Variant report

Variant	esv2752255
Chromosome Location	chr8:4226976-4328216
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	chr8:4299608-4299681	H1-hESC	embryonic stem cell:	n/a	n/a
2	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
3	CEBPB	chr8:4300849-4301101	K562	blood:	n/a	chr8:4300971-4300982
4	CEBPB	chr8:4242430-4242568	A549	lung:	n/a	n/a
5	CEBPB	chr8:4227032-4227320	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:4300804-4301145	HepG2	liver:	n/a	chr8:4300971-4300982
7	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
8	CEBPB	chr8:4227126-4227302	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:4300811-4301138	A549	lung:	n/a	chr8:4300971-4300982
10	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
11	CEBPB	chr8:4250895-4251106	HepG2	liver:	n/a	chr8:4250917-4250928
12	CEBPB	chr8:4300789-4301140	IMR90	lung:	n/a	chr8:4300971-4300982
13	CTCF	chr8:4257426-4257627	T-47D	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
14	CTCF	chr8:4257480-4257630	RPTEC	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
15	CTCF	chr8:4257388-4257676	HepG2	liver:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
16	CTCF	chr8:4257440-4257590	HEK293	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
17	CTCF	chr8:4257460-4257610	HepG2	liver:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
18	CTCF	chr8:4277420-4277570	AG04449	skin:	n/a	n/a
19	CTCF	chr8:4257480-4257630	WERI-Rb-1	eye:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
20	CTCF	chr8:4257480-4257630	HL-60	blood:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
21	CTCF	chr8:4257440-4257590	WERI-Rb-1	eye:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
22	CTCF	chr8:4257454-4257612	MCF-7	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
23	CTCF	chr8:4257460-4257610	A549	lung:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
24	CTCF	chr8:4253927-4253975	GM20000	blood:	n/a	n/a
25	CTCF	chr8:4257477-4257618	Kidney_OC	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
26	CTCF	chr8:4278070-4278412	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:4278209-4278325	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:4257460-4257610	HRE	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
29	CTCF	chr8:4257440-4257590	MCF-7	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
30	CTCF	chr8:4257493-4257566	Gliobla	brain:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
31	CTCF	chr8:4257479-4257619	Hela-S3	cervix:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
32	CTCF	chr8:4257440-4257590	NHEK	skin:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
33	CTCF	chr8:4257467-4257635	Lung_OC	lung:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
34	CTCF	chr8:4257440-4257590	HRE	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
35	CTCF	chr8:4257420-4257570	SK-N-SH_RA	brain:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
36	CTCF	chr8:4294452-4294500	GM13976	blood:	n/a	n/a
37	CTCF	chr8:4257440-4257590	HAc	cerebellar:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
38	CTCF	chr8:4257475-4257607	LNCaP	prostate:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
39	CTCF	chr8:4290960-4291110	HepG2	liver:	n/a	chr8:4291040-4291058
40	CTCF	chr8:4257440-4257590	Caco-2	colon:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
41	CTCF	chr8:4257444-4257629	LNCaP	prostate:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
42	CTCF	chr8:4257423-4257594	H1-hESC	embryonic stem cell:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
43	CTCF	chr8:4257464-4257602	HepG2	liver:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
44	CTCF	chr8:4257440-4257590	RPTEC	kidney:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
45	CTCF	chr8:4257440-4257590	HMEC	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
46	CTCF	chr8:4244652-4244790	Pancreas_OC	pancreas:	n/a	chr8:4244685-4244706 chr8:4244691-4244707 chr8:4244690-4244708
47	CTCF	chr8:4257441-4257652	Pancreas_OC	pancreas:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
48	CTCF	chr8:4257420-4257570	MCF-7	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
49	CTCF	chr8:4257472-4257613	Medullo	brain:	n/a	chr8:4257523-4257544 chr8:4257533-4257541
50	CTCF	chr8:4257485-4257570	MCF-7	breast:	n/a	chr8:4257523-4257544 chr8:4257533-4257541

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4238976-4239026	NT2-D1	testis:	n/a
2	chr8:4238976-4239026	PFSK-1	brain:	n/a
3	chr8:4238976-4239026	ProgFib	skin:	n/a
4	chr8:4238976-4239026	GM19239	blood:	n/a
5	chr8:4238976-4239026	HCPEpiC	choroid plexus:	n/a
6	chr8:4238976-4239026	Hela-S3	cervix:	n/a
7	chr8:4238976-4239026	AG04449	skin:	fetal
8	chr8:4238976-4239026	ovcar-3	ovarian:	n/a
9	chr8:4238976-4239026	HL-60	blood:	n/a
10	chr8:4238976-4239026	SAEC	small airway:	n/a
11	chr8:4238976-4239026	A549	lung:	n/a
12	chr8:4238976-4239026	ECC-1	luminal epithelium:	n/a
13	chr8:4238976-4239026	NB4	blood:	n/a
14	chr8:4238976-4239026	RPTEC	kidney:	n/a
15	chr8:4238976-4239026	SK-N-SH	brain:	n/a
16	chr8:4238976-4239026	HCT-116	colon:	n/a
17	chr8:4238976-4239026	HIPEpiC	eye:	n/a
18	chr8:4238976-4239026	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:4238976-4239026	Hepatocyte	liver:	n/a
20	chr8:4238976-4239026	MCF10A-Er-Src	breast:	n/a
21	chr8:4238976-4239026	HRCEpiC	kidney:	n/a
22	chr8:4238976-4239026	CMK	blood:	n/a
23	chr8:4238976-4239026	GM12878	blood:	n/a
24	chr8:4238976-4239026	U87	brain:	n/a
25	chr8:4238976-4239026	AG04450	lung:	fetal
26	chr8:4238976-4239026	SK-N-MC	brain:	n/a
27	chr8:4238976-4239026	SK-N-SH_RA	brain:	n/a
28	chr8:4238976-4239026	HRE	kidney:	n/a
29	chr8:4238976-4239026	HUVEC	blood vessel:	n/a
30	chr8:4238976-4239026	AG09309	skin:	n/a
31	chr8:4238976-4239026	GM06990	blood:	n/a
32	chr8:4238976-4239026	AoSMC	blood vessel:	n/a
33	chr8:4238976-4239026	HCM	heart:	n/a
34	chr8:4238976-4239026	SKMC	muscle:	n/a
35	chr8:4238976-4239026	HNPCEpiC	eye:	n/a
36	chr8:4238976-4239026	BE2_C	brain:	n/a
37	chr8:4238976-4239026	HRPEpiC	eye:	n/a
38	chr8:4238976-4239026	GM12892	blood:	n/a
39	chr8:4238976-4239026	PrEC	prostate:	n/a
40	chr8:4238976-4239026	Caco-2	colon:	n/a
41	chr8:4238976-4239026	K562	blood:	n/a
42	chr8:4238976-4239026	MCF-7	breast:	n/a
43	chr8:4238976-4239026	PANC-1	pancreas:	n/a
44	chr8:4238976-4239026	T-47D	breast:	n/a
45	chr8:4238976-4239026	LNCaP	prostate:	n/a
46	chr8:4238976-4239026	HepG2	liver:	n/a
47	chr8:4238976-4239026	NH-A	brain:	n/a
48	chr8:4238976-4239026	HEK293	kidney:	embryo
49	chr8:4238976-4239026	BJ	skin:	n/a
50	chr8:4238976-4239026	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:3141838..3142362-chr8:4257194..4257921,2	MCF-7	breast:
2	chr8:4092133..4092721-chr8:4257157..4257997,2	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: 4366 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:4366 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573831430	chr8:4229213-4229214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555585844	chr8:4229216-4229217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536254441	chr8:4229236-4229237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554494594	chr8:4229237-4229238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112214386	chr8:4229257-4229258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572897736	chr8:4229260-4229261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192650352	chr8:4229264-4229265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559371651	chr8:4229279-4229280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577795889	chr8:4229281-4229282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115215447	chr8:4229292-4229293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563382485	chr8:4229298-4229299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530574865	chr8:4229329-4229330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74530488	chr8:4229352-4229353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530960837	chr8:4229375-4229376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs66476968	chr8:4229379-4229380	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs528061319	chr8:4229389-4229390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142729264	chr8:4229392-4229393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571817912	chr8:4229421-4229422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532753333	chr8:4229430-4229431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533276100	chr8:4229432-4229433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547125492	chr8:4229439-4229440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1367320	chr8:4229456-4229457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs536393262	chr8:4229465-4229466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577976747	chr8:4229476-4229477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1367319	chr8:4229511-4229512	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1370731	chr8:4229522-4229523	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs533918829	chr8:4229532-4229533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367556146	chr8:4229545-4229546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145713991	chr8:4229551-4229552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577821157	chr8:4229562-4229563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545192894	chr8:4229566-4229567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548418948	chr8:4229570-4229571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1370730	chr8:4229573-4229574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376665902	chr8:4229578-4229579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79821450	chr8:4229582-4229583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560946471	chr8:4229583-4229584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570118452	chr8:4229603-4229604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562717451	chr8:4229613-4229614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539808311	chr8:4229631-4229632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147388754	chr8:4229635-4229636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532647398	chr8:4229642-4229643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557348918	chr8:4229664-4229665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576529629	chr8:4229665-4229666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185745107	chr8:4229668-4229669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530215190	chr8:4229698-4229699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549197316	chr8:4229700-4229701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79149025	chr8:4229724-4229725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566823332	chr8:4229736-4229737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139238040	chr8:4229757-4229758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563981049	chr8:4229759-4229760	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4229200-4229800	Enhancers	Liver	Liver
2	chr8:4232800-4233000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:4233000-4233800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr8:4235800-4236000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:4236000-4236200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:4236200-4238800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:4238800-4239200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:4238800-4239200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr8:4238800-4239400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:4238800-4239400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:4238800-4239400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:4239000-4239200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:4239000-4240000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:4240400-4240600	Enhancers	Psoas Muscle	Psoas
15	chr8:4252000-4253000	Enhancers	Dnd41	blood
16	chr8:4252200-4252600	Enhancers	Thymus	Thymus
17	chr8:4252400-4252600	Enhancers	Pancreas	Pancrea
18	chr8:4257400-4258000	Enhancers	Fetal Brain Female	brain
19	chr8:4257600-4260400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:4257800-4258200	Enhancers	Fetal Brain Male	brain
21	chr8:4258000-4260000	Weak transcription	Fetal Brain Female	brain
22	chr8:4258200-4265000	Weak transcription	Fetal Brain Male	brain
23	chr8:4259600-4259800	Enhancers	Fetal Heart	heart
24	chr8:4259800-4260200	Enhancers	Brain Germinal Matrix	brain
25	chr8:4259800-4260400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:4260000-4260200	Enhancers	Fetal Brain Female	brain
27	chr8:4260200-4263200	Weak transcription	Brain Germinal Matrix	brain
28	chr8:4260400-4263200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr8:4260400-4264200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:4262600-4262800	Enhancers	Brain Angular Gyrus	brain
31	chr8:4263000-4264400	Enhancers	Fetal Heart	heart
32	chr8:4263200-4263800	Enhancers	Brain Hippocampus Middle	brain
33	chr8:4263200-4264800	Enhancers	Fetal Muscle Leg	muscle
34	chr8:4263200-4266000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr8:4263200-4266000	Enhancers	Brain Germinal Matrix	brain
36	chr8:4263400-4263600	Enhancers	Brain Angular Gyrus	brain
37	chr8:4263800-4264200	Weak transcription	Brain Hippocampus Middle	brain
38	chr8:4264200-4264600	Enhancers	Brain Hippocampus Middle	brain
39	chr8:4264200-4264800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:4265000-4265800	Enhancers	Fetal Brain Male	brain
41	chr8:4265800-4274600	Weak transcription	Fetal Brain Male	brain
42	chr8:4269400-4270000	Enhancers	Gastric	stomach
43	chr8:4272800-4273000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:4278200-4279000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr8:4284600-4285000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:4285000-4285400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr8:4290000-4291000	Enhancers	Fetal Muscle Leg	muscle
48	chr8:4291000-4291800	Weak transcription	Fetal Muscle Leg	muscle
49	chr8:4292200-4292400	Enhancers	Fetal Muscle Leg	muscle
50	chr8:4293000-4293400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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