Variant report

Variant	nsv984234
Chromosome Location	chr16:31574751-31580250
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:368)
Chromatin interactive
region (count:0)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr16:31580242-31580402	IMR90	lung:	n/a	n/a
2	CTCF	chr16:31580200-31580378	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr16:31580248-31580403	Lung_OC	lung:	n/a	n/a
4	CTCF	chr16:31580240-31580390	HRE	kidney:	n/a	n/a
5	CTCF	chr16:31580194-31580418	K562	blood:	n/a	n/a
6	CTCF	chr16:31580183-31580504	K562	blood:	n/a	n/a
7	CTCF	chr16:31580234-31580418	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr16:31580200-31580350	K562	blood:	n/a	n/a
9	CTCF	chr16:31580220-31580370	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr16:31580187-31580453	K562	blood:	n/a	n/a
11	CTCF	chr16:31580220-31580370	AG04449	skin:	n/a	n/a
12	CTCF	chr16:31580246-31580387	NHEK	skin:	n/a	n/a
13	E2F6	chr16:31580034-31580170	K562	blood:	n/a	n/a
14	E2F6	chr16:31579936-31580289	H1-hESC	embryonic stem cell:	n/a	n/a
15	MAX	chr16:31580032-31580225	H1-hESC	embryonic stem cell:	n/a	chr16:31580094-31580109 chr16:31580095-31580106 chr16:31580092-31580107 chr16:31580096-31580105 chr16:31580097-31580106
16	MAX	chr16:31579907-31580169	H1-hESC	embryonic stem cell:	n/a	chr16:31580094-31580109 chr16:31580095-31580106 chr16:31580092-31580107 chr16:31580096-31580105 chr16:31580097-31580106
17	MAX	chr16:31579957-31580186	K562	blood:	n/a	chr16:31580094-31580109 chr16:31580095-31580106 chr16:31580092-31580107 chr16:31580096-31580105 chr16:31580097-31580106
18	POLR2A	chr16:31579807-31579912	MCF-7	breast:	n/a	n/a
19	POLR2A	chr16:31579921-31579928	MCF-7	breast:	n/a	n/a
20	POLR2A	chr16:31575237-31575414	Gliobla	brain:	n/a	n/a
21	RAD21	chr16:31580128-31580483	H1-hESC	embryonic stem cell:	n/a	n/a
22	RAD21	chr16:31580056-31580446	H1-hESC	embryonic stem cell:	n/a	n/a
23	RAD21	chr16:31580230-31580349	K562	blood:	n/a	n/a
24	RAD21	chr16:31580030-31580530	H1-hESC	embryonic stem cell:	n/a	n/a
25	RAD21	chr16:31580214-31580380	K562	blood:	n/a	n/a
26	SP1	chr16:31580212-31580469	H1-hESC	embryonic stem cell:	n/a	chr16:31580229-31580243
27	STAT3	chr16:31580009-31580044	MCF10A-Er-Src	breast:	n/a	n/a
28	USF1	chr16:31579994-31580239	H1-hESC	embryonic stem cell:	n/a	n/a
29	USF1	chr16:31579932-31580307	H1-hESC	embryonic stem cell:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31580150-31580200	SK-N-MC	brain:	n/a
2	chr16:31580150-31580200	MCF-7	breast:	n/a
3	chr16:31580150-31580200	SK-N-MC	brain:	n/a
4	chr16:31580150-31580200	MCF-7	breast:	n/a
5	chr16:31580153-31580203	HRCEpiC	kidney:	n/a
6	chr16:31579805-31579855	HNPCEpiC	eye:	n/a
7	chr16:31576872-31576922	AG04450	lung:	fetal
8	chr16:31576872-31576922	HAEpiC	amniotic membrane:	n/a
9	chr16:31576872-31576922	IMR90	lung:	fetal
10	chr16:31576339-31576389	K562	blood:	n/a
11	chr16:31579647-31579697	GM06990	blood:	n/a
12	chr16:31579647-31579697	SAEC	small airway:	n/a
13	chr16:31576339-31576389	BJ	skin:	n/a
14	chr16:31579805-31579855	HRE	kidney:	n/a
15	chr16:31580150-31580200	HRPEpiC	eye:	n/a
16	chr16:31580150-31580200	RPTEC	kidney:	n/a
17	chr16:31579805-31579855	SK-N-MC	brain:	n/a
18	chr16:31580150-31580200	GM12878	blood:	n/a
19	chr16:31576339-31576389	Hela-S3	cervix:	n/a
20	chr16:31576872-31576922	AG04449	skin:	fetal
21	chr16:31576339-31576389	A549	lung:	n/a
22	chr16:31576872-31576922	SK-N-SH_RA	brain:	n/a
23	chr16:31580153-31580203	AG04450	lung:	fetal
24	chr16:31579647-31579697	U87	brain:	n/a
25	chr16:31576339-31576389	GM12892	blood:	n/a
26	chr16:31579805-31579855	AG09309	skin:	n/a
27	chr16:31580150-31580200	AG09309	skin:	n/a
28	chr16:31576872-31576922	A549	lung:	n/a
29	chr16:31579805-31579855	H1-hESC	embryonic stem cell:	embryo
30	chr16:31580153-31580203	BJ	skin:	n/a
31	chr16:31576872-31576922	HEEpiC	esophagus:	n/a
32	chr16:31579647-31579697	ovcar-3	ovarian:	n/a
33	chr16:31579647-31579697	GM12878	blood:	n/a
34	chr16:31580150-31580200	U87	brain:	n/a
35	chr16:31579647-31579697	HCPEpiC	choroid plexus:	n/a
36	chr16:31580153-31580203	U87	brain:	n/a
37	chr16:31579647-31579697	BJ	skin:	n/a
38	chr16:31579805-31579855	ProgFib	skin:	n/a
39	chr16:31576872-31576922	SK-N-SH	brain:	n/a
40	chr16:31579805-31579855	HMEC	breast:	n/a
41	chr16:31579805-31579855	NT2-D1	testis:	n/a
42	chr16:31576339-31576389	NHDF-neo	bronchial:	n/a
43	chr16:31576872-31576922	SK-N-MC	brain:	n/a
44	chr16:31579647-31579697	AoSMC	blood vessel:	n/a
45	chr16:31580153-31580203	BE2_C	brain:	n/a
46	chr16:31580150-31580200	HCM	heart:	n/a
47	chr16:31576872-31576922	HL-60	blood:	n/a
48	chr16:31576339-31576389	MCF10A-Er-Src	breast:	n/a
49	chr16:31576872-31576922	GM12892	blood:	n/a
50	chr16:31576339-31576389	H1-hESC	embryonic stem cell:	embryo

No data

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141936
2	lnc-C16orf58-6	chr16:31575556-31575606	NONHSAT141935
3	lnc-C16orf58-6	chr16:31574506-31574955	NONHSAT141936
4	lnc-C16orf58-6	chr16:31575929-31576029	NONHSAT141934
5	lnc-C16orf58-6	chr16:31579088-31580845	NONHSAT141938
6	lnc-C16orf58-6	chr16:31575897-31576029	NONHSAT141937
7	lnc-C16orf58-6	chr16:31575929-31576029	NONHSAT141936
8	lnc-C16orf58-6	chr16:31578695-31579197	NONHSAT141937
9	lnc-C16orf58-6	chr16:31574154-31574955	NONHSAT141934
10	lnc-C16orf58-6	chr16:31575924-31576104	NONHSAT141935
11	lnc-C16orf58-6	chr16:31578695-31579037	NONHSAT141936
12	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141934
13	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141935
14	lnc-C16orf58-6	chr16:31574403-31574920	NONHSAT141935
15	lnc-C16orf58-6	chr16:31579707-31580796	NONHSAT141939

No data

Variant related genes	Relation type
ENSG00000261741	TF binding region
ENSG00000261741	CpG island

Extended variants
information (count: 220 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:220 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188473894	chr16:31574751-31574752	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs544132994	chr16:31574764-31574765	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs116973944	chr16:31574802-31574803	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs556268315	chr16:31574803-31574804	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs568568319	chr16:31574812-31574813	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs147153762	chr16:31574815-31574816	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs554789360	chr16:31574829-31574830	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs572662674	chr16:31574851-31574852	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs540141690	chr16:31574859-31574860	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs558402535	chr16:31574860-31574861	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs576447118	chr16:31574875-31574876	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs544232197	chr16:31574921-31574922	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs115422951	chr16:31574933-31574934	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs140398027	chr16:31574934-31574935	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs192214379	chr16:31574977-31574978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560668355	chr16:31575054-31575055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61353447	chr16:31575112-31575113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563612837	chr16:31575163-31575164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7192364	chr16:31575186-31575187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs111880416	chr16:31575211-31575212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184234678	chr16:31575275-31575276	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs149703472	chr16:31575310-31575311	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs550195258	chr16:31575430-31575431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57432109	chr16:31575450-31575451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572007578	chr16:31575485-31575486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535953163	chr16:31575508-31575509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190693292	chr16:31575518-31575519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181929991	chr16:31575560-31575561	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs533705573	chr16:31575572-31575573	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs57534078	chr16:31575583-31575584	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376937714	chr16:31575587-31575588	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs576757674	chr16:31575596-31575597	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs537748734	chr16:31575603-31575604	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs200230645	chr16:31575740-31575741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs55998443	chr16:31575767-31575768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs79128256	chr16:31575785-31575786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529122131	chr16:31575827-31575828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145802546	chr16:31575830-31575831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs8057029	chr16:31575900-31575901	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs560251869	chr16:31575914-31575915	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs572153343	chr16:31576025-31576026	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs546447798	chr16:31576040-31576041	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs187380124	chr16:31576048-31576049	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs189336725	chr16:31576054-31576055	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs550165619	chr16:31576073-31576074	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs562117410	chr16:31576081-31576082	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs34385075	chr16:31576130-31576131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72374895	chr16:31576131-31576132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs398058199	chr16:31576146-31576147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529244857	chr16:31576175-31576176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Lung cancer	18438408	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	18451855	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31573200-31579800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr16:31579600-31580000	Enhancers	Gastric	stomach
3	chr16:31579600-31580400	ZNF genes & repeats	Lung	lung
4	chr16:31579600-31581000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr16:31579600-31581000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
6	chr16:31579600-31581400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
7	chr16:31579800-31580000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr16:31579800-31580000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr16:31579800-31580000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr16:31579800-31580000	Enhancers	Pancreas	Pancrea
11	chr16:31579800-31580200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
12	chr16:31579800-31581000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
13	chr16:31579800-31581000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr16:31579800-31581200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
15	chr16:31579800-31581400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
16	chr16:31579800-31581400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
17	chr16:31580000-31580200	Enhancers	Primary hematopoietic stem cells	blood
18	chr16:31580000-31580200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr16:31580000-31580200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
20	chr16:31580000-31580200	Bivalent Enhancer	Fetal Stomach	stomach
21	chr16:31580000-31580200	Active TSS	Rectal Smooth Muscle	rectum
22	chr16:31580000-31580200	Active TSS	Right Atrium	heart
23	chr16:31580000-31580200	Active TSS	Right Ventricle	heart
24	chr16:31580000-31580200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
25	chr16:31580000-31580200	Bivalent Enhancer	Stomach Mucosa	stomach
26	chr16:31580000-31580200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
27	chr16:31580000-31580400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr16:31580000-31580400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
29	chr16:31580000-31580400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
30	chr16:31580000-31580400	Flanking Active TSS	Gastric	stomach
31	chr16:31580000-31580400	Flanking Active TSS	Pancreas	Pancrea
32	chr16:31580000-31580400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
33	chr16:31580000-31580600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
34	chr16:31580000-31580600	Bivalent Enhancer	Fetal Heart	heart
35	chr16:31580000-31580600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
36	chr16:31580000-31580600	Active TSS	Rectal Mucosa Donor 29	rectum
37	chr16:31580000-31580800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr16:31580000-31580800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr16:31580000-31580800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr16:31580000-31580800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr16:31580000-31580800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
42	chr16:31580000-31580800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
43	chr16:31580000-31580800	Bivalent/Poised TSS	Left Ventricle	heart
44	chr16:31580000-31581000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr16:31580000-31581000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr16:31580000-31581000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr16:31580000-31581000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
48	chr16:31580000-31581000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr16:31580000-31581000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr16:31580000-31581000	Bivalent/Poised TSS	Adipose Nuclei	Adipose

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