Variant report

Variant	nsv827755
Chromosome Location	chr16:76687126-76786702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:616)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
3	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
6	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
7	CEBPB	chr16:76687171-76687709	MCF-7	breast:	n/a	n/a
8	CEBPB	chr16:76714462-76714734	HepG2	liver:	n/a	chr16:76714617-76714628 chr16:76714616-76714629
9	CEBPB	chr16:76777703-76778010	IMR90	lung:	n/a	chr16:76777865-76777876
10	CEBPB	chr16:76782202-76782512	HepG2	liver:	n/a	chr16:76782369-76782380
11	CEBPB	chr16:76687256-76687678	A549	lung:	n/a	n/a
12	CEBPB	chr16:76756351-76756650	IMR90	lung:	n/a	chr16:76756489-76756502 chr16:76756490-76756501 chr16:76756620-76756631
13	CEBPB	chr16:76756458-76756533	K562	blood:	n/a	chr16:76756489-76756502 chr16:76756490-76756501
14	CEBPB	chr16:76737550-76737552	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr16:76710097-76710858	MCF-7	breast:	n/a	n/a
17	CEBPB	chr16:76687295-76687707	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
19	CEBPB	chr16:76777705-76778043	HepG2	liver:	n/a	chr16:76777865-76777876
20	CEBPB	chr16:76687291-76687702	HepG2	liver:	n/a	n/a
21	CEBPB	chr16:76700933-76701106	HepG2	liver:	n/a	chr16:76700935-76700946 chr16:76701040-76701051 chr16:76700935-76700946
22	CEBPB	chr16:76734178-76734430	IMR90	lung:	n/a	n/a
23	CEBPB	chr16:76687366-76687695	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:76698299-76698542	HepG2	liver:	n/a	n/a
25	CEBPB	chr16:76687301-76687681	IMR90	lung:	n/a	n/a
26	CEBPB	chr16:76777685-76778008	A549	lung:	n/a	chr16:76777865-76777876
27	CEBPB	chr16:76782214-76782511	A549	lung:	n/a	chr16:76782369-76782380
28	CEBPB	chr16:76687392-76687580	K562	blood:	n/a	n/a
29	CEBPB	chr16:76695763-76696093	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:76687305-76687716	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
32	CEBPB	chr16:76710451-76710670	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
34	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
35	CEBPB	chr16:76710226-76710819	MCF-7	breast:	n/a	n/a
36	CEBPB	chr16:76782215-76782526	IMR90	lung:	n/a	chr16:76782369-76782380
37	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
38	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a
39	CEBPB	chr16:76687200-76687807	A549	lung:	n/a	n/a
40	CEBPB	chr16:76756359-76756661	HepG2	liver:	n/a	chr16:76756489-76756502 chr16:76756490-76756501 chr16:76756620-76756631
41	CEBPB	chr16:76734138-76734455	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
43	CEBPZ	chr16:76708231-76708232	HepG2	liver:	n/a	n/a
44	CHD2	chr16:76717030-76717036	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr16:76687800-76687950	GM12873	blood:	n/a	n/a
46	CTCF	chr16:76702252-76702613	MCF-7	breast:	n/a	n/a
47	CTCF	chr16:76687480-76687630	HCM	heart:	n/a	chr16:76687510-76687531 chr16:76687516-76687532 chr16:76687520-76687528 chr16:76687515-76687533
48	CTCF	chr16:76687421-76687595	SK-N-SH_RA	brain:	n/a	chr16:76687510-76687531 chr16:76687516-76687532 chr16:76687520-76687528 chr16:76687515-76687533
49	CTCF	chr16:76700410-76700479	MCF-7	breast:	n/a	n/a
50	CTCF	chr16:76699600-76699750	HMEC	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76708064-76708114	NB4	blood:	n/a
2	chr16:76708064-76708114	AoSMC	blood vessel:	n/a
3	chr16:76708064-76708114	HMEC	breast:	n/a
4	chr16:76708064-76708114	SKMC	muscle:	n/a
5	chr16:76708064-76708114	SK-N-SH	brain:	n/a
6	chr16:76708064-76708114	Caco-2	colon:	n/a
7	chr16:76708064-76708114	HNPCEpiC	eye:	n/a
8	chr16:76708064-76708114	K562	blood:	n/a
9	chr16:76708064-76708114	NHBE	bronchial:	n/a
10	chr16:76708064-76708114	GM12878	blood:	n/a
11	chr16:76708064-76708114	HPAEpiC	pulmonary alveolar:	n/a
12	chr16:76708064-76708114	HCF	heart:	n/a
13	chr16:76708064-76708114	BJ	skin:	n/a
14	chr16:76708064-76708114	NHDF-neo	bronchial:	n/a
15	chr16:76708064-76708114	BE2_C	brain:	n/a
16	chr16:76708064-76708114	Hela-S3	cervix:	n/a
17	chr16:76708064-76708114	SK-N-SH_RA	brain:	n/a
18	chr16:76708064-76708114	U87	brain:	n/a
19	chr16:76708064-76708114	Hepatocyte	liver:	n/a
20	chr16:76708064-76708114	A549	lung:	n/a
21	chr16:76708064-76708114	MCF-7	breast:	n/a
22	chr16:76708064-76708114	AG04450	lung:	fetal
23	chr16:76708064-76708114	HCT-116	colon:	n/a
24	chr16:76708064-76708114	SAEC	small airway:	n/a
25	chr16:76708064-76708114	AG10803	skin:	n/a
26	chr16:76708064-76708114	RPTEC	kidney:	n/a
27	chr16:76708064-76708114	HCM	heart:	n/a
28	chr16:76708064-76708114	H1-hESC	embryonic stem cell:	embryo
29	chr16:76708064-76708114	HCPEpiC	choroid plexus:	n/a
30	chr16:76708064-76708114	SK-N-MC	brain:	n/a
31	chr16:76708064-76708114	AG09319	gingival:	n/a
32	chr16:76708064-76708114	ovcar-3	ovarian:	n/a
33	chr16:76708064-76708114	NT2-D1	testis:	n/a
34	chr16:76708064-76708114	HEEpiC	esophagus:	n/a
35	chr16:76708064-76708114	HIPEpiC	eye:	n/a
36	chr16:76708064-76708114	HEK293	kidney:	embryo
37	chr16:76708064-76708114	PrEC	prostate:	n/a
38	chr16:76708064-76708114	HRCEpiC	kidney:	n/a
39	chr16:76708064-76708114	LNCaP	prostate:	n/a
40	chr16:76708064-76708114	GM12892	blood:	n/a
41	chr16:76708064-76708114	CMK	blood:	n/a
42	chr16:76708064-76708114	Jurkat	blood:	n/a
43	chr16:76708064-76708114	HepG2	liver:	n/a
44	chr16:76708064-76708114	T-47D	breast:	n/a
45	chr16:76708064-76708114	MCF10A-Er-Src	breast:	n/a
46	chr16:76708064-76708114	PANC-1	pancreas:	n/a
47	chr16:76708064-76708114	AG09309	skin:	n/a
48	chr16:76708064-76708114	HAEpiC	amniotic membrane:	n/a
49	chr16:76708064-76708114	NH-A	brain:	n/a
50	chr16:76708064-76708114	HUVEC	blood vessel:	n/a

(count:25 , 50 per page) page: 1

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

(count:5 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2008 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2008 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142265759	chr16:76687206-76687207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190132786	chr16:76687223-76687224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76867794	chr16:76687310-76687311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs151330673	chr16:76687355-76687356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183491709	chr16:76687405-76687406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577995034	chr16:76687442-76687443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139396700	chr16:76687453-76687454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542997693	chr16:76687483-76687484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555420969	chr16:76687501-76687502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572306193	chr16:76687502-76687503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188499167	chr16:76687516-76687517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555683915	chr16:76687581-76687582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577892604	chr16:76687602-76687603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543580574	chr16:76687635-76687636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563458792	chr16:76687671-76687672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569030914	chr16:76687676-76687677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111946828	chr16:76687683-76687684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367765336	chr16:76687703-76687704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537911965	chr16:76687718-76687719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528931270	chr16:76687746-76687747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548967462	chr16:76687756-76687757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559047343	chr16:76687759-76687760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184226058	chr16:76687763-76687764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145559669	chr16:76687778-76687779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374096322	chr16:76687792-76687793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115707305	chr16:76687805-76687806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113321281	chr16:76687806-76687807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577795049	chr16:76687817-76687818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57193263	chr16:76687846-76687847	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77662748	chr16:76687881-76687882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187714029	chr16:76687918-76687919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553339257	chr16:76687923-76687924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573118473	chr16:76687945-76687946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77858215	chr16:76687947-76687948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574235099	chr16:76687971-76687972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142529256	chr16:76687994-76687995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191410532	chr16:76687995-76687996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543641441	chr16:76688007-76688008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146969736	chr16:76688014-76688015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146486492	chr16:76688029-76688030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370873091	chr16:76688031-76688032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374956314	chr16:76688115-76688116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573690441	chr16:76688131-76688132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144936372	chr16:76688155-76688156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551488699	chr16:76688170-76688171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367612022	chr16:76688183-76688184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183532851	chr16:76688184-76688185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73629988	chr16:76688211-76688212	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs138595063	chr16:76688235-76688236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565227720	chr16:76688269-76688270	Enhancers Weak transcription	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
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76687200-76687800	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr16:76687200-76688000	Enhancers	Brain Substantia Nigra	brain
3	chr16:76687200-76688200	Enhancers	Fetal Lung	lung
4	chr16:76687600-76688200	Enhancers	Brain Hippocampus Middle	brain
5	chr16:76687600-76689600	Enhancers	Brain Germinal Matrix	brain
6	chr16:76688200-76690600	Weak transcription	Fetal Lung	lung
7	chr16:76689600-76690400	Weak transcription	Brain Germinal Matrix	brain
8	chr16:76690000-76692000	Enhancers	Primary hematopoietic stem cells	blood
9	chr16:76690400-76692000	Enhancers	Brain Germinal Matrix	brain
10	chr16:76690600-76691800	Enhancers	Fetal Lung	lung
11	chr16:76690600-76692000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr16:76690600-76692000	Enhancers	Fetal Muscle Leg	muscle
13	chr16:76691400-76692000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr16:76692000-76694600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr16:76693400-76694000	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr16:76694000-76699400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr16:76694600-76696400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr16:76695000-76696200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr16:76696600-76714800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr16:76699400-76699600	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr16:76699600-76704000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr16:76699800-76700400	Enhancers	Primary hematopoietic stem cells	blood
23	chr16:76700400-76703200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr16:76703200-76703400	Active TSS	Primary hematopoietic stem cells	blood
25	chr16:76703400-76703600	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr16:76703600-76704600	Enhancers	Primary hematopoietic stem cells	blood
27	chr16:76703800-76704800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr16:76704000-76705200	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr16:76704800-76709400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:76707400-76708200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr16:76707600-76708000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr16:76708000-76709800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr16:76708000-76710800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr16:76708200-76710200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr16:76708600-76711400	Enhancers	Placenta Amnion	Placenta Amnion
36	chr16:76708800-76709000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr16:76708800-76709600	Enhancers	Fetal Lung	lung
38	chr16:76708800-76710800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr16:76709000-76710200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr16:76709200-76711200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr16:76709200-76711400	Enhancers	HMEC	breast
42	chr16:76709400-76711000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr16:76709400-76711400	Enhancers	Placenta	Placenta
44	chr16:76709800-76710600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr16:76710000-76710800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr16:76710200-76710800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr16:76710200-76710800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr16:76710200-76710800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr16:76710200-76710800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:76710400-76710800	Enhancers	H1 Cell Line	embryonic stem cell

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