Variant report

Variant	nsv1017276
Chromosome Location	chr8:3372977-3394737
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	chr8:3394062-3394294	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr8:3381143-3381992	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:3394202-3394634	HepG2	liver:	n/a	chr8:3394490-3394501 chr8:3394491-3394500
4	CEBPB	chr8:3394044-3394525	H1-hESC	embryonic stem cell:	n/a	chr8:3394490-3394501 chr8:3394491-3394500
5	CHD2	chr8:3394017-3394211	GM12878	blood:	n/a	n/a
6	CTCF	chr8:3394120-3394270	GM12874	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
7	CTCF	chr8:3394080-3394230	HMEC	breast:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
8	CTCF	chr8:3381234-3381357	GM19239	blood:	n/a	n/a
9	CTCF	chr8:3393960-3394210	GM12868	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
10	CTCF	chr8:3394105-3394270	GM10248	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
11	CTCF	chr8:3394102-3394278	GM19239	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
12	CTCF	chr8:3382003-3382134	GM19239	blood:	n/a	n/a
13	CTCF	chr8:3394100-3394250	MCF-7	breast:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
14	CTCF	chr8:3394120-3394270	GM12873	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
15	CTCF	chr8:3394100-3394250	HEEpiC	esophagus:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
16	CTCF	chr8:3381360-3381376	GM19239	blood:	n/a	n/a
17	CTCF	chr8:3394002-3394311	HepG2	liver:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
18	CTCF	chr8:3394120-3394270	GM12870	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
19	CTCF	chr8:3394020-3394170	HCT-116	colon:	n/a	n/a
20	CTCF	chr8:3394024-3394222	ECC-1	luminal epithelium:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
21	CTCF	chr8:3381755-3381840	GM19239	blood:	n/a	n/a
22	CTCF	chr8:3394080-3394230	BE2_C	brain:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
23	CTCF	chr8:3393968-3394385	GM12878	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
24	CTCF	chr8:3394080-3394230	HAc	cerebellar:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
25	CTCF	chr8:3394080-3394230	WERI-Rb-1	eye:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
26	CTCF	chr8:3394100-3394250	HEK293	kidney:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
27	CTCF	chr8:3394040-3394190	GM12871	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
28	CTCF	chr8:3394100-3394250	GM12873	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
29	CTCF	chr8:3394100-3394250	AG04449	skin:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
30	CTCF	chr8:3394060-3394210	GM06990	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
31	CTCF	chr8:3394060-3394210	SAEC	small airway:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
32	CTCF	chr8:3394073-3394285	Pancreas_OC	pancreas:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
33	CTCF	chr8:3394100-3394250	GM12872	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
34	CTCF	chr8:3394047-3394299	LNCaP	prostate:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
35	CTCF	chr8:3394080-3394230	GM12878	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
36	CTCF	chr8:3394068-3394249	SK-N-SH_RA	brain:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
37	CTCF	chr8:3394090-3394313	MCF-7	breast:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
38	CTCF	chr8:3394083-3394308	A549	lung:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
39	CTCF	chr8:3394109-3394312	H1-hESC	embryonic stem cell:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
40	CTCF	chr8:3394089-3394213	SK-N-SH_RA	brain:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
41	CTCF	chr8:3394080-3394230	GM12864	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
42	CTCF	chr8:3394054-3394256	IMR90	lung:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
43	CTCF	chr8:3394140-3394290	GM12868	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
44	CTCF	chr8:3394080-3394230	HRE	kidney:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
45	CTCF	chr8:3394450-3394516	Lung_OC	lung:	n/a	n/a
46	CTCF	chr8:3394046-3394319	Gliobla	brain:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174
47	CTCF	chr8:3394080-3394230	HepG2	liver:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
48	CTCF	chr8:3394080-3394230	GM12870	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
49	CTCF	chr8:3394080-3394230	HL-60	blood:	n/a	chr8:3394156-3394177 chr8:3394161-3394179 chr8:3394166-3394174
50	CTCF	chr8:3394160-3394310	GM12866	blood:	n/a	chr8:3394161-3394179 chr8:3394229-3394242 chr8:3394166-3394174

No.	Distal block	Cell Line	Cell type
1	chr8:3142221..3142747-chr8:3393835..3394631,2	MCF-7	breast:
2	chr8:2675575..2676101-chr8:3394089..3394683,2	MCF-7	breast:
3	chr8:3141218..3141916-chr8:3393869..3394656,2	MCF-7	breast:

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

Extended variants
information (count: 773 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11783295	chr8:3372977-3372978	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569944445	chr8:3372987-3372988	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs182236305	chr8:3372992-3372993	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs549382859	chr8:3373017-3373018	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs11447915	chr8:3373029-3373030	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs78800575	chr8:3373043-3373044	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs73503645	chr8:3373058-3373059	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs142373476	chr8:3373063-3373064	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs114052054	chr8:3373090-3373091	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs370768659	chr8:3373096-3373097	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575896605	chr8:3373108-3373109	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146356246	chr8:3373109-3373110	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs139378983	chr8:3373132-3373133	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs117398294	chr8:3373140-3373141	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs71521870	chr8:3373146-3373147	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs573643923	chr8:3373149-3373150	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs113455149	chr8:3373158-3373159	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs532850119	chr8:3373159-3373160	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs545193246	chr8:3373203-3373204	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs563313923	chr8:3373210-3373211	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs118083418	chr8:3373243-3373244	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs73658146	chr8:3373253-3373254	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs140596563	chr8:3373273-3373274	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs150473977	chr8:3373274-3373275	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546582272	chr8:3373293-3373294	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs545188743	chr8:3373309-3373310	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs538712015	chr8:3373337-3373338	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs557554019	chr8:3373380-3373381	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs558670220	chr8:3374512-3374513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577082727	chr8:3374547-3374548	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs151113587	chr8:3374550-3374551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs573715290	chr8:3374554-3374555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556166190	chr8:3374559-3374560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs546538789	chr8:3374612-3374613	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs11785154	chr8:3374624-3374625	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs560611141	chr8:3374645-3374646	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527747565	chr8:3374647-3374648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566283526	chr8:3375377-3375378	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs184721781	chr8:3375412-3375413	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs546297087	chr8:3377019-3377020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528608944	chr8:3377027-3377028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116356064	chr8:3377029-3377030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369819110	chr8:3377034-3377035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539531835	chr8:3377036-3377037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113969868	chr8:3377038-3377039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142909128	chr8:3377074-3377075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28688278	chr8:3377096-3377097	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs573077750	chr8:3377098-3377099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534127026	chr8:3377129-3377130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558549403	chr8:3377162-3377163	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3369000-3373000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:3371800-3373000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr8:3372800-3373000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
4	chr8:3372800-3373200	Enhancers	Brain Substantia Nigra	brain
5	chr8:3372800-3373400	Enhancers	Brain Angular Gyrus	brain
6	chr8:3372800-3373400	Active TSS	Brain Anterior Caudate	brain
7	chr8:3373000-3373200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:3373000-3373200	Enhancers	Brain Cingulate Gyrus	brain
9	chr8:3373000-3373400	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr8:3377000-3377200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:3377200-3381000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:3377200-3381000	Weak transcription	Pancreas	Pancrea
13	chr8:3378400-3381200	Weak transcription	Gastric	stomach
14	chr8:3380400-3381000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:3381000-3381800	ZNF genes & repeats	Fetal Heart	heart
16	chr8:3381000-3381800	ZNF genes & repeats	A549	lung
17	chr8:3381000-3382000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr8:3381000-3382000	ZNF genes & repeats	Fetal Lung	lung
19	chr8:3381000-3382200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:3381000-3382200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:3381000-3382200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
22	chr8:3381000-3382200	ZNF genes & repeats	Esophagus	oesophagus
23	chr8:3381000-3382200	ZNF genes & repeats	Fetal Kidney	kidney
24	chr8:3381000-3382200	ZNF genes & repeats	Pancreas	Pancrea
25	chr8:3381200-3381600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr8:3381200-3381600	Active TSS	Spleen	Spleen
27	chr8:3381200-3382000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:3381200-3382200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:3381200-3382200	ZNF genes & repeats	Gastric	stomach
30	chr8:3381200-3382400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:3381400-3382200	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr8:3381400-3382200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr8:3381600-3382200	ZNF genes & repeats	Fetal Brain Male	brain
34	chr8:3382000-3382400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:3382400-3382600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:3392600-3392800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:3393800-3394200	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr8:3393800-3394400	Enhancers	Brain Hippocampus Middle	brain
39	chr8:3393800-3394400	Enhancers	Brain Substantia Nigra	brain
40	chr8:3394000-3394200	Enhancers	Brain Cingulate Gyrus	brain
41	chr8:3394200-3395800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr8:3394400-3396400	Weak transcription	Brain Substantia Nigra	brain
43	chr8:3394400-3396600	Weak transcription	Brain Hippocampus Middle	brain

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