Variant report

Variant	esv1851140
Chromosome Location	chr16:31966787-32097285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
2	BATF	chr16:31967621-31968011	GM12878	blood:	n/a	n/a
3	BATF	chr16:32094016-32094261	GM12878	blood:	n/a	chr16:32094090-32094099
4	BATF	chr16:32007628-32007992	GM12878	blood:	n/a	n/a
5	BATF	chr16:32001426-32001621	GM12878	blood:	n/a	n/a
6	BATF	chr16:32050371-32050791	GM12878	blood:	n/a	n/a
7	BATF	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
8	BCL11A	chr16:32094551-32094763	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:32001120-32001954	GM12878	blood:	n/a	n/a
10	BCL11A	chr16:32059954-32060170	GM12878	blood:	n/a	n/a
11	BCL11A	chr16:32001344-32001697	GM12878	blood:	n/a	n/a
12	BCL11A	chr16:31967573-31967758	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:31985679-31985857	HepG2	liver:	n/a	chr16:31985733-31985749
14	CBX3	chr16:32050399-32050591	K562	blood:	n/a	n/a
15	CBX3	chr16:31967467-31967998	K562	blood:	n/a	n/a
16	CBX3	chr16:32050646-32050949	K562	blood:	n/a	n/a
17	CBX3	chr16:32007689-32008189	K562	blood:	n/a	n/a
18	CBX3	chr16:31967501-31967949	K562	blood:	n/a	n/a
19	CEBPB	chr16:31992189-31992618	K562	blood:	n/a	chr16:31992407-31992418
20	CEBPB	chr16:31992336-31992524	K562	blood:	n/a	chr16:31992407-31992418
21	CEBPB	chr16:31992231-31992592	K562	blood:	n/a	chr16:31992407-31992418
22	CEBPB	chr16:31992228-31992528	HepG2	liver:	n/a	chr16:31992407-31992418
23	CEBPB	chr16:32073025-32073229	HepG2	liver:	n/a	chr16:32073200-32073211
24	CHD2	chr16:32051321-32051488	HepG2	liver:	n/a	n/a
25	CTCF	chr16:31990450-31990642	A549	lung:	n/a	chr16:31990549-31990567 chr16:31990555-31990564
26	CTCF	chr16:31967620-31967770	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr16:31985540-31985690	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr16:32007760-32007910	MCF-7	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
29	CTCF	chr16:32054632-32054637	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr16:32007672-32007978	A549	lung:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
31	CTCF	chr16:31967960-31968110	GM12873	blood:	n/a	n/a
32	CTCF	chr16:31985677-31985824	GM13976	blood:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
33	CTCF	chr16:31967620-31967770	HCFaa	heart:	n/a	n/a
34	CTCF	chr16:32002008-32002088	GM20000	blood:	n/a	n/a
35	CTCF	chr16:32000585-32000748	GM19240	blood:	n/a	chr16:32000681-32000702 chr16:32000686-32000704 chr16:32000688-32000701 chr16:32000692-32000701
36	CTCF	chr16:32050560-32050710	GM12871	blood:	n/a	n/a
37	CTCF	chr16:32007752-32007954	T-47D	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
38	CTCF	chr16:32049969-32051693	K562	blood:	n/a	chr16:32051440-32051456 chr16:32050439-32050448 chr16:32051444-32051454
39	CTCF	chr16:31997538-31997580	GM20000	blood:	n/a	n/a
40	CTCF	chr16:31967513-31967834	HepG2	liver:	n/a	n/a
41	CTCF	chr16:32007728-32007949	GM10248	blood:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
42	CTCF	chr16:32007713-32007953	MCF-7	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
43	CTCF	chr16:32050180-32050330	GM12867	blood:	n/a	n/a
44	CTCF	chr16:32050436-32050653	H1-hESC	embryonic stem cell:	n/a	chr16:32050439-32050448
45	CTCF	chr16:31991246-31991322	GM20000	blood:	n/a	n/a
46	CTCF	chr16:32077618-32077836	Medullo	brain:	n/a	chr16:32077744-32077754 chr16:32077740-32077756
47	CTCF	chr16:32050434-32050627	GM13977	blood:	n/a	chr16:32050439-32050448
48	CTCF	chr16:32050915-32051060	Medullo	brain:	n/a	n/a
49	CTCF	chr16:32077699-32077806	GM19238	blood:	n/a	chr16:32077744-32077754 chr16:32077740-32077756
50	CTCF	chr16:32001989-32002005	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32037687-32037737	NH-A	brain:	n/a
2	chr16:32096623-32096673	SAEC	small airway:	n/a
3	chr16:32049224-32049274	Caco-2	colon:	n/a
4	chr16:31997067-31997117	GM06990	blood:	n/a
5	chr16:32095405-32095455	BE2_C	brain:	n/a
6	chr16:31993479-31993529	T-47D	breast:	n/a
7	chr16:31993231-31993281	HRCEpiC	kidney:	n/a
8	chr16:31993231-31993281	HPAEpiC	pulmonary alveolar:	n/a
9	chr16:31995423-31995473	RPTEC	kidney:	n/a
10	chr16:32049224-32049274	SAEC	small airway:	n/a
11	chr16:32096464-32096514	H1-hESC	embryonic stem cell:	embryo
12	chr16:32049224-32049274	IMR90	lung:	fetal
13	chr16:31997067-31997117	NT2-D1	testis:	n/a
14	chr16:32095405-32095455	LNCaP	prostate:	n/a
15	chr16:31990956-31991006	NT2-D1	testis:	n/a
16	chr16:31990956-31991006	H1-hESC	embryonic stem cell:	embryo
17	chr16:31993231-31993281	HRE	kidney:	n/a
18	chr16:32049224-32049274	T-47D	breast:	n/a
19	chr16:32037687-32037737	HCT-116	colon:	n/a
20	chr16:32037687-32037737	PFSK-1	brain:	n/a
21	chr16:31995423-31995473	AG09309	skin:	n/a
22	chr16:31993479-31993529	H1-hESC	embryonic stem cell:	embryo
23	chr16:31993479-31993529	HRPEpiC	eye:	n/a
24	chr16:31993479-31993529	HIPEpiC	eye:	n/a
25	chr16:31990956-31991006	GM06990	blood:	n/a
26	chr16:32049224-32049274	HCM	heart:	n/a
27	chr16:31993479-31993529	ProgFib	skin:	n/a
28	chr16:32049224-32049274	K562	blood:	n/a
29	chr16:32096464-32096514	HNPCEpiC	eye:	n/a
30	chr16:32096623-32096673	BJ	skin:	n/a
31	chr16:32049224-32049274	RPTEC	kidney:	n/a
32	chr16:31993231-31993281	HMEC	breast:	n/a
33	chr16:31995423-31995473	Hela-S3	cervix:	n/a
34	chr16:31993231-31993281	NHBE	bronchial:	n/a
35	chr16:32096623-32096673	HRCEpiC	kidney:	n/a
36	chr16:32037687-32037737	GM19239	blood:	n/a
37	chr16:32095405-32095455	IMR90	lung:	fetal
38	chr16:31995423-31995473	Jurkat	blood:	n/a
39	chr16:32096623-32096673	BE2_C	brain:	n/a
40	chr16:32037687-32037737	SK-N-MC	brain:	n/a
41	chr16:32049224-32049274	AG09319	gingival:	n/a
42	chr16:31997067-31997117	LNCaP	prostate:	n/a
43	chr16:31997067-31997117	HCM	heart:	n/a
44	chr16:32095405-32095455	RPTEC	kidney:	n/a
45	chr16:32049224-32049274	NH-A	brain:	n/a
46	chr16:32049224-32049274	PFSK-1	brain:	n/a
47	chr16:32095405-32095455	HIPEpiC	eye:	n/a
48	chr16:32096623-32096673	GM06990	blood:	n/a
49	chr16:31993479-31993529	HNPCEpiC	eye:	n/a
50	chr16:32096464-32096514	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:106598214..106598843-chr16:32050606..32051126,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF267-4	chr16:31972893-31972899	NONHSAT141979
2	lnc-ZNF267-4	chr16:31975124-31975400	NONHSAT141983
3	lnc-ZNF267-4	chr16:31973257-31973743	NONHSAT141979

Variant related genes	Relation type
ENSG00000223931	TF binding region
ENSG00000260628	TF binding region
ENSG00000197476	TF binding region
IGHV1OR16-1	TF binding region
IGHV3OR16-9	TF binding region
ENSG00000260218	TF binding region
ENSG00000261727	TF binding region
IGHV1OR16-3	TF binding region
ENSG00000223931	CpG island
ENSG00000260628	CpG island
ENSG00000197476	CpG island
IGHV1OR16-1	CpG island
IGHV3OR16-9	CpG island
ENSG00000260218	CpG island
ENSG00000261727	CpG island
IGHV1OR16-3	CpG island

Extended variants
information (count: 608 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7500857	chr16:31971070-31971071	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs7500861	chr16:31971086-31971087	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs113145928	chr16:31971135-31971136	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs369781302	chr16:31971179-31971180	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs201495592	chr16:31971198-31971199	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs182563267	chr16:31971220-31971221	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs150981497	chr16:31971289-31971290	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs552492481	chr16:31971328-31971329	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs571050649	chr16:31971349-31971350	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs199666081	chr16:31971402-31971403	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs537935002	chr16:31971410-31971411	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs556631553	chr16:31971411-31971412	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs568083602	chr16:31971412-31971413	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs535461715	chr16:31971424-31971425	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs536110357	chr16:31971436-31971437	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs554404995	chr16:31971456-31971457	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs554560419	chr16:31971457-31971458	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs572793658	chr16:31971551-31971552	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs368643290	chr16:31971561-31971562	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs371053439	chr16:31971577-31971578	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs187520711	chr16:31971581-31971582	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs577004096	chr16:31971602-31971603	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs543937629	chr16:31971603-31971604	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs537197577	chr16:31971606-31971607	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs367794934	chr16:31971624-31971625	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs62054095	chr16:31971632-31971633	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs62054096	chr16:31971645-31971646	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs574444679	chr16:31971648-31971649	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs188534962	chr16:31971682-31971683	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs191985872	chr16:31971693-31971694	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs113485616	chr16:31971702-31971703	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs147193440	chr16:31971705-31971706	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs149780526	chr16:31971707-31971708	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs62054097	chr16:31971719-31971720	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs146612375	chr16:31971728-31971729	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs199521268	chr16:31971786-31971787	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs527956073	chr16:31971787-31971788	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs552865248	chr16:31971793-31971794	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs564486076	chr16:31971798-31971799	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs367875121	chr16:31971810-31971811	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs558349153	chr16:31971869-31971870	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs112893548	chr16:31971875-31971876	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs71391231	chr16:31971891-31971892	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs568227210	chr16:31971896-31971897	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs535595404	chr16:31971900-31971901	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs375145432	chr16:31971928-31971929	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs370186280	chr16:31971960-31971961	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs565766577	chr16:31971999-31972000	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs533830393	chr16:31972001-31972002	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs558829995	chr16:31972002-31972003	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:127)

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
Breast cancer	21509527	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
Bladder cancer	21909424	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
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31971800-31972200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:32002400-32002800	Enhancers	HepG2	liver
3	chr16:32051200-32051600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr16:32051400-32051600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:32051400-32051600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr16:32077600-32078000	Enhancers	Dnd41	blood
7	chr16:32095200-32095400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
8	chr16:32095400-32096400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
9	chr16:32096000-32096200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr16:32096000-32096200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
12	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
13	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
14	chr16:32096200-32096600	Flanking Bivalent TSS/Enh	Placenta	Placenta
15	chr16:32096200-32096800	Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr16:32096200-32096800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr16:32096200-32097000	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
18	chr16:32096200-32097200	Active TSS	Primary T cells from cord blood	blood
19	chr16:32096200-32097200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
20	chr16:32096200-32097200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
21	chr16:32096200-32097200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr16:32096200-32097200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr16:32096200-32097400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr16:32096200-32097400	Active TSS	Right Atrium	heart
25	chr16:32096200-32097400	Bivalent/Poised TSS	A549	lung
26	chr16:32096200-32097400	Active TSS	Osteobl	bone
27	chr16:32096400-32096600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
28	chr16:32096400-32096600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
29	chr16:32096400-32096600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
30	chr16:32096400-32096800	Bivalent/Poised TSS	Primary B cells from peripheral blood	blood
31	chr16:32096400-32096800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr16:32096400-32096800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr16:32096400-32096800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr16:32096400-32096800	ZNF genes & repeats	Right Ventricle	heart
35	chr16:32096400-32096800	Active TSS	HSMM	muscle
36	chr16:32096400-32097000	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr16:32096400-32097200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:32096400-32097200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr16:32096400-32097200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr16:32096400-32097200	Active TSS	Rectal Smooth Muscle	rectum
41	chr16:32096400-32097400	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr16:32096400-32097600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr16:32096600-32096800	Bivalent Enhancer	Placenta	Placenta
44	chr16:32096600-32097000	Bivalent/Poised TSS	Primary monocytes fromperipheralblood	blood
45	chr16:32096600-32097000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
46	chr16:32096600-32097200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr16:32096800-32097000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
48	chr16:32096800-32097000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr16:32096800-32097000	Bivalent Enhancer	Dnd41	blood
50	chr16:32096800-32097200	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood

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