Variant report

Variant	nsv974811
Chromosome Location	chr16:47599013-47613849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:236)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:236 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47612461-47612663	K562	blood:	n/a	n/a
2	ATF1	chr16:47599472-47599607	K562	blood:	n/a	n/a
3	ATF2	chr16:47608501-47609078	GM12878	blood:	n/a	n/a
4	BATF	chr16:47599350-47599772	GM12878	blood:	n/a	chr16:47599551-47599561 chr16:47599546-47599557 chr16:47599547-47599557
5	BATF	chr16:47599987-47600257	GM12878	blood:	n/a	n/a
6	BCL3	chr16:47607971-47608367	GM12878	blood:	n/a	n/a
7	BHLHE40	chr16:47608662-47608921	GM12878	blood:	n/a	n/a
8	CEBPB	chr16:47608072-47608309	IMR90	lung:	n/a	n/a
9	CEBPB	chr16:47612424-47612741	K562	blood:	n/a	n/a
10	CEBPB	chr16:47599458-47599746	IMR90	lung:	n/a	n/a
11	CEBPB	chr16:47600982-47601173	HepG2	liver:	n/a	n/a
12	CEBPB	chr16:47612437-47612732	K562	blood:	n/a	n/a
13	CREB1	chr16:47599444-47599753	GM12878	blood:	n/a	n/a
14	CTCF	chr16:47605118-47605206	HepG2	liver:	n/a	n/a
15	CTCF	chr16:47605060-47605210	HMF	breast:	n/a	n/a
16	CTCF	chr16:47608100-47608250	HMEC	breast:	n/a	n/a
17	CTCF	chr16:47604980-47605130	RPTEC	kidney:	n/a	n/a
18	CTCF	chr16:47605089-47605228	GM13977	blood:	n/a	n/a
19	CTCF	chr16:47605040-47605190	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr16:47605060-47605210	GM12867	blood:	n/a	n/a
21	CTCF	chr16:47605133-47605269	GM19240	blood:	n/a	n/a
22	CTCF	chr16:47605140-47605281	GM19238	blood:	n/a	n/a
23	CTCF	chr16:47605071-47605250	HepG2	liver:	n/a	n/a
24	CTCF	chr16:47605100-47605250	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr16:47605140-47605290	GM12871	blood:	n/a	n/a
26	CTCF	chr16:47605120-47605270	GM12871	blood:	n/a	n/a
27	CTCF	chr16:47606111-47606133	GM19240	blood:	n/a	n/a
28	CTCF	chr16:47605020-47605250	HCFaa	heart:	n/a	n/a
29	CTCF	chr16:47599630-47599692	Lung_OC	lung:	n/a	n/a
30	CTCF	chr16:47605120-47605270	HCT-116	colon:	n/a	n/a
31	CTCF	chr16:47605120-47605270	K562	blood:	n/a	n/a
32	CTCF	chr16:47605200-47605350	A549	lung:	n/a	n/a
33	CTCF	chr16:47605060-47605210	HVMF	connective:	n/a	n/a
34	CTCF	chr16:47605160-47605310	GM12864	blood:	n/a	n/a
35	CTCF	chr16:47605160-47605310	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr16:47605220-47605370	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr16:47605100-47605250	GM12865	blood:	n/a	n/a
38	CTCF	chr16:47605199-47605210	GM10266	blood:	n/a	n/a
39	CTCF	chr16:47605280-47605430	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr16:47605180-47605330	HepG2	liver:	n/a	n/a
41	CTCF	chr16:47605120-47605270	HMEC	breast:	n/a	n/a
42	CTCF	chr16:47604983-47605281	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr16:47605152-47605268	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr16:47605100-47605250	GM12878	blood:	n/a	n/a
45	CTCF	chr16:47605120-47605270	GM12864	blood:	n/a	n/a
46	CTCF	chr16:47605180-47605330	RPTEC	kidney:	n/a	n/a
47	CTCF	chr16:47605120-47605270	GM12872	blood:	n/a	n/a
48	CTCF	chr16:47604960-47605110	BE2_C	brain:	n/a	n/a
49	CTCF	chr16:47605100-47605250	GM12875	blood:	n/a	n/a
50	CTCF	chr16:47605040-47605190	GM12872	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr16:47594118..47597140-chr16:47598345..47602068,5	K562	blood:
2	chr16:47603980..47606285-chr16:47608277..47609809,2	K562	blood:
3	chr16:47607769..47610118-chr16:47633916..47636393,2	K562	blood:
4	chr16:47496037..47497585-chr16:47610458..47612436,2	K562	blood:
5	chr16:47603980..47606285-chr16:47608277..47609809,2	K562	blood:
6	chr16:47613634..47615207-chr16:47619168..47621595,2	K562	blood:

No data

Variant related genes	Relation type
EIF4BP5	TF binding region
ENSG00000259866	TF binding region
ENSG00000259866	chromatin interactions
ENSG00000102893	chromatin interactions

Extended variants
information (count: 451 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568856431	chr16:47599015-47599016	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs186676544	chr16:47599036-47599037	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375087967	chr16:47599037-47599038	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574566798	chr16:47599093-47599094	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189906476	chr16:47599099-47599100	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554035721	chr16:47599248-47599249	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577374678	chr16:47599253-47599254	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs546128111	chr16:47599318-47599319	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544472440	chr16:47599379-47599380	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139368636	chr16:47599422-47599423	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182415405	chr16:47599429-47599430	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528743812	chr16:47599432-47599433	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs116913401	chr16:47599437-47599438	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs55705166	chr16:47599502-47599503	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs75303362	chr16:47599511-47599512	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546684082	chr16:47599524-47599525	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560043005	chr16:47599541-47599542	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532328730	chr16:47599542-47599543	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147694449	chr16:47599577-47599578	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546829112	chr16:47599605-47599606	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568794352	chr16:47599611-47599612	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs377441664	chr16:47599621-47599622	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548146437	chr16:47599622-47599623	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568126700	chr16:47599630-47599631	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533993283	chr16:47599769-47599770	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12926621	chr16:47599826-47599827	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577307039	chr16:47599833-47599834	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144712014	chr16:47599853-47599854	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535578854	chr16:47599898-47599899	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147884054	chr16:47599904-47599905	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs141526941	chr16:47599907-47599908	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77858344	chr16:47599925-47599926	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542554190	chr16:47599945-47599946	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554563464	chr16:47599967-47599968	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs143193514	chr16:47599972-47599973	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574377217	chr16:47599976-47599977	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs55972815	chr16:47599989-47599990	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539892887	chr16:47600050-47600051	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78200191	chr16:47600128-47600129	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368740447	chr16:47600163-47600164	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140297062	chr16:47600170-47600171	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545570066	chr16:47600202-47600203	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187801730	chr16:47600209-47600210	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1200996	chr16:47600240-47600241	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs193146844	chr16:47600271-47600272	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569183260	chr16:47600285-47600286	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150338787	chr16:47600293-47600294	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373232526	chr16:47600301-47600302	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs527676156	chr16:47600402-47600403	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547509334	chr16:47600409-47600410	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47548800-47605000	Weak transcription	Right Ventricle	heart
2	chr16:47580000-47599200	Weak transcription	Osteobl	bone
3	chr16:47581000-47615800	Weak transcription	Placenta	Placenta
4	chr16:47581000-47624200	Weak transcription	Brain Substantia Nigra	brain
5	chr16:47581200-47624600	Weak transcription	Colonic Mucosa	Colon
6	chr16:47581200-47627400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:47581400-47641800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:47581800-47621400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr16:47582000-47608200	Weak transcription	Fetal Thymus	thymus
10	chr16:47582000-47624200	Weak transcription	Fetal Kidney	kidney
11	chr16:47582200-47625000	Weak transcription	Fetal Heart	heart
12	chr16:47584600-47599200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr16:47584600-47599200	Weak transcription	K562	blood
14	chr16:47584600-47599200	Weak transcription	NH-A	brain
15	chr16:47584600-47599400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr16:47584600-47600600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr16:47584600-47604200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr16:47584600-47607000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr16:47584600-47624400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr16:47584600-47624400	Weak transcription	Colon Smooth Muscle	Colon
21	chr16:47584800-47599200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr16:47584800-47599200	Weak transcription	Left Ventricle	heart
23	chr16:47584800-47599600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr16:47584800-47601800	Weak transcription	Brain Hippocampus Middle	brain
25	chr16:47584800-47622600	Weak transcription	Brain Angular Gyrus	brain
26	chr16:47586200-47599200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr16:47586200-47605800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr16:47586800-47600600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr16:47587000-47599200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr16:47588000-47599600	Weak transcription	Brain Germinal Matrix	brain
31	chr16:47588000-47607400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr16:47588200-47599600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr16:47588200-47599800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr16:47588200-47599800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr16:47588200-47606600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr16:47588200-47622600	Weak transcription	Fetal Lung	lung
37	chr16:47588400-47599800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr16:47588400-47605200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr16:47588400-47608400	Weak transcription	Thymus	Thymus
40	chr16:47588400-47622600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr16:47588600-47599200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr16:47588600-47599600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr16:47588600-47599600	Weak transcription	Ovary	ovary
44	chr16:47588600-47615200	Weak transcription	Liver	Liver
45	chr16:47588600-47615800	Weak transcription	Fetal Muscle Trunk	muscle
46	chr16:47588600-47622600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr16:47588600-47622600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr16:47588800-47599200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr16:47588800-47605200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr16:47588800-47606400	Weak transcription	Lung	lung

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