Variant report

Variant	nsv1056212
Chromosome Location	chr16:76614276-76704216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:802)
CpG islands
(count:305)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
5	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
6	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
7	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
8	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
10	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
12	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
13	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
14	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
15	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
16	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
17	CEBPB	chr16:76640177-76640533	IMR90	lung:	n/a	chr16:76640353-76640364
18	CEBPB	chr16:76673910-76674162	K562	blood:	n/a	n/a
19	CEBPB	chr16:76687256-76687678	A549	lung:	n/a	n/a
20	CEBPB	chr16:76698299-76698542	HepG2	liver:	n/a	n/a
21	CEBPB	chr16:76666721-76666977	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:76700933-76701106	HepG2	liver:	n/a	chr16:76700935-76700946 chr16:76701040-76701051 chr16:76700935-76700946
23	CEBPB	chr16:76687301-76687681	IMR90	lung:	n/a	n/a
24	CEBPB	chr16:76640177-76640534	HepG2	liver:	n/a	chr16:76640353-76640364
25	CEBPB	chr16:76695763-76696093	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:76687366-76687695	HepG2	liver:	n/a	n/a
27	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
28	CEBPB	chr16:76687200-76687807	A549	lung:	n/a	n/a
29	CEBPB	chr16:76668970-76669641	K562	blood:	n/a	chr16:76669437-76669448
30	CEBPB	chr16:76669262-76669518	HepG2	liver:	n/a	chr16:76669437-76669448
31	CEBPB	chr16:76668991-76669576	K562	blood:	n/a	chr16:76669437-76669448
32	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:76626178-76626377	H1-hESC	embryonic stem cell:	n/a	chr16:76626265-76626276
34	CEBPB	chr16:76687291-76687702	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
36	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
37	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
38	CEBPB	chr16:76640302-76640497	H1-hESC	embryonic stem cell:	n/a	chr16:76640353-76640364
39	CEBPB	chr16:76626164-76626375	A549	lung:	n/a	chr16:76626265-76626276
40	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
41	CEBPB	chr16:76668375-76668595	HepG2	liver:	n/a	chr16:76668457-76668468
42	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:76640194-76640523	K562	blood:	n/a	chr16:76640353-76640364
44	CEBPB	chr16:76640219-76640497	Hela-S3	cervix:	n/a	chr16:76640353-76640364
45	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr16:76669283-76669515	K562	blood:	n/a	chr16:76669437-76669448
47	CEBPB	chr16:76687305-76687716	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr16:76687295-76687707	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr16:76687171-76687709	MCF-7	breast:	n/a	n/a
50	CEBPB	chr16:76687392-76687580	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76670197-76670247	Hela-S3	cervix:	n/a
2	chr16:76670197-76670247	HCT-116	colon:	n/a
3	chr16:76666860-76666910	NHDF-neo	bronchial:	n/a
4	chr16:76669151-76669201	HMEC	breast:	n/a
5	chr16:76669151-76669201	ovcar-3	ovarian:	n/a
6	chr16:76665665-76665715	IMR90	lung:	fetal
7	chr16:76668836-76668886	NB4	blood:	n/a
8	chr16:76666860-76666910	NHBE	bronchial:	n/a
9	chr16:76666860-76666910	MCF-7	breast:	n/a
10	chr16:76668836-76668886	GM19239	blood:	n/a
11	chr16:76668836-76668886	HRCEpiC	kidney:	n/a
12	chr16:76669151-76669201	Jurkat	blood:	n/a
13	chr16:76669151-76669201	H1-hESC	embryonic stem cell:	embryo
14	chr16:76666860-76666910	NT2-D1	testis:	n/a
15	chr16:76669151-76669201	HCM	heart:	n/a
16	chr16:76665665-76665715	PFSK-1	brain:	n/a
17	chr16:76668836-76668886	IMR90	lung:	fetal
18	chr16:76666860-76666910	SAEC	small airway:	n/a
19	chr16:76670197-76670247	HMEC	breast:	n/a
20	chr16:76668836-76668886	HEK293	kidney:	embryo
21	chr16:76669151-76669201	HEK293	kidney:	embryo
22	chr16:76670197-76670247	ovcar-3	ovarian:	n/a
23	chr16:76665665-76665715	SK-N-SH	brain:	n/a
24	chr16:76665665-76665715	SK-N-SH_RA	brain:	n/a
25	chr16:76669151-76669201	HCPEpiC	choroid plexus:	n/a
26	chr16:76670197-76670247	AG09319	gingival:	n/a
27	chr16:76670197-76670247	HUVEC	blood vessel:	n/a
28	chr16:76666860-76666910	HRCEpiC	kidney:	n/a
29	chr16:76670197-76670247	AG09309	skin:	n/a
30	chr16:76666860-76666910	PANC-1	pancreas:	n/a
31	chr16:76670197-76670247	HCM	heart:	n/a
32	chr16:76665665-76665715	GM06990	blood:	n/a
33	chr16:76669151-76669201	Caco-2	colon:	n/a
34	chr16:76670197-76670247	MCF10A-Er-Src	breast:	n/a
35	chr16:76670197-76670247	Caco-2	colon:	n/a
36	chr16:76669151-76669201	BE2_C	brain:	n/a
37	chr16:76670197-76670247	NB4	blood:	n/a
38	chr16:76668836-76668886	HCPEpiC	choroid plexus:	n/a
39	chr16:76668836-76668886	K562	blood:	n/a
40	chr16:76666860-76666910	HepG2	liver:	n/a
41	chr16:76668836-76668886	HPAEpiC	pulmonary alveolar:	n/a
42	chr16:76669151-76669201	Hela-S3	cervix:	n/a
43	chr16:76668836-76668886	BE2_C	brain:	n/a
44	chr16:76670197-76670247	HRE	kidney:	n/a
45	chr16:76665665-76665715	A549	lung:	n/a
46	chr16:76669151-76669201	SKMC	muscle:	n/a
47	chr16:76669151-76669201	HepG2	liver:	n/a
48	chr16:76668836-76668886	HCF	heart:	n/a
49	chr16:76666860-76666910	CMK	blood:	n/a
50	chr16:76665665-76665715	Hela-S3	cervix:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 1713 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1713 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547225721	chr16:76614406-76614407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189733201	chr16:76614421-76614422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373304033	chr16:76614438-76614439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs58304624	chr16:76614443-76614444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs562871426	chr16:76614446-76614447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72801238	chr16:76614450-76614451	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577727626	chr16:76614476-76614477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146813945	chr16:76614477-76614478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75186423	chr16:76614505-76614506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563394517	chr16:76614527-76614528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528886064	chr16:76614532-76614533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140551138	chr16:76614547-76614548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370053548	chr16:76614597-76614598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528784709	chr16:76614598-76614599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542326278	chr16:76615426-76615427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552638739	chr16:76615437-76615438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572794687	chr16:76615466-76615467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577979243	chr16:76615487-76615488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540619307	chr16:76615523-76615524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565472820	chr16:76615534-76615535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374401995	chr16:76615544-76615545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531250475	chr16:76615594-76615595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554013527	chr16:76615599-76615600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143528028	chr16:76615629-76615630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561469255	chr16:76615648-76615649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115549043	chr16:76615666-76615667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547162867	chr16:76615675-76615676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560547843	chr16:76615727-76615728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72801240	chr16:76615729-76615730	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs66746067	chr16:76615739-76615740	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138718701	chr16:76615740-76615741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537357456	chr16:76615779-76615780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141170113	chr16:76615827-76615828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567161091	chr16:76615854-76615855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184734950	chr16:76615879-76615880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189505104	chr16:76615908-76615909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150713728	chr16:76615911-76615912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538319293	chr16:76615920-76615921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533830998	chr16:76615942-76615943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553689987	chr16:76615976-76615977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180748180	chr16:76615988-76615989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374622066	chr16:76616005-76616006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74992252	chr16:76616113-76616114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186052362	chr16:76616121-76616122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371479495	chr16:76616138-76616139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575114450	chr16:76616199-76616200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540816123	chr16:76616219-76616220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61665891	chr16:76616241-76616242	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs139212126	chr16:76616244-76616245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149525370	chr16:76616259-76616260	Weak transcription	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:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76614400-76614600	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr16:76615400-76616200	Enhancers	Brain Germinal Matrix	brain
3	chr16:76616200-76616800	Weak transcription	Brain Germinal Matrix	brain
4	chr16:76616800-76617800	Enhancers	Brain Germinal Matrix	brain
5	chr16:76616800-76618000	Enhancers	Fetal Brain Male	brain
6	chr16:76616800-76618200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr16:76616800-76618400	Enhancers	Fetal Brain Female	brain
8	chr16:76617000-76617200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr16:76617000-76617200	Enhancers	Brain Angular Gyrus	brain
10	chr16:76617000-76617400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr16:76617000-76618000	Enhancers	Fetal Lung	lung
12	chr16:76617200-76617400	Flanking Active TSS	Brain Angular Gyrus	brain
13	chr16:76617200-76617600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr16:76617200-76617600	Enhancers	Adipose Nuclei	Adipose
15	chr16:76617200-76617600	Enhancers	Fetal Muscle Leg	muscle
16	chr16:76617200-76617600	Enhancers	Fetal Stomach	stomach
17	chr16:76617200-76617800	Active TSS	Brain Anterior Caudate	brain
18	chr16:76617200-76617800	Active TSS	Brain Cingulate Gyrus	brain
19	chr16:76617200-76617800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr16:76617200-76617800	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr16:76617200-76618000	Active TSS	Brain Hippocampus Middle	brain
22	chr16:76617200-76618200	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr16:76617200-76618200	Active TSS	Brain Substantia Nigra	brain
24	chr16:76617400-76617800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:76617400-76617800	Active TSS	Brain Angular Gyrus	brain
26	chr16:76617600-76618000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr16:76617800-76618200	Active TSS	Brain Germinal Matrix	brain
28	chr16:76617800-76618400	Enhancers	Brain Cingulate Gyrus	brain
29	chr16:76618000-76618200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr16:76618000-76618400	Enhancers	Brain Angular Gyrus	brain
31	chr16:76618000-76621000	Weak transcription	Fetal Lung	lung
32	chr16:76618200-76619600	Enhancers	Brain Germinal Matrix	brain
33	chr16:76618800-76619800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:76619600-76620600	Weak transcription	Brain Germinal Matrix	brain
35	chr16:76619800-76621000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr16:76620600-76620800	Enhancers	Brain Germinal Matrix	brain
37	chr16:76621000-76621200	Enhancers	Fetal Lung	lung
38	chr16:76621000-76621400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr16:76629200-76630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr16:76629600-76630000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr16:76645600-76645800	Enhancers	Placenta Amnion	Placenta Amnion
42	chr16:76646400-76647400	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr16:76647200-76650000	Enhancers	Brain Germinal Matrix	brain
44	chr16:76647400-76647800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr16:76647400-76647800	Enhancers	Placenta Amnion	Placenta Amnion
46	chr16:76647600-76648800	Enhancers	Brain Substantia Nigra	brain
47	chr16:76647800-76648200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr16:76647800-76649000	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr16:76647800-76649400	Enhancers	Fetal Brain Female	brain
50	chr16:76648000-76648600	Enhancers	Brain Hippocampus Middle	brain

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