Variant report

Variant	nsv457541
Chromosome Location	chr16:77353973-77389002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:77361518-77362088	GM12878	blood:	n/a	n/a
2	ATF3	chr16:77387406-77387935	A549	lung:	n/a	n/a
3	ATF3	chr16:77387390-77387946	A549	lung:	n/a	n/a
4	BACH1	chr16:77370568-77370892	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr16:77364729-77364750	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr16:77361605-77362055	GM12878	blood:	n/a	n/a
7	BATF	chr16:77361667-77361962	GM12878	blood:	n/a	n/a
8	BCL11A	chr16:77361671-77362022	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:77370621-77370777	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr16:77387277-77387969	A549	lung:	n/a	n/a
11	BCL3	chr16:77361644-77361903	GM12878	blood:	n/a	n/a
12	BCL3	chr16:77387257-77388009	A549	lung:	n/a	n/a
13	BHLHE40	chr16:77355073-77355181	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:77364267-77364567	GM12878	blood:	n/a	n/a
15	BRCA1	chr16:77362884-77362892	GM12878	blood:	n/a	n/a
16	CEBPB	chr16:77365690-77366105	MCF-7	breast:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
17	CEBPB	chr16:77365731-77365978	K562	blood:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
18	CEBPB	chr16:77387380-77387813	A549	lung:	n/a	chr16:77387440-77387452
19	CEBPB	chr16:77364165-77364551	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr16:77365722-77366066	H1-hESC	embryonic stem cell:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
21	CEBPB	chr16:77377560-77377832	HepG2	liver:	n/a	chr16:77377706-77377719 chr16:77377697-77377708
22	CEBPB	chr16:77361545-77362105	GM12878	blood:	n/a	chr16:77361698-77361711
23	CEBPB	chr16:77354682-77354845	A549	lung:	n/a	n/a
24	CEBPB	chr16:77365701-77366079	K562	blood:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
25	CEBPB	chr16:77365697-77366150	A549	lung:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
26	CEBPB	chr16:77365654-77366167	MCF-7	breast:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
27	CEBPB	chr16:77365712-77366070	ECC-1	luminal epithelium:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
28	CEBPB	chr16:77365713-77366093	A549	lung:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
29	CEBPB	chr16:77364214-77364593	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr16:77365710-77366093	Hela-S3	cervix:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
31	CEBPB	chr16:77365714-77366094	HepG2	liver:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
32	CEBPB	chr16:77365692-77366151	ECC-1	luminal epithelium:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
33	CEBPB	chr16:77365638-77366227	A549	lung:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
34	CEBPB	chr16:77365713-77366088	IMR90	lung:	n/a	chr16:77365874-77365885 chr16:77365895-77365906
35	CEBPB	chr16:77387365-77387920	A549	lung:	n/a	chr16:77387440-77387452
36	CEBPB	chr16:77354562-77354758	HepG2	liver:	n/a	n/a
37	CHD2	chr16:77361726-77361922	GM12878	blood:	n/a	n/a
38	CREB1	chr16:77387485-77387790	A549	lung:	n/a	n/a
39	CTCF	chr16:77354380-77354404	GM13976	blood:	n/a	n/a
40	CTCF	chr16:77369756-77369805	ProgFib	skin:	n/a	n/a
41	CTCF	chr16:77374267-77374361	GM13977	blood:	n/a	n/a
42	CTCF	chr16:77360323-77360429	Fibrobl	skin:	n/a	n/a
43	CTCF	chr16:77361531-77361595	Lung_OC	lung:	n/a	n/a
44	EBF1	chr16:77361654-77361926	GM12878	blood:	n/a	n/a
45	EBF1	chr16:77364363-77364526	GM12878	blood:	n/a	n/a
46	EGR1	chr16:77357191-77357401	K562	blood:	n/a	chr16:77357293-77357306 chr16:77357294-77357305 chr16:77357296-77357305 chr16:77357294-77357305 chr16:77357295-77357305 chr16:77357293-77357306 chr16:77357293-77357307 chr16:77357295-77357305 chr16:77357295-77357304 chr16:77357293-77357306
47	EP300	chr16:77361706-77361966	GM12878	blood:	n/a	chr16:77361771-77361785
48	EP300	chr16:77370443-77371064	ECC-1	luminal epithelium:	n/a	chr16:77370922-77370932 chr16:77370581-77370595
49	EP300	chr16:77370470-77370918	H1-hESC	embryonic stem cell:	n/a	chr16:77370581-77370595
50	EP300	chr16:77387285-77388123	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:77370171-77370221	HNPCEpiC	eye:	n/a
2	chr16:77370171-77370221	HNPCEpiC	eye:	n/a
3	chr16:77370171-77370221	GM12891	blood:	n/a
4	chr16:77367200-77367250	NHDF-neo	bronchial:	n/a
5	chr16:77370171-77370221	HepG2	liver:	n/a
6	chr16:77369724-77369774	BJ	skin:	n/a
7	chr16:77369724-77369774	AG09319	gingival:	n/a
8	chr16:77370171-77370221	GM12892	blood:	n/a
9	chr16:77369724-77369774	PANC-1	pancreas:	n/a
10	chr16:77370171-77370221	HEK293	kidney:	embryo
11	chr16:77370171-77370221	PANC-1	pancreas:	n/a
12	chr16:77367200-77367250	K562	blood:	n/a
13	chr16:77370171-77370221	AG04450	lung:	fetal
14	chr16:77370171-77370221	HRE	kidney:	n/a
15	chr16:77370171-77370221	Hepatocyte	liver:	n/a
16	chr16:77369724-77369774	A549	lung:	n/a
17	chr16:77370171-77370221	MCF10A-Er-Src	breast:	n/a
18	chr16:77370171-77370221	NHBE	bronchial:	n/a
19	chr16:77367200-77367250	SKMC	muscle:	n/a
20	chr16:77367200-77367250	PANC-1	pancreas:	n/a
21	chr16:77370171-77370221	HCT-116	colon:	n/a
22	chr16:77369724-77369774	HAEpiC	amniotic membrane:	n/a
23	chr16:77367200-77367250	GM12891	blood:	n/a
24	chr16:77369724-77369774	AG09309	skin:	n/a
25	chr16:77367200-77367250	BE2_C	brain:	n/a
26	chr16:77370171-77370221	HUVEC	blood vessel:	n/a
27	chr16:77370171-77370221	SK-N-MC	brain:	n/a
28	chr16:77369724-77369774	SK-N-MC	brain:	n/a
29	chr16:77367200-77367250	GM12892	blood:	n/a
30	chr16:77369724-77369774	HEK293	kidney:	embryo
31	chr16:77367200-77367250	HCT-116	colon:	n/a
32	chr16:77369724-77369774	K562	blood:	n/a
33	chr16:77369724-77369774	NHBE	bronchial:	n/a
34	chr16:77369724-77369774	CMK	blood:	n/a
35	chr16:77370171-77370221	SK-N-SH	brain:	n/a
36	chr16:77369724-77369774	NT2-D1	testis:	n/a
37	chr16:77369724-77369774	H1-hESC	embryonic stem cell:	embryo
38	chr16:77370171-77370221	HCPEpiC	choroid plexus:	n/a
39	chr16:77367200-77367250	ovcar-3	ovarian:	n/a
40	chr16:77367200-77367250	CMK	blood:	n/a
41	chr16:77370171-77370221	A549	lung:	n/a
42	chr16:77370171-77370221	GM06990	blood:	n/a
43	chr16:77369724-77369774	AoSMC	blood vessel:	n/a
44	chr16:77367200-77367250	T-47D	breast:	n/a
45	chr16:77370171-77370221	Jurkat	blood:	n/a
46	chr16:77367200-77367250	Jurkat	blood:	n/a
47	chr16:77369724-77369774	HCM	heart:	n/a
48	chr16:77370171-77370221	HPAEpiC	pulmonary alveolar:	n/a
49	chr16:77369724-77369774	NHDF-neo	bronchial:	n/a
50	chr16:77367200-77367250	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:77364104..77366895-chr16:77412752..77415656,2	K562	blood:
2	chr16:77364163..77366855-chr16:77389238..77390900,2	MCF-7	breast:
3	chr12:75336977..75337697-chr16:77358943..77359755,2	MCF-7	breast:
4	chr16:77376619..77379177-chr16:77392341..77394728,2	MCF-7	breast:

Variant related genes	Relation type
ADAMTS18	TF binding region
ADAMTS18	CpG island

Extended variants
information (count: 1819 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9930984	chr16:77353973-77353974	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149346461	chr16:77353980-77353981	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533859064	chr16:77353996-77353997	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372489082	chr16:77354039-77354040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553517875	chr16:77354055-77354056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570325339	chr16:77354061-77354062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146342853	chr16:77354091-77354092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533080203	chr16:77354146-77354147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575733931	chr16:77354153-77354154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191402900	chr16:77354193-77354194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554968682	chr16:77354209-77354210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139611140	chr16:77354210-77354211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540937025	chr16:77354263-77354264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560621619	chr16:77354306-77354307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577508129	chr16:77354310-77354311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576504700	chr16:77354314-77354315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545425038	chr16:77354384-77354385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111667954	chr16:77354423-77354424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144237440	chr16:77354437-77354438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78194045	chr16:77354522-77354523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546617807	chr16:77354536-77354537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397805437	chr16:77354547-77354548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183588757	chr16:77354556-77354557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9746317	chr16:77354562-77354563	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs547658144	chr16:77354584-77354585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188490996	chr16:77354647-77354648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527544996	chr16:77354665-77354666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547295318	chr16:77354667-77354668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570460079	chr16:77354668-77354669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77618698	chr16:77354690-77354691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549983662	chr16:77354705-77354706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541236352	chr16:77354717-77354718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113076476	chr16:77354730-77354731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554625137	chr16:77354742-77354743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574889684	chr16:77354754-77354755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78487510	chr16:77354779-77354780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554493781	chr16:77354783-77354784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577643907	chr16:77354791-77354792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373245677	chr16:77354804-77354805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183143558	chr16:77354842-77354843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76875909	chr16:77354891-77354892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149221603	chr16:77354896-77354897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541919238	chr16:77354907-77354908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142440298	chr16:77354908-77354909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191414543	chr16:77354923-77354924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183562226	chr16:77354932-77354933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369845142	chr16:77354938-77354939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564024738	chr16:77354950-77354951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151306394	chr16:77354983-77354984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188168666	chr16:77355022-77355023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77328000-77357600	Weak transcription	Adipose Nuclei	Adipose
2	chr16:77329200-77389800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr16:77343800-77356200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr16:77346000-77354000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:77349200-77355400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:77351000-77369800	Weak transcription	Brain Substantia Nigra	brain
7	chr16:77354000-77360200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr16:77355400-77358800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:77356000-77356200	Enhancers	Ovary	ovary
10	chr16:77356200-77357000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr16:77356200-77357400	Weak transcription	Ovary	ovary
12	chr16:77356600-77357200	Enhancers	Fetal Lung	lung
13	chr16:77357000-77357400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr16:77357400-77358200	Enhancers	Ovary	ovary
15	chr16:77357400-77358400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr16:77357600-77357800	Enhancers	Adipose Nuclei	Adipose
17	chr16:77358000-77359200	Enhancers	Dnd41	blood
18	chr16:77358400-77359600	Enhancers	Primary T cells from cord blood	blood
19	chr16:77358800-77362000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr16:77359400-77392800	Weak transcription	HUVEC	blood vessel
21	chr16:77360200-77362000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr16:77361200-77361800	Enhancers	Brain Cingulate Gyrus	brain
23	chr16:77361400-77362200	Enhancers	GM12878-XiMat	blood
24	chr16:77361600-77361800	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr16:77361800-77364200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr16:77361800-77364200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr16:77362000-77364000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr16:77362000-77364200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr16:77362200-77362800	Enhancers	Fetal Stomach	stomach
30	chr16:77362200-77364200	Weak transcription	GM12878-XiMat	blood
31	chr16:77362400-77362800	Enhancers	Colon Smooth Muscle	Colon
32	chr16:77362800-77363000	Enhancers	Brain Angular Gyrus	brain
33	chr16:77364000-77364600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:77364000-77365400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr16:77364200-77364400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:77364200-77364800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr16:77364200-77364800	Enhancers	GM12878-XiMat	blood
38	chr16:77364200-77365000	Enhancers	Brain Cingulate Gyrus	brain
39	chr16:77364200-77365000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr16:77364400-77364600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr16:77364400-77364600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr16:77364400-77364800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr16:77364600-77364800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr16:77364600-77364800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr16:77364600-77365600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr16:77364600-77365600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr16:77364800-77365000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr16:77364800-77365000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr16:77364800-77369600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr16:77364800-77369600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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