Variant report

Variant	nsv598563
Chromosome Location	chr5:70257155-70424031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:777)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:70362121-70362600	GM12878	blood:	n/a	n/a
2	BATF	chr5:70363259-70363809	GM12878	blood:	n/a	n/a
3	BATF	chr5:70362170-70362374	GM12878	blood:	n/a	n/a
4	BATF	chr5:70363439-70363749	GM12878	blood:	n/a	n/a
5	BATF	chr5:70280725-70281071	GM12878	blood:	n/a	n/a
6	BATF	chr5:70363039-70363251	GM12878	blood:	n/a	n/a
7	BATF	chr5:70405611-70405957	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:70363241-70363801	GM12878	blood:	n/a	chr5:70363563-70363572
9	BCL11A	chr5:70362110-70362487	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:70363265-70363860	GM12878	blood:	n/a	chr5:70363563-70363572
11	BCL11A	chr5:70321231-70321752	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:70280732-70280977	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:70405618-70405863	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:70321346-70321632	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:70308373-70308538	K562	blood:	n/a	n/a
16	BHLHE40	chr5:70309992-70310192	K562	blood:	n/a	n/a
17	BHLHE40	chr5:70363384-70363696	HepG2	liver:	n/a	chr5:70363608-70363624 chr5:70363624-70363640
18	CBX3	chr5:70363327-70363979	K562	blood:	n/a	n/a
19	CBX3	chr5:70362704-70364093	K562	blood:	n/a	n/a
20	CEBPB	chr5:70362066-70362404	K562	blood:	n/a	n/a
21	CEBPB	chr5:70362104-70362275	K562	blood:	n/a	n/a
22	CEBPB	chr5:70393343-70393363	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:70362898-70363936	GM12878	blood:	n/a	n/a
24	CEBPB	chr5:70302942-70303152	HepG2	liver:	n/a	chr5:70303123-70303134 chr5:70303121-70303132 chr5:70303121-70303134
25	CEBPB	chr5:70310098-70310378	HepG2	liver:	n/a	chr5:70310216-70310227
26	CEBPB	chr5:70303102-70303296	IMR90	lung:	n/a	chr5:70303123-70303134 chr5:70303121-70303132 chr5:70303121-70303134
27	CEBPB	chr5:70310102-70310319	K562	blood:	n/a	chr5:70310216-70310227
28	CEBPD	chr5:70363322-70363798	K562	blood:	n/a	n/a
29	CEBPD	chr5:70301831-70302230	K562	blood:	n/a	n/a
30	CTCF	chr5:70363503-70363739	LNCaP	prostate:	n/a	n/a
31	CTCF	chr5:70363389-70363760	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr5:70309500-70309650	NB4	blood:	n/a	n/a
33	CTCF	chr5:70363591-70363716	GM19240	blood:	n/a	n/a
34	CTCF	chr5:70365343-70365393	GM10248	blood:	n/a	n/a
35	CTCF	chr5:70360806-70360877	GM10248	blood:	n/a	n/a
36	CTCF	chr5:70363587-70363704	ProgFib	skin:	n/a	n/a
37	CTCF	chr5:70406640-70406790	HepG2	liver:	n/a	n/a
38	CTCF	chr5:70309552-70309659	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr5:70363570-70363716	GM12891	blood:	n/a	n/a
40	CTCF	chr5:70380705-70380760	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr5:70363614-70363699	K562	blood:	n/a	n/a
42	CTCF	chr5:70343924-70344029	GM13976	blood:	n/a	n/a
43	CTCF	chr5:70268281-70268370	K562	blood:	n/a	n/a
44	CTCF	chr5:70268288-70268379	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:70345229-70345253	Medullo	brain:	n/a	n/a
46	CTCF	chr5:70363515-70363720	GM20000	blood:	n/a	n/a
47	CTCF	chr5:70363567-70363714	GM19239	blood:	n/a	n/a
48	CTCF	chr5:70309424-70309700	K562	blood:	n/a	n/a
49	CTCF	chr5:70330328-70330378	GM10248	blood:	n/a	n/a
50	CTCF	chr5:70335083-70335203	Medullo	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70320693-70320743	ProgFib	skin:	n/a
2	chr5:70372505-70372555	ovcar-3	ovarian:	n/a
3	chr5:70372505-70372555	NHDF-neo	bronchial:	n/a
4	chr5:70320693-70320743	PFSK-1	brain:	n/a
5	chr5:70308497-70308547	H1-hESC	embryonic stem cell:	embryo
6	chr5:70308497-70308547	ProgFib	skin:	n/a
7	chr5:70309843-70309893	A549	lung:	n/a
8	chr5:70309843-70309893	BJ	skin:	n/a
9	chr5:70320693-70320743	AG04449	skin:	fetal
10	chr5:70308497-70308547	Caco-2	colon:	n/a
11	chr5:70372505-70372555	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:70320693-70320743	K562	blood:	n/a
13	chr5:70308497-70308547	U87	brain:	n/a
14	chr5:70320693-70320743	HepG2	liver:	n/a
15	chr5:70309843-70309893	U87	brain:	n/a
16	chr5:70309843-70309893	T-47D	breast:	n/a
17	chr5:70320693-70320743	AoSMC	blood vessel:	n/a
18	chr5:70309843-70309893	SKMC	muscle:	n/a
19	chr5:70320693-70320743	AG10803	skin:	n/a
20	chr5:70309843-70309893	GM06990	blood:	n/a
21	chr5:70309843-70309893	AG04450	lung:	fetal
22	chr5:70320693-70320743	ECC-1	luminal epithelium:	n/a
23	chr5:70372505-70372555	GM12878	blood:	n/a
24	chr5:70372505-70372555	AG10803	skin:	n/a
25	chr5:70372505-70372555	HEEpiC	esophagus:	n/a
26	chr5:70308497-70308547	RPTEC	kidney:	n/a
27	chr5:70308497-70308547	LNCaP	prostate:	n/a
28	chr5:70308497-70308547	SK-N-SH_RA	brain:	n/a
29	chr5:70308497-70308547	SKMC	muscle:	n/a
30	chr5:70372505-70372555	SK-N-MC	brain:	n/a
31	chr5:70308497-70308547	Hepatocyte	liver:	n/a
32	chr5:70308497-70308547	AG09319	gingival:	n/a
33	chr5:70309843-70309893	AoSMC	blood vessel:	n/a
34	chr5:70372505-70372555	PFSK-1	brain:	n/a
35	chr5:70320693-70320743	AG09319	gingival:	n/a
36	chr5:70372505-70372555	GM12891	blood:	n/a
37	chr5:70308497-70308547	NHBE	bronchial:	n/a
38	chr5:70309843-70309893	NHBE	bronchial:	n/a
39	chr5:70308497-70308547	NB4	blood:	n/a
40	chr5:70320693-70320743	HIPEpiC	eye:	n/a
41	chr5:70309843-70309893	HNPCEpiC	eye:	n/a
42	chr5:70308497-70308547	SK-N-SH	brain:	n/a
43	chr5:70320693-70320743	HMEC	breast:	n/a
44	chr5:70308497-70308547	AoSMC	blood vessel:	n/a
45	chr5:70372505-70372555	SKMC	muscle:	n/a
46	chr5:70308497-70308547	SK-N-MC	brain:	n/a
47	chr5:70309843-70309893	NH-A	brain:	n/a
48	chr5:70309843-70309893	CMK	blood:	n/a
49	chr5:70320693-70320743	PrEC	prostate:	n/a
50	chr5:70320693-70320743	GM12892	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-1	chr5:70328995-70329470	ENSG00000254353
2	lnc-NAIP-1	chr5:70363123-70363465	NONHSAT101997
3	lnc-NAIP-1	chr5:70358579-70358623	NONHSAT101997
4	lnc-GTF2H2-1	chr5:70329997-70330227	ENSG00000254353
5	lnc-NAIP-1	chr5:70360952-70361049	NONHSAT101997
6	lnc-SMN1-2	chr5:70378669-70379081	NONHSAT101998

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2	hsa-miR-30a-5p	chr5:70331287-70331308

Variant related genes	Relation type
NAIP	TF binding region
ENSG00000238451	TF binding region
ENSG00000230847	TF binding region
CDH12P4	TF binding region
GTF2H2	TF binding region
ENSG00000254353	TF binding region
NAIP	CpG island
ENSG00000238451	CpG island
ENSG00000230847	CpG island
CDH12P4	CpG island
GTF2H2	CpG island
ENSG00000254353	CpG island

Extended variants
information (count: 874 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199753900	chr5:70259075-70259076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376411853	chr5:70259650-70259651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576887647	chr5:70259892-70259893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546897948	chr5:70259918-70259919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543884504	chr5:70259928-70259929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562180901	chr5:70259939-70259940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1636861	chr5:70260002-70260003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139722200	chr5:70260902-70260903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574087889	chr5:70265597-70265598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542165302	chr5:70265611-70265612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201481029	chr5:70265644-70265645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs211492	chr5:70273653-70273654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571435701	chr5:70273678-70273679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150442	chr5:70273694-70273695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534066850	chr5:70273695-70273696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558502066	chr5:70273748-70273749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs211491	chr5:70273794-70273795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575104	chr5:70273809-70273810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573577756	chr5:70273823-70273824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575909	chr5:70273877-70273878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538559	chr5:70273880-70273881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111917576	chr5:70273930-70273931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2528566	chr5:70273957-70273958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192949650	chr5:70273963-70273964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370581403	chr5:70273972-70273973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2528565	chr5:70273982-70273983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570612327	chr5:70274222-70274223	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150290	chr5:70274486-70274487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550791016	chr5:70274600-70274601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150441	chr5:70274656-70274657	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs374701035	chr5:70275414-70275415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201535866	chr5:70275417-70275418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200151814	chr5:70275420-70275421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555839981	chr5:70275436-70275437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574152089	chr5:70275437-70275438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369050727	chr5:70275441-70275442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370927985	chr5:70275668-70275669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541439010	chr5:70275696-70275697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76228942	chr5:70275720-70275721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546461257	chr5:70285107-70285108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs564565003	chr5:70285154-70285155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs531938128	chr5:70285179-70285180	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs543985590	chr5:70285186-70285187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs562174945	chr5:70285189-70285190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs207733	chr5:70302824-70302825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527627190	chr5:70302839-70302840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373135264	chr5:70303128-70303129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533533482	chr5:70303146-70303147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201940132	chr5:70303157-70303158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560838077	chr5:70303470-70303471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70238000-70257800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr5:70245000-70257600	Weak transcription	Fetal Stomach	stomach
3	chr5:70245200-70258200	Weak transcription	Fetal Thymus	thymus
4	chr5:70246400-70258200	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr5:70247000-70259600	Weak transcription	Fetal Muscle Leg	muscle
6	chr5:70249200-70258200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:70249200-70266400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:70249400-70257600	Weak transcription	Dnd41	blood
9	chr5:70249600-70257800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr5:70251200-70257800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:70273600-70276000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr5:70302800-70303400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr5:70303400-70303600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr5:70303400-70305200	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr5:70303600-70305200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr5:70303600-70305200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr5:70303600-70305400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr5:70305200-70308200	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr5:70305200-70308600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr5:70305200-70309600	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr5:70305400-70308200	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr5:70305600-70310200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr5:70306400-70309000	Weak transcription	Adipose Nuclei	Adipose
24	chr5:70306400-70309000	Weak transcription	Liver	Liver
25	chr5:70306800-70307000	Enhancers	HepG2	liver
26	chr5:70307000-70307800	Flanking Active TSS	HepG2	liver
27	chr5:70307800-70310000	Enhancers	HepG2	liver
28	chr5:70308200-70309200	Genic enhancers	Primary monocytes fromperipheralblood	blood
29	chr5:70308200-70311000	Genic enhancers	Monocytes-CD14+_RO01746	blood
30	chr5:70308400-70308800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:70308600-70310200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr5:70309200-70310000	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr5:70309600-70311000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
34	chr5:70310000-70311200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr5:70311000-70313600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr5:70311000-70314000	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr5:70311200-70313200	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr5:70313200-70313800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr5:70313600-70313800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr5:70313800-70314000	Active TSS	Monocytes-CD14+_RO01746	blood
41	chr5:70314000-70314400	Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr5:70325000-70325400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr5:70325000-70325400	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr5:70325200-70325600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr5:70325400-70327600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr5:70325400-70327800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr5:70325400-70327800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr5:70327600-70328000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr5:70327800-70328000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr5:70340200-70351400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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