Variant report

Variant	nsv905763
Chromosome Location	chr16:31937596-32069996
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	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
2	BATF	chr16:32001426-32001621	GM12878	blood:	n/a	n/a
3	BATF	chr16:31967621-31968011	GM12878	blood:	n/a	n/a
4	BATF	chr16:32007628-32007992	GM12878	blood:	n/a	n/a
5	BATF	chr16:32050371-32050791	GM12878	blood:	n/a	n/a
6	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
7	BCL11A	chr16:32059954-32060170	GM12878	blood:	n/a	n/a
8	BCL11A	chr16:32001120-32001954	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:32001344-32001697	GM12878	blood:	n/a	n/a
10	BCL11A	chr16:31967573-31967758	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:31985679-31985857	HepG2	liver:	n/a	chr16:31985733-31985749
12	CBX3	chr16:32050399-32050591	K562	blood:	n/a	n/a
13	CBX3	chr16:31967467-31967998	K562	blood:	n/a	n/a
14	CBX3	chr16:32007689-32008189	K562	blood:	n/a	n/a
15	CBX3	chr16:32050646-32050949	K562	blood:	n/a	n/a
16	CBX3	chr16:31967501-31967949	K562	blood:	n/a	n/a
17	CEBPB	chr16:31992336-31992524	K562	blood:	n/a	chr16:31992407-31992418
18	CEBPB	chr16:31992231-31992592	K562	blood:	n/a	chr16:31992407-31992418
19	CEBPB	chr16:31992228-31992528	HepG2	liver:	n/a	chr16:31992407-31992418
20	CEBPB	chr16:31939618-31939872	HepG2	liver:	n/a	n/a
21	CEBPB	chr16:31992189-31992618	K562	blood:	n/a	chr16:31992407-31992418
22	CHD2	chr16:32051321-32051488	HepG2	liver:	n/a	n/a
23	CTCF	chr16:32051880-32051891	Lung_OC	lung:	n/a	n/a
24	CTCF	chr16:32049979-32051581	K562	blood:	n/a	chr16:32051440-32051456 chr16:32050439-32050448 chr16:32051444-32051454
25	CTCF	chr16:31967960-31968110	BE2_C	brain:	n/a	n/a
26	CTCF	chr16:31985680-31985830	HCT-116	colon:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
27	CTCF	chr16:32007692-32007970	Medullo	brain:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
28	CTCF	chr16:32050411-32050840	GM12878	blood:	n/a	chr16:32050439-32050448
29	CTCF	chr16:32007770-32007974	MCF-7	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
30	CTCF	chr16:32050280-32050430	GM12864	blood:	n/a	n/a
31	CTCF	chr16:31967680-31967830	Caco-2	colon:	n/a	n/a
32	CTCF	chr16:32007752-32007954	T-47D	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
33	CTCF	chr16:32007740-32007890	AG09309	skin:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854
34	CTCF	chr16:32007740-32007890	HCPEpiC	choroid plexus:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854
35	CTCF	chr16:32000585-32000748	GM19240	blood:	n/a	chr16:32000681-32000702 chr16:32000686-32000704 chr16:32000688-32000701 chr16:32000692-32000701
36	CTCF	chr16:32007589-32008234	A549	lung:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
37	CTCF	chr16:31967620-31967770	GM12864	blood:	n/a	n/a
38	CTCF	chr16:32000574-32000751	GM19238	blood:	n/a	chr16:32000681-32000702 chr16:32000686-32000704 chr16:32000688-32000701 chr16:32000692-32000701
39	CTCF	chr16:32000969-32001112	GM13976	blood:	n/a	n/a
40	CTCF	chr16:32010559-32010596	Lung_OC	lung:	n/a	n/a
41	CTCF	chr16:32050520-32050670	GM12801	blood:	n/a	n/a
42	CTCF	chr16:32007672-32007978	A549	lung:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
43	CTCF	chr16:31975415-31975483	GM10248	blood:	n/a	n/a
44	CTCF	chr16:31985667-31985825	HepG2	liver:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
45	CTCF	chr16:32050560-32050710	GM12866	blood:	n/a	n/a
46	CTCF	chr16:32007760-32007910	GM12869	blood:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901
47	CTCF	chr16:31967620-31967770	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr16:32008148-32008247	LNCaP	prostate:	n/a	n/a
49	CTCF	chr16:31985562-31985918	A549	lung:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
50	CTCF	chr16:31967640-31967790	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31993479-31993529	AG09319	gingival:	n/a
2	chr16:32037687-32037737	NB4	blood:	n/a
3	chr16:31993479-31993529	AG09319	gingival:	n/a
4	chr16:32037687-32037737	NB4	blood:	n/a
5	chr16:31995423-31995473	SK-N-MC	brain:	n/a
6	chr16:32037687-32037737	A549	lung:	n/a
7	chr16:32049224-32049274	Jurkat	blood:	n/a
8	chr16:31995423-31995473	HL-60	blood:	n/a
9	chr16:31993231-31993281	HRPEpiC	eye:	n/a
10	chr16:32037687-32037737	SKMC	muscle:	n/a
11	chr16:31997067-31997117	HRCEpiC	kidney:	n/a
12	chr16:31993231-31993281	NHDF-neo	bronchial:	n/a
13	chr16:31993231-31993281	SK-N-MC	brain:	n/a
14	chr16:31997067-31997117	RPTEC	kidney:	n/a
15	chr16:31993479-31993529	LNCaP	prostate:	n/a
16	chr16:31997067-31997117	IMR90	lung:	fetal
17	chr16:31993479-31993529	MCF-7	breast:	n/a
18	chr16:31997067-31997117	Jurkat	blood:	n/a
19	chr16:31993479-31993529	SAEC	small airway:	n/a
20	chr16:31997067-31997117	HPAEpiC	pulmonary alveolar:	n/a
21	chr16:32049224-32049274	ProgFib	skin:	n/a
22	chr16:32049224-32049274	H1-hESC	embryonic stem cell:	embryo
23	chr16:31997067-31997117	AG09319	gingival:	n/a
24	chr16:32049224-32049274	GM12892	blood:	n/a
25	chr16:31997067-31997117	HEEpiC	esophagus:	n/a
26	chr16:31993479-31993529	GM06990	blood:	n/a
27	chr16:32049224-32049274	Caco-2	colon:	n/a
28	chr16:31993479-31993529	HCM	heart:	n/a
29	chr16:31993231-31993281	SK-N-SH_RA	brain:	n/a
30	chr16:31997067-31997117	HepG2	liver:	n/a
31	chr16:31997067-31997117	SK-N-MC	brain:	n/a
32	chr16:31990956-31991006	U87	brain:	n/a
33	chr16:31995423-31995473	HCPEpiC	choroid plexus:	n/a
34	chr16:32037687-32037737	Hepatocyte	liver:	n/a
35	chr16:31995423-31995473	AG09319	gingival:	n/a
36	chr16:31995423-31995473	T-47D	breast:	n/a
37	chr16:31997067-31997117	BE2_C	brain:	n/a
38	chr16:31997067-31997117	HUVEC	blood vessel:	n/a
39	chr16:31995423-31995473	LNCaP	prostate:	n/a
40	chr16:31990956-31991006	MCF-7	breast:	n/a
41	chr16:32049224-32049274	HCPEpiC	choroid plexus:	n/a
42	chr16:32037687-32037737	AG09309	skin:	n/a
43	chr16:31993231-31993281	AG10803	skin:	n/a
44	chr16:31993231-31993281	GM12878	blood:	n/a
45	chr16:32037687-32037737	IMR90	lung:	fetal
46	chr16:32049224-32049274	RPTEC	kidney:	n/a
47	chr16:32037687-32037737	U87	brain:	n/a
48	chr16:31995423-31995473	GM12892	blood:	n/a
49	chr16:31993231-31993281	SK-N-SH	brain:	n/a
50	chr16:31993479-31993529	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:31926461..31927983-chr16:31935855..31938647,2	K562	blood:
2	chr14:106598214..106598843-chr16:32050606..32051126,2	MCF-7	breast:
3	chr16:31932491..31936311-chr16:31936605..31941493,6	K562	blood:
4	chr16:31932903..31935520-chr16:31946813..31948460,2	K562	blood:
5	chr16:31931465..31935999-chr16:31936605..31940603,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF267-4	chr16:31975124-31975400	NONHSAT141983
2	lnc-ZNF267-3	chr16:31963481-31963794	NONHSAT141978
3	lnc-ZNF267-4	chr16:31972893-31972899	NONHSAT141979
4	lnc-ZNF267-4	chr16:31973257-31973743	NONHSAT141979

Variant related genes	Relation type
ENSG00000261289	TF binding region
ENSG00000223931	TF binding region
ENSG00000260628	TF binding region
ENSG00000197476	TF binding region
IGHV1OR16-1	TF binding region
ENSG00000260218	TF binding region
IGHV1OR16-3	TF binding region
ENSG00000261289	CpG island
ENSG00000223931	CpG island
ENSG00000260628	CpG island
ENSG00000197476	CpG island
IGHV1OR16-1	CpG island
ENSG00000260218	CpG island
IGHV1OR16-3	CpG island

Extended variants
information (count: 569 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12444740	chr16:31937596-31937597	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189501485	chr16:31937628-31937629	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs531775839	chr16:31937654-31937655	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs550577895	chr16:31937750-31937751	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs8057397	chr16:31937762-31937763	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs181042905	chr16:31937826-31937827	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs536005667	chr16:31937827-31937828	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs12599066	chr16:31937829-31937830	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78092483	chr16:31937879-31937880	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs537363480	chr16:31937896-31937897	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs566193842	chr16:31937897-31937898	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs533634188	chr16:31937903-31937904	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs552181304	chr16:31937914-31937915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs184451863	chr16:31937956-31937957	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs188648306	chr16:31937975-31937976	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs181130188	chr16:31937982-31937983	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs537882758	chr16:31938025-31938026	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs556545413	chr16:31938061-31938062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs575233635	chr16:31938079-31938080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs374172140	chr16:31938083-31938084	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs376668483	chr16:31938097-31938098	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs141036807	chr16:31938103-31938104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs560676556	chr16:31938107-31938108	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs534583125	chr16:31938120-31938121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs560849375	chr16:31938147-31938148	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs576690047	chr16:31938185-31938186	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs572717824	chr16:31938197-31938198	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs572685026	chr16:31938198-31938199	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs545976282	chr16:31938212-31938213	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs371572233	chr16:31938214-31938215	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs202113898	chr16:31938227-31938228	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs142950763	chr16:31938242-31938243	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs560694889	chr16:31938285-31938286	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs150827194	chr16:31938303-31938304	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs550162275	chr16:31938307-31938308	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs139275732	chr16:31938319-31938320	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs529950389	chr16:31938372-31938373	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs548120226	chr16:31938452-31938453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs1857943	chr16:31938455-31938456	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533767450	chr16:31938485-31938486	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs551971167	chr16:31938486-31938487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs570543508	chr16:31938517-31938518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs537416413	chr16:31938521-31938522	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs557540412	chr16:31938542-31938543	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs531432751	chr16:31938548-31938549	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs556126489	chr16:31938675-31938676	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs568730057	chr16:31938765-31938766	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs536145626	chr16:31938766-31938767	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs554551042	chr16:31938773-31938774	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs185925388	chr16:31938810-31938811	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31937000-31941600	ZNF genes & repeats	Liver	Liver
2	chr16:31956400-31956800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:31957000-31958800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr16:31962600-31963000	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr16:31962600-31963400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr16:31962800-31963400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr16:31962800-31963600	Enhancers	Primary T cells fromperipheralblood	blood
8	chr16:31962800-31963600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr16:31963200-31963400	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr16:31963200-31964000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr16:31963600-31964200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr16:31964200-31964400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr16:31964200-31964400	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr16:31971800-31972200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr16:32002400-32002800	Enhancers	HepG2	liver
16	chr16:32051200-32051600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr16:32051400-32051600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr16:32051400-32051600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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