Variant report

Variant	nsv890837
Chromosome Location	chr8:39507869-39609626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:239)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:239 , 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	ARID3A	chr8:39547188-39547606	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:39599175-39599222	K562	blood:	n/a	n/a
3	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
4	ATF1	chr8:39552789-39552868	K562	blood:	n/a	n/a
5	ATF2	chr8:39542169-39542470	GM12878	blood:	n/a	n/a
6	BACH1	chr8:39601076-39601099	K562	blood:	n/a	n/a
7	BACH1	chr8:39601010-39601037	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
9	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
10	BATF	chr8:39542225-39542523	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:39542183-39542620	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:39542248-39542605	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:39542279-39542596	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
16	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
17	CEBPB	chr8:39562626-39562905	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:39550934-39551155	IMR90	lung:	n/a	chr8:39551018-39551029
19	CEBPB	chr8:39545791-39545917	A549	lung:	n/a	n/a
20	CEBPB	chr8:39589214-39589269	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:39589146-39589277	A549	lung:	n/a	chr8:39589190-39589201
22	CEBPB	chr8:39562647-39562945	A549	lung:	n/a	n/a
23	CEBPB	chr8:39550875-39551134	HepG2	liver:	n/a	chr8:39551018-39551029
24	CEBPB	chr8:39562606-39562938	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:39536157-39536372	HepG2	liver:	n/a	chr8:39536260-39536272
26	CEBPB	chr8:39584624-39585155	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:39562615-39562959	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:39550893-39551144	K562	blood:	n/a	chr8:39551018-39551029
29	CHD1	chr8:39544449-39544453	GM12878	blood:	n/a	n/a
30	CHD1	chr8:39542597-39542843	GM12878	blood:	n/a	n/a
31	CHD1	chr8:39543635-39543758	GM12878	blood:	n/a	n/a
32	CHD2	chr8:39511704-39511832	K562	blood:	n/a	n/a
33	CHD2	chr8:39541932-39543050	GM12878	blood:	n/a	n/a
34	CTCF	chr8:39530060-39530210	BE2_C	brain:	n/a	n/a
35	CTCF	chr8:39545941-39545950	GM10248	blood:	n/a	n/a
36	CTCF	chr8:39531405-39531462	GM13976	blood:	n/a	n/a
37	CTCF	chr8:39547760-39547804	GM19239	blood:	n/a	n/a
38	CTCF	chr8:39564300-39564450	BE2_C	brain:	n/a	n/a
39	CUX1	chr8:39542010-39542700	GM12878	blood:	n/a	n/a
40	CUX1	chr8:39538255-39538344	GM12878	blood:	n/a	n/a
41	CUX1	chr8:39544201-39544276	GM12878	blood:	n/a	n/a
42	CUX1	chr8:39520617-39520682	GM12878	blood:	n/a	n/a
43	CUX1	chr8:39575767-39575867	GM12878	blood:	n/a	n/a
44	E2F4	chr8:39580670-39581154	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr8:39546889-39546908	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr8:39518243-39518366	GM12878	blood:	n/a	n/a
47	EBF1	chr8:39540745-39540901	GM12878	blood:	n/a	n/a
48	EBF1	chr8:39542004-39542259	GM12878	blood:	n/a	n/a
49	EBF1	chr8:39543841-39544373	GM12878	blood:	n/a	n/a
50	EBF1	chr8:39530578-39530587	GM12878	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
2	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
3	chr8:39602749..39604278-chr8:39604368..39606576,2	K562	blood:
4	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
5	chr8:39602749..39604278-chr8:39604368..39606576,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ADAM18	TF binding region

Extended variants
information (count: 2444 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6474162	chr8:39507869-39507870	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544070259	chr8:39507949-39507950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559677530	chr8:39507981-39507982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562377295	chr8:39508010-39508011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184608562	chr8:39508025-39508026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544820584	chr8:39508085-39508086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189376093	chr8:39508182-39508183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138617228	chr8:39508218-39508219	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs141577285	chr8:39508222-39508223	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567104190	chr8:39508229-39508230	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs529971994	chr8:39508233-39508234	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs550041748	chr8:39508248-39508249	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569997687	chr8:39508251-39508252	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs577757858	chr8:39508270-39508271	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs538977210	chr8:39508277-39508278	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs558792541	chr8:39508283-39508284	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs373077905	chr8:39508311-39508312	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs376294477	chr8:39508327-39508328	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs370421096	chr8:39508328-39508329	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs114848501	chr8:39508331-39508332	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs562681924	chr8:39508333-39508334	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs372975548	chr8:39508353-39508354	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs375970057	chr8:39508354-39508355	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs535251742	chr8:39508357-39508358	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs555228561	chr8:39508358-39508359	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116650231	chr8:39508359-39508360	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs370014671	chr8:39508365-39508366	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs543800050	chr8:39508391-39508392	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs146180264	chr8:39508392-39508393	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs147390015	chr8:39508405-39508406	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs191113209	chr8:39508409-39508410	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs138661117	chr8:39508411-39508412	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs144867981	chr8:39508422-39508423	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs544957084	chr8:39508430-39508431	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs145786764	chr8:39508433-39508434	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs149345894	chr8:39508434-39508435	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs145101116	chr8:39508436-39508437	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs145887248	chr8:39508447-39508448	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148318882	chr8:39508448-39508449	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs142843854	chr8:39508456-39508457	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs564663977	chr8:39508458-39508459	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs141155856	chr8:39508461-39508462	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs140143321	chr8:39508469-39508470	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs571838686	chr8:39508479-39508480	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs145781204	chr8:39508480-39508481	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138460748	chr8:39508484-39508485	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs139235024	chr8:39508485-39508486	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs146188078	chr8:39508498-39508499	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs77663729	chr8:39508505-39508506	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs113116224	chr8:39508507-39508508	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Medulloblastoma	21979893	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39506200-39509000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:39506600-39508200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:39506800-39508200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr8:39507000-39508400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:39507000-39509000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:39507000-39509600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:39507600-39508400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr8:39507600-39508800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:39507800-39508200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr8:39507800-39508200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:39508200-39508600	Enhancers	Placenta	Placenta
12	chr8:39508200-39509000	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr8:39508200-39509000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:39508200-39509000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr8:39508200-39509000	Enhancers	K562	blood
16	chr8:39508400-39508800	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr8:39508400-39509200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr8:39508800-39509000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:39508800-39509000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr8:39509000-39509400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:39509000-39515800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr8:39509400-39510600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:39510400-39510600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr8:39510800-39511200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:39515600-39516400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:39515800-39516200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr8:39515800-39516400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:39515800-39516400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr8:39516000-39516400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr8:39525200-39525800	Enhancers	Fetal Lung	lung
31	chr8:39525800-39529200	Weak transcription	Fetal Lung	lung
32	chr8:39529200-39530800	Enhancers	Fetal Lung	lung
33	chr8:39529400-39530600	Enhancers	Colon Smooth Muscle	Colon
34	chr8:39533400-39534200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:39533600-39534000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:39534000-39542000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:39537600-39539400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:39538600-39539000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr8:39538600-39539200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr8:39538800-39539200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr8:39539400-39539800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:39539800-39541600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:39541600-39542400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:39542000-39542800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:39542000-39543000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:39542000-39543000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:39542000-39543000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:39542000-39543000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:39542000-39543000	Enhancers	Placenta	Placenta
50	chr8:39542000-39543600	Enhancers	Placenta Amnion	Placenta Amnion

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