Variant report

Variant	nsv1020460
Chromosome Location	chr8:53867769-53917467
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	ARID3A	chr8:53878433-53878817	K562	blood:	n/a	n/a
2	ARID3A	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
3	ATF2	chr8:53909866-53910228	GM12878	blood:	n/a	n/a
4	BATF	chr8:53909878-53910230	GM12878	blood:	n/a	chr8:53910027-53910037 chr8:53910026-53910037
5	BCL11A	chr8:53909839-53910302	GM12878	blood:	n/a	chr8:53910131-53910140
6	BCL11A	chr8:53909858-53910582	GM12878	blood:	n/a	chr8:53910131-53910140 chr8:53910301-53910310
7	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:53883301-53883728	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:53909862-53910567	GM12878	blood:	n/a	n/a
10	BRCA1	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:53916865-53917369	A549	lung:	n/a	n/a
12	CEBPB	chr8:53917155-53917454	K562	blood:	n/a	n/a
13	CEBPB	chr8:53907958-53908021	K562	blood:	n/a	n/a
14	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
15	CEBPB	chr8:53910786-53911069	K562	blood:	n/a	chr8:53910933-53910944 chr8:53910931-53910944 chr8:53910931-53910944 chr8:53910933-53910944
16	CHD1	chr8:53910064-53910138	GM12878	blood:	n/a	n/a
17	CHD2	chr8:53909815-53910522	GM12878	blood:	n/a	n/a
18	CHD2	chr8:53886601-53886615	GM12878	blood:	n/a	n/a
19	CREB1	chr8:53886223-53886639	HepG2	liver:	n/a	n/a
20	CTCF	chr8:53878460-53878610	GM12866	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
21	CTCF	chr8:53883260-53883410	GM12864	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
22	CTCF	chr8:53878460-53878610	Caco-2	colon:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
23	CTCF	chr8:53878480-53878630	AG09319	gingival:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
24	CTCF	chr8:53878500-53878650	HUVEC	blood vessel:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
25	CTCF	chr8:53878460-53878610	WI-38	lung:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
26	CTCF	chr8:53878480-53878630	Caco-2	colon:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
27	CTCF	chr8:53917460-53917610	GM12873	blood:	n/a	n/a
28	CTCF	chr8:53878480-53878630	HEEpiC	esophagus:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
29	CTCF	chr8:53878060-53878210	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr8:53878500-53878650	HEEpiC	esophagus:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
31	CTCF	chr8:53878440-53878590	MCF-7	breast:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
32	CTCF	chr8:53878500-53878650	HA-sp	spinal cord:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
33	CTCF	chr8:53878060-53878210	Caco-2	colon:	n/a	n/a
34	CTCF	chr8:53878400-53878550	HCT-116	colon:	n/a	n/a
35	CTCF	chr8:53883240-53883390	GM12864	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
36	CTCF	chr8:53883300-53883398	Gliobla	brain:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
37	CTCF	chr8:53878504-53878603	A549	lung:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
38	CTCF	chr8:53878500-53878650	Hela-S3	cervix:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
39	CTCF	chr8:53878300-53878450	SAEC	small airway:	n/a	n/a
40	CTCF	chr8:53878307-53878823	HCT-116	colon:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
41	CTCF	chr8:53883263-53883448	K562	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
42	CTCF	chr8:53883268-53883421	Pancreas_OC	pancreas:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
43	CTCF	chr8:53883355-53883375	GM13977	blood:	n/a	n/a
44	CTCF	chr8:53878340-53878490	GM12872	blood:	n/a	n/a
45	CTCF	chr8:53878416-53878700	Medullo	brain:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
46	CTCF	chr8:53883240-53883390	Hela-S3	cervix:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
47	CTCF	chr8:53878158-53878848	SK-N-SH	brain:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
48	CTCF	chr8:53878499-53878637	GM20000	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
49	CTCF	chr8:53883281-53883424	GM19238	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
50	CTCF	chr8:53883278-53883426	GM12878	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53883763-53883813	NB4	blood:	n/a
2	chr8:53883763-53883813	ECC-1	luminal epithelium:	n/a
3	chr8:53883763-53883813	NT2-D1	testis:	n/a
4	chr8:53883763-53883813	HepG2	liver:	n/a
5	chr8:53883763-53883813	PANC-1	pancreas:	n/a
6	chr8:53883763-53883813	PFSK-1	brain:	n/a
7	chr8:53883763-53883813	HIPEpiC	eye:	n/a
8	chr8:53883763-53883813	SK-N-SH_RA	brain:	n/a
9	chr8:53883763-53883813	BJ	skin:	n/a
10	chr8:53883763-53883813	T-47D	breast:	n/a
11	chr8:53883763-53883813	Hepatocyte	liver:	n/a
12	chr8:53883763-53883813	Caco-2	colon:	n/a
13	chr8:53883763-53883813	SAEC	small airway:	n/a
14	chr8:53883763-53883813	Jurkat	blood:	n/a
15	chr8:53883763-53883813	ProgFib	skin:	n/a
16	chr8:53883763-53883813	AG04450	lung:	fetal
17	chr8:53883763-53883813	HRPEpiC	eye:	n/a
18	chr8:53883763-53883813	HEK293	kidney:	embryo
19	chr8:53883763-53883813	K562	blood:	n/a
20	chr8:53883763-53883813	ovcar-3	ovarian:	n/a
21	chr8:53883763-53883813	Hela-S3	cervix:	n/a
22	chr8:53883763-53883813	SK-N-MC	brain:	n/a
23	chr8:53883763-53883813	HMEC	breast:	n/a
24	chr8:53883763-53883813	GM19239	blood:	n/a
25	chr8:53883763-53883813	HRE	kidney:	n/a
26	chr8:53883763-53883813	AG04449	skin:	fetal
27	chr8:53883763-53883813	SKMC	muscle:	n/a
28	chr8:53883763-53883813	HCF	heart:	n/a
29	chr8:53883763-53883813	PrEC	prostate:	n/a
30	chr8:53883763-53883813	HNPCEpiC	eye:	n/a
31	chr8:53883763-53883813	HCPEpiC	choroid plexus:	n/a
32	chr8:53883763-53883813	AG09319	gingival:	n/a
33	chr8:53883763-53883813	GM06990	blood:	n/a
34	chr8:53883763-53883813	GM12892	blood:	n/a
35	chr8:53883763-53883813	HRCEpiC	kidney:	n/a
36	chr8:53883763-53883813	GM12891	blood:	n/a
37	chr8:53883763-53883813	GM12878	blood:	n/a
38	chr8:53883763-53883813	AG10803	skin:	n/a
39	chr8:53883763-53883813	AG09309	skin:	n/a
40	chr8:53883763-53883813	NH-A	brain:	n/a
41	chr8:53883763-53883813	HL-60	blood:	n/a
42	chr8:53883763-53883813	SK-N-SH	brain:	n/a
43	chr8:53883763-53883813	H1-hESC	embryonic stem cell:	embryo
44	chr8:53883763-53883813	HEEpiC	esophagus:	n/a
45	chr8:53883763-53883813	U87	brain:	n/a
46	chr8:53883763-53883813	NHBE	bronchial:	n/a
47	chr8:53883763-53883813	HCM	heart:	n/a
48	chr8:53883763-53883813	LNCaP	prostate:	n/a
49	chr8:53883763-53883813	AoSMC	blood vessel:	n/a
50	chr8:53883763-53883813	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
2	chr8:53878057..53878612-chr8:54775599..54776413,2	K562	blood:
3	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
4	chr8:53878521..53879036-chr8:54398874..54399575,2	MCF-7	breast:
5	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:

Variant related genes	Relation type
ENSG00000248911	TF binding region
ENSG00000265835	TF binding region
ENSG00000248911	CpG island
ENSG00000265835	CpG island

Extended variants
information (count: 1419 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565051268	chr8:53867781-53867782	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186721537	chr8:53867805-53867806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191323276	chr8:53867806-53867807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540244287	chr8:53867817-53867818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375408011	chr8:53867832-53867833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564712354	chr8:53867835-53867836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11991536	chr8:53867860-53867861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374245304	chr8:53867865-53867866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551785644	chr8:53867912-53867913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563595291	chr8:53867952-53867953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531018934	chr8:53867955-53867956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183342158	chr8:53867957-53867958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550504101	chr8:53867967-53867968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561111589	chr8:53867968-53867969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113832111	chr8:53867984-53867985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547005386	chr8:53868029-53868030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571540319	chr8:53868031-53868032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538969230	chr8:53868032-53868033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557296001	chr8:53868039-53868040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569129357	chr8:53868056-53868057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187786727	chr8:53868058-53868059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554774319	chr8:53868064-53868065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572921237	chr8:53868065-53868066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539943758	chr8:53868078-53868079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529902517	chr8:53868095-53868096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193199248	chr8:53868097-53868098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546752080	chr8:53868147-53868148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576769187	chr8:53868167-53868168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543765232	chr8:53868171-53868172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs386725405	chr8:53868200-53868201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531082356	chr8:53868201-53868202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542842032	chr8:53868208-53868209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561129097	chr8:53868209-53868210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528625017	chr8:53868225-53868226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72648424	chr8:53868226-53868227	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs58231387	chr8:53868231-53868232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532408698	chr8:53868232-53868233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552115125	chr8:53868249-53868250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140531897	chr8:53868270-53868271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550957897	chr8:53868298-53868299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374339638	chr8:53868314-53868315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113906680	chr8:53868320-53868321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377482414	chr8:53868334-53868335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536526971	chr8:53868339-53868340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562490868	chr8:53868359-53868360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554845987	chr8:53868382-53868383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531493694	chr8:53868404-53868405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149727273	chr8:53868411-53868412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533944307	chr8:53868440-53868441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185120285	chr8:53868465-53868466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53866800-53868400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:53866800-53868600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:53867600-53867800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:53867800-53868800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:53868200-53869200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:53868600-53868800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:53868600-53869000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:53868600-53869200	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr8:53868800-53869400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr8:53872400-53873000	Enhancers	Dnd41	blood
11	chr8:53873000-53874600	Weak transcription	Dnd41	blood
12	chr8:53873800-53874400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:53874600-53876800	Enhancers	Dnd41	blood
14	chr8:53876800-53877800	Weak transcription	Dnd41	blood
15	chr8:53877800-53878800	Enhancers	Dnd41	blood
16	chr8:53878000-53878400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:53878200-53878600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr8:53878800-53882400	Weak transcription	Dnd41	blood
19	chr8:53881400-53881600	Enhancers	Thymus	Thymus
20	chr8:53881600-53883400	Weak transcription	Thymus	Thymus
21	chr8:53882200-53883000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:53882400-53882600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr8:53882400-53884800	Enhancers	Dnd41	blood
24	chr8:53882600-53887200	Enhancers	Fetal Intestine Small	intestine
25	chr8:53882800-53884800	Enhancers	Fetal Thymus	thymus
26	chr8:53882800-53887600	Enhancers	Fetal Intestine Large	intestine
27	chr8:53883000-53883400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr8:53883000-53884200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr8:53883200-53883800	Enhancers	Duodenum Mucosa	Duodenum
30	chr8:53883200-53884600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:53883200-53885000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:53883200-53885200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:53883200-53885200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:53883400-53883600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:53883400-53883800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr8:53883400-53884000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:53883400-53884000	Enhancers	Thymus	Thymus
38	chr8:53883400-53884400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr8:53883400-53884600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:53883400-53884600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr8:53883400-53885000	Enhancers	Primary B cells from peripheral blood	blood
42	chr8:53883400-53885200	Enhancers	H1 Cell Line	embryonic stem cell
43	chr8:53883400-53885400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:53883400-53885400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr8:53883400-53885400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr8:53883600-53883800	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr8:53883600-53883800	Enhancers	Stomach Mucosa	stomach
48	chr8:53883600-53883800	Enhancers	HepG2	liver
49	chr8:53883600-53884000	Enhancers	Small Intestine	intestine
50	chr8:53883600-53884200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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