Variant report

Variant	nsv1057982
Chromosome Location	chr16:69988374-70110034
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1467)
CpG islands
(count:1040)
Chromatin interactive
region (count:6)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70052402-70052407	K562	blood:	n/a	n/a
2	ARID3A	chr16:70099725-70099826	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70094518-70094975	HepG2	liver:	n/a	n/a
4	ATF1	chr16:70052291-70052494	K562	blood:	n/a	n/a
5	BACH1	chr16:70099644-70099802	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr16:70098884-70099108	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr16:70092399-70092762	GM12878	blood:	n/a	chr16:70092632-70092641 chr16:70092580-70092591
8	BATF	chr16:70098660-70098957	GM12878	blood:	n/a	n/a
9	BATF	chr16:70097361-70097563	GM12878	blood:	n/a	n/a
10	BATF	chr16:70030873-70031085	GM12878	blood:	n/a	n/a
11	BATF	chr16:70098689-70098984	GM12878	blood:	n/a	n/a
12	BATF	chr16:70030809-70031132	GM12878	blood:	n/a	n/a
13	BATF	chr16:70099910-70100113	GM12878	blood:	n/a	n/a
14	BATF	chr16:70027831-70028579	GM12878	blood:	n/a	n/a
15	BATF	chr16:70027465-70028625	GM12878	blood:	n/a	chr16:70027829-70027838
16	BATF	chr16:70027141-70027316	GM12878	blood:	n/a	n/a
17	BATF	chr16:70092492-70092730	GM12878	blood:	n/a	chr16:70092632-70092641 chr16:70092580-70092591
18	BCL11A	chr16:70099915-70100185	GM12878	blood:	n/a	chr16:70100085-70100094 chr16:70100119-70100132
19	BCL11A	chr16:70036802-70037068	GM12878	blood:	n/a	n/a
20	BCL11A	chr16:70092397-70092736	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:70027834-70028563	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:70036786-70037039	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:70092531-70092705	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70027757-70028623	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70028667-70028869	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70031808-70032044	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70030931-70031131	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70030895-70031136	GM12878	blood:	n/a	n/a
29	BHLHE40	chr16:70099632-70100195	K562	blood:	n/a	chr16:70099817-70099833 chr16:70099820-70099836 chr16:70099730-70099746
30	BHLHE40	chr16:70052228-70052498	K562	blood:	n/a	n/a
31	BHLHE40	chr16:70052248-70052459	HepG2	liver:	n/a	n/a
32	BHLHE40	chr16:70099815-70100204	HepG2	liver:	n/a	chr16:70099817-70099833 chr16:70099820-70099836
33	BHLHE40	chr16:70099730-70100199	GM12878	blood:	n/a	chr16:70099817-70099833 chr16:70099820-70099836 chr16:70099730-70099746
34	BHLHE40	chr16:70099019-70099091	GM12878	blood:	n/a	n/a
35	BHLHE40	chr16:70060262-70060448	GM12878	blood:	n/a	n/a
36	BRCA1	chr16:70099741-70100015	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr16:70086442-70086763	K562	blood:	n/a	n/a
38	CBX3	chr16:70099843-70100158	K562	blood:	n/a	n/a
39	CEBPB	chr16:70096700-70097190	K562	blood:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
40	CEBPB	chr16:70100348-70100388	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr16:70096864-70097083	Hela-S3	cervix:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
42	CEBPB	chr16:70100657-70100922	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr16:70040001-70040200	H1-hESC	embryonic stem cell:	n/a	chr16:70040028-70040041
44	CEBPB	chr16:70096851-70097218	K562	blood:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
45	CEBPB	chr16:70101779-70101854	A549	lung:	n/a	n/a
46	CEBPB	chr16:70096860-70097217	IMR90	lung:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
47	CEBPB	chr16:70100568-70100970	K562	blood:	n/a	n/a
48	CEBPB	chr16:70096855-70097220	HepG2	liver:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
49	CEBPB	chr16:70083652-70083863	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:70083694-70083816	K562	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70099078-70099128	HIPEpiC	eye:	n/a
2	chr16:69988428-69988478	ovcar-3	ovarian:	n/a
3	chr16:70099275-70099325	HRCEpiC	kidney:	n/a
4	chr16:70099078-70099128	HIPEpiC	eye:	n/a
5	chr16:69988428-69988478	ovcar-3	ovarian:	n/a
6	chr16:70099275-70099325	HRCEpiC	kidney:	n/a
7	chr16:70098757-70098807	GM12892	blood:	n/a
8	chr16:70100199-70100249	AG09309	skin:	n/a
9	chr16:70098757-70098807	HNPCEpiC	eye:	n/a
10	chr16:69999425-69999475	MCF10A-Er-Src	breast:	n/a
11	chr16:70099275-70099325	MCF-7	breast:	n/a
12	chr16:70100756-70100806	Hepatocyte	liver:	n/a
13	chr16:70099968-70100018	ECC-1	luminal epithelium:	n/a
14	chr16:70099078-70099128	HNPCEpiC	eye:	n/a
15	chr16:70096420-70096470	HCM	heart:	n/a
16	chr16:70099968-70100018	CMK	blood:	n/a
17	chr16:69999425-69999475	Hela-S3	cervix:	n/a
18	chr16:70100319-70100369	HEK293	kidney:	embryo
19	chr16:70100193-70100243	A549	lung:	n/a
20	chr16:70099275-70099325	AG04450	lung:	fetal
21	chr16:70099608-70099658	ECC-1	luminal epithelium:	n/a
22	chr16:70099275-70099325	RPTEC	kidney:	n/a
23	chr16:70100756-70100806	HEEpiC	esophagus:	n/a
24	chr16:69997368-69997418	NB4	blood:	n/a
25	chr16:70099275-70099325	K562	blood:	n/a
26	chr16:70099968-70100018	HepG2	liver:	n/a
27	chr16:69999425-69999475	NH-A	brain:	n/a
28	chr16:70004872-70004922	BE2_C	brain:	n/a
29	chr16:70099275-70099325	HCF	heart:	n/a
30	chr16:70099078-70099128	HEK293	kidney:	embryo
31	chr16:69999425-69999475	GM06990	blood:	n/a
32	chr16:70098757-70098807	T-47D	breast:	n/a
33	chr16:70099078-70099128	NB4	blood:	n/a
34	chr16:70099608-70099658	Caco-2	colon:	n/a
35	chr16:70099608-70099658	HIPEpiC	eye:	n/a
36	chr16:70096420-70096470	HepG2	liver:	n/a
37	chr16:70100199-70100249	HUVEC	blood vessel:	n/a
38	chr16:70100213-70100263	HPAEpiC	pulmonary alveolar:	n/a
39	chr16:70099608-70099658	AoSMC	blood vessel:	n/a
40	chr16:70100199-70100249	NB4	blood:	n/a
41	chr16:70100213-70100263	ovcar-3	ovarian:	n/a
42	chr16:70100213-70100263	AG09319	gingival:	n/a
43	chr16:70102342-70102392	ECC-1	luminal epithelium:	n/a
44	chr16:70099968-70100018	PANC-1	pancreas:	n/a
45	chr16:70099078-70099128	T-47D	breast:	n/a
46	chr16:70100199-70100249	SK-N-SH	brain:	n/a
47	chr16:69999859-69999909	H1-hESC	embryonic stem cell:	embryo
48	chr16:69999425-69999475	HCF	heart:	n/a
49	chr16:70096420-70096470	BJ	skin:	n/a
50	chr16:70099078-70099128	NH-A	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:54673381..54674330-chr16:70099343..70100334,2	Hela-S3	cervix:
2	chr16:70093516..70095725-chr16:70099039..70100582,2	MCF-7	breast:
3	chr16:70098076..70099819-chr16:70146086..70148783,2	MCF-7	breast:
4	chr16:70098870..70100734-chr16:70105028..70107884,2	MCF-7	breast:
5	chr16:15068623..15069146-chr16:70099345..70100020,4	MCF-7	breast:
6	chr16:15066889..15068819-chr16:70099825..70101888,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC6-3	chr16:70098574-70098679	NONHSAT143385
2	lnc-RP11-419C5.2.1-1	chr16:70100122-70100332	NONHSAT143386
3	lnc-RP11-419C5.2.1-1	chr16:70099907-70100013	NONHSAT143386
4	lnc-EXOSC6-3	chr16:70011509-70011906	NONHSAT143378
5	lnc-EXOSC6-3	chr16:70012125-70012185	NONHSAT143378
6	lnc-EXOSC6-3	chr16:70099659-70099688	NONHSAT143385
7	lnc-EXOSC6-3	chr16:70096958-70097591	NONHSAT143385
8	lnc-EXOSC6-3	chr16:70011980-70012015	NONHSAT143378
9	lnc-EXOSC6-3	chr16:70051793-70053313	ENSG00000196696.7
10	lnc-EXOSC6-3	chr16:70016253-70016368	NONHSAT143378

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1972	chr16:70064296-70064317	MIMAT0009447_1

No data

Variant related genes	Relation type
ENSG00000226232	TF binding region
ENSG00000255185	TF binding region
MIR1972-2	TF binding region
PDXDC2P	TF binding region
ENSG00000226232	CpG island
ENSG00000255185	CpG island
MIR1972-2	CpG island
PDXDC2P	CpG island
ENSG00000255185	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000179889	chromatin interactions
ENSG00000196696	chromatin interactions
ENSG00000090857	chromatin interactions

Extended variants
information (count: 4621 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4621 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191870515	chr16:69988384-69988385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559431400	chr16:69988414-69988415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533136482	chr16:69988418-69988419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60310934	chr16:69988429-69988430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140422967	chr16:69988430-69988431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530536080	chr16:69988431-69988432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144215595	chr16:69988459-69988460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78531533	chr16:69988463-69988464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566927520	chr16:69988464-69988465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75776403	chr16:69988472-69988473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs80122082	chr16:69988473-69988474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371517431	chr16:69988481-69988482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377363932	chr16:69988497-69988498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370839883	chr16:69988501-69988502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201281743	chr16:69988502-69988503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374226494	chr16:69988520-69988521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571880756	chr16:69988524-69988525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200179844	chr16:69988549-69988550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539200638	chr16:69988601-69988602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557292654	chr16:69988608-69988609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201040913	chr16:69988618-69988619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575656840	chr16:69988627-69988628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183972621	chr16:69988646-69988647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554954987	chr16:69988653-69988654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149909666	chr16:69988667-69988668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542100080	chr16:69988687-69988688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555991976	chr16:69988689-69988690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4985468	chr16:69988713-69988714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540667513	chr16:69988720-69988721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559578560	chr16:69988767-69988768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113328607	chr16:69988792-69988793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533100690	chr16:69988793-69988794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs55862211	chr16:69988812-69988813	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs200906931	chr16:69988830-69988831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563347029	chr16:69988838-69988839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530475906	chr16:69988845-69988846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548667098	chr16:69988863-69988864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187896819	chr16:69988874-69988875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528060277	chr16:69988881-69988882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546307338	chr16:69988886-69988887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571880695	chr16:69988895-69988896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192064976	chr16:69988896-69988897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533146486	chr16:69988935-69988936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557486936	chr16:69988945-69988946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569475991	chr16:69988972-69988973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78466083	chr16:69988981-69988982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536892261	chr16:69988989-69988990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555087474	chr16:69988990-69988991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573405153	chr16:69989006-69989007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540599192	chr16:69989007-69989008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	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
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

Chromatin state (count:2065 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69976800-69998600	Weak transcription	Spleen	Spleen
2	chr16:69977400-69988800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr16:69985600-69991000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:69988800-69989800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr16:69989800-69998800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr16:69995400-69998600	Weak transcription	Gastric	stomach
7	chr16:69998400-69998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr16:69998400-69998600	Enhancers	Adipose Nuclei	Adipose
9	chr16:69998600-69998800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr16:69998600-69998800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr16:69998600-69998800	Enhancers	Liver	Liver
12	chr16:69998600-69998800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr16:69998600-69998800	Enhancers	Fetal Muscle Leg	muscle
14	chr16:69998600-69998800	Enhancers	Gastric	stomach
15	chr16:69998600-69998800	Enhancers	Left Ventricle	heart
16	chr16:69998600-69998800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr16:69998600-69999000	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr16:69998600-69999000	Enhancers	HUVEC	blood vessel
19	chr16:69998600-69999200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr16:69998600-69999400	Enhancers	Spleen	Spleen
21	chr16:69998600-69999600	Active TSS	Duodenum Mucosa	Duodenum
22	chr16:69998600-69999600	Active TSS	HSMM	muscle
23	chr16:69998800-69999000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr16:69998800-69999000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr16:69998800-69999000	Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr16:69998800-69999000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr16:69998800-69999000	Active TSS	Fetal Muscle Trunk	muscle
28	chr16:69998800-69999000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
29	chr16:69998800-69999200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr16:69998800-69999200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
31	chr16:69998800-69999200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr16:69998800-69999200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr16:69998800-69999200	Flanking Active TSS	Liver	Liver
34	chr16:69998800-69999200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr16:69998800-69999200	Flanking Active TSS	Left Ventricle	heart
36	chr16:69998800-69999200	Active TSS	Placenta Amnion	Placenta Amnion
37	chr16:69998800-69999200	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr16:69998800-69999400	Active TSS	Brain Anterior Caudate	brain
39	chr16:69998800-69999400	Active TSS	Brain Hippocampus Middle	brain
40	chr16:69998800-69999400	Active TSS	Colon Smooth Muscle	Colon
41	chr16:69998800-69999400	Active TSS	Fetal Intestine Large	intestine
42	chr16:69998800-69999400	Active TSS	Gastric	stomach
43	chr16:69998800-69999600	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr16:69998800-69999600	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr16:69998800-69999600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr16:69998800-69999600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr16:69998800-69999600	Active TSS	Primary hematopoietic stem cells	blood
48	chr16:69998800-69999600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr16:69998800-69999600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr16:69998800-69999600	Active TSS	Muscle Satellite Cultured Cells	--

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