Variant report

Variant	nsv1057164
Chromosome Location	chr16:76610695-76704216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:857)
CpG islands
(count:305)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
3	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
4	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
5	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
6	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
7	ATF1	chr16:76687134-76687664	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	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
12	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
13	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
14	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
16	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a
17	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
18	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
19	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
20	CEBPB	chr16:76668375-76668595	HepG2	liver:	n/a	chr16:76668457-76668468
21	CEBPB	chr16:76640219-76640497	Hela-S3	cervix:	n/a	chr16:76640353-76640364
22	CEBPB	chr16:76626164-76626375	A549	lung:	n/a	chr16:76626265-76626276
23	CEBPB	chr16:76668991-76669576	K562	blood:	n/a	chr16:76669437-76669448
24	CEBPB	chr16:76698299-76698542	HepG2	liver:	n/a	n/a
25	CEBPB	chr16:76687366-76687695	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:76640227-76640508	A549	lung:	n/a	chr16:76640353-76640364
27	CEBPB	chr16:76687301-76687681	IMR90	lung:	n/a	n/a
28	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
29	CEBPB	chr16:76687256-76687678	A549	lung:	n/a	n/a
30	CEBPB	chr16:76687392-76687580	K562	blood:	n/a	n/a
31	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
32	CEBPB	chr16:76687295-76687707	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr16:76626105-76626409	HepG2	liver:	n/a	chr16:76626265-76626276
34	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
35	CEBPB	chr16:76673910-76674162	K562	blood:	n/a	n/a
36	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
38	CEBPB	chr16:76668970-76669641	K562	blood:	n/a	chr16:76669437-76669448
39	CEBPB	chr16:76640177-76640533	IMR90	lung:	n/a	chr16:76640353-76640364
40	CEBPB	chr16:76695763-76696093	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:76666721-76666977	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:76669262-76669518	HepG2	liver:	n/a	chr16:76669437-76669448
44	CEBPB	chr16:76626178-76626377	H1-hESC	embryonic stem cell:	n/a	chr16:76626265-76626276
45	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
46	CEBPB	chr16:76687171-76687709	MCF-7	breast:	n/a	n/a
47	CEBPB	chr16:76640302-76640497	H1-hESC	embryonic stem cell:	n/a	chr16:76640353-76640364
48	CEBPB	chr16:76687291-76687702	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr16:76669283-76669515	K562	blood:	n/a	chr16:76669437-76669448

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76668836-76668886	NHBE	bronchial:	n/a
2	chr16:76668836-76668886	ProgFib	skin:	n/a
3	chr16:76668836-76668886	HCF	heart:	n/a
4	chr16:76668836-76668886	HCM	heart:	n/a
5	chr16:76666860-76666910	LNCaP	prostate:	n/a
6	chr16:76668836-76668886	ECC-1	luminal epithelium:	n/a
7	chr16:76665665-76665715	IMR90	lung:	fetal
8	chr16:76666860-76666910	PFSK-1	brain:	n/a
9	chr16:76668836-76668886	PFSK-1	brain:	n/a
10	chr16:76670197-76670247	MCF-7	breast:	n/a
11	chr16:76670197-76670247	Hepatocyte	liver:	n/a
12	chr16:76666860-76666910	AG09309	skin:	n/a
13	chr16:76669151-76669201	HRCEpiC	kidney:	n/a
14	chr16:76668836-76668886	K562	blood:	n/a
15	chr16:76669151-76669201	GM06990	blood:	n/a
16	chr16:76666860-76666910	NH-A	brain:	n/a
17	chr16:76669151-76669201	HL-60	blood:	n/a
18	chr16:76670197-76670247	U87	brain:	n/a
19	chr16:76670197-76670247	AG04449	skin:	fetal
20	chr16:76669151-76669201	NHDF-neo	bronchial:	n/a
21	chr16:76665665-76665715	SKMC	muscle:	n/a
22	chr16:76668836-76668886	GM12892	blood:	n/a
23	chr16:76670197-76670247	NHBE	bronchial:	n/a
24	chr16:76668836-76668886	GM12878	blood:	n/a
25	chr16:76669151-76669201	GM19239	blood:	n/a
26	chr16:76666860-76666910	NT2-D1	testis:	n/a
27	chr16:76670197-76670247	NT2-D1	testis:	n/a
28	chr16:76669151-76669201	H1-hESC	embryonic stem cell:	embryo
29	chr16:76665665-76665715	HRPEpiC	eye:	n/a
30	chr16:76669151-76669201	IMR90	lung:	fetal
31	chr16:76669151-76669201	RPTEC	kidney:	n/a
32	chr16:76665665-76665715	HCT-116	colon:	n/a
33	chr16:76666860-76666910	HIPEpiC	eye:	n/a
34	chr16:76666860-76666910	AG09319	gingival:	n/a
35	chr16:76668836-76668886	AG09309	skin:	n/a
36	chr16:76668836-76668886	HIPEpiC	eye:	n/a
37	chr16:76665665-76665715	PrEC	prostate:	n/a
38	chr16:76669151-76669201	NB4	blood:	n/a
39	chr16:76665665-76665715	PANC-1	pancreas:	n/a
40	chr16:76668836-76668886	SK-N-SH	brain:	n/a
41	chr16:76669151-76669201	AG10803	skin:	n/a
42	chr16:76668836-76668886	HEEpiC	esophagus:	n/a
43	chr16:76668836-76668886	GM06990	blood:	n/a
44	chr16:76665665-76665715	HAEpiC	amniotic membrane:	n/a
45	chr16:76665665-76665715	H1-hESC	embryonic stem cell:	embryo
46	chr16:76665665-76665715	HRE	kidney:	n/a
47	chr16:76669151-76669201	HepG2	liver:	n/a
48	chr16:76665665-76665715	NT2-D1	testis:	n/a
49	chr16:76665665-76665715	SAEC	small airway:	n/a
50	chr16:76669151-76669201	HUVEC	blood vessel:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
2	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
3	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
4	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
5	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
6	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
7	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
8	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
9	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
10	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
11	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
12	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
13	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
14	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
15	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
16	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
17	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
18	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
19	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
20	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
21	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
2	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514
3	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
4	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514

No data

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

Extended variants
information (count: 1778 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7194038	chr16:76610695-76610696	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs561615152	chr16:76610697-76610698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530260574	chr16:76610703-76610704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547201591	chr16:76610733-76610734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567036314	chr16:76610800-76610801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373836167	chr16:76610809-76610810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569204867	chr16:76610810-76610811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569170919	chr16:76610846-76610847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538231089	chr16:76610896-76610897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557022956	chr16:76610979-76610980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567528375	chr16:76611012-76611013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550829521	chr16:76611023-76611024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536075036	chr16:76611032-76611033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376370351	chr16:76611036-76611037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572670955	chr16:76611044-76611045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188366645	chr16:76611045-76611046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558581197	chr16:76611048-76611049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575170924	chr16:76611056-76611057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544191330	chr16:76611070-76611071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570642775	chr16:76611080-76611081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537488408	chr16:76611086-76611087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529690801	chr16:76611155-76611156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561461980	chr16:76611182-76611183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148164451	chr16:76611241-76611242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531644260	chr16:76611253-76611254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74721259	chr16:76611263-76611264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193019343	chr16:76611312-76611313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571195409	chr16:76611328-76611329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532715036	chr16:76611330-76611331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548348616	chr16:76611373-76611374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183484023	chr16:76611385-76611386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531638348	chr16:76611438-76611439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569755809	chr16:76611442-76611443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188931050	chr16:76611451-76611452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141964281	chr16:76611490-76611491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192600807	chr16:76611511-76611512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552801739	chr16:76611526-76611527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9929705	chr16:76611530-76611531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62045791	chr16:76611562-76611563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558413728	chr16:76611588-76611589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114306439	chr16:76611629-76611630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375725264	chr16:76611696-76611697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150239420	chr16:76611787-76611788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537510218	chr16:76611802-76611803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554572693	chr16:76611815-76611816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373818970	chr16:76611861-76611862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574438713	chr16:76611864-76611865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530576728	chr16:76611879-76611880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368176199	chr16:76611881-76611882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560760286	chr16:76611894-76611895	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76610200-76612200	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr16:76610400-76611200	Enhancers	Fetal Lung	lung
3	chr16:76610400-76611200	Enhancers	HepG2	liver
4	chr16:76610400-76611400	Enhancers	Primary hematopoietic stem cells	blood
5	chr16:76610400-76611800	Enhancers	GM12878-XiMat	blood
6	chr16:76611200-76611800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr16:76614400-76614600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr16:76615400-76616200	Enhancers	Brain Germinal Matrix	brain
9	chr16:76616200-76616800	Weak transcription	Brain Germinal Matrix	brain
10	chr16:76616800-76617800	Enhancers	Brain Germinal Matrix	brain
11	chr16:76616800-76618000	Enhancers	Fetal Brain Male	brain
12	chr16:76616800-76618200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr16:76616800-76618400	Enhancers	Fetal Brain Female	brain
14	chr16:76617000-76617200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr16:76617000-76617200	Enhancers	Brain Angular Gyrus	brain
16	chr16:76617000-76617400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr16:76617000-76618000	Enhancers	Fetal Lung	lung
18	chr16:76617200-76617400	Flanking Active TSS	Brain Angular Gyrus	brain
19	chr16:76617200-76617600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:76617200-76617600	Enhancers	Adipose Nuclei	Adipose
21	chr16:76617200-76617600	Enhancers	Fetal Muscle Leg	muscle
22	chr16:76617200-76617600	Enhancers	Fetal Stomach	stomach
23	chr16:76617200-76617800	Active TSS	Brain Anterior Caudate	brain
24	chr16:76617200-76617800	Active TSS	Brain Cingulate Gyrus	brain
25	chr16:76617200-76617800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr16:76617200-76617800	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr16:76617200-76618000	Active TSS	Brain Hippocampus Middle	brain
28	chr16:76617200-76618200	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr16:76617200-76618200	Active TSS	Brain Substantia Nigra	brain
30	chr16:76617400-76617800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr16:76617400-76617800	Active TSS	Brain Angular Gyrus	brain
32	chr16:76617600-76618000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr16:76617800-76618200	Active TSS	Brain Germinal Matrix	brain
34	chr16:76617800-76618400	Enhancers	Brain Cingulate Gyrus	brain
35	chr16:76618000-76618200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr16:76618000-76618400	Enhancers	Brain Angular Gyrus	brain
37	chr16:76618000-76621000	Weak transcription	Fetal Lung	lung
38	chr16:76618200-76619600	Enhancers	Brain Germinal Matrix	brain
39	chr16:76618800-76619800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr16:76619600-76620600	Weak transcription	Brain Germinal Matrix	brain
41	chr16:76619800-76621000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr16:76620600-76620800	Enhancers	Brain Germinal Matrix	brain
43	chr16:76621000-76621200	Enhancers	Fetal Lung	lung
44	chr16:76621000-76621400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr16:76629200-76630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr16:76629600-76630000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr16:76645600-76645800	Enhancers	Placenta Amnion	Placenta Amnion
48	chr16:76646400-76647400	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr16:76647200-76650000	Enhancers	Brain Germinal Matrix	brain
50	chr16:76647400-76647800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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