Variant report

Variant	nsv4847
Chromosome Location	chr5:59523591-59569307
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59553354-59554437	HepG2	liver:	n/a	n/a
2	ATF1	chr5:59560365-59560521	K562	blood:	n/a	n/a
3	BATF	chr5:59544689-59545104	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:59558736-59559148	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:59544756-59545152	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:59544746-59545162	GM12878	blood:	n/a	n/a
7	BCLAF1	chr5:59544682-59545205	GM12878	blood:	n/a	n/a
8	BHLHE40	chr5:59558766-59559019	GM12878	blood:	n/a	n/a
9	CEBPB	chr5:59565465-59565782	A549	lung:	n/a	chr5:59565595-59565606
10	CEBPB	chr5:59553690-59554010	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:59565445-59565762	HepG2	liver:	n/a	chr5:59565595-59565606
12	CEBPB	chr5:59527681-59528564	HepG2	liver:	n/a	chr5:59528086-59528097 chr5:59528085-59528098
13	CEBPB	chr5:59553612-59553900	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:59565540-59565728	Hela-S3	cervix:	n/a	chr5:59565595-59565606
15	CEBPB	chr5:59528003-59528544	A549	lung:	n/a	chr5:59528086-59528097 chr5:59528085-59528098
16	CEBPB	chr5:59553635-59554049	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:59553573-59554113	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:59553554-59554400	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:59529845-59530043	HepG2	liver:	n/a	chr5:59529862-59529873
20	CEBPB	chr5:59556410-59556925	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:59553591-59554148	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:59553595-59554042	A549	lung:	n/a	n/a
23	CHD2	chr5:59556375-59556860	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr5:59558446-59558598	GM12878	blood:	n/a	n/a
25	CHD2	chr5:59544752-59545126	GM12878	blood:	n/a	n/a
26	CTCF	chr5:59565860-59566010	RPTEC	kidney:	n/a	n/a
27	CTCF	chr5:59533040-59533190	AG10803	skin:	n/a	n/a
28	CUX1	chr5:59558612-59558686	GM12878	blood:	n/a	n/a
29	CUX1	chr5:59558896-59558954	GM12878	blood:	n/a	n/a
30	CUX1	chr5:59544872-59545018	GM12878	blood:	n/a	n/a
31	E2F4	chr5:59553366-59553473	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr5:59535303-59535545	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr5:59529675-59530090	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr5:59557596-59557932	GM12878	blood:	n/a	n/a
35	EBF1	chr5:59544773-59545177	GM12878	blood:	n/a	n/a
36	EBF1	chr5:59558684-59559077	GM12878	blood:	n/a	chr5:59558876-59558885 chr5:59558862-59558873 chr5:59558874-59558887 chr5:59558875-59558886 chr5:59558876-59558886 chr5:59558876-59558885
37	EBF1	chr5:59558436-59559161	GM12878	blood:	n/a	chr5:59558876-59558885 chr5:59558862-59558873 chr5:59558874-59558887 chr5:59558875-59558886 chr5:59558876-59558886 chr5:59558876-59558885
38	EBF1	chr5:59544669-59545246	GM12878	blood:	n/a	n/a
39	EP300	chr5:59553193-59553696	SK-N-SH	brain:	n/a	n/a
40	EP300	chr5:59556407-59557061	Hela-S3	cervix:	n/a	chr5:59556562-59556572
41	EP300	chr5:59556299-59557127	SK-N-SH	brain:	n/a	chr5:59556562-59556572
42	EP300	chr5:59558455-59559047	GM12878	blood:	n/a	n/a
43	EP300	chr5:59544736-59545140	GM12878	blood:	n/a	chr5:59544989-59544998 chr5:59544879-59544888
44	EP300	chr5:59553700-59554106	HepG2	liver:	n/a	n/a
45	EP300	chr5:59556366-59557210	SK-N-SH	brain:	n/a	chr5:59556562-59556572
46	EP300	chr5:59525261-59525268	K562	blood:	n/a	n/a
47	EP300	chr5:59558407-59559381	GM12878	blood:	n/a	n/a
48	EP300	chr5:59558765-59558838	GM12878	blood:	n/a	n/a
49	EP300	chr5:59544695-59545189	GM12878	blood:	n/a	chr5:59544989-59544998 chr5:59544879-59544888
50	FOS	chr5:59556400-59556913	Hela-S3	cervix:	n/a	chr5:59556765-59556776 chr5:59556767-59556779 chr5:59556769-59556777

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59559218-59559268	GM12891	blood:	n/a
2	chr5:59559062-59559112	CMK	blood:	n/a
3	chr5:59559218-59559268	GM12878	blood:	n/a
4	chr5:59559218-59559268	H1-hESC	embryonic stem cell:	embryo
5	chr5:59559218-59559268	HEEpiC	esophagus:	n/a
6	chr5:59559218-59559268	RPTEC	kidney:	n/a
7	chr5:59559062-59559112	HCM	heart:	n/a
8	chr5:59559062-59559112	GM12892	blood:	n/a
9	chr5:59559218-59559268	AG04449	skin:	fetal
10	chr5:59559218-59559268	IMR90	lung:	fetal
11	chr5:59559180-59559230	SKMC	muscle:	n/a
12	chr5:59559180-59559230	HIPEpiC	eye:	n/a
13	chr5:59559062-59559112	PrEC	prostate:	n/a
14	chr5:59559180-59559230	BE2_C	brain:	n/a
15	chr5:59559062-59559112	AG04449	skin:	fetal
16	chr5:59559180-59559230	PFSK-1	brain:	n/a
17	chr5:59559180-59559230	LNCaP	prostate:	n/a
18	chr5:59559218-59559268	NT2-D1	testis:	n/a
19	chr5:59559218-59559268	HRE	kidney:	n/a
20	chr5:59559218-59559268	ProgFib	skin:	n/a
21	chr5:59559218-59559268	U87	brain:	n/a
22	chr5:59559062-59559112	ECC-1	luminal epithelium:	n/a
23	chr5:59559180-59559230	GM06990	blood:	n/a
24	chr5:59559180-59559230	GM12892	blood:	n/a
25	chr5:59559218-59559268	AG10803	skin:	n/a
26	chr5:59559180-59559230	HCF	heart:	n/a
27	chr5:59559218-59559268	HCPEpiC	choroid plexus:	n/a
28	chr5:59559062-59559112	NHBE	bronchial:	n/a
29	chr5:59559180-59559230	GM12891	blood:	n/a
30	chr5:59559062-59559112	GM12878	blood:	n/a
31	chr5:59559062-59559112	GM19239	blood:	n/a
32	chr5:59559180-59559230	ProgFib	skin:	n/a
33	chr5:59559180-59559230	HL-60	blood:	n/a
34	chr5:59559062-59559112	HRE	kidney:	n/a
35	chr5:59559218-59559268	AG09309	skin:	n/a
36	chr5:59559180-59559230	SK-N-SH_RA	brain:	n/a
37	chr5:59559180-59559230	HRPEpiC	eye:	n/a
38	chr5:59559062-59559112	HCT-116	colon:	n/a
39	chr5:59559218-59559268	HepG2	liver:	n/a
40	chr5:59559218-59559268	SK-N-SH	brain:	n/a
41	chr5:59559180-59559230	U87	brain:	n/a
42	chr5:59559180-59559230	SAEC	small airway:	n/a
43	chr5:59559180-59559230	IMR90	lung:	fetal
44	chr5:59559218-59559268	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:59559218-59559268	SK-N-MC	brain:	n/a
46	chr5:59559180-59559230	T-47D	breast:	n/a
47	chr5:59559180-59559230	NH-A	brain:	n/a
48	chr5:59559180-59559230	HEK293	kidney:	embryo
49	chr5:59559218-59559268	HEK293	kidney:	embryo
50	chr5:59559062-59559112	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:59549482..59552233-chr5:59553881..59555409,2	K562	blood:
2	chr11:288802..289567-chr5:59528126..59528944,2	NB4	blood:
3	chr5:59525141..59527803-chr5:59530452..59533157,2	MCF-7	breast:
4	chr5:59525141..59527803-chr5:59530452..59533157,2	MCF-7	breast:
5	chr5:59549482..59552233-chr5:59553881..59555409,2	K562	blood:

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island
ENSG00000142102	chromatin interactions

Extended variants
information (count: 1504 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373720912	chr5:59523617-59523618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572699725	chr5:59523716-59523717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541816748	chr5:59523731-59523732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs67787424	chr5:59523749-59523750	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575519912	chr5:59523830-59523831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544129769	chr5:59523863-59523864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563926142	chr5:59523894-59523895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533001544	chr5:59523899-59523900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546686902	chr5:59523937-59523938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142160225	chr5:59523973-59523974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369708314	chr5:59523984-59523985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187079335	chr5:59523986-59523987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549380427	chr5:59523990-59523991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577436596	chr5:59524036-59524037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76899179	chr5:59524219-59524220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10066896	chr5:59524259-59524260	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7721457	chr5:59524275-59524276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs56215414	chr5:59524280-59524281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs76705426	chr5:59524330-59524331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201794036	chr5:59524336-59524337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111930630	chr5:59524462-59524463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553060854	chr5:59524477-59524478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572907300	chr5:59524487-59524488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77371742	chr5:59524519-59524520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553737067	chr5:59524522-59524523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555324035	chr5:59524531-59524532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373159550	chr5:59524549-59524550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572236440	chr5:59524573-59524574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544092021	chr5:59524582-59524583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564088140	chr5:59524628-59524629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545889696	chr5:59524634-59524635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79285349	chr5:59524661-59524662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540047426	chr5:59524686-59524687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555940337	chr5:59524702-59524703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560354579	chr5:59524748-59524749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140173792	chr5:59524759-59524760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549243255	chr5:59524773-59524774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562891346	chr5:59524804-59524805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149914623	chr5:59524837-59524838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576572311	chr5:59524854-59524855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552054405	chr5:59524877-59524878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113012925	chr5:59524941-59524942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181560088	chr5:59524960-59524961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547994691	chr5:59525048-59525049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567794100	chr5:59525067-59525068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186275028	chr5:59525083-59525084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555213407	chr5:59525086-59525087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71627995	chr5:59525153-59525154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs562265849	chr5:59525158-59525159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112062828	chr5:59525192-59525193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	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
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59506800-59528000	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59520000-59525200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:59522400-59523600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr5:59523600-59524000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr5:59524000-59525800	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr5:59525200-59528400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:59525400-59526200	Enhancers	Adipose Nuclei	Adipose
8	chr5:59525800-59526000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:59525800-59526600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr5:59525800-59528000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr5:59525800-59531400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr5:59526000-59528200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:59526200-59527600	Weak transcription	Adipose Nuclei	Adipose
14	chr5:59526600-59529200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr5:59527600-59529000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr5:59527600-59529000	Enhancers	Adipose Nuclei	Adipose
17	chr5:59528000-59528400	Active TSS	Primary B cells from cord blood	blood
18	chr5:59528000-59528800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
19	chr5:59528200-59529200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:59528400-59528600	Weak transcription	Primary B cells from cord blood	blood
21	chr5:59528600-59529400	Enhancers	Primary B cells from cord blood	blood
22	chr5:59528800-59530600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr5:59529200-59529800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr5:59529400-59536000	Weak transcription	Primary B cells from cord blood	blood
25	chr5:59529800-59536000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr5:59536000-59537000	ZNF genes & repeats	Primary B cells from cord blood	blood
27	chr5:59536000-59537800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
28	chr5:59536200-59536600	ZNF genes & repeats	Lung	lung
29	chr5:59537000-59543600	Weak transcription	Primary B cells from cord blood	blood
30	chr5:59538400-59538600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr5:59539400-59544000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr5:59540400-59541000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr5:59541000-59542200	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr5:59542200-59544800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr5:59542400-59542600	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr5:59542600-59543000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr5:59542600-59546200	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr5:59543000-59543400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr5:59543400-59543600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr5:59543400-59544000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr5:59543600-59543800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr5:59543600-59546400	Enhancers	Primary B cells from cord blood	blood
43	chr5:59543800-59545600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr5:59544000-59544600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr5:59544000-59545600	Enhancers	Primary hematopoietic stem cells	blood
46	chr5:59544000-59545600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:59544000-59545600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:59544200-59545600	Enhancers	GM12878-XiMat	blood
49	chr5:59544600-59545600	Enhancers	Primary B cells from peripheral blood	blood
50	chr5:59544600-59546400	Enhancers	Primary hematopoietic stem cells short term culture	blood

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