Variant report

Variant	esv3444439
Chromosome Location	chr16:30209251-30219549
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	BHLHE40	chr16:30210902-30211673	HepG2	liver:	n/a	n/a
2	BHLHE40	chr16:30218877-30219112	HepG2	liver:	n/a	n/a
3	BHLHE40	chr16:30219470-30219887	HepG2	liver:	n/a	n/a
4	CBX3	chr16:30210416-30211329	K562	blood:	n/a	n/a
5	CEBPB	chr16:30210926-30211366	K562	blood:	n/a	n/a
6	CEBPB	chr16:30211021-30211237	K562	blood:	n/a	n/a
7	CTCF	chr16:30218747-30218886	GM12892	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
8	CTCF	chr16:30218710-30219003	K562	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
9	CTCF	chr16:30218729-30218894	GM19238	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
10	CTCF	chr16:30218784-30218852	GM10248	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
11	CTCF	chr16:30218780-30218855	GM12891	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
12	CTCF	chr16:30218221-30219075	A549	lung:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
13	CTCF	chr16:30218628-30218968	A549	lung:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
14	CTCF	chr16:30218683-30218911	K562	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
15	CTCF	chr16:30218735-30218909	MCF-7	breast:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
16	CTCF	chr16:30218893-30218938	GM20000	blood:	n/a	n/a
17	CTCF	chr16:30218765-30218876	H1-hESC	embryonic stem cell:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
18	CTCF	chr16:30218761-30218863	GM10266	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
19	CTCF	chr16:30218749-30218894	NHEK	skin:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
20	CTCF	chr16:30218735-30218868	K562	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
21	CTCF	chr16:30218788-30218829	GM13977	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
22	CTCF	chr16:30218807-30218861	Fibrobl	skin:	n/a	n/a
23	CTCF	chr16:30218740-30218888	GM19240	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
24	CTCF	chr16:30218805-30218861	GM13976	blood:	n/a	n/a
25	CTCF	chr16:30218761-30218879	GM12878	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
26	CTCF	chr16:30218748-30218899	A549	lung:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
27	CTCF	chr16:30218769-30218849	ProgFib	skin:	n/a	chr16:30218793-30218811 chr16:30218788-30218809
28	CTCF	chr16:30218744-30218893	Medullo	brain:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
29	CTCF	chr16:30218759-30218888	GM19239	blood:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
30	CTCF	chr16:30218760-30218891	MCF-7	breast:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
31	CTCF	chr16:30218757-30218905	MCF-7	breast:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
32	CTCF	chr16:30210610-30210616	Lung_OC	lung:	n/a	n/a
33	CTCF	chr16:30218726-30218911	Hela-S3	cervix:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
34	CTCF	chr16:30218745-30218912	MCF-7	breast:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
35	CTCF	chr16:30218746-30218879	HUVEC	blood vessel:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
36	CTCF	chr16:30218711-30218892	HepG2	liver:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
37	CTCF	chr16:30210589-30210638	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr16:30218740-30218900	MCF-7	breast:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
39	CTCF	chr16:30218598-30218932	A549	lung:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
40	CTCF	chr16:30218742-30218897	Gliobla	brain:	n/a	chr16:30218793-30218811 chr16:30218788-30218809 chr16:30218864-30218877
41	EBF1	chr16:30218447-30218739	GM12878	blood:	n/a	n/a
42	EBF1	chr16:30216604-30216872	GM12878	blood:	n/a	chr16:30216744-30216757 chr16:30216622-30216632 chr16:30216622-30216631
43	EBF1	chr16:30218416-30218714	GM12878	blood:	n/a	n/a
44	EBF1	chr16:30216618-30216928	GM12878	blood:	n/a	chr16:30216744-30216757 chr16:30216622-30216632 chr16:30216622-30216631
45	EP300	chr16:30218013-30218163	GM12878	blood:	n/a	n/a
46	FOS	chr16:30218464-30218652	MCF10A-Er-Src	breast:	n/a	chr16:30218565-30218573
47	FOSL2	chr16:30217553-30218235	HepG2	liver:	n/a	n/a
48	FOSL2	chr16:30210066-30211862	HepG2	liver:	n/a	chr16:30211119-30211131 chr16:30211120-30211130 chr16:30211120-30211129 chr16:30211122-30211129 chr16:30211121-30211130 chr16:30211121-30211129
49	FOSL2	chr16:30209584-30210019	HepG2	liver:	n/a	n/a
50	FOSL2	chr16:30219264-30220030	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30217452-30217502	IMR90	lung:	fetal
2	chr16:30217452-30217502	SK-N-MC	brain:	n/a
3	chr16:30209202-30209252	AG09319	gingival:	n/a
4	chr16:30209202-30209252	ProgFib	skin:	n/a
5	chr16:30217452-30217502	HRE	kidney:	n/a
6	chr16:30209202-30209252	H1-hESC	embryonic stem cell:	embryo
7	chr16:30217452-30217502	PrEC	prostate:	n/a
8	chr16:30209202-30209252	ovcar-3	ovarian:	n/a
9	chr16:30217452-30217502	HPAEpiC	pulmonary alveolar:	n/a
10	chr16:30217452-30217502	HL-60	blood:	n/a
11	chr16:30209202-30209252	NB4	blood:	n/a
12	chr16:30217452-30217502	Jurkat	blood:	n/a
13	chr16:30209202-30209252	HPAEpiC	pulmonary alveolar:	n/a
14	chr16:30217452-30217502	HepG2	liver:	n/a
15	chr16:30209202-30209252	IMR90	lung:	fetal
16	chr16:30217452-30217502	HCPEpiC	choroid plexus:	n/a
17	chr16:30209202-30209252	HCPEpiC	choroid plexus:	n/a
18	chr16:30217452-30217502	GM06990	blood:	n/a
19	chr16:30209202-30209252	LNCaP	prostate:	n/a
20	chr16:30209202-30209252	A549	lung:	n/a
21	chr16:30209202-30209252	HUVEC	blood vessel:	n/a
22	chr16:30209202-30209252	BJ	skin:	n/a
23	chr16:30209202-30209252	HRE	kidney:	n/a
24	chr16:30209202-30209252	U87	brain:	n/a
25	chr16:30209202-30209252	ECC-1	luminal epithelium:	n/a
26	chr16:30217452-30217502	HCM	heart:	n/a
27	chr16:30217452-30217502	Hela-S3	cervix:	n/a
28	chr16:30209202-30209252	NHBE	bronchial:	n/a
29	chr16:30217452-30217502	T-47D	breast:	n/a
30	chr16:30209202-30209252	K562	blood:	n/a
31	chr16:30217452-30217502	NHDF-neo	bronchial:	n/a
32	chr16:30217452-30217502	ovcar-3	ovarian:	n/a
33	chr16:30209202-30209252	MCF10A-Er-Src	breast:	n/a
34	chr16:30209202-30209252	SK-N-MC	brain:	n/a
35	chr16:30209202-30209252	MCF-7	breast:	n/a
36	chr16:30209202-30209252	HCM	heart:	n/a
37	chr16:30217452-30217502	SKMC	muscle:	n/a
38	chr16:30217452-30217502	NH-A	brain:	n/a
39	chr16:30217452-30217502	AoSMC	blood vessel:	n/a
40	chr16:30209202-30209252	GM06990	blood:	n/a
41	chr16:30209202-30209252	GM12878	blood:	n/a
42	chr16:30217452-30217502	NT2-D1	testis:	n/a
43	chr16:30217452-30217502	MCF10A-Er-Src	breast:	n/a
44	chr16:30217452-30217502	ECC-1	luminal epithelium:	n/a
45	chr16:30209202-30209252	HIPEpiC	eye:	n/a
46	chr16:30209202-30209252	HNPCEpiC	eye:	n/a
47	chr16:30217452-30217502	AG04449	skin:	fetal
48	chr16:30209202-30209252	RPTEC	kidney:	n/a
49	chr16:30209202-30209252	CMK	blood:	n/a
50	chr16:30217452-30217502	SK-N-SH_RA	brain:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SULT1A3.1-1	chr16:30214329-30214825	NONHSAT141723
2	lnc-BOLA2B-2	chr16:30215638-30216007	NONHSAT141724
3	lnc-BOLA2B-2	chr16:30218197-30218221	NONHSAT141726
4	lnc-BOLA2B-2	chr16:30217575-30218248	NONHSAT141724
5	lnc-BOLA2B-2	chr16:30216148-30216211	NONHSAT141724
6	lnc-BOLA2B-2	chr16:30216282-30216411	NONHSAT141724
7	lnc-BOLA2B-2	chr16:30217246-30217485	NONHSAT141724

Variant related genes	Relation type
BOLA2B	TF binding region
SULT1A3	TF binding region
ENSG00000258130	TF binding region
BOLA2B	CpG island
SULT1A3	CpG island
ENSG00000258130	CpG island

Extended variants
information (count: 35 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79070527	chr16:30209530-30209531	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs541013055	chr16:30211887-30211888	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs371560738	chr16:30211957-30211958	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs151163643	chr16:30211975-30211976	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553050853	chr16:30212101-30212102	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs577982762	chr16:30212223-30212224	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs545355986	chr16:30212542-30212543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370051437	chr16:30212776-30212777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563589661	chr16:30212839-30212840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530694556	chr16:30212900-30212901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561391603	chr16:30212901-30212902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528615885	chr16:30212902-30212903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546967167	chr16:30212916-30212917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571332999	chr16:30212941-30212942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532388992	chr16:30212983-30212984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540306192	chr16:30213019-30213020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140113532	chr16:30213032-30213033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372875504	chr16:30213100-30213101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569213725	chr16:30213159-30213160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112327790	chr16:30213175-30213176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536815344	chr16:30215169-30215170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548541512	chr16:30215187-30215188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567352508	chr16:30215591-30215592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76641670	chr16:30215621-30215622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537614769	chr16:30215660-30215661	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs552989163	chr16:30215662-30215663	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs577676862	chr16:30215890-30215891	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs538659318	chr16:30216054-30216055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557244878	chr16:30217373-30217374	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs575456643	chr16:30217474-30217475	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs540757932	chr16:30218615-30218616	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs373853736	chr16:30218634-30218635	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371826537	chr16:30218635-30218636	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542795482	chr16:30218642-30218643	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs560968816	chr16:30218788-30218789	Weak transcription	TF binding region	1 gene(s)	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
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
low-grade B-cell lymphoma tumor	18367492	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
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
autism	21731881	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30199800-30217200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr16:30199800-30217200	Weak transcription	Placenta	Placenta
3	chr16:30199800-30217200	Weak transcription	Fetal Stomach	stomach
4	chr16:30200000-30217200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr16:30206200-30217200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:30206200-30217200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr16:30206200-30217200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr16:30206200-30217200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr16:30206200-30217200	Weak transcription	Fetal Intestine Large	intestine
10	chr16:30206200-30217200	Weak transcription	Fetal Intestine Small	intestine
11	chr16:30206200-30217200	Weak transcription	Fetal Thymus	thymus
12	chr16:30216800-30217000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr16:30217000-30217200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr16:30217000-30217200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr16:30217200-30217400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:30217200-30217400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:30217200-30217400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr16:30217200-30217400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
19	chr16:30217200-30217400	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr16:30217200-30217400	Active TSS	Colonic Mucosa	Colon
21	chr16:30217200-30217400	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
22	chr16:30217200-30217400	Flanking Active TSS	Fetal Intestine Small	intestine
23	chr16:30217200-30217400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
24	chr16:30217200-30217400	Enhancers	Fetal Muscle Leg	muscle
25	chr16:30217200-30217400	Flanking Active TSS	Placenta	Placenta
26	chr16:30217200-30217400	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
27	chr16:30217200-30217400	Bivalent Enhancer	Fetal Thymus	thymus
28	chr16:30217200-30217400	Enhancers	Lung	lung
29	chr16:30217200-30217400	Active TSS	Psoas Muscle	Psoas
30	chr16:30217200-30217400	Enhancers	HMEC	breast
31	chr16:30217200-30217400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr16:30217200-30217600	Active TSS	H1 Cell Line	embryonic stem cell
33	chr16:30217200-30217600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr16:30217200-30217600	Active TSS	H9 Cell Line	embryonic stem cell
35	chr16:30217200-30217600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr16:30217200-30217600	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr16:30217200-30217600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr16:30217200-30217600	Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr16:30217200-30217600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr16:30217200-30217600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr16:30217200-30217600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr16:30217200-30217600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr16:30217200-30217600	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr16:30217200-30217600	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr16:30217200-30217600	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr16:30217200-30217600	Enhancers	Primary B cells from cord blood	blood
47	chr16:30217200-30217600	Active TSS	Primary B cells from peripheral blood	blood
48	chr16:30217200-30217600	Active TSS	Primary T cells fromperipheralblood	blood
49	chr16:30217200-30217600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr16:30217200-30217600	Active TSS	Primary T helper cells PMA-I stimulated	--

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