Variant report

Variant	nsv457569
Chromosome Location	chr16:81080366-81095091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr16:81082537-81082870	K562	blood:	n/a	n/a
2	CBX3	chr16:81082503-81082901	K562	blood:	n/a	n/a
3	CTCF	chr16:81088263-81088340	LNCaP	prostate:	n/a	n/a
4	E2F4	chr16:81083215-81083373	MCF10A-Er-Src	breast:	n/a	n/a
5	ELF1	chr16:81081832-81082188	GM12878	blood:	n/a	n/a
6	FOXA1	chr16:81087368-81087742	T-47D	breast:	n/a	n/a
7	FOXA1	chr16:81086672-81086942	T-47D	breast:	n/a	n/a
8	FOXA1	chr16:81086707-81086943	T-47D	breast:	n/a	n/a
9	FOXA1	chr16:81087287-81087663	T-47D	breast:	n/a	n/a
10	GATA3	chr16:81087414-81087823	T-47D	breast:	n/a	n/a
11	GATA3	chr16:81087431-81087916	MCF-7	breast:	n/a	n/a
12	GATA3	chr16:81087416-81087782	T-47D	breast:	n/a	n/a
13	IRF1	chr16:81087517-81087847	K562	blood:	n/a	n/a
14	JUND	chr16:81085648-81085725	HepG2	liver:	n/a	chr16:81085682-81085693
15	KAP1	chr16:81082165-81083514	K562	blood:	n/a	n/a
16	MYC	chr16:81091480-81091544	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr16:81081534-81081719	MCF-7	breast:	n/a	n/a
18	POLR2A	chr16:81081471-81082002	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr16:81080059-81080446	GM12892	blood:	n/a	n/a
20	POLR2A	chr16:81080275-81080392	MCF-7	breast:	n/a	n/a
21	POLR2A	chr16:81080385-81080531	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr16:81080170-81080492	HepG2	liver:	n/a	n/a
23	POLR2A	chr16:81081801-81082172	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr16:81080163-81080583	HepG2	liver:	n/a	n/a
25	POLR2A	chr16:81085329-81085529	GM12878	blood:	n/a	n/a
26	POLR2A	chr16:81081720-81081985	MCF-7	breast:	n/a	n/a
27	POLR2A	chr16:81080298-81080452	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr16:81079055-81080554	K562	blood:	n/a	n/a
29	POLR2A	chr16:81080229-81080394	K562	blood:	n/a	n/a
30	POLR2A	chr16:81087504-81087542	Gliobla	brain:	n/a	n/a
31	SETDB1	chr16:81082326-81083989	U2OS	brain:	n/a	n/a
32	SPI1	chr16:81083989-81084204	GM12891	blood:	n/a	n/a
33	SPI1	chr16:81083965-81084149	GM12878	blood:	n/a	n/a
34	STAT3	chr16:81080527-81080785	MCF10A-Er-Src	breast:	n/a	n/a
35	TBL1XR1	chr16:81087157-81087160	K562	blood:	n/a	n/a
36	ZNF143	chr16:81082619-81082789	K562	blood:	n/a	n/a
37	ZNF384	chr16:81082551-81082864	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81094757-81094807	AG04449	skin:	fetal
2	chr16:81094757-81094807	HUVEC	blood vessel:	n/a
3	chr16:81095002-81095052	SK-N-SH_RA	brain:	n/a
4	chr16:81094757-81094807	GM12892	blood:	n/a
5	chr16:81094757-81094807	MCF10A-Er-Src	breast:	n/a
6	chr16:81095002-81095052	RPTEC	kidney:	n/a
7	chr16:81095002-81095052	MCF10A-Er-Src	breast:	n/a
8	chr16:81095002-81095052	BJ	skin:	n/a
9	chr16:81095002-81095052	GM12891	blood:	n/a
10	chr16:81095002-81095052	AG04449	skin:	fetal
11	chr16:81094757-81094807	MCF-7	breast:	n/a
12	chr16:81094757-81094807	HepG2	liver:	n/a
13	chr16:81095002-81095052	SAEC	small airway:	n/a
14	chr16:81095002-81095052	NT2-D1	testis:	n/a
15	chr16:81095002-81095052	AoSMC	blood vessel:	n/a
16	chr16:81095002-81095052	ProgFib	skin:	n/a
17	chr16:81094757-81094807	GM12891	blood:	n/a
18	chr16:81095002-81095052	HRPEpiC	eye:	n/a
19	chr16:81094757-81094807	NHBE	bronchial:	n/a
20	chr16:81094757-81094807	GM06990	blood:	n/a
21	chr16:81094757-81094807	K562	blood:	n/a
22	chr16:81094757-81094807	IMR90	lung:	fetal
23	chr16:81095002-81095052	HMEC	breast:	n/a
24	chr16:81095002-81095052	AG09309	skin:	n/a
25	chr16:81094757-81094807	Hepatocyte	liver:	n/a
26	chr16:81095002-81095052	Hela-S3	cervix:	n/a
27	chr16:81094757-81094807	ECC-1	luminal epithelium:	n/a
28	chr16:81094757-81094807	HL-60	blood:	n/a
29	chr16:81095002-81095052	AG09319	gingival:	n/a
30	chr16:81095002-81095052	GM12878	blood:	n/a
31	chr16:81094757-81094807	SK-N-SH_RA	brain:	n/a
32	chr16:81095002-81095052	HCM	heart:	n/a
33	chr16:81095002-81095052	U87	brain:	n/a
34	chr16:81094757-81094807	HEEpiC	esophagus:	n/a
35	chr16:81094757-81094807	BE2_C	brain:	n/a
36	chr16:81095002-81095052	PrEC	prostate:	n/a
37	chr16:81094757-81094807	PFSK-1	brain:	n/a
38	chr16:81094757-81094807	HCF	heart:	n/a
39	chr16:81095002-81095052	CMK	blood:	n/a
40	chr16:81094757-81094807	HAEpiC	amniotic membrane:	n/a
41	chr16:81094757-81094807	HIPEpiC	eye:	n/a
42	chr16:81095002-81095052	HCPEpiC	choroid plexus:	n/a
43	chr16:81095002-81095052	Caco-2	colon:	n/a
44	chr16:81095002-81095052	LNCaP	prostate:	n/a
45	chr16:81094757-81094807	NT2-D1	testis:	n/a
46	chr16:81095002-81095052	HEEpiC	esophagus:	n/a
47	chr16:81094757-81094807	HRE	kidney:	n/a
48	chr16:81095002-81095052	ovcar-3	ovarian:	n/a
49	chr16:81095002-81095052	HL-60	blood:	n/a
50	chr16:81095002-81095052	IMR90	lung:	fetal

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81081881..81083637-chr16:81109528..81112357,2	K562	blood:
2	chr16:81079864..81081981-chr16:81082304..81084589,2	MCF-7	breast:
3	chr16:81071649..81074411-chr16:81077568..81081037,5	K562	blood:
4	chr16:81083064..81085165-chr16:81098548..81100699,2	MCF-7	breast:
5	chr16:81076434..81078165-chr16:81078716..81082306,3	MCF-7	breast:
6	chr16:81090262..81092172-chr16:81110435..81112277,2	K562	blood:
7	chr16:81079864..81081981-chr16:81082304..81084589,2	MCF-7	breast:
8	chr16:81079124..81081324-chr16:81108585..81111174,2	K562	blood:
9	chr16:81039673..81042304-chr16:81079605..81082488,2	MCF-7	breast:
10	chr16:81080745..81083107-chr16:81231797..81233650,2	MCF-7	breast:
11	chr16:81078691..81081572-chr16:81082090..81085180,4	K562	blood:
12	chr16:81082050..81083642-chr16:81085268..81087006,2	K562	blood:
13	chr16:81082050..81083642-chr16:81085268..81087006,2	K562	blood:
14	chr16:81094141..81096818-chr16:81110183..81111758,2	K562	blood:
15	chr16:81073681..81077156-chr16:81081079..81084155,3	MCF-7	breast:
16	chr16:81078751..81080848-chr16:81181095..81182686,2	K562	blood:
17	chr16:81069446..81072291-chr16:81077678..81081761,3	K562	blood:
18	chr16:81081030..81085437-chr16:81085906..81090062,5	MCF-7	breast:
19	chr16:81091735..81094640-chr16:81096464..81099185,2	K562	blood:
20	chr16:81082137..81086308-chr16:81108446..81111994,4	K562	blood:
21	chr16:81083129..81085319-chr16:81095819..81098738,2	K562	blood:
22	chr16:81068550..81071158-chr16:81085432..81087364,3	K562	blood:
23	chr16:81093718..81096458-chr16:81477922..81479889,2	K562	blood:
24	chr16:81068994..81072999-chr16:81079171..81083841,7	MCF-7	breast:
25	chr16:81072851..81076497-chr16:81077627..81082197,6	K562	blood:
26	chr16:81093322..81097410-chr16:81102754..81106923,4	MCF-7	breast:
27	chr16:81080653..81082343-chr16:81109748..81111286,2	MCF-7	breast:
28	chr16:81068052..81071215-chr16:81080209..81082319,3	MCF-7	breast:
29	chr16:81067876..81070786-chr16:81085396..81086928,2	MCF-7	breast:
30	chr16:81093754..81095861-chr16:81110102..81112383,2	MCF-7	breast:
31	chr16:81078691..81081572-chr16:81082090..81085180,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATMIN-2	chr16:81089601-81090031	ENSG00000261141.1
2	lnc-ATMIN-2	chr16:81088906-81089067	ENSG00000261141.1
3	lnc-C16orf46-1	chr16:81087103-81087699	NONHSAT143931

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C16orf46	hsa-miR-192-5p	chr16:81087192-81087214
2	ATMIN	hsa-miR-19b-3p	chr16:81080380-81080402

Variant related genes	Relation type
ENSG00000261141	TF binding region
ENSG00000261141	CpG island
ENSG00000153815	chromatin interactions
ENSG00000103121	chromatin interactions
ENSG00000166451	chromatin interactions
ENSG00000166473	chromatin interactions
ENSG00000261141	chromatin interactions
ENSG00000245059	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000261838	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000166455	chromatin interactions

Extended variants
information (count: 716 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2549891	chr16:81080366-81080367	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148726332	chr16:81080370-81080371	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs532783992	chr16:81080385-81080386	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	7 gene(s)	Overlapped CNVs	n/a
4	rs12932856	chr16:81080395-81080396	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	7 gene(s)	Overlapped CNVs	n/a
5	rs551071858	chr16:81080398-81080399	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	7 gene(s)	Overlapped CNVs	n/a
6	rs547736754	chr16:81080421-81080422	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs559770245	chr16:81080463-81080464	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs192167215	chr16:81080471-81080472	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs533974620	chr16:81080479-81080480	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs570993714	chr16:81080497-81080498	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs11537	chr16:81080499-81080500	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs567325475	chr16:81080514-81080515	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs185089000	chr16:81080518-81080519	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs189772710	chr16:81080522-81080523	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs34529307	chr16:81080528-81080529	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539794637	chr16:81080634-81080635	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs142668128	chr16:81080656-81080657	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs151015599	chr16:81080685-81080686	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs534270130	chr16:81080689-81080690	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs555958051	chr16:81080692-81080693	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs574151020	chr16:81080725-81080726	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs544932425	chr16:81080756-81080757	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs563002121	chr16:81080788-81080789	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs555950435	chr16:81080789-81080790	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs563273056	chr16:81080844-81080845	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs556536314	chr16:81080883-81080884	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs544577645	chr16:81080886-81080887	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs140810443	chr16:81080893-81080894	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs527421210	chr16:81080929-81080930	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs192888426	chr16:81080952-81080953	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs78062698	chr16:81080972-81080973	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs184487004	chr16:81081001-81081002	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs561176591	chr16:81081080-81081081	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs2549892	chr16:81081163-81081164	Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147784962	chr16:81081186-81081187	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs9806860	chr16:81081187-81081188	Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs373111822	chr16:81081203-81081204	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs188197349	chr16:81081224-81081225	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs551832701	chr16:81081305-81081306	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs146967271	chr16:81081328-81081329	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs534337539	chr16:81081332-81081333	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs571996959	chr16:81081341-81081342	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs369563878	chr16:81081398-81081399	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs59245959	chr16:81081427-81081428	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs397807809	chr16:81081445-81081446	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs180757491	chr16:81081471-81081472	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs374857372	chr16:81081495-81081496	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs201615108	chr16:81081498-81081499	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs79736561	chr16:81081508-81081509	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs74030503	chr16:81081525-81081526	Weak transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

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
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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 lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81070800-81081800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:81071200-81080400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr16:81071200-81080400	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr16:81071200-81080600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr16:81071200-81082000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr16:81071200-81082400	Weak transcription	Stomach Mucosa	stomach
7	chr16:81071600-81080600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:81071800-81081800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr16:81074000-81080400	Strong transcription	Primary B cells from cord blood	blood
10	chr16:81074000-81080400	Strong transcription	Duodenum Mucosa	Duodenum
11	chr16:81074000-81082400	Weak transcription	Fetal Heart	heart
12	chr16:81074600-81080400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr16:81074600-81080600	Strong transcription	Fetal Brain Female	brain
14	chr16:81074600-81080800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr16:81075000-81080400	Strong transcription	Brain Germinal Matrix	brain
16	chr16:81075000-81080400	Strong transcription	Duodenum Smooth Muscle	Duodenum
17	chr16:81075000-81080400	Strong transcription	Ovary	ovary
18	chr16:81075000-81080600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr16:81075000-81080600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:81075400-81080400	Strong transcription	Brain Anterior Caudate	brain
21	chr16:81076200-81080400	Strong transcription	Placenta	Placenta
22	chr16:81076200-81081400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr16:81077000-81094600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr16:81077200-81081000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr16:81077200-81082200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr16:81077400-81081600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr16:81077600-81080600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr16:81077600-81080800	Weak transcription	Rectal Smooth Muscle	rectum
29	chr16:81077600-81081400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr16:81077800-81081400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr16:81077800-81081600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr16:81077800-81081600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr16:81077800-81081800	Weak transcription	Hela-S3	cervix
34	chr16:81078000-81081800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr16:81078000-81083600	Weak transcription	Brain Angular Gyrus	brain
36	chr16:81078200-81080600	Weak transcription	Psoas Muscle	Psoas
37	chr16:81078400-81081400	Weak transcription	GM12878-XiMat	blood
38	chr16:81078600-81080600	Weak transcription	NH-A	brain
39	chr16:81078600-81081200	Weak transcription	Right Ventricle	heart
40	chr16:81078800-81081000	Weak transcription	NHEK	skin
41	chr16:81078800-81081600	Weak transcription	NHLF	lung
42	chr16:81078800-81082000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr16:81078800-81083800	Weak transcription	Colon Smooth Muscle	Colon
44	chr16:81079000-81081600	Weak transcription	NHDF-Ad	bronchial
45	chr16:81079200-81080800	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr16:81079200-81081000	Weak transcription	Brain Cingulate Gyrus	brain
47	chr16:81079200-81081600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr16:81079200-81081600	Weak transcription	Esophagus	oesophagus
49	chr16:81079200-81081800	Weak transcription	Fetal Brain Male	brain
50	chr16:81079200-81082000	Weak transcription	Brain Substantia Nigra	brain

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