Variant report

Variant	esv1809452
Chromosome Location	chr16:72094757-72109354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:505)
CpG islands
(count:306)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:72106772-72107045	K562	blood:	n/a	n/a
2	ARID3A	chr16:72096768-72097017	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:72106673-72107165	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:72100631-72100890	HepG2	liver:	n/a	n/a
5	ATF1	chr16:72106727-72107177	K562	blood:	n/a	n/a
6	BHLHE40	chr16:72106822-72107057	K562	blood:	n/a	n/a
7	BHLHE40	chr16:72100638-72100838	GM12878	blood:	n/a	n/a
8	BHLHE40	chr16:72098374-72098413	HepG2	liver:	n/a	n/a
9	BHLHE40	chr16:72100614-72101032	K562	blood:	n/a	n/a
10	CBX3	chr16:72106469-72107388	K562	blood:	n/a	n/a
11	CCNT2	chr16:72106794-72107083	K562	blood:	n/a	n/a
12	CEBPB	chr16:72096826-72097080	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
13	CEBPB	chr16:72098298-72098582	HepG2	liver:	n/a	n/a
14	CEBPB	chr16:72106854-72107148	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr16:72096795-72097213	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
16	CEBPB	chr16:72106867-72107147	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:72096800-72097221	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
18	CEBPB	chr16:72100481-72100866	K562	blood:	n/a	n/a
19	CEBPB	chr16:72096774-72097113	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
20	CEBPD	chr16:72106811-72107187	K562	blood:	n/a	n/a
21	CEBPD	chr16:72096833-72097096	HepG2	liver:	n/a	chr16:72097055-72097066
22	CEBPD	chr16:72096830-72097104	HepG2	liver:	n/a	chr16:72097055-72097066
23	CHD2	chr16:72106869-72107069	K562	blood:	n/a	n/a
24	CHD2	chr16:72106961-72107085	HepG2	liver:	n/a	n/a
25	CTCF	chr16:72102740-72102890	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr16:72100720-72100870	GM12865	blood:	n/a	n/a
27	CTCF	chr16:72100666-72100869	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr16:72100612-72100933	K562	blood:	n/a	n/a
29	CTCF	chr16:72101360-72101510	RPTEC	kidney:	n/a	n/a
30	CTCF	chr16:72100691-72100859	Fibrobl	skin:	n/a	n/a
31	CTCF	chr16:72100680-72100830	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr16:72100700-72100850	GM12866	blood:	n/a	n/a
33	CTCF	chr16:72100080-72100230	HMF	breast:	n/a	n/a
34	CTCF	chr16:72100660-72100810	GM12864	blood:	n/a	n/a
35	CTCF	chr16:72100700-72100850	GM12864	blood:	n/a	n/a
36	CTCF	chr16:72100680-72100830	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr16:72100490-72101067	HepG2	liver:	n/a	n/a
38	CTCF	chr16:72100691-72100845	GM20000	blood:	n/a	n/a
39	CTCF	chr16:72100680-72100830	GM12865	blood:	n/a	n/a
40	CTCF	chr16:72100637-72100876	GM12878	blood:	n/a	n/a
41	CTCF	chr16:72100564-72100947	A549	lung:	n/a	n/a
42	CTCF	chr16:72100240-72100390	GM12864	blood:	n/a	n/a
43	CTCF	chr16:72099860-72100010	HPF	lung:	n/a	n/a
44	CTCF	chr16:72100633-72100906	Medullo	brain:	n/a	n/a
45	CTCF	chr16:72100623-72100966	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr16:72101600-72101750	RPTEC	kidney:	n/a	n/a
47	CTCF	chr16:72100610-72100895	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr16:72099040-72099190	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr16:72099158-72099181	HepG2	liver:	n/a	n/a
50	CTCF	chr16:72104960-72105110	AoAF	blood vessel:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:72097718-72097768	T-47D	breast:	n/a
2	chr16:72097718-72097768	T-47D	breast:	n/a
3	chr16:72096944-72096994	HCT-116	colon:	n/a
4	chr16:72096944-72096994	Caco-2	colon:	n/a
5	chr16:72096498-72096548	AG09319	gingival:	n/a
6	chr16:72096608-72096658	HEK293	kidney:	embryo
7	chr16:72096498-72096548	AoSMC	blood vessel:	n/a
8	chr16:72096449-72096499	Caco-2	colon:	n/a
9	chr16:72096449-72096499	AG04449	skin:	fetal
10	chr16:72096944-72096994	AG09319	gingival:	n/a
11	chr16:72096608-72096658	HAEpiC	amniotic membrane:	n/a
12	chr16:72096449-72096499	MCF10A-Er-Src	breast:	n/a
13	chr16:72096498-72096548	HRCEpiC	kidney:	n/a
14	chr16:72096608-72096658	Jurkat	blood:	n/a
15	chr16:72096449-72096499	T-47D	breast:	n/a
16	chr16:72096608-72096658	HL-60	blood:	n/a
17	chr16:72096608-72096658	PANC-1	pancreas:	n/a
18	chr16:72096449-72096499	HEEpiC	esophagus:	n/a
19	chr16:72096498-72096548	AG10803	skin:	n/a
20	chr16:72096449-72096499	ProgFib	skin:	n/a
21	chr16:72096498-72096548	HMEC	breast:	n/a
22	chr16:72097718-72097768	AG09309	skin:	n/a
23	chr16:72097718-72097768	HCT-116	colon:	n/a
24	chr16:72096944-72096994	ECC-1	luminal epithelium:	n/a
25	chr16:72097718-72097768	HAEpiC	amniotic membrane:	n/a
26	chr16:72096498-72096548	Hepatocyte	liver:	n/a
27	chr16:72096498-72096548	HCPEpiC	choroid plexus:	n/a
28	chr16:72097718-72097768	Caco-2	colon:	n/a
29	chr16:72096944-72096994	ovcar-3	ovarian:	n/a
30	chr16:72097718-72097768	HNPCEpiC	eye:	n/a
31	chr16:72096449-72096499	NB4	blood:	n/a
32	chr16:72096944-72096994	AG04449	skin:	fetal
33	chr16:72096608-72096658	PrEC	prostate:	n/a
34	chr16:72096608-72096658	K562	blood:	n/a
35	chr16:72096498-72096548	IMR90	lung:	fetal
36	chr16:72096608-72096658	H1-hESC	embryonic stem cell:	embryo
37	chr16:72096608-72096658	SKMC	muscle:	n/a
38	chr16:72096498-72096548	HEEpiC	esophagus:	n/a
39	chr16:72096498-72096548	MCF10A-Er-Src	breast:	n/a
40	chr16:72096608-72096658	GM06990	blood:	n/a
41	chr16:72096608-72096658	AG04450	lung:	fetal
42	chr16:72097718-72097768	HUVEC	blood vessel:	n/a
43	chr16:72096498-72096548	PrEC	prostate:	n/a
44	chr16:72096449-72096499	AG09319	gingival:	n/a
45	chr16:72096449-72096499	HCM	heart:	n/a
46	chr16:72096944-72096994	AG04450	lung:	fetal
47	chr16:72096944-72096994	PFSK-1	brain:	n/a
48	chr16:72096608-72096658	GM12878	blood:	n/a
49	chr16:72096608-72096658	NHDF-neo	bronchial:	n/a
50	chr16:72096944-72096994	IMR90	lung:	fetal

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:72103326..72105153-chr16:72117441..72120370,2	MCF-7	breast:
2	chr16:72103116..72104667-chr16:72127883..72129694,2	K562	blood:
3	chr16:72098840..72102253-chr16:72104146..72107637,4	K562	blood:
4	chr16:72098664..72100530-chr16:72126789..72129168,2	K562	blood:
5	chr16:72098170..72103448-chr16:72104419..72108463,5	K562	blood:
6	chr16:72093537..72095716-chr16:72125964..72128665,2	MCF-7	breast:
7	chr16:72107601..72110331-chr16:72118448..72121540,3	MCF-7	breast:
8	chr16:72100293..72101113-chr16:72132931..72133757,5	MCF-7	breast:
9	chr16:72098664..72102766-chr16:72126373..72129232,5	K562	blood:
10	chr16:72100778..72101306-chr16:72127117..72128039,2	K562	blood:
11	chr16:72100358..72100998-chr16:72130881..72131518,2	MCF-7	breast:
12	chr16:72100387..72101200-chr16:72132899..72133926,7	MCF-7	breast:
13	chr16:72097383..72100653-chr16:72133488..72135199,3	MCF-7	breast:
14	chr16:72041551..72044328-chr16:72098859..72101646,2	K562	blood:
15	chr16:72100206..72101351-chr16:72132899..72134129,9	K562	blood:
16	chr16:72098840..72102253-chr16:72104146..72107637,4	K562	blood:
17	chr16:72099750..72107853-chr16:72126502..72131093,10	MCF-7	breast:

No data

Variant related genes	Relation type
HPR	TF binding region
HPR	CpG island
ENSG00000140829	chromatin interactions
ENSG00000140830	chromatin interactions
ENSG00000260252	chromatin interactions
ENSG00000102967	chromatin interactions
ENSG00000261701	chromatin interactions

Extended variants
information (count: 666 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189115161	chr16:72094757-72094758	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs370924206	chr16:72094801-72094802	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200016253	chr16:72094802-72094803	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs368140185	chr16:72094803-72094804	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs568578319	chr16:72094905-72094906	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs142946429	chr16:72094909-72094910	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs367785929	chr16:72094917-72094918	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs535475176	chr16:72094934-72094935	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs554186466	chr16:72094976-72094977	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs535412039	chr16:72095113-72095114	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546049335	chr16:72095136-72095137	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs558046283	chr16:72095141-72095142	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs113234131	chr16:72095240-72095241	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs192568258	chr16:72095273-72095274	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs28610193	chr16:72095312-72095313	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs8056409	chr16:72095314-72095315	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148393568	chr16:72095331-72095332	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529024075	chr16:72095338-72095339	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs2854693	chr16:72095345-72095346	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs540664928	chr16:72095346-72095347	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs559342498	chr16:72095359-72095360	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs532966131	chr16:72095404-72095405	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs551664949	chr16:72095405-72095406	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs182011635	chr16:72095429-72095430	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs386791985	chr16:72095452-72095453	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs398580	chr16:72095453-72095454	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs368099907	chr16:72095468-72095469	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs186354506	chr16:72095480-72095481	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs535896535	chr16:72095490-72095491	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs547495064	chr16:72095502-72095503	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs2854694	chr16:72095520-72095521	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs564123263	chr16:72095531-72095532	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs565703250	chr16:72095553-72095554	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs539470879	chr16:72095556-72095557	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs558007188	chr16:72095574-72095575	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576361866	chr16:72095586-72095587	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537239575	chr16:72095602-72095603	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs190704783	chr16:72095608-72095609	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs75444904	chr16:72095650-72095651	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs541078276	chr16:72095656-72095657	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs62055634	chr16:72095676-72095677	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs577859676	chr16:72095691-72095692	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs182894966	chr16:72095707-72095708	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs186369767	chr16:72095711-72095712	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs545058299	chr16:72095735-72095736	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs10451118	chr16:72095772-72095773	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs530883215	chr16:72095812-72095813	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549010702	chr16:72095835-72095836	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561097321	chr16:72095849-72095850	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs528291295	chr16:72095882-72095883	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923524	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:72060200-72095600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr16:72060200-72110600	Weak transcription	Esophagus	oesophagus
3	chr16:72076200-72098200	Weak transcription	Fetal Heart	heart
4	chr16:72077000-72107400	Weak transcription	Right Ventricle	heart
5	chr16:72077400-72102400	Weak transcription	Brain Substantia Nigra	brain
6	chr16:72077400-72107400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr16:72077600-72107400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr16:72078000-72100800	Weak transcription	Brain Hippocampus Middle	brain
9	chr16:72078000-72103200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr16:72078200-72095600	Weak transcription	Brain Anterior Caudate	brain
11	chr16:72078200-72105200	Weak transcription	Brain Angular Gyrus	brain
12	chr16:72078400-72098400	Weak transcription	Primary T cells from cord blood	blood
13	chr16:72078400-72105400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr16:72078400-72108000	Weak transcription	Aorta	Aorta
15	chr16:72084600-72106800	Weak transcription	Psoas Muscle	Psoas
16	chr16:72084800-72098200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr16:72088400-72098400	Weak transcription	Adipose Nuclei	Adipose
18	chr16:72089000-72096200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr16:72090000-72107600	Weak transcription	Primary B cells from cord blood	blood
20	chr16:72090200-72107600	Weak transcription	Gastric	stomach
21	chr16:72090200-72118400	Weak transcription	Lung	lung
22	chr16:72092800-72094800	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr16:72093200-72097200	Weak transcription	Liver	Liver
24	chr16:72093200-72118000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr16:72093800-72107400	Weak transcription	Fetal Stomach	stomach
26	chr16:72093800-72118400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr16:72093800-72118400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr16:72094000-72094800	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr16:72094200-72094800	Strong transcription	Spleen	Spleen
30	chr16:72094200-72095800	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr16:72094200-72096000	Enhancers	HepG2	liver
32	chr16:72094400-72094800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
33	chr16:72094400-72094800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr16:72094600-72096400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr16:72094800-72097400	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr16:72094800-72099800	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr16:72094800-72106800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr16:72094800-72108000	Weak transcription	Fetal Muscle Leg	muscle
39	chr16:72094800-72110600	Weak transcription	Spleen	Spleen
40	chr16:72095600-72095800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr16:72095600-72096000	Strong transcription	Brain Anterior Caudate	brain
42	chr16:72095800-72111800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr16:72096000-72097000	Flanking Active TSS	HepG2	liver
44	chr16:72096000-72105400	Weak transcription	Brain Anterior Caudate	brain
45	chr16:72096200-72105200	Weak transcription	Ovary	ovary
46	chr16:72096400-72096800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr16:72096800-72102400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr16:72096800-72118200	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr16:72097000-72097200	Enhancers	HepG2	liver
50	chr16:72097200-72098200	Active TSS	Liver	Liver

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