Variant report

Variant	nsv572294
Chromosome Location	chr16:33795687-33903652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3019)
CpG islands
(count:793)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3019 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

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	chr16:33866004-33866743	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:33901370-33901374	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:33892139-33892507	HepG2	liver:	n/a	n/a
5	ATF1	chr16:33867010-33867345	K562	blood:	n/a	n/a
6	ATF1	chr16:33887468-33887983	K562	blood:	n/a	n/a
7	ATF1	chr16:33888415-33888877	K562	blood:	n/a	n/a
8	ATF1	chr16:33873877-33874488	K562	blood:	n/a	n/a
9	ATF1	chr16:33894835-33895202	K562	blood:	n/a	n/a
10	ATF1	chr16:33876587-33876956	K562	blood:	n/a	n/a
11	ATF1	chr16:33899829-33900096	K562	blood:	n/a	n/a
12	ATF1	chr16:33868495-33868781	K562	blood:	n/a	n/a
13	ATF1	chr16:33881172-33881547	K562	blood:	n/a	n/a
14	ATF1	chr16:33892137-33892513	K562	blood:	n/a	n/a
15	ATF1	chr16:33864913-33866753	K562	blood:	n/a	n/a
16	ATF1	chr16:33897239-33897401	K562	blood:	n/a	n/a
17	ATF1	chr16:33901083-33901942	K562	blood:	n/a	n/a
18	ATF3	chr16:33865168-33865377	K562	blood:	n/a	n/a
19	ATF3	chr16:33866335-33866504	K562	blood:	n/a	n/a
20	ATF3	chr16:33865448-33865613	K562	blood:	n/a	n/a
21	BACH1	chr16:33897806-33898180	K562	blood:	n/a	n/a
22	BACH1	chr16:33882407-33882780	K562	blood:	n/a	n/a
23	BACH1	chr16:33878317-33878646	K562	blood:	n/a	n/a
24	BACH1	chr16:33893536-33894076	K562	blood:	n/a	n/a
25	BACH1	chr16:33898568-33899292	K562	blood:	n/a	n/a
26	BATF	chr16:33867583-33868446	GM12878	blood:	n/a	n/a
27	BATF	chr16:33901240-33901937	GM12878	blood:	n/a	n/a
28	BATF	chr16:33894776-33898245	GM12878	blood:	n/a	n/a
29	BATF	chr16:33901075-33902389	GM12878	blood:	n/a	n/a
30	BATF	chr16:33875433-33876983	GM12878	blood:	n/a	n/a
31	BATF	chr16:33869540-33870442	GM12878	blood:	n/a	n/a
32	BATF	chr16:33889778-33891707	GM12878	blood:	n/a	n/a
33	BATF	chr16:33875367-33876259	GM12878	blood:	n/a	n/a
34	BATF	chr16:33880912-33881916	GM12878	blood:	n/a	n/a
35	BATF	chr16:33877955-33879121	GM12878	blood:	n/a	n/a
36	BATF	chr16:33898612-33900916	GM12878	blood:	n/a	n/a
37	BATF	chr16:33895519-33897145	GM12878	blood:	n/a	n/a
38	BATF	chr16:33882407-33883225	GM12878	blood:	n/a	n/a
39	BATF	chr16:33864717-33866793	GM12878	blood:	n/a	n/a
40	BATF	chr16:33867631-33869299	GM12878	blood:	n/a	n/a
41	BATF	chr16:33873918-33875113	GM12878	blood:	n/a	n/a
42	BATF	chr16:33880945-33881911	GM12878	blood:	n/a	n/a
43	BATF	chr16:33871196-33873362	GM12878	blood:	n/a	n/a
44	BATF	chr16:33886617-33887161	GM12878	blood:	n/a	n/a
45	BATF	chr16:33887300-33888728	GM12878	blood:	n/a	n/a
46	BATF	chr16:33884688-33885990	GM12878	blood:	n/a	n/a
47	BATF	chr16:33876484-33877068	GM12878	blood:	n/a	n/a
48	BATF	chr16:33881917-33883249	GM12878	blood:	n/a	n/a
49	BATF	chr16:33864424-33867460	GM12878	blood:	n/a	n/a
50	BATF	chr16:33892544-33893480	GM12878	blood:	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	chr16:33853544-33853594	SK-N-SH_RA	brain:	n/a
2	chr16:33852801-33852851	K562	blood:	n/a
3	chr16:33852823-33852873	MCF10A-Er-Src	breast:	n/a
4	chr16:33853473-33853523	HL-60	blood:	n/a
5	chr16:33853544-33853594	HAEpiC	amniotic membrane:	n/a
6	chr16:33853473-33853523	PANC-1	pancreas:	n/a
7	chr16:33854086-33854136	T-47D	breast:	n/a
8	chr16:33821339-33821389	HL-60	blood:	n/a
9	chr16:33815990-33816040	HCF	heart:	n/a
10	chr16:33854086-33854136	HL-60	blood:	n/a
11	chr16:33853176-33853226	HNPCEpiC	eye:	n/a
12	chr16:33854086-33854136	H1-hESC	embryonic stem cell:	embryo
13	chr16:33852823-33852873	AoSMC	blood vessel:	n/a
14	chr16:33815990-33816040	ECC-1	luminal epithelium:	n/a
15	chr16:33852823-33852873	PFSK-1	brain:	n/a
16	chr16:33853176-33853226	GM19239	blood:	n/a
17	chr16:33853544-33853594	AG10803	skin:	n/a
18	chr16:33852801-33852851	HNPCEpiC	eye:	n/a
19	chr16:33853176-33853226	NT2-D1	testis:	n/a
20	chr16:33821339-33821389	T-47D	breast:	n/a
21	chr16:33815990-33816040	GM06990	blood:	n/a
22	chr16:33821339-33821389	HepG2	liver:	n/a
23	chr16:33821339-33821389	AG09309	skin:	n/a
24	chr16:33853473-33853523	HIPEpiC	eye:	n/a
25	chr16:33853544-33853594	U87	brain:	n/a
26	chr16:33853473-33853523	NHBE	bronchial:	n/a
27	chr16:33853176-33853226	ProgFib	skin:	n/a
28	chr16:33821339-33821389	Hepatocyte	liver:	n/a
29	chr16:33852801-33852851	AG09309	skin:	n/a
30	chr16:33854086-33854136	U87	brain:	n/a
31	chr16:33818253-33818303	HRCEpiC	kidney:	n/a
32	chr16:33852801-33852851	HEEpiC	esophagus:	n/a
33	chr16:33853176-33853226	T-47D	breast:	n/a
34	chr16:33852823-33852873	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:33853473-33853523	RPTEC	kidney:	n/a
36	chr16:33852823-33852873	HEEpiC	esophagus:	n/a
37	chr16:33851284-33851334	U87	brain:	n/a
38	chr16:33818253-33818303	SK-N-SH	brain:	n/a
39	chr16:33853176-33853226	LNCaP	prostate:	n/a
40	chr16:33817992-33818042	BE2_C	brain:	n/a
41	chr16:33817992-33818042	BJ	skin:	n/a
42	chr16:33851284-33851334	SK-N-SH_RA	brain:	n/a
43	chr16:33852823-33852873	LNCaP	prostate:	n/a
44	chr16:33851284-33851334	GM06990	blood:	n/a
45	chr16:33853544-33853594	GM06990	blood:	n/a
46	chr16:33852801-33852851	MCF-7	breast:	n/a
47	chr16:33852801-33852851	MCF10A-Er-Src	breast:	n/a
48	chr16:33815990-33816040	NT2-D1	testis:	n/a
49	chr16:33821339-33821389	GM12891	blood:	n/a
50	chr16:33821339-33821389	AG09319	gingival:	n/a

(count:3 , 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:

No data

Variant related genes	Relation type
ENSG00000261217	TF binding region
ENSG00000261197	TF binding region
ENSG00000259990	TF binding region
ENSG00000261217	CpG island
ENSG00000261197	CpG island
ENSG00000259990	CpG island

Extended variants
information (count: 5724 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:5724 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386790385	chr16:33795687-33795688	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2562076	chr16:33795689-33795690	Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574781020	chr16:33795697-33795698	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541455725	chr16:33795717-33795718	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs559741469	chr16:33795748-33795749	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs527247862	chr16:33795756-33795757	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577017051	chr16:33795772-33795773	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564163102	chr16:33795786-33795787	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377449908	chr16:33795791-33795792	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs371189028	chr16:33795800-33795801	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549993619	chr16:33795806-33795807	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs376007631	chr16:33795864-33795865	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2549345	chr16:33795894-33795895	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs2549344	chr16:33795939-33795940	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs690328	chr16:33795964-33795965	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs535726991	chr16:33795974-33795975	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs547685263	chr16:33795978-33795979	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs605259	chr16:33795987-33795988	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs566767241	chr16:33795988-33795989	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534155980	chr16:33795998-33795999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558784833	chr16:33796002-33796003	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs577262784	chr16:33796016-33796017	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs538086626	chr16:33796026-33796027	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs370662572	chr16:33796082-33796083	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs541265496	chr16:33796087-33796088	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs139642113	chr16:33796098-33796099	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs553031483	chr16:33796102-33796103	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs574818838	chr16:33796103-33796104	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs574619347	chr16:33796125-33796126	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542134694	chr16:33796156-33796157	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs181628480	chr16:33796157-33796158	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs571952524	chr16:33796197-33796198	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545783638	chr16:33796209-33796210	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs564067000	chr16:33796222-33796223	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs531419690	chr16:33796337-33796338	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs146256097	chr16:33796384-33796385	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs139121598	chr16:33796387-33796388	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs561887748	chr16:33796400-33796401	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs541832101	chr16:33796434-33796435	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547721581	chr16:33796471-33796472	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs565919966	chr16:33796495-33796496	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113985667	chr16:33796521-33796522	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs527730298	chr16:33796543-33796544	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs552530702	chr16:33796544-33796545	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs570888490	chr16:33796552-33796553	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537925836	chr16:33796605-33796606	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs556209517	chr16:33796661-33796662	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs568326734	chr16:33796662-33796663	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs535609634	chr16:33796707-33796708	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554218115	chr16:33796708-33796709	Active TSS	TF binding region	1 gene(s)	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	22297974	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
Medulloblastoma	21163964	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33795600-33797400	Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr16:33795600-33798000	Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr16:33797400-33798000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr16:33798000-33798200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr16:33798000-33798400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr16:33803800-33804600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr16:33804400-33804800	Enhancers	Left Ventricle	heart
8	chr16:33817000-33817200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
9	chr16:33817000-33817400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:33817000-33818000	Bivalent Enhancer	Placenta	Placenta
11	chr16:33817600-33817800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
12	chr16:33836400-33836800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr16:33852200-33852400	Active TSS	Brain Hippocampus Middle	brain
14	chr16:33852400-33852600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
15	chr16:33852600-33853400	Flanking Bivalent TSS/Enh	Placenta	Placenta
16	chr16:33852800-33854000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:33853000-33853600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
18	chr16:33853400-33853600	Bivalent Enhancer	Placenta	Placenta
19	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr16:33856800-33857800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr16:33862200-33862400	Enhancers	Esophagus	oesophagus
23	chr16:33862400-33864600	Weak transcription	Esophagus	oesophagus
24	chr16:33864400-33868800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
25	chr16:33864400-33868800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr16:33864600-33868800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr16:33864600-33868800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
28	chr16:33864600-33868800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr16:33864600-33868800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
30	chr16:33864600-33868800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr16:33864600-33868800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
32	chr16:33864600-33868800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
33	chr16:33864600-33868800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
34	chr16:33864600-33868800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
35	chr16:33864600-33868800	ZNF genes & repeats	Adipose Nuclei	Adipose
36	chr16:33864600-33868800	ZNF genes & repeats	Brain Anterior Caudate	brain
37	chr16:33864600-33868800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
38	chr16:33864600-33868800	ZNF genes & repeats	Colonic Mucosa	Colon
39	chr16:33864600-33868800	ZNF genes & repeats	Colon Smooth Muscle	Colon
40	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
41	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
42	chr16:33864600-33868800	ZNF genes & repeats	Esophagus	oesophagus
43	chr16:33864600-33868800	ZNF genes & repeats	Fetal Kidney	kidney
44	chr16:33864600-33868800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
45	chr16:33864600-33868800	ZNF genes & repeats	Gastric	stomach
46	chr16:33864600-33868800	ZNF genes & repeats	Dnd41	blood
47	chr16:33864600-33868800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
48	chr16:33864800-33866800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr16:33864800-33866800	ZNF genes & repeats	HSMMtube	muscle
50	chr16:33864800-33866800	ZNF genes & repeats	NHEK	skin

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