Variant report

Variant	nsv542907
Chromosome Location	chr16:34956840-35147509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:408)
CpG islands
(count:793)
Chromatin interactive
region (count:1)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr16:35047591-35047687	A549	lung:	n/a	chr16:35047601-35047612
2	CEBPB	chr16:34973700-34973888	HepG2	liver:	n/a	chr16:34973763-34973774
3	CEBPB	chr16:35044569-35044729	K562	blood:	n/a	n/a
4	CEBPB	chr16:35047511-35047736	HepG2	liver:	n/a	chr16:35047601-35047612
5	CEBPB	chr16:35044630-35044830	HepG2	liver:	n/a	chr16:35044752-35044763
6	CEBPB	chr16:35102752-35102851	A549	lung:	n/a	n/a
7	CEBPB	chr16:35138106-35138159	HepG2	liver:	n/a	n/a
8	CEBPB	chr16:35106622-35106825	A549	lung:	n/a	chr16:35106739-35106750
9	CEBPB	chr16:35106565-35106888	HepG2	liver:	n/a	chr16:35106739-35106750
10	CEBPB	chr16:35044480-35044659	IMR90	lung:	n/a	n/a
11	CEBPB	chr16:35087390-35087614	HepG2	liver:	n/a	n/a
12	CEBPB	chr16:35106627-35106872	IMR90	lung:	n/a	chr16:35106739-35106750
13	CTCF	chr16:35143447-35143618	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr16:35143440-35143590	GM06990	blood:	n/a	n/a
15	CTCF	chr16:35043520-35043670	HCT-116	colon:	n/a	n/a
16	CTCF	chr16:35071360-35071510	GM12874	blood:	n/a	n/a
17	CTCF	chr16:35043500-35043650	RPTEC	kidney:	n/a	n/a
18	CTCF	chr16:35143413-35143616	GM12878	blood:	n/a	n/a
19	CTCF	chr16:35143480-35143630	HRE	kidney:	n/a	n/a
20	CTCF	chr16:35128505-35128569	GM13976	blood:	n/a	n/a
21	CTCF	chr16:35143340-35143490	HRE	kidney:	n/a	n/a
22	CTCF	chr16:35043460-35043610	HEK293	kidney:	n/a	n/a
23	CTCF	chr16:35143440-35143590	BE2_C	brain:	n/a	n/a
24	CTCF	chr16:35143440-35143590	K562	blood:	n/a	n/a
25	CTCF	chr16:35143040-35143190	NB4	blood:	n/a	n/a
26	CTCF	chr16:35043580-35043730	NHEK	skin:	n/a	n/a
27	CTCF	chr16:35143460-35143610	K562	blood:	n/a	n/a
28	CTCF	chr16:35143492-35143562	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr16:35135074-35135181	Gliobla	brain:	n/a	n/a
30	CTCF	chr16:35143460-35143610	GM12873	blood:	n/a	n/a
31	CTCF	chr16:35143500-35143650	HPF	lung:	n/a	n/a
32	CTCF	chr16:35043560-35043710	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr16:35043420-35043570	RPTEC	kidney:	n/a	n/a
34	CTCF	chr16:35043840-35043990	HCT-116	colon:	n/a	n/a
35	CTCF	chr16:35043560-35043710	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr16:35038420-35038454	GM10248	blood:	n/a	n/a
37	CTCF	chr16:35143420-35143570	HEK293	kidney:	n/a	n/a
38	CTCF	chr16:35103380-35103530	NHLF	lung:	n/a	n/a
39	CTCF	chr16:35143440-35143590	HL-60	blood:	n/a	n/a
40	CTCF	chr16:35043500-35043650	NB4	blood:	n/a	n/a
41	CTCF	chr16:35143440-35143590	HepG2	liver:	n/a	n/a
42	CTCF	chr16:35143420-35143570	AG10803	skin:	n/a	n/a
43	CTCF	chr16:35143419-35143584	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr16:35143376-35143629	LNCaP	prostate:	n/a	n/a
45	CTCF	chr16:35143360-35143510	HMF	breast:	n/a	n/a
46	CTCF	chr16:35043631-35043636	HepG2	liver:	n/a	n/a
47	CTCF	chr16:35143480-35143630	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr16:35143420-35143570	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr16:35143492-35143571	GM12892	blood:	n/a	n/a
50	CTCF	chr16:35043560-35043710	HEK293	kidney:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34983912-34983962	GM19239	blood:	n/a
2	chr16:35027026-35027076	NH-A	brain:	n/a
3	chr16:35026985-35027035	BE2_C	brain:	n/a
4	chr16:35026985-35027035	SK-N-SH	brain:	n/a
5	chr16:35037569-35037619	AoSMC	blood vessel:	n/a
6	chr16:35027026-35027076	AG04450	lung:	fetal
7	chr16:35037569-35037619	SAEC	small airway:	n/a
8	chr16:35026985-35027035	SAEC	small airway:	n/a
9	chr16:35027418-35027468	SK-N-SH_RA	brain:	n/a
10	chr16:35026985-35027035	SKMC	muscle:	n/a
11	chr16:35027026-35027076	AoSMC	blood vessel:	n/a
12	chr16:34979671-34979721	LNCaP	prostate:	n/a
13	chr16:34979671-34979721	GM12891	blood:	n/a
14	chr16:34983384-34983434	HepG2	liver:	n/a
15	chr16:35037569-35037619	HL-60	blood:	n/a
16	chr16:34979575-34979625	GM12878	blood:	n/a
17	chr16:34983912-34983962	HAEpiC	amniotic membrane:	n/a
18	chr16:35037569-35037619	AG04450	lung:	fetal
19	chr16:34979575-34979625	GM12892	blood:	n/a
20	chr16:34984121-34984171	HEEpiC	esophagus:	n/a
21	chr16:34983384-34983434	MCF-7	breast:	n/a
22	chr16:34984121-34984171	GM12878	blood:	n/a
23	chr16:35026985-35027035	HRCEpiC	kidney:	n/a
24	chr16:35026985-35027035	Hepatocyte	liver:	n/a
25	chr16:35027418-35027468	MCF-7	breast:	n/a
26	chr16:34983384-34983434	PANC-1	pancreas:	n/a
27	chr16:35030232-35030282	SK-N-SH	brain:	n/a
28	chr16:34983615-34983665	H1-hESC	embryonic stem cell:	embryo
29	chr16:35027418-35027468	PFSK-1	brain:	n/a
30	chr16:35030232-35030282	HEEpiC	esophagus:	n/a
31	chr16:35029890-35029940	GM12892	blood:	n/a
32	chr16:35027026-35027076	HEK293	kidney:	embryo
33	chr16:35029997-35030047	RPTEC	kidney:	n/a
34	chr16:34983912-34983962	HCPEpiC	choroid plexus:	n/a
35	chr16:34983912-34983962	AG09309	skin:	n/a
36	chr16:35027026-35027076	ovcar-3	ovarian:	n/a
37	chr16:34979671-34979721	HCF	heart:	n/a
38	chr16:34983615-34983665	HCM	heart:	n/a
39	chr16:35027418-35027468	Hela-S3	cervix:	n/a
40	chr16:34983384-34983434	Hepatocyte	liver:	n/a
41	chr16:35029890-35029940	HMEC	breast:	n/a
42	chr16:34979671-34979721	MCF-7	breast:	n/a
43	chr16:34979575-34979625	SK-N-MC	brain:	n/a
44	chr16:35030232-35030282	ECC-1	luminal epithelium:	n/a
45	chr16:35027418-35027468	HRE	kidney:	n/a
46	chr16:34979575-34979625	LNCaP	prostate:	n/a
47	chr16:34979575-34979625	Jurkat	blood:	n/a
48	chr16:35026985-35027035	Hela-S3	cervix:	n/a
49	chr16:34984121-34984171	Hepatocyte	liver:	n/a
50	chr16:34979671-34979721	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:35133889..35136586-chr16:35136893..35138863,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-30	chr16:34956639-34956900	NONHSAT142221
2	lnc-CTD-2144E22.5.1-35	chr16:35071257-35072103	NONHSAT142246
3	lnc-CTD-2144E22.5.1-36	chr16:35146491-35146887	NONHSAT142249
4	lnc-LINC00273-9	chr16:35019940-35021258	ENSG00000260611.1
5	lnc-LINC00273-33	chr16:35113407-35113869	NONHSAT142247
6	lnc-LINC00273-31	chr16:35036459-35037041	NONHSAT142244

No data

Variant related genes	Relation type
VN1R70P	TF binding region
RNA5SP417	TF binding region
ENSG00000260611	TF binding region
ENSG00000261122	TF binding region
ENSG00000221580	TF binding region
RNA5SP409	TF binding region
RNA5SP419	TF binding region
RNA5SP407	TF binding region
RNA5SP421	TF binding region
RNA5SP406	TF binding region
RNA5SP408	TF binding region
RNA5SP416	TF binding region
RNA5SP410	TF binding region
RNA5SP413	TF binding region
ENSG00000261782	TF binding region
ENSG00000260522	TF binding region
RNA5SP420	TF binding region
RNA5SP423	TF binding region
RNA5SP415	TF binding region
RNA5SP418	TF binding region
RNA5SP422	TF binding region
HMGN2P41	TF binding region
PPP1R1AP2	TF binding region
VN1R70P	CpG island
RNA5SP417	CpG island
ENSG00000260611	CpG island
ENSG00000261122	CpG island
ENSG00000221580	CpG island
RNA5SP409	CpG island
RNA5SP419	CpG island
RNA5SP407	CpG island
RNA5SP421	CpG island
RNA5SP406	CpG island
RNA5SP408	CpG island
RNA5SP416	CpG island
RNA5SP410	CpG island
RNA5SP413	CpG island
ENSG00000261782	CpG island
ENSG00000260522	CpG island
RNA5SP420	CpG island
RNA5SP423	CpG island
RNA5SP415	CpG island
RNA5SP418	CpG island
RNA5SP422	CpG island
HMGN2P41	CpG island
PPP1R1AP2	CpG island
ENSG00000221580	chromatin interactions

Extended variants
information (count: 3916 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3916 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559711053	chr16:34956841-34956842	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs577694980	chr16:34956849-34956850	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs561049469	chr16:34956858-34956859	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs531502736	chr16:34956882-34956883	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs563230413	chr16:34956887-34956888	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs530630536	chr16:34956897-34956898	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs547069855	chr16:34957202-34957203	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs193047928	chr16:34957210-34957211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs116647427	chr16:34957211-34957212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs377044719	chr16:34957224-34957225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs147385997	chr16:34957249-34957250	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs184494769	chr16:34957262-34957263	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs530838257	chr16:34957263-34957264	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs189012954	chr16:34957269-34957270	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs567693257	chr16:34957329-34957330	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs371325824	chr16:34957370-34957371	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs534806031	chr16:34957400-34957401	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs375296012	chr16:34957401-34957402	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs553204134	chr16:34957403-34957404	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs571524645	chr16:34957404-34957405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs181570857	chr16:34957414-34957415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs565717706	chr16:34957444-34957445	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs557004989	chr16:34957469-34957470	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs575163239	chr16:34957484-34957485	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs530306385	chr16:34957488-34957489	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs554646665	chr16:34957491-34957492	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs572609450	chr16:34957499-34957500	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs139437698	chr16:34957526-34957527	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs548503870	chr16:34957531-34957532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs559537350	chr16:34957549-34957550	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs533418351	chr16:34957557-34957558	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs375080012	chr16:34957569-34957570	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs545661245	chr16:34957574-34957575	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs185469069	chr16:34957594-34957595	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs77247399	chr16:34957595-34957596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs549153437	chr16:34957603-34957604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs567713096	chr16:34957616-34957617	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs369888125	chr16:34957665-34957666	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs117676846	chr16:34957687-34957688	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs116059374	chr16:34957693-34957694	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs538872037	chr16:34957694-34957695	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs557213504	chr16:34957712-34957713	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs371843511	chr16:34957718-34957719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs570813172	chr16:34957742-34957743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs535158073	chr16:34957764-34957765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs554277653	chr16:34957845-34957846	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs62059094	chr16:34957865-34957866	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs141651020	chr16:34957875-34957876	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs189058610	chr16:34957888-34957889	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs558258789	chr16:34957898-34957899	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34957200-34958400	ZNF genes & repeats	Dnd41	blood
2	chr16:34959200-34960400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr16:34959400-34959600	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr16:34959600-34965000	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr16:34960200-34960600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr16:34960600-34961000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr16:34960800-34961200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
8	chr16:34961000-34961200	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr16:34961200-34963000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr16:34963000-34964400	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr16:34964400-34965400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr16:34965000-34965800	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr16:34965400-34967400	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr16:34965800-34966800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr16:34966800-34968000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr16:34967200-34969200	Enhancers	NHEK	skin
17	chr16:34968000-34970800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr16:34969000-34970200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:34970000-34971200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr16:34978800-34980400	Enhancers	NHEK	skin
21	chr16:34979800-34989600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr16:34980400-34989000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:34983000-34988400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
24	chr16:34983600-34986400	ZNF genes & repeats	Fetal Stomach	stomach
25	chr16:34984200-34986200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr16:34985600-34986600	Enhancers	NHEK	skin
27	chr16:34987000-34989000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr16:34988800-34989000	ZNF genes & repeats	Brain Germinal Matrix	brain
29	chr16:34999000-35000000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr16:35006800-35009000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr16:35013200-35014000	ZNF genes & repeats	Dnd41	blood
32	chr16:35015200-35015800	Active TSS	Liver	Liver
33	chr16:35017200-35020600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:35018200-35018800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
35	chr16:35021400-35025800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr16:35022000-35023600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr16:35025200-35026200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr16:35025600-35026400	Enhancers	NHEK	skin
39	chr16:35026400-35026600	ZNF genes & repeats	Fetal Brain Female	brain
40	chr16:35029000-35029600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr16:35029600-35030400	ZNF genes & repeats	Placenta	Placenta
42	chr16:35029800-35030000	Enhancers	Stomach Mucosa	stomach
43	chr16:35029800-35030200	ZNF genes & repeats	Lung	lung
44	chr16:35030200-35030400	ZNF genes & repeats	Gastric	stomach
45	chr16:35030400-35031600	Weak transcription	Gastric	stomach
46	chr16:35031600-35031800	Enhancers	Gastric	stomach
47	chr16:35032000-35033000	Enhancers	Stomach Mucosa	stomach
48	chr16:35033200-35033600	Enhancers	Dnd41	blood
49	chr16:35033400-35033600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr16:35033600-35035800	Weak transcription	Dnd41	blood

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