Variant report

Variant	nsv882118
Chromosome Location	chr5:70251701-70415804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:739)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:70405611-70405957	GM12878	blood:	n/a	n/a
2	BATF	chr5:70362121-70362600	GM12878	blood:	n/a	n/a
3	BATF	chr5:70280725-70281071	GM12878	blood:	n/a	n/a
4	BATF	chr5:70363259-70363809	GM12878	blood:	n/a	n/a
5	BATF	chr5:70362170-70362374	GM12878	blood:	n/a	n/a
6	BATF	chr5:70363039-70363251	GM12878	blood:	n/a	n/a
7	BATF	chr5:70363439-70363749	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:70362110-70362487	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:70321231-70321752	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:70363265-70363860	GM12878	blood:	n/a	chr5:70363563-70363572
11	BCL11A	chr5:70405618-70405863	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:70363241-70363801	GM12878	blood:	n/a	chr5:70363563-70363572
13	BCL11A	chr5:70321346-70321632	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:70280732-70280977	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:70363384-70363696	HepG2	liver:	n/a	chr5:70363608-70363624 chr5:70363624-70363640
16	BHLHE40	chr5:70309992-70310192	K562	blood:	n/a	n/a
17	BHLHE40	chr5:70308373-70308538	K562	blood:	n/a	n/a
18	CBX3	chr5:70362704-70364093	K562	blood:	n/a	n/a
19	CBX3	chr5:70363327-70363979	K562	blood:	n/a	n/a
20	CEBPB	chr5:70393343-70393363	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:70302942-70303152	HepG2	liver:	n/a	chr5:70303123-70303134 chr5:70303121-70303132 chr5:70303121-70303134
22	CEBPB	chr5:70310102-70310319	K562	blood:	n/a	chr5:70310216-70310227
23	CEBPB	chr5:70362066-70362404	K562	blood:	n/a	n/a
24	CEBPB	chr5:70303102-70303296	IMR90	lung:	n/a	chr5:70303123-70303134 chr5:70303121-70303132 chr5:70303121-70303134
25	CEBPB	chr5:70362104-70362275	K562	blood:	n/a	n/a
26	CEBPB	chr5:70362898-70363936	GM12878	blood:	n/a	n/a
27	CEBPB	chr5:70310098-70310378	HepG2	liver:	n/a	chr5:70310216-70310227
28	CEBPD	chr5:70301831-70302230	K562	blood:	n/a	n/a
29	CEBPD	chr5:70363322-70363798	K562	blood:	n/a	n/a
30	CTCF	chr5:70309500-70309650	HEK293	kidney:	n/a	n/a
31	CTCF	chr5:70309552-70309659	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:70302004-70302064	Medullo	brain:	n/a	n/a
33	CTCF	chr5:70309429-70309737	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr5:70366045-70366103	GM10248	blood:	n/a	n/a
35	CTCF	chr5:70360806-70360877	GM10248	blood:	n/a	n/a
36	CTCF	chr5:70309471-70309695	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:70325992-70326059	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr5:70309522-70309653	HepG2	liver:	n/a	n/a
39	CTCF	chr5:70325271-70325356	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr5:70302453-70302558	GM13976	blood:	n/a	n/a
41	CTCF	chr5:70343924-70344029	GM13976	blood:	n/a	n/a
42	CTCF	chr5:70363469-70363742	Medullo	brain:	n/a	n/a
43	CTCF	chr5:70309424-70309700	K562	blood:	n/a	n/a
44	CTCF	chr5:70363334-70363784	A549	lung:	n/a	n/a
45	CTCF	chr5:70363357-70363771	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr5:70268289-70268356	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:70363591-70363716	GM19240	blood:	n/a	n/a
48	CTCF	chr5:70344962-70345001	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr5:70309500-70309650	NB4	blood:	n/a	n/a
50	CTCF	chr5:70309461-70309730	K562	blood:	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	AG04449	skin:	fetal
2	chr5:70372505-70372555	HEEpiC	esophagus:	n/a
3	chr5:70320693-70320743	GM12878	blood:	n/a
4	chr5:70372505-70372555	HEK293	kidney:	embryo
5	chr5:70309843-70309893	ECC-1	luminal epithelium:	n/a
6	chr5:70320693-70320743	SKMC	muscle:	n/a
7	chr5:70308497-70308547	U87	brain:	n/a
8	chr5:70320693-70320743	HRPEpiC	eye:	n/a
9	chr5:70308497-70308547	PFSK-1	brain:	n/a
10	chr5:70308497-70308547	HEEpiC	esophagus:	n/a
11	chr5:70320693-70320743	GM12891	blood:	n/a
12	chr5:70320693-70320743	HNPCEpiC	eye:	n/a
13	chr5:70320693-70320743	HCT-116	colon:	n/a
14	chr5:70372505-70372555	MCF10A-Er-Src	breast:	n/a
15	chr5:70308497-70308547	NH-A	brain:	n/a
16	chr5:70372505-70372555	SK-N-MC	brain:	n/a
17	chr5:70308497-70308547	HL-60	blood:	n/a
18	chr5:70308497-70308547	ProgFib	skin:	n/a
19	chr5:70320693-70320743	ECC-1	luminal epithelium:	n/a
20	chr5:70308497-70308547	BJ	skin:	n/a
21	chr5:70309843-70309893	SK-N-SH_RA	brain:	n/a
22	chr5:70372505-70372555	MCF-7	breast:	n/a
23	chr5:70308497-70308547	K562	blood:	n/a
24	chr5:70320693-70320743	HCF	heart:	n/a
25	chr5:70309843-70309893	HCPEpiC	choroid plexus:	n/a
26	chr5:70320693-70320743	SK-N-SH	brain:	n/a
27	chr5:70372505-70372555	HUVEC	blood vessel:	n/a
28	chr5:70372505-70372555	U87	brain:	n/a
29	chr5:70372505-70372555	PANC-1	pancreas:	n/a
30	chr5:70372505-70372555	AG10803	skin:	n/a
31	chr5:70309843-70309893	HCM	heart:	n/a
32	chr5:70320693-70320743	ovcar-3	ovarian:	n/a
33	chr5:70308497-70308547	MCF10A-Er-Src	breast:	n/a
34	chr5:70308497-70308547	NB4	blood:	n/a
35	chr5:70308497-70308547	NHBE	bronchial:	n/a
36	chr5:70308497-70308547	Hepatocyte	liver:	n/a
37	chr5:70308497-70308547	AG04450	lung:	fetal
38	chr5:70308497-70308547	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:70372505-70372555	NT2-D1	testis:	n/a
40	chr5:70309843-70309893	RPTEC	kidney:	n/a
41	chr5:70372505-70372555	HCPEpiC	choroid plexus:	n/a
42	chr5:70308497-70308547	SKMC	muscle:	n/a
43	chr5:70308497-70308547	HCM	heart:	n/a
44	chr5:70320693-70320743	NHDF-neo	bronchial:	n/a
45	chr5:70308497-70308547	AG09309	skin:	n/a
46	chr5:70308497-70308547	HRE	kidney:	n/a
47	chr5:70308497-70308547	GM12891	blood:	n/a
48	chr5:70320693-70320743	SK-N-MC	brain:	n/a
49	chr5:70309843-70309893	PFSK-1	brain:	n/a
50	chr5:70372505-70372555	HL-60	blood:	n/a

No data

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

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

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
GTF2H2	TF binding region
ENSG00000254353	TF binding region
NAIP	CpG island
ENSG00000238451	CpG island
ENSG00000230847	CpG island
GTF2H2	CpG island
ENSG00000254353	CpG island

Extended variants
information (count: 925 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:925 , 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	rs530298016	chr5:70252528-70252529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs212203	chr5:70252538-70252539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548396854	chr5:70252613-70252614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111517196	chr5:70252750-70252751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531459148	chr5:70253131-70253132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375323635	chr5:70253313-70253314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs58088657	chr5:70253347-70253348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57680718	chr5:70253741-70253742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs55935101	chr5:70254469-70254470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566702996	chr5:70254601-70254602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183404027	chr5:70254648-70254649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534338174	chr5:70254657-70254658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558774534	chr5:70254665-70254666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570876792	chr5:70254675-70254676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537860998	chr5:70254796-70254797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56214652	chr5:70254797-70254798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575632540	chr5:70254827-70254828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28611118	chr5:70254828-70254829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554835690	chr5:70254829-70254830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572940515	chr5:70254837-70254838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192340054	chr5:70254853-70254854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564834364	chr5:70254933-70254934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576834229	chr5:70254977-70254978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543823954	chr5:70255072-70255073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201408382	chr5:70255140-70255141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562116696	chr5:70255208-70255209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200869337	chr5:70255362-70255363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200610490	chr5:70255470-70255471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56675508	chr5:70255485-70255486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138956981	chr5:70255780-70255781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530357152	chr5:70255880-70255881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561300592	chr5:70255937-70255938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150493	chr5:70255946-70255947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537290440	chr5:70255997-70255998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548459842	chr5:70256004-70256005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560357341	chr5:70256005-70256006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547357998	chr5:70256064-70256065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527882676	chr5:70256081-70256082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74776405	chr5:70256200-70256201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570870140	chr5:70256215-70256216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538307076	chr5:70256222-70256223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550226484	chr5:70256237-70256238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568448281	chr5:70256260-70256261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79376862	chr5:70256275-70256276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554898581	chr5:70256296-70256297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573046825	chr5:70256487-70256488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112521587	chr5:70256591-70256592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533758684	chr5:70256616-70256617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369525336	chr5:70256621-70256622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558684555	chr5:70256666-70256667	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:123 , 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	chr5:70239000-70252400	Weak transcription	Liver	Liver
3	chr5:70239400-70252000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr5:70244400-70253000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:70244800-70256200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:70245000-70253000	Weak transcription	Fetal Intestine Small	intestine
7	chr5:70245000-70257600	Weak transcription	Fetal Stomach	stomach
8	chr5:70245200-70258200	Weak transcription	Fetal Thymus	thymus
9	chr5:70245400-70252600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr5:70246400-70252400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:70246400-70252800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr5:70246400-70256000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:70246400-70258200	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr5:70246600-70252800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:70247000-70259600	Weak transcription	Fetal Muscle Leg	muscle
16	chr5:70247600-70253000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:70248200-70256800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr5:70249200-70258200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr5:70249200-70266400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr5:70249400-70257600	Weak transcription	Dnd41	blood
21	chr5:70249600-70257800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr5:70249800-70252200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:70249800-70252200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr5:70249800-70252200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr5:70249800-70252200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr5:70251200-70257800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:70251600-70256600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:70256600-70256800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr5:70273600-70276000	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr5:70302800-70303400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr5:70303400-70303600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr5:70303400-70305200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr5:70303600-70305200	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr5:70303600-70305200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:70303600-70305400	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr5:70305200-70308200	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr5:70305200-70308600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr5:70305200-70309600	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr5:70305400-70308200	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr5:70305600-70310200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr5:70306400-70309000	Weak transcription	Adipose Nuclei	Adipose
42	chr5:70306400-70309000	Weak transcription	Liver	Liver
43	chr5:70306800-70307000	Enhancers	HepG2	liver
44	chr5:70307000-70307800	Flanking Active TSS	HepG2	liver
45	chr5:70307800-70310000	Enhancers	HepG2	liver
46	chr5:70308200-70309200	Genic enhancers	Primary monocytes fromperipheralblood	blood
47	chr5:70308200-70311000	Genic enhancers	Monocytes-CD14+_RO01746	blood
48	chr5:70308400-70308800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr5:70308600-70310200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr5:70309200-70310000	Weak transcription	Primary monocytes fromperipheralblood	blood

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