Variant report

Variant	nsv517376
Chromosome Location	chr19:51260989-51280756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:51275680-51276017	GM12878	blood:	n/a	n/a
2	ATF3	chr19:51263161-51263447	K562	blood:	n/a	n/a
3	ATF3	chr19:51263192-51263431	GM12878	blood:	n/a	n/a
4	ATF3	chr19:51263137-51263443	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr19:51276768-51277056	K562	blood:	n/a	n/a
6	BHLHE40	chr19:51275771-51275935	K562	blood:	n/a	n/a
7	CBX3	chr19:51263013-51263594	K562	blood:	n/a	n/a
8	CBX3	chr19:51275556-51276151	K562	blood:	n/a	n/a
9	CEBPB	chr19:51263204-51263640	MCF-7	breast:	n/a	chr19:51263448-51263459
10	CEBPB	chr19:51263161-51263648	MCF-7	breast:	n/a	chr19:51263448-51263459
11	CEBPB	chr19:51263143-51263622	K562	blood:	n/a	chr19:51263448-51263459
12	CEBPB	chr19:51266996-51267088	K562	blood:	n/a	n/a
13	CEBPB	chr19:51263273-51263642	ECC-1	luminal epithelium:	n/a	chr19:51263448-51263459
14	CEBPB	chr19:51263301-51263537	K562	blood:	n/a	chr19:51263448-51263459
15	CEBPB	chr19:51263261-51263636	HepG2	liver:	n/a	chr19:51263448-51263459
16	CEBPB	chr19:51279835-51279887	K562	blood:	n/a	n/a
17	CEBPB	chr19:51263182-51263643	A549	lung:	n/a	chr19:51263448-51263459
18	CEBPB	chr19:51263262-51263640	IMR90	lung:	n/a	chr19:51263448-51263459
19	CEBPB	chr19:51263175-51263636	Hela-S3	cervix:	n/a	chr19:51263448-51263459
20	CEBPB	chr19:51263226-51263641	H1-hESC	embryonic stem cell:	n/a	chr19:51263448-51263459
21	CEBPB	chr19:51263228-51263684	A549	lung:	n/a	chr19:51263448-51263459
22	CEBPB	chr19:51266871-51267131	K562	blood:	n/a	n/a
23	CEBPB	chr19:51263279-51263520	ECC-1	luminal epithelium:	n/a	chr19:51263448-51263459
24	CEBPB	chr19:51263149-51263649	K562	blood:	n/a	chr19:51263448-51263459
25	CEBPB	chr19:51263101-51263642	A549	lung:	n/a	chr19:51263448-51263459
26	CEBPB	chr19:51264181-51264359	K562	blood:	n/a	n/a
27	CHD2	chr19:51275712-51276030	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr19:51275781-51276028	K562	blood:	n/a	n/a
29	CHD2	chr19:51263138-51263480	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr19:51263145-51263466	K562	blood:	n/a	n/a
31	CTCF	chr19:51265892-51265951	GM20000	blood:	n/a	n/a
32	CTCF	chr19:51276352-51276414	LNCaP	prostate:	n/a	n/a
33	CTCF	chr19:51270501-51270562	Kidney_OC	kidney:	n/a	n/a
34	EGR1	chr19:51265307-51265507	K562	blood:	n/a	n/a
35	EGR1	chr19:51265351-51265495	K562	blood:	n/a	n/a
36	ELF1	chr19:51263096-51263583	K562	blood:	n/a	n/a
37	ELF1	chr19:51275683-51276005	HepG2	liver:	n/a	n/a
38	ELF1	chr19:51263180-51263554	A549	lung:	n/a	n/a
39	ELF1	chr19:51263104-51263493	A549	lung:	n/a	n/a
40	ELF1	chr19:51262976-51263639	HCT-116	colon:	n/a	n/a
41	ELF1	chr19:51263226-51263485	GM12878	blood:	n/a	n/a
42	ELF1	chr19:51275703-51275984	HepG2	liver:	n/a	n/a
43	ELF1	chr19:51263195-51263521	SK-N-SH	brain:	n/a	n/a
44	ELF1	chr19:51263221-51263490	K562	blood:	n/a	n/a
45	ELF1	chr19:51275677-51276136	K562	blood:	n/a	n/a
46	ELF1	chr19:51263160-51263539	MCF-7	breast:	n/a	n/a
47	ELF1	chr19:51275620-51276088	MCF-7	breast:	n/a	n/a
48	ELF1	chr19:51275659-51276001	A549	lung:	n/a	n/a
49	EP300	chr19:51277391-51277467	K562	blood:	n/a	n/a
50	EP300	chr19:51263177-51263465	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51273924-51273974	HCF	heart:	n/a
2	chr19:51273924-51273974	PANC-1	pancreas:	n/a
3	chr19:51273924-51273974	GM06990	blood:	n/a
4	chr19:51273924-51273974	HL-60	blood:	n/a
5	chr19:51273924-51273974	AG09319	gingival:	n/a
6	chr19:51273924-51273974	MCF-7	breast:	n/a
7	chr19:51273924-51273974	HepG2	liver:	n/a
8	chr19:51273924-51273974	HRCEpiC	kidney:	n/a
9	chr19:51273924-51273974	HCT-116	colon:	n/a
10	chr19:51273924-51273974	SK-N-SH_RA	brain:	n/a
11	chr19:51273924-51273974	MCF10A-Er-Src	breast:	n/a
12	chr19:51273924-51273974	A549	lung:	n/a
13	chr19:51273924-51273974	HNPCEpiC	eye:	n/a
14	chr19:51273924-51273974	PrEC	prostate:	n/a
15	chr19:51273924-51273974	RPTEC	kidney:	n/a
16	chr19:51273924-51273974	ovcar-3	ovarian:	n/a
17	chr19:51273924-51273974	HEK293	kidney:	embryo
18	chr19:51273924-51273974	HCM	heart:	n/a
19	chr19:51273924-51273974	HIPEpiC	eye:	n/a
20	chr19:51273924-51273974	PFSK-1	brain:	n/a
21	chr19:51273924-51273974	HEEpiC	esophagus:	n/a
22	chr19:51273924-51273974	AG04450	lung:	fetal
23	chr19:51273924-51273974	Jurkat	blood:	n/a
24	chr19:51273924-51273974	Caco-2	colon:	n/a
25	chr19:51273924-51273974	NHBE	bronchial:	n/a
26	chr19:51273924-51273974	GM12892	blood:	n/a
27	chr19:51273924-51273974	U87	brain:	n/a
28	chr19:51273924-51273974	AG10803	skin:	n/a
29	chr19:51273924-51273974	HUVEC	blood vessel:	n/a
30	chr19:51273924-51273974	LNCaP	prostate:	n/a
31	chr19:51273924-51273974	HCPEpiC	choroid plexus:	n/a
32	chr19:51273924-51273974	HRPEpiC	eye:	n/a
33	chr19:51273924-51273974	NB4	blood:	n/a
34	chr19:51273924-51273974	GM19239	blood:	n/a
35	chr19:51273924-51273974	H1-hESC	embryonic stem cell:	embryo
36	chr19:51273924-51273974	AoSMC	blood vessel:	n/a
37	chr19:51273924-51273974	Hepatocyte	liver:	n/a
38	chr19:51273924-51273974	SK-N-MC	brain:	n/a
39	chr19:51273924-51273974	NT2-D1	testis:	n/a
40	chr19:51273924-51273974	CMK	blood:	n/a
41	chr19:51273924-51273974	HRE	kidney:	n/a
42	chr19:51273924-51273974	ECC-1	luminal epithelium:	n/a
43	chr19:51273924-51273974	IMR90	lung:	fetal
44	chr19:51273924-51273974	BE2_C	brain:	n/a
45	chr19:51273924-51273974	HAEpiC	amniotic membrane:	n/a
46	chr19:51273924-51273974	AG04449	skin:	fetal
47	chr19:51273924-51273974	BJ	skin:	n/a
48	chr19:51273924-51273974	SK-N-SH	brain:	n/a
49	chr19:51273924-51273974	AG09309	skin:	n/a
50	chr19:51273924-51273974	K562	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51260685..51263505-chr19:51269843..51271574,2	MCF-7	breast:
2	chr19:51227797..51230409-chr19:51278794..51284248,7	K562	blood:
3	chr19:51226684..51231742-chr19:51279891..51284185,9	K562	blood:
4	chr19:51261730..51264544-chr19:51297937..51299631,2	K562	blood:
5	chr19:51229051..51231656-chr19:51279475..51282410,2	MCF-7	breast:
6	chr19:51230541..51232764-chr19:51276781..51279069,2	K562	blood:
7	chr19:51275157..51278581-chr19:51280878..51283315,4	K562	blood:
8	chr19:51264409..51266482-chr19:51295781..51298327,2	MCF-7	breast:
9	chr19:51230514..51232764-chr19:51275727..51278281,2	K562	blood:
10	chr19:51220442..51223100-chr19:51275794..51278297,2	K562	blood:
11	chr19:51279277..51281371-chr19:51297725..51300722,2	K562	blood:
12	chr19:51229843..51232257-chr19:51279365..51282359,2	MCF-7	breast:
13	chr19:51159187..51161941-chr19:51274551..51277312,2	K562	blood:
14	chr19:51210289..51212000-chr19:51274505..51277258,2	K562	blood:
15	chr19:51276888..51279753-chr19:51305550..51307754,2	K562	blood:
16	chr19:51162574..51165243-chr19:51279759..51282961,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C19orf48-4	chr19:51272118-51272727	ucscGeneNc_uc002pdz_1

No data

Variant related genes	Relation type
GPR32P1	TF binding region
GPR32	TF binding region
GPR32P1	CpG island
GPR32	CpG island
ENSG00000235034	chromatin interactions
ENSG00000105472	chromatin interactions
ENSG00000161681	chromatin interactions
ENSG00000268375	chromatin interactions
ENSG00000269565	chromatin interactions
ENSG00000167747	chromatin interactions
ENSG00000220988	chromatin interactions

Extended variants
information (count: 1060 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7245984	chr19:51260989-51260990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200773575	chr19:51261048-51261049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7246110	chr19:51261051-51261052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs114451447	chr19:51261075-51261076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576469630	chr19:51261085-51261086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7246125	chr19:51261095-51261096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs555824491	chr19:51261108-51261109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574641215	chr19:51261133-51261134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542147758	chr19:51261145-51261146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560049288	chr19:51261146-51261147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572209108	chr19:51261173-51261174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545553204	chr19:51261209-51261210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563856056	chr19:51261210-51261211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531340459	chr19:51261251-51261252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372790573	chr19:51261260-51261261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146065264	chr19:51261274-51261275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189242303	chr19:51261281-51261282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548069466	chr19:51261329-51261330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149510523	chr19:51261339-51261340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143115148	chr19:51261342-51261343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138876408	chr19:51261383-51261384	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs193099312	chr19:51261386-51261387	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs374665601	chr19:51261395-51261396	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs374700998	chr19:51261396-51261397	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs202184085	chr19:51261408-51261409	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs376978246	chr19:51261410-51261411	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs146327260	chr19:51261411-51261412	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs535343242	chr19:51261424-51261425	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs535231459	chr19:51261433-51261434	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs185119552	chr19:51261448-51261449	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs545580117	chr19:51261466-51261467	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs557561252	chr19:51261472-51261473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs112233711	chr19:51261507-51261508	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs568502652	chr19:51261522-51261523	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs372086691	chr19:51261546-51261547	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561310778	chr19:51261564-51261565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376075025	chr19:51261624-51261625	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73046514	chr19:51261635-51261636	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs141836767	chr19:51261645-51261646	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112749815	chr19:51261654-51261655	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570310740	chr19:51261684-51261685	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139938743	chr19:51261735-51261736	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116022451	chr19:51261744-51261745	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371890980	chr19:51261747-51261748	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567517741	chr19:51261769-51261770	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575030665	chr19:51261795-51261796	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117611112	chr19:51261825-51261826	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188996701	chr19:51261828-51261829	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73046516	chr19:51261829-51261830	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557524811	chr19:51261841-51261842	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51243800-51261600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:51252200-51263000	Weak transcription	K562	blood
3	chr19:51260200-51261600	Weak transcription	Placenta	Placenta
4	chr19:51261600-51261800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:51261600-51268000	Enhancers	Placenta	Placenta
6	chr19:51261800-51262000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:51261800-51262000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:51262000-51262200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:51262000-51263000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:51262200-51273800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:51263000-51263200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:51263000-51264600	Enhancers	K562	blood
13	chr19:51264600-51269000	Weak transcription	K562	blood
14	chr19:51265800-51266000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr19:51266000-51267000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:51266600-51267000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr19:51267000-51267400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr19:51267000-51267400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr19:51267000-51267600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr19:51267400-51267800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr19:51267400-51269400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr19:51267600-51270600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr19:51267800-51269200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr19:51268000-51269400	Weak transcription	Placenta	Placenta
25	chr19:51269000-51270000	Enhancers	K562	blood
26	chr19:51269200-51270400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr19:51269400-51270400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:51269400-51271600	Enhancers	Placenta	Placenta
29	chr19:51269600-51270400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr19:51269800-51270200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr19:51270000-51270400	Weak transcription	K562	blood
32	chr19:51270400-51271400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr19:51270400-51271800	Enhancers	K562	blood
34	chr19:51270400-51281000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr19:51270600-51271000	Enhancers	HUVEC	blood vessel
36	chr19:51270600-51271400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr19:51270600-51271400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr19:51271200-51272200	Enhancers	Primary hematopoietic stem cells	blood
39	chr19:51271400-51271600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr19:51271400-51271800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr19:51271400-51272000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:51271600-51275200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr19:51271600-51280200	Weak transcription	Placenta	Placenta
44	chr19:51271800-51272400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr19:51271800-51275600	Weak transcription	K562	blood
46	chr19:51272000-51272200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:51273800-51274200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:51275200-51275400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr19:51275600-51275800	Enhancers	K562	blood
50	chr19:51275800-51276200	Weak transcription	K562	blood

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