Variant report

Variant	nsv891355
Chromosome Location	chr8:115285808-115395451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:115309455-115309795	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr8:115309934-115311300	GM12878	blood:	n/a	n/a
3	ATF2	chr8:115309885-115311242	GM12878	blood:	n/a	n/a
4	ATF2	chr8:115310219-115310638	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:115332200-115332247	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:115330646-115330834	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:115309992-115310599	GM12878	blood:	n/a	n/a
8	BATF	chr8:115310001-115310427	GM12878	blood:	n/a	n/a
9	BATF	chr8:115318701-115318964	GM12878	blood:	n/a	chr8:115318871-115318882
10	BATF	chr8:115310578-115311176	GM12878	blood:	n/a	n/a
11	BATF	chr8:115310640-115310938	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:115310015-115310397	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:115310567-115311162	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:115310650-115310937	GM12878	blood:	n/a	n/a
15	BCL3	chr8:115310631-115311217	GM12878	blood:	n/a	n/a
16	BCL3	chr8:115310042-115310348	GM12878	blood:	n/a	n/a
17	BCLAF1	chr8:115310652-115311196	GM12878	blood:	n/a	n/a
18	BCLAF1	chr8:115310053-115311206	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:115310002-115311236	GM12878	blood:	n/a	n/a
20	CEBPB	chr8:115364657-115364877	HepG2	liver:	n/a	chr8:115364727-115364738 chr8:115364728-115364737 chr8:115364726-115364737 chr8:115364726-115364739
21	CEBPB	chr8:115317512-115317686	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:115336098-115336490	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:115320912-115321273	HepG2	liver:	n/a	chr8:115321083-115321092 chr8:115321081-115321092
24	CEBPB	chr8:115361911-115362139	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:115364696-115364815	A549	lung:	n/a	chr8:115364727-115364738 chr8:115364728-115364737 chr8:115364726-115364737 chr8:115364726-115364739
26	CEBPB	chr8:115309955-115311248	GM12878	blood:	n/a	n/a
27	CEBPB	chr8:115320971-115321265	IMR90	lung:	n/a	chr8:115321083-115321092 chr8:115321081-115321092
28	CEBPB	chr8:115363238-115363247	K562	blood:	n/a	n/a
29	CHD1	chr8:115309334-115309357	GM12878	blood:	n/a	n/a
30	CHD1	chr8:115310831-115311197	GM12878	blood:	n/a	n/a
31	CHD1	chr8:115309936-115310551	GM12878	blood:	n/a	n/a
32	CHD1	chr8:115300469-115300758	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr8:115296505-115296527	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr8:115302427-115302502	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr8:115301554-115301725	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr8:115309954-115311224	GM12878	blood:	n/a	n/a
37	CHD2	chr8:115343589-115343696	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr8:115310193-115311155	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr8:115310500-115311284	GM12878	blood:	n/a	n/a
40	CREB1	chr8:115310513-115311295	GM12878	blood:	n/a	n/a
41	CTCF	chr8:115310680-115310796	GM10248	blood:	n/a	n/a
42	CTCF	chr8:115310680-115310830	GM12873	blood:	n/a	n/a
43	CTCF	chr8:115360785-115360827	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr8:115386660-115386810	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr8:115310722-115310767	GM10266	blood:	n/a	n/a
46	CTCF	chr8:115310588-115310949	GM12878	blood:	n/a	n/a
47	CTCF	chr8:115341549-115341599	GM20000	blood:	n/a	n/a
48	CTCF	chr8:115330540-115330690	HPF	lung:	n/a	n/a
49	CTCF	chr8:115290015-115290102	ProgFib	skin:	n/a	n/a
50	CTCF	chr8:115370571-115370644	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:115301887-115301937	SKMC	muscle:	n/a
2	chr8:115301887-115301937	HRCEpiC	kidney:	n/a
3	chr8:115301887-115301937	Hepatocyte	liver:	n/a
4	chr8:115301887-115301937	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:115301887-115301937	BJ	skin:	n/a
6	chr8:115301887-115301937	AoSMC	blood vessel:	n/a
7	chr8:115301887-115301937	PrEC	prostate:	n/a
8	chr8:115301887-115301937	HCF	heart:	n/a
9	chr8:115301887-115301937	GM12878	blood:	n/a
10	chr8:115301887-115301937	NT2-D1	testis:	n/a
11	chr8:115301887-115301937	ECC-1	luminal epithelium:	n/a
12	chr8:115301887-115301937	SK-N-MC	brain:	n/a
13	chr8:115301887-115301937	HRPEpiC	eye:	n/a
14	chr8:115301887-115301937	BE2_C	brain:	n/a
15	chr8:115301887-115301937	GM12891	blood:	n/a
16	chr8:115301887-115301937	HEEpiC	esophagus:	n/a
17	chr8:115301887-115301937	MCF10A-Er-Src	breast:	n/a
18	chr8:115301887-115301937	NHDF-neo	bronchial:	n/a
19	chr8:115301887-115301937	LNCaP	prostate:	n/a
20	chr8:115301887-115301937	MCF-7	breast:	n/a
21	chr8:115301887-115301937	NB4	blood:	n/a
22	chr8:115301887-115301937	SK-N-SH	brain:	n/a
23	chr8:115301887-115301937	HUVEC	blood vessel:	n/a
24	chr8:115301887-115301937	AG04450	lung:	fetal
25	chr8:115301887-115301937	RPTEC	kidney:	n/a
26	chr8:115301887-115301937	PANC-1	pancreas:	n/a
27	chr8:115301887-115301937	Caco-2	colon:	n/a
28	chr8:115301887-115301937	ovcar-3	ovarian:	n/a
29	chr8:115301887-115301937	HIPEpiC	eye:	n/a
30	chr8:115301887-115301937	ProgFib	skin:	n/a
31	chr8:115301887-115301937	NH-A	brain:	n/a
32	chr8:115301887-115301937	HMEC	breast:	n/a
33	chr8:115301887-115301937	HCT-116	colon:	n/a
34	chr8:115301887-115301937	IMR90	lung:	fetal
35	chr8:115301887-115301937	AG09319	gingival:	n/a
36	chr8:115301887-115301937	HL-60	blood:	n/a
37	chr8:115301887-115301937	U87	brain:	n/a
38	chr8:115301887-115301937	HNPCEpiC	eye:	n/a
39	chr8:115301887-115301937	H1-hESC	embryonic stem cell:	embryo
40	chr8:115301887-115301937	HCPEpiC	choroid plexus:	n/a
41	chr8:115301887-115301937	NHBE	bronchial:	n/a
42	chr8:115301887-115301937	GM12892	blood:	n/a
43	chr8:115301887-115301937	HepG2	liver:	n/a
44	chr8:115301887-115301937	HCM	heart:	n/a
45	chr8:115301887-115301937	SK-N-SH_RA	brain:	n/a
46	chr8:115301887-115301937	PFSK-1	brain:	n/a
47	chr8:115301887-115301937	A549	lung:	n/a
48	chr8:115301887-115301937	AG10803	skin:	n/a
49	chr8:115301887-115301937	HAEpiC	amniotic membrane:	n/a
50	chr8:115301887-115301937	T-47D	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
2	chr8:115327227..115329633-chr8:115330616..115333275,2	MCF-7	breast:
3	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
4	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
5	chr8:115308430..115310814-chr8:115329605..115331962,2	MCF-7	breast:
6	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
7	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
8	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD3-1	chr8:115315119-115315373	XLOC_007184
2	lnc-CSMD3-1	chr8:115323322-115323497	XLOC_007184
3	lnc-CSMD3-5	chr8:115308063-115308898	NONHSAT128356
4	lnc-CSMD3-1	chr8:115316636-115316724	XLOC_007184
5	lnc-CSMD3-6	chr8:115330629-115331140	NONHSAT128358
6	lnc-CSMD3-5	chr8:115299951-115300072	NONHSAT128356
7	lnc-CSMD3-5	chr8:115309415-115309984	NONHSAT128356

No data

Variant related genes	Relation type
ENSG00000254339	TF binding region
ENSG00000253499	TF binding region
ENSG00000254339	CpG island
ENSG00000253499	CpG island
ENSG00000253499	chromatin interactions
MAFK	miRNA target sites
MAGT1	miRNA target sites

Extended variants
information (count: 2174 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2174 , 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	rs6469517	chr8:115288220-115288221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573465277	chr8:115288247-115288248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540542247	chr8:115288283-115288284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191774039	chr8:115288301-115288302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116536155	chr8:115288302-115288303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541484149	chr8:115288321-115288322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17633801	chr8:115288332-115288333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530569660	chr8:115288354-115288355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76447447	chr8:115288383-115288384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79533035	chr8:115288387-115288388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541863047	chr8:115288396-115288397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564140720	chr8:115288413-115288414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562076416	chr8:115288431-115288432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546917452	chr8:115288475-115288476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183185934	chr8:115288526-115288527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188120550	chr8:115288534-115288535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371545754	chr8:115288541-115288542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547751811	chr8:115288627-115288628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72684142	chr8:115288633-115288634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147853119	chr8:115288650-115288651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7829397	chr8:115288672-115288673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs75345559	chr8:115288687-115288688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77886831	chr8:115288710-115288711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140933390	chr8:115288732-115288733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570936750	chr8:115288749-115288750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35158603	chr8:115288754-115288755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574038818	chr8:115288781-115288782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548321993	chr8:115288814-115288815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367715136	chr8:115288815-115288816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192953729	chr8:115288864-115288865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556712576	chr8:115288876-115288877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs16892696	chr8:115288890-115288891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545600375	chr8:115288905-115288906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564258689	chr8:115288973-115288974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6469518	chr8:115289019-115289020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs72684144	chr8:115289026-115289027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368461529	chr8:115289069-115289070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182100036	chr8:115289117-115289118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186823514	chr8:115289144-115289145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566793441	chr8:115289195-115289196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111913094	chr8:115289210-115289211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6985983	chr8:115289224-115289225	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs372495004	chr8:115289237-115289238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533439413	chr8:115289273-115289274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376696676	chr8:115289301-115289302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150203396	chr8:115289308-115289309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534117193	chr8:115289336-115289337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549215957	chr8:115289355-115289356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55880805	chr8:115289356-115289357	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148962311	chr8:115289357-115289358	Weak transcription	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:115288200-115290600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:115290600-115293000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:115291200-115292400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr8:115291200-115292400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr8:115291200-115293600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:115291600-115293000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:115291800-115292200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:115291800-115292400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr8:115291800-115292400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:115291800-115292600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:115291800-115293600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:115291800-115293800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr8:115292200-115294000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:115292400-115293600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr8:115292400-115293600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr8:115292400-115293800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:115292400-115293800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:115292600-115293800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:115293000-115293400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr8:115293000-115293400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr8:115293400-115293800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:115293400-115293800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr8:115293600-115294000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr8:115293600-115294000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr8:115293600-115294000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr8:115293600-115297000	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr8:115293800-115294000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr8:115293800-115294000	Flanking Active TSS	H9 Cell Line	embryonic stem cell
29	chr8:115293800-115294000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:115293800-115294000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr8:115293800-115294000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr8:115293800-115297400	Active TSS	H1 Cell Line	embryonic stem cell
33	chr8:115294000-115294800	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr8:115294000-115296400	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr8:115294000-115296400	Active TSS	H9 Cell Line	embryonic stem cell
36	chr8:115294000-115296400	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr8:115294000-115297000	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr8:115294000-115297000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr8:115294000-115297400	Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr8:115294000-115298400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:115294000-115298600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:115294000-115300000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr8:115294200-115295600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:115294400-115295200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr8:115294800-115298400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
46	chr8:115296400-115297000	Transcr. at gene 5' and 3'	H9 Cell Line	embryonic stem cell
47	chr8:115296400-115298400	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
48	chr8:115296400-115298600	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
49	chr8:115297000-115297600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr8:115297000-115300000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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