Variant report

Variant	nsv1063704
Chromosome Location	chr16:70179331-70272696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1764)
CpG islands
(count:795)
Chromatin interactive
region (count:19)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1764 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70199076-70199303	K562	blood:	n/a	n/a
2	ARID3A	chr16:70186462-70187162	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70195992-70196417	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70191181-70192253	HepG2	liver:	n/a	n/a
5	ATF1	chr16:70199108-70199250	K562	blood:	n/a	n/a
6	ATF1	chr16:70195925-70196369	K562	blood:	n/a	n/a
7	BACH1	chr16:70190168-70190514	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr16:70243288-70243494	GM12878	blood:	n/a	n/a
9	BATF	chr16:70199070-70199298	GM12878	blood:	n/a	n/a
10	BATF	chr16:70269207-70269408	GM12878	blood:	n/a	n/a
11	BATF	chr16:70272693-70272978	GM12878	blood:	n/a	n/a
12	BATF	chr16:70269196-70269455	GM12878	blood:	n/a	n/a
13	BATF	chr16:70251089-70251362	GM12878	blood:	n/a	n/a
14	BATF	chr16:70242991-70243230	GM12878	blood:	n/a	n/a
15	BATF	chr16:70265769-70265977	GM12878	blood:	n/a	n/a
16	BATF	chr16:70266143-70266490	GM12878	blood:	n/a	n/a
17	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
18	BATF	chr16:70266179-70266523	GM12878	blood:	n/a	n/a
19	BATF	chr16:70251010-70251261	GM12878	blood:	n/a	n/a
20	BATF	chr16:70252521-70252845	GM12878	blood:	n/a	chr16:70252736-70252746
21	BATF	chr16:70272645-70272986	GM12878	blood:	n/a	n/a
22	BATF	chr16:70249268-70249471	GM12878	blood:	n/a	n/a
23	BATF	chr16:70270340-70270551	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70242982-70243227	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70272603-70273149	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70264796-70265164	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70256507-70256821	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70267253-70267439	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70256979-70257253	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70266128-70266474	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:70266040-70266508	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:70249059-70249253	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:70252607-70252876	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:70252674-70252910	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:70265235-70265407	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:70247717-70247954	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:70253466-70253640	GM12878	blood:	n/a	n/a
40	BHLHE40	chr16:70256452-70256822	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:70198964-70199392	HepG2	liver:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
42	BHLHE40	chr16:70198955-70199421	K562	blood:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
43	BHLHE40	chr16:70264795-70265113	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:70247348-70248139	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:70242201-70242419	HepG2	liver:	n/a	n/a
46	BHLHE40	chr16:70249020-70249505	HepG2	liver:	n/a	n/a
47	BHLHE40	chr16:70242942-70243167	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:70256978-70257194	HepG2	liver:	n/a	n/a
49	BHLHE40	chr16:70254937-70255237	HepG2	liver:	n/a	n/a
50	BHLHE40	chr16:70254336-70254859	HepG2	liver:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70196247-70196297	HL-60	blood:	n/a
2	chr16:70207304-70207354	HNPCEpiC	eye:	n/a
3	chr16:70196247-70196297	HL-60	blood:	n/a
4	chr16:70207304-70207354	HNPCEpiC	eye:	n/a
5	chr16:70190513-70190563	HCT-116	colon:	n/a
6	chr16:70220191-70220241	PANC-1	pancreas:	n/a
7	chr16:70220191-70220241	RPTEC	kidney:	n/a
8	chr16:70222502-70222552	NH-A	brain:	n/a
9	chr16:70259186-70259236	NT2-D1	testis:	n/a
10	chr16:70259186-70259236	AoSMC	blood vessel:	n/a
11	chr16:70207304-70207354	Hela-S3	cervix:	n/a
12	chr16:70222502-70222552	U87	brain:	n/a
13	chr16:70190513-70190563	HNPCEpiC	eye:	n/a
14	chr16:70196247-70196297	HIPEpiC	eye:	n/a
15	chr16:70207722-70207772	HepG2	liver:	n/a
16	chr16:70226235-70226285	HCF	heart:	n/a
17	chr16:70226235-70226285	GM12878	blood:	n/a
18	chr16:70193705-70193755	T-47D	breast:	n/a
19	chr16:70190398-70190448	IMR90	lung:	fetal
20	chr16:70193705-70193755	GM12892	blood:	n/a
21	chr16:70190398-70190448	U87	brain:	n/a
22	chr16:70196247-70196297	ovcar-3	ovarian:	n/a
23	chr16:70207722-70207772	Hepatocyte	liver:	n/a
24	chr16:70196247-70196297	HCPEpiC	choroid plexus:	n/a
25	chr16:70207801-70207851	Jurkat	blood:	n/a
26	chr16:70222502-70222552	NHBE	bronchial:	n/a
27	chr16:70207801-70207851	GM19239	blood:	n/a
28	chr16:70196247-70196297	Hepatocyte	liver:	n/a
29	chr16:70220191-70220241	NHDF-neo	bronchial:	n/a
30	chr16:70207722-70207772	NT2-D1	testis:	n/a
31	chr16:70190513-70190563	HL-60	blood:	n/a
32	chr16:70207722-70207772	HCM	heart:	n/a
33	chr16:70226235-70226285	NHBE	bronchial:	n/a
34	chr16:70220191-70220241	NT2-D1	testis:	n/a
35	chr16:70193705-70193755	NB4	blood:	n/a
36	chr16:70207297-70207347	RPTEC	kidney:	n/a
37	chr16:70190513-70190563	SK-N-MC	brain:	n/a
38	chr16:70190398-70190448	HNPCEpiC	eye:	n/a
39	chr16:70226235-70226285	RPTEC	kidney:	n/a
40	chr16:70190329-70190379	HUVEC	blood vessel:	n/a
41	chr16:70259186-70259236	GM12878	blood:	n/a
42	chr16:70207304-70207354	AoSMC	blood vessel:	n/a
43	chr16:70207801-70207851	A549	lung:	n/a
44	chr16:70207801-70207851	HepG2	liver:	n/a
45	chr16:70207722-70207772	HIPEpiC	eye:	n/a
46	chr16:70207801-70207851	HIPEpiC	eye:	n/a
47	chr16:70207801-70207851	GM12878	blood:	n/a
48	chr16:70207722-70207772	HEK293	kidney:	embryo
49	chr16:70207304-70207354	ECC-1	luminal epithelium:	n/a
50	chr16:70190329-70190379	HMEC	breast:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70190124..70192979-chr16:70192985..70196334,3	MCF-7	breast:
2	chr16:70198641..70199632-chr16:74343397..74344233,2	K562	blood:
3	chr16:70189713..70191262-chr16:70193819..70195441,2	MCF-7	breast:
4	chr16:70192894..70195380-chr16:70284264..70288568,4	MCF-7	breast:
5	chr16:70195628..70198229-chr16:70323197..70325854,2	MCF-7	breast:
6	chr16:70185026..70185664-chr16:74657267..74657783,2	MCF-7	breast:
7	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:
8	chr16:70185001..70186006-chr16:74463672..74464734,4	MCF-7	breast:
9	chr16:70245449..70247912-chr16:70284379..70285973,2	MCF-7	breast:
10	chr16:70189713..70191262-chr16:70193819..70195441,2	MCF-7	breast:
11	chr16:70194744..70197032-chr16:70317749..70321532,3	K562	blood:
12	chr16:70194900..70197913-chr16:70284304..70286530,3	MCF-7	breast:
13	chr16:70190723..70192786-chr16:74330377..74332345,2	K562	blood:
14	chr16:70190180..70193178-chr16:70320490..70323768,3	K562	blood:
15	chr16:70185546..70188215-chr16:74330413..74333077,2	K562	blood:
16	chr16:70190124..70192979-chr16:70192985..70196334,3	MCF-7	breast:
17	chr16:70183960..70187287-chr16:70187613..70192158,4	MCF-7	breast:
18	chr16:70197328..70198092-chr16:70301268..70302134,2	MCF-7	breast:
19	chr16:70183960..70187287-chr16:70187613..70192158,4	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC6-2	chr16:70192860-70193983	ENSG00000247228
2	lnc-EXOSC6-2	chr16:70207031-70207322	ENSG00000247228.2
3	lnc-EXOSC6-2	chr16:70194638-70194844	ENSG00000247228
4	lnc-EXOSC6-2	chr16:70207031-70207351	ENSG00000247228
5	lnc-EXOSC6-2	chr16:70190243-70190407	ENSG00000247228.2
6	lnc-EXOSC6-2	chr16:70195347-70195796	ENSG00000247228
7	lnc-EXOSC6-2	chr16:70194075-70194214	ENSG00000247228
8	lnc-EXOSC6-2	chr16:70192708-70192792	ENSG00000247228.2

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PDPR	hsa-miR-155-5p	chr16:70192265-70192271
2	PDPR	hsa-let-7b-5p	chr16:70191336-70191343
3	PDPR	hsa-let-7b-5p	chr16:70191322-70191343
4	PDPR	hsa-miR-16-5p	chr16:70191655-70191661

Variant related genes	Relation type
PDPR	TF binding region
ENSG00000247228	TF binding region
ENSG00000238734	TF binding region
ENSG00000269866	TF binding region
ENSG00000269746	TF binding region
CLEC18C	TF binding region
ENSG00000261145	TF binding region
ENSG00000261556	TF binding region
PDPR	CpG island
ENSG00000247228	CpG island
ENSG00000238734	CpG island
ENSG00000269866	CpG island
ENSG00000269746	CpG island
CLEC18C	CpG island
ENSG00000261145	CpG island
ENSG00000261556	CpG island
ENSG00000157349	chromatin interactions
ENSG00000090861	chromatin interactions
ENSG00000259972	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000261404	chromatin interactions
ZNRF3	miRNA target sites
ARHGDIA	miRNA target sites
ACOT8	miRNA target sites
ATAD5	miRNA target sites
FAM122B	miRNA target sites

Extended variants
information (count: 3052 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3052 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375495616	chr16:70179352-70179353	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536415034	chr16:70179388-70179389	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554490087	chr16:70179389-70179390	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188322583	chr16:70179396-70179397	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539937501	chr16:70179443-70179444	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564680406	chr16:70179458-70179459	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369828966	chr16:70179494-70179495	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576380940	chr16:70179510-70179511	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543813593	chr16:70179556-70179557	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562806862	chr16:70179592-70179593	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372211173	chr16:70179595-70179596	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548889453	chr16:70179669-70179670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560502395	chr16:70179706-70179707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527924402	chr16:70179709-70179710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552703264	chr16:70179718-70179719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570963130	chr16:70179835-70179836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538205459	chr16:70179867-70179868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550216365	chr16:70179982-70179983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376273126	chr16:70180005-70180006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569145681	chr16:70180011-70180012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369952107	chr16:70180019-70180020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368469864	chr16:70180045-70180046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371349256	chr16:70180063-70180064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2287978	chr16:70180088-70180089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200665951	chr16:70180090-70180091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371559790	chr16:70180110-70180111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572944301	chr16:70180151-70180152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149247484	chr16:70180158-70180159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2549254	chr16:70180196-70180197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78267352	chr16:70180220-70180221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79911222	chr16:70180223-70180224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558189076	chr16:70180271-70180272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576545125	chr16:70180325-70180326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543777463	chr16:70180353-70180354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562120691	chr16:70180510-70180511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574405433	chr16:70180606-70180607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542147553	chr16:70180941-70180942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368687475	chr16:70180994-70180995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560885853	chr16:70181026-70181027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527836934	chr16:70181134-70181135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371791881	chr16:70181142-70181143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3903115	chr16:70181232-70181233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546431464	chr16:70181278-70181279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564539690	chr16:70181307-70181308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531866283	chr16:70181332-70181333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550326192	chr16:70181350-70181351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112468928	chr16:70181355-70181356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568348332	chr16:70181423-70181424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529330822	chr16:70181432-70181433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548185072	chr16:70181445-70181446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1312 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70149000-70185200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr16:70149000-70185600	Weak transcription	Stomach Mucosa	stomach
3	chr16:70151200-70180600	Strong transcription	Fetal Stomach	stomach
4	chr16:70152800-70181600	Weak transcription	Psoas Muscle	Psoas
5	chr16:70154000-70180600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr16:70154000-70180600	Strong transcription	Fetal Intestine Small	intestine
7	chr16:70154000-70180600	Strong transcription	Lung	lung
8	chr16:70154000-70196800	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr16:70154200-70180200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr16:70154200-70180200	Strong transcription	Fetal Muscle Leg	muscle
11	chr16:70154200-70180200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr16:70154200-70180400	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr16:70154200-70180600	Strong transcription	Fetal Muscle Trunk	muscle
14	chr16:70154200-70196800	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr16:70154200-70197000	Strong transcription	Adipose Nuclei	Adipose
16	chr16:70154400-70179600	Strong transcription	Primary B cells from peripheral blood	blood
17	chr16:70154400-70180200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr16:70154400-70180200	Strong transcription	Thymus	Thymus
19	chr16:70154400-70180600	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr16:70154400-70180600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr16:70154400-70180600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr16:70154400-70185600	Strong transcription	Liver	Liver
23	chr16:70154400-70185600	Strong transcription	Duodenum Mucosa	Duodenum
24	chr16:70154600-70180400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr16:70155000-70180200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr16:70155400-70180200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr16:70155400-70180400	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr16:70155400-70180600	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr16:70155400-70180600	Strong transcription	Fetal Intestine Large	intestine
30	chr16:70155600-70179800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr16:70156400-70190600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr16:70156600-70185200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr16:70159200-70180600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr16:70159400-70179600	Strong transcription	Fetal Thymus	thymus
35	chr16:70159400-70180400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr16:70159600-70180600	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr16:70159600-70196800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr16:70159800-70180600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr16:70159800-70185400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr16:70160200-70180400	Strong transcription	Brain Anterior Caudate	brain
41	chr16:70160200-70180600	Strong transcription	Ovary	ovary
42	chr16:70160400-70187000	Weak transcription	Fetal Heart	heart
43	chr16:70160600-70179600	Strong transcription	Fetal Brain Female	brain
44	chr16:70160600-70180200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
45	chr16:70160600-70180600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr16:70160600-70180600	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr16:70160600-70180600	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr16:70160600-70197000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr16:70160800-70179600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr16:70160800-70180400	Strong transcription	Duodenum Smooth Muscle	Duodenum

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