Variant report

Variant	nsv891344
Chromosome Location	chr8:114956591-115003742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:114982076-114982307	H1-hESC	embryonic stem cell:	n/a	chr8:114982190-114982201
2	CEBPB	chr8:114958974-114959125	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:114975102-114975441	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr8:114958993-114959150	K562	blood:	n/a	n/a
5	CEBPB	chr8:114988802-114989057	HepG2	liver:	n/a	chr8:114988981-114988994
6	CEBPB	chr8:114982038-114982329	HepG2	liver:	n/a	chr8:114982190-114982201
7	CEBPB	chr8:114975231-114975400	A549	lung:	n/a	n/a
8	CHD2	chr8:114992512-114992515	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:114993131-114993266	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr8:114993180-114993330	Caco-2	colon:	n/a	n/a
11	CTCF	chr8:114992583-114992658	MCF-7	breast:	n/a	n/a
12	CTCF	chr8:114993098-114993291	Gliobla	brain:	n/a	n/a
13	CTCF	chr8:114993098-114993305	T-47D	breast:	n/a	n/a
14	CTCF	chr8:114992540-114992690	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:114993120-114993270	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr8:114992590-114992669	MCF-7	breast:	n/a	n/a
17	CTCF	chr8:114993235-114993280	GM13977	blood:	n/a	n/a
18	CTCF	chr8:114993100-114993302	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:114993089-114993276	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:114965001-114965077	GM13976	blood:	n/a	n/a
21	CTCF	chr8:114993080-114993230	GM12874	blood:	n/a	n/a
22	CTCF	chr8:114992560-114992710	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr8:114993080-114993230	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr8:114992970-114993358	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:114993028-114993371	GM12878	blood:	n/a	n/a
26	CTCF	chr8:114992590-114992665	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:114992520-114992670	HEK293	kidney:	n/a	n/a
28	CTCF	chr8:114993135-114993285	LNCaP	prostate:	n/a	n/a
29	CTCF	chr8:114993143-114993144	LNCaP	prostate:	n/a	n/a
30	CTCF	chr8:114992380-114992530	BE2_C	brain:	n/a	n/a
31	CTCF	chr8:114992580-114992730	GM12865	blood:	n/a	n/a
32	CTCF	chr8:114993078-114993319	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:114992580-114992730	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:114992547-114992723	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:114992555-114992694	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:114993160-114993310	BE2_C	brain:	n/a	n/a
37	CTCF	chr8:114992582-114992701	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:114992600-114992750	GM12866	blood:	n/a	n/a
39	CTCF	chr8:114966214-114966286	GM12878	blood:	n/a	n/a
40	CTCF	chr8:114993140-114993290	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:114993151-114993215	LNCaP	prostate:	n/a	n/a
42	CTCF	chr8:114993160-114993310	HCT-116	colon:	n/a	n/a
43	CTCF	chr8:114993400-114993550	GM12872	blood:	n/a	n/a
44	CTCF	chr8:114992500-114992650	BE2_C	brain:	n/a	n/a
45	CTCF	chr8:114992937-114993449	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:114993153-114993290	HepG2	liver:	n/a	n/a
47	E2F4	chr8:114997380-114997468	MCF10A-Er-Src	breast:	n/a	n/a
48	EP300	chr8:114974288-114974410	K562	blood:	n/a	n/a
49	EP300	chr8:114960214-114960492	HepG2	liver:	n/a	n/a
50	EP300	chr8:114974497-114974791	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:114992667-114992717	A549	lung:	n/a
2	chr8:114992667-114992717	SK-N-MC	brain:	n/a
3	chr8:114992667-114992717	T-47D	breast:	n/a
4	chr8:114992667-114992717	HMEC	breast:	n/a
5	chr8:114992667-114992717	BE2_C	brain:	n/a
6	chr8:114992667-114992717	GM12891	blood:	n/a
7	chr8:114992667-114992717	K562	blood:	n/a
8	chr8:114992667-114992717	HAEpiC	amniotic membrane:	n/a
9	chr8:114992667-114992717	GM12878	blood:	n/a
10	chr8:114992667-114992717	HEK293	kidney:	embryo
11	chr8:114992667-114992717	AG04449	skin:	fetal
12	chr8:114992667-114992717	HCM	heart:	n/a
13	chr8:114992667-114992717	HRPEpiC	eye:	n/a
14	chr8:114992667-114992717	NH-A	brain:	n/a
15	chr8:114992667-114992717	HUVEC	blood vessel:	n/a
16	chr8:114992667-114992717	AG09319	gingival:	n/a
17	chr8:114992667-114992717	HCPEpiC	choroid plexus:	n/a
18	chr8:114992667-114992717	RPTEC	kidney:	n/a
19	chr8:114992667-114992717	HepG2	liver:	n/a
20	chr8:114992667-114992717	AG09309	skin:	n/a
21	chr8:114992667-114992717	NB4	blood:	n/a
22	chr8:114992667-114992717	Hepatocyte	liver:	n/a
23	chr8:114992667-114992717	H1-hESC	embryonic stem cell:	embryo
24	chr8:114992667-114992717	SK-N-SH	brain:	n/a
25	chr8:114992667-114992717	MCF-7	breast:	n/a
26	chr8:114992667-114992717	LNCaP	prostate:	n/a
27	chr8:114992667-114992717	HRE	kidney:	n/a
28	chr8:114992667-114992717	AG10803	skin:	n/a
29	chr8:114992667-114992717	AG04450	lung:	fetal
30	chr8:114992667-114992717	U87	brain:	n/a
31	chr8:114992667-114992717	BJ	skin:	n/a
32	chr8:114992667-114992717	ECC-1	luminal epithelium:	n/a
33	chr8:114992667-114992717	NHDF-neo	bronchial:	n/a
34	chr8:114992667-114992717	MCF10A-Er-Src	breast:	n/a
35	chr8:114992667-114992717	HL-60	blood:	n/a
36	chr8:114992667-114992717	HIPEpiC	eye:	n/a
37	chr8:114992667-114992717	SKMC	muscle:	n/a
38	chr8:114992667-114992717	GM19239	blood:	n/a
39	chr8:114992667-114992717	HPAEpiC	pulmonary alveolar:	n/a
40	chr8:114992667-114992717	HEEpiC	esophagus:	n/a
41	chr8:114992667-114992717	HRCEpiC	kidney:	n/a
42	chr8:114992667-114992717	GM06990	blood:	n/a
43	chr8:114992667-114992717	SAEC	small airway:	n/a
44	chr8:114992667-114992717	PrEC	prostate:	n/a
45	chr8:114992667-114992717	HCF	heart:	n/a
46	chr8:114992667-114992717	Jurkat	blood:	n/a
47	chr8:114992667-114992717	HNPCEpiC	eye:	n/a
48	chr8:114992667-114992717	PANC-1	pancreas:	n/a
49	chr8:114992667-114992717	CMK	blood:	n/a
50	chr8:114992667-114992717	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:114966861..114968820-chr8:114970401..114973108,2	MCF-7	breast:
2	chr8:114384438..114385053-chr8:114992865..114993457,2	MCF-7	breast:
3	chr8:114966861..114968820-chr8:114970401..114973108,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000206719	TF binding region
ENSG00000206719	CpG island

Extended variants
information (count: 527 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2458064	chr8:114956591-114956592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561238720	chr8:114956600-114956601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147885244	chr8:114956632-114956633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28534753	chr8:114956658-114956659	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566884229	chr8:114956678-114956679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532355554	chr8:114956679-114956680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552091914	chr8:114956692-114956693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186337757	chr8:114956693-114956694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537652195	chr8:114956697-114956698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547940660	chr8:114956699-114956700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568078978	chr8:114956721-114956722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72677784	chr8:114956725-114956726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577959632	chr8:114956756-114956757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576813716	chr8:114956842-114956843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143734324	chr8:114956849-114956850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376739476	chr8:114956881-114956882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191188432	chr8:114956898-114956899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372252757	chr8:114956935-114956936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544838196	chr8:114956952-114956953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561507262	chr8:114956984-114956985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574910674	chr8:114956993-114956994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149483590	chr8:114959008-114959009	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548660081	chr8:114959048-114959049	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568750589	chr8:114959076-114959077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs143956105	chr8:114959095-114959096	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs369025699	chr8:114959147-114959148	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558084630	chr8:114960162-114960163	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577967983	chr8:114960184-114960185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs73344282	chr8:114960195-114960196	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs181611334	chr8:114960213-114960214	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs573758091	chr8:114960217-114960218	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527437803	chr8:114960237-114960238	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186961112	chr8:114960240-114960241	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs191380406	chr8:114960244-114960245	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs528077110	chr8:114960260-114960261	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567189640	chr8:114960278-114960279	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs149999269	chr8:114960281-114960282	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs564454146	chr8:114960321-114960322	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533416470	chr8:114960347-114960348	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs550037324	chr8:114960365-114960366	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs538982790	chr8:114960393-114960394	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570185711	chr8:114960418-114960419	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs7833523	chr8:114960436-114960437	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs77939223	chr8:114960518-114960519	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs569583179	chr8:114960526-114960527	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs542810184	chr8:114960531-114960532	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs115577091	chr8:114960561-114960562	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs535027396	chr8:114960567-114960568	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145257274	chr8:114960605-114960606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578016545	chr8:114960624-114960625	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114956400-114956800	Enhancers	Dnd41	blood
2	chr8:114956600-114957000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr8:114960200-114960400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:114960200-114960400	Enhancers	Pancreas	Pancrea
5	chr8:114960200-114960600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:114960200-114960800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:114960400-114961000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:114960600-114961000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:114960600-114961200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr8:114960800-114961200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:114967800-114968800	Enhancers	Dnd41	blood
12	chr8:114973000-114973200	ZNF genes & repeats	Fetal Lung	lung
13	chr8:114973200-114974400	Weak transcription	Fetal Lung	lung
14	chr8:114974400-114974800	Enhancers	Fetal Lung	lung
15	chr8:114974400-114975800	Enhancers	Hela-S3	cervix
16	chr8:114975800-114978000	Weak transcription	Hela-S3	cervix
17	chr8:114976600-114976800	Enhancers	Fetal Lung	lung
18	chr8:114976800-114978400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:114978000-114978600	Enhancers	Hela-S3	cervix
20	chr8:114991000-114991800	Enhancers	Dnd41	blood
21	chr8:114992400-114993200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr8:114992400-114993200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:114992400-114994600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr8:114992600-114993000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr8:114992600-114993000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr8:114992600-114993000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr8:114992600-114993000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:114992600-114993600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr8:114992600-114993600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:114992600-114993600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr8:114992600-114993600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr8:114992600-114993600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:114993000-114993200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr8:114993000-114994000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:114993200-114993400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr8:114993400-114993600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr8:114993600-114993800	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr8:114993800-114994200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr8:114994000-114994600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:114994200-114994600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr8:115001800-115002200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr8:115002000-115002200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:115002000-115002200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr8:115002200-115003200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr8:115002200-115005800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr8:115002200-115006000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr8:115003200-115003400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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