Variant report

Variant	nsv824633
Chromosome Location	chr8:53739971-53866329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:927)
CpG islands
(count:1282)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:53849646-53849868	K562	blood:	n/a	n/a
2	ATF1	chr8:53835080-53835117	K562	blood:	n/a	n/a
3	ATF1	chr8:53808152-53808289	K562	blood:	n/a	n/a
4	BACH1	chr8:53852611-53852810	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:53752697-53752724	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:53752228-53752795	GM12878	blood:	n/a	n/a
10	BCL3	chr8:53752546-53752884	GM12878	blood:	n/a	chr8:53752683-53752692
11	BHLHE40	chr8:53854274-53854336	GM12878	blood:	n/a	n/a
12	BRCA1	chr8:53809465-53809560	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
15	BRCA1	chr8:53810109-53810437	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr8:53756167-53756690	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:53831668-53832176	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:53827418-53827672	Hela-S3	cervix:	n/a	chr8:53827575-53827587
20	CEBPB	chr8:53752507-53752849	A549	lung:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
21	CEBPB	chr8:53830968-53831268	HepG2	liver:	n/a	chr8:53831113-53831124
22	CEBPB	chr8:53744670-53745012	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:53850499-53850779	K562	blood:	n/a	n/a
24	CEBPB	chr8:53752543-53752843	Hela-S3	cervix:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
25	CEBPB	chr8:53752549-53752841	MCF-7	breast:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
26	CEBPB	chr8:53772929-53773042	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:53830927-53831156	K562	blood:	n/a	chr8:53831113-53831124
28	CEBPB	chr8:53763008-53763208	HepG2	liver:	n/a	chr8:53763044-53763055
29	CEBPB	chr8:53772883-53773063	A549	lung:	n/a	n/a
30	CEBPB	chr8:53756219-53756752	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:53744690-53745080	A549	lung:	n/a	n/a
32	CEBPB	chr8:53850582-53850783	A549	lung:	n/a	n/a
33	CEBPB	chr8:53809910-53810405	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:53763040-53763050	K562	blood:	n/a	n/a
35	CEBPB	chr8:53798967-53799236	A549	lung:	n/a	chr8:53799062-53799073
36	CEBPB	chr8:53834940-53834973	A549	lung:	n/a	n/a
37	CEBPB	chr8:53744852-53744928	A549	lung:	n/a	n/a
38	CEBPB	chr8:53798977-53799209	HepG2	liver:	n/a	chr8:53799062-53799073
39	CEBPB	chr8:53854282-53854519	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:53783054-53783127	HepG2	liver:	n/a	chr8:53783077-53783088
41	CEBPB	chr8:53830972-53831278	IMR90	lung:	n/a	chr8:53831113-53831124
42	CHD1	chr8:53854039-53854723	IMR90	lung:	n/a	n/a
43	CHD1	chr8:53853898-53854325	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr8:53854213-53854389	GM12878	blood:	n/a	n/a
45	CHD2	chr8:53854284-53854530	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr8:53756407-53756770	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr8:53810013-53810448	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr8:53851260-53851279	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:53853125-53853738	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr8:53854239-53854481	HepG2	liver:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53852030-53852080	SAEC	small airway:	n/a
2	chr8:53852030-53852080	SAEC	small airway:	n/a
3	chr8:53852446-53852496	U87	brain:	n/a
4	chr8:53853444-53853494	GM12892	blood:	n/a
5	chr8:53864533-53864583	ECC-1	luminal epithelium:	n/a
6	chr8:53853112-53853162	SK-N-MC	brain:	n/a
7	chr8:53852661-53852711	GM19239	blood:	n/a
8	chr8:53854425-53854475	CMK	blood:	n/a
9	chr8:53851707-53851757	SK-N-MC	brain:	n/a
10	chr8:53849059-53849109	GM06990	blood:	n/a
11	chr8:53852030-53852080	IMR90	lung:	fetal
12	chr8:53852446-53852496	AoSMC	blood vessel:	n/a
13	chr8:53852030-53852080	CMK	blood:	n/a
14	chr8:53852274-53852324	AG09319	gingival:	n/a
15	chr8:53852274-53852324	AG04450	lung:	fetal
16	chr8:53849059-53849109	PANC-1	pancreas:	n/a
17	chr8:53854425-53854475	HCF	heart:	n/a
18	chr8:53852446-53852496	SKMC	muscle:	n/a
19	chr8:53849059-53849109	HEK293	kidney:	embryo
20	chr8:53852184-53852234	GM06990	blood:	n/a
21	chr8:53854172-53854222	SK-N-MC	brain:	n/a
22	chr8:53854495-53854545	HepG2	liver:	n/a
23	chr8:53852422-53852472	AoSMC	blood vessel:	n/a
24	chr8:53851707-53851757	SK-N-SH_RA	brain:	n/a
25	chr8:53854495-53854545	GM06990	blood:	n/a
26	chr8:53864533-53864583	GM12891	blood:	n/a
27	chr8:53853659-53853709	HIPEpiC	eye:	n/a
28	chr8:53854425-53854475	HEEpiC	esophagus:	n/a
29	chr8:53851613-53851663	BE2_C	brain:	n/a
30	chr8:53851613-53851663	PrEC	prostate:	n/a
31	chr8:53853659-53853709	MCF10A-Er-Src	breast:	n/a
32	chr8:53857047-53857097	GM19239	blood:	n/a
33	chr8:53852030-53852080	Hepatocyte	liver:	n/a
34	chr8:53853659-53853709	AoSMC	blood vessel:	n/a
35	chr8:53851707-53851757	ovcar-3	ovarian:	n/a
36	chr8:53857047-53857097	HRCEpiC	kidney:	n/a
37	chr8:53854495-53854545	NH-A	brain:	n/a
38	chr8:53853604-53853654	GM06990	blood:	n/a
39	chr8:53864533-53864583	H1-hESC	embryonic stem cell:	embryo
40	chr8:53852274-53852324	SK-N-MC	brain:	n/a
41	chr8:53852446-53852496	HAEpiC	amniotic membrane:	n/a
42	chr8:53854172-53854222	LNCaP	prostate:	n/a
43	chr8:53853444-53853494	HEEpiC	esophagus:	n/a
44	chr8:53852274-53852324	HMEC	breast:	n/a
45	chr8:53851156-53851206	SK-N-SH	brain:	n/a
46	chr8:53852422-53852472	NT2-D1	testis:	n/a
47	chr8:53854495-53854545	SAEC	small airway:	n/a
48	chr8:53851156-53851206	NH-A	brain:	n/a
49	chr8:53854425-53854475	NH-A	brain:	n/a
50	chr8:53864533-53864583	SKMC	muscle:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53649708..53650309-chr8:53861493..53862325,2	MCF-7	breast:
2	chr8:53634696..53637064-chr8:53861267..53863053,2	MCF-7	breast:
3	chr8:53649371..53650945-chr8:53853868..53854778,6	MCF-7	breast:
4	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:
5	chr8:53742557..53744441-chr8:53753816..53756483,2	MCF-7	breast:
6	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
7	chr8:53763900..53765944-chr8:53767253..53769124,2	MCF-7	breast:
8	chr8:53653974..53655794-chr8:53756951..53758784,2	MCF-7	breast:
9	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
10	chr8:53751467..53754365-chr8:53754550..53756405,2	MCF-7	breast:
11	chr14:88237597..88238206-chr8:53793496..53793998,3	MCF-7	breast:
12	chr8:53805931..53807978-chr8:53816689..53818778,2	K562	blood:
13	chr8:53636506..53637243-chr8:53861404..53862378,2	MCF-7	breast:
14	chr8:53784191..53786210-chr8:53800399..53802685,2	K562	blood:
15	chr8:53763900..53765944-chr8:53767253..53769124,2	MCF-7	breast:
16	chr8:53797993..53800966-chr8:53802377..53805640,4	K562	blood:
17	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
18	chr8:53805931..53807978-chr8:53816689..53818778,2	K562	blood:
19	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
20	chr8:53775937..53778409-chr8:53784460..53787182,3	MCF-7	breast:
21	chr8:53797993..53800966-chr8:53802377..53805640,4	K562	blood:
22	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
23	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
24	chr8:53775937..53778409-chr8:53784460..53787182,3	MCF-7	breast:
25	chr8:53784191..53786210-chr8:53800399..53802685,2	K562	blood:
26	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
27	chr8:53742557..53744441-chr8:53753816..53756483,2	MCF-7	breast:
28	chr8:53649723..53650709-chr8:53861922..53862952,3	MCF-7	breast:
29	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
30	chr8:53738269..53739834-chr8:53754081..53756709,2	MCF-7	breast:
31	chr8:53751467..53754365-chr8:53754550..53756405,2	MCF-7	breast:
32	chr8:53627445..53629464-chr8:53852538..53854621,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPBWR1	TF binding region
NPBWR1	CpG island
ENSG00000271555	chromatin interactions

Extended variants
information (count: 2963 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2963 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs118129803	chr8:53739984-53739985	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs149543377	chr8:53739999-53740000	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs181627762	chr8:53740011-53740012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532151131	chr8:53740031-53740032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186776435	chr8:53740050-53740051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564013204	chr8:53740062-53740063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531221301	chr8:53740063-53740064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113787253	chr8:53740102-53740103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567871107	chr8:53740105-53740106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534871012	chr8:53740109-53740110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546692625	chr8:53740226-53740227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571404081	chr8:53740255-53740256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62501747	chr8:53740259-53740260	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556919583	chr8:53740278-53740279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542267004	chr8:53740312-53740313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192100109	chr8:53740334-53740335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536567418	chr8:53740356-53740357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143128953	chr8:53740357-53740358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183995620	chr8:53740413-53740414	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs540010231	chr8:53740417-53740418	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs200657215	chr8:53740419-53740420	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187695284	chr8:53740421-53740422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs368117714	chr8:53740448-53740449	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs189803066	chr8:53740480-53740481	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs544260110	chr8:53740517-53740518	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs532239880	chr8:53740551-53740552	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs2360242	chr8:53740565-53740566	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs182101930	chr8:53740616-53740617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187051771	chr8:53740617-53740618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148257172	chr8:53740685-53740686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561376235	chr8:53740811-53740812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528730064	chr8:53740825-53740826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191503062	chr8:53740850-53740851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4487798	chr8:53740860-53740861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112663583	chr8:53740961-53740962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376427899	chr8:53740985-53740986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146796007	chr8:53740992-53740993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569247292	chr8:53740996-53740997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536209179	chr8:53740999-53741000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4242482	chr8:53741061-53741062	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185364956	chr8:53741065-53741066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534022806	chr8:53741085-53741086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567469808	chr8:53741095-53741096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111583122	chr8:53741117-53741118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568631062	chr8:53741248-53741249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188612982	chr8:53741276-53741277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534175746	chr8:53741293-53741294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111746829	chr8:53741294-53741295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373607945	chr8:53741329-53741330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574383618	chr8:53741392-53741393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53731800-53740200	Enhancers	HMEC	breast
2	chr8:53737200-53740600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:53737400-53740000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:53737800-53740600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr8:53737800-53740600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:53738000-53740600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:53738400-53740000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:53738600-53740000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr8:53738600-53740200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:53738800-53740200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:53739400-53740600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:53739600-53740800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:53739800-53740000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:53739800-53740000	Bivalent Enhancer	GM12878-XiMat	blood
15	chr8:53739800-53740200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:53739800-53740400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr8:53739800-53740600	Enhancers	Hela-S3	cervix
18	chr8:53740000-53740400	Enhancers	GM12878-XiMat	blood
19	chr8:53740000-53743200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:53740000-53743200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:53740400-53740600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr8:53740400-53740600	Flanking Active TSS	GM12878-XiMat	blood
23	chr8:53740800-53743200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:53743000-53743600	Enhancers	Fetal Thymus	thymus
25	chr8:53743000-53743800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr8:53743000-53744200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr8:53743000-53744400	Enhancers	Primary T cells from cord blood	blood
28	chr8:53743000-53744800	Enhancers	Dnd41	blood
29	chr8:53743200-53743400	ZNF genes & repeats	Pancreas	Pancrea
30	chr8:53743200-53743400	Enhancers	GM12878-XiMat	blood
31	chr8:53743200-53743600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:53743200-53743600	Weak transcription	HMEC	breast
33	chr8:53743200-53744000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:53743200-53744600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:53743200-53744600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr8:53743200-53744600	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr8:53743200-53744800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr8:53743200-53744800	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr8:53743400-53743600	Enhancers	Primary T cells fromperipheralblood	blood
40	chr8:53743600-53749400	Weak transcription	Fetal Thymus	thymus
41	chr8:53743800-53744200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr8:53743800-53744800	Enhancers	NHEK	skin
43	chr8:53744000-53744800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr8:53744000-53744800	Enhancers	HMEC	breast
45	chr8:53744200-53744600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr8:53744200-53744800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr8:53744400-53744800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr8:53744400-53748200	Weak transcription	Primary T cells from cord blood	blood
49	chr8:53744600-53744800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr8:53744600-53745000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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