Variant report

Variant	nsv890836
Chromosome Location	chr8:39480366-39650940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:368)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39621219-39621517	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:39599175-39599222	K562	blood:	n/a	n/a
3	ARID3A	chr8:39547188-39547606	HepG2	liver:	n/a	n/a
4	ATF1	chr8:39552789-39552868	K562	blood:	n/a	n/a
5	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
6	ATF2	chr8:39542169-39542470	GM12878	blood:	n/a	n/a
7	BACH1	chr8:39601010-39601037	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:39601076-39601099	K562	blood:	n/a	n/a
9	BATF	chr8:39637507-39637695	GM12878	blood:	n/a	n/a
10	BATF	chr8:39542225-39542523	GM12878	blood:	n/a	n/a
11	BATF	chr8:39637507-39637697	GM12878	blood:	n/a	n/a
12	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
13	BATF	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
14	BCL11A	chr8:39542248-39542605	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:39542183-39542620	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:39542279-39542596	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
19	CBX3	chr8:39498734-39499015	HCT-116	colon:	n/a	n/a
20	CCNT2	chr8:39613824-39613995	K562	blood:	n/a	n/a
21	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
22	CEBPB	chr8:39610769-39611092	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:39621751-39621950	H1-hESC	embryonic stem cell:	n/a	chr8:39621879-39621890
24	CEBPB	chr8:39562647-39562945	A549	lung:	n/a	n/a
25	CEBPB	chr8:39562615-39562959	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:39589146-39589277	A549	lung:	n/a	chr8:39589190-39589201
27	CEBPB	chr8:39647716-39648001	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:39562606-39562938	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:39647685-39647955	A549	lung:	n/a	n/a
30	CEBPB	chr8:39621736-39621988	A549	lung:	n/a	chr8:39621879-39621890
31	CEBPB	chr8:39550934-39551155	IMR90	lung:	n/a	chr8:39551018-39551029
32	CEBPB	chr8:39621750-39622030	HepG2	liver:	n/a	chr8:39621879-39621890
33	CEBPB	chr8:39550875-39551134	HepG2	liver:	n/a	chr8:39551018-39551029
34	CEBPB	chr8:39550893-39551144	K562	blood:	n/a	chr8:39551018-39551029
35	CEBPB	chr8:39545791-39545917	A549	lung:	n/a	n/a
36	CEBPB	chr8:39584624-39585155	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:39562626-39562905	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:39610912-39610941	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:39536157-39536372	HepG2	liver:	n/a	chr8:39536260-39536272
40	CEBPB	chr8:39635155-39635197	A549	lung:	n/a	n/a
41	CEBPB	chr8:39589214-39589269	HepG2	liver:	n/a	n/a
42	CHD1	chr8:39543635-39543758	GM12878	blood:	n/a	n/a
43	CHD1	chr8:39542597-39542843	GM12878	blood:	n/a	n/a
44	CHD1	chr8:39544449-39544453	GM12878	blood:	n/a	n/a
45	CHD2	chr8:39511704-39511832	K562	blood:	n/a	n/a
46	CHD2	chr8:39541932-39543050	GM12878	blood:	n/a	n/a
47	CTCF	chr8:39564300-39564450	BE2_C	brain:	n/a	n/a
48	CTCF	chr8:39501960-39502110	GM12868	blood:	n/a	n/a
49	CTCF	chr8:39530060-39530210	BE2_C	brain:	n/a	n/a
50	CTCF	chr8:39484841-39484900	GM20000	blood:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39622412..39624554-chr8:39628340..39630731,2	MCF-7	breast:
2	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
3	chr8:39629924..39632128-chr8:39633892..39635911,2	MCF-7	breast:
4	chr8:39622412..39624554-chr8:39628340..39630731,2	MCF-7	breast:
5	chr8:39602749..39604278-chr8:39604368..39606576,2	K562	blood:
6	chr8:39629008..39630969-chr8:39633550..39635113,2	K562	blood:
7	chr8:39602749..39604278-chr8:39604368..39606576,2	K562	blood:
8	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
9	chr8:39610203..39611775-chr8:39614895..39616496,2	K562	blood:
10	chr8:39629008..39630969-chr8:39633550..39635113,2	K562	blood:
11	chr8:39629924..39632128-chr8:39633892..39635911,2	MCF-7	breast:
12	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
13	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
14	chr8:39610203..39611775-chr8:39614895..39616496,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDO1-3	chr8:39587417-39587581	NONHSAT126179
2	lnc-IDO1-3	chr8:39542649-39542931	NONHSAT126179
3	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126180
4	lnc-IDO1-3	chr8:39542693-39542931	NONHSAT126180
5	lnc-IDO1-2	chr8:39549919-39550084	l_3583_chr8:39549918-39556807_testes
6	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126179
7	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126179
8	lnc-IDO1-2	chr8:39556704-39556807	l_3583_chr8:39549918-39556807_testes
9	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126180
10	lnc-IDO1-3	chr8:39581267-39581477	NONHSAT126180
11	lnc-IDO1-2	chr8:39552257-39552314	l_3583_chr8:39549918-39556807_testes
12	lnc-IDO1-2	chr8:39556641-39556699	l_3583_chr8:39549918-39556807_testes
13	lnc-IDO1-3	chr8:39581267-39581426	NONHSAT126179

No data

Variant related genes	Relation type
ADAM2	TF binding region
ENSG00000221018	TF binding region
ADAM18	TF binding region

Extended variants
information (count: 3238 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:3238 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138455034	chr8:39491671-39491672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115496491	chr8:39491697-39491698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538060176	chr8:39491701-39491702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557900746	chr8:39491733-39491734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192918944	chr8:39491744-39491745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571620566	chr8:39491758-39491759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558743696	chr8:39491769-39491770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534252582	chr8:39491821-39491822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114500287	chr8:39491883-39491884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572796972	chr8:39491890-39491891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535421138	chr8:39491904-39491905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555178450	chr8:39491914-39491915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575251661	chr8:39491917-39491918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544442327	chr8:39491925-39491926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564239670	chr8:39491934-39491935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201815583	chr8:39491955-39491956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577326897	chr8:39491956-39491957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62511900	chr8:39491982-39491983	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540562137	chr8:39491987-39491988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs3735880	chr8:39505826-39505827	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs145386216	chr8:39505831-39505832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201596679	chr8:39505884-39505885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148130296	chr8:39505898-39505899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376114324	chr8:39505905-39505906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190997988	chr8:39505915-39505916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141902185	chr8:39505929-39505930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377343312	chr8:39505954-39505955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146631509	chr8:39506014-39506015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139133869	chr8:39506018-39506019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35422112	chr8:39506031-39506032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577825306	chr8:39506034-39506035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533952131	chr8:39506062-39506063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371248394	chr8:39506069-39506070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368877868	chr8:39506070-39506071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142344298	chr8:39506081-39506082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573679793	chr8:39506153-39506154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114697553	chr8:39506190-39506191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562797966	chr8:39506192-39506193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7011969	chr8:39506213-39506214	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs545239428	chr8:39506245-39506246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565594422	chr8:39506275-39506276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528004968	chr8:39506300-39506301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530762354	chr8:39506320-39506321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374072193	chr8:39506394-39506395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548094972	chr8:39506408-39506409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377629993	chr8:39506442-39506443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549213156	chr8:39506475-39506476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550333970	chr8:39506517-39506518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560232029	chr8:39506543-39506544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552886113	chr8:39506552-39506553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	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
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Cancer	21249187	CNVD
Autism	19287141	CNVD
Rett syndrome	21593744	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39491600-39492000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:39505800-39506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:39506000-39506600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:39506200-39506600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:39506200-39509000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:39506600-39507000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr8:39506600-39508200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:39506800-39508200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr8:39507000-39507600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:39507000-39508400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr8:39507000-39509000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:39507000-39509600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:39507200-39507600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:39507200-39507800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr8:39507600-39508400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr8:39507600-39508800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:39507800-39508200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr8:39507800-39508200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:39508200-39508600	Enhancers	Placenta	Placenta
20	chr8:39508200-39509000	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr8:39508200-39509000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:39508200-39509000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr8:39508200-39509000	Enhancers	K562	blood
24	chr8:39508400-39508800	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr8:39508400-39509200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr8:39508800-39509000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:39508800-39509000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr8:39509000-39509400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:39509000-39515800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr8:39509400-39510600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:39510400-39510600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr8:39510800-39511200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr8:39515600-39516400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:39515800-39516200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr8:39515800-39516400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:39515800-39516400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:39516000-39516400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:39525200-39525800	Enhancers	Fetal Lung	lung
39	chr8:39525800-39529200	Weak transcription	Fetal Lung	lung
40	chr8:39529200-39530800	Enhancers	Fetal Lung	lung
41	chr8:39529400-39530600	Enhancers	Colon Smooth Muscle	Colon
42	chr8:39533400-39534200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:39533600-39534000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:39534000-39542000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:39537600-39539400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:39538600-39539000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr8:39538600-39539200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:39538800-39539200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr8:39539400-39539800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:39539800-39541600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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