Variant report

Variant	nsv906602
Chromosome Location	chr16:33769308-33922285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3428)
CpG islands
(count:1038)
Chromatin interactive
region (count:4)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3428 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33901370-33901374	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33881018-33881666	K562	blood:	n/a	n/a
3	ARID3A	chr16:33892139-33892507	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:33866004-33866743	HepG2	liver:	n/a	n/a
5	ATF1	chr16:33887468-33887983	K562	blood:	n/a	n/a
6	ATF1	chr16:33894835-33895202	K562	blood:	n/a	n/a
7	ATF1	chr16:33873877-33874488	K562	blood:	n/a	n/a
8	ATF1	chr16:33888415-33888877	K562	blood:	n/a	n/a
9	ATF1	chr16:33867010-33867345	K562	blood:	n/a	n/a
10	ATF1	chr16:33881172-33881547	K562	blood:	n/a	n/a
11	ATF1	chr16:33901083-33901942	K562	blood:	n/a	n/a
12	ATF1	chr16:33892137-33892513	K562	blood:	n/a	n/a
13	ATF1	chr16:33897239-33897401	K562	blood:	n/a	n/a
14	ATF1	chr16:33876587-33876956	K562	blood:	n/a	n/a
15	ATF1	chr16:33864913-33866753	K562	blood:	n/a	n/a
16	ATF1	chr16:33899829-33900096	K562	blood:	n/a	n/a
17	ATF1	chr16:33868495-33868781	K562	blood:	n/a	n/a
18	ATF3	chr16:33865448-33865613	K562	blood:	n/a	n/a
19	ATF3	chr16:33865168-33865377	K562	blood:	n/a	n/a
20	ATF3	chr16:33866335-33866504	K562	blood:	n/a	n/a
21	BACH1	chr16:33922161-33923902	K562	blood:	n/a	n/a
22	BACH1	chr16:33893536-33894076	K562	blood:	n/a	n/a
23	BACH1	chr16:33878317-33878646	K562	blood:	n/a	n/a
24	BACH1	chr16:33882407-33882780	K562	blood:	n/a	n/a
25	BACH1	chr16:33897806-33898180	K562	blood:	n/a	n/a
26	BACH1	chr16:33898568-33899292	K562	blood:	n/a	n/a
27	BATF	chr16:33884688-33885990	GM12878	blood:	n/a	n/a
28	BATF	chr16:33880912-33881916	GM12878	blood:	n/a	n/a
29	BATF	chr16:33871196-33873362	GM12878	blood:	n/a	n/a
30	BATF	chr16:33894302-33894717	GM12878	blood:	n/a	n/a
31	BATF	chr16:33899064-33900897	GM12878	blood:	n/a	n/a
32	BATF	chr16:33871808-33872802	GM12878	blood:	n/a	n/a
33	BATF	chr16:33889778-33891707	GM12878	blood:	n/a	n/a
34	BATF	chr16:33875433-33876983	GM12878	blood:	n/a	n/a
35	BATF	chr16:33898612-33900916	GM12878	blood:	n/a	n/a
36	BATF	chr16:33869540-33870442	GM12878	blood:	n/a	n/a
37	BATF	chr16:33880945-33881911	GM12878	blood:	n/a	n/a
38	BATF	chr16:33867631-33869299	GM12878	blood:	n/a	n/a
39	BATF	chr16:33887300-33888728	GM12878	blood:	n/a	n/a
40	BATF	chr16:33876484-33877068	GM12878	blood:	n/a	n/a
41	BATF	chr16:33901240-33901937	GM12878	blood:	n/a	n/a
42	BATF	chr16:33897169-33898148	GM12878	blood:	n/a	n/a
43	BATF	chr16:33882407-33883225	GM12878	blood:	n/a	n/a
44	BATF	chr16:33894776-33898245	GM12878	blood:	n/a	n/a
45	BATF	chr16:33864717-33866793	GM12878	blood:	n/a	n/a
46	BATF	chr16:33873961-33875126	GM12878	blood:	n/a	n/a
47	BATF	chr16:33887249-33889708	GM12878	blood:	n/a	n/a
48	BATF	chr16:33895519-33897145	GM12878	blood:	n/a	n/a
49	BATF	chr16:33894028-33894772	GM12878	blood:	n/a	n/a
50	BATF	chr16:33864424-33867460	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33853176-33853226	SK-N-SH	brain:	n/a
2	chr16:33853176-33853226	SK-N-SH	brain:	n/a
3	chr16:33817992-33818042	GM06990	blood:	n/a
4	chr16:33776910-33776960	NT2-D1	testis:	n/a
5	chr16:33821339-33821389	GM12892	blood:	n/a
6	chr16:33852801-33852851	HCF	heart:	n/a
7	chr16:33851284-33851334	HepG2	liver:	n/a
8	chr16:33853544-33853594	Hepatocyte	liver:	n/a
9	chr16:33851284-33851334	HRE	kidney:	n/a
10	chr16:33815990-33816040	Caco-2	colon:	n/a
11	chr16:33776910-33776960	HEEpiC	esophagus:	n/a
12	chr16:33776910-33776960	HUVEC	blood vessel:	n/a
13	chr16:33776910-33776960	NB4	blood:	n/a
14	chr16:33783802-33783852	U87	brain:	n/a
15	chr16:33852801-33852851	Caco-2	colon:	n/a
16	chr16:33853473-33853523	U87	brain:	n/a
17	chr16:33779917-33779967	ECC-1	luminal epithelium:	n/a
18	chr16:33853544-33853594	HAEpiC	amniotic membrane:	n/a
19	chr16:33783802-33783852	MCF-7	breast:	n/a
20	chr16:33852801-33852851	HAEpiC	amniotic membrane:	n/a
21	chr16:33821339-33821389	HCM	heart:	n/a
22	chr16:33853473-33853523	AoSMC	blood vessel:	n/a
23	chr16:33817992-33818042	AG04450	lung:	fetal
24	chr16:33817992-33818042	HL-60	blood:	n/a
25	chr16:33853544-33853594	LNCaP	prostate:	n/a
26	chr16:33818253-33818303	HMEC	breast:	n/a
27	chr16:33851284-33851334	AoSMC	blood vessel:	n/a
28	chr16:33852801-33852851	U87	brain:	n/a
29	chr16:33852823-33852873	HMEC	breast:	n/a
30	chr16:33815990-33816040	RPTEC	kidney:	n/a
31	chr16:33852823-33852873	LNCaP	prostate:	n/a
32	chr16:33783802-33783852	Caco-2	colon:	n/a
33	chr16:33817457-33817507	Jurkat	blood:	n/a
34	chr16:33817457-33817507	Caco-2	colon:	n/a
35	chr16:33781365-33781415	SK-N-MC	brain:	n/a
36	chr16:33821339-33821389	GM06990	blood:	n/a
37	chr16:33783802-33783852	HRE	kidney:	n/a
38	chr16:33817457-33817507	RPTEC	kidney:	n/a
39	chr16:33817129-33817179	HUVEC	blood vessel:	n/a
40	chr16:33817129-33817179	NHDF-neo	bronchial:	n/a
41	chr16:33817992-33818042	SK-N-MC	brain:	n/a
42	chr16:33853473-33853523	GM12892	blood:	n/a
43	chr16:33853176-33853226	HepG2	liver:	n/a
44	chr16:33817992-33818042	HRCEpiC	kidney:	n/a
45	chr16:33852823-33852873	K562	blood:	n/a
46	chr16:33853544-33853594	Jurkat	blood:	n/a
47	chr16:33853544-33853594	BE2_C	brain:	n/a
48	chr16:33817129-33817179	AG09309	skin:	n/a
49	chr16:33817129-33817179	SKMC	muscle:	n/a
50	chr16:33818253-33818303	LNCaP	prostate:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:42387171..42387692-chr16:33888891..33889406,2	MCF-7	breast:
2	chr16:33883354..33883854-chr16:33895502..33896105,2	MCF-7	breast:
3	chr16:33883354..33883854-chr16:33895502..33896105,2	MCF-7	breast:
4	chr13:95260054..95260733-chr16:33908997..33909498,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
2	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
3	lnc-AC140658.1-6	chr16:33777416-33777550	ENSG00000205452.4
4	lnc-AC140658.1-6	chr16:33776448-33776670	ENSG00000205452.4
5	lnc-AC140658.1-6	chr16:33776833-33776957	ENSG00000205452.4
6	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4
7	lnc-AC140658.1-6	chr16:33775514-33776189	ENSG00000205452.4
8	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4
9	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4

No data

Variant related genes	Relation type
ENSG00000205452	TF binding region
ENSG00000262561	TF binding region
ENSG00000198555	TF binding region
ENSG00000270401	TF binding region
ENSG00000261217	TF binding region
ENSG00000261197	TF binding region
ENSG00000259990	TF binding region
ENSG00000205452	CpG island
ENSG00000262561	CpG island
ENSG00000198555	CpG island
ENSG00000270401	CpG island
ENSG00000261217	CpG island
ENSG00000261197	CpG island
ENSG00000259990	CpG island

Extended variants
information (count: 7967 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:7967 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541840304	chr16:33771130-33771131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs560673638	chr16:33771136-33771137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572444661	chr16:33771152-33771153	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs546381419	chr16:33771189-33771190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs564299158	chr16:33771281-33771282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572510294	chr16:33771832-33771833	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs545856935	chr16:33771849-33771850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146869809	chr16:33773732-33773733	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs62040311	chr16:33773747-33773748	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571979498	chr16:33773771-33773772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs539304768	chr16:33773839-33773840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs661389	chr16:33773854-33773855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs557016262	chr16:33773861-33773862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575339732	chr16:33773865-33773866	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542593134	chr16:33773879-33773880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs554410282	chr16:33773893-33773894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs561485544	chr16:33773894-33773895	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs368912729	chr16:33773922-33773923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs531790216	chr16:33773924-33773925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs79432092	chr16:33773925-33773926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs369055419	chr16:33773963-33773964	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564700764	chr16:33774006-33774007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs532291897	chr16:33774046-33774047	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201262271	chr16:33774981-33774982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs561300849	chr16:33775535-33775536	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs186003612	chr16:33775668-33775669	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs140141409	chr16:33775689-33775690	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs112810909	chr16:33775705-33775706	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs547142553	chr16:33775711-33775712	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs571753228	chr16:33775717-33775718	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs532796546	chr16:33775721-33775722	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs563659230	chr16:33775780-33775781	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs138319629	chr16:33775828-33775829	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs551193887	chr16:33775868-33775869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs569454140	chr16:33775891-33775892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs536910778	chr16:33775901-33775902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs201238756	chr16:33775931-33775932	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs566438695	chr16:33775988-33775989	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs533533693	chr16:33776088-33776089	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs381097	chr16:33776093-33776094	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs369423794	chr16:33776125-33776126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs558267041	chr16:33776163-33776164	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs200462161	chr16:33776205-33776206	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs576525015	chr16:33776221-33776222	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs537651964	chr16:33776428-33776429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs555897262	chr16:33776448-33776449	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs574657292	chr16:33776534-33776535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs189793013	chr16:33776864-33776865	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs560165485	chr16:33778670-33778671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs573222040	chr16:33778689-33778690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:905 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33784400-33784800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr16:33784400-33784800	Active TSS	HSMM	muscle
3	chr16:33794600-33795000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr16:33794600-33795600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr16:33795000-33795600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr16:33795600-33797400	Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr16:33795600-33798000	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr16:33797400-33798000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr16:33798000-33798200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr16:33798000-33798400	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr16:33803800-33804600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr16:33804400-33804800	Enhancers	Left Ventricle	heart
13	chr16:33817000-33817200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
14	chr16:33817000-33817400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:33817000-33818000	Bivalent Enhancer	Placenta	Placenta
16	chr16:33817600-33817800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
17	chr16:33836400-33836800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr16:33852200-33852400	Active TSS	Brain Hippocampus Middle	brain
19	chr16:33852400-33852600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
20	chr16:33852600-33853400	Flanking Bivalent TSS/Enh	Placenta	Placenta
21	chr16:33852800-33854000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:33853000-33853600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
23	chr16:33853400-33853600	Bivalent Enhancer	Placenta	Placenta
24	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:33856800-33857800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr16:33862200-33862400	Enhancers	Esophagus	oesophagus
28	chr16:33862400-33864600	Weak transcription	Esophagus	oesophagus
29	chr16:33864400-33868800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr16:33864400-33868800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:33864600-33868800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr16:33864600-33868800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
33	chr16:33864600-33868800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:33864600-33868800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr16:33864600-33868800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr16:33864600-33868800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
37	chr16:33864600-33868800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
38	chr16:33864600-33868800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr16:33864600-33868800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
40	chr16:33864600-33868800	ZNF genes & repeats	Adipose Nuclei	Adipose
41	chr16:33864600-33868800	ZNF genes & repeats	Brain Anterior Caudate	brain
42	chr16:33864600-33868800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
43	chr16:33864600-33868800	ZNF genes & repeats	Colonic Mucosa	Colon
44	chr16:33864600-33868800	ZNF genes & repeats	Colon Smooth Muscle	Colon
45	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
46	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
47	chr16:33864600-33868800	ZNF genes & repeats	Esophagus	oesophagus
48	chr16:33864600-33868800	ZNF genes & repeats	Fetal Kidney	kidney
49	chr16:33864600-33868800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
50	chr16:33864600-33868800	ZNF genes & repeats	Gastric	stomach

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