Variant report

Variant	nsv598533
Chromosome Location	chr5:69688350-70379466
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7283)
CpG islands
(count:732)
Chromatin interactive
region (count:0)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:7283 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:69696778-69696970	K562	blood:	n/a	n/a
2	ATF3	chr5:69696877-69696999	K562	blood:	n/a	n/a
3	BATF	chr5:69841101-69841327	GM12878	blood:	n/a	n/a
4	BATF	chr5:69819391-69819676	GM12878	blood:	n/a	n/a
5	BATF	chr5:69853617-69853832	GM12878	blood:	n/a	n/a
6	BATF	chr5:70019070-70019445	GM12878	blood:	n/a	n/a
7	BATF	chr5:69905747-69905950	GM12878	blood:	n/a	n/a
8	BATF	chr5:69692268-69692558	GM12878	blood:	n/a	chr5:69692405-69692416 chr5:69692406-69692416
9	BATF	chr5:70043249-70043524	GM12878	blood:	n/a	chr5:70043459-70043468
10	BATF	chr5:70015604-70016219	GM12878	blood:	n/a	n/a
11	BATF	chr5:70025579-70025765	GM12878	blood:	n/a	chr5:70025663-70025674 chr5:70025664-70025674
12	BATF	chr5:69879818-69880025	GM12878	blood:	n/a	n/a
13	BATF	chr5:70018776-70019002	GM12878	blood:	n/a	n/a
14	BATF	chr5:69868700-69868944	GM12878	blood:	n/a	n/a
15	BATF	chr5:69881032-69881681	GM12878	blood:	n/a	n/a
16	BATF	chr5:70046680-70046878	GM12878	blood:	n/a	chr5:70046762-70046773
17	BATF	chr5:69700337-69700589	GM12878	blood:	n/a	n/a
18	BATF	chr5:70056763-70057190	GM12878	blood:	n/a	n/a
19	BATF	chr5:69998345-69998574	GM12878	blood:	n/a	n/a
20	BATF	chr5:70018767-70018986	GM12878	blood:	n/a	n/a
21	BATF	chr5:69798110-69798395	GM12878	blood:	n/a	n/a
22	BATF	chr5:69877858-69878274	GM12878	blood:	n/a	n/a
23	BATF	chr5:69698885-69699248	GM12878	blood:	n/a	n/a
24	BATF	chr5:69854534-69854815	GM12878	blood:	n/a	chr5:69854638-69854647
25	BATF	chr5:69703633-69704665	GM12878	blood:	n/a	n/a
26	BATF	chr5:69700343-69700605	GM12878	blood:	n/a	n/a
27	BATF	chr5:69699561-69699834	GM12878	blood:	n/a	n/a
28	BATF	chr5:69880455-69880768	GM12878	blood:	n/a	n/a
29	BATF	chr5:69854149-69854431	GM12878	blood:	n/a	n/a
30	BATF	chr5:69799993-69800148	GM12878	blood:	n/a	n/a
31	BATF	chr5:69712289-69712493	GM12878	blood:	n/a	n/a
32	BATF	chr5:69699525-69699963	GM12878	blood:	n/a	n/a
33	BATF	chr5:69897698-69897890	GM12878	blood:	n/a	n/a
34	BATF	chr5:70017925-70018198	GM12878	blood:	n/a	n/a
35	BATF	chr5:69837674-69838451	GM12878	blood:	n/a	n/a
36	BATF	chr5:69712063-69712542	GM12878	blood:	n/a	chr5:69712253-69712264
37	BATF	chr5:70220674-70221170	GM12878	blood:	n/a	n/a
38	BATF	chr5:70111545-70111758	GM12878	blood:	n/a	n/a
39	BATF	chr5:70021119-70021411	GM12878	blood:	n/a	n/a
40	BATF	chr5:69877438-69877843	GM12878	blood:	n/a	n/a
41	BATF	chr5:69896750-69896954	GM12878	blood:	n/a	n/a
42	BATF	chr5:69839605-69840032	GM12878	blood:	n/a	n/a
43	BATF	chr5:70079574-70079848	GM12878	blood:	n/a	n/a
44	BATF	chr5:70014362-70014876	GM12878	blood:	n/a	n/a
45	BATF	chr5:69882386-69883123	GM12878	blood:	n/a	n/a
46	BATF	chr5:70060839-70061183	GM12878	blood:	n/a	n/a
47	BATF	chr5:69878947-69879374	GM12878	blood:	n/a	n/a
48	BATF	chr5:70079571-70079936	GM12878	blood:	n/a	n/a
49	BATF	chr5:70028362-70028636	GM12878	blood:	n/a	n/a
50	BATF	chr5:69695976-69696490	GM12878	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70372505-70372555	HCT-116	colon:	n/a
2	chr5:70309843-70309893	NHBE	bronchial:	n/a
3	chr5:70372505-70372555	NB4	blood:	n/a
4	chr5:69803286-69803336	Jurkat	blood:	n/a
5	chr5:70220559-70220609	ECC-1	luminal epithelium:	n/a
6	chr5:69784092-69784142	PrEC	prostate:	n/a
7	chr5:69783979-69784029	Jurkat	blood:	n/a
8	chr5:69804518-69804568	HCPEpiC	choroid plexus:	n/a
9	chr5:69804518-69804568	AG04449	skin:	fetal
10	chr5:70309843-70309893	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:70308497-70308547	PrEC	prostate:	n/a
12	chr5:69697369-69697419	ECC-1	luminal epithelium:	n/a
13	chr5:69803286-69803336	Hepatocyte	liver:	n/a
14	chr5:69804518-69804568	AG04450	lung:	fetal
15	chr5:69783979-69784029	AG09319	gingival:	n/a
16	chr5:69804518-69804568	HUVEC	blood vessel:	n/a
17	chr5:69804518-69804568	HRCEpiC	kidney:	n/a
18	chr5:70372505-70372555	A549	lung:	n/a
19	chr5:69783979-69784029	Caco-2	colon:	n/a
20	chr5:69697369-69697419	RPTEC	kidney:	n/a
21	chr5:69784092-69784142	HRE	kidney:	n/a
22	chr5:69784092-69784142	NHBE	bronchial:	n/a
23	chr5:69804518-69804568	Hela-S3	cervix:	n/a
24	chr5:70218963-70219013	AG10803	skin:	n/a
25	chr5:70246896-70246946	HRPEpiC	eye:	n/a
26	chr5:70320693-70320743	GM19239	blood:	n/a
27	chr5:70320693-70320743	Jurkat	blood:	n/a
28	chr5:70320693-70320743	H1-hESC	embryonic stem cell:	embryo
29	chr5:70220559-70220609	HepG2	liver:	n/a
30	chr5:69784092-69784142	HIPEpiC	eye:	n/a
31	chr5:70308497-70308547	PFSK-1	brain:	n/a
32	chr5:69783979-69784029	LNCaP	prostate:	n/a
33	chr5:70309843-70309893	BE2_C	brain:	n/a
34	chr5:70220559-70220609	AG10803	skin:	n/a
35	chr5:69697369-69697419	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:69783979-69784029	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:69783979-69784029	SK-N-MC	brain:	n/a
38	chr5:70308497-70308547	LNCaP	prostate:	n/a
39	chr5:70246896-70246946	NHBE	bronchial:	n/a
40	chr5:70320693-70320743	Caco-2	colon:	n/a
41	chr5:70308497-70308547	HCT-116	colon:	n/a
42	chr5:69783979-69784029	ovcar-3	ovarian:	n/a
43	chr5:69804518-69804568	BE2_C	brain:	n/a
44	chr5:70320693-70320743	NH-A	brain:	n/a
45	chr5:70372505-70372555	BE2_C	brain:	n/a
46	chr5:69803286-69803336	SKMC	muscle:	n/a
47	chr5:69803286-69803336	K562	blood:	n/a
48	chr5:70309843-70309893	ECC-1	luminal epithelium:	n/a
49	chr5:70308497-70308547	GM12878	blood:	n/a
50	chr5:69804518-69804568	MCF10A-Er-Src	breast:	n/a

No data

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-1	chr5:70328995-70329470	ENSG00000254353
2	lnc-SERF1A-2	chr5:70146637-70146751	NONHSAT101987
3	lnc-NAIP-1	chr5:70358579-70358623	NONHSAT101997
4	lnc-NAIP-1	chr5:70363123-70363465	NONHSAT101997
5	lnc-NAIP-2	chr5:69776697-69777165	NONHSAT101978
6	lnc-NAIP-1	chr5:70360952-70361049	NONHSAT101997
7	lnc-NAIP-3	chr5:69733322-69734405	NONHSAT101975
8	lnc-GTF2H2-1	chr5:70329997-70330227	ENSG00000254353
9	lnc-SERF1A-2	chr5:70091602-70091743	NONHSAT101987
10	lnc-SERF1A-2	chr5:70149363-70149508	NONHSAT101987
11	lnc-SMN1-2	chr5:70378669-70379081	NONHSAT101998
12	lnc-SMN2-2	chr5:69745463-69746180	ENSG00000269983.1

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GTF2H2	hsa-miR-30a-5p	chr5:70331287-70331308
2	SMN2	hsa-miR-186-5p	chr5:70248811-70248834
3	SMN2	hsa-miR-30a-5p	chr5:70248784-70248805
4	SMN2	hsa-miR-132-3p	chr5:70248617-70248638

Variant related genes	Relation type
NAIP	TF binding region
GTF2H2	TF binding region
ENSG00000196302	TF binding region
ENSG00000253333	TF binding region
ENSG00000197284	TF binding region
ENSG00000254353	TF binding region
ENSG00000238451	TF binding region
CDH12P1	TF binding region
SMN1	TF binding region
ENSG00000250687	TF binding region
ENSG00000237075	TF binding region
GTF2H2B	TF binding region
SERF1A	TF binding region
ENSG00000205565	TF binding region
ENSG00000253366	TF binding region
ENSG00000250918	TF binding region
ENSG00000269983	TF binding region
NAIP	CpG island
GTF2H2	CpG island
ENSG00000196302	CpG island
ENSG00000253333	CpG island
ENSG00000197284	CpG island
ENSG00000254353	CpG island
ENSG00000238451	CpG island
CDH12P1	CpG island
SMN1	CpG island
ENSG00000250687	CpG island
ENSG00000237075	CpG island
GTF2H2B	CpG island
SERF1A	CpG island
ENSG00000205565	CpG island
ENSG00000253366	CpG island
ENSG00000250918	CpG island
ENSG00000269983	CpG island

Extended variants
information (count: 1348 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9686698	chr5:69696886-69696887	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs543369208	chr5:69696912-69696913	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs561546174	chr5:69696923-69696924	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573422186	chr5:69696927-69696928	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540465982	chr5:69696931-69696932	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs2770558	chr5:69696932-69696933	Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs370492909	chr5:69696940-69696941	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs550626290	chr5:69696952-69696953	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs562572464	chr5:69696955-69696956	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs2770556	chr5:69696960-69696961	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548907365	chr5:69696982-69696983	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs567446090	chr5:69696992-69696993	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs534874377	chr5:69696998-69696999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs576253945	chr5:69697583-69697584	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs2568288	chr5:69697679-69697680	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs113337270	chr5:69697804-69697805	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs202126299	chr5:69697992-69697993	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs2770554	chr5:69698035-69698036	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs147672694	chr5:69698101-69698102	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs546489574	chr5:69698143-69698144	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs199499960	chr5:69698195-69698196	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs571387063	chr5:69698198-69698199	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs546409096	chr5:69698289-69698290	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200075777	chr5:69708295-69708296	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2576908	chr5:69709684-69709685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs75940579	chr5:69711410-69711411	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs183085846	chr5:69714630-69714631	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544641956	chr5:69714637-69714638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs561663403	chr5:69714780-69714781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs162959	chr5:69730040-69730041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369710412	chr5:69730060-69730061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374166345	chr5:69730061-69730062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542277748	chr5:69730101-69730102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560309346	chr5:69730535-69730536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527665863	chr5:69730574-69730575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540190388	chr5:69730621-69730622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565166103	chr5:69730630-69730631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532391605	chr5:69730638-69730639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113946828	chr5:69730655-69730656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189881023	chr5:69730662-69730663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550795344	chr5:69730680-69730681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569032542	chr5:69730691-69730692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529829837	chr5:69730692-69730693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548238596	chr5:69730706-69730707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566372366	chr5:69730745-69730746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201304231	chr5:69730786-69730787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533775031	chr5:69730822-69730823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150151999	chr5:69731407-69731408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62371808	chr5:69732068-69732069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559035040	chr5:69732256-69732257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	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
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21364760	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Spinal muscular atrophy	17647030	CNVD
Spinal muscular atrophy	20937953	CNVD
Spinal muscular atrophy	20442745	CNVD
Spinal muscular atrophy	21227393	CNVD
Breast cancer	21509527	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Autism	22549408	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:69696800-69697600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr5:69696800-69697600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
3	chr5:69696800-69697600	Active TSS	Primary T helper cells fromperipheralblood	blood
4	chr5:69696800-69697600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr5:69696800-69697600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:69696800-69697600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:69696800-69697600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:69696800-69697600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:69696800-69697600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
10	chr5:69696800-69697600	Active TSS	Colonic Mucosa	Colon
11	chr5:69696800-69697600	Active TSS	Pancreas	Pancrea
12	chr5:69696800-69697600	Active TSS	Thymus	Thymus
13	chr5:69697000-69697400	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr5:69697000-69697400	Active TSS	Primary hematopoietic stem cells	blood
15	chr5:69697000-69697400	Active TSS	Aorta	Aorta
16	chr5:69697000-69697400	Active TSS	Fetal Brain Female	brain
17	chr5:69697000-69697400	Active TSS	Sigmoid Colon	Sigmoid Colon
18	chr5:69697000-69697600	Active TSS	H1 Cell Line	embryonic stem cell
19	chr5:69697000-69697600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr5:69697000-69697600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:69697000-69697600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:69697000-69697600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:69697000-69697600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr5:69697000-69697600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:69697000-69697600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:69697000-69697600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr5:69697000-69697600	Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr5:69697000-69697600	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr5:69697000-69697600	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr5:69697000-69697600	Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr5:69697000-69697600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr5:69697000-69697600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:69697000-69697600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:69697000-69697600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:69697000-69697600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr5:69697000-69697600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr5:69697000-69697600	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr5:69697000-69697600	Active TSS	Primary monocytes fromperipheralblood	blood
39	chr5:69697000-69697600	Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr5:69697000-69697600	Active TSS	Primary B cells from peripheral blood	blood
41	chr5:69697000-69697600	Active TSS	Primary T cells fromperipheralblood	blood
42	chr5:69697000-69697600	Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr5:69697000-69697600	Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr5:69697000-69697600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr5:69697000-69697600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr5:69697000-69697600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr5:69697000-69697600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
48	chr5:69697000-69697600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:69697000-69697600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:69697000-69697600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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