Variant report

Variant	nsv465684
Chromosome Location	chr8:53880247-53917467
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	ATF2	chr8:53909866-53910228	GM12878	blood:	n/a	n/a
2	BATF	chr8:53909878-53910230	GM12878	blood:	n/a	chr8:53910027-53910037 chr8:53910026-53910037
3	BCL11A	chr8:53909839-53910302	GM12878	blood:	n/a	chr8:53910131-53910140
4	BCL11A	chr8:53909858-53910582	GM12878	blood:	n/a	chr8:53910131-53910140 chr8:53910301-53910310
5	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:53909862-53910567	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:53883301-53883728	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:53910786-53911069	K562	blood:	n/a	chr8:53910933-53910944 chr8:53910931-53910944 chr8:53910931-53910944 chr8:53910933-53910944
10	CEBPB	chr8:53917155-53917454	K562	blood:	n/a	n/a
11	CEBPB	chr8:53916865-53917369	A549	lung:	n/a	n/a
12	CEBPB	chr8:53907958-53908021	K562	blood:	n/a	n/a
13	CHD1	chr8:53910064-53910138	GM12878	blood:	n/a	n/a
14	CHD2	chr8:53909815-53910522	GM12878	blood:	n/a	n/a
15	CHD2	chr8:53886601-53886615	GM12878	blood:	n/a	n/a
16	CREB1	chr8:53886223-53886639	HepG2	liver:	n/a	n/a
17	CTCF	chr8:53899383-53899448	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr8:53883260-53883410	MCF-7	breast:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
19	CTCF	chr8:53883203-53883564	MCF-7	breast:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
20	CTCF	chr8:53883280-53883430	GM12868	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
21	CTCF	chr8:53883320-53883470	NHEK	skin:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
22	CTCF	chr8:53883300-53883450	GM12873	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
23	CTCF	chr8:53883240-53883390	NHEK	skin:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
24	CTCF	chr8:53917440-53917758	K562	blood:	n/a	n/a
25	CTCF	chr8:53917420-53917570	NB4	blood:	n/a	n/a
26	CTCF	chr8:53883320-53883470	HRPEpiC	eye:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
27	CTCF	chr8:53883240-53883390	GM12864	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
28	CTCF	chr8:53883281-53883424	GM19238	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
29	CTCF	chr8:53883240-53883390	Hela-S3	cervix:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
30	CTCF	chr8:53883165-53883543	GM12878	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
31	CTCF	chr8:53883295-53883418	HepG2	liver:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
32	CTCF	chr8:53917411-53917687	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr8:53883240-53883390	GM12872	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
34	CTCF	chr8:53883355-53883375	GM13977	blood:	n/a	n/a
35	CTCF	chr8:53883275-53883452	GM12892	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
36	CTCF	chr8:53883260-53883410	GM12864	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
37	CTCF	chr8:53883275-53883453	MCF-7	breast:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
38	CTCF	chr8:53883280-53883430	WERI-Rb-1	eye:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
39	CTCF	chr8:53917460-53917610	NHEK	skin:	n/a	n/a
40	CTCF	chr8:53883241-53883458	LNCaP	prostate:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
41	CTCF	chr8:53883288-53883429	Hela-S3	cervix:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
42	CTCF	chr8:53883295-53883394	GM10248	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
43	CTCF	chr8:53883266-53883445	MCF-7	breast:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
44	CTCF	chr8:53883241-53883473	Medullo	brain:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
45	CTCF	chr8:53892072-53892100	Lung_OC	lung:	n/a	n/a
46	CTCF	chr8:53883240-53883390	SAEC	small airway:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
47	CTCF	chr8:53883288-53883408	Spleen_OC	spleen:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
48	CTCF	chr8:53917460-53917610	GM12870	blood:	n/a	n/a
49	CTCF	chr8:53883335-53883344	GM13977	blood:	n/a	n/a
50	CTCF	chr8:53883271-53883438	GM19240	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	HRPEpiC	eye:	n/a
2	chr8:53883763-53883813	NH-A	brain:	n/a
3	chr8:53883763-53883813	AoSMC	blood vessel:	n/a
4	chr8:53883763-53883813	IMR90	lung:	fetal
5	chr8:53883763-53883813	SK-N-SH_RA	brain:	n/a
6	chr8:53883763-53883813	SAEC	small airway:	n/a
7	chr8:53883763-53883813	PrEC	prostate:	n/a
8	chr8:53883763-53883813	GM12891	blood:	n/a
9	chr8:53883763-53883813	HCM	heart:	n/a
10	chr8:53883763-53883813	Jurkat	blood:	n/a
11	chr8:53883763-53883813	BJ	skin:	n/a
12	chr8:53883763-53883813	GM19239	blood:	n/a
13	chr8:53883763-53883813	HMEC	breast:	n/a
14	chr8:53883763-53883813	U87	brain:	n/a
15	chr8:53883763-53883813	NHDF-neo	bronchial:	n/a
16	chr8:53883763-53883813	GM06990	blood:	n/a
17	chr8:53883763-53883813	GM12892	blood:	n/a
18	chr8:53883763-53883813	HEK293	kidney:	embryo
19	chr8:53883763-53883813	ECC-1	luminal epithelium:	n/a
20	chr8:53883763-53883813	HRCEpiC	kidney:	n/a
21	chr8:53883763-53883813	ProgFib	skin:	n/a
22	chr8:53883763-53883813	NT2-D1	testis:	n/a
23	chr8:53883763-53883813	HepG2	liver:	n/a
24	chr8:53883763-53883813	HL-60	blood:	n/a
25	chr8:53883763-53883813	NB4	blood:	n/a
26	chr8:53883763-53883813	H1-hESC	embryonic stem cell:	embryo
27	chr8:53883763-53883813	AG10803	skin:	n/a
28	chr8:53883763-53883813	PFSK-1	brain:	n/a
29	chr8:53883763-53883813	HCT-116	colon:	n/a
30	chr8:53883763-53883813	SK-N-MC	brain:	n/a
31	chr8:53883763-53883813	SKMC	muscle:	n/a
32	chr8:53883763-53883813	HEEpiC	esophagus:	n/a
33	chr8:53883763-53883813	AG09319	gingival:	n/a
34	chr8:53883763-53883813	Hepatocyte	liver:	n/a
35	chr8:53883763-53883813	HCF	heart:	n/a
36	chr8:53883763-53883813	ovcar-3	ovarian:	n/a
37	chr8:53883763-53883813	AG04450	lung:	fetal
38	chr8:53883763-53883813	Hela-S3	cervix:	n/a
39	chr8:53883763-53883813	K562	blood:	n/a
40	chr8:53883763-53883813	HRE	kidney:	n/a
41	chr8:53883763-53883813	CMK	blood:	n/a
42	chr8:53883763-53883813	HNPCEpiC	eye:	n/a
43	chr8:53883763-53883813	NHBE	bronchial:	n/a
44	chr8:53883763-53883813	HIPEpiC	eye:	n/a
45	chr8:53883763-53883813	BE2_C	brain:	n/a
46	chr8:53883763-53883813	AG09309	skin:	n/a
47	chr8:53883763-53883813	LNCaP	prostate:	n/a
48	chr8:53883763-53883813	MCF-7	breast:	n/a
49	chr8:53883763-53883813	AG04449	skin:	fetal
50	chr8:53883763-53883813	RPTEC	kidney:	n/a

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

Extended variants
information (count: 960 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16918381	chr8:53880247-53880248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377566138	chr8:53880268-53880269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577161992	chr8:53880314-53880315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547436185	chr8:53880363-53880364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545322350	chr8:53880370-53880371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190525242	chr8:53880461-53880462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539781442	chr8:53880476-53880477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200480848	chr8:53880486-53880487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551402839	chr8:53880487-53880488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17257407	chr8:53880510-53880511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192413625	chr8:53880524-53880525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555591797	chr8:53880577-53880578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560714871	chr8:53880654-53880655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184601891	chr8:53880696-53880697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534710661	chr8:53880702-53880703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370190787	chr8:53880750-53880751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs628746	chr8:53880777-53880778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs188224548	chr8:53880778-53880779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139115244	chr8:53880810-53880811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564650590	chr8:53880828-53880829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576656256	chr8:53880874-53880875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149877130	chr8:53880875-53880876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77702840	chr8:53880879-53880880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529402401	chr8:53880881-53880882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73603250	chr8:53880882-53880883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs559388450	chr8:53880920-53880921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533194809	chr8:53880925-53880926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77136085	chr8:53880934-53880935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2360238	chr8:53880944-53880945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs537348945	chr8:53880951-53880952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549250521	chr8:53880970-53880971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530524957	chr8:53880977-53880978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567478108	chr8:53880989-53880990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62507156	chr8:53881034-53881035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180708266	chr8:53881048-53881049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546374742	chr8:53881100-53881101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141938710	chr8:53881103-53881104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534773664	chr8:53881120-53881121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2625583	chr8:53881131-53881132	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577643360	chr8:53881154-53881155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538288189	chr8:53881155-53881156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62507157	chr8:53881167-53881168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112878727	chr8:53881245-53881246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556909773	chr8:53881266-53881267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72648436	chr8:53881267-53881268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs144894459	chr8:53881269-53881270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562006418	chr8:53881291-53881292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77948345	chr8:53881299-53881300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76190899	chr8:53881300-53881301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77046262	chr8:53881301-53881302	Weak transcription	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:111 , 50 per page) page: 1 2 3

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

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