chr8:4183726-4183776	AG09309	skin:	n/a
9	chr8:4183726-4183776	ProgFib	skin:	n/a
10	chr8:4183642-4183692	NH-A	brain:	n/a
11	chr8:4183642-4183692	GM06990	blood:	n/a
12	chr8:4238976-4239026	AG09319	gingival:	n/a
13	chr8:4188646-4188696	AG09319	gingival:	n/a
14	chr8:4183642-4183692	HCF	heart:	n/a
15	chr8:4183642-4183692	GM12891	blood:	n/a
16	chr8:4183880-4183930	K562	blood:	n/a
17	chr8:4183880-4183930	MCF10A-Er-Src	breast:	n/a
18	chr8:4238976-4239026	BJ	skin:	n/a
19	chr8:4183880-4183930	SK-N-SH_RA	brain:	n/a
20	chr8:4183726-4183776	HUVEC	blood vessel:	n/a
21	chr8:4183880-4183930	HNPCEpiC	eye:	n/a
22	chr8:4183726-4183776	ECC-1	luminal epithelium:	n/a
23	chr8:4183726-4183776	K562	blood:	n/a
24	chr8:4183642-4183692	AoSMC	blood vessel:	n/a
25	chr8:4183880-4183930	SKMC	muscle:	n/a
26	chr8:4183880-4183930	H1-hESC	embryonic stem cell:	embryo
27	chr8:4183726-4183776	SAEC	small airway:	n/a
28	chr8:4238976-4239026	HRE	kidney:	n/a
29	chr8:4188646-4188696	Hepatocyte	liver:	n/a
30	chr8:4238976-4239026	Hela-S3	cervix:	n/a
31	chr8:4238976-4239026	ProgFib	skin:	n/a
32	chr8:4188646-4188696	Jurkat	blood:	n/a
33	chr8:4183726-4183776	MCF10A-Er-Src	breast:	n/a
34	chr8:4183642-4183692	T-47D	breast:	n/a
35	chr8:4188646-4188696	SKMC	muscle:	n/a
36	chr8:4183880-4183930	HEK293	kidney:	embryo
37	chr8:4238976-4239026	AG09309	skin:	n/a
38	chr8:4183880-4183930	SK-N-SH	brain:	n/a
39	chr8:4183642-4183692	Caco-2	colon:	n/a
40	chr8:4183880-4183930	MCF-7	breast:	n/a
41	chr8:4238976-4239026	SK-N-MC	brain:	n/a
42	chr8:4188646-4188696	AG09309	skin:	n/a
43	chr8:4183726-4183776	PrEC	prostate:	n/a
44	chr8:4238976-4239026	AG04450	lung:	fetal
45	chr8:4183642-4183692	ovcar-3	ovarian:	n/a
46	chr8:4238976-4239026	HRCEpiC	kidney:	n/a
47	chr8:4238976-4239026	SK-N-SH	brain:	n/a
48	chr8:4183880-4183930	Jurkat	blood:	n/a
49	chr8:4183642-4183692	GM12878	blood:	n/a
50	chr8:4188646-4188696	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr8:4138578..4139163-chr8:4399169..4399679,2	MCF-7	breast:
2	chr8:4092133..4092721-chr8:4257157..4257997,2	MCF-7	breast:
3	chr1:103323089..103325462-chr8:4135925..4138695,2	MCF-7	breast:
4	chr8:4092133..4092721-chr8:4257157..4257997,2	MCF-7	breast:
5	chr8:4091582..4092324-chr8:4399511..4400398,2	MCF-7	breast:
6	chr8:4091951..4092554-chr8:4399113..4400010,2	MCF-7	breast:
7	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: 10477 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:10477 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549508178	chr8:4072840-4072841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570280519	chr8:4072847-4072848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537614940	chr8:4072864-4072865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192963428	chr8:4072877-4072878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185135900	chr8:4072893-4072894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149704516	chr8:4072897-4072898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553332993	chr8:4072899-4072900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577915540	chr8:4072914-4072915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538542463	chr8:4072927-4072928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17069495	chr8:4072933-4072934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs189603060	chr8:4072942-4072943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575858360	chr8:4072947-4072948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144312120	chr8:4072959-4072960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148772454	chr8:4072972-4072973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529184114	chr8:4072988-4072989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547328496	chr8:4072997-4072998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192815289	chr8:4073006-4073007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532759653	chr8:4073008-4073009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200138801	chr8:4073030-4073031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201124149	chr8:4073031-4073032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs398067515	chr8:4073040-4073041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551476922	chr8:4073045-4073046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571881571	chr8:4073048-4073049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537678311	chr8:4073055-4073056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548049849	chr8:4073059-4073060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549592592	chr8:4073082-4073083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568010035	chr8:4073084-4073085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535333235	chr8:4073089-4073090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1714716	chr8:4073091-4073092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183970884	chr8:4073098-4073099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9792308	chr8:4073102-4073103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557066539	chr8:4073113-4073114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188312196	chr8:4073135-4073136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543260678	chr8:4073150-4073151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561548594	chr8:4073165-4073166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573714075	chr8:4073168-4073169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541334899	chr8:4073194-4073195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559358682	chr8:4073195-4073196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532973835	chr8:4073203-4073204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144889932	chr8:4073210-4073211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530520113	chr8:4073214-4073215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180783188	chr8:4073219-4073220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2407312	chr8:4073225-4073226	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs1714717	chr8:4073265-4073266	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs9792313	chr8:4073271-4073272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571764984	chr8:4073280-4073281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372189704	chr8:4073296-4073297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539083482	chr8:4073297-4073298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116392736	chr8:4073326-4073327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376647730	chr8:4073330-4073331	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:132)

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
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	22315472	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4070400-4074600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:4070600-4074600	Enhancers	Fetal Brain Male	brain
3	chr8:4071600-4073200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:4072200-4074400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:4072600-4073600	Enhancers	Brain Germinal Matrix	brain
6	chr8:4072600-4074200	Enhancers	Fetal Muscle Leg	muscle
7	chr8:4072600-4074400	Enhancers	Fetal Brain Female	brain
8	chr8:4072800-4073200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:4073200-4074000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:4073200-4074200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:4073400-4074400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr8:4074600-4078200	Weak transcription	Fetal Brain Male	brain
13	chr8:4078200-4078600	Enhancers	Fetal Brain Male	brain
14	chr8:4089800-4092800	Enhancers	Dnd41	blood
15	chr8:4092000-4092600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:4092000-4092600	Enhancers	Fetal Heart	heart
17	chr8:4092200-4092800	Enhancers	Fetal Muscle Leg	muscle
18	chr8:4092800-4093400	Weak transcription	Fetal Muscle Leg	muscle
19	chr8:4093400-4093600	Enhancers	Fetal Muscle Leg	muscle
20	chr8:4100400-4102000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr8:4100600-4101800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr8:4100800-4101400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr8:4101400-4101600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr8:4101400-4101800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr8:4107400-4108600	Bivalent Enhancer	Fetal Heart	heart
26	chr8:4119800-4120200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr8:4119800-4120200	Enhancers	Dnd41	blood
28	chr8:4128000-4128400	Active TSS	Duodenum Mucosa	Duodenum
29	chr8:4128000-4128400	Enhancers	Fetal Intestine Small	intestine
30	chr8:4128000-4128400	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr8:4128000-4132600	Bivalent Enhancer	Fetal Heart	heart
32	chr8:4139400-4140000	Enhancers	Fetal Brain Female	brain
33	chr8:4145600-4146000	Enhancers	Dnd41	blood
34	chr8:4146800-4148000	Enhancers	Fetal Brain Male	brain
35	chr8:4147400-4148200	Enhancers	Fetal Brain Female	brain
36	chr8:4148000-4149000	Weak transcription	Fetal Brain Male	brain
37	chr8:4149000-4149200	Enhancers	Fetal Brain Male	brain
38	chr8:4150600-4150800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:4170400-4171200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr8:4170600-4171000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:4170800-4171000	Enhancers	Pancreas	Pancrea
42	chr8:4171000-4172400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:4171000-4188800	Weak transcription	Pancreas	Pancrea
44	chr8:4172400-4172600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:4175000-4175400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
46	chr8:4180800-4182400	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr8:4181200-4183000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr8:4181400-4181800	Enhancers	Stomach Mucosa	stomach
49	chr8:4181800-4182000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:4181800-4182200	Enhancers	Rectal Mucosa Donor 29	rectum

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