Variant report

Variant	nsv457530
Chromosome Location	chr16:76248410-76295598
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	ARID3A	chr16:76256042-76256283	HepG2	liver:	n/a	n/a
2	CEBPB	chr16:76266652-76266909	H1-hESC	embryonic stem cell:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
3	CEBPB	chr16:76256857-76257120	HepG2	liver:	n/a	chr16:76257002-76257013
4	CEBPB	chr16:76266660-76266961	HepG2	liver:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
5	CEBPB	chr16:76256803-76257198	H1-hESC	embryonic stem cell:	n/a	chr16:76257002-76257013
6	CEBPB	chr16:76266739-76266878	K562	blood:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
7	CEBPB	chr16:76266667-76266981	IMR90	lung:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
8	CEBPB	chr16:76276619-76276914	HepG2	liver:	n/a	chr16:76276751-76276762
9	CEBPB	chr16:76266695-76266926	A549	lung:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
10	CTCF	chr16:76253820-76253970	GM12872	blood:	n/a	n/a
11	CTCF	chr16:76261160-76261310	SAEC	small airway:	n/a	n/a
12	CTCF	chr16:76263161-76263202	Kidney_OC	kidney:	n/a	n/a
13	E2F4	chr16:76276713-76276959	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr16:76259558-76259746	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr16:76259965-76260724	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr16:76259949-76260248	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr16:76259967-76260199	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr16:76260430-76260726	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr16:76259967-76260192	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr16:76260397-76260652	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr16:76260449-76260740	MCF10A-Er-Src	breast:	n/a	n/a
22	FOXA1	chr16:76255956-76256327	HepG2	liver:	n/a	n/a
23	FOXA1	chr16:76256830-76257066	HepG2	liver:	n/a	n/a
24	FOXA1	chr16:76256745-76257085	HepG2	liver:	n/a	n/a
25	FOXA2	chr16:76256799-76257037	HepG2	liver:	n/a	n/a
26	FOXA2	chr16:76288729-76289045	A549	lung:	n/a	n/a
27	GATA2	chr16:76256782-76257088	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr16:76262491-76262776	MCF-7	breast:	n/a	n/a
29	GATA3	chr16:76256788-76257033	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr16:76248681-76248928	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr16:76262530-76262772	T-47D	breast:	n/a	n/a
32	HNF4A	chr16:76256016-76256306	HepG2	liver:	n/a	chr16:76256137-76256150 chr16:76256157-76256165 chr16:76256137-76256150 chr16:76256133-76256155 chr16:76256137-76256151
33	JUN	chr16:76278777-76279058	HepG2	liver:	n/a	chr16:76278894-76278907 chr16:76278895-76278904
34	JUND	chr16:76278802-76279074	HepG2	liver:	n/a	chr16:76278895-76278904
35	JUND	chr16:76251468-76251777	HepG2	liver:	n/a	n/a
36	MAFF	chr16:76256004-76256302	HepG2	liver:	n/a	chr16:76256116-76256134
37	MAFF	chr16:76280641-76280735	K562	blood:	n/a	chr16:76280670-76280688
38	MAFF	chr16:76266623-76266925	K562	blood:	n/a	chr16:76266780-76266798
39	MAFF	chr16:76280510-76280831	HepG2	liver:	n/a	chr16:76280670-76280688
40	MAFF	chr16:76277534-76277901	HepG2	liver:	n/a	chr16:76277705-76277723 chr16:76277711-76277725
41	MAFF	chr16:76277560-76277872	K562	blood:	n/a	chr16:76277705-76277723 chr16:76277711-76277725
42	MAFF	chr16:76266605-76266963	HepG2	liver:	n/a	chr16:76266780-76266798
43	MAFF	chr16:76268363-76268489	HepG2	liver:	n/a	n/a
44	MAFK	chr16:76280538-76280833	IMR90	lung:	n/a	chr16:76280671-76280686
45	MAFK	chr16:76266604-76266961	HepG2	liver:	n/a	chr16:76266781-76266796 chr16:76266781-76266797 chr16:76266776-76266796
46	MAFK	chr16:76290521-76290586	HepG2	liver:	n/a	n/a
47	MAFK	chr16:76266618-76266951	IMR90	lung:	n/a	chr16:76266781-76266796 chr16:76266781-76266797 chr16:76266776-76266796
48	MAFK	chr16:76266652-76266915	K562	blood:	n/a	chr16:76266781-76266796 chr16:76266781-76266797 chr16:76266776-76266796
49	MAFK	chr16:76277549-76278089	H1-hESC	embryonic stem cell:	n/a	chr16:76277708-76277728 chr16:76277710-76277726 chr16:76277711-76277725 chr16:76277707-76277722
50	MAFK	chr16:76266628-76266947	Hela-S3	cervix:	n/a	chr16:76266781-76266796 chr16:76266781-76266797 chr16:76266776-76266796

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76269184-76269234	HRPEpiC	eye:	n/a
2	chr16:76256948-76256998	HRCEpiC	kidney:	n/a
3	chr16:76269409-76269459	LNCaP	prostate:	n/a
4	chr16:76269184-76269234	HRPEpiC	eye:	n/a
5	chr16:76256948-76256998	HRCEpiC	kidney:	n/a
6	chr16:76269409-76269459	LNCaP	prostate:	n/a
7	chr16:76268785-76268835	Hepatocyte	liver:	n/a
8	chr16:76256948-76256998	NB4	blood:	n/a
9	chr16:76269184-76269234	SK-N-MC	brain:	n/a
10	chr16:76272351-76272401	BE2_C	brain:	n/a
11	chr16:76268785-76268835	HepG2	liver:	n/a
12	chr16:76269409-76269459	BJ	skin:	n/a
13	chr16:76269297-76269347	HUVEC	blood vessel:	n/a
14	chr16:76269297-76269347	LNCaP	prostate:	n/a
15	chr16:76269043-76269093	AoSMC	blood vessel:	n/a
16	chr16:76269297-76269347	GM19239	blood:	n/a
17	chr16:76269192-76269242	GM12891	blood:	n/a
18	chr16:76256948-76256998	T-47D	breast:	n/a
19	chr16:76256948-76256998	HAEpiC	amniotic membrane:	n/a
20	chr16:76269043-76269093	ECC-1	luminal epithelium:	n/a
21	chr16:76269297-76269347	ECC-1	luminal epithelium:	n/a
22	chr16:76256948-76256998	IMR90	lung:	fetal
23	chr16:76269192-76269242	Hela-S3	cervix:	n/a
24	chr16:76269043-76269093	CMK	blood:	n/a
25	chr16:76269297-76269347	HL-60	blood:	n/a
26	chr16:76266534-76266584	PFSK-1	brain:	n/a
27	chr16:76272351-76272401	SK-N-SH	brain:	n/a
28	chr16:76256948-76256998	H1-hESC	embryonic stem cell:	embryo
29	chr16:76269043-76269093	HPAEpiC	pulmonary alveolar:	n/a
30	chr16:76269409-76269459	GM12878	blood:	n/a
31	chr16:76269184-76269234	AG04450	lung:	fetal
32	chr16:76269192-76269242	MCF10A-Er-Src	breast:	n/a
33	chr16:76269184-76269234	NHDF-neo	bronchial:	n/a
34	chr16:76266534-76266584	A549	lung:	n/a
35	chr16:76256948-76256998	SK-N-SH_RA	brain:	n/a
36	chr16:76272351-76272401	K562	blood:	n/a
37	chr16:76269043-76269093	U87	brain:	n/a
38	chr16:76272351-76272401	BJ	skin:	n/a
39	chr16:76269184-76269234	U87	brain:	n/a
40	chr16:76269297-76269347	SK-N-SH	brain:	n/a
41	chr16:76256948-76256998	HEEpiC	esophagus:	n/a
42	chr16:76266534-76266584	AG09319	gingival:	n/a
43	chr16:76256948-76256998	HUVEC	blood vessel:	n/a
44	chr16:76269297-76269347	SKMC	muscle:	n/a
45	chr16:76269297-76269347	GM06990	blood:	n/a
46	chr16:76272351-76272401	H1-hESC	embryonic stem cell:	embryo
47	chr16:76269192-76269242	HCPEpiC	choroid plexus:	n/a
48	chr16:76266534-76266584	HEEpiC	esophagus:	n/a
49	chr16:76269184-76269234	HCPEpiC	choroid plexus:	n/a
50	chr16:76256948-76256998	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr16:76267035..76268706-chr16:76269783..76271539,2	K562	blood:
2	chr16:76264260..76266317-chr16:76268267..76270250,2	MCF-7	breast:
3	chr16:76267035..76268706-chr16:76269783..76271539,2	K562	blood:
4	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
5	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC025287.1-3	chr16:76268585-76269326	NONHSAT143776
2	lnc-AC025287.1-3	chr16:76262283-76262757	ENSG00000260983.1
3	lnc-AC025287.1-3	chr16:76265215-76265343	ENSG00000260983.1
4	lnc-AC025287.1-3	chr16:76268953-76269521	NONHSAT143777

Variant related genes	Relation type
RPL18P13	TF binding region
RPL18P13	CpG island
ENSG00000244485	chromatin interactions

Extended variants
information (count: 1123 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2161638	chr16:76248410-76248411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553090557	chr16:76248422-76248423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190239504	chr16:76248454-76248455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538650270	chr16:76248455-76248456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140211916	chr16:76248510-76248511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557534062	chr16:76248531-76248532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145258629	chr16:76248541-76248542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549623947	chr16:76248549-76248550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563477981	chr16:76248585-76248586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573917211	chr16:76248588-76248589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183199747	chr16:76248603-76248604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531239622	chr16:76248606-76248607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550951581	chr16:76248643-76248644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188311287	chr16:76248712-76248713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528047136	chr16:76248723-76248724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372910955	chr16:76248759-76248760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545001723	chr16:76248805-76248806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191405945	chr16:76248819-76248820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531211062	chr16:76248865-76248866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551022728	chr16:76248896-76248897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571058120	chr16:76248918-76248919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183748029	chr16:76248935-76248936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62052003	chr16:76248953-76248954	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9928834	chr16:76249019-76249020	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532422217	chr16:76249020-76249021	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs79762145	chr16:76249040-76249041	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs373953531	chr16:76249041-76249042	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs566634472	chr16:76249075-76249076	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs538621493	chr16:76249080-76249081	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558933228	chr16:76249086-76249087	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs569186777	chr16:76249095-76249096	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs9928916	chr16:76249115-76249116	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs187586319	chr16:76249127-76249128	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536180024	chr16:76249224-76249225	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs138076330	chr16:76249244-76249245	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs192634960	chr16:76249248-76249249	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs556528607	chr16:76249269-76249270	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs553066942	chr16:76249275-76249276	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs73615421	chr16:76249281-76249282	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544801620	chr16:76249288-76249289	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs183546436	chr16:76249338-76249339	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs149545818	chr16:76249351-76249352	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs112742914	chr16:76249355-76249356	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs561248249	chr16:76249405-76249406	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs11644607	chr16:76249497-76249498	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs372144078	chr16:76249508-76249509	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs546806513	chr16:76249512-76249513	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs186814984	chr16:76249518-76249519	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs73615422	chr16:76249557-76249558	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552426555	chr16:76249575-76249576	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Breast cancer	21364760	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
Schizophrenia	23813976	CNVD
Lung cancer	24585490	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76241600-76257400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:76247600-76248600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr16:76247800-76248600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr16:76248000-76249200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr16:76248200-76248600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr16:76248600-76249000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:76248600-76249000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr16:76248600-76249400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr16:76248600-76249400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr16:76248600-76249600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr16:76248600-76249800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr16:76248800-76249200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr16:76248800-76249400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr16:76248800-76249800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr16:76249000-76249600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr16:76249000-76254400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr16:76249600-76250800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr16:76249800-76250800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr16:76249800-76257400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr16:76250800-76251200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr16:76250800-76252000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr16:76251200-76251400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr16:76251400-76251600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr16:76251400-76251800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr16:76251600-76251800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
26	chr16:76251800-76255400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr16:76252800-76253400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr16:76253400-76254600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr16:76253800-76254800	Enhancers	Small Intestine	intestine
30	chr16:76254000-76254200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr16:76254200-76254400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr16:76254400-76254600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr16:76254400-76254600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr16:76254600-76255200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr16:76254600-76255800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr16:76255200-76256800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr16:76255400-76256400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr16:76255600-76256000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr16:76255600-76257000	Enhancers	Liver	Liver
40	chr16:76255800-76256200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr16:76255800-76256600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
42	chr16:76255800-76256800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
43	chr16:76255800-76257000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr16:76255800-76258200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
45	chr16:76256000-76256200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr16:76256000-76256200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr16:76256000-76257000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
48	chr16:76256000-76257000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr16:76256000-76257000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr16:76256000-76257200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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