Variant report

Variant	nsv427813
Chromosome Location	chr8:3339350-3501515
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	chr8:3348537-3348542	K562	blood:	n/a	n/a
2	BACH1	chr8:3491473-3491649	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:3414459-3414512	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:3394062-3394294	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr8:3381143-3381992	GM12878	blood:	n/a	n/a
6	BCL3	chr8:3456830-3457201	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:3371087-3371103	K562	blood:	n/a	n/a
8	CEBPB	chr8:3486970-3487053	HepG2	liver:	n/a	chr8:3487017-3487028 chr8:3487015-3487026
9	CEBPB	chr8:3430609-3430796	HepG2	liver:	n/a	chr8:3430696-3430709 chr8:3430698-3430707 chr8:3430698-3430707 chr8:3430698-3430707
10	CEBPB	chr8:3430118-3430309	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:3497558-3497809	A549	lung:	n/a	chr8:3497574-3497587
12	CEBPB	chr8:3425975-3426122	K562	blood:	n/a	chr8:3426039-3426050
13	CEBPB	chr8:3365631-3365922	H1-hESC	embryonic stem cell:	n/a	chr8:3365776-3365787
14	CEBPB	chr8:3371778-3371955	H1-hESC	embryonic stem cell:	n/a	chr8:3371791-3371804
15	CEBPB	chr8:3475205-3475329	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:3425923-3426210	HepG2	liver:	n/a	chr8:3426039-3426050
17	CEBPB	chr8:3475245-3475445	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:3430118-3430337	A549	lung:	n/a	n/a
19	CEBPB	chr8:3365772-3365816	HepG2	liver:	n/a	chr8:3365776-3365787
20	CEBPB	chr8:3394044-3394525	H1-hESC	embryonic stem cell:	n/a	chr8:3394490-3394501 chr8:3394491-3394500
21	CEBPB	chr8:3430078-3430383	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:3497527-3497833	HepG2	liver:	n/a	chr8:3497574-3497587
23	CEBPB	chr8:3497489-3497769	H1-hESC	embryonic stem cell:	n/a	chr8:3497574-3497587
24	CEBPB	chr8:3371181-3371448	HepG2	liver:	n/a	chr8:3371286-3371298
25	CEBPB	chr8:3425939-3426206	A549	lung:	n/a	chr8:3426039-3426050
26	CEBPB	chr8:3394202-3394634	HepG2	liver:	n/a	chr8:3394490-3394501 chr8:3394491-3394500
27	CEBPB	chr8:3420332-3420336	A549	lung:	n/a	n/a
28	CEBPB	chr8:3430569-3430821	H1-hESC	embryonic stem cell:	n/a	chr8:3430696-3430709 chr8:3430698-3430707 chr8:3430698-3430707 chr8:3430698-3430707
29	CEBPB	chr8:3458334-3458381	A549	lung:	n/a	n/a
30	CEBPB	chr8:3371790-3371990	A549	lung:	n/a	chr8:3371791-3371804
31	CEBPD	chr8:3449018-3449462	K562	blood:	n/a	n/a
32	CHD2	chr8:3394017-3394211	GM12878	blood:	n/a	n/a
33	CTCF	chr8:3394095-3394311	GM12891	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
34	CTCF	chr8:3442540-3442690	HRE	kidney:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
35	CTCF	chr8:3394020-3394170	HCT-116	colon:	n/a	n/a
36	CTCF	chr8:3442560-3442710	GM12874	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
37	CTCF	chr8:3442560-3442710	GM12869	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
38	CTCF	chr8:3394120-3394270	GM06990	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
39	CTCF	chr8:3412340-3412490	A549	lung:	n/a	n/a
40	CTCF	chr8:3442453-3442729	K562	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
41	CTCF	chr8:3394450-3394516	Lung_OC	lung:	n/a	n/a
42	CTCF	chr8:3442520-3442670	GM12873	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
43	CTCF	chr8:3442560-3442710	Caco-2	colon:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
44	CTCF	chr8:3394073-3394285	Pancreas_OC	pancreas:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
45	CTCF	chr8:3442380-3442530	HFF	foreskin:	n/a	n/a
46	CTCF	chr8:3394059-3394308	MCF-7	breast:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
47	CTCF	chr8:3374500-3374650	GM12865	blood:	n/a	n/a
48	CTCF	chr8:3381410-3381479	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:3394060-3394210	Caco-2	colon:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
50	CTCF	chr8:3442565-3442722	SK-N-SH_RA	brain:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:3429480-3429530	IMR90	lung:	fetal
2	chr8:3429428-3429478	HRE	kidney:	n/a
3	chr8:3429480-3429530	HRPEpiC	eye:	n/a
4	chr8:3429382-3429432	PFSK-1	brain:	n/a
5	chr8:3429428-3429478	SK-N-SH_RA	brain:	n/a
6	chr8:3429382-3429432	HAEpiC	amniotic membrane:	n/a
7	chr8:3412728-3412778	HUVEC	blood vessel:	n/a
8	chr8:3416080-3416130	AoSMC	blood vessel:	n/a
9	chr8:3429382-3429432	HCT-116	colon:	n/a
10	chr8:3412728-3412778	AG09319	gingival:	n/a
11	chr8:3429428-3429478	AG10803	skin:	n/a
12	chr8:3416209-3416259	GM12878	blood:	n/a
13	chr8:3429382-3429432	CMK	blood:	n/a
14	chr8:3416080-3416130	PFSK-1	brain:	n/a
15	chr8:3416209-3416259	MCF10A-Er-Src	breast:	n/a
16	chr8:3429382-3429432	ovcar-3	ovarian:	n/a
17	chr8:3429428-3429478	PANC-1	pancreas:	n/a
18	chr8:3412728-3412778	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:3429480-3429530	HCPEpiC	choroid plexus:	n/a
20	chr8:3416209-3416259	CMK	blood:	n/a
21	chr8:3416209-3416259	HEK293	kidney:	embryo
22	chr8:3412728-3412778	GM06990	blood:	n/a
23	chr8:3412728-3412778	ECC-1	luminal epithelium:	n/a
24	chr8:3429382-3429432	AG10803	skin:	n/a
25	chr8:3429480-3429530	HAEpiC	amniotic membrane:	n/a
26	chr8:3429428-3429478	ProgFib	skin:	n/a
27	chr8:3412728-3412778	HRPEpiC	eye:	n/a
28	chr8:3416209-3416259	GM19239	blood:	n/a
29	chr8:3429382-3429432	HRE	kidney:	n/a
30	chr8:3416209-3416259	SK-N-SH_RA	brain:	n/a
31	chr8:3429480-3429530	Caco-2	colon:	n/a
32	chr8:3429428-3429478	GM12891	blood:	n/a
33	chr8:3429480-3429530	Hepatocyte	liver:	n/a
34	chr8:3429480-3429530	SKMC	muscle:	n/a
35	chr8:3429480-3429530	AG04449	skin:	fetal
36	chr8:3429428-3429478	ECC-1	luminal epithelium:	n/a
37	chr8:3412728-3412778	HEK293	kidney:	embryo
38	chr8:3412728-3412778	CMK	blood:	n/a
39	chr8:3412728-3412778	BJ	skin:	n/a
40	chr8:3416221-3416271	GM12878	blood:	n/a
41	chr8:3416080-3416130	HL-60	blood:	n/a
42	chr8:3416209-3416259	U87	brain:	n/a
43	chr8:3412728-3412778	MCF-7	breast:	n/a
44	chr8:3416221-3416271	HCM	heart:	n/a
45	chr8:3416209-3416259	HIPEpiC	eye:	n/a
46	chr8:3416221-3416271	GM12892	blood:	n/a
47	chr8:3429428-3429478	Jurkat	blood:	n/a
48	chr8:3416221-3416271	T-47D	breast:	n/a
49	chr8:3429382-3429432	T-47D	breast:	n/a
50	chr8:3416080-3416130	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:3142043..3142754-chr8:3442196..3443079,3	K562	blood:
2	chr8:3357251..3359656-chr8:3362174..3364772,2	K562	blood:
3	chr8:3357251..3359656-chr8:3362174..3364772,2	K562	blood:
4	chr8:3482781..3484971-chr8:3489836..3491508,2	K562	blood:
5	chr8:2675575..2676101-chr8:3394089..3394683,2	MCF-7	breast:
6	chr8:3141218..3141916-chr8:3393869..3394656,2	MCF-7	breast:
7	chr8:3142221..3142747-chr8:3393835..3394631,2	MCF-7	breast:
8	chr8:3482781..3484971-chr8:3489836..3491508,2	K562	blood:
9	chr12:58159481..58160161-chr8:3442277..3442945,2	HCT-116	colon:

Variant related genes	Relation type
CSMD1	TF binding region
CSMD1	CpG island
ENSG00000183117	chromatin interactions

Extended variants
information (count: 7626 )
Associated
traits (count: 129 )

Variant overlapped rSNPs/rCNVs (count:7626 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141399197	chr8:3339360-3339361	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs551084086	chr8:3339373-3339374	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs558438661	chr8:3339383-3339384	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs577082147	chr8:3339397-3339398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs549518951	chr8:3346603-3346604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571990033	chr8:3346606-3346607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145970363	chr8:3346625-3346626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2055338	chr8:3346630-3346631	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs185424749	chr8:3346650-3346651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375582308	chr8:3346656-3346657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138559521	chr8:3346657-3346658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1392145	chr8:3346681-3346682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs28568619	chr8:3346688-3346689	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534532114	chr8:3346690-3346691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534212831	chr8:3346692-3346693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552706031	chr8:3346723-3346724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554036005	chr8:3346730-3346731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114039304	chr8:3346731-3346732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375779132	chr8:3346737-3346738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566728749	chr8:3346738-3346739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545017086	chr8:3346766-3346767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111439804	chr8:3346835-3346836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6999448	chr8:3346860-3346861	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543027378	chr8:3346881-3346882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149255591	chr8:3346886-3346887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371285865	chr8:3346901-3346902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535055324	chr8:3346908-3346909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144440014	chr8:3346916-3346917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148490962	chr8:3346917-3346918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142707889	chr8:3346918-3346919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551034710	chr8:3346923-3346924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569509098	chr8:3346924-3346925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9657393	chr8:3346928-3346929	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs150581880	chr8:3346930-3346931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567026739	chr8:3346945-3346946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537675138	chr8:3346958-3346959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534376316	chr8:3346962-3346963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552642702	chr8:3346971-3346972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577809074	chr8:3346978-3346979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538806280	chr8:3346981-3346982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188571465	chr8:3346986-3346987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9314493	chr8:3347003-3347004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140509977	chr8:3347005-3347006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144369805	chr8:3347013-3347014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573382997	chr8:3347030-3347031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180675683	chr8:3347037-3347038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112862831	chr8:3347038-3347039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185156860	chr8:3347040-3347041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532621058	chr8:3347042-3347043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551122185	chr8:3347045-3347046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:129)

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
Ovarian cancer	22355333	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
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3339000-3339400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:3346600-3347000	Enhancers	Brain Hippocampus Middle	brain
3	chr8:3346600-3347000	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr8:3346600-3347000	Enhancers	Brain Substantia Nigra	brain
5	chr8:3347000-3361000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr8:3347800-3349000	Weak transcription	Stomach Mucosa	stomach
7	chr8:3349000-3351200	Enhancers	Stomach Mucosa	stomach
8	chr8:3351200-3352200	Weak transcription	Stomach Mucosa	stomach
9	chr8:3352200-3352400	Enhancers	Stomach Mucosa	stomach
10	chr8:3352800-3353000	Enhancers	Fetal Brain Male	brain
11	chr8:3353000-3360000	Weak transcription	Fetal Brain Male	brain
12	chr8:3356800-3357600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:3357000-3357600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
14	chr8:3357600-3360000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr8:3357600-3363600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:3360000-3361600	Enhancers	Fetal Brain Male	brain
17	chr8:3360000-3362000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:3360200-3360800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr8:3360200-3361200	Enhancers	Brain Anterior Caudate	brain
20	chr8:3360200-3361200	Enhancers	Brain Hippocampus Middle	brain
21	chr8:3360200-3361200	Enhancers	Fetal Brain Female	brain
22	chr8:3360200-3361400	Enhancers	Fetal Stomach	stomach
23	chr8:3360200-3362200	Enhancers	Brain Germinal Matrix	brain
24	chr8:3360200-3362400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:3360400-3360800	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr8:3360400-3361200	Enhancers	Brain Angular Gyrus	brain
27	chr8:3360600-3361000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:3360600-3361200	Enhancers	Fetal Heart	heart
29	chr8:3360800-3361200	Enhancers	Brain Cingulate Gyrus	brain
30	chr8:3361000-3361200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr8:3361000-3361600	Enhancers	Fetal Muscle Leg	muscle
32	chr8:3361200-3362200	Weak transcription	Brain Hippocampus Middle	brain
33	chr8:3362000-3368600	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:3362200-3362400	Enhancers	Brain Hippocampus Middle	brain
35	chr8:3363600-3364000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:3368600-3369000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
37	chr8:3369000-3373000	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:3371200-3371600	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr8:3371200-3371800	Enhancers	Brain Cingulate Gyrus	brain
40	chr8:3371600-3372000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
41	chr8:3371600-3372000	Active TSS	Brain Substantia Nigra	brain
42	chr8:3371800-3372000	Enhancers	Brain Angular Gyrus	brain
43	chr8:3371800-3373000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr8:3372000-3372200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr8:3372000-3372800	Weak transcription	Brain Angular Gyrus	brain
46	chr8:3372000-3372800	Weak transcription	Brain Substantia Nigra	brain
47	chr8:3372200-3372600	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr8:3372600-3372800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr8:3372800-3373000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr8:3372800-3373200	Enhancers	Brain Substantia Nigra	brain

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