Variant report

Variant	nsv827630
Chromosome Location	chr16:33773075-33859790
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	CEBPB	chr16:33820888-33821000	K562	blood:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
2	CEBPB	chr16:33820719-33821164	HepG2	liver:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
3	CEBPB	chr16:33857091-33857092	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr16:33820812-33821002	Hela-S3	cervix:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
5	CEBPB	chr16:33856598-33857932	A549	lung:	n/a	chr16:33857668-33857679
6	CEBPB	chr16:33857525-33857711	Hela-S3	cervix:	n/a	chr16:33857668-33857679
7	CEBPB	chr16:33820733-33821084	K562	blood:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
8	CEBPB	chr16:33820735-33821142	IMR90	lung:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
9	CEBPB	chr16:33856667-33857782	IMR90	lung:	n/a	chr16:33857668-33857679
10	CEBPB	chr16:33820727-33821192	A549	lung:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
11	CEBPB	chr16:33856594-33857899	HepG2	liver:	n/a	chr16:33857668-33857679
12	CTCF	chr16:33798360-33798510	K562	blood:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
13	CTCF	chr16:33798483-33798567	GM12891	blood:	n/a	n/a
14	CTCF	chr16:33777103-33777311	LNCaP	prostate:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
15	CTCF	chr16:33801008-33801084	MCF-7	breast:	n/a	chr16:33801062-33801075 chr16:33801059-33801077 chr16:33801062-33801071
16	CTCF	chr16:33775676-33775735	MCF-7	breast:	n/a	n/a
17	CTCF	chr16:33793195-33793267	LNCaP	prostate:	n/a	chr16:33793210-33793223
18	CTCF	chr16:33798426-33798582	HepG2	liver:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
19	CTCF	chr16:33777164-33777274	MCF-7	breast:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
20	CTCF	chr16:33777113-33777282	HepG2	liver:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
21	CTCF	chr16:33806206-33806287	MCF-7	breast:	n/a	chr16:33806238-33806256
22	CTCF	chr16:33798380-33798530	MCF-7	breast:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
23	CTCF	chr16:33798396-33798610	MCF-7	breast:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
24	CTCF	chr16:33798376-33798553	T-47D	breast:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
25	CTCF	chr16:33798273-33798589	K562	blood:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459 chr16:33798345-33798353
26	CTCF	chr16:33798460-33798579	A549	lung:	n/a	chr16:33798476-33798494 chr16:33798471-33798492
27	CTCF	chr16:33798393-33798598	K562	blood:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
28	CTCF	chr16:33777064-33777413	K562	blood:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
29	CTCF	chr16:33777119-33777292	K562	blood:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
30	CTCF	chr16:33777204-33777276	GM20000	blood:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
31	CTCF	chr16:33798404-33798611	MCF-7	breast:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
32	CTCF	chr16:33798314-33798569	K562	blood:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459 chr16:33798345-33798353
33	CTCF	chr16:33789695-33789754	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr16:33798380-33798530	NHEK	skin:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
35	CTCF	chr16:33798340-33798490	HCT-116	colon:	n/a	chr16:33798446-33798459 chr16:33798345-33798353
36	CTCF	chr16:33775620-33775770	HepG2	liver:	n/a	n/a
37	CTCF	chr16:33777112-33777275	MCF-7	breast:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
38	CTCF	chr16:33795656-33795789	HepG2	liver:	n/a	chr16:33795713-33795734 chr16:33795724-33795733 chr16:33795719-33795735 chr16:33795721-33795731 chr16:33795718-33795736
39	CTCF	chr16:33798508-33798565	GM19240	blood:	n/a	n/a
40	CTCF	chr16:33798374-33798534	HepG2	liver:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459
41	CTCF	chr16:33777136-33777266	Hela-S3	cervix:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
42	CTCF	chr16:33775771-33775782	LNCaP	prostate:	n/a	n/a
43	CTCF	chr16:33795600-33795750	HepG2	liver:	n/a	chr16:33795713-33795734 chr16:33795724-33795733 chr16:33795719-33795735 chr16:33795721-33795731 chr16:33795718-33795736
44	CTCF	chr16:33839561-33839619	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr16:33775688-33775730	MCF-7	breast:	n/a	n/a
46	CTCF	chr16:33795400-33795550	WERI-Rb-1	eye:	n/a	chr16:33795495-33795513 chr16:33795455-33795468
47	CTCF	chr16:33806085-33806400	K562	blood:	n/a	chr16:33806238-33806256
48	CTCF	chr16:33777165-33777243	H1-hESC	embryonic stem cell:	n/a	chr16:33777212-33777230 chr16:33777217-33777227 chr16:33777215-33777224 chr16:33777215-33777228
49	CTCF	chr16:33782687-33782712	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr16:33798295-33798540	HepG2	liver:	n/a	chr16:33798476-33798494 chr16:33798471-33798492 chr16:33798446-33798459 chr16:33798345-33798353

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33779917-33779967	HRPEpiC	eye:	n/a
2	chr16:33815990-33816040	IMR90	lung:	fetal
3	chr16:33821339-33821389	HRPEpiC	eye:	n/a
4	chr16:33783802-33783852	HEEpiC	esophagus:	n/a
5	chr16:33817129-33817179	HNPCEpiC	eye:	n/a
6	chr16:33817992-33818042	Jurkat	blood:	n/a
7	chr16:33817457-33817507	GM19239	blood:	n/a
8	chr16:33821339-33821389	Hela-S3	cervix:	n/a
9	chr16:33852823-33852873	T-47D	breast:	n/a
10	chr16:33852823-33852873	AG09319	gingival:	n/a
11	chr16:33783802-33783852	HCM	heart:	n/a
12	chr16:33854086-33854136	HMEC	breast:	n/a
13	chr16:33852823-33852873	GM12892	blood:	n/a
14	chr16:33776910-33776960	HCM	heart:	n/a
15	chr16:33853473-33853523	HL-60	blood:	n/a
16	chr16:33815990-33816040	MCF-7	breast:	n/a
17	chr16:33853544-33853594	HIPEpiC	eye:	n/a
18	chr16:33818253-33818303	T-47D	breast:	n/a
19	chr16:33821339-33821389	GM19239	blood:	n/a
20	chr16:33818253-33818303	CMK	blood:	n/a
21	chr16:33817992-33818042	MCF10A-Er-Src	breast:	n/a
22	chr16:33821339-33821389	PANC-1	pancreas:	n/a
23	chr16:33852801-33852851	GM12892	blood:	n/a
24	chr16:33815990-33816040	T-47D	breast:	n/a
25	chr16:33853544-33853594	SK-N-SH	brain:	n/a
26	chr16:33853544-33853594	PFSK-1	brain:	n/a
27	chr16:33783802-33783852	GM06990	blood:	n/a
28	chr16:33781365-33781415	MCF-7	breast:	n/a
29	chr16:33776910-33776960	HepG2	liver:	n/a
30	chr16:33817457-33817507	ovcar-3	ovarian:	n/a
31	chr16:33852823-33852873	HCPEpiC	choroid plexus:	n/a
32	chr16:33776910-33776960	AG04450	lung:	fetal
33	chr16:33851284-33851334	SK-N-MC	brain:	n/a
34	chr16:33851284-33851334	SK-N-SH	brain:	n/a
35	chr16:33821339-33821389	GM12892	blood:	n/a
36	chr16:33854086-33854136	SAEC	small airway:	n/a
37	chr16:33815990-33816040	GM12891	blood:	n/a
38	chr16:33779917-33779967	NB4	blood:	n/a
39	chr16:33821339-33821389	U87	brain:	n/a
40	chr16:33783802-33783852	SK-N-SH	brain:	n/a
41	chr16:33817457-33817507	PFSK-1	brain:	n/a
42	chr16:33852823-33852873	NHBE	bronchial:	n/a
43	chr16:33817992-33818042	ProgFib	skin:	n/a
44	chr16:33779917-33779967	AG09319	gingival:	n/a
45	chr16:33853473-33853523	HCF	heart:	n/a
46	chr16:33818253-33818303	AG04450	lung:	fetal
47	chr16:33852823-33852873	GM12878	blood:	n/a
48	chr16:33853176-33853226	HepG2	liver:	n/a
49	chr16:33818253-33818303	PFSK-1	brain:	n/a
50	chr16:33821339-33821389	HL-60	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-6	chr16:33777416-33777550	ENSG00000205452.4
2	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4
3	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4
4	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
5	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
6	lnc-AC140658.1-6	chr16:33775514-33776189	ENSG00000205452.4
7	lnc-AC140658.1-6	chr16:33776448-33776670	ENSG00000205452.4
8	lnc-AC140658.1-6	chr16:33776833-33776957	ENSG00000205452.4
9	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4

Variant related genes	Relation type
ENSG00000205452	TF binding region
ENSG00000198555	TF binding region
ENSG00000270401	TF binding region
ENSG00000261217	TF binding region
ENSG00000261197	TF binding region
ENSG00000259990	TF binding region
ENSG00000205452	CpG island
ENSG00000198555	CpG island
ENSG00000270401	CpG island
ENSG00000261217	CpG island
ENSG00000261197	CpG island
ENSG00000259990	CpG island

Extended variants
information (count: 888 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146869809	chr16:33773732-33773733	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs62040311	chr16:33773747-33773748	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs571979498	chr16:33773771-33773772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs539304768	chr16:33773839-33773840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs661389	chr16:33773854-33773855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs557016262	chr16:33773861-33773862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs575339732	chr16:33773865-33773866	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542593134	chr16:33773879-33773880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs554410282	chr16:33773893-33773894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs561485544	chr16:33773894-33773895	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs368912729	chr16:33773922-33773923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531790216	chr16:33773924-33773925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs79432092	chr16:33773925-33773926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs369055419	chr16:33773963-33773964	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs564700764	chr16:33774006-33774007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs532291897	chr16:33774046-33774047	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs201262271	chr16:33774981-33774982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs561300849	chr16:33775535-33775536	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs186003612	chr16:33775668-33775669	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs140141409	chr16:33775689-33775690	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs112810909	chr16:33775705-33775706	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs547142553	chr16:33775711-33775712	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs571753228	chr16:33775717-33775718	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs532796546	chr16:33775721-33775722	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs563659230	chr16:33775780-33775781	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs138319629	chr16:33775828-33775829	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs551193887	chr16:33775868-33775869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs569454140	chr16:33775891-33775892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs536910778	chr16:33775901-33775902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs201238756	chr16:33775931-33775932	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs566438695	chr16:33775988-33775989	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs533533693	chr16:33776088-33776089	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs381097	chr16:33776093-33776094	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs369423794	chr16:33776125-33776126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs558267041	chr16:33776163-33776164	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs200462161	chr16:33776205-33776206	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs576525015	chr16:33776221-33776222	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs537651964	chr16:33776428-33776429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs555897262	chr16:33776448-33776449	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs574657292	chr16:33776534-33776535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs189793013	chr16:33776864-33776865	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs560165485	chr16:33778670-33778671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573222040	chr16:33778689-33778690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540621157	chr16:33778698-33778699	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs201251085	chr16:33778710-33778711	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs181307183	chr16:33778714-33778715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs565427080	chr16:33778725-33778726	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs532605097	chr16:33778731-33778732	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551205938	chr16:33778739-33778740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs563064386	chr16:33778787-33778788	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Ductal carcinoma	22052326	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
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33784400-33784800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr16:33784400-33784800	Active TSS	HSMM	muscle
3	chr16:33794600-33795000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr16:33794600-33795600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr16:33795000-33795600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr16:33795600-33797400	Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr16:33795600-33798000	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr16:33797400-33798000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr16:33798000-33798200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr16:33798000-33798400	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr16:33803800-33804600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr16:33804400-33804800	Enhancers	Left Ventricle	heart
13	chr16:33817000-33817200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
14	chr16:33817000-33817400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:33817000-33818000	Bivalent Enhancer	Placenta	Placenta
16	chr16:33817600-33817800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
17	chr16:33836400-33836800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr16:33852200-33852400	Active TSS	Brain Hippocampus Middle	brain
19	chr16:33852400-33852600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
20	chr16:33852600-33853400	Flanking Bivalent TSS/Enh	Placenta	Placenta
21	chr16:33852800-33854000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:33853000-33853600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
23	chr16:33853400-33853600	Bivalent Enhancer	Placenta	Placenta
24	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:33856800-33857800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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