Variant report

Variant	nsv572832
Chromosome Location	chr16:59578561-59756567
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	ATF3	chr16:59607268-59608238	A549	lung:	n/a	chr16:59607669-59607680 chr16:59607669-59607680 chr16:59607671-59607679 chr16:59607669-59607682
2	ATF3	chr16:59607286-59608197	A549	lung:	n/a	chr16:59607669-59607680 chr16:59607669-59607680 chr16:59607671-59607679 chr16:59607669-59607682
3	BACH1	chr16:59637252-59637310	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr16:59607250-59608289	A549	lung:	n/a	chr16:59607950-59607959
5	BCL3	chr16:59607280-59608220	A549	lung:	n/a	chr16:59607950-59607959
6	CEBPB	chr16:59611123-59611379	HepG2	liver:	n/a	chr16:59611239-59611250
7	CEBPB	chr16:59652494-59652790	HepG2	liver:	n/a	chr16:59652665-59652676
8	CEBPB	chr16:59699603-59699905	HepG2	liver:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
9	CEBPB	chr16:59639640-59639961	HepG2	liver:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
10	CEBPB	chr16:59728890-59729203	IMR90	lung:	n/a	chr16:59729056-59729067
11	CEBPB	chr16:59728966-59729119	K562	blood:	n/a	chr16:59729056-59729067
12	CEBPB	chr16:59639635-59639988	IMR90	lung:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
13	CEBPB	chr16:59638295-59638509	HepG2	liver:	n/a	chr16:59638376-59638387 chr16:59638376-59638389 chr16:59638376-59638387 chr16:59638377-59638388
14	CEBPB	chr16:59699560-59699871	IMR90	lung:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
15	CEBPB	chr16:59728909-59729189	HepG2	liver:	n/a	chr16:59729056-59729067
16	CEBPB	chr16:59731195-59731541	IMR90	lung:	n/a	n/a
17	CEBPB	chr16:59728926-59729209	A549	lung:	n/a	chr16:59729056-59729067
18	CEBPB	chr16:59639781-59639958	K562	blood:	n/a	chr16:59639806-59639817
19	CEBPB	chr16:59607839-59608171	A549	lung:	n/a	n/a
20	CEBPB	chr16:59702500-59702739	IMR90	lung:	n/a	chr16:59702597-59702608
21	CEBPB	chr16:59752932-59753285	A549	lung:	n/a	chr16:59753078-59753089
22	CEBPB	chr16:59607305-59607809	A549	lung:	n/a	chr16:59607756-59607768
23	CEBPB	chr16:59752998-59753271	K562	blood:	n/a	chr16:59753078-59753089
24	CEBPB	chr16:59674581-59674822	A549	lung:	n/a	chr16:59674679-59674690 chr16:59674668-59674679
25	CEBPB	chr16:59732911-59733165	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:59640531-59640537	A549	lung:	n/a	n/a
27	CEBPB	chr16:59702527-59702671	HepG2	liver:	n/a	chr16:59702597-59702608
28	CEBPB	chr16:59606859-59607041	A549	lung:	n/a	n/a
29	CEBPB	chr16:59672961-59673060	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr16:59607451-59607761	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:59614762-59614870	A549	lung:	n/a	n/a
32	CEBPB	chr16:59638167-59638644	A549	lung:	n/a	chr16:59638376-59638387 chr16:59638376-59638389 chr16:59638185-59638197 chr16:59638376-59638387 chr16:59638377-59638388
33	CEBPB	chr16:59674551-59674832	HepG2	liver:	n/a	chr16:59674679-59674690 chr16:59674668-59674679
34	CEBPB	chr16:59667835-59668479	IMR90	lung:	n/a	n/a
35	CEBPB	chr16:59641136-59641336	A549	lung:	n/a	n/a
36	CEBPB	chr16:59607352-59608186	IMR90	lung:	n/a	chr16:59607756-59607768
37	CEBPB	chr16:59752968-59753260	Hela-S3	cervix:	n/a	chr16:59753078-59753089
38	CEBPB	chr16:59619057-59619288	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:59627070-59627695	IMR90	lung:	n/a	chr16:59627251-59627264
40	CEBPB	chr16:59652522-59652789	IMR90	lung:	n/a	chr16:59652665-59652676
41	CEBPB	chr16:59752911-59753298	HepG2	liver:	n/a	chr16:59753078-59753089
42	CEBPB	chr16:59717805-59717880	A549	lung:	n/a	n/a
43	CEBPB	chr16:59752926-59753295	IMR90	lung:	n/a	chr16:59753078-59753089
44	CEBPB	chr16:59699676-59699852	A549	lung:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
45	CEBPB	chr16:59607195-59608611	A549	lung:	n/a	chr16:59608246-59608258 chr16:59607756-59607768
46	CEBPB	chr16:59639646-59640003	A549	lung:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
47	CEBPB	chr16:59607369-59608128	A549	lung:	n/a	chr16:59607756-59607768
48	CREB1	chr16:59607478-59607800	A549	lung:	n/a	n/a
49	CTCF	chr16:59625433-59625613	ProgFib	skin:	n/a	n/a
50	CTCF	chr16:59627520-59627670	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:59656293-59656343	HCM	heart:	n/a
2	chr16:59602460-59602510	PFSK-1	brain:	n/a
3	chr16:59656293-59656343	HPAEpiC	pulmonary alveolar:	n/a
4	chr16:59656293-59656343	SK-N-SH	brain:	n/a
5	chr16:59627519-59627569	HMEC	breast:	n/a
6	chr16:59656293-59656343	Hela-S3	cervix:	n/a
7	chr16:59627519-59627569	GM12892	blood:	n/a
8	chr16:59627519-59627569	HepG2	liver:	n/a
9	chr16:59602460-59602510	HRCEpiC	kidney:	n/a
10	chr16:59627519-59627569	HCF	heart:	n/a
11	chr16:59656293-59656343	NHDF-neo	bronchial:	n/a
12	chr16:59602460-59602510	GM12878	blood:	n/a
13	chr16:59627519-59627569	HEEpiC	esophagus:	n/a
14	chr16:59627519-59627569	T-47D	breast:	n/a
15	chr16:59627519-59627569	AG09309	skin:	n/a
16	chr16:59656293-59656343	U87	brain:	n/a
17	chr16:59602460-59602510	HIPEpiC	eye:	n/a
18	chr16:59627519-59627569	H1-hESC	embryonic stem cell:	embryo
19	chr16:59602460-59602510	ECC-1	luminal epithelium:	n/a
20	chr16:59602460-59602510	Jurkat	blood:	n/a
21	chr16:59656293-59656343	SKMC	muscle:	n/a
22	chr16:59627519-59627569	GM19239	blood:	n/a
23	chr16:59656293-59656343	PFSK-1	brain:	n/a
24	chr16:59602460-59602510	HCT-116	colon:	n/a
25	chr16:59602460-59602510	AoSMC	blood vessel:	n/a
26	chr16:59627519-59627569	HCM	heart:	n/a
27	chr16:59627519-59627569	GM12891	blood:	n/a
28	chr16:59627519-59627569	HRCEpiC	kidney:	n/a
29	chr16:59656293-59656343	NH-A	brain:	n/a
30	chr16:59627519-59627569	PANC-1	pancreas:	n/a
31	chr16:59602460-59602510	SAEC	small airway:	n/a
32	chr16:59627519-59627569	HRE	kidney:	n/a
33	chr16:59602460-59602510	GM06990	blood:	n/a
34	chr16:59627519-59627569	HUVEC	blood vessel:	n/a
35	chr16:59627519-59627569	AG04450	lung:	fetal
36	chr16:59602460-59602510	CMK	blood:	n/a
37	chr16:59602460-59602510	AG04449	skin:	fetal
38	chr16:59656293-59656343	AG04450	lung:	fetal
39	chr16:59656293-59656343	SAEC	small airway:	n/a
40	chr16:59656293-59656343	ProgFib	skin:	n/a
41	chr16:59602460-59602510	NHBE	bronchial:	n/a
42	chr16:59656293-59656343	PrEC	prostate:	n/a
43	chr16:59656293-59656343	PANC-1	pancreas:	n/a
44	chr16:59656293-59656343	AG09309	skin:	n/a
45	chr16:59602460-59602510	NB4	blood:	n/a
46	chr16:59656293-59656343	Caco-2	colon:	n/a
47	chr16:59656293-59656343	CMK	blood:	n/a
48	chr16:59627519-59627569	HCPEpiC	choroid plexus:	n/a
49	chr16:59656293-59656343	T-47D	breast:	n/a
50	chr16:59627519-59627569	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:59581382..59583967-chr16:59590690..59593280,2	MCF-7	breast:
2	chr16:59710678..59713121-chr16:59778438..59780009,2	K562	blood:
3	chr16:59635524..59637585-chr16:59638803..59640976,2	K562	blood:
4	chr16:59581382..59583967-chr16:59590690..59593280,2	MCF-7	breast:
5	chr16:59635524..59637585-chr16:59638803..59640976,2	K562	blood:
6	chr16:59730238..59732939-chr3:97563003..97565712,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETD6-13	chr16:59689506-59689824	NONHSAT142891
2	lnc-RP11-105C20.2.1-5	chr16:59744120-59744199	NONHSAT142892
3	lnc-RP11-105C20.2.1-5	chr16:59743897-59744027	NONHSAT142892
4	lnc-SETD6-13	chr16:59690034-59690240	NONHSAT142891

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

Extended variants
information (count: 4839 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4839 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8063487	chr16:59578561-59578562	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575939043	chr16:59578667-59578668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546079335	chr16:59578685-59578686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564842484	chr16:59578702-59578703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141473601	chr16:59578726-59578727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144962355	chr16:59578748-59578749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13380644	chr16:59578821-59578822	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs148307303	chr16:59578895-59578896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140478832	chr16:59578927-59578928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113195018	chr16:59578984-59578985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569006428	chr16:59578992-59578993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150435913	chr16:59579011-59579012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138011313	chr16:59579089-59579090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7185029	chr16:59579103-59579104	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533865750	chr16:59579115-59579116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549266459	chr16:59579195-59579196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7185216	chr16:59579232-59579233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs34762091	chr16:59579270-59579271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143640885	chr16:59579272-59579273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186800202	chr16:59579277-59579278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577657086	chr16:59579312-59579313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147203758	chr16:59579318-59579319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192484634	chr16:59579390-59579391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111711732	chr16:59579418-59579419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540602229	chr16:59579428-59579429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34948782	chr16:59579449-59579450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs543576560	chr16:59579489-59579490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73558736	chr16:59579501-59579502	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs78252693	chr16:59579517-59579518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562501199	chr16:59579520-59579521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77021061	chr16:59579539-59579540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551823939	chr16:59579584-59579585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560106379	chr16:59579630-59579631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527466543	chr16:59579693-59579694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549327918	chr16:59579721-59579722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34148903	chr16:59579744-59579745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188320228	chr16:59579769-59579770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147652466	chr16:59579786-59579787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62057579	chr16:59579823-59579824	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs72798428	chr16:59579836-59579837	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs193046116	chr16:59579838-59579839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538368049	chr16:59579855-59579856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143456675	chr16:59579887-59579888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77925617	chr16:59579888-59579889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202201575	chr16:59579891-59579892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528027894	chr16:59579947-59579948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553813070	chr16:59579967-59579968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573383716	chr16:59580010-59580011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534121277	chr16:59580024-59580025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555680029	chr16:59580056-59580057	Weak transcription 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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:59575200-59581400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr16:59576200-59580000	Enhancers	HSMM	muscle
3	chr16:59577000-59579800	Enhancers	NH-A	brain
4	chr16:59577200-59578800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr16:59577600-59580000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr16:59577800-59578800	Enhancers	NHDF-Ad	bronchial
7	chr16:59578200-59578600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr16:59578200-59579200	Weak transcription	HUVEC	blood vessel
9	chr16:59578600-59578800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr16:59578800-59579800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr16:59579200-59579600	Enhancers	HUVEC	blood vessel
12	chr16:59579400-59579600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr16:59579600-59581000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr16:59579800-59580200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr16:59579800-59580200	Enhancers	Fetal Lung	lung
16	chr16:59580000-59580400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr16:59580200-59586400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr16:59581000-59581200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr16:59581200-59581800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr16:59581400-59581800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr16:59586200-59586600	Enhancers	HepG2	liver
22	chr16:59586400-59586800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr16:59586400-59586800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr16:59586800-59587800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr16:59587800-59588000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr16:59587800-59588000	Enhancers	NHDF-Ad	bronchial
27	chr16:59587800-59588400	Enhancers	HSMM	muscle
28	chr16:59601400-59602000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr16:59601400-59602200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr16:59601600-59602800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr16:59601800-59602600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr16:59602400-59602800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr16:59602400-59603600	Enhancers	Fetal Heart	heart
34	chr16:59603600-59604800	Weak transcription	Fetal Heart	heart
35	chr16:59604800-59605400	Enhancers	Fetal Heart	heart
36	chr16:59605400-59606400	Weak transcription	Fetal Heart	heart
37	chr16:59606400-59606800	ZNF genes & repeats	A549	lung
38	chr16:59606600-59606800	Enhancers	Fetal Heart	heart
39	chr16:59606600-59609000	Enhancers	HSMM	muscle
40	chr16:59606800-59607200	Flanking Active TSS	A549	lung
41	chr16:59607000-59608800	Enhancers	Osteobl	bone
42	chr16:59607200-59607400	Active TSS	A549	lung
43	chr16:59607200-59608800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr16:59607200-59608800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr16:59607200-59608800	Enhancers	NH-A	brain
46	chr16:59607400-59607600	Flanking Active TSS	A549	lung
47	chr16:59607400-59608400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr16:59607400-59608600	Enhancers	NHDF-Ad	bronchial
49	chr16:59607600-59608000	Active TSS	A549	lung
50	chr16:59608000-59608800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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