Variant report

Variant	nsv529566
Chromosome Location	chr5:69732192-70309855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5748)
CpG islands
(count:551)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:5748 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:70016506-70016819	GM12878	blood:	n/a	n/a
2	BATF	chr5:70025027-70025309	GM12878	blood:	n/a	n/a
3	BATF	chr5:70022457-70022912	GM12878	blood:	n/a	n/a
4	BATF	chr5:69905747-69905950	GM12878	blood:	n/a	n/a
5	BATF	chr5:70046623-70046836	GM12878	blood:	n/a	chr5:70046762-70046773
6	BATF	chr5:70002912-70003149	GM12878	blood:	n/a	n/a
7	BATF	chr5:70017925-70018198	GM12878	blood:	n/a	n/a
8	BATF	chr5:70019070-70019445	GM12878	blood:	n/a	n/a
9	BATF	chr5:69835627-69835971	GM12878	blood:	n/a	n/a
10	BATF	chr5:70079574-70079848	GM12878	blood:	n/a	n/a
11	BATF	chr5:69831042-69831257	GM12878	blood:	n/a	n/a
12	BATF	chr5:70280725-70281071	GM12878	blood:	n/a	n/a
13	BATF	chr5:70046680-70046878	GM12878	blood:	n/a	chr5:70046762-70046773
14	BATF	chr5:70020537-70020793	GM12878	blood:	n/a	n/a
15	BATF	chr5:70000353-70000557	GM12878	blood:	n/a	n/a
16	BATF	chr5:70079571-70079936	GM12878	blood:	n/a	n/a
17	BATF	chr5:70111545-70111758	GM12878	blood:	n/a	n/a
18	BATF	chr5:69819313-69819679	GM12878	blood:	n/a	n/a
19	BATF	chr5:70028362-70028636	GM12878	blood:	n/a	n/a
20	BATF	chr5:70014973-70015556	GM12878	blood:	n/a	n/a
21	BATF	chr5:69840039-69840196	GM12878	blood:	n/a	n/a
22	BATF	chr5:70043256-70043537	GM12878	blood:	n/a	chr5:70043459-70043468
23	BATF	chr5:69753018-69753328	GM12878	blood:	n/a	n/a
24	BATF	chr5:70060822-70061246	GM12878	blood:	n/a	n/a
25	BATF	chr5:69799993-69800148	GM12878	blood:	n/a	n/a
26	BATF	chr5:70044205-70044406	GM12878	blood:	n/a	n/a
27	BATF	chr5:69999361-69999611	GM12878	blood:	n/a	chr5:69999369-69999378
28	BATF	chr5:69871949-69872278	GM12878	blood:	n/a	n/a
29	BATF	chr5:70019639-70019850	GM12878	blood:	n/a	n/a
30	BATF	chr5:69975886-69976112	GM12878	blood:	n/a	n/a
31	BATF	chr5:69874391-69874846	GM12878	blood:	n/a	n/a
32	BATF	chr5:70017900-70018327	GM12878	blood:	n/a	n/a
33	BATF	chr5:70021119-70021411	GM12878	blood:	n/a	n/a
34	BATF	chr5:69839605-69840032	GM12878	blood:	n/a	n/a
35	BATF	chr5:69880455-69880768	GM12878	blood:	n/a	n/a
36	BATF	chr5:70058356-70059133	GM12878	blood:	n/a	n/a
37	BATF	chr5:70077815-70077970	GM12878	blood:	n/a	n/a
38	BATF	chr5:69998345-69998574	GM12878	blood:	n/a	n/a
39	BATF	chr5:69854149-69854431	GM12878	blood:	n/a	n/a
40	BATF	chr5:69841101-69841327	GM12878	blood:	n/a	n/a
41	BATF	chr5:69877858-69878274	GM12878	blood:	n/a	n/a
42	BATF	chr5:69834700-69835099	GM12878	blood:	n/a	n/a
43	BATF	chr5:70015590-70016239	GM12878	blood:	n/a	n/a
44	BATF	chr5:69881708-69882291	GM12878	blood:	n/a	n/a
45	BATF	chr5:69837679-69838460	GM12878	blood:	n/a	n/a
46	BATF	chr5:70044239-70044454	GM12878	blood:	n/a	n/a
47	BATF	chr5:70027009-70027232	GM12878	blood:	n/a	n/a
48	BATF	chr5:69876412-69876763	GM12878	blood:	n/a	n/a
49	BATF	chr5:70049738-70050013	GM12878	blood:	n/a	n/a
50	BATF	chr5:70015604-70016219	GM12878	blood:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:69784092-69784142	GM12891	blood:	n/a
2	chr5:69804518-69804568	HEK293	kidney:	embryo
3	chr5:69784092-69784142	GM12891	blood:	n/a
4	chr5:69804518-69804568	HEK293	kidney:	embryo
5	chr5:70246896-70246946	HUVEC	blood vessel:	n/a
6	chr5:70218963-70219013	RPTEC	kidney:	n/a
7	chr5:70308497-70308547	GM12878	blood:	n/a
8	chr5:69783979-69784029	AG04449	skin:	fetal
9	chr5:69803286-69803336	HRPEpiC	eye:	n/a
10	chr5:70218963-70219013	AG04450	lung:	fetal
11	chr5:70308497-70308547	CMK	blood:	n/a
12	chr5:69803286-69803336	Hela-S3	cervix:	n/a
13	chr5:70308497-70308547	AG04449	skin:	fetal
14	chr5:70246896-70246946	RPTEC	kidney:	n/a
15	chr5:70218963-70219013	PrEC	prostate:	n/a
16	chr5:69784092-69784142	K562	blood:	n/a
17	chr5:69803286-69803336	GM19239	blood:	n/a
18	chr5:69783979-69784029	GM19239	blood:	n/a
19	chr5:70246896-70246946	NHBE	bronchial:	n/a
20	chr5:70218963-70219013	LNCaP	prostate:	n/a
21	chr5:70220559-70220609	AG09319	gingival:	n/a
22	chr5:70220559-70220609	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:70220559-70220609	ProgFib	skin:	n/a
24	chr5:69804518-69804568	Hela-S3	cervix:	n/a
25	chr5:69783979-69784029	HMEC	breast:	n/a
26	chr5:70246896-70246946	T-47D	breast:	n/a
27	chr5:69784092-69784142	RPTEC	kidney:	n/a
28	chr5:70309843-70309893	HNPCEpiC	eye:	n/a
29	chr5:69784092-69784142	NB4	blood:	n/a
30	chr5:70218963-70219013	MCF10A-Er-Src	breast:	n/a
31	chr5:70308497-70308547	AG09309	skin:	n/a
32	chr5:70309843-70309893	ECC-1	luminal epithelium:	n/a
33	chr5:69803286-69803336	HAEpiC	amniotic membrane:	n/a
34	chr5:70220559-70220609	T-47D	breast:	n/a
35	chr5:69804518-69804568	HRPEpiC	eye:	n/a
36	chr5:70308497-70308547	U87	brain:	n/a
37	chr5:69804518-69804568	AG09319	gingival:	n/a
38	chr5:70309843-70309893	NHDF-neo	bronchial:	n/a
39	chr5:69784092-69784142	HCM	heart:	n/a
40	chr5:70308497-70308547	BJ	skin:	n/a
41	chr5:69804518-69804568	PrEC	prostate:	n/a
42	chr5:70246896-70246946	Hepatocyte	liver:	n/a
43	chr5:70246896-70246946	A549	lung:	n/a
44	chr5:70309843-70309893	AG09319	gingival:	n/a
45	chr5:70246896-70246946	HepG2	liver:	n/a
46	chr5:70309843-70309893	SKMC	muscle:	n/a
47	chr5:69803286-69803336	SK-N-SH_RA	brain:	n/a
48	chr5:69784092-69784142	ECC-1	luminal epithelium:	n/a
49	chr5:70308497-70308547	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:70309843-70309893	Hela-S3	cervix:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMN2-2	chr5:69745463-69746180	ENSG00000269983.1
2	lnc-SERF1A-2	chr5:70146637-70146751	NONHSAT101987
3	lnc-SERF1A-2	chr5:70091602-70091743	NONHSAT101987
4	lnc-NAIP-3	chr5:69733322-69734405	NONHSAT101975
5	lnc-NAIP-2	chr5:69776697-69777165	NONHSAT101978
6	lnc-SERF1A-2	chr5:70149363-70149508	NONHSAT101987

No data

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

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

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

Extended variants
information (count: 903 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559035040	chr5:69732256-69732257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570813514	chr5:69732271-69732272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532525452	chr5:69732299-69732300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200609467	chr5:69732470-69732471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559587515	chr5:69733097-69733098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538109565	chr5:69733102-69733103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556356955	chr5:69733283-69733284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574666645	chr5:69733460-69733461	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs78077434	chr5:69733811-69733812	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs541989489	chr5:69733818-69733819	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs374579489	chr5:69734769-69734770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56237803	chr5:69734825-69734826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554221360	chr5:69734927-69734928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116401657	chr5:69734934-69734935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs154420	chr5:69734947-69734948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368777271	chr5:69735127-69735128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572386468	chr5:69735199-69735200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202077936	chr5:69735272-69735273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61188665	chr5:69735342-69735343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150262	chr5:69735706-69735707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546173780	chr5:69735794-69735795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564424034	chr5:69736066-69736067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577218051	chr5:69736127-69736128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112589744	chr5:69736157-69736158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544483158	chr5:69736222-69736223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199976069	chr5:69736477-69736478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529875518	chr5:69736837-69736838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548020987	chr5:69736913-69736914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113487058	chr5:69737103-69737104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78485424	chr5:69737299-69737300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560190389	chr5:69737973-69737974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527350135	chr5:69738026-69738027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552161784	chr5:69738027-69738028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561858732	chr5:69738169-69738170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377375549	chr5:69738170-69738171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183333142	chr5:69738224-69738225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560413075	chr5:69738226-69738227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527513532	chr5:69738228-69738229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538171249	chr5:69738259-69738260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188077334	chr5:69738337-69738338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550043273	chr5:69738338-69738339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145211065	chr5:69738375-69738376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568352971	chr5:69738409-69738410	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536036213	chr5:69738421-69738422	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62371809	chr5:69738496-69738497	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs257503	chr5:69738544-69738545	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57076635	chr5:69738674-69738675	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142062193	chr5:69738698-69738699	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539506874	chr5:69738732-69738733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151155473	chr5:69738774-69738775	Strong transcription 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:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:69729400-69738200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:69729400-69739800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr5:69729400-69745200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:69729600-69740000	Weak transcription	Liver	Liver
5	chr5:69731800-69738000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:69734200-69740000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:69734200-69745000	Weak transcription	Fetal Stomach	stomach
8	chr5:69734400-69740200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:69734400-69740200	Weak transcription	Osteobl	bone
10	chr5:69734400-69740800	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr5:69734400-69741400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr5:69734400-69744000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:69734600-69745000	Weak transcription	Fetal Intestine Small	intestine
14	chr5:69734800-69745000	Weak transcription	Fetal Thymus	thymus
15	chr5:69735800-69736200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr5:69735800-69736200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr5:69735800-69738400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:69736000-69738600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr5:69736200-69738200	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr5:69736200-69740400	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr5:69736400-69738200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:69736600-69738200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr5:69736600-69738200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr5:69737200-69739600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:69737200-69739600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:69737400-69739600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:69737400-69739800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:69737400-69739800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr5:69738000-69738800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:69738200-69738800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:69738200-69738800	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr5:69738200-69738800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
33	chr5:69738200-69738800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr5:69738200-69739800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:69738800-69740400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr5:69738800-69740400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:69738800-69741200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:69738800-69744000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:69738800-69748800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr5:69739800-69741400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:69748800-69749000	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr5:69754800-69755400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr5:69755000-69755400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr5:69755400-69758600	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr5:69755400-69758600	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr5:69758600-69759000	Active TSS	Primary monocytes fromperipheralblood	blood
47	chr5:69758600-69759000	Enhancers	Primary B cells from peripheral blood	blood
48	chr5:69758600-69759000	Active TSS	Monocytes-CD14+_RO01746	blood
49	chr5:69758600-69759600	Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr5:69759000-69767800	Weak transcription	Primary monocytes fromperipheralblood	blood

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