Variant report

Variant	nsv1027250
Chromosome Location	chr8:53341086-53400608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:366)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53379534-53379715	HepG2	liver:	n/a	n/a
2	ATF1	chr8:53359120-53359225	K562	blood:	n/a	n/a
3	ATF3	chr8:53380751-53380920	K562	blood:	n/a	n/a
4	BHLHE40	chr8:53381891-53381969	HepG2	liver:	n/a	n/a
5	BHLHE40	chr8:53379663-53380117	HepG2	liver:	n/a	n/a
6	BHLHE40	chr8:53379829-53380010	K562	blood:	n/a	n/a
7	BRCA1	chr8:53379588-53380167	Hela-S3	cervix:	n/a	chr8:53380042-53380051
8	BRCA1	chr8:53378991-53379357	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr8:53396527-53396846	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr8:53372746-53373386	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr8:53379508-53380052	HCT-116	colon:	n/a	n/a
12	CEBPB	chr8:53380702-53380961	A549	lung:	n/a	chr8:53380846-53380857
13	CEBPB	chr8:53363255-53363417	K562	blood:	n/a	chr8:53363360-53363371
14	CEBPB	chr8:53380703-53381035	K562	blood:	n/a	chr8:53380846-53380857
15	CEBPB	chr8:53380720-53380951	Hela-S3	cervix:	n/a	chr8:53380846-53380857
16	CEBPB	chr8:53379594-53379970	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr8:53345345-53345411	K562	blood:	n/a	chr8:53345360-53345371
18	CEBPB	chr8:53379541-53380152	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:53380743-53381004	H1-hESC	embryonic stem cell:	n/a	chr8:53380846-53380857
20	CEBPB	chr8:53380704-53380931	IMR90	lung:	n/a	chr8:53380846-53380857
21	CEBPB	chr8:53396446-53396903	MCF-7	breast:	n/a	chr8:53396452-53396464 chr8:53396637-53396650
22	CEBPB	chr8:53390851-53391216	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:53396438-53396902	MCF-7	breast:	n/a	chr8:53396452-53396464 chr8:53396637-53396650
24	CEBPB	chr8:53372644-53373068	A549	lung:	n/a	n/a
25	CEBPB	chr8:53379757-53380001	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:53395946-53395953	A549	lung:	n/a	n/a
27	CEBPB	chr8:53396522-53396810	H1-hESC	embryonic stem cell:	n/a	chr8:53396637-53396650
28	CEBPB	chr8:53390896-53391184	K562	blood:	n/a	n/a
29	CEBPB	chr8:53383876-53384104	HepG2	liver:	n/a	chr8:53384002-53384013
30	CEBPB	chr8:53396457-53396894	A549	lung:	n/a	chr8:53396637-53396650
31	CEBPB	chr8:53396469-53396829	Hela-S3	cervix:	n/a	chr8:53396637-53396650
32	CEBPB	chr8:53396460-53396843	IMR90	lung:	n/a	chr8:53396637-53396650
33	CEBPB	chr8:53381863-53382286	MCF-7	breast:	n/a	n/a
34	CEBPB	chr8:53372293-53373280	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr8:53396531-53396797	K562	blood:	n/a	chr8:53396637-53396650
36	CEBPB	chr8:53366024-53366229	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:53383928-53384094	A549	lung:	n/a	chr8:53384002-53384013
38	CEBPB	chr8:53372721-53373146	MCF-7	breast:	n/a	n/a
39	CEBPB	chr8:53363290-53363497	HepG2	liver:	n/a	chr8:53363360-53363371
40	CEBPB	chr8:53390857-53391216	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:53380669-53381024	HepG2	liver:	n/a	chr8:53380846-53380857 chr8:53380675-53380688
42	CEBPB	chr8:53396464-53396816	A549	lung:	n/a	chr8:53396637-53396650
43	CEBPB	chr8:53390859-53391231	A549	lung:	n/a	n/a
44	CEBPB	chr8:53386645-53386969	HepG2	liver:	n/a	chr8:53386814-53386831
45	CEBPB	chr8:53390956-53391156	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr8:53379012-53380164	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr8:53379510-53380065	MCF-7	breast:	n/a	n/a
48	CEBPB	chr8:53366626-53366812	HepG2	liver:	n/a	chr8:53366685-53366696
49	CHD2	chr8:53379613-53380244	Hela-S3	cervix:	n/a	chr8:53380042-53380051
50	CHD2	chr8:53379864-53380167	H1-hESC	embryonic stem cell:	n/a	chr8:53380042-53380051

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53352237-53352287	SKMC	muscle:	n/a
2	chr8:53392286-53392336	HL-60	blood:	n/a
3	chr8:53352237-53352287	Caco-2	colon:	n/a
4	chr8:53397932-53397982	Hela-S3	cervix:	n/a
5	chr8:53352275-53352325	HAEpiC	amniotic membrane:	n/a
6	chr8:53397932-53397982	BJ	skin:	n/a
7	chr8:53397932-53397982	CMK	blood:	n/a
8	chr8:53397932-53397982	ovcar-3	ovarian:	n/a
9	chr8:53397932-53397982	HIPEpiC	eye:	n/a
10	chr8:53352275-53352325	HCM	heart:	n/a
11	chr8:53361893-53361943	SK-N-MC	brain:	n/a
12	chr8:53392286-53392336	IMR90	lung:	fetal
13	chr8:53397932-53397982	PANC-1	pancreas:	n/a
14	chr8:53352237-53352287	CMK	blood:	n/a
15	chr8:53352237-53352287	GM12892	blood:	n/a
16	chr8:53397932-53397982	H1-hESC	embryonic stem cell:	embryo
17	chr8:53361893-53361943	SK-N-SH_RA	brain:	n/a
18	chr8:53361936-53361986	SK-N-MC	brain:	n/a
19	chr8:53352237-53352287	HMEC	breast:	n/a
20	chr8:53361893-53361943	AoSMC	blood vessel:	n/a
21	chr8:53361893-53361943	HepG2	liver:	n/a
22	chr8:53397932-53397982	AG04449	skin:	fetal
23	chr8:53392286-53392336	SAEC	small airway:	n/a
24	chr8:53361936-53361986	GM12892	blood:	n/a
25	chr8:53361936-53361986	AG04450	lung:	fetal
26	chr8:53361936-53361986	RPTEC	kidney:	n/a
27	chr8:53361893-53361943	HAEpiC	amniotic membrane:	n/a
28	chr8:53361936-53361986	HMEC	breast:	n/a
29	chr8:53392286-53392336	GM12892	blood:	n/a
30	chr8:53352275-53352325	Jurkat	blood:	n/a
31	chr8:53392286-53392336	T-47D	breast:	n/a
32	chr8:53352237-53352287	SK-N-MC	brain:	n/a
33	chr8:53352237-53352287	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:53361936-53361986	SAEC	small airway:	n/a
35	chr8:53392286-53392336	HCF	heart:	n/a
36	chr8:53397932-53397982	GM06990	blood:	n/a
37	chr8:53352275-53352325	HRE	kidney:	n/a
38	chr8:53392286-53392336	HUVEC	blood vessel:	n/a
39	chr8:53361936-53361986	AG10803	skin:	n/a
40	chr8:53397932-53397982	HRPEpiC	eye:	n/a
41	chr8:53352275-53352325	NH-A	brain:	n/a
42	chr8:53361893-53361943	Hepatocyte	liver:	n/a
43	chr8:53397932-53397982	RPTEC	kidney:	n/a
44	chr8:53352237-53352287	HCF	heart:	n/a
45	chr8:53397932-53397982	HepG2	liver:	n/a
46	chr8:53361936-53361986	MCF10A-Er-Src	breast:	n/a
47	chr8:53352237-53352287	GM06990	blood:	n/a
48	chr8:53352275-53352325	GM12892	blood:	n/a
49	chr8:53392286-53392336	K562	blood:	n/a
50	chr8:53361936-53361986	AG04449	skin:	fetal

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:52810955..52812797-chr8:53371753..53374505,2	MCF-7	breast:
2	chr8:53333225..53333725-chr8:53388714..53389585,2	MCF-7	breast:
3	chr8:53384050..53386139-chr8:53390786..53392939,2	MCF-7	breast:
4	chr8:53379300..53382260-chr8:53389036..53391579,2	MCF-7	breast:
5	chr8:53372582..53373541-chr9:86594741..86595608,2	Hela-S3	cervix:
6	chr8:53396327..53397778-chr8:53408319..53409731,6	MCF-7	breast:
7	chr8:53377547..53380484-chr8:53382020..53384595,2	MCF-7	breast:
8	chr8:53372593..53375156-chr8:53377269..53381843,6	MCF-7	breast:
9	chr8:53379006..53383439-chr8:53384188..53388259,4	MCF-7	breast:
10	chr8:53354328..53356957-chr8:53358190..53360419,2	MCF-7	breast:
11	chr8:53379300..53382260-chr8:53389036..53391579,2	MCF-7	breast:
12	chr8:53395676..53397810-chr8:53399596..53402225,2	MCF-7	breast:
13	chr8:53384050..53386139-chr8:53390786..53392939,2	MCF-7	breast:
14	chr8:53379006..53383439-chr8:53384188..53388259,4	MCF-7	breast:
15	chr8:53395676..53397810-chr8:53399596..53402225,2	MCF-7	breast:
16	chr8:53377547..53380484-chr8:53382020..53384595,2	MCF-7	breast:
17	chr8:53354328..53356957-chr8:53358190..53360419,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCMTD1-4	chr8:53373445-53373519	NONHSAT126569

No data

Variant related genes	Relation type
ST18	TF binding region
ST18	CpG island
ENSG00000168300	chromatin interactions
ENSG00000147488	chromatin interactions
ENSG00000228801	chromatin interactions
ENSG00000165119	chromatin interactions

Extended variants
information (count: 1994 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1994 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554375752	chr8:53341095-53341096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572492918	chr8:53341109-53341110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539886813	chr8:53341113-53341114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559593834	chr8:53341115-53341116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192109275	chr8:53341123-53341124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545401942	chr8:53341132-53341133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563861388	chr8:53341133-53341134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369296979	chr8:53341134-53341135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531022638	chr8:53341155-53341156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549450068	chr8:53341171-53341172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561415319	chr8:53341172-53341173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528474931	chr8:53341183-53341184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138979491	chr8:53341186-53341187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567285013	chr8:53341194-53341195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571684346	chr8:53341195-53341196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533652162	chr8:53341236-53341237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs284812	chr8:53341242-53341243	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs369081565	chr8:53341245-53341246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12542734	chr8:53341248-53341249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs386725374	chr8:53341255-53341256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113033221	chr8:53341257-53341258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145957552	chr8:53341258-53341259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568991008	chr8:53341267-53341268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536096405	chr8:53341339-53341340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552645652	chr8:53341449-53341450	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554239115	chr8:53341485-53341486	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572630137	chr8:53341522-53341523	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533526816	chr8:53341541-53341542	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569449389	chr8:53341578-53341579	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77102756	chr8:53341587-53341588	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs58578956	chr8:53341600-53341601	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs530822859	chr8:53341621-53341622	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs13279773	chr8:53341622-53341623	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs144805573	chr8:53341662-53341663	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73587328	chr8:53341740-53341741	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542881782	chr8:53341759-53341760	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75974581	chr8:53341780-53341781	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376517972	chr8:53341781-53341782	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528562844	chr8:53341807-53341808	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs284811	chr8:53341828-53341829	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs182622370	chr8:53341867-53341868	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532409039	chr8:53341878-53341879	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139847846	chr8:53341886-53341887	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569101716	chr8:53341896-53341897	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143293275	chr8:53341938-53341939	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545341732	chr8:53341968-53341969	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187745502	chr8:53341969-53341970	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191782804	chr8:53341972-53341973	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558242497	chr8:53341982-53341983	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182635290	chr8:53342049-53342050	Weak transcription Enhancers	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
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
low-grade B-cell lymphoma tumor	18367492	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
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53336800-53341400	Weak transcription	Brain Anterior Caudate	brain
2	chr8:53337600-53341600	Weak transcription	Brain Angular Gyrus	brain
3	chr8:53337600-53341600	Weak transcription	Brain Germinal Matrix	brain
4	chr8:53337800-53341400	Weak transcription	Brain Substantia Nigra	brain
5	chr8:53337800-53341800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr8:53338000-53341400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr8:53338000-53341600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr8:53340200-53343400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:53340400-53343200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:53340600-53341400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr8:53340600-53341400	Weak transcription	Brain Hippocampus Middle	brain
12	chr8:53341400-53342000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr8:53341400-53342400	Enhancers	Brain Anterior Caudate	brain
14	chr8:53341400-53342600	Enhancers	Brain Hippocampus Middle	brain
15	chr8:53341400-53342600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr8:53341400-53342800	Enhancers	Brain Substantia Nigra	brain
17	chr8:53341600-53342400	Enhancers	Brain Germinal Matrix	brain
18	chr8:53341600-53342600	Enhancers	Brain Angular Gyrus	brain
19	chr8:53341600-53342600	Enhancers	Brain Cingulate Gyrus	brain
20	chr8:53341800-53342200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr8:53342000-53343200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr8:53343200-53343600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:53343200-53344600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr8:53343400-53343800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:53344600-53351000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr8:53350800-53351000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:53351000-53351200	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:53351000-53351200	Enhancers	Gastric	stomach
29	chr8:53351000-53351600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr8:53351000-53351600	Enhancers	Fetal Kidney	kidney
31	chr8:53351000-53352400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:53351000-53352800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr8:53351200-53351400	Flanking Active TSS	Gastric	stomach
34	chr8:53351200-53351400	Enhancers	Pancreas	Pancrea
35	chr8:53351200-53351600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:53351200-53351600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
37	chr8:53351200-53351800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:53351200-53352400	Enhancers	Spleen	Spleen
39	chr8:53351200-53352800	Enhancers	Esophagus	oesophagus
40	chr8:53351400-53351800	Active TSS	Gastric	stomach
41	chr8:53351400-53352000	ZNF genes & repeats	Pancreas	Pancrea
42	chr8:53351600-53351800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:53351600-53351800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:53351600-53351800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:53351800-53352000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr8:53352000-53352200	Weak transcription	Pancreas	Pancrea
47	chr8:53352800-53360000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr8:53360000-53360400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
49	chr8:53360400-53371200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr8:53361200-53363800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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