Variant report

Variant	nsv827695
Chromosome Location	chr16:59617082-59700873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:59637252-59637310	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr16:59672961-59673060	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr16:59639635-59639988	IMR90	lung:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
4	CEBPB	chr16:59627070-59627695	IMR90	lung:	n/a	chr16:59627251-59627264
5	CEBPB	chr16:59699603-59699905	HepG2	liver:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
6	CEBPB	chr16:59639640-59639961	HepG2	liver:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
7	CEBPB	chr16:59619057-59619288	HepG2	liver:	n/a	n/a
8	CEBPB	chr16:59638295-59638509	HepG2	liver:	n/a	chr16:59638376-59638387 chr16:59638376-59638389 chr16:59638376-59638387 chr16:59638377-59638388
9	CEBPB	chr16:59674551-59674832	HepG2	liver:	n/a	chr16:59674679-59674690 chr16:59674668-59674679
10	CEBPB	chr16:59640531-59640537	A549	lung:	n/a	n/a
11	CEBPB	chr16:59652522-59652789	IMR90	lung:	n/a	chr16:59652665-59652676
12	CEBPB	chr16:59641136-59641336	A549	lung:	n/a	n/a
13	CEBPB	chr16:59667835-59668479	IMR90	lung:	n/a	n/a
14	CEBPB	chr16:59699560-59699871	IMR90	lung:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
15	CEBPB	chr16:59638167-59638644	A549	lung:	n/a	chr16:59638376-59638387 chr16:59638376-59638389 chr16:59638185-59638197 chr16:59638376-59638387 chr16:59638377-59638388
16	CEBPB	chr16:59652494-59652790	HepG2	liver:	n/a	chr16:59652665-59652676
17	CEBPB	chr16:59639646-59640003	A549	lung:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
18	CEBPB	chr16:59699676-59699852	A549	lung:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
19	CEBPB	chr16:59674581-59674822	A549	lung:	n/a	chr16:59674679-59674690 chr16:59674668-59674679
20	CEBPB	chr16:59639781-59639958	K562	blood:	n/a	chr16:59639806-59639817
21	CTCF	chr16:59625460-59625610	AG09309	skin:	n/a	n/a
22	CTCF	chr16:59625484-59625633	LNCaP	prostate:	n/a	n/a
23	CTCF	chr16:59662481-59662515	GM20000	blood:	n/a	n/a
24	CTCF	chr16:59625440-59625590	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr16:59625500-59625650	BJ	skin:	n/a	n/a
26	CTCF	chr16:59625440-59625590	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr16:59625440-59625590	AG09309	skin:	n/a	n/a
28	CTCF	chr16:59627300-59627450	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr16:59625460-59625610	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr16:59625460-59625610	AG10803	skin:	n/a	n/a
31	CTCF	chr16:59625480-59625630	AG09319	gingival:	n/a	n/a
32	CTCF	chr16:59625420-59625570	HAc	cerebellar:	n/a	n/a
33	CTCF	chr16:59632960-59633110	GM12865	blood:	n/a	n/a
34	CTCF	chr16:59641611-59641652	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr16:59625480-59625630	AG10803	skin:	n/a	n/a
36	CTCF	chr16:59625473-59625652	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr16:59640000-59640150	AG10803	skin:	n/a	n/a
38	CTCF	chr16:59625480-59625630	BJ	skin:	n/a	n/a
39	CTCF	chr16:59625433-59625613	ProgFib	skin:	n/a	n/a
40	CTCF	chr16:59625500-59625650	HCFaa	heart:	n/a	n/a
41	CTCF	chr16:59625360-59625510	HVMF	connective:	n/a	n/a
42	CTCF	chr16:59625520-59625670	HCM	heart:	n/a	n/a
43	CTCF	chr16:59689220-59689370	BJ	skin:	n/a	n/a
44	CTCF	chr16:59625520-59625670	AG09319	gingival:	n/a	n/a
45	CTCF	chr16:59625540-59625690	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr16:59625506-59625517	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr16:59679660-59679810	HCPEpiC	choroid plexus:	n/a	chr16:59679685-59679701 chr16:59679684-59679702
48	CTCF	chr16:59625360-59625510	WI-38	lung:	n/a	n/a
49	CTCF	chr16:59625530-59625635	LNCaP	prostate:	n/a	n/a
50	CTCF	chr16:59625600-59625750	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:59656293-59656343	AG09319	gingival:	n/a
2	chr16:59656293-59656343	AG09319	gingival:	n/a
3	chr16:59627519-59627569	A549	lung:	n/a
4	chr16:59656293-59656343	K562	blood:	n/a
5	chr16:59627519-59627569	SK-N-SH_RA	brain:	n/a
6	chr16:59656293-59656343	GM12892	blood:	n/a
7	chr16:59627519-59627569	T-47D	breast:	n/a
8	chr16:59656293-59656343	NHBE	bronchial:	n/a
9	chr16:59656293-59656343	A549	lung:	n/a
10	chr16:59656293-59656343	ProgFib	skin:	n/a
11	chr16:59656293-59656343	Caco-2	colon:	n/a
12	chr16:59627519-59627569	BE2_C	brain:	n/a
13	chr16:59656293-59656343	AoSMC	blood vessel:	n/a
14	chr16:59627519-59627569	GM06990	blood:	n/a
15	chr16:59627519-59627569	GM12891	blood:	n/a
16	chr16:59656293-59656343	RPTEC	kidney:	n/a
17	chr16:59656293-59656343	AG09309	skin:	n/a
18	chr16:59656293-59656343	T-47D	breast:	n/a
19	chr16:59656293-59656343	HCM	heart:	n/a
20	chr16:59656293-59656343	Jurkat	blood:	n/a
21	chr16:59627519-59627569	HUVEC	blood vessel:	n/a
22	chr16:59627519-59627569	AG10803	skin:	n/a
23	chr16:59656293-59656343	HAEpiC	amniotic membrane:	n/a
24	chr16:59627519-59627569	HL-60	blood:	n/a
25	chr16:59656293-59656343	IMR90	lung:	fetal
26	chr16:59656293-59656343	NB4	blood:	n/a
27	chr16:59656293-59656343	NHDF-neo	bronchial:	n/a
28	chr16:59656293-59656343	SKMC	muscle:	n/a
29	chr16:59656293-59656343	HRPEpiC	eye:	n/a
30	chr16:59627519-59627569	H1-hESC	embryonic stem cell:	embryo
31	chr16:59656293-59656343	AG10803	skin:	n/a
32	chr16:59656293-59656343	PFSK-1	brain:	n/a
33	chr16:59656293-59656343	H1-hESC	embryonic stem cell:	embryo
34	chr16:59627519-59627569	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:59656293-59656343	U87	brain:	n/a
36	chr16:59627519-59627569	NT2-D1	testis:	n/a
37	chr16:59627519-59627569	Jurkat	blood:	n/a
38	chr16:59627519-59627569	NB4	blood:	n/a
39	chr16:59627519-59627569	HCF	heart:	n/a
40	chr16:59627519-59627569	HRE	kidney:	n/a
41	chr16:59627519-59627569	HRPEpiC	eye:	n/a
42	chr16:59627519-59627569	SK-N-SH	brain:	n/a
43	chr16:59627519-59627569	HCPEpiC	choroid plexus:	n/a
44	chr16:59627519-59627569	HEK293	kidney:	embryo
45	chr16:59656293-59656343	HepG2	liver:	n/a
46	chr16:59656293-59656343	SK-N-SH_RA	brain:	n/a
47	chr16:59656293-59656343	HRCEpiC	kidney:	n/a
48	chr16:59627519-59627569	K562	blood:	n/a
49	chr16:59627519-59627569	RPTEC	kidney:	n/a
50	chr16:59627519-59627569	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:59635524..59637585-chr16:59638803..59640976,2	K562	blood:
2	chr16:59635524..59637585-chr16:59638803..59640976,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETD6-13	chr16:59690034-59690240	NONHSAT142891
2	lnc-SETD6-13	chr16:59689506-59689824	NONHSAT142891

Variant related genes	Relation type
ENSG00000270222	TF binding region
ENSG00000270222	CpG island

Extended variants
information (count: 2330 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2330 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563695822	chr16:59617103-59617104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573010394	chr16:59617107-59617108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564119529	chr16:59617113-59617114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528099485	chr16:59617148-59617149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6500046	chr16:59617171-59617172	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs185989386	chr16:59617194-59617195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75364378	chr16:59617208-59617209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371331536	chr16:59617250-59617251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546060989	chr16:59617287-59617288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570219962	chr16:59617397-59617398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531154477	chr16:59617427-59617428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528181778	chr16:59617430-59617431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141179078	chr16:59617435-59617436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190987573	chr16:59617465-59617466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376088430	chr16:59617525-59617526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534709455	chr16:59617535-59617536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150747732	chr16:59617547-59617548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568487300	chr16:59617556-59617557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535927345	chr16:59617583-59617584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139116146	chr16:59617591-59617592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73558791	chr16:59617608-59617609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539600093	chr16:59617612-59617613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558092902	chr16:59617617-59617618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540175761	chr16:59617680-59617681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17258603	chr16:59617744-59617745	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs371280131	chr16:59617752-59617753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200901244	chr16:59617833-59617834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35451281	chr16:59617849-59617850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376623156	chr16:59617872-59617873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561704018	chr16:59617886-59617887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528245821	chr16:59617912-59617913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34287900	chr16:59617960-59617961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149824480	chr16:59618007-59618008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532237104	chr16:59618110-59618111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562396520	chr16:59618165-59618166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531018852	chr16:59618189-59618190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367907306	chr16:59618270-59618271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12935627	chr16:59618321-59618322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12921844	chr16:59618322-59618323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182075648	chr16:59618402-59618403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564458439	chr16:59618411-59618412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146857800	chr16:59618420-59618421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139739746	chr16:59618425-59618426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11312077	chr16:59618472-59618473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77273658	chr16:59618485-59618486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs80232528	chr16:59618487-59618488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568435128	chr16:59618538-59618539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535623229	chr16:59618575-59618576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551058920	chr16:59618597-59618598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144530905	chr16:59618615-59618616	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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	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
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	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
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Infertility	21528002	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Neurodevelopmental disorder	22521361	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	18414403	CNVD
Breast cancer	20409316	CNVD
Chordoma	18071362	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
Ovarian clear cell carcinoma	21343371	CNVD
Ovarian cancer	21720365	CNVD
Leiomyosarcoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20972252	CNVD
Invasive breast cancer	20972252	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:59615000-59619400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr16:59617200-59617800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr16:59619400-59621200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr16:59621200-59622000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr16:59622000-59622600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr16:59624600-59625000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:59625000-59625400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr16:59625000-59628200	Enhancers	NHDF-Ad	bronchial
9	chr16:59625200-59627200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr16:59625200-59627400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr16:59625200-59627400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr16:59625400-59625600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr16:59625400-59626000	Enhancers	NHLF	lung
14	chr16:59625400-59627400	Enhancers	Osteobl	bone
15	chr16:59625600-59639400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr16:59625800-59626800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr16:59625800-59628000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr16:59625800-59628000	Enhancers	HSMM	muscle
19	chr16:59625800-59628800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr16:59626000-59626400	Weak transcription	NHLF	lung
21	chr16:59626400-59628200	Enhancers	NHLF	lung
22	chr16:59626600-59627600	Enhancers	HSMMtube	muscle
23	chr16:59626600-59628000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr16:59626800-59627800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr16:59626800-59627800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr16:59626800-59628000	Enhancers	NH-A	brain
27	chr16:59627000-59627800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr16:59627200-59627400	Enhancers	A549	lung
29	chr16:59627200-59627600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:59627400-59627800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr16:59627400-59627800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr16:59627400-59627800	Flanking Active TSS	Osteobl	bone
33	chr16:59627600-59627800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr16:59627600-59631200	Weak transcription	HSMMtube	muscle
35	chr16:59627800-59628000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr16:59627800-59628200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr16:59627800-59628400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:59627800-59628600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr16:59627800-59628800	Enhancers	Osteobl	bone
40	chr16:59628000-59631000	Weak transcription	HSMM	muscle
41	chr16:59628000-59631200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr16:59628000-59631200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr16:59628200-59631000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr16:59628200-59631000	Weak transcription	NHDF-Ad	bronchial
45	chr16:59628200-59631200	Weak transcription	NHLF	lung
46	chr16:59628400-59628800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr16:59628600-59630800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr16:59628800-59629000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr16:59628800-59631000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr16:59628800-59631000	Weak transcription	Osteobl	bone

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