Variant report

Variant	nsv1059932
Chromosome Location	chr16:32058483-32244472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1691)
CpG islands
(count:1222)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1691 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32131861-32132041	HepG2	liver:	n/a	n/a
2	ATF1	chr16:32194699-32194908	K562	blood:	n/a	n/a
3	BATF	chr16:32144456-32144674	GM12878	blood:	n/a	n/a
4	BATF	chr16:32098574-32098849	GM12878	blood:	n/a	n/a
5	BATF	chr16:32150053-32150293	GM12878	blood:	n/a	n/a
6	BATF	chr16:32102770-32103216	GM12878	blood:	n/a	n/a
7	BATF	chr16:32101215-32101624	GM12878	blood:	n/a	chr16:32101437-32101448
8	BATF	chr16:32100565-32100763	GM12878	blood:	n/a	n/a
9	BATF	chr16:32099023-32099501	GM12878	blood:	n/a	n/a
10	BATF	chr16:32140974-32141195	GM12878	blood:	n/a	n/a
11	BATF	chr16:32144482-32144672	GM12878	blood:	n/a	n/a
12	BATF	chr16:32139079-32139319	GM12878	blood:	n/a	n/a
13	BATF	chr16:32099644-32100206	GM12878	blood:	n/a	n/a
14	BATF	chr16:32133941-32134130	GM12878	blood:	n/a	n/a
15	BATF	chr16:32101090-32101595	GM12878	blood:	n/a	chr16:32101437-32101448
16	BATF	chr16:32108354-32108543	GM12878	blood:	n/a	n/a
17	BATF	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
18	BATF	chr16:32108268-32108476	GM12878	blood:	n/a	n/a
19	BATF	chr16:32105349-32105637	GM12878	blood:	n/a	n/a
20	BATF	chr16:32148154-32148425	GM12878	blood:	n/a	n/a
21	BATF	chr16:32094016-32094261	GM12878	blood:	n/a	chr16:32094090-32094099
22	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
23	BATF	chr16:32102790-32103063	GM12878	blood:	n/a	n/a
24	BATF	chr16:32133244-32133444	GM12878	blood:	n/a	n/a
25	BATF	chr16:32099142-32100510	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:32102926-32103117	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:32148075-32148453	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:32102705-32103427	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:32103295-32103464	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:32118418-32118587	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:32059954-32060170	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:32094551-32094763	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:32148143-32148447	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:32140967-32141255	GM12878	blood:	n/a	chr16:32141015-32141024
35	BCL11A	chr16:32097964-32098220	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:32098612-32098854	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:32099658-32100165	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:32105603-32105910	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:32105229-32105525	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:32106782-32107034	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:32108319-32108554	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:32145107-32145410	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:32135113-32135283	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:32105207-32105577	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:32099052-32099504	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:32099046-32100495	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:32100955-32101646	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:32146932-32147161	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:32133201-32133502	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:32229562-32229735	GM12878	blood:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32127313-32127363	HEEpiC	esophagus:	n/a
2	chr16:32165196-32165246	HIPEpiC	eye:	n/a
3	chr16:32127313-32127363	HEEpiC	esophagus:	n/a
4	chr16:32165196-32165246	HIPEpiC	eye:	n/a
5	chr16:32123983-32124033	NHDF-neo	bronchial:	n/a
6	chr16:32096464-32096514	Hela-S3	cervix:	n/a
7	chr16:32213913-32213963	Hela-S3	cervix:	n/a
8	chr16:32165225-32165275	A549	lung:	n/a
9	chr16:32213944-32213994	MCF-7	breast:	n/a
10	chr16:32127656-32127706	NH-A	brain:	n/a
11	chr16:32201912-32201962	GM12878	blood:	n/a
12	chr16:32212399-32212449	HepG2	liver:	n/a
13	chr16:32095405-32095455	CMK	blood:	n/a
14	chr16:32096464-32096514	PrEC	prostate:	n/a
15	chr16:32097291-32097341	HNPCEpiC	eye:	n/a
16	chr16:32128349-32128399	HCF	heart:	n/a
17	chr16:32096623-32096673	BJ	skin:	n/a
18	chr16:32130303-32130353	HCF	heart:	n/a
19	chr16:32201912-32201962	HepG2	liver:	n/a
20	chr16:32213913-32213963	HCF	heart:	n/a
21	chr16:32178973-32179023	SAEC	small airway:	n/a
22	chr16:32201912-32201962	K562	blood:	n/a
23	chr16:32213913-32213963	SK-N-SH_RA	brain:	n/a
24	chr16:32097291-32097341	AG09319	gingival:	n/a
25	chr16:32212399-32212449	Hepatocyte	liver:	n/a
26	chr16:32127659-32127709	HPAEpiC	pulmonary alveolar:	n/a
27	chr16:32165196-32165246	HCF	heart:	n/a
28	chr16:32165196-32165246	HRCEpiC	kidney:	n/a
29	chr16:32127078-32127128	GM12878	blood:	n/a
30	chr16:32213913-32213963	T-47D	breast:	n/a
31	chr16:32127659-32127709	HCM	heart:	n/a
32	chr16:32097291-32097341	HCPEpiC	choroid plexus:	n/a
33	chr16:32127656-32127706	NT2-D1	testis:	n/a
34	chr16:32165153-32165203	NB4	blood:	n/a
35	chr16:32127078-32127128	NB4	blood:	n/a
36	chr16:32127313-32127363	AG09309	skin:	n/a
37	chr16:32201912-32201962	ovcar-3	ovarian:	n/a
38	chr16:32212399-32212449	IMR90	lung:	fetal
39	chr16:32213944-32213994	IMR90	lung:	fetal
40	chr16:32127659-32127709	AG09319	gingival:	n/a
41	chr16:32127313-32127363	U87	brain:	n/a
42	chr16:32127313-32127363	HCT-116	colon:	n/a
43	chr16:32178973-32179023	NB4	blood:	n/a
44	chr16:32096623-32096673	ovcar-3	ovarian:	n/a
45	chr16:32127656-32127706	A549	lung:	n/a
46	chr16:32127656-32127706	HL-60	blood:	n/a
47	chr16:32096623-32096673	Jurkat	blood:	n/a
48	chr16:32095405-32095455	NHDF-neo	bronchial:	n/a
49	chr16:32127656-32127706	ECC-1	luminal epithelium:	n/a
50	chr16:32127078-32127128	AoSMC	blood vessel:	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC133485.1.1-1	chr16:32199654-32199738	ENSG00000260847.1
2	lnc-AC133485.1.1-1	chr16:32204071-32204851	ENSG00000260847.1
3	lnc-AC133485.1.1-7	chr16:32200583-32200802	NONHSAT141994

No data

Variant related genes	Relation type
ENSG00000223931	TF binding region
ENSG00000260540	TF binding region
ENSG00000260344	TF binding region
ENSG00000260584	TF binding region
ENSG00000260649	TF binding region
IGHV3OR16-9	TF binding region
HERC2P4	TF binding region
ENSG00000260847	TF binding region
ENSG00000261727	TF binding region
IGHV1OR16-3	TF binding region
ENSG00000223931	CpG island
ENSG00000260540	CpG island
ENSG00000260344	CpG island
ENSG00000260584	CpG island
ENSG00000260649	CpG island
IGHV3OR16-9	CpG island
HERC2P4	CpG island
ENSG00000260847	CpG island
ENSG00000261727	CpG island
IGHV1OR16-3	CpG island

Extended variants
information (count: 1425 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:1425 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546319081	chr16:32058660-32058661	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551814989	chr16:32059209-32059210	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs570457121	chr16:32059210-32059211	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531309151	chr16:32059264-32059265	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs549526887	chr16:32059417-32059418	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs568084109	chr16:32059431-32059432	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536135465	chr16:32059469-32059470	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs554554866	chr16:32059521-32059522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs566270669	chr16:32059586-32059587	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs540050697	chr16:32059587-32059588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs558252279	chr16:32059619-32059620	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs113469618	chr16:32059959-32059960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574023865	chr16:32060122-32060123	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs377053334	chr16:32062924-32062925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532997278	chr16:32062943-32062944	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs545334297	chr16:32062944-32062945	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs371442372	chr16:32062951-32062952	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs373351129	chr16:32062956-32062957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs564010297	chr16:32062960-32062961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs530984039	chr16:32063006-32063007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs549568926	chr16:32063090-32063091	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs62052107	chr16:32067876-32067877	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201163368	chr16:32068004-32068005	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113709791	chr16:32068078-32068079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs62052113	chr16:32073093-32073094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs557539597	chr16:32073105-32073106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576064304	chr16:32073218-32073219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs560013468	chr16:32073514-32073515	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199791045	chr16:32073533-32073534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs533338837	chr16:32073540-32073541	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs551930674	chr16:32073567-32073568	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs570191397	chr16:32073582-32073583	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs555476032	chr16:32076566-32076567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573760957	chr16:32076591-32076592	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200177579	chr16:32076624-32076625	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs534456706	chr16:32076675-32076676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs552926487	chr16:32076693-32076694	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs577614284	chr16:32076734-32076735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528285106	chr16:32077605-32077606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546641146	chr16:32077607-32077608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571275471	chr16:32077613-32077614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538754726	chr16:32077628-32077629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200744708	chr16:32077650-32077651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144576359	chr16:32077657-32077658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556521963	chr16:32077658-32077659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113360397	chr16:32077675-32077676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188963603	chr16:32077684-32077685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536542030	chr16:32077696-32077697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554844239	chr16:32077702-32077703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2215566	chr16:32077740-32077741	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:132)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

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

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