Variant report

Variant	nsv881899
Chromosome Location	chr5:69336461-69507207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1069)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1069 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:69504985-69505250	GM12878	blood:	n/a	n/a
2	BATF	chr5:69345256-69345752	GM12878	blood:	n/a	n/a
3	BATF	chr5:69456322-69456651	GM12878	blood:	n/a	n/a
4	BATF	chr5:69456351-69456586	GM12878	blood:	n/a	n/a
5	BATF	chr5:69472886-69473188	GM12878	blood:	n/a	n/a
6	BATF	chr5:69504951-69505253	GM12878	blood:	n/a	n/a
7	BATF	chr5:69405258-69405604	GM12878	blood:	n/a	n/a
8	BATF	chr5:69473052-69473265	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:69492919-69493140	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:69465859-69466029	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:69497191-69497380	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:69465861-69466202	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:69405265-69405510	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:69500307-69500526	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:69456435-69456617	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:69499831-69500109	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:69504989-69505217	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:69504953-69505182	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:69456419-69456658	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:69467031-69467204	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:69345206-69345974	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:69494961-69495194	HepG2	liver:	n/a	n/a
23	BHLHE40	chr5:69475972-69476211	HepG2	liver:	n/a	n/a
24	BHLHE40	chr5:69345312-69345640	HepG2	liver:	n/a	n/a
25	BHLHE40	chr5:69473355-69473594	HepG2	liver:	n/a	n/a
26	BHLHE40	chr5:69466847-69467258	HepG2	liver:	n/a	n/a
27	BHLHE40	chr5:69434991-69435233	HepG2	liver:	n/a	n/a
28	CBX3	chr5:69383773-69384177	K562	blood:	n/a	n/a
29	CBX3	chr5:69344863-69345946	K562	blood:	n/a	n/a
30	CBX3	chr5:69344975-69345864	K562	blood:	n/a	n/a
31	CEBPB	chr5:69342760-69343019	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:69342820-69343110	K562	blood:	n/a	n/a
33	CEBPB	chr5:69485735-69486086	HepG2	liver:	n/a	chr5:69485899-69485910
34	CEBPB	chr5:69356219-69356621	K562	blood:	n/a	n/a
35	CEBPB	chr5:69356368-69356612	K562	blood:	n/a	n/a
36	CEBPB	chr5:69342787-69343015	A549	lung:	n/a	n/a
37	CEBPB	chr5:69345203-69345698	K562	blood:	n/a	n/a
38	CEBPD	chr5:69345151-69345751	K562	blood:	n/a	n/a
39	CTCF	chr5:69345520-69345558	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr5:69392824-69392942	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:69338869-69338905	GM13976	blood:	n/a	n/a
42	CTCF	chr5:69345429-69345481	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr5:69392833-69392948	K562	blood:	n/a	n/a
44	CTCF	chr5:69423717-69424058	K562	blood:	n/a	n/a
45	CTCF	chr5:69469459-69469519	GM10266	blood:	n/a	n/a
46	CTCF	chr5:69423890-69423987	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr5:69423765-69423949	A549	lung:	n/a	n/a
48	CTCF	chr5:69345509-69345519	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr5:69337345-69337534	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:69392838-69392910	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:69371421-69371471	Hela-S3	cervix:	n/a
2	chr5:69483768-69483818	LNCaP	prostate:	n/a
3	chr5:69371421-69371471	MCF-7	breast:	n/a
4	chr5:69345099-69345149	NHDF-neo	bronchial:	n/a
5	chr5:69483768-69483818	AG09309	skin:	n/a
6	chr5:69371421-69371471	A549	lung:	n/a
7	chr5:69483768-69483818	Caco-2	colon:	n/a
8	chr5:69483768-69483818	NHBE	bronchial:	n/a
9	chr5:69483768-69483818	MCF10A-Er-Src	breast:	n/a
10	chr5:69345099-69345149	HEEpiC	esophagus:	n/a
11	chr5:69345099-69345149	HAEpiC	amniotic membrane:	n/a
12	chr5:69483768-69483818	RPTEC	kidney:	n/a
13	chr5:69483768-69483818	AG09319	gingival:	n/a
14	chr5:69483768-69483818	HAEpiC	amniotic membrane:	n/a
15	chr5:69345099-69345149	ECC-1	luminal epithelium:	n/a
16	chr5:69483768-69483818	HCPEpiC	choroid plexus:	n/a
17	chr5:69345099-69345149	Jurkat	blood:	n/a
18	chr5:69371421-69371471	NHBE	bronchial:	n/a
19	chr5:69345099-69345149	SK-N-SH	brain:	n/a
20	chr5:69371421-69371471	HCT-116	colon:	n/a
21	chr5:69371421-69371471	BJ	skin:	n/a
22	chr5:69371421-69371471	NB4	blood:	n/a
23	chr5:69483768-69483818	T-47D	breast:	n/a
24	chr5:69483768-69483818	BJ	skin:	n/a
25	chr5:69345099-69345149	HIPEpiC	eye:	n/a
26	chr5:69483768-69483818	SKMC	muscle:	n/a
27	chr5:69483768-69483818	GM12891	blood:	n/a
28	chr5:69345099-69345149	AG04449	skin:	fetal
29	chr5:69345099-69345149	AG10803	skin:	n/a
30	chr5:69371421-69371471	HAEpiC	amniotic membrane:	n/a
31	chr5:69483768-69483818	HRPEpiC	eye:	n/a
32	chr5:69371421-69371471	HUVEC	blood vessel:	n/a
33	chr5:69371421-69371471	H1-hESC	embryonic stem cell:	embryo
34	chr5:69483768-69483818	HUVEC	blood vessel:	n/a
35	chr5:69371421-69371471	HMEC	breast:	n/a
36	chr5:69371421-69371471	U87	brain:	n/a
37	chr5:69371421-69371471	AG09319	gingival:	n/a
38	chr5:69345099-69345149	HCF	heart:	n/a
39	chr5:69345099-69345149	ProgFib	skin:	n/a
40	chr5:69345099-69345149	NHBE	bronchial:	n/a
41	chr5:69371421-69371471	SK-N-SH_RA	brain:	n/a
42	chr5:69371421-69371471	GM06990	blood:	n/a
43	chr5:69483768-69483818	NT2-D1	testis:	n/a
44	chr5:69345099-69345149	HCPEpiC	choroid plexus:	n/a
45	chr5:69345099-69345149	H1-hESC	embryonic stem cell:	embryo
46	chr5:69345099-69345149	GM19239	blood:	n/a
47	chr5:69345099-69345149	HL-60	blood:	n/a
48	chr5:69371421-69371471	AG04450	lung:	fetal
49	chr5:69483768-69483818	HRCEpiC	kidney:	n/a
50	chr5:69371421-69371471	SAEC	small airway:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAIP-5	chr5:69435402-69435547	NONHSAT101964
2	lnc-SERF1B-3	chr5:69370673-69370944	NONHSAT101959
3	lnc-TAF9-8	chr5:69351645-69353243	NONHSAT101952
4	lnc-NAIP-5	chr5:69493082-69493223	NONHSAT101964
5	lnc-NAIP-5	chr5:69438158-69438272	NONHSAT101964
6	lnc-SERF1B-2	chr5:69372740-69373356	NONHSAT101960

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SMN2	hsa-miR-132-3p	chr5:69373197-69373218
2	SMN2	hsa-miR-30a-5p	chr5:69373364-69373385
3	SMN2	hsa-miR-186-5p	chr5:69373391-69373414

Variant related genes	Relation type
ENSG00000251007	TF binding region
CDH12P3	TF binding region
SMN2	TF binding region
ENSG00000254701	TF binding region
RN7SL9P	TF binding region
ENSG00000179978	TF binding region
ENSG00000251007	CpG island
CDH12P3	CpG island
SMN2	CpG island
ENSG00000254701	CpG island
RN7SL9P	CpG island
ENSG00000179978	CpG island
GLCE	miRNA target sites

Extended variants
information (count: 370 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571198504	chr5:69336799-69336800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191224979	chr5:69336803-69336804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183507639	chr5:69337171-69337172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187955345	chr5:69337184-69337185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542721796	chr5:69337278-69337279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554674343	chr5:69337355-69337356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572901729	chr5:69337439-69337440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540215706	chr5:69337504-69337505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565616053	chr5:69337568-69337569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532860249	chr5:69337615-69337616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544541368	chr5:69337674-69337675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563114343	chr5:69337692-69337693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374435968	chr5:69337750-69337751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532104012	chr5:69338198-69338199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372408064	chr5:69339392-69339393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373202721	chr5:69339491-69339492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551938643	chr5:69339521-69339522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530206641	chr5:69339524-69339525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548692264	chr5:69339550-69339551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566612167	chr5:69339831-69339832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527720408	chr5:69339839-69339840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552151100	chr5:69339894-69339895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570465906	chr5:69339910-69339911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538934041	chr5:69339921-69339922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556941193	chr5:69339922-69339923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569054219	chr5:69339965-69339966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs152153	chr5:69339977-69339978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377318612	chr5:69340227-69340228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552105243	chr5:69340246-69340247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536035840	chr5:69340247-69340248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554737546	chr5:69340268-69340269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572962400	chr5:69340599-69340600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201179698	chr5:69341301-69341302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200933232	chr5:69341303-69341304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540274865	chr5:69341377-69341378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202073068	chr5:69341595-69341596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200264876	chr5:69341603-69341604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62374803	chr5:69342217-69342218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111696362	chr5:69342220-69342221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558597741	chr5:69342303-69342304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570091162	chr5:69342581-69342582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544913781	chr5:69342608-69342609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530909557	chr5:69342622-69342623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530353598	chr5:69342734-69342735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542010665	chr5:69342756-69342757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373536155	chr5:69342821-69342822	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144759210	chr5:69342881-69342882	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs552212530	chr5:69342937-69342938	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs570527045	chr5:69342982-69342983	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370293168	chr5:69342995-69342996	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Spinal muscular atrophy	17647030	CNVD
Spinal muscular atrophy	20937953	CNVD
Spinal muscular atrophy	20442745	CNVD
Spinal muscular atrophy	21227393	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Disease	19212409	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:69323600-69345000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr5:69325200-69344800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr5:69325800-69344800	Weak transcription	Brain Anterior Caudate	brain
4	chr5:69336600-69345000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:69342600-69345000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:69342600-69345000	Weak transcription	Fetal Muscle Leg	muscle
7	chr5:69343000-69345000	Weak transcription	Fetal Lung	lung
8	chr5:69344000-69344600	Weak transcription	Dnd41	blood
9	chr5:69344600-69344800	Enhancers	Primary T cells fromperipheralblood	blood
10	chr5:69344600-69344800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:69344600-69344800	Enhancers	Dnd41	blood
12	chr5:69344800-69345000	Enhancers	Primary B cells from cord blood	blood
13	chr5:69344800-69345000	Enhancers	Primary B cells from peripheral blood	blood
14	chr5:69344800-69345000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr5:69344800-69345000	Flanking Active TSS	Brain Anterior Caudate	brain
16	chr5:69344800-69345000	Enhancers	Fetal Thymus	thymus
17	chr5:69344800-69345000	Enhancers	Pancreas	Pancrea
18	chr5:69344800-69345200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
19	chr5:69344800-69345200	Flanking Active TSS	Dnd41	blood
20	chr5:69344800-69345400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:69344800-69345400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:69344800-69345400	Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr5:69344800-69345400	Active TSS	Primary monocytes fromperipheralblood	blood
24	chr5:69344800-69345400	Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr5:69344800-69345400	Active TSS	Primary T cells from cord blood	blood
26	chr5:69344800-69345400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr5:69344800-69345400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr5:69344800-69345400	Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr5:69344800-69345400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr5:69344800-69345400	Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr5:69344800-69345400	Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr5:69344800-69345400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
33	chr5:69344800-69345400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr5:69344800-69345400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr5:69344800-69345400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr5:69344800-69345400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:69344800-69345400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:69344800-69345400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:69344800-69345400	Active TSS	Adipose Nuclei	Adipose
40	chr5:69344800-69345400	Active TSS	Liver	Liver
41	chr5:69344800-69345400	Active TSS	Brain Angular Gyrus	brain
42	chr5:69344800-69345400	Active TSS	Brain Cingulate Gyrus	brain
43	chr5:69344800-69345400	Active TSS	Brain Hippocampus Middle	brain
44	chr5:69344800-69345400	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr5:69344800-69345400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr5:69344800-69345400	Active TSS	Brain Substantia Nigra	brain
47	chr5:69344800-69345400	Active TSS	Duodenum Mucosa	Duodenum
48	chr5:69344800-69345400	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr5:69344800-69345400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr5:69344800-69345400	Active TSS	Pancreatic Islets	Pancreatic Islet

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