Variant report

Variant	esv2761913
Chromosome Location	chr16:74828988-74876348
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:61)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:74847065-74847363	K562	blood:	n/a	n/a
2	ARID3A	chr16:74847066-74847411	HepG2	liver:	n/a	n/a
3	ATF2	chr16:74846983-74847410	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr16:74864547-74864824	K562	blood:	n/a	n/a
5	BACH1	chr16:74847029-74847367	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr16:74846938-74847406	GM12878	blood:	n/a	chr16:74847373-74847382
7	BHLHE40	chr16:74867477-74867655	K562	blood:	n/a	n/a
8	BHLHE40	chr16:74863622-74863804	HepG2	liver:	n/a	n/a
9	BHLHE40	chr16:74847028-74847577	K562	blood:	n/a	n/a
10	BHLHE40	chr16:74875983-74876148	HepG2	liver:	n/a	n/a
11	BHLHE40	chr16:74875936-74876280	K562	blood:	n/a	n/a
12	BHLHE40	chr16:74865907-74865908	K562	blood:	n/a	n/a
13	BHLHE40	chr16:74847126-74847339	GM12878	blood:	n/a	n/a
14	BRCA1	chr16:74847039-74847322	HepG2	liver:	n/a	n/a
15	BRCA1	chr16:74847018-74847377	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr16:74847010-74847522	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr16:74846955-74847408	K562	blood:	n/a	n/a
18	CBX3	chr16:74840873-74841256	K562	blood:	n/a	n/a
19	CCNT2	chr16:74847014-74847419	K562	blood:	n/a	n/a
20	CEBPB	chr16:74867448-74867761	A549	lung:	n/a	n/a
21	CEBPB	chr16:74873527-74873554	A549	lung:	n/a	n/a
22	CEBPB	chr16:74874704-74874904	HepG2	liver:	n/a	chr16:74874833-74874844
23	CEBPB	chr16:74867390-74867732	K562	blood:	n/a	n/a
24	CEBPB	chr16:74867422-74867783	K562	blood:	n/a	n/a
25	CEBPB	chr16:74867432-74867799	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:74863582-74863827	H1-hESC	embryonic stem cell:	n/a	chr16:74863710-74863723
27	CEBPB	chr16:74847039-74847365	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr16:74863551-74863880	HepG2	liver:	n/a	chr16:74863710-74863723
29	CEBPB	chr16:74867455-74867680	K562	blood:	n/a	n/a
30	CEBPB	chr16:74863535-74863895	HepG2	liver:	n/a	chr16:74863710-74863723
31	CEBPB	chr16:74863524-74863919	Hela-S3	cervix:	n/a	chr16:74863710-74863723
32	CEBPB	chr16:74841912-74842288	A549	lung:	n/a	chr16:74842126-74842137
33	CEBPB	chr16:74874804-74874902	K562	blood:	n/a	chr16:74874833-74874844
34	CEBPB	chr16:74863571-74863852	K562	blood:	n/a	chr16:74863710-74863723
35	CEBPB	chr16:74831234-74831474	HepG2	liver:	n/a	chr16:74831330-74831341
36	CEBPB	chr16:74863576-74863847	A549	lung:	n/a	chr16:74863710-74863723
37	CEBPB	chr16:74831257-74831463	Hela-S3	cervix:	n/a	chr16:74831330-74831341
38	CEBPB	chr16:74867437-74867781	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr16:74863552-74863895	A549	lung:	n/a	chr16:74863710-74863723
40	CEBPB	chr16:74863473-74863925	A549	lung:	n/a	chr16:74863710-74863723
41	CEBPB	chr16:74863529-74863893	K562	blood:	n/a	chr16:74863710-74863723
42	CEBPB	chr16:74856654-74856747	HepG2	liver:	n/a	chr16:74856692-74856703 chr16:74856694-74856705
43	CEBPB	chr16:74847031-74847433	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr16:74841958-74842304	K562	blood:	n/a	chr16:74842126-74842137
45	CEBPB	chr16:74863549-74863890	IMR90	lung:	n/a	chr16:74863710-74863723
46	CEBPB	chr16:74867496-74867767	IMR90	lung:	n/a	n/a
47	CEBPB	chr16:74841949-74842299	HepG2	liver:	n/a	chr16:74842126-74842137
48	CEBPB	chr16:74863576-74863771	HepG2	liver:	n/a	chr16:74863710-74863723
49	CEBPB	chr16:74863524-74863904	HepG2	liver:	n/a	chr16:74863710-74863723
50	CEBPB	chr16:74841965-74842275	A549	lung:	n/a	chr16:74842126-74842137

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74847234-74847284	NT2-D1	testis:	n/a
2	chr16:74847234-74847284	HIPEpiC	eye:	n/a
3	chr16:74847234-74847284	Hela-S3	cervix:	n/a
4	chr16:74847234-74847284	HUVEC	blood vessel:	n/a
5	chr16:74847234-74847284	HAEpiC	amniotic membrane:	n/a
6	chr16:74847234-74847284	AG10803	skin:	n/a
7	chr16:74847234-74847284	HCM	heart:	n/a
8	chr16:74847234-74847284	PANC-1	pancreas:	n/a
9	chr16:74847234-74847284	A549	lung:	n/a
10	chr16:74847234-74847284	NHDF-neo	bronchial:	n/a
11	chr16:74847234-74847284	HRPEpiC	eye:	n/a
12	chr16:74847234-74847284	SK-N-SH_RA	brain:	n/a
13	chr16:74847234-74847284	U87	brain:	n/a
14	chr16:74847234-74847284	GM06990	blood:	n/a
15	chr16:74847234-74847284	HRE	kidney:	n/a
16	chr16:74847234-74847284	NH-A	brain:	n/a
17	chr16:74847234-74847284	MCF10A-Er-Src	breast:	n/a
18	chr16:74847234-74847284	BE2_C	brain:	n/a
19	chr16:74847234-74847284	HL-60	blood:	n/a
20	chr16:74847234-74847284	Jurkat	blood:	n/a
21	chr16:74847234-74847284	HCT-116	colon:	n/a
22	chr16:74847234-74847284	IMR90	lung:	fetal
23	chr16:74847234-74847284	BJ	skin:	n/a
24	chr16:74847234-74847284	HMEC	breast:	n/a
25	chr16:74847234-74847284	SK-N-SH	brain:	n/a
26	chr16:74847234-74847284	ovcar-3	ovarian:	n/a
27	chr16:74847234-74847284	H1-hESC	embryonic stem cell:	embryo
28	chr16:74847234-74847284	SKMC	muscle:	n/a
29	chr16:74847234-74847284	RPTEC	kidney:	n/a
30	chr16:74847234-74847284	GM12878	blood:	n/a
31	chr16:74847234-74847284	AG04450	lung:	fetal
32	chr16:74847234-74847284	GM12892	blood:	n/a
33	chr16:74847234-74847284	Caco-2	colon:	n/a
34	chr16:74847234-74847284	HNPCEpiC	eye:	n/a
35	chr16:74847234-74847284	SK-N-MC	brain:	n/a
36	chr16:74847234-74847284	PrEC	prostate:	n/a
37	chr16:74847234-74847284	AoSMC	blood vessel:	n/a
38	chr16:74847234-74847284	HCF	heart:	n/a
39	chr16:74847234-74847284	MCF-7	breast:	n/a
40	chr16:74847234-74847284	Hepatocyte	liver:	n/a
41	chr16:74847234-74847284	HepG2	liver:	n/a
42	chr16:74847234-74847284	HEK293	kidney:	embryo
43	chr16:74847234-74847284	ECC-1	luminal epithelium:	n/a
44	chr16:74847234-74847284	HPAEpiC	pulmonary alveolar:	n/a
45	chr16:74847234-74847284	LNCaP	prostate:	n/a
46	chr16:74847234-74847284	AG09309	skin:	n/a
47	chr16:74847234-74847284	GM19239	blood:	n/a
48	chr16:74847234-74847284	SAEC	small airway:	n/a
49	chr16:74847234-74847284	PFSK-1	brain:	n/a
50	chr16:74847234-74847284	HCPEpiC	choroid plexus:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:74808038..74810939-chr16:74829216..74831740,2	MCF-7	breast:
2	chr16:74742777..74743959-chr16:74846396..74847939,16	MCF-7	breast:
3	chr16:74847751..74849473-chr16:74850843..74852737,2	K562	blood:
4	chr16:74846831..74847572-chr16:74877008..74877733,2	MCF-7	breast:
5	chr16:74846710..74847551-chr16:75232890..75233892,3	K562	blood:
6	chr16:74860827..74863318-chr16:74864140..74866083,2	K562	blood:
7	chr16:74855986..74858386-chr16:74860798..74864514,4	K562	blood:
8	chr16:74743093..74743916-chr16:74851394..74852427,4	MCF-7	breast:
9	chr16:74859894..74862181-chr16:74872505..74874523,2	MCF-7	breast:
10	chr16:74343503..74344314-chr16:74847131..74847664,2	MCF-7	breast:
11	chr16:74780872..74781750-chr16:74846558..74847234,2	MCF-7	breast:
12	chr16:74855986..74858386-chr16:74860798..74864514,4	K562	blood:
13	chr16:74743044..74744187-chr16:74846300..74847985,46	MCF-7	breast:
14	chr16:74846668..74847725-chr16:74896168..74897246,10	MCF-7	breast:
15	chr16:74743065..74743952-chr16:74848682..74849480,2	MCF-7	breast:
16	chr16:74858319..74860749-chr16:74866182..74868876,2	K562	blood:
17	chr16:74846943..74848881-chr16:75143299..75145856,2	MCF-7	breast:
18	chr16:74860827..74863318-chr16:74864140..74866083,2	K562	blood:
19	chr16:74847095..74847642-chr20:56197443..56198071,2	MCF-7	breast:
20	chr16:74858744..74860802-chr16:74886371..74889370,2	MCF-7	breast:
21	chr16:74851640..74852331-chr16:74896396..74897214,3	MCF-7	breast:
22	chr16:74850480..74851199-chr20:57230832..57231666,2	MCF-7	breast:
23	chr16:74743004..74743985-chr16:74846664..74847648,5	K562	blood:
24	chr16:74850528..74853540-chr16:74856738..74859364,3	MCF-7	breast:
25	chr16:74846819..74847580-chr16:74875766..74876759,2	K562	blood:
26	chr16:74859894..74862181-chr16:74872505..74874523,2	MCF-7	breast:
27	chr16:74733905..74734725-chr16:74846845..74847676,2	MCF-7	breast:
28	chr16:74811119..74813847-chr16:74847570..74850500,2	MCF-7	breast:
29	chr16:74858319..74860749-chr16:74866182..74868876,2	K562	blood:
30	chr16:74846696..74847406-chr16:74895112..74895797,2	MCF-7	breast:
31	chr16:74847751..74849473-chr16:74850843..74852737,2	K562	blood:
32	chr16:74846723..74847755-chr16:74896368..74897323,9	K562	blood:
33	chr16:74743104..74743954-chr16:74851839..74852353,2	MCF-7	breast:
34	chr16:74701971..74704127-chr16:74845160..74847638,2	MCF-7	breast:
35	chr16:74847093..74847652-chr16:75164460..75164989,2	MCF-7	breast:
36	chr16:74850528..74853540-chr16:74856738..74859364,3	MCF-7	breast:
37	chr16:74808159..74809197-chr16:74846688..74848115,4	K562	blood:
38	chr16:74800666..74801203-chr16:74846970..74847645,2	MCF-7	breast:
39	chr16:74846665..74847640-chr16:74896133..74897263,15	MCF-7	breast:
40	chr16:74825438..74827028-chr16:74828952..74830642,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000261458	TF binding region
ENSG00000261458	CpG island
ENSG00000261458	chromatin interactions
ENSG00000103089	chromatin interactions
ENSG00000247033	chromatin interactions
ENSG00000259972	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000263661	chromatin interactions

Extended variants
information (count: 2016 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147268937	chr16:74829005-74829006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185577025	chr16:74829007-74829008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376199493	chr16:74829017-74829018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140830738	chr16:74829027-74829028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386792132	chr16:74829050-74829051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111672471	chr16:74829051-74829052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1557906	chr16:74829052-74829053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs141398816	chr16:74829056-74829057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565487821	chr16:74829066-74829067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76714925	chr16:74829068-74829069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557367290	chr16:74829069-74829070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571415373	chr16:74829112-74829113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537371678	chr16:74829115-74829116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139387786	chr16:74829159-74829160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557168738	chr16:74829264-74829265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113714001	chr16:74829282-74829283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189306290	chr16:74829299-74829300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145432886	chr16:74829314-74829315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573401288	chr16:74829315-74829316	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566725180	chr16:74829329-74829330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565303589	chr16:74829340-74829341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1013978	chr16:74829373-74829374	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs544899628	chr16:74829375-74829376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs180829314	chr16:74829445-74829446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1557907	chr16:74829450-74829451	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546821160	chr16:74829461-74829462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140117777	chr16:74829500-74829501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528191308	chr16:74829505-74829506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143835226	chr16:74829590-74829591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571223746	chr16:74829629-74829630	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536905462	chr16:74829652-74829653	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146445688	chr16:74829655-74829656	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544090055	chr16:74829664-74829665	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567495653	chr16:74829729-74829730	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186285194	chr16:74829735-74829736	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190149408	chr16:74829738-74829739	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs8054422	chr16:74829765-74829766	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs557077582	chr16:74829769-74829770	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76887555	chr16:74829779-74829780	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181381560	chr16:74829813-74829814	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140908386	chr16:74829938-74829939	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576862519	chr16:74829975-74829976	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575587075	chr16:74829994-74829995	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545825392	chr16:74830077-74830078	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544329012	chr16:74830090-74830091	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561606822	chr16:74830108-74830109	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185948145	chr16:74830115-74830116	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs540396550	chr16:74830178-74830179	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190713144	chr16:74830180-74830181	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528126406	chr16:74830242-74830243	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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	21364760	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
Epilepsy	20502679	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74813000-74829800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:74826600-74831000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr16:74827800-74831000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr16:74828200-74829600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr16:74829600-74833400	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr16:74830600-74833000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:74831000-74831400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr16:74831000-74831600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr16:74831200-74833000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
10	chr16:74831400-74833400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr16:74831600-74833400	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr16:74831800-74833000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr16:74832000-74833000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr16:74832200-74833400	Active TSS	iPS-18 Cell Line	embryonic stem cell
15	chr16:74832400-74832800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:74832800-74833400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr16:74833400-74834200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr16:74833400-74834400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr16:74834200-74834600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
20	chr16:74834200-74835000	Enhancers	HepG2	liver
21	chr16:74834400-74834600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr16:74834400-74835000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
23	chr16:74838600-74845200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr16:74841000-74841600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr16:74841000-74841800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr16:74841000-74842600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
27	chr16:74841200-74841400	ZNF genes & repeats	Thymus	Thymus
28	chr16:74841200-74841800	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr16:74841600-74842000	Weak transcription	Thymus	Thymus
30	chr16:74841800-74846000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:74841800-74846800	Weak transcription	Fetal Intestine Small	intestine
32	chr16:74842000-74842400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
33	chr16:74844400-74847200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr16:74844600-74847600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr16:74844800-74845000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr16:74844800-74845400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr16:74845000-74845200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
38	chr16:74845000-74845200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr16:74845000-74845200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr16:74845000-74846000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr16:74845200-74845400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr16:74845200-74845400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
43	chr16:74845200-74845400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr16:74845200-74845400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr16:74845200-74845800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr16:74845400-74845600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr16:74845400-74845600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr16:74845400-74845600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
49	chr16:74845400-74845600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr16:74845400-74845800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell

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