Variant report

Variant	esv3514165
Chromosome Location	chr8:51416583-51923545
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	chr8:51448363-51448441	K562	blood:	n/a	n/a
2	BACH1	chr8:51549746-51549863	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:51622516-51622751	H1-hESC	embryonic stem cell:	n/a	chr8:51622657-51622671
4	BACH1	chr8:51760452-51760813	K562	blood:	n/a	n/a
5	BACH1	chr8:51551406-51551486	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:51760453-51760811	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr8:51553900-51554065	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:51771806-51771914	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:51417307-51417674	H1-hESC	embryonic stem cell:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
10	CEBPB	chr8:51815003-51815238	HepG2	liver:	n/a	chr8:51815099-51815110
11	CEBPB	chr8:51733412-51733627	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:51767482-51767716	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:51853745-51854060	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:51629219-51629277	IMR90	lung:	n/a	chr8:51629252-51629261 chr8:51629250-51629261
15	CEBPB	chr8:51853777-51854033	A549	lung:	n/a	n/a
16	CEBPB	chr8:51442847-51443072	HepG2	liver:	n/a	chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
17	CEBPB	chr8:51774506-51774533	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:51647559-51647802	HepG2	liver:	n/a	chr8:51647683-51647694
19	CEBPB	chr8:51755059-51755254	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:51417321-51417664	Hela-S3	cervix:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
21	CEBPB	chr8:51647578-51647778	K562	blood:	n/a	chr8:51647683-51647694
22	CEBPB	chr8:51483855-51484159	HepG2	liver:	n/a	chr8:51483989-51484000
23	CEBPB	chr8:51647599-51647828	IMR90	lung:	n/a	chr8:51647683-51647694
24	CEBPB	chr8:51463003-51463270	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:51440554-51440643	HepG2	liver:	n/a	chr8:51440566-51440577
26	CEBPB	chr8:51590751-51591040	HepG2	liver:	n/a	chr8:51590858-51590871 chr8:51590858-51590869
27	CEBPB	chr8:51417365-51417636	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
28	CEBPB	chr8:51576308-51576662	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:51658383-51658644	IMR90	lung:	n/a	chr8:51658514-51658525
30	CEBPB	chr8:51442889-51443030	H1-hESC	embryonic stem cell:	n/a	chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
31	CEBPB	chr8:51741406-51741719	A549	lung:	n/a	chr8:51741562-51741573 chr8:51741528-51741539
32	CEBPB	chr8:51755011-51755229	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:51544182-51544382	IMR90	lung:	n/a	chr8:51544270-51544279 chr8:51544268-51544279
34	CEBPB	chr8:51658455-51658661	HepG2	liver:	n/a	chr8:51658514-51658525
35	CEBPB	chr8:51815008-51815301	Hela-S3	cervix:	n/a	chr8:51815099-51815110
36	CEBPB	chr8:51417299-51417672	IMR90	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
37	CEBPB	chr8:51417314-51417678	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
38	CEBPB	chr8:51754975-51755240	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:51442567-51443109	Hela-S3	cervix:	n/a	chr8:51442578-51442589 chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
40	CEBPB	chr8:51417303-51417661	K562	blood:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
41	CEBPB	chr8:51741486-51741631	H1-hESC	embryonic stem cell:	n/a	chr8:51741562-51741573 chr8:51741528-51741539
42	CEBPB	chr8:51741395-51741592	K562	blood:	n/a	chr8:51741562-51741573 chr8:51741528-51741539
43	CEBPB	chr8:51463151-51463193	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:51594361-51594688	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:51741473-51741716	IMR90	lung:	n/a	chr8:51741562-51741573 chr8:51741528-51741539
46	CEBPB	chr8:51853747-51854039	IMR90	lung:	n/a	n/a
47	CEBPB	chr8:51417301-51417674	HepG2	liver:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
48	CEBPB	chr8:51741424-51741726	HepG2	liver:	n/a	chr8:51741562-51741573 chr8:51741528-51741539
49	CEBPZ	chr8:51529649-51529754	HepG2	liver:	n/a	n/a
50	CTCF	chr8:51721480-51721630	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51449266-51449316	MCF10A-Er-Src	breast:	n/a
2	chr8:51449266-51449316	SAEC	small airway:	n/a
3	chr8:51449266-51449316	HCM	heart:	n/a
4	chr8:51449266-51449316	AG09309	skin:	n/a
5	chr8:51528401-51528451	T-47D	breast:	n/a
6	chr8:51555740-51555790	RPTEC	kidney:	n/a
7	chr8:51555740-51555790	SK-N-SH	brain:	n/a
8	chr8:51528401-51528451	SK-N-SH_RA	brain:	n/a
9	chr8:51576109-51576159	AG10803	skin:	n/a
10	chr8:51449266-51449316	GM12892	blood:	n/a
11	chr8:51576109-51576159	ProgFib	skin:	n/a
12	chr8:51528401-51528451	AG09319	gingival:	n/a
13	chr8:51576109-51576159	GM19239	blood:	n/a
14	chr8:51553739-51553789	AoSMC	blood vessel:	n/a
15	chr8:51528401-51528451	RPTEC	kidney:	n/a
16	chr8:51555740-51555790	HCT-116	colon:	n/a
17	chr8:51555740-51555790	ProgFib	skin:	n/a
18	chr8:51528401-51528451	AG09309	skin:	n/a
19	chr8:51528401-51528451	Hepatocyte	liver:	n/a
20	chr8:51576109-51576159	K562	blood:	n/a
21	chr8:51555740-51555790	NT2-D1	testis:	n/a
22	chr8:51528401-51528451	PFSK-1	brain:	n/a
23	chr8:51576109-51576159	AG09309	skin:	n/a
24	chr8:51555740-51555790	AG09309	skin:	n/a
25	chr8:51576109-51576159	AG04450	lung:	fetal
26	chr8:51528401-51528451	BE2_C	brain:	n/a
27	chr8:51553739-51553789	SK-N-MC	brain:	n/a
28	chr8:51576109-51576159	BJ	skin:	n/a
29	chr8:51576109-51576159	Hela-S3	cervix:	n/a
30	chr8:51555740-51555790	GM06990	blood:	n/a
31	chr8:51576109-51576159	SK-N-SH_RA	brain:	n/a
32	chr8:51553739-51553789	ovcar-3	ovarian:	n/a
33	chr8:51553739-51553789	HCF	heart:	n/a
34	chr8:51528401-51528451	HCPEpiC	choroid plexus:	n/a
35	chr8:51555740-51555790	HCPEpiC	choroid plexus:	n/a
36	chr8:51449266-51449316	GM19239	blood:	n/a
37	chr8:51553739-51553789	T-47D	breast:	n/a
38	chr8:51555740-51555790	AoSMC	blood vessel:	n/a
39	chr8:51449266-51449316	AG10803	skin:	n/a
40	chr8:51555740-51555790	GM12878	blood:	n/a
41	chr8:51528401-51528451	AG10803	skin:	n/a
42	chr8:51576109-51576159	HRPEpiC	eye:	n/a
43	chr8:51555740-51555790	HNPCEpiC	eye:	n/a
44	chr8:51449266-51449316	NB4	blood:	n/a
45	chr8:51449266-51449316	SK-N-SH	brain:	n/a
46	chr8:51576109-51576159	SAEC	small airway:	n/a
47	chr8:51555740-51555790	HepG2	liver:	n/a
48	chr8:51553739-51553789	AG09309	skin:	n/a
49	chr8:51528401-51528451	HepG2	liver:	n/a
50	chr8:51528401-51528451	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
2	chr7:135846774..135848617-chr8:51481190..51483855,2	MCF-7	breast:
3	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
4	chr8:51715941..51718504-chr8:51718568..51721133,2	K562	blood:
5	chr8:51715941..51718504-chr8:51718568..51721133,2	K562	blood:
6	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
7	chr8:51767065..51768781-chr8:51770684..51773527,2	MCF-7	breast:
8	chr8:51464363..51466671-chr8:51475999..51477985,2	K562	blood:
9	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
10	chr8:51711545..51713227-chr8:51715658..51718026,2	K562	blood:
11	chr8:51854395..51855974-chr8:51858657..51860193,2	K562	blood:
12	chr8:51854395..51855974-chr8:51858657..51860193,2	K562	blood:
13	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
14	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
15	chr8:51711545..51713227-chr8:51715658..51718026,2	K562	blood:
16	chr1:116959143..116962126-chr8:51573809..51576471,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNTG1-2	chr8:51772090-51772622	NONHSAT126530
2	lnc-PXDNL-4	chr8:51675020-51675358	NONHSAT126529

Variant related genes	Relation type
CYCSP22	TF binding region
ENSG00000253340	TF binding region
SNTG1	TF binding region
ENSG00000201316	TF binding region
CYCSP22	CpG island
ENSG00000253340	CpG island
SNTG1	CpG island
ENSG00000201316	CpG island
ENSG00000147481	chromatin interactions
ENSG00000203865	chromatin interactions
ENSG00000253340	chromatin interactions

Extended variants
information (count: 10550 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:10550 , 50 per page) page: 1 2 3 4 5 6 7 ... 211

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139675620	chr8:51426431-51426432	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs532946168	chr8:51426440-51426441	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs184523467	chr8:51426457-51426458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs189235419	chr8:51426458-51426459	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs545625901	chr8:51426467-51426468	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs539650051	chr8:51426500-51426501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs377640734	chr8:51426505-51426506	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs549471506	chr8:51426510-51426511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs117176344	chr8:51426534-51426535	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs377562835	chr8:51426546-51426547	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs576155414	chr8:51426552-51426553	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs181884240	chr8:51426563-51426564	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs145200416	chr8:51426564-51426565	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs574499042	chr8:51426597-51426598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs541810323	chr8:51426616-51426617	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs560260148	chr8:51426625-51426626	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs527756868	chr8:51426650-51426651	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs552771562	chr8:51426667-51426668	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs528928103	chr8:51426688-51426689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs530139288	chr8:51426690-51426691	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs564546692	chr8:51426732-51426733	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs2467205	chr8:51426748-51426749	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs186529880	chr8:51426805-51426806	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs78655974	chr8:51426814-51426815	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs568762294	chr8:51426837-51426838	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs535491306	chr8:51426838-51426839	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs375128751	chr8:51426846-51426847	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs547396511	chr8:51426866-51426867	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs565817835	chr8:51426877-51426878	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs57988555	chr8:51426899-51426900	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576667292	chr8:51426931-51426932	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs62515747	chr8:51426939-51426940	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs371436413	chr8:51426954-51426955	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs576158851	chr8:51426962-51426963	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs537207919	chr8:51426996-51426997	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs4873462	chr8:51427070-51427071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs555280343	chr8:51427088-51427089	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs192040621	chr8:51427139-51427140	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs374574599	chr8:51427142-51427143	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs367583574	chr8:51427149-51427150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs118073411	chr8:51427193-51427194	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs560098845	chr8:51427197-51427198	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs180748254	chr8:51427199-51427200	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs183159063	chr8:51428408-51428409	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs533657481	chr8:51428432-51428433	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs117361706	chr8:51428433-51428434	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs563312458	chr8:51428434-51428435	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs530397499	chr8:51428448-51428449	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs540304526	chr8:51428452-51428453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs188939708	chr8:51428453-51428454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51426400-51427200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr8:51428400-51429800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:51441000-51469200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:51444200-51444400	Enhancers	Gastric	stomach
5	chr8:51451200-51452000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:51452000-51452200	Enhancers	Spleen	Spleen
7	chr8:51452000-51452400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:51457200-51457400	Enhancers	Brain Germinal Matrix	brain
9	chr8:51457400-51469400	Weak transcription	Brain Germinal Matrix	brain
10	chr8:51458200-51469400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:51469200-51470200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:51469400-51470400	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:51470200-51471200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:51470400-51472000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr8:51471200-51489400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:51483600-51484000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:51483600-51484200	Enhancers	Liver	Liver
18	chr8:51491800-51493200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:51492200-51493200	ZNF genes & repeats	Brain Germinal Matrix	brain
20	chr8:51493200-51499000	Weak transcription	Brain Germinal Matrix	brain
21	chr8:51499000-51499200	Enhancers	Brain Germinal Matrix	brain
22	chr8:51504400-51504600	Enhancers	Gastric	stomach
23	chr8:51516200-51520400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr8:51517600-51518200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:51518200-51529000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr8:51528200-51529400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:51528200-51530000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr8:51528200-51530200	Enhancers	Brain Germinal Matrix	brain
29	chr8:51528200-51530200	Enhancers	HUVEC	blood vessel
30	chr8:51528400-51530200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:51528800-51529600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:51528800-51529600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr8:51528800-51529600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:51528800-51529600	Enhancers	Brain Angular Gyrus	brain
35	chr8:51528800-51529800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:51528800-51529800	Enhancers	Fetal Lung	lung
37	chr8:51528800-51530200	Enhancers	Fetal Brain Female	brain
38	chr8:51529000-51529600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:51529000-51529600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr8:51529000-51529600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr8:51529000-51529800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr8:51529000-51529800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:51529200-51529600	Enhancers	Duodenum Mucosa	Duodenum
44	chr8:51529200-51529800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr8:51529200-51530600	Enhancers	Hela-S3	cervix
46	chr8:51529400-51538800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:51529600-51530000	Enhancers	Fetal Kidney	kidney
48	chr8:51529600-51530200	Weak transcription	Duodenum Mucosa	Duodenum
49	chr8:51530200-51530600	Active TSS	Duodenum Mucosa	Duodenum
50	chr8:51530200-51533000	Weak transcription	HUVEC	blood vessel

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