Variant report

Variant	nsv573051
Chromosome Location	chr16:76650543-76798980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:963)
CpG islands
(count:367)
Chromatin interactive
region (count:32)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
2	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
5	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
6	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
7	ATF1	chr16:76789952-76789998	K562	blood:	n/a	n/a
8	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
9	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
12	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
13	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
14	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
15	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
16	CEBPB	chr16:76669283-76669515	K562	blood:	n/a	chr16:76669437-76669448
17	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a
18	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
19	CEBPB	chr16:76666721-76666977	HepG2	liver:	n/a	n/a
20	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
21	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr16:76687256-76687678	A549	lung:	n/a	n/a
23	CEBPB	chr16:76710451-76710670	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:76714462-76714734	HepG2	liver:	n/a	chr16:76714617-76714628 chr16:76714616-76714629
25	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
26	CEBPB	chr16:76777705-76778043	HepG2	liver:	n/a	chr16:76777865-76777876
27	CEBPB	chr16:76687305-76687716	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr16:76695763-76696093	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:76794135-76794428	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:76777685-76778008	A549	lung:	n/a	chr16:76777865-76777876
31	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
32	CEBPB	chr16:76734178-76734430	IMR90	lung:	n/a	n/a
33	CEBPB	chr16:76668991-76669576	K562	blood:	n/a	chr16:76669437-76669448
34	CEBPB	chr16:76687366-76687695	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:76710097-76710858	MCF-7	breast:	n/a	n/a
36	CEBPB	chr16:76700933-76701106	HepG2	liver:	n/a	chr16:76700935-76700946 chr16:76701040-76701051 chr16:76700935-76700946
37	CEBPB	chr16:76687301-76687681	IMR90	lung:	n/a	n/a
38	CEBPB	chr16:76782202-76782512	HepG2	liver:	n/a	chr16:76782369-76782380
39	CEBPB	chr16:76687291-76687702	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
41	CEBPB	chr16:76734138-76734455	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:76687171-76687709	MCF-7	breast:	n/a	n/a
43	CEBPB	chr16:76794239-76794437	A549	lung:	n/a	n/a
44	CEBPB	chr16:76687392-76687580	K562	blood:	n/a	n/a
45	CEBPB	chr16:76756458-76756533	K562	blood:	n/a	chr16:76756489-76756502 chr16:76756490-76756501
46	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
47	CEBPB	chr16:76777703-76778010	IMR90	lung:	n/a	chr16:76777865-76777876
48	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
49	CEBPB	chr16:76756351-76756650	IMR90	lung:	n/a	chr16:76756489-76756502 chr16:76756490-76756501 chr16:76756620-76756631
50	CEBPB	chr16:76756359-76756661	HepG2	liver:	n/a	chr16:76756489-76756502 chr16:76756490-76756501 chr16:76756620-76756631

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76669151-76669201	HIPEpiC	eye:	n/a
2	chr16:76669151-76669201	HIPEpiC	eye:	n/a
3	chr16:76666860-76666910	LNCaP	prostate:	n/a
4	chr16:76708064-76708114	Caco-2	colon:	n/a
5	chr16:76668836-76668886	K562	blood:	n/a
6	chr16:76666860-76666910	CMK	blood:	n/a
7	chr16:76665665-76665715	MCF10A-Er-Src	breast:	n/a
8	chr16:76665665-76665715	HCPEpiC	choroid plexus:	n/a
9	chr16:76708064-76708114	K562	blood:	n/a
10	chr16:76708064-76708114	MCF10A-Er-Src	breast:	n/a
11	chr16:76670197-76670247	Jurkat	blood:	n/a
12	chr16:76670197-76670247	HIPEpiC	eye:	n/a
13	chr16:76669151-76669201	HCPEpiC	choroid plexus:	n/a
14	chr16:76669151-76669201	HMEC	breast:	n/a
15	chr16:76708064-76708114	CMK	blood:	n/a
16	chr16:76669151-76669201	HPAEpiC	pulmonary alveolar:	n/a
17	chr16:76668836-76668886	CMK	blood:	n/a
18	chr16:76668836-76668886	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:76708064-76708114	HIPEpiC	eye:	n/a
20	chr16:76708064-76708114	LNCaP	prostate:	n/a
21	chr16:76668836-76668886	T-47D	breast:	n/a
22	chr16:76670197-76670247	Hela-S3	cervix:	n/a
23	chr16:76670197-76670247	AG09319	gingival:	n/a
24	chr16:76670197-76670247	HCM	heart:	n/a
25	chr16:76708064-76708114	AG10803	skin:	n/a
26	chr16:76666860-76666910	HCT-116	colon:	n/a
27	chr16:76666860-76666910	Jurkat	blood:	n/a
28	chr16:76669151-76669201	SK-N-MC	brain:	n/a
29	chr16:76708064-76708114	AG09319	gingival:	n/a
30	chr16:76668836-76668886	NHDF-neo	bronchial:	n/a
31	chr16:76668836-76668886	Hepatocyte	liver:	n/a
32	chr16:76708064-76708114	HRCEpiC	kidney:	n/a
33	chr16:76666860-76666910	HCF	heart:	n/a
34	chr16:76668836-76668886	U87	brain:	n/a
35	chr16:76708064-76708114	SAEC	small airway:	n/a
36	chr16:76708064-76708114	GM06990	blood:	n/a
37	chr16:76665665-76665715	GM12878	blood:	n/a
38	chr16:76668836-76668886	BE2_C	brain:	n/a
39	chr16:76708064-76708114	HEEpiC	esophagus:	n/a
40	chr16:76669151-76669201	K562	blood:	n/a
41	chr16:76670197-76670247	CMK	blood:	n/a
42	chr16:76668836-76668886	SK-N-SH	brain:	n/a
43	chr16:76670197-76670247	HCT-116	colon:	n/a
44	chr16:76708064-76708114	ProgFib	skin:	n/a
45	chr16:76669151-76669201	NH-A	brain:	n/a
46	chr16:76668836-76668886	HNPCEpiC	eye:	n/a
47	chr16:76669151-76669201	RPTEC	kidney:	n/a
48	chr16:76668836-76668886	SAEC	small airway:	n/a
49	chr16:76670197-76670247	SK-N-SH_RA	brain:	n/a
50	chr16:76708064-76708114	GM12878	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
2	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
3	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
4	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
5	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
6	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
7	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
8	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
9	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
10	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
11	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
12	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
13	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
14	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
15	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
16	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
17	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
18	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
19	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
20	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
21	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
22	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
23	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
24	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
25	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
26	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
27	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
28	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
29	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
30	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
31	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
32	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-4	chr16:76770239-76770376	ENSG00000259995.1
2	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
3	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
4	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
5	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792
6	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514
7	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792

No data

Variant related genes	Relation type
ENSG00000259995	TF binding region
ENSG00000250514	TF binding region
ENSG00000259995	CpG island
ENSG00000250514	CpG island
ENSG00000250514	chromatin interactions
CDKN1A	miRNA target sites
CDV3	miRNA target sites
DDX3Y	miRNA target sites
SPRYD3	miRNA target sites

Extended variants
information (count: 2529 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2529 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34537081	chr16:76653600-76653601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528882780	chr16:76653621-76653622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147919611	chr16:76653666-76653667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142069755	chr16:76653697-76653698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117927180	chr16:76653708-76653709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73629928	chr16:76653715-76653716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs180919847	chr16:76653718-76653719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531094859	chr16:76653719-76653720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79725127	chr16:76653780-76653781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577412099	chr16:76653824-76653825	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs531130723	chr16:76653840-76653841	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs73629931	chr16:76653843-76653844	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551030490	chr16:76653854-76653855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs571131542	chr16:76653864-76653865	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs533398973	chr16:76653910-76653911	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs116909832	chr16:76653973-76653974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs565668150	chr16:76653986-76653987	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs141253300	chr16:76656017-76656018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79798771	chr16:76656028-76656029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76823714	chr16:76656042-76656043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150860049	chr16:76656119-76656120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75405284	chr16:76656123-76656124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184576104	chr16:76656129-76656130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568442488	chr16:76656136-76656137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534218677	chr16:76656146-76656147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111809541	chr16:76656154-76656155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546870352	chr16:76656174-76656175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577376972	chr16:76656211-76656212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546053883	chr16:76656213-76656214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566161535	chr16:76656276-76656277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188471595	chr16:76656311-76656312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181316975	chr16:76656312-76656313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576443850	chr16:76656338-76656339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185845448	chr16:76656349-76656350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562063121	chr16:76656367-76656368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115915125	chr16:76656391-76656392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375930419	chr16:76656394-76656395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540544150	chr16:76656459-76656460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139294872	chr16:76656501-76656502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149568196	chr16:76656529-76656530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147236500	chr16:76656555-76656556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558137115	chr16:76656605-76656606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141032355	chr16:76656622-76656623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531283999	chr16:76656637-76656638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547828690	chr16:76656680-76656681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567707257	chr16:76656701-76656702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146761485	chr16:76656732-76656733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533504201	chr16:76656758-76656759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73629936	chr16:76656772-76656773	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs568943943	chr16:76656800-76656801	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76653600-76653800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:76653600-76653800	Enhancers	Pancreas	Pancrea
3	chr16:76653800-76654000	ZNF genes & repeats	Pancreas	Pancrea
4	chr16:76656000-76659000	Enhancers	Fetal Lung	lung
5	chr16:76657000-76657600	Enhancers	Fetal Brain Male	brain
6	chr16:76657200-76657800	Enhancers	Fetal Brain Female	brain
7	chr16:76660400-76660800	Enhancers	K562	blood
8	chr16:76668600-76668800	Enhancers	Pancreas	Pancrea
9	chr16:76668600-76669800	Active TSS	K562	blood
10	chr16:76668800-76669200	Active TSS	Gastric	stomach
11	chr16:76668800-76669200	Flanking Active TSS	Pancreas	Pancrea
12	chr16:76669000-76669400	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr16:76669000-76669400	Active TSS	Duodenum Mucosa	Duodenum
14	chr16:76673400-76674600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr16:76673600-76674000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr16:76673800-76674400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr16:76684400-76685200	Flanking Active TSS	A549	lung
18	chr16:76684600-76685200	Enhancers	HepG2	liver
19	chr16:76685200-76685400	Enhancers	A549	lung
20	chr16:76686600-76687000	Enhancers	Fetal Brain Male	brain
21	chr16:76687200-76687800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr16:76687200-76688000	Enhancers	Brain Substantia Nigra	brain
23	chr16:76687200-76688200	Enhancers	Fetal Lung	lung
24	chr16:76687600-76688200	Enhancers	Brain Hippocampus Middle	brain
25	chr16:76687600-76689600	Enhancers	Brain Germinal Matrix	brain
26	chr16:76688200-76690600	Weak transcription	Fetal Lung	lung
27	chr16:76689600-76690400	Weak transcription	Brain Germinal Matrix	brain
28	chr16:76690000-76692000	Enhancers	Primary hematopoietic stem cells	blood
29	chr16:76690400-76692000	Enhancers	Brain Germinal Matrix	brain
30	chr16:76690600-76691800	Enhancers	Fetal Lung	lung
31	chr16:76690600-76692000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr16:76690600-76692000	Enhancers	Fetal Muscle Leg	muscle
33	chr16:76691400-76692000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr16:76692000-76694600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr16:76693400-76694000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr16:76694000-76699400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr16:76694600-76696400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:76695000-76696200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr16:76696600-76714800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr16:76699400-76699600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr16:76699600-76704000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr16:76699800-76700400	Enhancers	Primary hematopoietic stem cells	blood
43	chr16:76700400-76703200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr16:76703200-76703400	Active TSS	Primary hematopoietic stem cells	blood
45	chr16:76703400-76703600	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr16:76703600-76704600	Enhancers	Primary hematopoietic stem cells	blood
47	chr16:76703800-76704800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr16:76704000-76705200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr16:76704800-76709400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr16:76707400-76708200	Enhancers	HUES48 Cell Line	embryonic stem cell

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