Variant report

Variant	nsv429925
Chromosome Location	chr8:86473348-86535448
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:123)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:86494789-86495026	K562	blood:	n/a	n/a
2	BACH1	chr8:86477700-86478018	K562	blood:	n/a	n/a
3	BACH1	chr8:86477707-86478028	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
5	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
6	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
7	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
8	CEBPB	chr8:86475730-86475860	HepG2	liver:	n/a	chr8:86475757-86475770
9	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
10	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
11	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
12	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
13	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
14	CEBPB	chr8:86483060-86483308	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
16	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
17	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
18	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
19	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
20	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
21	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr8:86482894-86483257	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr8:86501940-86502090	HRE	kidney:	n/a	n/a
24	CTCF	chr8:86494374-86494479	GM19239	blood:	n/a	n/a
25	CTCF	chr8:86480580-86480730	HRE	kidney:	n/a	n/a
26	CTCF	chr8:86488842-86488876	GM19238	blood:	n/a	n/a
27	CTCF	chr8:86520432-86520511	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr8:86488790-86488916	Fibrobl	skin:	n/a	n/a
29	CTCF	chr8:86488811-86488916	A549	lung:	n/a	n/a
30	CTCF	chr8:86488813-86488918	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a
32	CTCF	chr8:86500740-86500890	HCT-116	colon:	n/a	n/a
33	CTCF	chr8:86488825-86488916	GM12891	blood:	n/a	n/a
34	CTCF	chr8:86488840-86488915	GM19240	blood:	n/a	n/a
35	CTCF	chr8:86494371-86494488	GM12878	blood:	n/a	n/a
36	CTCF	chr8:86509421-86509521	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr8:86488877-86488897	GM19238	blood:	n/a	n/a
38	CTCF	chr8:86488799-86488917	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:86488806-86488916	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:86488793-86488916	ProgFib	skin:	n/a	n/a
41	CTCF	chr8:86488826-86488917	MCF-7	breast:	n/a	n/a
42	CUX1	chr8:86483144-86483243	K562	blood:	n/a	n/a
43	E2F4	chr8:86505700-86505895	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr8:86528535-86528749	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr8:86502777-86502819	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F6	chr8:86487592-86487938	H1-hESC	embryonic stem cell:	n/a	n/a
47	EP300	chr8:86530109-86530133	K562	blood:	n/a	n/a
48	EP300	chr8:86488817-86488952	GM12878	blood:	n/a	n/a
49	EP300	chr8:86477858-86477902	HepG2	liver:	n/a	n/a
50	FOS	chr8:86483834-86484314	MCF10A-Er-Src	breast:	n/a	chr8:86484011-86484019

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86504072-86504122	BJ	skin:	n/a
2	chr8:86504072-86504122	BJ	skin:	n/a
3	chr8:86504072-86504122	GM12891	blood:	n/a
4	chr8:86486097-86486147	AG09309	skin:	n/a
5	chr8:86504072-86504122	HMEC	breast:	n/a
6	chr8:86486097-86486147	AG04449	skin:	fetal
7	chr8:86504072-86504122	HAEpiC	amniotic membrane:	n/a
8	chr8:86486097-86486147	GM06990	blood:	n/a
9	chr8:86504072-86504122	ProgFib	skin:	n/a
10	chr8:86504072-86504122	LNCaP	prostate:	n/a
11	chr8:86504072-86504122	HL-60	blood:	n/a
12	chr8:86504072-86504122	SAEC	small airway:	n/a
13	chr8:86486097-86486147	HRPEpiC	eye:	n/a
14	chr8:86504072-86504122	T-47D	breast:	n/a
15	chr8:86486097-86486147	T-47D	breast:	n/a
16	chr8:86504072-86504122	NB4	blood:	n/a
17	chr8:86504072-86504122	PFSK-1	brain:	n/a
18	chr8:86486097-86486147	HCT-116	colon:	n/a
19	chr8:86504072-86504122	NH-A	brain:	n/a
20	chr8:86486097-86486147	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:86486097-86486147	HEK293	kidney:	embryo
22	chr8:86486097-86486147	SK-N-MC	brain:	n/a
23	chr8:86504072-86504122	SKMC	muscle:	n/a
24	chr8:86486097-86486147	Hepatocyte	liver:	n/a
25	chr8:86486097-86486147	NH-A	brain:	n/a
26	chr8:86504072-86504122	HCM	heart:	n/a
27	chr8:86486097-86486147	HMEC	breast:	n/a
28	chr8:86486097-86486147	RPTEC	kidney:	n/a
29	chr8:86504072-86504122	Hepatocyte	liver:	n/a
30	chr8:86486097-86486147	SK-N-SH	brain:	n/a
31	chr8:86504072-86504122	AG04449	skin:	fetal
32	chr8:86486097-86486147	PANC-1	pancreas:	n/a
33	chr8:86504072-86504122	HEEpiC	esophagus:	n/a
34	chr8:86486097-86486147	HL-60	blood:	n/a
35	chr8:86486097-86486147	NHBE	bronchial:	n/a
36	chr8:86504072-86504122	NT2-D1	testis:	n/a
37	chr8:86486097-86486147	HRE	kidney:	n/a
38	chr8:86486097-86486147	AG10803	skin:	n/a
39	chr8:86504072-86504122	PrEC	prostate:	n/a
40	chr8:86504072-86504122	SK-N-MC	brain:	n/a
41	chr8:86486097-86486147	BJ	skin:	n/a
42	chr8:86504072-86504122	AG09309	skin:	n/a
43	chr8:86504072-86504122	K562	blood:	n/a
44	chr8:86504072-86504122	A549	lung:	n/a
45	chr8:86504072-86504122	GM06990	blood:	n/a
46	chr8:86486097-86486147	PrEC	prostate:	n/a
47	chr8:86486097-86486147	NT2-D1	testis:	n/a
48	chr8:86504072-86504122	H1-hESC	embryonic stem cell:	embryo
49	chr8:86504072-86504122	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:86504072-86504122	AG10803	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
2	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
3	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
4	chr8:86468837..86470919-chr8:86472571..86475543,2	MCF-7	breast:
5	chr8:86439507..86442336-chr8:86514176..86515935,2	MCF-7	breast:
6	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
7	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
8	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
9	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
10	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
11	chr8:86375239..86377397-chr8:86481535..86484020,2	MCF-7	breast:
12	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537
2	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537

No data

Variant related genes	Relation type
ENSG00000253680	TF binding region
ENSG00000253680	CpG island
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 1718 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1718 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535737458	chr8:86473351-86473352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555674001	chr8:86473395-86473396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs650498	chr8:86473397-86473398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs402295	chr8:86473459-86473460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs376130020	chr8:86473489-86473490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557935198	chr8:86473517-86473518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs578055083	chr8:86473545-86473546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559030692	chr8:86473557-86473558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116754475	chr8:86473648-86473649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111541113	chr8:86473657-86473658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557385970	chr8:86473734-86473735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574119715	chr8:86473810-86473811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs648286	chr8:86473852-86473853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559707159	chr8:86473899-86473900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148170142	chr8:86473900-86473901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552960124	chr8:86473903-86473904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141928626	chr8:86473926-86473927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530626143	chr8:86473958-86473959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550301179	chr8:86473983-86473984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566906888	chr8:86473990-86473991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374797434	chr8:86474142-86474143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs398067996	chr8:86474144-86474145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541562699	chr8:86474157-86474158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200023266	chr8:86474224-86474225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74677430	chr8:86474225-86474226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377678844	chr8:86474242-86474243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189373234	chr8:86474264-86474265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150673219	chr8:86474293-86474294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556975821	chr8:86474303-86474304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551951120	chr8:86474304-86474305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140954224	chr8:86474325-86474326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112237425	chr8:86474335-86474336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573298168	chr8:86474371-86474372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147494942	chr8:86474400-86474401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574056901	chr8:86474453-86474454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139818800	chr8:86474457-86474458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575170972	chr8:86474458-86474459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545779843	chr8:86474459-86474460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370846213	chr8:86474481-86474482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182328969	chr8:86474499-86474500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528376623	chr8:86474520-86474521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545021477	chr8:86474544-86474545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149985780	chr8:86474592-86474593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185645097	chr8:86474593-86474594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368566480	chr8:86474605-86474606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543880435	chr8:86474616-86474617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190019414	chr8:86474624-86474625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145056113	chr8:86474666-86474667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540496900	chr8:86474707-86474708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545152480	chr8:86474736-86474737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86469400-86474600	Weak transcription	Fetal Intestine Small	intestine
2	chr8:86469400-86475000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr8:86469400-86475000	Weak transcription	Brain Anterior Caudate	brain
4	chr8:86469800-86474800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:86470000-86475400	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:86470200-86474800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:86472200-86474600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:86472200-86474800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:86472200-86474800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:86473800-86474600	Weak transcription	Brain Substantia Nigra	brain
11	chr8:86474400-86475400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr8:86474600-86475200	Enhancers	Psoas Muscle	Psoas
13	chr8:86474600-86475400	Enhancers	Fetal Intestine Large	intestine
14	chr8:86474600-86475400	Enhancers	Fetal Intestine Small	intestine
15	chr8:86474600-86475400	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr8:86474600-86476000	Enhancers	Brain Substantia Nigra	brain
17	chr8:86474600-86476600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:86474800-86475000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:86474800-86475000	Enhancers	Left Ventricle	heart
20	chr8:86474800-86475200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr8:86474800-86475200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:86474800-86475200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:86475000-86475200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr8:86475000-86475200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr8:86475000-86475400	Enhancers	Brain Anterior Caudate	brain
26	chr8:86475400-86476200	Enhancers	Brain Hippocampus Middle	brain
27	chr8:86475400-86480600	Weak transcription	Fetal Intestine Small	intestine
28	chr8:86475400-86480800	Weak transcription	Fetal Intestine Large	intestine
29	chr8:86475400-86481000	Weak transcription	Brain Anterior Caudate	brain
30	chr8:86475800-86476000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr8:86476000-86477200	Enhancers	HMEC	breast
32	chr8:86476000-86480600	Weak transcription	Brain Substantia Nigra	brain
33	chr8:86476200-86480600	Weak transcription	Brain Hippocampus Middle	brain
34	chr8:86476600-86481200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr8:86476800-86477600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr8:86477000-86477400	Enhancers	Esophagus	oesophagus
37	chr8:86477200-86482600	Weak transcription	HMEC	breast
38	chr8:86479000-86482400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:86480400-86480800	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr8:86480400-86481200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr8:86480400-86481600	Enhancers	Brain Cingulate Gyrus	brain
42	chr8:86480600-86481000	Enhancers	Brain Substantia Nigra	brain
43	chr8:86480600-86481600	Enhancers	Brain Angular Gyrus	brain
44	chr8:86480600-86482200	Enhancers	Brain Hippocampus Middle	brain
45	chr8:86480600-86482200	Enhancers	Fetal Intestine Small	intestine
46	chr8:86480800-86481600	Enhancers	Fetal Lung	lung
47	chr8:86480800-86482200	Enhancers	Fetal Intestine Large	intestine
48	chr8:86480800-86487000	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr8:86481000-86481200	Enhancers	Brain Anterior Caudate	brain
50	chr8:86481000-86481400	Flanking Active TSS	Brain Substantia Nigra	brain

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