Variant report

Variant	nsv1016720
Chromosome Location	chr8:89819473-89878186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr8:89851926-89852130	GM12878	blood:	n/a	n/a
2	BATF	chr8:89851958-89852146	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:89855829-89856039	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr8:89823940-89824090	Caco-2	colon:	n/a	n/a
5	CTCF	chr8:89824021-89824117	LNCaP	prostate:	n/a	n/a
6	CTCF	chr8:89823902-89824239	GM12878	blood:	n/a	n/a
7	CTCF	chr8:89823980-89824130	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr8:89823960-89824110	GM12871	blood:	n/a	n/a
9	CTCF	chr8:89872803-89872995	MCF-7	breast:	n/a	n/a
10	CTCF	chr8:89855900-89856050	HCT-116	colon:	n/a	n/a
11	CTCF	chr8:89855995-89856069	Gliobla	brain:	n/a	n/a
12	CTCF	chr8:89823884-89824342	HCT-116	colon:	n/a	n/a
13	CTCF	chr8:89823923-89824195	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:89824000-89824150	SAEC	small airway:	n/a	n/a
15	CTCF	chr8:89841760-89841910	MCF-7	breast:	n/a	n/a
16	CTCF	chr8:89855880-89856030	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr8:89855860-89856010	MCF-7	breast:	n/a	n/a
18	CTCF	chr8:89872742-89873024	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:89872738-89873021	MCF-7	breast:	n/a	n/a
20	CTCF	chr8:89872838-89872965	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:89823960-89824110	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr8:89823923-89824185	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:89823940-89824090	HEK293	kidney:	n/a	n/a
24	CTCF	chr8:89824040-89824135	HepG2	liver:	n/a	n/a
25	CTCF	chr8:89855880-89856030	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr8:89872901-89872951	HepG2	liver:	n/a	n/a
27	CTCF	chr8:89824000-89824150	HMEC	breast:	n/a	n/a
28	CTCF	chr8:89845680-89845830	GM12869	blood:	n/a	n/a
29	CTCF	chr8:89872857-89872945	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:89824020-89824170	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr8:89872871-89872898	HepG2	liver:	n/a	n/a
32	CTCF	chr8:89855956-89856098	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:89855900-89856050	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:89823929-89824190	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:89872451-89872529	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr8:89823943-89824092	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:89823960-89824110	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr8:89855920-89856070	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr8:89823920-89824070	HCT-116	colon:	n/a	n/a
40	CTCF	chr8:89847120-89847270	HMEC	breast:	n/a	n/a
41	CTCF	chr8:89823960-89824110	HFF	foreskin:	n/a	n/a
42	CTCF	chr8:89824000-89824150	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr8:89855974-89856064	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:89824000-89824150	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:89824000-89824150	HRE	kidney:	n/a	n/a
46	CTCF	chr8:89823900-89824050	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr8:89855948-89856089	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:89823920-89824070	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr8:89823940-89824090	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr8:89872840-89872990	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:89856205-89856255	NHBE	bronchial:	n/a
2	chr8:89856205-89856255	PFSK-1	brain:	n/a
3	chr8:89856205-89856255	GM12878	blood:	n/a
4	chr8:89856205-89856255	Jurkat	blood:	n/a
5	chr8:89856205-89856255	HAEpiC	amniotic membrane:	n/a
6	chr8:89856205-89856255	NHDF-neo	bronchial:	n/a
7	chr8:89856205-89856255	GM12892	blood:	n/a
8	chr8:89856205-89856255	BJ	skin:	n/a
9	chr8:89856205-89856255	NH-A	brain:	n/a
10	chr8:89856205-89856255	Hepatocyte	liver:	n/a
11	chr8:89856205-89856255	SKMC	muscle:	n/a
12	chr8:89856205-89856255	AG04449	skin:	fetal
13	chr8:89856205-89856255	HL-60	blood:	n/a
14	chr8:89856205-89856255	CMK	blood:	n/a
15	chr8:89856205-89856255	HCT-116	colon:	n/a
16	chr8:89856205-89856255	HRCEpiC	kidney:	n/a
17	chr8:89856205-89856255	AG09319	gingival:	n/a
18	chr8:89856205-89856255	BE2_C	brain:	n/a
19	chr8:89856205-89856255	SK-N-SH	brain:	n/a
20	chr8:89856205-89856255	HCF	heart:	n/a
21	chr8:89856205-89856255	HMEC	breast:	n/a
22	chr8:89856205-89856255	HNPCEpiC	eye:	n/a
23	chr8:89856205-89856255	GM06990	blood:	n/a
24	chr8:89856205-89856255	H1-hESC	embryonic stem cell:	embryo
25	chr8:89856205-89856255	GM19239	blood:	n/a
26	chr8:89856205-89856255	ECC-1	luminal epithelium:	n/a
27	chr8:89856205-89856255	T-47D	breast:	n/a
28	chr8:89856205-89856255	SAEC	small airway:	n/a
29	chr8:89856205-89856255	NB4	blood:	n/a
30	chr8:89856205-89856255	SK-N-MC	brain:	n/a
31	chr8:89856205-89856255	AG04450	lung:	fetal
32	chr8:89856205-89856255	LNCaP	prostate:	n/a
33	chr8:89856205-89856255	PrEC	prostate:	n/a
34	chr8:89856205-89856255	PANC-1	pancreas:	n/a
35	chr8:89856205-89856255	AG10803	skin:	n/a
36	chr8:89856205-89856255	MCF-7	breast:	n/a
37	chr8:89856205-89856255	HCM	heart:	n/a
38	chr8:89856205-89856255	MCF10A-Er-Src	breast:	n/a
39	chr8:89856205-89856255	K562	blood:	n/a
40	chr8:89856205-89856255	IMR90	lung:	fetal
41	chr8:89856205-89856255	RPTEC	kidney:	n/a
42	chr8:89856205-89856255	HEEpiC	esophagus:	n/a
43	chr8:89856205-89856255	ovcar-3	ovarian:	n/a
44	chr8:89856205-89856255	HRPEpiC	eye:	n/a
45	chr8:89856205-89856255	GM12891	blood:	n/a
46	chr8:89856205-89856255	SK-N-SH_RA	brain:	n/a
47	chr8:89856205-89856255	NT2-D1	testis:	n/a
48	chr8:89856205-89856255	AG09309	skin:	n/a
49	chr8:89856205-89856255	HCPEpiC	choroid plexus:	n/a
50	chr8:89856205-89856255	Caco-2	colon:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:89848601..89851264-chr8:89852497..89854514,2	MCF-7	breast:
2	chr8:89826530..89828949-chr8:89832664..89834256,2	MCF-7	breast:
3	chr8:89304192..89305173-chr8:89823627..89824192,2	MCF-7	breast:
4	chr8:89818784..89820369-chr8:89820936..89822501,2	MCF-7	breast:
5	chr8:89848601..89851264-chr8:89852497..89854514,2	MCF-7	breast:
6	chr8:89826530..89828949-chr8:89832664..89834256,2	MCF-7	breast:
7	chr8:89340717..89341497-chr8:89823523..89824135,2	MCF-7	breast:
8	chr8:89877780..89878499-chrX:117700612..117701483,2	MCF-7	breast:
9	chr8:89566591..89567525-chr8:89823590..89824198,2	MCF-7	breast:
10	chr8:89724996..89725850-chr8:89855566..89856466,2	MCF-7	breast:
11	chr8:89725334..89726635-chr8:89823867..89824656,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP16-4	chr8:89820547-89821137	ENSG00000271156.1

No data

Variant related genes	Relation type
ENSG00000271156	TF binding region
ENSG00000271156	CpG island
ENSG00000271156	chromatin interactions

Extended variants
information (count: 493 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534412131	chr8:89819474-89819475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs36091824	chr8:89819523-89819524	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114837276	chr8:89819592-89819593	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs117995939	chr8:89819665-89819666	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372569381	chr8:89819728-89819729	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7821061	chr8:89819763-89819764	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs187598738	chr8:89819842-89819843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190918766	chr8:89819843-89819844	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs113221788	chr8:89819847-89819848	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs78040517	chr8:89819870-89819871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544322782	chr8:89819935-89819936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562886982	chr8:89819945-89819946	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533495456	chr8:89819980-89819981	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551927662	chr8:89820019-89820020	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116110647	chr8:89820023-89820024	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574551482	chr8:89820038-89820039	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111261644	chr8:89820050-89820051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116361126	chr8:89820089-89820090	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546769183	chr8:89820123-89820124	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557056837	chr8:89820159-89820160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376749522	chr8:89820194-89820195	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568304030	chr8:89820236-89820237	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115050547	chr8:89820259-89820260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143274666	chr8:89820261-89820262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182040908	chr8:89820288-89820289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs1391628	chr8:89820552-89820553	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs543577711	chr8:89820578-89820579	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs555921523	chr8:89820660-89820661	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs574287424	chr8:89820684-89820685	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs10102082	chr8:89820691-89820692	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563014454	chr8:89820737-89820738	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs34919276	chr8:89820788-89820789	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs531320589	chr8:89820789-89820790	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs545382358	chr8:89820794-89820795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs560614984	chr8:89820814-89820815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs77149063	chr8:89820819-89820820	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs546510081	chr8:89820831-89820832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs139136732	chr8:89820849-89820850	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs143986852	chr8:89820892-89820893	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs188052032	chr8:89820937-89820938	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs568768045	chr8:89820943-89820944	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs192677145	chr8:89821094-89821095	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs145880140	chr8:89821097-89821098	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs566274316	chr8:89821131-89821132	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs553871714	chr8:89821141-89821142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533872697	chr8:89821231-89821232	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs555713189	chr8:89821277-89821278	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs13251035	chr8:89821286-89821287	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs538022143	chr8:89821340-89821341	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs556906029	chr8:89821405-89821406	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89821200-89821400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:89823600-89823800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:89823600-89823800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:89823800-89824000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:89823800-89825000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:89833600-89834400	Enhancers	Fetal Heart	heart
7	chr8:89835600-89836200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:89853800-89854000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr8:89854200-89855400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr8:89855400-89856400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:89855400-89856400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:89855400-89856600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:89855600-89856400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:89855600-89856400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr8:89855600-89856600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr8:89855600-89856600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:89855800-89856200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr8:89855800-89856600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:89864400-89864800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:89864600-89865000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr8:89872200-89873000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr8:89872200-89873200	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr8:89872600-89873000	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr8:89872600-89873000	Active TSS	H9 Cell Line	embryonic stem cell
25	chr8:89872600-89873000	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr8:89872600-89873200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr8:89873000-89873200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr8:89873000-89874600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr8:89873200-89873600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr8:89873600-89873800	Enhancers	H9 Cell Line	embryonic stem cell
31	chr8:89874600-89874800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr8:89876000-89877000	Enhancers	Fetal Heart	heart

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