Variant report

Variant	nsv531502
Chromosome Location	chr8:51390997-51703556
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	chr8:51622516-51622751	H1-hESC	embryonic stem cell:	n/a	chr8:51622657-51622671
2	BACH1	chr8:51448363-51448441	K562	blood:	n/a	n/a
3	BACH1	chr8:51549746-51549863	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:51551406-51551486	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:51553900-51554065	GM12878	blood:	n/a	n/a
6	CEBPB	chr8:51417321-51417664	Hela-S3	cervix:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
7	CEBPB	chr8:51442847-51443072	HepG2	liver:	n/a	chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
8	CEBPB	chr8:51647559-51647802	HepG2	liver:	n/a	chr8:51647683-51647694
9	CEBPB	chr8:51544182-51544382	IMR90	lung:	n/a	chr8:51544270-51544279 chr8:51544268-51544279
10	CEBPB	chr8:51594361-51594688	IMR90	lung:	n/a	n/a
11	CEBPB	chr8:51658383-51658644	IMR90	lung:	n/a	chr8:51658514-51658525
12	CEBPB	chr8:51417307-51417674	H1-hESC	embryonic stem cell:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
13	CEBPB	chr8:51576308-51576662	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:51629219-51629277	IMR90	lung:	n/a	chr8:51629252-51629261 chr8:51629250-51629261
15	CEBPB	chr8:51463003-51463270	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:51658455-51658661	HepG2	liver:	n/a	chr8:51658514-51658525
17	CEBPB	chr8:51417299-51417672	IMR90	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
18	CEBPB	chr8:51417303-51417661	K562	blood:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
19	CEBPB	chr8:51440554-51440643	HepG2	liver:	n/a	chr8:51440566-51440577
20	CEBPB	chr8:51417314-51417678	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
21	CEBPB	chr8:51442889-51443030	H1-hESC	embryonic stem cell:	n/a	chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
22	CEBPB	chr8:51417301-51417674	HepG2	liver:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
23	CEBPB	chr8:51483855-51484159	HepG2	liver:	n/a	chr8:51483989-51484000
24	CEBPB	chr8:51647599-51647828	IMR90	lung:	n/a	chr8:51647683-51647694
25	CEBPB	chr8:51647578-51647778	K562	blood:	n/a	chr8:51647683-51647694
26	CEBPB	chr8:51463151-51463193	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:51590751-51591040	HepG2	liver:	n/a	chr8:51590858-51590871 chr8:51590858-51590869
28	CEBPB	chr8:51417365-51417636	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
29	CEBPB	chr8:51442567-51443109	Hela-S3	cervix:	n/a	chr8:51442578-51442589 chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
30	CEBPZ	chr8:51529649-51529754	HepG2	liver:	n/a	n/a
31	CTCF	chr8:51426120-51426270	GM12874	blood:	n/a	n/a
32	CTCF	chr8:51539241-51539324	Lung_OC	lung:	n/a	n/a
33	CTCF	chr8:51438640-51438790	HRPEpiC	eye:	n/a	chr8:51438697-51438705
34	CTCF	chr8:51438600-51438750	Hela-S3	cervix:	n/a	chr8:51438697-51438705
35	CTCF	chr8:51517840-51517990	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr8:51575980-51576065	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr8:51640780-51640930	MCF-7	breast:	n/a	chr8:51640877-51640884
38	CTCF	chr8:51617225-51617257	ProgFib	skin:	n/a	n/a
39	CTCF	chr8:51604662-51604756	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr8:51627682-51627802	GM19240	blood:	n/a	n/a
41	CTCF	chr8:51632013-51632105	GM20000	blood:	n/a	n/a
42	CTCF	chr8:51653842-51653896	LNCaP	prostate:	n/a	n/a
43	CTCF	chr8:51671556-51671652	GM20000	blood:	n/a	n/a
44	CTCF	chr8:51627650-51627837	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:51640800-51640950	MCF-7	breast:	n/a	chr8:51640877-51640884
46	CTCF	chr8:51438580-51438730	Caco-2	colon:	n/a	chr8:51438697-51438705
47	CTCF	chr8:51627634-51627867	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:51426040-51426190	HepG2	liver:	n/a	n/a
49	CTCF	chr8:51438480-51438630	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:51627632-51627869	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51449266-51449316	HCM	heart:	n/a
2	chr8:51404066-51404116	BE2_C	brain:	n/a
3	chr8:51404179-51404229	AoSMC	blood vessel:	n/a
4	chr8:51553739-51553789	HRPEpiC	eye:	n/a
5	chr8:51404106-51404156	HNPCEpiC	eye:	n/a
6	chr8:51404106-51404156	HAEpiC	amniotic membrane:	n/a
7	chr8:51449266-51449316	HIPEpiC	eye:	n/a
8	chr8:51528401-51528451	HCT-116	colon:	n/a
9	chr8:51449266-51449316	AG04450	lung:	fetal
10	chr8:51404179-51404229	GM06990	blood:	n/a
11	chr8:51576109-51576159	BJ	skin:	n/a
12	chr8:51555740-51555790	BE2_C	brain:	n/a
13	chr8:51553739-51553789	K562	blood:	n/a
14	chr8:51404066-51404116	Jurkat	blood:	n/a
15	chr8:51576109-51576159	HEEpiC	esophagus:	n/a
16	chr8:51449266-51449316	AG04449	skin:	fetal
17	chr8:51528401-51528451	MCF-7	breast:	n/a
18	chr8:51528401-51528451	HRE	kidney:	n/a
19	chr8:51576109-51576159	BE2_C	brain:	n/a
20	chr8:51404179-51404229	HNPCEpiC	eye:	n/a
21	chr8:51555740-51555790	HRE	kidney:	n/a
22	chr8:51404066-51404116	GM12878	blood:	n/a
23	chr8:51555740-51555790	LNCaP	prostate:	n/a
24	chr8:51553739-51553789	MCF10A-Er-Src	breast:	n/a
25	chr8:51404106-51404156	BJ	skin:	n/a
26	chr8:51404066-51404116	GM19239	blood:	n/a
27	chr8:51404066-51404116	HL-60	blood:	n/a
28	chr8:51576109-51576159	SK-N-MC	brain:	n/a
29	chr8:51404179-51404229	NT2-D1	testis:	n/a
30	chr8:51404179-51404229	AG09319	gingival:	n/a
31	chr8:51576109-51576159	RPTEC	kidney:	n/a
32	chr8:51404179-51404229	HCF	heart:	n/a
33	chr8:51576109-51576159	HUVEC	blood vessel:	n/a
34	chr8:51553739-51553789	Jurkat	blood:	n/a
35	chr8:51528401-51528451	AoSMC	blood vessel:	n/a
36	chr8:51404106-51404156	T-47D	breast:	n/a
37	chr8:51404179-51404229	K562	blood:	n/a
38	chr8:51404106-51404156	HRPEpiC	eye:	n/a
39	chr8:51555740-51555790	HRCEpiC	kidney:	n/a
40	chr8:51404106-51404156	MCF-7	breast:	n/a
41	chr8:51576109-51576159	A549	lung:	n/a
42	chr8:51553739-51553789	HCT-116	colon:	n/a
43	chr8:51404066-51404116	NH-A	brain:	n/a
44	chr8:51404179-51404229	HepG2	liver:	n/a
45	chr8:51404106-51404156	Caco-2	colon:	n/a
46	chr8:51404106-51404156	NHDF-neo	bronchial:	n/a
47	chr8:51404179-51404229	U87	brain:	n/a
48	chr8:51404106-51404156	NHBE	bronchial:	n/a
49	chr8:51553739-51553789	SK-N-SH_RA	brain:	n/a
50	chr8:51404106-51404156	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
2	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
3	chr7:135846774..135848617-chr8:51481190..51483855,2	MCF-7	breast:
4	chr1:116959143..116962126-chr8:51573809..51576471,2	MCF-7	breast:
5	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
6	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
7	chr8:51464363..51466671-chr8:51475999..51477985,2	K562	blood:
8	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PXDNL-4	chr8:51675020-51675358	NONHSAT126529

Variant related genes	Relation type
CYCSP22	TF binding region
ENSG00000254392	TF binding region
SNTG1	TF binding region
CYCSP22	CpG island
ENSG00000254392	CpG island
SNTG1	CpG island
ENSG00000203865	chromatin interactions
ENSG00000147481	chromatin interactions

Extended variants
information (count: 8874 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8874 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61046978	chr8:51391011-51391012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35498338	chr8:51391035-51391036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565127804	chr8:51391041-51391042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532194456	chr8:51391057-51391058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189012546	chr8:51391065-51391066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs57342544	chr8:51391074-51391075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1904996	chr8:51391161-51391162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149656504	chr8:51391170-51391171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115889785	chr8:51391199-51391200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548968726	chr8:51391300-51391301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567318307	chr8:51391331-51391332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535157886	chr8:51391339-51391340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12543066	chr8:51391369-51391370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528124463	chr8:51391374-51391375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145521605	chr8:51391397-51391398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538885205	chr8:51391413-51391414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571010693	chr8:51391494-51391495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79027686	chr8:51391511-51391512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181843505	chr8:51391592-51391593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543300072	chr8:51391614-51391615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7830079	chr8:51391629-51391630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567881295	chr8:51391632-51391633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572741092	chr8:51391742-51391743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536422259	chr8:51391767-51391768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559721912	chr8:51391820-51391821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185380424	chr8:51391830-51391831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540358936	chr8:51391850-51391851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190260566	chr8:51391855-51391856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532197702	chr8:51391873-51391874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200538426	chr8:51391902-51391903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371650459	chr8:51391928-51391929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538163089	chr8:51391938-51391939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562295588	chr8:51391981-51391982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145109208	chr8:51391987-51391988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548068439	chr8:51392012-51392013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73676170	chr8:51392023-51392024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368721762	chr8:51392041-51392042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74740579	chr8:51392101-51392102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571668331	chr8:51392119-51392120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539083700	chr8:51392184-51392185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557595284	chr8:51392201-51392202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534431629	chr8:51392287-51392288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147624307	chr8:51392296-51392297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541635898	chr8:51392335-51392336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564724307	chr8:51392364-51392365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182434334	chr8:51392407-51392408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377026562	chr8:51392428-51392429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142166102	chr8:51392465-51392466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184901332	chr8:51392483-51392484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368096536	chr8:51392493-51392494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51389000-51394600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:51393000-51393200	Enhancers	Brain Germinal Matrix	brain
3	chr8:51393000-51393200	Enhancers	Fetal Brain Female	brain
4	chr8:51393400-51394600	Weak transcription	Brain Germinal Matrix	brain
5	chr8:51393400-51394600	Weak transcription	Fetal Brain Female	brain
6	chr8:51393800-51394400	Enhancers	Dnd41	blood
7	chr8:51394400-51394600	Active TSS	Fetal Brain Male	brain
8	chr8:51394400-51394800	Flanking Active TSS	Dnd41	blood
9	chr8:51394600-51394800	Flanking Active TSS	Fetal Brain Male	brain
10	chr8:51394600-51395000	Enhancers	Brain Germinal Matrix	brain
11	chr8:51394600-51395000	Enhancers	Ovary	ovary
12	chr8:51394600-51395200	Enhancers	Fetal Brain Female	brain
13	chr8:51394600-51395400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:51394800-51395200	Enhancers	Fetal Brain Male	brain
15	chr8:51394800-51395400	Enhancers	Dnd41	blood
16	chr8:51395400-51403000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:51402600-51403200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:51403000-51404200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:51403200-51403400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:51403200-51404200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
21	chr8:51403400-51404000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:51403600-51404200	ZNF genes & repeats	Fetal Brain Female	brain
23	chr8:51404000-51404200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:51404200-51407400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:51413400-51413800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:51426400-51427200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
27	chr8:51428400-51429800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:51441000-51469200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:51444200-51444400	Enhancers	Gastric	stomach
30	chr8:51451200-51452000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:51452000-51452200	Enhancers	Spleen	Spleen
32	chr8:51452000-51452400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:51457200-51457400	Enhancers	Brain Germinal Matrix	brain
34	chr8:51457400-51469400	Weak transcription	Brain Germinal Matrix	brain
35	chr8:51458200-51469400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:51469200-51470200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:51469400-51470400	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:51470200-51471200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:51470400-51472000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr8:51471200-51489400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:51483600-51484000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:51483600-51484200	Enhancers	Liver	Liver
43	chr8:51491800-51493200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr8:51492200-51493200	ZNF genes & repeats	Brain Germinal Matrix	brain
45	chr8:51493200-51499000	Weak transcription	Brain Germinal Matrix	brain
46	chr8:51499000-51499200	Enhancers	Brain Germinal Matrix	brain
47	chr8:51504400-51504600	Enhancers	Gastric	stomach
48	chr8:51516200-51520400	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr8:51517600-51518200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:51518200-51529000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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