Variant report

Variant	nsv890911
Chromosome Location	chr8:53788331-53880054
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:978)
CpG islands
(count:1404)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53878433-53878817	K562	blood:	n/a	n/a
2	ARID3A	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
3	ATF1	chr8:53808152-53808289	K562	blood:	n/a	n/a
4	ATF1	chr8:53835080-53835117	K562	blood:	n/a	n/a
5	ATF1	chr8:53849646-53849868	K562	blood:	n/a	n/a
6	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:53852611-53852810	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr8:53854274-53854336	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
12	BRCA1	chr8:53810109-53810437	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr8:53809465-53809560	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:53831668-53832176	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:53830927-53831156	K562	blood:	n/a	chr8:53831113-53831124
18	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
19	CEBPB	chr8:53830972-53831278	IMR90	lung:	n/a	chr8:53831113-53831124
20	CEBPB	chr8:53809910-53810405	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr8:53827418-53827672	Hela-S3	cervix:	n/a	chr8:53827575-53827587
22	CEBPB	chr8:53834940-53834973	A549	lung:	n/a	n/a
23	CEBPB	chr8:53854282-53854519	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:53798967-53799236	A549	lung:	n/a	chr8:53799062-53799073
25	CEBPB	chr8:53850582-53850783	A549	lung:	n/a	n/a
26	CEBPB	chr8:53850499-53850779	K562	blood:	n/a	n/a
27	CEBPB	chr8:53830968-53831268	HepG2	liver:	n/a	chr8:53831113-53831124
28	CEBPB	chr8:53798977-53799209	HepG2	liver:	n/a	chr8:53799062-53799073
29	CHD1	chr8:53853898-53854325	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr8:53854039-53854723	IMR90	lung:	n/a	n/a
31	CHD1	chr8:53854213-53854389	GM12878	blood:	n/a	n/a
32	CHD2	chr8:53810013-53810448	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr8:53854284-53854530	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr8:53851260-53851279	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr8:53854239-53854481	HepG2	liver:	n/a	n/a
36	CHD2	chr8:53853125-53853738	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr8:53854182-53854464	A549	lung:	n/a	n/a
38	CREB1	chr8:53853639-53854000	A549	lung:	n/a	n/a
39	CREB1	chr8:53852360-53853460	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr8:53851626-53854473	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:53813680-53813830	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr8:53878400-53878550	GM12868	blood:	n/a	n/a
43	CTCF	chr8:53854220-53854370	GM12878	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
44	CTCF	chr8:53854214-53854471	K562	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
45	CTCF	chr8:53853820-53853970	GM12871	blood:	n/a	chr8:53853894-53853907
46	CTCF	chr8:53878480-53878630	NHEK	skin:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
47	CTCF	chr8:53853819-53853943	GM12891	blood:	n/a	chr8:53853894-53853907
48	CTCF	chr8:53853800-53853950	HCT-116	colon:	n/a	chr8:53853894-53853907
49	CTCF	chr8:53854320-53854470	HCM	heart:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
50	CTCF	chr8:53854260-53854410	Hela-S3	cervix:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53851707-53851757	HL-60	blood:	n/a
2	chr8:53851707-53851757	HL-60	blood:	n/a
3	chr8:53851613-53851663	HL-60	blood:	n/a
4	chr8:53853112-53853162	SK-N-SH_RA	brain:	n/a
5	chr8:53853112-53853162	NHBE	bronchial:	n/a
6	chr8:53864533-53864583	Caco-2	colon:	n/a
7	chr8:53866689-53866739	GM12878	blood:	n/a
8	chr8:53854172-53854222	GM12892	blood:	n/a
9	chr8:53854425-53854475	AG09319	gingival:	n/a
10	chr8:53851156-53851206	H1-hESC	embryonic stem cell:	embryo
11	chr8:53852443-53852493	ovcar-3	ovarian:	n/a
12	chr8:53852446-53852496	SK-N-SH	brain:	n/a
13	chr8:53851613-53851663	ProgFib	skin:	n/a
14	chr8:53866689-53866739	U87	brain:	n/a
15	chr8:53851156-53851206	PrEC	prostate:	n/a
16	chr8:53866689-53866739	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:53854172-53854222	K562	blood:	n/a
18	chr8:53854495-53854545	NT2-D1	testis:	n/a
19	chr8:53851156-53851206	HCM	heart:	n/a
20	chr8:53854172-53854222	PFSK-1	brain:	n/a
21	chr8:53866529-53866579	HMEC	breast:	n/a
22	chr8:53852101-53852151	SK-N-MC	brain:	n/a
23	chr8:53851707-53851757	HCT-116	colon:	n/a
24	chr8:53852030-53852080	SKMC	muscle:	n/a
25	chr8:53853604-53853654	HCT-116	colon:	n/a
26	chr8:53853444-53853494	NH-A	brain:	n/a
27	chr8:53849059-53849109	CMK	blood:	n/a
28	chr8:53853659-53853709	AG09309	skin:	n/a
29	chr8:53852184-53852234	SKMC	muscle:	n/a
30	chr8:53852661-53852711	AG09319	gingival:	n/a
31	chr8:53854425-53854475	A549	lung:	n/a
32	chr8:53854172-53854222	AG04450	lung:	fetal
33	chr8:53854495-53854545	MCF10A-Er-Src	breast:	n/a
34	chr8:53852101-53852151	CMK	blood:	n/a
35	chr8:53864533-53864583	NT2-D1	testis:	n/a
36	chr8:53852184-53852234	CMK	blood:	n/a
37	chr8:53851707-53851757	T-47D	breast:	n/a
38	chr8:53857047-53857097	HCM	heart:	n/a
39	chr8:53852030-53852080	GM12878	blood:	n/a
40	chr8:53854172-53854222	Hepatocyte	liver:	n/a
41	chr8:53853112-53853162	ovcar-3	ovarian:	n/a
42	chr8:53854495-53854545	PFSK-1	brain:	n/a
43	chr8:53857047-53857097	HL-60	blood:	n/a
44	chr8:53853444-53853494	A549	lung:	n/a
45	chr8:53851613-53851663	CMK	blood:	n/a
46	chr8:53854172-53854222	MCF10A-Er-Src	breast:	n/a
47	chr8:53864533-53864583	HRE	kidney:	n/a
48	chr8:53866689-53866739	PFSK-1	brain:	n/a
49	chr8:53851156-53851206	SK-N-SH	brain:	n/a
50	chr8:53852101-53852151	AG10803	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53878057..53878612-chr8:54775599..54776413,2	K562	blood:
2	chr8:53649371..53650945-chr8:53853868..53854778,6	MCF-7	breast:
3	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
4	chr14:88237597..88238206-chr8:53793496..53793998,3	MCF-7	breast:
5	chr8:53649708..53650309-chr8:53861493..53862325,2	MCF-7	breast:
6	chr8:53784191..53786210-chr8:53800399..53802685,2	K562	blood:
7	chr8:53878521..53879036-chr8:54398874..54399575,2	MCF-7	breast:
8	chr8:53636506..53637243-chr8:53861404..53862378,2	MCF-7	breast:
9	chr8:53649723..53650709-chr8:53861922..53862952,3	MCF-7	breast:
10	chr8:53805931..53807978-chr8:53816689..53818778,2	K562	blood:
11	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
12	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
13	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
14	chr8:53634696..53637064-chr8:53861267..53863053,2	MCF-7	breast:
15	chr8:53797993..53800966-chr8:53802377..53805640,4	K562	blood:
16	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
17	chr8:53805931..53807978-chr8:53816689..53818778,2	K562	blood:
18	chr8:53797993..53800966-chr8:53802377..53805640,4	K562	blood:
19	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
20	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
21	chr8:53627445..53629464-chr8:53852538..53854621,2	MCF-7	breast:
22	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:
23	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
24	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2102 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2102 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76684636	chr8:53788331-53788332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551599079	chr8:53788337-53788338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs55714807	chr8:53788450-53788451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181834885	chr8:53788510-53788511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549439956	chr8:53788514-53788515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79804045	chr8:53788519-53788520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535036018	chr8:53788630-53788631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553353355	chr8:53788642-53788643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571577152	chr8:53788655-53788656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558767686	chr8:53788700-53788701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538927783	chr8:53788705-53788706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185193852	chr8:53788716-53788717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189805218	chr8:53788853-53788854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372821640	chr8:53788865-53788866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575375383	chr8:53788894-53788895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569064654	chr8:53788896-53788897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542392949	chr8:53788906-53788907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554666734	chr8:53788908-53788909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572823358	chr8:53788970-53788971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538007459	chr8:53788982-53788983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73681212	chr8:53789015-53789016	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs376450564	chr8:53789030-53789031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564528892	chr8:53789038-53789039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533491994	chr8:53789059-53789060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548661651	chr8:53789110-53789111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182100688	chr8:53789118-53789119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563761952	chr8:53789216-53789217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531148422	chr8:53789300-53789301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7826925	chr8:53789349-53789350	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs116032090	chr8:53789376-53789377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185513433	chr8:53789378-53789379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6473759	chr8:53789397-53789398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs143692639	chr8:53789445-53789446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191244037	chr8:53789454-53789455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538965731	chr8:53789492-53789493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183627774	chr8:53789508-53789509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188624907	chr8:53789514-53789515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144915113	chr8:53789521-53789522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554422482	chr8:53789568-53789569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6473760	chr8:53789603-53789604	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576960529	chr8:53789621-53789622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117816858	chr8:53789680-53789681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192051160	chr8:53789742-53789743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563157187	chr8:53789819-53789820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148690087	chr8:53789823-53789824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13438870	chr8:53789924-53789925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117550176	chr8:53789942-53789943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs386725394	chr8:53789943-53789944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs72637496	chr8:53789944-53789945	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs561317937	chr8:53789959-53789960	Enhancers	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:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53781800-53788800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:53784600-53789000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:53788800-53790200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:53789000-53789400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:53789400-53789600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:53789600-53790200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:53793400-53794000	ZNF genes & repeats	Dnd41	blood
8	chr8:53795200-53796400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:53796400-53796600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:53804800-53805400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:53804800-53805400	Enhancers	HMEC	breast
12	chr8:53805400-53809600	Weak transcription	HMEC	breast
13	chr8:53805600-53805800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:53805800-53806400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:53806400-53807400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:53807400-53808200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:53807800-53808200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr8:53809600-53811200	Enhancers	HMEC	breast
19	chr8:53809800-53810400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:53809800-53810600	Enhancers	NHEK	skin
21	chr8:53809800-53810800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:53809800-53810800	Enhancers	Hela-S3	cervix
23	chr8:53811200-53811800	Weak transcription	HMEC	breast
24	chr8:53811800-53812000	Enhancers	HMEC	breast
25	chr8:53818400-53819000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:53818400-53819600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:53818800-53819800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:53818800-53819800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr8:53818800-53819800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:53819400-53819800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:53820800-53821800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:53825200-53825600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:53825200-53825600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:53825200-53825800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:53825200-53825800	Enhancers	HMEC	breast
36	chr8:53825400-53825600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr8:53825400-53825600	Enhancers	Hela-S3	cervix
38	chr8:53825400-53825600	Enhancers	HSMMtube	muscle
39	chr8:53825400-53825800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:53825800-53831200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:53826000-53831000	Weak transcription	Hela-S3	cervix
42	chr8:53831000-53832400	Enhancers	Hela-S3	cervix
43	chr8:53831000-53832400	Enhancers	HSMMtube	muscle
44	chr8:53831200-53832000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:53831200-53832000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:53831200-53832200	Enhancers	HSMM	muscle
47	chr8:53831200-53832600	Enhancers	Liver	Liver
48	chr8:53831400-53831800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:53831600-53832200	Enhancers	Dnd41	blood
50	chr8:53832000-53836600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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