Variant report

Variant	nsv465682
Chromosome Location	chr8:53874753-53917467
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	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53878433-53878817	K562	blood:	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	chr8:53909862-53910567	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:53883301-53883728	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	chr8:53910786-53911069	K562	blood:	n/a	chr8:53910933-53910944 chr8:53910931-53910944 chr8:53910931-53910944 chr8:53910933-53910944
13	CEBPB	chr8:53907958-53908021	K562	blood:	n/a	n/a
14	CEBPB	chr8:53917155-53917454	K562	blood:	n/a	n/a
15	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
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	chr8:53878500-53878650	RPTEC	kidney:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
21	CTCF	chr8:53883280-53883430	WERI-Rb-1	eye:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
22	CTCF	chr8:53878504-53878603	A549	lung:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
23	CTCF	chr8:53883380-53883530	HMEC	breast:	n/a	n/a
24	CTCF	chr8:53883307-53883429	GM12891	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
25	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
26	CTCF	chr8:53878500-53878650	Hela-S3	cervix:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
27	CTCF	chr8:53878454-53878664	Gliobla	brain:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
28	CTCF	chr8:53883300-53883398	Gliobla	brain:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
29	CTCF	chr8:53878480-53878630	AG09319	gingival:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
30	CTCF	chr8:53878324-53878703	HepG2	liver:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
31	CTCF	chr8:53878460-53878610	GM12871	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
32	CTCF	chr8:53882357-53882428	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr8:53878400-53878550	GM12878	blood:	n/a	n/a
34	CTCF	chr8:53878540-53878690	GM12874	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
35	CTCF	chr8:53878480-53878638	MCF-7	breast:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
36	CTCF	chr8:53883066-53883608	MCF-7	breast:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
37	CTCF	chr8:53883295-53883418	HepG2	liver:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
38	CTCF	chr8:53878440-53878590	WERI-Rb-1	eye:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
39	CTCF	chr8:53883271-53883438	GM19240	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
40	CTCF	chr8:53883200-53883350	A549	lung:	n/a	n/a
41	CTCF	chr8:53878416-53878679	HepG2	liver:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
42	CTCF	chr8:53883266-53883462	MCF-7	breast:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
43	CTCF	chr8:53878460-53878610	GM12867	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
44	CTCF	chr8:53883220-53883370	GM06990	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
45	CTCF	chr8:53878460-53878610	K562	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
46	CTCF	chr8:53878307-53878823	HCT-116	colon:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
47	CTCF	chr8:53878540-53878690	HAc	cerebellar:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
48	CTCF	chr8:53878080-53878230	AG04450	lung:	n/a	n/a
49	CTCF	chr8:53883260-53883410	HEEpiC	esophagus:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
50	CTCF	chr8:53878460-53878610	Caco-2	colon:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53883763-53883813	Jurkat	blood:	n/a
2	chr8:53883763-53883813	HRCEpiC	kidney:	n/a
3	chr8:53883763-53883813	AG04449	skin:	fetal
4	chr8:53883763-53883813	HNPCEpiC	eye:	n/a
5	chr8:53883763-53883813	ovcar-3	ovarian:	n/a
6	chr8:53883763-53883813	ECC-1	luminal epithelium:	n/a
7	chr8:53883763-53883813	BJ	skin:	n/a
8	chr8:53883763-53883813	AoSMC	blood vessel:	n/a
9	chr8:53883763-53883813	Hepatocyte	liver:	n/a
10	chr8:53883763-53883813	GM12878	blood:	n/a
11	chr8:53883763-53883813	GM06990	blood:	n/a
12	chr8:53883763-53883813	PFSK-1	brain:	n/a
13	chr8:53883763-53883813	HL-60	blood:	n/a
14	chr8:53883763-53883813	LNCaP	prostate:	n/a
15	chr8:53883763-53883813	Hela-S3	cervix:	n/a
16	chr8:53883763-53883813	HCF	heart:	n/a
17	chr8:53883763-53883813	IMR90	lung:	fetal
18	chr8:53883763-53883813	PANC-1	pancreas:	n/a
19	chr8:53883763-53883813	HepG2	liver:	n/a
20	chr8:53883763-53883813	NHDF-neo	bronchial:	n/a
21	chr8:53883763-53883813	GM12891	blood:	n/a
22	chr8:53883763-53883813	AG09319	gingival:	n/a
23	chr8:53883763-53883813	HEK293	kidney:	embryo
24	chr8:53883763-53883813	NH-A	brain:	n/a
25	chr8:53883763-53883813	AG09309	skin:	n/a
26	chr8:53883763-53883813	HIPEpiC	eye:	n/a
27	chr8:53883763-53883813	SK-N-SH_RA	brain:	n/a
28	chr8:53883763-53883813	U87	brain:	n/a
29	chr8:53883763-53883813	GM12892	blood:	n/a
30	chr8:53883763-53883813	HCPEpiC	choroid plexus:	n/a
31	chr8:53883763-53883813	NB4	blood:	n/a
32	chr8:53883763-53883813	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:53883763-53883813	HAEpiC	amniotic membrane:	n/a
34	chr8:53883763-53883813	RPTEC	kidney:	n/a
35	chr8:53883763-53883813	H1-hESC	embryonic stem cell:	embryo
36	chr8:53883763-53883813	HUVEC	blood vessel:	n/a
37	chr8:53883763-53883813	NHBE	bronchial:	n/a
38	chr8:53883763-53883813	PrEC	prostate:	n/a
39	chr8:53883763-53883813	BE2_C	brain:	n/a
40	chr8:53883763-53883813	T-47D	breast:	n/a
41	chr8:53883763-53883813	ProgFib	skin:	n/a
42	chr8:53883763-53883813	AG04450	lung:	fetal
43	chr8:53883763-53883813	K562	blood:	n/a
44	chr8:53883763-53883813	HMEC	breast:	n/a
45	chr8:53883763-53883813	SK-N-MC	brain:	n/a
46	chr8:53883763-53883813	A549	lung:	n/a
47	chr8:53883763-53883813	HRPEpiC	eye:	n/a
48	chr8:53883763-53883813	SKMC	muscle:	n/a
49	chr8:53883763-53883813	MCF-7	breast:	n/a
50	chr8:53883763-53883813	Caco-2	colon:	n/a

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

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

Extended variants
information (count: 1196 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1196 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7843363	chr8:53874753-53874754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149506031	chr8:53874784-53874785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569967433	chr8:53874798-53874799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111594256	chr8:53874804-53874805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549833800	chr8:53874819-53874820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138864712	chr8:53874825-53874826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541186947	chr8:53874831-53874832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553126447	chr8:53874837-53874838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111398369	chr8:53874847-53874848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146292619	chr8:53874865-53874866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7014874	chr8:53874866-53874867	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148513821	chr8:53874867-53874868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7826923	chr8:53874894-53874895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs562364461	chr8:53874919-53874920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529476403	chr8:53874969-53874970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537149177	chr8:53874976-53874977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565863101	chr8:53874988-53874989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6473774	chr8:53875003-53875004	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs6473775	chr8:53875047-53875048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558590209	chr8:53875058-53875059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6473776	chr8:53875125-53875126	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs537413344	chr8:53875138-53875139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555390691	chr8:53875156-53875157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112532509	chr8:53875189-53875190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577595894	chr8:53875192-53875193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191731093	chr8:53875333-53875334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553191476	chr8:53875359-53875360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372144324	chr8:53875376-53875377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112952729	chr8:53875392-53875393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545124647	chr8:53875407-53875408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556967132	chr8:53875420-53875421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577996690	chr8:53875428-53875429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575138212	chr8:53875434-53875435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542572344	chr8:53875532-53875533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6473777	chr8:53875544-53875545	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529567659	chr8:53875674-53875675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183954452	chr8:53875698-53875699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527238	chr8:53875701-53875702	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376430645	chr8:53875743-53875744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35757671	chr8:53875768-53875769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75580398	chr8:53875796-53875797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372570978	chr8:53875813-53875814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150689507	chr8:53875847-53875848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188905878	chr8:53875862-53875863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560038440	chr8:53875868-53875869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528488163	chr8:53875882-53875883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534909047	chr8:53875892-53875893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546866363	chr8:53875893-53875894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571473220	chr8:53875898-53875899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370676302	chr8:53875922-53875923	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:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53874600-53876800	Enhancers	Dnd41	blood
2	chr8:53876800-53877800	Weak transcription	Dnd41	blood
3	chr8:53877800-53878800	Enhancers	Dnd41	blood
4	chr8:53878000-53878400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:53878200-53878600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr8:53878800-53882400	Weak transcription	Dnd41	blood
7	chr8:53881400-53881600	Enhancers	Thymus	Thymus
8	chr8:53881600-53883400	Weak transcription	Thymus	Thymus
9	chr8:53882200-53883000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:53882400-53882600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr8:53882400-53884800	Enhancers	Dnd41	blood
12	chr8:53882600-53887200	Enhancers	Fetal Intestine Small	intestine
13	chr8:53882800-53884800	Enhancers	Fetal Thymus	thymus
14	chr8:53882800-53887600	Enhancers	Fetal Intestine Large	intestine
15	chr8:53883000-53883400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr8:53883000-53884200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr8:53883200-53883800	Enhancers	Duodenum Mucosa	Duodenum
18	chr8:53883200-53884600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:53883200-53885000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:53883200-53885200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:53883200-53885200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:53883400-53883600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr8:53883400-53883800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr8:53883400-53884000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:53883400-53884000	Enhancers	Thymus	Thymus
26	chr8:53883400-53884400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr8:53883400-53884600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:53883400-53884600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr8:53883400-53885000	Enhancers	Primary B cells from peripheral blood	blood
30	chr8:53883400-53885200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr8:53883400-53885400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:53883400-53885400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr8:53883400-53885400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:53883600-53883800	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr8:53883600-53883800	Enhancers	Stomach Mucosa	stomach
36	chr8:53883600-53883800	Enhancers	HepG2	liver
37	chr8:53883600-53884000	Enhancers	Small Intestine	intestine
38	chr8:53883600-53884200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr8:53883600-53884200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr8:53883600-53884600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:53883600-53884800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:53883600-53885400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr8:53883800-53885000	Enhancers	Primary B cells from cord blood	blood
44	chr8:53883800-53886200	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr8:53883800-53886200	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr8:53883800-53886200	Weak transcription	Stomach Mucosa	stomach
47	chr8:53883800-53886200	Weak transcription	HepG2	liver
48	chr8:53884200-53884600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr8:53884200-53885000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr8:53884200-53885000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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