Variant report

Variant	nsv968877
Chromosome Location	chr5:16901612-16905258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:16903930-16904377	H1-hESC	embryonic stem cell:	n/a	chr5:16904017-16904028
2	CEBPB	chr5:16903839-16904417	HepG2	liver:	n/a	chr5:16904017-16904028
3	CEBPB	chr5:16903822-16904440	MCF-7	breast:	n/a	chr5:16904017-16904028
4	CEBPB	chr5:16903839-16904418	IMR90	lung:	n/a	chr5:16904017-16904028
5	CEBPB	chr5:16903830-16904437	A549	lung:	n/a	chr5:16904017-16904028
6	CEBPB	chr5:16903858-16904453	A549	lung:	n/a	chr5:16904017-16904028
7	CEBPB	chr5:16903853-16904325	K562	blood:	n/a	chr5:16904017-16904028
8	CEBPB	chr5:16903807-16904506	A549	lung:	n/a	chr5:16904017-16904028
9	CEBPB	chr5:16903852-16904421	Hela-S3	cervix:	n/a	chr5:16904017-16904028
10	FOS	chr5:16902992-16903328	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr5:16902907-16903423	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr5:16904053-16904218	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr5:16904052-16904268	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr5:16904116-16904254	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr5:16902927-16903383	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr5:16902918-16903407	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr5:16903904-16904255	MCF10A-Er-Src	breast:	n/a	n/a
18	MAX	chr5:16904059-16904229	Hela-S3	cervix:	n/a	n/a
19	MYC	chr5:16902927-16903400	MCF10A-Er-Src	breast:	n/a	n/a
20	MYC	chr5:16905164-16905261	H1-hESC	embryonic stem cell:	n/a	n/a
21	MYC	chr5:16902920-16903394	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr5:16903062-16903259	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr5:16904500-16904559	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr5:16901641-16902178	SK-N-MC	brain:	n/a	n/a
25	POLR2A	chr5:16905114-16906934	A549	lung:	n/a	n/a
26	POLR2A	chr5:16905258-16905398	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr5:16902601-16902703	GM12878	blood:	n/a	n/a
28	POLR2A	chr5:16899221-16902124	A549	lung:	n/a	n/a
29	POLR2A	chr5:16903205-16903213	A549	lung:	n/a	n/a
30	POLR2A	chr5:16903692-16904644	A549	lung:	n/a	n/a
31	POLR2A	chr5:16902277-16903286	SK-N-MC	brain:	n/a	n/a
32	POLR2A	chr5:16903776-16907066	SK-N-MC	brain:	n/a	n/a
33	STAT3	chr5:16902996-16903392	MCF10A-Er-Src	breast:	n/a	n/a
34	STAT3	chr5:16903944-16904106	MCF10A-Er-Src	breast:	n/a	n/a
35	STAT3	chr5:16904053-16904057	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT3	chr5:16903098-16903366	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr5:16902997-16903319	MCF10A-Er-Src	breast:	n/a	n/a
38	TCF7L2	chr5:16904369-16904520	PANC-1	pancreas:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16902633-16902683	HRE	kidney:	n/a
2	chr5:16902573-16902623	GM06990	blood:	n/a
3	chr5:16902573-16902623	Jurkat	blood:	n/a
4	chr5:16902633-16902683	HRCEpiC	kidney:	n/a
5	chr5:16902573-16902623	HRCEpiC	kidney:	n/a
6	chr5:16904764-16904814	NB4	blood:	n/a
7	chr5:16902633-16902683	NHDF-neo	bronchial:	n/a
8	chr5:16902573-16902623	CMK	blood:	n/a
9	chr5:16904764-16904814	NH-A	brain:	n/a
10	chr5:16904764-16904814	HNPCEpiC	eye:	n/a
11	chr5:16902573-16902623	IMR90	lung:	fetal
12	chr5:16902573-16902623	BE2_C	brain:	n/a
13	chr5:16902633-16902683	AG10803	skin:	n/a
14	chr5:16902633-16902683	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:16902633-16902683	BE2_C	brain:	n/a
16	chr5:16902573-16902623	PrEC	prostate:	n/a
17	chr5:16902573-16902623	HUVEC	blood vessel:	n/a
18	chr5:16904764-16904814	AG10803	skin:	n/a
19	chr5:16904764-16904814	GM12892	blood:	n/a
20	chr5:16902633-16902683	HCT-116	colon:	n/a
21	chr5:16902573-16902623	AG10803	skin:	n/a
22	chr5:16902633-16902683	AG04450	lung:	fetal
23	chr5:16904764-16904814	AG04450	lung:	fetal
24	chr5:16902573-16902623	SAEC	small airway:	n/a
25	chr5:16902573-16902623	HCF	heart:	n/a
26	chr5:16902633-16902683	NT2-D1	testis:	n/a
27	chr5:16904764-16904814	MCF10A-Er-Src	breast:	n/a
28	chr5:16902633-16902683	SK-N-MC	brain:	n/a
29	chr5:16904764-16904814	HL-60	blood:	n/a
30	chr5:16902633-16902683	SAEC	small airway:	n/a
31	chr5:16902633-16902683	AG09319	gingival:	n/a
32	chr5:16902633-16902683	GM06990	blood:	n/a
33	chr5:16902633-16902683	LNCaP	prostate:	n/a
34	chr5:16904764-16904814	ProgFib	skin:	n/a
35	chr5:16902573-16902623	MCF-7	breast:	n/a
36	chr5:16902573-16902623	ECC-1	luminal epithelium:	n/a
37	chr5:16902633-16902683	HAEpiC	amniotic membrane:	n/a
38	chr5:16904764-16904814	NT2-D1	testis:	n/a
39	chr5:16902573-16902623	Caco-2	colon:	n/a
40	chr5:16904764-16904814	NHDF-neo	bronchial:	n/a
41	chr5:16904764-16904814	PFSK-1	brain:	n/a
42	chr5:16902573-16902623	PFSK-1	brain:	n/a
43	chr5:16902633-16902683	GM12891	blood:	n/a
44	chr5:16902573-16902623	T-47D	breast:	n/a
45	chr5:16904764-16904814	HUVEC	blood vessel:	n/a
46	chr5:16904764-16904814	SAEC	small airway:	n/a
47	chr5:16902633-16902683	U87	brain:	n/a
48	chr5:16902573-16902623	HRPEpiC	eye:	n/a
49	chr5:16902573-16902623	RPTEC	kidney:	n/a
50	chr5:16902573-16902623	BJ	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16894491..16896403-chr5:16903844..16905936,2	MCF-7	breast:
2	chr5:16903174..16906084-chr5:16912041..16914007,3	MCF-7	breast:
3	chr5:16899974..16902321-chr5:16904564..16907062,3	MCF-7	breast:
4	chr5:16892933..16897070-chr5:16897498..16901971,5	MCF-7	breast:
5	chr5:16899974..16902321-chr5:16904564..16907062,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000243538	TF binding region
ENSG00000243538	CpG island

Extended variants
information (count: 163 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:163 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567132060	chr5:16901648-16901649	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370424651	chr5:16901649-16901650	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557248040	chr5:16901682-16901683	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535782718	chr5:16901740-16901741	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10520846	chr5:16901752-16901753	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572306705	chr5:16901806-16901807	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566607005	chr5:16901834-16901835	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545947992	chr5:16901863-16901864	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77117684	chr5:16901891-16901892	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527360931	chr5:16901914-16901915	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185522432	chr5:16901926-16901927	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543529351	chr5:16901944-16901945	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562145479	chr5:16901983-16901984	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529268907	chr5:16901996-16901997	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62371018	chr5:16902051-16902052	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189598145	chr5:16902062-16902063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533171382	chr5:16902085-16902086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570086590	chr5:16902094-16902095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143745825	chr5:16902100-16902101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569749790	chr5:16902123-16902124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376515405	chr5:16902144-16902145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530659361	chr5:16902148-16902149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2560844	chr5:16902229-16902230	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2562356	chr5:16902248-16902249	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs2562357	chr5:16902257-16902258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534272863	chr5:16902259-16902260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554051007	chr5:16902312-16902313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2560843	chr5:16902315-16902316	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34050297	chr5:16902321-16902322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397881550	chr5:16902334-16902335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199677567	chr5:16902335-16902336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74544852	chr5:16902348-16902349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559510830	chr5:16902371-16902372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576543382	chr5:16902401-16902402	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543911879	chr5:16902404-16902405	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191195388	chr5:16902408-16902409	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574087445	chr5:16902416-16902417	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183528149	chr5:16902439-16902440	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573046045	chr5:16902457-16902458	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs151192590	chr5:16902461-16902462	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544956348	chr5:16902486-16902487	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2560842	chr5:16902512-16902513	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs61742953	chr5:16902536-16902537	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549063827	chr5:16902574-16902575	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149898337	chr5:16902583-16902584	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573931553	chr5:16902616-16902617	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528161774	chr5:16902663-16902664	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546233118	chr5:16902664-16902665	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188581415	chr5:16902669-16902670	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562768757	chr5:16902686-16902687	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16895000-16903000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr5:16895600-16902000	Enhancers	Hela-S3	cervix
3	chr5:16896000-16912400	Weak transcription	Esophagus	oesophagus
4	chr5:16897000-16902800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:16897600-16902000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr5:16898000-16901800	Weak transcription	HSMMtube	muscle
7	chr5:16898000-16902800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:16898000-16902800	Weak transcription	HSMM	muscle
9	chr5:16898200-16902600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr5:16898200-16902800	Weak transcription	Colon Smooth Muscle	Colon
11	chr5:16898200-16903000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:16898200-16903400	Weak transcription	Placenta	Placenta
13	chr5:16898200-16903800	Weak transcription	Osteobl	bone
14	chr5:16898200-16904000	Weak transcription	NHLF	lung
15	chr5:16898200-16906200	Weak transcription	Psoas Muscle	Psoas
16	chr5:16898200-16912600	Weak transcription	NH-A	brain
17	chr5:16898400-16903000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:16898400-16903000	Weak transcription	Fetal Stomach	stomach
19	chr5:16898400-16903000	Weak transcription	Ovary	ovary
20	chr5:16898400-16903800	Weak transcription	Small Intestine	intestine
21	chr5:16898400-16904600	Weak transcription	Fetal Intestine Small	intestine
22	chr5:16899200-16902000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:16899400-16902200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:16899400-16907000	Enhancers	Pancreas	Pancrea
25	chr5:16899600-16902000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:16899600-16902000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:16899800-16905600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr5:16899800-16910000	Weak transcription	HUVEC	blood vessel
29	chr5:16899800-16910800	Weak transcription	HMEC	breast
30	chr5:16900200-16902200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:16900200-16902200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr5:16900200-16902200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr5:16900400-16901800	Enhancers	Fetal Brain Male	brain
34	chr5:16900400-16905400	Enhancers	Fetal Muscle Leg	muscle
35	chr5:16900600-16903800	Weak transcription	NHDF-Ad	bronchial
36	chr5:16900600-16903800	Weak transcription	NHEK	skin
37	chr5:16900800-16903200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:16900800-16903200	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr5:16901000-16901800	Enhancers	Stomach Mucosa	stomach
40	chr5:16901000-16902000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr5:16901200-16901800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:16901200-16901800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr5:16901200-16902000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:16901200-16902000	Enhancers	Duodenum Mucosa	Duodenum
45	chr5:16901200-16902000	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr5:16901200-16902000	Enhancers	Spleen	Spleen
47	chr5:16901200-16902000	Flanking Active TSS	A549	lung
48	chr5:16901200-16902400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:16901200-16904400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:16901200-16904800	Enhancers	Fetal Muscle Trunk	muscle

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