Variant report

Variant	esv2757103
Chromosome Location	chr5:8701920-8790546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr5:8756822-8756872	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr5:8765963-8766369	IMR90	lung:	n/a	n/a
3	CEBPB	chr5:8719257-8719401	HepG2	liver:	n/a	chr5:8719311-8719328
4	CEBPB	chr5:8707373-8707645	HepG2	liver:	n/a	chr5:8707511-8707522 chr5:8707511-8707524
5	CEBPB	chr5:8730286-8730703	IMR90	lung:	n/a	n/a
6	CEBPB	chr5:8788385-8788712	IMR90	lung:	n/a	chr5:8788537-8788548
7	CEBPB	chr5:8719943-8720185	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:8775924-8775984	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:8775599-8776116	IMR90	lung:	n/a	n/a
10	CTCF	chr5:8756720-8756970	A549	lung:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
11	CTCF	chr5:8756760-8756910	NHEK	skin:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
12	CTCF	chr5:8756780-8756930	GM12868	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
13	CTCF	chr5:8756740-8756890	GM12864	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
14	CTCF	chr5:8752840-8752990	AG04449	skin:	n/a	n/a
15	CTCF	chr5:8756640-8756790	HAc	cerebellar:	n/a	n/a
16	CTCF	chr5:8756760-8756910	SAEC	small airway:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
17	CTCF	chr5:8756720-8756870	HRPEpiC	eye:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
18	CTCF	chr5:8756715-8756903	GM12892	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
19	CTCF	chr5:8752920-8753070	AG10803	skin:	n/a	n/a
20	CTCF	chr5:8756720-8756870	HPAF	blood vessel:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
21	CTCF	chr5:8756704-8756907	Fibrobl	skin:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
22	CTCF	chr5:8756680-8756830	GM12870	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
23	CTCF	chr5:8752900-8753050	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr5:8756700-8756850	HVMF	connective:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
25	CTCF	chr5:8756700-8756850	HPF	lung:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
26	CTCF	chr5:8752900-8753050	HMEC	breast:	n/a	n/a
27	CTCF	chr5:8740234-8740319	GM20000	blood:	n/a	n/a
28	CTCF	chr5:8752980-8753130	HVMF	connective:	n/a	n/a
29	CTCF	chr5:8756729-8756896	Medullo	brain:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
30	CTCF	chr5:8752900-8753050	RPTEC	kidney:	n/a	n/a
31	CTCF	chr5:8756720-8756870	AG04449	skin:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
32	CTCF	chr5:8705049-8705110	GM20000	blood:	n/a	n/a
33	CTCF	chr5:8756716-8756871	K562	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
34	CTCF	chr5:8756700-8756850	HMEC	breast:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
35	CTCF	chr5:8756720-8756870	AG04450	lung:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
36	CTCF	chr5:8756720-8756870	BJ	skin:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
37	CTCF	chr5:8756660-8756810	GM12869	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810
38	CTCF	chr5:8756749-8756833	GM13976	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
39	CTCF	chr5:8756669-8756928	Gliobla	brain:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
40	CTCF	chr5:8756700-8756850	GM12865	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
41	CTCF	chr5:8756680-8756830	GM12878	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
42	CTCF	chr5:8705068-8705070	GM10248	blood:	n/a	n/a
43	CTCF	chr5:8752900-8753050	HCM	heart:	n/a	n/a
44	CTCF	chr5:8752880-8753030	HVMF	connective:	n/a	n/a
45	CTCF	chr5:8756720-8756870	GM12870	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
46	CTCF	chr5:8756740-8756890	HA-sp	spinal cord:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
47	CTCF	chr5:8752860-8753010	RPTEC	kidney:	n/a	n/a
48	CTCF	chr5:8756730-8756852	GM20000	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
49	CTCF	chr5:8756697-8756881	GM19239	blood:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812
50	CTCF	chr5:8756723-8756865	MCF-7	breast:	n/a	chr5:8756797-8756805 chr5:8756797-8756810 chr5:8756796-8756817 chr5:8756794-8756812

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:8767041-8767091	HAEpiC	amniotic membrane:	n/a
2	chr5:8767041-8767091	Jurkat	blood:	n/a
3	chr5:8767041-8767091	ECC-1	luminal epithelium:	n/a
4	chr5:8767041-8767091	NHDF-neo	bronchial:	n/a
5	chr5:8767041-8767091	AG04449	skin:	fetal
6	chr5:8767041-8767091	HCPEpiC	choroid plexus:	n/a
7	chr5:8767041-8767091	MCF-7	breast:	n/a
8	chr5:8767041-8767091	IMR90	lung:	fetal
9	chr5:8767041-8767091	PANC-1	pancreas:	n/a
10	chr5:8767041-8767091	H1-hESC	embryonic stem cell:	embryo
11	chr5:8767041-8767091	T-47D	breast:	n/a
12	chr5:8767041-8767091	GM12878	blood:	n/a
13	chr5:8767041-8767091	HL-60	blood:	n/a
14	chr5:8767041-8767091	HUVEC	blood vessel:	n/a
15	chr5:8767041-8767091	SK-N-SH	brain:	n/a
16	chr5:8767041-8767091	BE2_C	brain:	n/a
17	chr5:8767041-8767091	MCF10A-Er-Src	breast:	n/a
18	chr5:8767041-8767091	ovcar-3	ovarian:	n/a
19	chr5:8767041-8767091	CMK	blood:	n/a
20	chr5:8767041-8767091	SK-N-SH_RA	brain:	n/a
21	chr5:8767041-8767091	GM06990	blood:	n/a
22	chr5:8767041-8767091	NH-A	brain:	n/a
23	chr5:8767041-8767091	HRPEpiC	eye:	n/a
24	chr5:8767041-8767091	BJ	skin:	n/a
25	chr5:8767041-8767091	Hepatocyte	liver:	n/a
26	chr5:8767041-8767091	Hela-S3	cervix:	n/a
27	chr5:8767041-8767091	AG09319	gingival:	n/a
28	chr5:8767041-8767091	K562	blood:	n/a
29	chr5:8767041-8767091	HCM	heart:	n/a
30	chr5:8767041-8767091	SKMC	muscle:	n/a
31	chr5:8767041-8767091	HCT-116	colon:	n/a
32	chr5:8767041-8767091	U87	brain:	n/a
33	chr5:8767041-8767091	HRE	kidney:	n/a
34	chr5:8767041-8767091	PFSK-1	brain:	n/a
35	chr5:8767041-8767091	AG04450	lung:	fetal
36	chr5:8767041-8767091	HRCEpiC	kidney:	n/a
37	chr5:8767041-8767091	NT2-D1	testis:	n/a
38	chr5:8767041-8767091	SK-N-MC	brain:	n/a
39	chr5:8767041-8767091	NB4	blood:	n/a
40	chr5:8767041-8767091	HEK293	kidney:	embryo
41	chr5:8767041-8767091	HepG2	liver:	n/a
42	chr5:8767041-8767091	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:8767041-8767091	HNPCEpiC	eye:	n/a
44	chr5:8767041-8767091	GM12892	blood:	n/a
45	chr5:8767041-8767091	HEEpiC	esophagus:	n/a
46	chr5:8767041-8767091	ProgFib	skin:	n/a
47	chr5:8767041-8767091	RPTEC	kidney:	n/a
48	chr5:8767041-8767091	GM12891	blood:	n/a
49	chr5:8767041-8767091	GM19239	blood:	n/a
50	chr5:8767041-8767091	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:8756316..8757349-chr5:9207756..9208446,4	MCF-7	breast:
2	chr5:8756767..8757357-chr5:9208108..9208626,2	MCF-7	breast:
3	chr15:63747394..63747975-chr5:8748090..8749028,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRR-16	chr5:8754981-8755271	NONHSAT100310
2	lnc-MTRR-16	chr5:8754981-8756996	NONHSAT100311
3	lnc-SEMA5A-2	chr5:8785154-8785580	ENSG00000260981.1
4	lnc-SEMA5A-2	chr5:8785277-8785578	NONHSAT100313

Variant related genes	Relation type
ENSG00000260981	TF binding region
ENSG00000260981	CpG island

Extended variants
information (count: 2171 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2171 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199997	chr5:8701920-8701921	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570065951	chr5:8701964-8701965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78958607	chr5:8701977-8701978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372196983	chr5:8701993-8701994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559030639	chr5:8702000-8702001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553111124	chr5:8702142-8702143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572585856	chr5:8702263-8702264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533107983	chr5:8702265-8702266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541293698	chr5:8702284-8702285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553559251	chr5:8702310-8702311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555168500	chr5:8702313-8702314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574162101	chr5:8702357-8702358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115153946	chr5:8702363-8702364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4701817	chr5:8702372-8702373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs560369054	chr5:8702430-8702431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528505740	chr5:8702475-8702476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546063197	chr5:8702484-8702485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199996	chr5:8702492-8702493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs6875808	chr5:8702522-8702523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs376812673	chr5:8702523-8702524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181289490	chr5:8702539-8702540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375139113	chr5:8702549-8702550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138863446	chr5:8702550-8702551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530527204	chr5:8702551-8702552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7702803	chr5:8702555-8702556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35547465	chr5:8702573-8702574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186498970	chr5:8702579-8702580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550342395	chr5:8702596-8702597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60422362	chr5:8702605-8702606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs376045912	chr5:8702610-8702611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55779915	chr5:8702612-8702613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386685289	chr5:8702618-8702619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559184528	chr5:8702619-8702620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569484073	chr5:8702626-8702627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186131857	chr5:8702635-8702636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190935557	chr5:8702637-8702638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs172044	chr5:8702638-8702639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182732014	chr5:8702642-8702643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543103593	chr5:8702643-8702644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112132872	chr5:8702649-8702650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576406541	chr5:8702650-8702651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190624092	chr5:8702658-8702659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559313616	chr5:8702670-8702671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557559950	chr5:8702679-8702680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528332174	chr5:8702681-8702682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567135541	chr5:8702694-8702695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111747810	chr5:8702701-8702702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376117192	chr5:8702703-8702704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561859249	chr5:8702705-8702706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188062221	chr5:8702706-8702707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
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
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
T-cell prolymphocytic leukemia	17713554	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8699600-8702200	Enhancers	Fetal Lung	lung
2	chr5:8702200-8710600	Weak transcription	Fetal Lung	lung
3	chr5:8710600-8711800	Enhancers	Fetal Lung	lung
4	chr5:8717600-8718000	Active TSS	Right Ventricle	heart
5	chr5:8721000-8722200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:8722200-8727200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:8723400-8726400	Enhancers	Dnd41	blood
8	chr5:8725400-8730200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr5:8726400-8726600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:8726400-8726800	Flanking Active TSS	Dnd41	blood
11	chr5:8726600-8726800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:8726600-8727200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:8726600-8728200	Enhancers	Fetal Stomach	stomach
14	chr5:8726800-8727000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:8726800-8727400	Enhancers	Dnd41	blood
16	chr5:8727000-8728000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:8727200-8727400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:8727200-8727600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr5:8727400-8727800	Active TSS	Osteobl	bone
20	chr5:8727400-8728200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:8727400-8728400	Flanking Active TSS	Dnd41	blood
22	chr5:8727600-8727800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr5:8727600-8728000	Active TSS	NHDF-Ad	bronchial
24	chr5:8727800-8728000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:8727800-8728200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:8727800-8728200	Flanking Active TSS	Osteobl	bone
27	chr5:8727800-8728400	Enhancers	Fetal Lung	lung
28	chr5:8727800-8728800	Enhancers	NHLF	lung
29	chr5:8728000-8728800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:8728000-8728800	Enhancers	NHDF-Ad	bronchial
31	chr5:8728000-8729000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:8728200-8728800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr5:8728200-8730800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:8728200-8730800	Enhancers	Osteobl	bone
35	chr5:8728400-8729400	Enhancers	Dnd41	blood
36	chr5:8728800-8730000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:8728800-8730000	Weak transcription	NHDF-Ad	bronchial
38	chr5:8728800-8730000	Weak transcription	NHLF	lung
39	chr5:8728800-8730200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:8729000-8730400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:8729000-8730400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:8729400-8730400	Weak transcription	Dnd41	blood
43	chr5:8729800-8730800	Enhancers	NH-A	brain
44	chr5:8730000-8730600	Enhancers	NHDF-Ad	bronchial
45	chr5:8730000-8730800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:8730000-8730800	Enhancers	NHLF	lung
47	chr5:8730200-8730600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr5:8730200-8731200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:8730400-8730600	ZNF genes & repeats	Dnd41	blood
50	chr5:8748600-8751000	Enhancers	Dnd41	blood

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