Variant report

Variant	nsv906609
Chromosome Location	chr16:33808566-33922285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3218)
CpG islands
(count:794)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3218 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33881018-33881666	K562	blood:	n/a	n/a
2	ARID3A	chr16:33901370-33901374	HepG2	liver:	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	chr16:33897239-33897401	K562	blood:	n/a	n/a
6	ATF1	chr16:33901083-33901942	K562	blood:	n/a	n/a
7	ATF1	chr16:33887468-33887983	K562	blood:	n/a	n/a
8	ATF1	chr16:33867010-33867345	K562	blood:	n/a	n/a
9	ATF1	chr16:33868495-33868781	K562	blood:	n/a	n/a
10	ATF1	chr16:33864913-33866753	K562	blood:	n/a	n/a
11	ATF1	chr16:33876587-33876956	K562	blood:	n/a	n/a
12	ATF1	chr16:33892137-33892513	K562	blood:	n/a	n/a
13	ATF1	chr16:33873877-33874488	K562	blood:	n/a	n/a
14	ATF1	chr16:33881172-33881547	K562	blood:	n/a	n/a
15	ATF1	chr16:33899829-33900096	K562	blood:	n/a	n/a
16	ATF1	chr16:33888415-33888877	K562	blood:	n/a	n/a
17	ATF1	chr16:33894835-33895202	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	chr16:33882407-33882780	K562	blood:	n/a	n/a
22	BACH1	chr16:33878317-33878646	K562	blood:	n/a	n/a
23	BACH1	chr16:33897806-33898180	K562	blood:	n/a	n/a
24	BACH1	chr16:33898568-33899292	K562	blood:	n/a	n/a
25	BACH1	chr16:33922161-33923902	K562	blood:	n/a	n/a
26	BACH1	chr16:33893536-33894076	K562	blood:	n/a	n/a
27	BATF	chr16:33869606-33871000	GM12878	blood:	n/a	n/a
28	BATF	chr16:33894776-33898245	GM12878	blood:	n/a	n/a
29	BATF	chr16:33910292-33910548	GM12878	blood:	n/a	n/a
30	BATF	chr16:33867631-33869299	GM12878	blood:	n/a	n/a
31	BATF	chr16:33901240-33901937	GM12878	blood:	n/a	n/a
32	BATF	chr16:33887249-33889708	GM12878	blood:	n/a	n/a
33	BATF	chr16:33882407-33883225	GM12878	blood:	n/a	n/a
34	BATF	chr16:33880912-33881916	GM12878	blood:	n/a	n/a
35	BATF	chr16:33867583-33868446	GM12878	blood:	n/a	n/a
36	BATF	chr16:33881917-33883249	GM12878	blood:	n/a	n/a
37	BATF	chr16:33871196-33873362	GM12878	blood:	n/a	n/a
38	BATF	chr16:33892544-33893480	GM12878	blood:	n/a	n/a
39	BATF	chr16:33875433-33876983	GM12878	blood:	n/a	n/a
40	BATF	chr16:33886617-33887161	GM12878	blood:	n/a	n/a
41	BATF	chr16:33879131-33880895	GM12878	blood:	n/a	n/a
42	BATF	chr16:33868456-33869286	GM12878	blood:	n/a	n/a
43	BATF	chr16:33913665-33913949	GM12878	blood:	n/a	n/a
44	BATF	chr16:33876484-33877068	GM12878	blood:	n/a	n/a
45	BATF	chr16:33875367-33876259	GM12878	blood:	n/a	n/a
46	BATF	chr16:33887300-33888728	GM12878	blood:	n/a	n/a
47	BATF	chr16:33873918-33875113	GM12878	blood:	n/a	n/a
48	BATF	chr16:33877955-33879121	GM12878	blood:	n/a	n/a
49	BATF	chr16:33880945-33881911	GM12878	blood:	n/a	n/a
50	BATF	chr16:33864717-33866793	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33853473-33853523	U87	brain:	n/a
2	chr16:33853473-33853523	U87	brain:	n/a
3	chr16:33815990-33816040	PrEC	prostate:	n/a
4	chr16:33853473-33853523	AoSMC	blood vessel:	n/a
5	chr16:33851284-33851334	SK-N-SH_RA	brain:	n/a
6	chr16:33852801-33852851	HepG2	liver:	n/a
7	chr16:33853473-33853523	NHDF-neo	bronchial:	n/a
8	chr16:33817129-33817179	HL-60	blood:	n/a
9	chr16:33817457-33817507	SK-N-SH_RA	brain:	n/a
10	chr16:33852801-33852851	NHBE	bronchial:	n/a
11	chr16:33818253-33818303	HL-60	blood:	n/a
12	chr16:33852801-33852851	HRPEpiC	eye:	n/a
13	chr16:33818253-33818303	T-47D	breast:	n/a
14	chr16:33817457-33817507	HRCEpiC	kidney:	n/a
15	chr16:33817992-33818042	BE2_C	brain:	n/a
16	chr16:33817457-33817507	Jurkat	blood:	n/a
17	chr16:33817992-33818042	T-47D	breast:	n/a
18	chr16:33818253-33818303	HCF	heart:	n/a
19	chr16:33853544-33853594	HepG2	liver:	n/a
20	chr16:33853544-33853594	NT2-D1	testis:	n/a
21	chr16:33817129-33817179	MCF10A-Er-Src	breast:	n/a
22	chr16:33817129-33817179	GM06990	blood:	n/a
23	chr16:33815990-33816040	HPAEpiC	pulmonary alveolar:	n/a
24	chr16:33818253-33818303	HepG2	liver:	n/a
25	chr16:33815990-33816040	RPTEC	kidney:	n/a
26	chr16:33815990-33816040	ProgFib	skin:	n/a
27	chr16:33851284-33851334	PrEC	prostate:	n/a
28	chr16:33818253-33818303	SKMC	muscle:	n/a
29	chr16:33821339-33821389	GM06990	blood:	n/a
30	chr16:33817129-33817179	Hela-S3	cervix:	n/a
31	chr16:33852823-33852873	PFSK-1	brain:	n/a
32	chr16:33851284-33851334	Hela-S3	cervix:	n/a
33	chr16:33852801-33852851	RPTEC	kidney:	n/a
34	chr16:33853176-33853226	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:33853473-33853523	HepG2	liver:	n/a
36	chr16:33817129-33817179	HCT-116	colon:	n/a
37	chr16:33852823-33852873	NHBE	bronchial:	n/a
38	chr16:33851284-33851334	HUVEC	blood vessel:	n/a
39	chr16:33854086-33854136	NHBE	bronchial:	n/a
40	chr16:33815990-33816040	CMK	blood:	n/a
41	chr16:33851284-33851334	HEEpiC	esophagus:	n/a
42	chr16:33815990-33816040	Hepatocyte	liver:	n/a
43	chr16:33817129-33817179	HepG2	liver:	n/a
44	chr16:33818253-33818303	AG09309	skin:	n/a
45	chr16:33853473-33853523	MCF10A-Er-Src	breast:	n/a
46	chr16:33854086-33854136	HEK293	kidney:	embryo
47	chr16:33821339-33821389	HL-60	blood:	n/a
48	chr16:33821339-33821389	ovcar-3	ovarian:	n/a
49	chr16:33853176-33853226	NHBE	bronchial:	n/a
50	chr16:33852823-33852873	NT2-D1	testis:	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	chr13:95260054..95260733-chr16:33908997..33909498,2	MCF-7	breast:
3	chr16:33883354..33883854-chr16:33895502..33896105,2	MCF-7	breast:
4	chr16:33883354..33883854-chr16:33895502..33896105,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000262561	TF binding region
ENSG00000261197	TF binding region
ENSG00000259990	TF binding region
ENSG00000262561	CpG island
ENSG00000261197	CpG island
ENSG00000259990	CpG island

Extended variants
information (count: 7539 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:7539 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113202404	chr16:33813348-33813349	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs368811882	chr16:33815716-33815717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536173785	chr16:33815725-33815726	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554806010	chr16:33815816-33815817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573952170	chr16:33815865-33815866	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs62041135	chr16:33815893-33815894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs535011745	chr16:33815896-33815897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs578132416	chr16:33816036-33816037	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs575758900	chr16:33816183-33816184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs542955433	chr16:33816186-33816187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs561625067	chr16:33816187-33816188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs528114998	chr16:33816210-33816211	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs546172834	chr16:33816227-33816228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs564670084	chr16:33816233-33816234	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532102047	chr16:33816238-33816239	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs550229256	chr16:33816254-33816255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs199824958	chr16:33816260-33816261	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs543197040	chr16:33816433-33816434	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs554998176	chr16:33816436-33816437	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs573463160	chr16:33816441-33816442	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs148229689	chr16:33816486-33816487	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs368226338	chr16:33816530-33816531	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs368080201	chr16:33817016-33817017	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs536474830	chr16:33817066-33817067	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs558927606	chr16:33817138-33817139	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
26	rs555168909	chr16:33817142-33817143	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
27	rs112036591	chr16:33817150-33817151	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
28	rs113386231	chr16:33817152-33817153	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
29	rs9937206	chr16:33817159-33817160	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
30	rs187637957	chr16:33817166-33817167	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
31	rs540536201	chr16:33817174-33817175	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
32	rs558781098	chr16:33817199-33817200	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs576475326	chr16:33817211-33817212	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs543793595	chr16:33817234-33817235	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs562476059	chr16:33817243-33817244	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs529773985	chr16:33817250-33817251	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs371797177	chr16:33817258-33817259	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs560310216	chr16:33817273-33817274	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs113789033	chr16:33817276-33817277	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs527440563	chr16:33817305-33817306	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs192779443	chr16:33817341-33817342	ZNF genes & repeats Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs144669438	chr16:33817391-33817392	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs4887714	chr16:33817400-33817401	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs532584746	chr16:33817411-33817412	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs111668882	chr16:33817429-33817430	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs148544522	chr16:33817480-33817481	Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs550931853	chr16:33817490-33817491	Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs151198174	chr16:33817519-33817520	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs569132225	chr16:33817553-33817554	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs536770104	chr16:33817554-33817555	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33817000-33817200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
2	chr16:33817000-33817400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:33817000-33818000	Bivalent Enhancer	Placenta	Placenta
4	chr16:33817600-33817800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
5	chr16:33836400-33836800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:33852200-33852400	Active TSS	Brain Hippocampus Middle	brain
7	chr16:33852400-33852600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
8	chr16:33852600-33853400	Flanking Bivalent TSS/Enh	Placenta	Placenta
9	chr16:33852800-33854000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:33853000-33853600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
11	chr16:33853400-33853600	Bivalent Enhancer	Placenta	Placenta
12	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr16:33856800-33857800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr16:33862200-33862400	Enhancers	Esophagus	oesophagus
16	chr16:33862400-33864600	Weak transcription	Esophagus	oesophagus
17	chr16:33864400-33868800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr16:33864400-33868800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr16:33864600-33868800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr16:33864600-33868800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr16:33864600-33868800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr16:33864600-33868800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr16:33864600-33868800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr16:33864600-33868800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
25	chr16:33864600-33868800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
26	chr16:33864600-33868800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr16:33864600-33868800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
28	chr16:33864600-33868800	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr16:33864600-33868800	ZNF genes & repeats	Brain Anterior Caudate	brain
30	chr16:33864600-33868800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
31	chr16:33864600-33868800	ZNF genes & repeats	Colonic Mucosa	Colon
32	chr16:33864600-33868800	ZNF genes & repeats	Colon Smooth Muscle	Colon
33	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
34	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
35	chr16:33864600-33868800	ZNF genes & repeats	Esophagus	oesophagus
36	chr16:33864600-33868800	ZNF genes & repeats	Fetal Kidney	kidney
37	chr16:33864600-33868800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
38	chr16:33864600-33868800	ZNF genes & repeats	Gastric	stomach
39	chr16:33864600-33868800	ZNF genes & repeats	Dnd41	blood
40	chr16:33864600-33868800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
41	chr16:33864800-33866800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr16:33864800-33866800	ZNF genes & repeats	HSMMtube	muscle
43	chr16:33864800-33866800	ZNF genes & repeats	NHEK	skin
44	chr16:33864800-33868600	ZNF genes & repeats	Primary B cells from cord blood	blood
45	chr16:33864800-33868600	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
46	chr16:33864800-33868600	ZNF genes & repeats	Fetal Muscle Leg	muscle
47	chr16:33864800-33868600	ZNF genes & repeats	Fetal Stomach	stomach
48	chr16:33864800-33868600	ZNF genes & repeats	Lung	lung
49	chr16:33864800-33868600	ZNF genes & repeats	Hela-S3	cervix
50	chr16:33864800-33868800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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