Variant report

Variant	esv1832105
Chromosome Location	chr16:47223418-47347780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:565)
CpG islands
(count:122)
Chromatin interactive
region (count:39)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:47344576-47345243	GM12878	blood:	n/a	n/a
2	BATF	chr16:47344674-47344855	GM12878	blood:	n/a	n/a
3	BCL11A	chr16:47345681-47345863	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr16:47344674-47344906	GM12878	blood:	n/a	n/a
5	CEBPB	chr16:47281027-47281314	IMR90	lung:	n/a	chr16:47281152-47281163 chr16:47281154-47281165
6	CEBPB	chr16:47279161-47279476	HepG2	liver:	n/a	chr16:47279302-47279311
7	CEBPB	chr16:47274852-47274872	IMR90	lung:	n/a	n/a
8	CEBPB	chr16:47279181-47279381	K562	blood:	n/a	chr16:47279302-47279311
9	CEBPB	chr16:47231474-47231853	K562	blood:	n/a	chr16:47231609-47231620
10	CEBPB	chr16:47259215-47259434	HepG2	liver:	n/a	chr16:47259271-47259282
11	CEBPB	chr16:47334783-47334834	HepG2	liver:	n/a	chr16:47334787-47334798 chr16:47334787-47334800 chr16:47334787-47334800 chr16:47334788-47334799
12	CEBPB	chr16:47231505-47231771	H1-hESC	embryonic stem cell:	n/a	chr16:47231609-47231620
13	CEBPB	chr16:47343568-47343827	IMR90	lung:	n/a	n/a
14	CEBPB	chr16:47275941-47276087	K562	blood:	n/a	chr16:47275959-47275970
15	CEBPB	chr16:47274841-47274874	K562	blood:	n/a	n/a
16	CEBPB	chr16:47248040-47248319	HepG2	liver:	n/a	chr16:47248141-47248152
17	CEBPB	chr16:47335027-47335082	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr16:47280999-47281338	K562	blood:	n/a	chr16:47281152-47281163 chr16:47281154-47281165
19	CEBPB	chr16:47279201-47279444	A549	lung:	n/a	chr16:47279302-47279311
20	CEBPB	chr16:47318928-47319316	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr16:47275884-47276019	IMR90	lung:	n/a	chr16:47275959-47275970
22	CEBPB	chr16:47279159-47279476	IMR90	lung:	n/a	chr16:47279302-47279311
23	CEBPB	chr16:47248073-47248238	A549	lung:	n/a	chr16:47248141-47248152
24	CEBPB	chr16:47268376-47268555	K562	blood:	n/a	n/a
25	CEBPB	chr16:47338272-47338613	IMR90	lung:	n/a	n/a
26	CEBPB	chr16:47340948-47341071	K562	blood:	n/a	n/a
27	CEBPB	chr16:47340109-47340380	HepG2	liver:	n/a	chr16:47340253-47340264 chr16:47340251-47340262
28	CEBPB	chr16:47231440-47231788	HepG2	liver:	n/a	chr16:47231609-47231620
29	CEBPB	chr16:47284635-47284814	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr16:47283243-47283529	HepG2	liver:	n/a	chr16:47283377-47283386 chr16:47283376-47283387
31	CEBPB	chr16:47281025-47281260	HepG2	liver:	n/a	chr16:47281152-47281163 chr16:47281154-47281165
32	CEBPB	chr16:47231529-47231781	Hela-S3	cervix:	n/a	chr16:47231609-47231620
33	CEBPB	chr16:47248007-47248285	IMR90	lung:	n/a	chr16:47248141-47248152
34	CEBPB	chr16:47231446-47231805	IMR90	lung:	n/a	chr16:47231609-47231620
35	CEBPB	chr16:47275943-47276030	HepG2	liver:	n/a	chr16:47275959-47275970
36	CEBPB	chr16:47289349-47289645	IMR90	lung:	n/a	n/a
37	CEBPB	chr16:47340142-47340339	K562	blood:	n/a	chr16:47340253-47340264 chr16:47340251-47340262
38	CEBPB	chr16:47279246-47279458	Hela-S3	cervix:	n/a	chr16:47279302-47279311
39	CEBPB	chr16:47259184-47259394	A549	lung:	n/a	chr16:47259271-47259282
40	CHD1	chr16:47343397-47344272	IMR90	lung:	n/a	n/a
41	CTCF	chr16:47292840-47292990	GM12871	blood:	n/a	n/a
42	CTCF	chr16:47292860-47293010	A549	lung:	n/a	n/a
43	CTCF	chr16:47292872-47293035	GM10248	blood:	n/a	n/a
44	CTCF	chr16:47239060-47239210	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr16:47292920-47293070	HAc	cerebellar:	n/a	n/a
46	CTCF	chr16:47292920-47293070	HFF	foreskin:	n/a	n/a
47	CTCF	chr16:47292736-47293149	HCT-116	colon:	n/a	n/a
48	CTCF	chr16:47292876-47293066	HepG2	liver:	n/a	n/a
49	CTCF	chr16:47292886-47293063	MCF-7	breast:	n/a	n/a
50	CTCF	chr16:47239040-47239190	HRE	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47344826-47344876	SK-N-SH	brain:	n/a
2	chr16:47338451-47338501	GM19239	blood:	n/a
3	chr16:47338451-47338501	HRCEpiC	kidney:	n/a
4	chr16:47344826-47344876	GM12892	blood:	n/a
5	chr16:47344826-47344876	HepG2	liver:	n/a
6	chr16:47338451-47338501	HCT-116	colon:	n/a
7	chr16:47344826-47344876	GM06990	blood:	n/a
8	chr16:47344826-47344876	A549	lung:	n/a
9	chr16:47344826-47344876	Jurkat	blood:	n/a
10	chr16:47338451-47338501	HNPCEpiC	eye:	n/a
11	chr16:47338451-47338501	HIPEpiC	eye:	n/a
12	chr16:47338451-47338501	HEEpiC	esophagus:	n/a
13	chr16:47344826-47344876	K562	blood:	n/a
14	chr16:47338451-47338501	HCPEpiC	choroid plexus:	n/a
15	chr16:47344826-47344876	HCT-116	colon:	n/a
16	chr16:47344826-47344876	HL-60	blood:	n/a
17	chr16:47344826-47344876	CMK	blood:	n/a
18	chr16:47338451-47338501	GM12892	blood:	n/a
19	chr16:47338451-47338501	SK-N-SH	brain:	n/a
20	chr16:47338451-47338501	GM06990	blood:	n/a
21	chr16:47344826-47344876	IMR90	lung:	fetal
22	chr16:47338451-47338501	AoSMC	blood vessel:	n/a
23	chr16:47338451-47338501	HPAEpiC	pulmonary alveolar:	n/a
24	chr16:47338451-47338501	SAEC	small airway:	n/a
25	chr16:47344826-47344876	GM12878	blood:	n/a
26	chr16:47344826-47344876	NT2-D1	testis:	n/a
27	chr16:47338451-47338501	Caco-2	colon:	n/a
28	chr16:47338451-47338501	GM12878	blood:	n/a
29	chr16:47344826-47344876	HUVEC	blood vessel:	n/a
30	chr16:47338451-47338501	T-47D	breast:	n/a
31	chr16:47344826-47344876	HAEpiC	amniotic membrane:	n/a
32	chr16:47338451-47338501	NHBE	bronchial:	n/a
33	chr16:47338451-47338501	U87	brain:	n/a
34	chr16:47338451-47338501	HUVEC	blood vessel:	n/a
35	chr16:47344826-47344876	PrEC	prostate:	n/a
36	chr16:47344826-47344876	U87	brain:	n/a
37	chr16:47344826-47344876	GM12891	blood:	n/a
38	chr16:47344826-47344876	HCPEpiC	choroid plexus:	n/a
39	chr16:47338451-47338501	Jurkat	blood:	n/a
40	chr16:47344826-47344876	HEK293	kidney:	embryo
41	chr16:47344826-47344876	HRE	kidney:	n/a
42	chr16:47338451-47338501	HCM	heart:	n/a
43	chr16:47344826-47344876	MCF10A-Er-Src	breast:	n/a
44	chr16:47338451-47338501	SK-N-MC	brain:	n/a
45	chr16:47344826-47344876	NB4	blood:	n/a
46	chr16:47338451-47338501	NT2-D1	testis:	n/a
47	chr16:47344826-47344876	T-47D	breast:	n/a
48	chr16:47338451-47338501	NH-A	brain:	n/a
49	chr16:47344826-47344876	AG09319	gingival:	n/a
50	chr16:47344826-47344876	H1-hESC	embryonic stem cell:	embryo

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:47264762..47266642-chr16:47266702..47269300,2	K562	blood:
2	chr16:47310628..47312888-chr16:47313901..47316020,2	K562	blood:
3	chr16:47269900..47272616-chr16:47277828..47281996,3	K562	blood:
4	chr16:47282712..47286365-chr16:47287931..47291615,3	K562	blood:
5	chr16:47298562..47302472-chr16:47302634..47305844,3	K562	blood:
6	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
7	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
8	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
9	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
10	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
11	chr16:47282712..47286365-chr16:47287931..47291615,3	K562	blood:
12	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
13	chr16:47263413..47265450-chr16:47271876..47274264,2	K562	blood:
14	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:
15	chr16:47298562..47302472-chr16:47302634..47305844,3	K562	blood:
16	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
17	chr16:47264762..47266642-chr16:47266702..47269300,2	K562	blood:
18	chr16:47288247..47290542-chr16:47297549..47300017,2	K562	blood:
19	chr16:47288247..47290542-chr16:47297549..47300017,2	K562	blood:
20	chr16:47305590..47308851-chr16:47316493..47319236,3	K562	blood:
21	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
22	chr16:47305590..47308851-chr16:47316493..47319236,3	K562	blood:
23	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
24	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
25	chr16:47239252..47239752-chr3:67770876..67771427,2	Hela-S3	cervix:
26	chr16:47315203..47316940-chr16:47529898..47531487,2	K562	blood:
27	chr16:47281267..47281944-chr3:111725286..111725871,2	MCF-7	breast:
28	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
29	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
30	chr16:47337967..47339829-chr16:47344000..47345924,2	K562	blood:
31	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
32	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
33	chr16:47290686..47293346-chr16:47302878..47305751,2	K562	blood:
34	chr16:47238697..47239501-chr16:48151319..48151975,2	MCF-7	breast:
35	chr16:47290498..47293236-chr16:47492799..47495777,2	MCF-7	breast:
36	chr16:47310628..47312888-chr16:47313901..47316020,2	K562	blood:
37	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
38	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
39	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHKB-1	chr16:47333358-47333859	ENSG00000261369.1
2	lnc-PHKB-1	chr16:47346550-47346651	ENSG00000261369.1
3	lnc-NETO2-2	chr16:47296678-47296925	NONHSAT142288
4	lnc-NETO2-3	chr16:47310408-47311851	NONHSAT142289
5	lnc-NETO2-2	chr16:47294571-47294606	NONHSAT142288
6	lnc-PHKB-3	chr16:47235986-47236340	ENSG00000260744.1
7	lnc-PHKB-3	chr16:47230222-47230630	ENSG00000260744.1

No data

Variant related genes	Relation type
ITFG1	TF binding region
ENSG00000261369	TF binding region
ENSG00000222767	TF binding region
ENSG00000260012	TF binding region
ENSG00000260744	TF binding region
ITFG1	CpG island
ENSG00000261369	CpG island
ENSG00000222767	CpG island
ENSG00000260012	CpG island
ENSG00000260744	CpG island
ENSG00000102893	chromatin interactions
ENSG00000129636	chromatin interactions

Extended variants
information (count: 3825 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3825 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9928466	chr16:47223418-47223419	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116019505	chr16:47223460-47223461	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs537401786	chr16:47223495-47223496	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs557533983	chr16:47223502-47223503	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs557654045	chr16:47223504-47223505	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs118053604	chr16:47223527-47223528	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs59318658	chr16:47223560-47223561	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs554912915	chr16:47223570-47223571	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs573468563	chr16:47223571-47223572	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs546411352	chr16:47223573-47223574	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs146018973	chr16:47223584-47223585	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs559049812	chr16:47223702-47223703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192498193	chr16:47223755-47223756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573353696	chr16:47223759-47223760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570076016	chr16:47223766-47223767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544583560	chr16:47223779-47223780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72814503	chr16:47223811-47223812	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs116359600	chr16:47223833-47223834	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs574673509	chr16:47223839-47223840	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs540656600	chr16:47223938-47223939	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs201761716	chr16:47223955-47223956	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs542102961	chr16:47223961-47223962	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs560128902	chr16:47223966-47223967	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs527443234	chr16:47224066-47224067	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs376009972	chr16:47224135-47224136	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs551858194	chr16:47224140-47224141	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs573619174	chr16:47224142-47224143	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs563807287	chr16:47224172-47224173	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs115743316	chr16:47224187-47224188	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs148247922	chr16:47224230-47224231	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs374926392	chr16:47224258-47224259	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs568024183	chr16:47224271-47224272	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs75500474	chr16:47224311-47224312	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs548824415	chr16:47224355-47224356	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs35738391	chr16:47224361-47224362	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs561902638	chr16:47224491-47224492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567075278	chr16:47224515-47224516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534364631	chr16:47224575-47224576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190200118	chr16:47224630-47224631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1362567	chr16:47224693-47224694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs538315676	chr16:47224730-47224731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181858607	chr16:47224741-47224742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141294811	chr16:47224751-47224752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373607568	chr16:47224797-47224798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150769895	chr16:47224858-47224859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571931152	chr16:47224913-47224914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545556003	chr16:47224917-47224918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563921936	chr16:47224950-47224951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531331944	chr16:47224956-47224957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563154099	chr16:47224980-47224981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1386 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47178800-47231400	Weak transcription	Psoas Muscle	Psoas
2	chr16:47178800-47296600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:47186600-47231400	Weak transcription	Aorta	Aorta
4	chr16:47187800-47223800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr16:47187800-47243800	Weak transcription	HSMM	muscle
6	chr16:47192000-47252000	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr16:47192400-47231800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr16:47194800-47231000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr16:47195400-47244200	Weak transcription	Liver	Liver
10	chr16:47209800-47232000	Weak transcription	Gastric	stomach
11	chr16:47210600-47240200	Weak transcription	Primary B cells from cord blood	blood
12	chr16:47216800-47225800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr16:47216800-47230400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr16:47216800-47247200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr16:47217200-47243600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr16:47221400-47225200	Weak transcription	Fetal Stomach	stomach
17	chr16:47222800-47250600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr16:47223000-47223600	ZNF genes & repeats	Fetal Lung	lung
19	chr16:47223200-47231600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr16:47223200-47237600	Weak transcription	Lung	lung
21	chr16:47223400-47247600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr16:47223400-47250000	Weak transcription	Ovary	ovary
23	chr16:47223600-47230600	Weak transcription	Fetal Muscle Leg	muscle
24	chr16:47223600-47231400	Weak transcription	Fetal Lung	lung
25	chr16:47223600-47232200	Weak transcription	Dnd41	blood
26	chr16:47223600-47250200	Weak transcription	Fetal Intestine Small	intestine
27	chr16:47223800-47224400	ZNF genes & repeats	Primary T cells from cord blood	blood
28	chr16:47224200-47230400	Weak transcription	Brain Hippocampus Middle	brain
29	chr16:47224200-47263000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr16:47224400-47225400	Strong transcription	Primary T cells from cord blood	blood
31	chr16:47224400-47250200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr16:47224400-47265600	Weak transcription	HSMMtube	muscle
33	chr16:47224600-47249400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr16:47224800-47251200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr16:47225000-47227600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr16:47225000-47250200	Weak transcription	Fetal Intestine Large	intestine
37	chr16:47225200-47225800	ZNF genes & repeats	Fetal Stomach	stomach
38	chr16:47225400-47237200	Weak transcription	Primary T cells from cord blood	blood
39	chr16:47225400-47247600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr16:47225600-47226800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr16:47225800-47226200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
42	chr16:47225800-47226600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
43	chr16:47225800-47250000	Weak transcription	Fetal Stomach	stomach
44	chr16:47226000-47226200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
45	chr16:47226200-47231400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr16:47226200-47249800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr16:47226200-47250000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr16:47226400-47227000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr16:47226400-47230400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr16:47226600-47230400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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