Variant report

Variant	nsv1060026
Chromosome Location	chr19:51751123-51773175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 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	ARID3A	chr19:51763490-51763571	K562	blood:	n/a	n/a
2	ATF1	chr19:51761509-51761788	K562	blood:	n/a	n/a
3	ATF1	chr19:51762606-51762965	K562	blood:	n/a	n/a
4	ATF2	chr19:51754581-51755015	GM12878	blood:	n/a	n/a
5	BATF	chr19:51754691-51755046	GM12878	blood:	n/a	chr19:51754839-51754850
6	BATF	chr19:51754605-51755151	GM12878	blood:	n/a	chr19:51754839-51754850
7	BCL11A	chr19:51754668-51755111	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:51754830-51754937	GM12878	blood:	n/a	n/a
9	CEBPB	chr19:51760842-51760975	K562	blood:	n/a	n/a
10	CTCF	chr19:51762720-51762870	AG04449	skin:	n/a	n/a
11	CTCF	chr19:51762720-51762870	HMF	breast:	n/a	n/a
12	CTCF	chr19:51762669-51762949	Gliobla	brain:	n/a	n/a
13	CTCF	chr19:51757820-51757970	HMF	breast:	n/a	n/a
14	CTCF	chr19:51762760-51762910	NB4	blood:	n/a	n/a
15	CTCF	chr19:51762675-51762922	HepG2	liver:	n/a	n/a
16	CTCF	chr19:51762740-51762890	GM12865	blood:	n/a	n/a
17	CTCF	chr19:51762720-51762870	AG10803	skin:	n/a	n/a
18	CTCF	chr19:51762715-51762881	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr19:51762685-51762923	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr19:51762740-51762890	HMEC	breast:	n/a	n/a
21	CTCF	chr19:51762980-51763130	Caco-2	colon:	n/a	n/a
22	CTCF	chr19:51762631-51762999	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr19:51762740-51762890	GM12868	blood:	n/a	n/a
24	CTCF	chr19:51762700-51762850	HRE	kidney:	n/a	n/a
25	CTCF	chr19:51762700-51762850	GM12870	blood:	n/a	n/a
26	CTCF	chr19:51762720-51762870	HRE	kidney:	n/a	n/a
27	CTCF	chr19:51762760-51762910	GM12865	blood:	n/a	n/a
28	CTCF	chr19:51763040-51763190	HMF	breast:	n/a	n/a
29	CTCF	chr19:51762720-51762870	GM12866	blood:	n/a	n/a
30	CTCF	chr19:51762590-51763003	GM12878	blood:	n/a	n/a
31	CTCF	chr19:51754500-51754650	GM12865	blood:	n/a	chr19:51754607-51754616
32	CTCF	chr19:51762720-51762870	GM12869	blood:	n/a	n/a
33	CTCF	chr19:51762720-51762870	GM12875	blood:	n/a	n/a
34	CTCF	chr19:51762605-51762950	K562	blood:	n/a	n/a
35	CTCF	chr19:51757760-51757910	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr19:51762720-51762870	BE2_C	brain:	n/a	n/a
37	CTCF	chr19:51762560-51763069	HCT-116	colon:	n/a	n/a
38	CTCF	chr19:51762740-51762890	K562	blood:	n/a	n/a
39	CTCF	chr19:51762720-51762870	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr19:51762720-51762870	HEK293	kidney:	n/a	n/a
41	CTCF	chr19:51762683-51762911	A549	lung:	n/a	n/a
42	CTCF	chr19:51762700-51762850	GM12874	blood:	n/a	n/a
43	CTCF	chr19:51762667-51762941	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr19:51754560-51754710	GM06990	blood:	n/a	chr19:51754607-51754616
45	CTCF	chr19:51762691-51762923	ProgFib	skin:	n/a	n/a
46	CTCF	chr19:51762740-51762890	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr19:51762740-51762890	GM12874	blood:	n/a	n/a
48	CTCF	chr19:51762680-51762830	HVMF	connective:	n/a	n/a
49	CTCF	chr19:51762720-51762870	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr19:51763257-51763314	GM10266	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	chr19:51771923-51771973	HepG2	liver:	n/a
2	chr19:51761116-51761166	SK-N-MC	brain:	n/a
3	chr19:51762753-51762803	PrEC	prostate:	n/a
4	chr19:51771923-51771973	HL-60	blood:	n/a
5	chr19:51770775-51770825	HEEpiC	esophagus:	n/a
6	chr19:51770775-51770825	BE2_C	brain:	n/a
7	chr19:51762753-51762803	HMEC	breast:	n/a
8	chr19:51761116-51761166	HepG2	liver:	n/a
9	chr19:51771923-51771973	PFSK-1	brain:	n/a
10	chr19:51770775-51770825	GM06990	blood:	n/a
11	chr19:51770775-51770825	HCM	heart:	n/a
12	chr19:51761116-51761166	NT2-D1	testis:	n/a
13	chr19:51771923-51771973	T-47D	breast:	n/a
14	chr19:51761116-51761166	AoSMC	blood vessel:	n/a
15	chr19:51771923-51771973	PrEC	prostate:	n/a
16	chr19:51761116-51761166	HRCEpiC	kidney:	n/a
17	chr19:51762753-51762803	HCF	heart:	n/a
18	chr19:51771923-51771973	SAEC	small airway:	n/a
19	chr19:51762753-51762803	Jurkat	blood:	n/a
20	chr19:51770775-51770825	HCT-116	colon:	n/a
21	chr19:51762753-51762803	NHBE	bronchial:	n/a
22	chr19:51761116-51761166	K562	blood:	n/a
23	chr19:51770775-51770825	PrEC	prostate:	n/a
24	chr19:51771923-51771973	HCF	heart:	n/a
25	chr19:51761116-51761166	SKMC	muscle:	n/a
26	chr19:51761116-51761166	NH-A	brain:	n/a
27	chr19:51770775-51770825	CMK	blood:	n/a
28	chr19:51770775-51770825	SK-N-SH_RA	brain:	n/a
29	chr19:51761116-51761166	U87	brain:	n/a
30	chr19:51771923-51771973	SK-N-SH_RA	brain:	n/a
31	chr19:51771923-51771973	PANC-1	pancreas:	n/a
32	chr19:51771923-51771973	GM19239	blood:	n/a
33	chr19:51762753-51762803	HCPEpiC	choroid plexus:	n/a
34	chr19:51762753-51762803	GM12891	blood:	n/a
35	chr19:51762753-51762803	SAEC	small airway:	n/a
36	chr19:51770775-51770825	K562	blood:	n/a
37	chr19:51771923-51771973	A549	lung:	n/a
38	chr19:51761116-51761166	GM12878	blood:	n/a
39	chr19:51762753-51762803	HCT-116	colon:	n/a
40	chr19:51762753-51762803	HL-60	blood:	n/a
41	chr19:51770775-51770825	U87	brain:	n/a
42	chr19:51771923-51771973	HUVEC	blood vessel:	n/a
43	chr19:51770775-51770825	A549	lung:	n/a
44	chr19:51771923-51771973	HCPEpiC	choroid plexus:	n/a
45	chr19:51770775-51770825	AG09309	skin:	n/a
46	chr19:51771923-51771973	ECC-1	luminal epithelium:	n/a
47	chr19:51762753-51762803	LNCaP	prostate:	n/a
48	chr19:51770775-51770825	HUVEC	blood vessel:	n/a
49	chr19:51770775-51770825	HAEpiC	amniotic membrane:	n/a
50	chr19:51771923-51771973	Jurkat	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51661493..51662394-chr19:51762311..51762910,6	MCF-7	breast:
2	chr19:51770892..51772482-chr19:51774022..51775700,2	K562	blood:
3	chr19:51770888..51773726-chr19:51775825..51777713,2	K562	blood:
4	chr19:51765820..51768667-chr19:51769261..51772147,2	K562	blood:
5	chr19:51661431..51662712-chr19:51761692..51763149,12	K562	blood:
6	chr19:51770982..51772847-chr19:51774200..51775938,2	K562	blood:
7	chr19:51762812..51764543-chr19:51765982..51768235,3	K562	blood:
8	chr19:51600353..51600887-chr19:51762311..51762872,2	K562	blood:
9	chr19:51763432..51765236-chr19:51768339..51771020,2	K562	blood:
10	chr19:51661388..51662622-chr19:51761876..51763512,12	MCF-7	breast:
11	chr19:51747857..51749540-chr19:51750009..51752859,2	K562	blood:
12	chr19:51763432..51765236-chr19:51768339..51771020,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C19orf75-1	chr19:51754503-51754799	NONHSAT067426
2	lnc-C19orf75-1	chr19:51769031-51769136	NONHSAT067424
3	lnc-C19orf75-1	chr19:51770627-51770783	NONHSAT067424
4	lnc-C19orf75-1	chr19:51767137-51767357	NONHSAT067424
5	lnc-VSIG10L-1	chr19:51754485-51754788	ENSG00000268595.1
6	lnc-C19orf75-1	chr19:51759188-51759286	NONHSAT067426
7	lnc-C19orf75-1	chr19:51771825-51772582	NONHSAT067424
8	lnc-C19orf75-1	chr19:51754332-51754799	NONHSAT067424
9	lnc-C19orf75-1	chr19:51767137-51767303	NONHSAT067426

No data

Variant related genes	Relation type
ENSG00000268318	TF binding region
SIGLECL1	TF binding region
ENSG00000268318	CpG island
SIGLECL1	CpG island
ENSG00000268595	chromatin interactions
ENSG00000179213	chromatin interactions
ENSG00000268318	chromatin interactions

Extended variants
information (count: 899 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:899 , 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	rs11084063	chr19:51751123-51751124	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546111285	chr19:51751216-51751217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557803389	chr19:51751219-51751220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193058167	chr19:51751236-51751237	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs35931165	chr19:51751285-51751286	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs368671729	chr19:51751315-51751316	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113903697	chr19:51751372-51751373	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs549646561	chr19:51751373-51751374	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs561350056	chr19:51751381-51751382	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs57490406	chr19:51751417-51751418	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs183078952	chr19:51751425-51751426	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201627505	chr19:51751437-51751438	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs74197505	chr19:51751439-51751440	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs79854485	chr19:51751440-51751441	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs72509605	chr19:51751441-51751442	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs571428988	chr19:51751458-51751459	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs538700927	chr19:51751477-51751478	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550571399	chr19:51751497-51751498	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs568904736	chr19:51751544-51751545	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536994072	chr19:51751559-51751560	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs543075717	chr19:51751566-51751567	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs989504	chr19:51751650-51751651	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs528991419	chr19:51751708-51751709	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs573791087	chr19:51751755-51751756	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369951074	chr19:51751793-51751794	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs375754832	chr19:51751801-51751802	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs138570250	chr19:51751804-51751805	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs373373932	chr19:51751812-51751813	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs140617834	chr19:51751814-51751815	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563319106	chr19:51751835-51751836	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs575289298	chr19:51751848-51751849	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs273647	chr19:51751858-51751859	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs10426210	chr19:51751887-51751888	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145668762	chr19:51751925-51751926	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs989502	chr19:51751934-51751935	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs34606577	chr19:51751950-51751951	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs1319675	chr19:51751951-51751952	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs550659400	chr19:51751973-51751974	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs188106512	chr19:51752025-51752026	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs557930027	chr19:51752036-51752037	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs273646	chr19:51752059-51752060	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138214599	chr19:51752083-51752084	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567552747	chr19:51752098-51752099	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs12971800	chr19:51752217-51752218	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs386810318	chr19:51752270-51752271	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs192341043	chr19:51752271-51752272	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538765555	chr19:51752298-51752299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142760765	chr19:51752304-51752305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575214000	chr19:51752318-51752319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542629894	chr19:51752337-51752338	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
Adenoid cystic carcinoma	18698036	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
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
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
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51745400-51753200	Enhancers	Primary hematopoietic stem cells	blood
2	chr19:51745800-51754000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr19:51749400-51753400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr19:51749800-51751400	Weak transcription	Fetal Thymus	thymus
5	chr19:51749800-51753400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr19:51749800-51753400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:51750600-51754000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr19:51751400-51752800	Enhancers	Fetal Thymus	thymus
9	chr19:51751600-51752200	Enhancers	GM12878-XiMat	blood
10	chr19:51751600-51752400	Enhancers	Thymus	Thymus
11	chr19:51753200-51756400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr19:51753400-51754200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr19:51753400-51755600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:51753400-51755600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr19:51754000-51755800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr19:51754200-51754600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
17	chr19:51754200-51754800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:51754600-51754800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr19:51754600-51755600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr19:51755600-51757400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr19:51755600-51757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:51755600-51757600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:51755800-51757400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr19:51756000-51757600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr19:51756200-51757600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr19:51756400-51757000	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr19:51756400-51757400	Enhancers	Primary hematopoietic stem cells	blood
28	chr19:51757400-51759400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr19:51757400-51759400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr19:51757400-51759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr19:51757400-51761000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr19:51757600-51758800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr19:51757600-51759400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:51757600-51761200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr19:51758800-51759400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr19:51759400-51761400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr19:51759400-51761400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr19:51759400-51762800	Enhancers	Primary hematopoietic stem cells	blood
39	chr19:51759400-51762800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr19:51759600-51761600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr19:51761000-51761600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr19:51761000-51761800	Enhancers	K562	blood
43	chr19:51761000-51762200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr19:51761200-51762400	Enhancers	Fetal Thymus	thymus
45	chr19:51761200-51762800	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr19:51761400-51762000	Enhancers	GM12878-XiMat	blood
47	chr19:51761400-51762400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr19:51761400-51762600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:51761600-51761800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr19:51761600-51762000	Enhancers	Primary neutrophils fromperipheralblood	blood

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