Variant report

Variant	nsv465680
Chromosome Location	chr8:53416951-53505755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:647)
CpG islands
(count:1465)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53490268-53490616	K562	blood:	n/a	n/a
2	ARID3A	chr8:53490305-53490673	HepG2	liver:	n/a	n/a
3	ATF2	chr8:53502312-53502692	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:53474425-53474625	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:53502214-53502830	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:53476807-53478567	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr8:53502345-53502607	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr8:53490163-53490169	K562	blood:	n/a	n/a
9	CBX3	chr8:53459232-53459585	K562	blood:	n/a	n/a
10	CCNT2	chr8:53436081-53436281	K562	blood:	n/a	n/a
11	CEBPB	chr8:53484150-53484340	HepG2	liver:	n/a	chr8:53484205-53484216
12	CEBPB	chr8:53500260-53500488	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:53504545-53504779	K562	blood:	n/a	chr8:53504612-53504623
14	CEBPB	chr8:53500301-53500400	K562	blood:	n/a	n/a
15	CEBPB	chr8:53473645-53474169	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:53473661-53473959	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:53473671-53473965	K562	blood:	n/a	n/a
18	CEBPB	chr8:53473675-53474000	A549	lung:	n/a	n/a
19	CEBPB	chr8:53475202-53475451	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:53473588-53474038	A549	lung:	n/a	n/a
21	CEBPB	chr8:53482232-53482516	HepG2	liver:	n/a	chr8:53482355-53482366
22	CEBPB	chr8:53475278-53475403	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:53482192-53482440	A549	lung:	n/a	chr8:53482355-53482366
24	CEBPB	chr8:53473626-53474007	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:53504508-53504688	HepG2	liver:	n/a	chr8:53504612-53504623
26	CEBPB	chr8:53500247-53500519	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:53504483-53504758	IMR90	lung:	n/a	chr8:53504612-53504623
28	CEBPB	chr8:53473666-53473994	HepG2	liver:	n/a	n/a
29	CHD1	chr8:53490413-53490437	GM12878	blood:	n/a	n/a
30	CHD1	chr8:53478215-53478807	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr8:53474867-53474966	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr8:53476833-53478582	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr8:53436120-53436270	HepG2	liver:	n/a	n/a
34	CTCF	chr8:53490400-53490550	HBMEC	blood vessel:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
35	CTCF	chr8:53436060-53436210	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr8:53490205-53490232	GM13977	blood:	n/a	n/a
37	CTCF	chr8:53490060-53490210	GM12875	blood:	n/a	n/a
38	CTCF	chr8:53500280-53500430	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr8:53500370-53500431	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:53490356-53490528	SK-N-SH_RA	brain:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
41	CTCF	chr8:53490060-53490210	GM06990	blood:	n/a	n/a
42	CTCF	chr8:53490268-53490553	K562	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
43	CTCF	chr8:53490380-53490530	AG10803	skin:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
44	CTCF	chr8:53436056-53436321	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:53490080-53490230	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr8:53490400-53490550	HRE	kidney:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
47	CTCF	chr8:53436120-53436270	K562	blood:	n/a	n/a
48	CTCF	chr8:53500256-53500471	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr8:53500304-53500480	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr8:53490240-53490390	NHLF	lung:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53485704-53485754	HEK293	kidney:	embryo
2	chr8:53485704-53485754	HEK293	kidney:	embryo
3	chr8:53478624-53478674	HUVEC	blood vessel:	n/a
4	chr8:53478624-53478674	PFSK-1	brain:	n/a
5	chr8:53476943-53476993	BJ	skin:	n/a
6	chr8:53478074-53478124	U87	brain:	n/a
7	chr8:53474030-53474080	PFSK-1	brain:	n/a
8	chr8:53478023-53478073	AG04449	skin:	fetal
9	chr8:53490251-53490301	HNPCEpiC	eye:	n/a
10	chr8:53490251-53490301	HUVEC	blood vessel:	n/a
11	chr8:53490251-53490301	AG10803	skin:	n/a
12	chr8:53478074-53478124	AoSMC	blood vessel:	n/a
13	chr8:53477218-53477268	PFSK-1	brain:	n/a
14	chr8:53478023-53478073	BJ	skin:	n/a
15	chr8:53474030-53474080	HRCEpiC	kidney:	n/a
16	chr8:53474030-53474080	NHDF-neo	bronchial:	n/a
17	chr8:53477264-53477314	GM12892	blood:	n/a
18	chr8:53490251-53490301	AoSMC	blood vessel:	n/a
19	chr8:53478023-53478073	SK-N-SH	brain:	n/a
20	chr8:53478102-53478152	GM12878	blood:	n/a
21	chr8:53476865-53476915	NT2-D1	testis:	n/a
22	chr8:53485670-53485720	RPTEC	kidney:	n/a
23	chr8:53478053-53478103	HIPEpiC	eye:	n/a
24	chr8:53485670-53485720	U87	brain:	n/a
25	chr8:53499582-53499632	GM06990	blood:	n/a
26	chr8:53478053-53478103	MCF10A-Er-Src	breast:	n/a
27	chr8:53471884-53471934	Hela-S3	cervix:	n/a
28	chr8:53499582-53499632	Jurkat	blood:	n/a
29	chr8:53477545-53477595	H1-hESC	embryonic stem cell:	embryo
30	chr8:53478074-53478124	HCPEpiC	choroid plexus:	n/a
31	chr8:53485704-53485754	NT2-D1	testis:	n/a
32	chr8:53478624-53478674	HRCEpiC	kidney:	n/a
33	chr8:53450729-53450779	T-47D	breast:	n/a
34	chr8:53478053-53478103	SAEC	small airway:	n/a
35	chr8:53490251-53490301	RPTEC	kidney:	n/a
36	chr8:53474030-53474080	SK-N-MC	brain:	n/a
37	chr8:53471884-53471934	A549	lung:	n/a
38	chr8:53477545-53477595	SK-N-SH_RA	brain:	n/a
39	chr8:53485704-53485754	MCF10A-Er-Src	breast:	n/a
40	chr8:53452398-53452448	HCT-116	colon:	n/a
41	chr8:53478074-53478124	CMK	blood:	n/a
42	chr8:53499558-53499608	NHDF-neo	bronchial:	n/a
43	chr8:53478102-53478152	PFSK-1	brain:	n/a
44	chr8:53478624-53478674	HRE	kidney:	n/a
45	chr8:53477264-53477314	ECC-1	luminal epithelium:	n/a
46	chr8:53450729-53450779	SK-N-MC	brain:	n/a
47	chr8:53477545-53477595	NH-A	brain:	n/a
48	chr8:53478624-53478674	LNCaP	prostate:	n/a
49	chr8:53456003-53456053	HUVEC	blood vessel:	n/a
50	chr8:53471884-53471934	NHDF-neo	bronchial:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53490108..53490739-chr8:53649694..53650429,2	MCF-7	breast:
2	chr8:53408834..53411625-chr8:53415197..53417909,2	MCF-7	breast:
3	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:

No data

Variant related genes	Relation type
FAM150A	TF binding region
FAM150A	CpG island

Extended variants
information (count: 2166 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2166 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534733164	chr8:53436203-53436204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552985345	chr8:53436238-53436239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11987780	chr8:53436288-53436289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560304042	chr8:53436334-53436335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150466729	chr8:53436354-53436355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573242645	chr8:53436466-53436467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564846695	chr8:53436552-53436553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145490081	chr8:53436566-53436567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532529182	chr8:53436586-53436587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543569206	chr8:53436591-53436592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531592937	chr8:53436625-53436626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76514637	chr8:53436626-53436627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186202886	chr8:53436627-53436628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188324090	chr8:53436628-53436629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548084108	chr8:53436666-53436667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552357598	chr8:53436683-53436684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547513049	chr8:53436749-53436750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559470554	chr8:53436799-53436800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533403724	chr8:53436816-53436817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180835168	chr8:53436888-53436889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569883982	chr8:53436898-53436899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374126160	chr8:53436921-53436922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148850950	chr8:53436932-53436933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534100135	chr8:53436941-53436942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6981711	chr8:53436954-53436955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185471430	chr8:53436955-53436956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553075481	chr8:53436981-53436982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571153038	chr8:53436986-53436987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113300529	chr8:53437026-53437027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7826531	chr8:53437037-53437038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs576294562	chr8:53437050-53437051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543727098	chr8:53437082-53437083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555651334	chr8:53437090-53437091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568469885	chr8:53437119-53437120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541116445	chr8:53437155-53437156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536153244	chr8:53437161-53437162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191251038	chr8:53437173-53437174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533267611	chr8:53437182-53437183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373805661	chr8:53437211-53437212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181770591	chr8:53437249-53437250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs137893788	chr8:53437345-53437346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566277779	chr8:53437379-53437380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186849913	chr8:53437387-53437388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377062113	chr8:53437407-53437408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369449782	chr8:53437415-53437416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191489310	chr8:53437465-53437466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528343919	chr8:53437513-53437514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566779228	chr8:53437524-53437525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546481323	chr8:53437570-53437571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571281016	chr8:53437617-53437618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Pancreatic endocrine tumor	17639061	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
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53436200-53436400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:53436400-53444000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:53444000-53444800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:53444800-53446000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:53445400-53446400	Enhancers	Fetal Lung	lung
6	chr8:53446000-53446400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:53446000-53446600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:53446400-53453200	Weak transcription	Fetal Lung	lung
9	chr8:53446600-53448400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:53448400-53448800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:53448800-53453000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:53453000-53454000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:53453200-53453400	Enhancers	Fetal Lung	lung
14	chr8:53454000-53455200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:53455200-53456200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:53455800-53456800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:53455800-53457200	Bivalent Enhancer	Dnd41	blood
18	chr8:53456200-53456400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr8:53456400-53457200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:53457200-53458600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:53458600-53460800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:53460800-53467800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:53467600-53475000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:53467800-53468600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr8:53467800-53468600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr8:53468200-53468400	Enhancers	H9 Cell Line	embryonic stem cell
27	chr8:53468200-53468400	Enhancers	Esophagus	oesophagus
28	chr8:53468400-53471600	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr8:53468600-53469600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr8:53469600-53470000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:53470000-53471000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:53470800-53471400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr8:53471000-53471400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:53471000-53471400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:53471000-53472000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:53471000-53472400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr8:53471000-53472400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:53471200-53471600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:53471200-53471600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr8:53471200-53471800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr8:53471200-53471800	Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr8:53471200-53472000	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr8:53471400-53471600	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr8:53471400-53471600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
45	chr8:53471400-53472000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:53471600-53471800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr8:53471600-53471800	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr8:53471600-53472000	Active TSS	H9 Cell Line	embryonic stem cell
49	chr8:53471600-53472000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr8:53471600-53472000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell

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