Variant report

Variant	nsv907007
Chromosome Location	chr16:81157521-81181423
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:62)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:81175001-81175341	K562	blood:	n/a	n/a
2	BACH1	chr16:81174746-81175382	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr16:81168205-81168486	GM12878	blood:	n/a	n/a
4	BCL11A	chr16:81168284-81168501	GM12878	blood:	n/a	n/a
5	BHLHE40	chr16:81170261-81170322	K562	blood:	n/a	chr16:81170312-81170321
6	BHLHE40	chr16:81170170-81170518	HepG2	liver:	n/a	chr16:81170312-81170321
7	BHLHE40	chr16:81163135-81163164	K562	blood:	n/a	n/a
8	CBX3	chr16:81177298-81178299	HCT-116	colon:	n/a	n/a
9	CBX3	chr16:81174969-81175313	K562	blood:	n/a	n/a
10	CBX3	chr16:81177278-81178302	HCT-116	colon:	n/a	n/a
11	CEBPB	chr16:81175038-81175238	HepG2	liver:	n/a	n/a
12	CEBPB	chr16:81177423-81178286	MCF-7	breast:	n/a	n/a
13	CEBPB	chr16:81172505-81172638	K562	blood:	n/a	n/a
14	CEBPB	chr16:81179993-81180304	HepG2	liver:	n/a	n/a
15	CEBPB	chr16:81177444-81178184	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr16:81160709-81161083	IMR90	lung:	n/a	n/a
17	CEBPB	chr16:81177379-81178318	MCF-7	breast:	n/a	n/a
18	CEBPB	chr16:81175032-81175221	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr16:81177405-81178293	HCT-116	colon:	n/a	n/a
20	CEBPB	chr16:81177354-81178428	HCT-116	colon:	n/a	n/a
21	CEBPB	chr16:81180062-81180209	HepG2	liver:	n/a	n/a
22	CHD2	chr16:81175179-81175253	K562	blood:	n/a	n/a
23	CHD2	chr16:81174697-81174833	HepG2	liver:	n/a	n/a
24	CREB1	chr16:81174880-81175333	A549	lung:	n/a	n/a
25	CTCF	chr16:81176660-81176810	HCT-116	colon:	n/a	n/a
26	CTCF	chr16:81175140-81175290	HepG2	liver:	n/a	n/a
27	CTCF	chr16:81175140-81175290	MCF-7	breast:	n/a	n/a
28	CTCF	chr16:81175132-81175301	GM19240	blood:	n/a	n/a
29	CTCF	chr16:81175120-81175270	GM12869	blood:	n/a	n/a
30	CTCF	chr16:81175120-81175270	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr16:81175120-81175270	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr16:81175160-81175310	AG04450	lung:	n/a	n/a
33	CTCF	chr16:81174980-81175130	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr16:81172918-81173026	K562	blood:	n/a	n/a
35	CTCF	chr16:81175340-81175490	HCM	heart:	n/a	n/a
36	CTCF	chr16:81175140-81175290	HMEC	breast:	n/a	n/a
37	CTCF	chr16:81176600-81176750	NHEK	skin:	n/a	n/a
38	CTCF	chr16:81175001-81175413	HepG2	liver:	n/a	n/a
39	CTCF	chr16:81175140-81175290	AG09319	gingival:	n/a	n/a
40	CTCF	chr16:81175160-81175310	HVMF	connective:	n/a	n/a
41	CTCF	chr16:81175080-81175230	RPTEC	kidney:	n/a	n/a
42	CTCF	chr16:81175150-81175262	GM10248	blood:	n/a	n/a
43	CTCF	chr16:81175160-81175310	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr16:81172763-81173214	MCF-7	breast:	n/a	n/a
45	CTCF	chr16:81175120-81175270	HCT-116	colon:	n/a	n/a
46	CTCF	chr16:81175080-81175230	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr16:81175060-81175210	HMEC	breast:	n/a	n/a
48	CTCF	chr16:81175080-81175230	HFF	foreskin:	n/a	n/a
49	CTCF	chr16:81175080-81175230	AG09319	gingival:	n/a	n/a
50	CTCF	chr16:81175120-81175270	AG04449	skin:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81170527-81170577	PFSK-1	brain:	n/a
2	chr16:81170527-81170577	PFSK-1	brain:	n/a
3	chr16:81170527-81170577	HEK293	kidney:	embryo
4	chr16:81170527-81170577	Jurkat	blood:	n/a
5	chr16:81170527-81170577	PANC-1	pancreas:	n/a
6	chr16:81170527-81170577	NHBE	bronchial:	n/a
7	chr16:81170527-81170577	HPAEpiC	pulmonary alveolar:	n/a
8	chr16:81170527-81170577	Hepatocyte	liver:	n/a
9	chr16:81170527-81170577	GM12878	blood:	n/a
10	chr16:81170527-81170577	AoSMC	blood vessel:	n/a
11	chr16:81170527-81170577	NB4	blood:	n/a
12	chr16:81170527-81170577	K562	blood:	n/a
13	chr16:81170527-81170577	SK-N-SH_RA	brain:	n/a
14	chr16:81170527-81170577	SKMC	muscle:	n/a
15	chr16:81170527-81170577	HRPEpiC	eye:	n/a
16	chr16:81170527-81170577	AG10803	skin:	n/a
17	chr16:81170527-81170577	SAEC	small airway:	n/a
18	chr16:81170527-81170577	BE2_C	brain:	n/a
19	chr16:81170527-81170577	ProgFib	skin:	n/a
20	chr16:81170527-81170577	U87	brain:	n/a
21	chr16:81170527-81170577	AG04449	skin:	fetal
22	chr16:81170527-81170577	HCM	heart:	n/a
23	chr16:81170527-81170577	HEEpiC	esophagus:	n/a
24	chr16:81170527-81170577	HCT-116	colon:	n/a
25	chr16:81170527-81170577	GM19239	blood:	n/a
26	chr16:81170527-81170577	T-47D	breast:	n/a
27	chr16:81170527-81170577	HCF	heart:	n/a
28	chr16:81170527-81170577	NH-A	brain:	n/a
29	chr16:81170527-81170577	AG04450	lung:	fetal
30	chr16:81170527-81170577	LNCaP	prostate:	n/a
31	chr16:81170527-81170577	HRCEpiC	kidney:	n/a
32	chr16:81170527-81170577	ovcar-3	ovarian:	n/a
33	chr16:81170527-81170577	HAEpiC	amniotic membrane:	n/a
34	chr16:81170527-81170577	PrEC	prostate:	n/a
35	chr16:81170527-81170577	SK-N-MC	brain:	n/a
36	chr16:81170527-81170577	HL-60	blood:	n/a
37	chr16:81170527-81170577	BJ	skin:	n/a
38	chr16:81170527-81170577	NT2-D1	testis:	n/a
39	chr16:81170527-81170577	HRE	kidney:	n/a
40	chr16:81170527-81170577	HIPEpiC	eye:	n/a
41	chr16:81170527-81170577	SK-N-SH	brain:	n/a
42	chr16:81170527-81170577	MCF-7	breast:	n/a
43	chr16:81170527-81170577	A549	lung:	n/a
44	chr16:81170527-81170577	RPTEC	kidney:	n/a
45	chr16:81170527-81170577	GM12891	blood:	n/a
46	chr16:81170527-81170577	HCPEpiC	choroid plexus:	n/a
47	chr16:81170527-81170577	CMK	blood:	n/a
48	chr16:81170527-81170577	Hela-S3	cervix:	n/a
49	chr16:81170527-81170577	GM12892	blood:	n/a
50	chr16:81170527-81170577	Caco-2	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81133429..81135383-chr16:81162672..81165434,2	K562	blood:
2	chr16:81155345..81157687-chr16:81159354..81162522,3	MCF-7	breast:
3	chr16:81181423..81183511-chr16:81191451..81193447,2	MCF-7	breast:
4	chr16:81167266..81170181-chr16:81212814..81215037,2	MCF-7	breast:
5	chr16:81170203..81172478-chr16:81173151..81175133,2	MCF-7	breast:
6	chr16:81078751..81080848-chr16:81181095..81182686,2	K562	blood:
7	chr16:81159689..81161686-chr16:81165248..81167111,2	MCF-7	breast:
8	chr16:81163789..81165490-chr16:81205338..81207838,2	MCF-7	breast:
9	chr16:81168888..81171592-chr16:81175504..81177098,2	MCF-7	breast:
10	chr16:81160894..81162615-chr16:81168602..81170831,2	MCF-7	breast:
11	chr16:81128511..81130849-chr16:81169835..81172966,4	MCF-7	breast:
12	chr16:81159689..81161686-chr16:81165248..81167111,2	MCF-7	breast:
13	chr16:81165301..81167307-chr16:81169163..81170985,2	MCF-7	breast:
14	chr16:81068953..81069797-chr16:81176232..81177093,2	K562	blood:
15	chr16:81152674..81158113-chr16:81158859..81162763,5	K562	blood:
16	chr16:81176050..81179014-chr16:81206703..81209353,3	MCF-7	breast:
17	chr16:81152674..81158113-chr16:81158859..81162763,5	K562	blood:
18	chr16:81174893..81175517-chr16:81231737..81232731,3	MCF-7	breast:
19	chr16:81155345..81157687-chr16:81159354..81162522,3	MCF-7	breast:
20	chr16:81172576..81173403-chr16:81248138..81248840,3	MCF-7	breast:
21	chr16:81068581..81070765-chr16:81177689..81179201,2	MCF-7	breast:
22	chr16:81177157..81179228-chr16:81223964..81225695,2	MCF-7	breast:
23	chr16:81110384..81110935-chr16:81169785..81170782,2	MCF-7	breast:
24	chr16:81177178..81179005-chr16:81180841..81182912,2	MCF-7	breast:
25	chr16:81177178..81179005-chr16:81180841..81182912,2	MCF-7	breast:
26	chr16:81160768..81163700-chr16:81169451..81173770,5	MCF-7	breast:
27	chr16:81172499..81173473-chr16:81231950..81233302,5	MCF-7	breast:
28	chr16:71843029..71844532-chr16:81169189..81171698,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCSH-2	chr16:81166255-81166565	l_1369_chr16:81136436-81166565_testes
2	lnc-GCSH-2	chr16:81165896-81166137	l_1369_chr16:81136436-81166565_testes

No data

Variant related genes	Relation type
PKD1L2	TF binding region
PKD1L2	CpG island
ENSG00000166747	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000140905	chromatin interactions
ENSG00000166473	chromatin interactions
ENSG00000245059	chromatin interactions
ENSG00000166455	chromatin interactions
ENSG00000166454	chromatin interactions

Extended variants
information (count: 1652 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4889242	chr16:81157521-81157522	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188379259	chr16:81157564-81157565	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs562057158	chr16:81157565-81157566	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs529446638	chr16:81157573-81157574	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs57043371	chr16:81157576-81157577	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs76970623	chr16:81157577-81157578	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs376836455	chr16:81157588-81157589	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs533382164	chr16:81157603-81157604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551916357	chr16:81157684-81157685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180988921	chr16:81157690-81157691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527933115	chr16:81157697-81157698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548615954	chr16:81157713-81157714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566915104	chr16:81157744-81157745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185931118	chr16:81157749-81157750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377164663	chr16:81157762-81157763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555819998	chr16:81157795-81157796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571295254	chr16:81157803-81157804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538474670	chr16:81157805-81157806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11641929	chr16:81157812-81157813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs572295237	chr16:81157827-81157828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373022685	chr16:81157833-81157834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190736704	chr16:81157834-81157835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555830579	chr16:81157917-81157918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146520650	chr16:81157925-81157926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544589265	chr16:81157935-81157936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562857005	chr16:81157943-81157944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560817067	chr16:81157971-81157972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545274454	chr16:81157979-81157980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560735043	chr16:81157987-81157988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528019578	chr16:81158005-81158006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112766979	chr16:81158010-81158011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560581021	chr16:81158033-81158034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11647547	chr16:81158053-81158054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549718073	chr16:81158066-81158067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571265916	chr16:81158077-81158078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71400145	chr16:81158098-81158099	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532055838	chr16:81158107-81158108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111754208	chr16:81158120-81158121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551652008	chr16:81158146-81158147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182192937	chr16:81158178-81158179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565849871	chr16:81158221-81158222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375746444	chr16:81158227-81158228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552867028	chr16:81158230-81158231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11642410	chr16:81158256-81158257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs8058053	chr16:81158260-81158261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs529320216	chr16:81158266-81158267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs8051756	chr16:81158267-81158268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143508858	chr16:81158273-81158274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545475605	chr16:81158280-81158281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560558576	chr16:81158282-81158283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81130000-81187600	Weak transcription	Right Atrium	heart
2	chr16:81141200-81169600	Weak transcription	Brain Anterior Caudate	brain
3	chr16:81141400-81169600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr16:81141400-81169600	Weak transcription	Brain Hippocampus Middle	brain
5	chr16:81151400-81173000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:81154000-81198800	Weak transcription	Right Ventricle	heart
7	chr16:81154400-81169800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr16:81155000-81161000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr16:81155400-81174600	Weak transcription	Left Ventricle	heart
10	chr16:81155600-81160200	Weak transcription	Ovary	ovary
11	chr16:81155600-81160400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr16:81156400-81157600	Enhancers	Placenta	Placenta
13	chr16:81156600-81157600	Enhancers	Liver	Liver
14	chr16:81156800-81157600	Strong transcription	Adipose Nuclei	Adipose
15	chr16:81156800-81157600	Bivalent Enhancer	K562	blood
16	chr16:81157200-81157600	Enhancers	Fetal Intestine Large	intestine
17	chr16:81157400-81157800	Enhancers	HepG2	liver
18	chr16:81157600-81159600	Weak transcription	Adipose Nuclei	Adipose
19	chr16:81157600-81160200	Weak transcription	Placenta	Placenta
20	chr16:81157800-81160600	Weak transcription	HepG2	liver
21	chr16:81158200-81169800	Weak transcription	A549	lung
22	chr16:81159400-81162400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr16:81159600-81162200	Strong transcription	Adipose Nuclei	Adipose
24	chr16:81160200-81161400	Enhancers	NHEK	skin
25	chr16:81160200-81161600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr16:81160200-81161600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr16:81160200-81161600	Enhancers	Placenta	Placenta
28	chr16:81160200-81161600	Strong transcription	Ovary	ovary
29	chr16:81160200-81161800	Enhancers	HMEC	breast
30	chr16:81160400-81161200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr16:81160400-81161400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr16:81160400-81161600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr16:81160400-81161800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr16:81160400-81162200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr16:81160600-81162000	Strong transcription	HepG2	liver
36	chr16:81161000-81161400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr16:81161000-81162000	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr16:81161400-81161600	Bivalent Enhancer	NHEK	skin
39	chr16:81161600-81169800	Weak transcription	Ovary	ovary
40	chr16:81162000-81169600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr16:81162000-81169800	Weak transcription	HepG2	liver
42	chr16:81162200-81162600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr16:81162200-81169600	Weak transcription	Adipose Nuclei	Adipose
44	chr16:81162400-81164000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr16:81162600-81162800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr16:81162800-81163800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr16:81163800-81164400	Enhancers	Placenta	Placenta
48	chr16:81163800-81164600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr16:81163800-81170600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr16:81164400-81167200	Weak transcription	Placenta	Placenta

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