Variant report

Variant	nsv1058277
Chromosome Location	chr19:51488544-51509847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:855)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 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	ATF1	chr19:51505893-51506332	K562	blood:	n/a	n/a
2	ATF2	chr19:51505874-51506266	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr19:51505869-51506247	K562	blood:	n/a	n/a
4	ATF3	chr19:51505767-51506301	K562	blood:	n/a	n/a
5	ATF3	chr19:51497455-51497721	K562	blood:	n/a	n/a
6	ATF3	chr19:51497422-51497699	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:51505857-51506062	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr19:51504227-51504502	K562	blood:	n/a	n/a
9	BHLHE40	chr19:51505735-51506365	K562	blood:	n/a	n/a
10	CBX3	chr19:51497347-51497781	K562	blood:	n/a	n/a
11	CBX3	chr19:51505605-51506348	K562	blood:	n/a	n/a
12	CBX3	chr19:51497320-51497896	K562	blood:	n/a	n/a
13	CCNT2	chr19:51505837-51506215	K562	blood:	n/a	n/a
14	CEBPB	chr19:51505625-51506268	K562	blood:	n/a	n/a
15	CHD2	chr19:51497464-51497689	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr19:51505866-51506159	K562	blood:	n/a	n/a
17	CREB1	chr19:51505718-51506458	K562	blood:	n/a	n/a
18	CREB1	chr19:51505827-51506320	A549	lung:	n/a	n/a
19	CREB1	chr19:51505675-51506406	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr19:51505739-51506327	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr19:51502607-51502708	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr19:51497320-51497470	A549	lung:	n/a	n/a
23	CTCF	chr19:51505700-51505850	K562	blood:	n/a	n/a
24	CTCF	chr19:51504389-51504405	MCF-7	breast:	n/a	n/a
25	CTCF	chr19:51508482-51508582	Lung_OC	lung:	n/a	n/a
26	CTCF	chr19:51504360-51504510	K562	blood:	n/a	chr19:51504462-51504475
27	CTCF	chr19:51503280-51503430	GM12866	blood:	n/a	n/a
28	CTCF	chr19:51503786-51504058	NHEK	skin:	n/a	n/a
29	CTCF	chr19:51504247-51504518	NHEK	skin:	n/a	chr19:51504462-51504475
30	CTCF	chr19:51498280-51498430	MCF-7	breast:	n/a	chr19:51498308-51498321 chr19:51498306-51498322 chr19:51498307-51498328 chr19:51498305-51498323
31	CTCF	chr19:51505965-51506204	K562	blood:	n/a	n/a
32	CTCF	chr19:51497400-51497550	BE2_C	brain:	n/a	n/a
33	CTCF	chr19:51497520-51497670	A549	lung:	n/a	n/a
34	CTCF	chr19:51504320-51504470	NHEK	skin:	n/a	n/a
35	CTCF	chr19:51504253-51504602	H1-hESC	embryonic stem cell:	n/a	chr19:51504462-51504475
36	CTCF	chr19:51498240-51498390	HMEC	breast:	n/a	chr19:51498308-51498321 chr19:51498306-51498322 chr19:51498307-51498328 chr19:51498305-51498323
37	CTCF	chr19:51505620-51505770	HMEC	breast:	n/a	n/a
38	CTCF	chr19:51503940-51504090	NHEK	skin:	n/a	n/a
39	CTCF	chr19:51497360-51497510	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr19:51504314-51504447	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr19:51504343-51504474	K562	blood:	n/a	n/a
42	CTCF	chr19:51498283-51498335	MCF-7	breast:	n/a	chr19:51498308-51498321 chr19:51498306-51498322 chr19:51498307-51498328 chr19:51498305-51498323
43	CTCF	chr19:51503080-51503230	HMEC	breast:	n/a	n/a
44	CTCF	chr19:51504340-51504490	HCT-116	colon:	n/a	chr19:51504462-51504475
45	CTCF	chr19:51504356-51504442	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:51498120-51498270	HMEC	breast:	n/a	n/a
47	CTCF	chr19:51505740-51505890	HMEC	breast:	n/a	n/a
48	CTCF	chr19:51498265-51498345	LNCaP	prostate:	n/a	chr19:51498308-51498321 chr19:51498306-51498322 chr19:51498307-51498328 chr19:51498305-51498323
49	CTCF	chr19:51504269-51504563	H1-hESC	embryonic stem cell:	n/a	chr19:51504462-51504475
50	CTCF	chr19:51504289-51504563	K562	blood:	n/a	chr19:51504462-51504475

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51508927-51508977	GM12878	blood:	n/a
2	chr19:51508927-51508977	GM12878	blood:	n/a
3	chr19:51504516-51504566	HAEpiC	amniotic membrane:	n/a
4	chr19:51505001-51505051	GM12878	blood:	n/a
5	chr19:51504516-51504566	SK-N-SH_RA	brain:	n/a
6	chr19:51502695-51502745	GM12878	blood:	n/a
7	chr19:51504234-51504284	HRE	kidney:	n/a
8	chr19:51499358-51499408	HRE	kidney:	n/a
9	chr19:51505507-51505557	A549	lung:	n/a
10	chr19:51505001-51505051	AG04449	skin:	fetal
11	chr19:51504234-51504284	HRPEpiC	eye:	n/a
12	chr19:51504823-51504873	NHBE	bronchial:	n/a
13	chr19:51506358-51506408	NT2-D1	testis:	n/a
14	chr19:51505507-51505557	HIPEpiC	eye:	n/a
15	chr19:51506888-51506938	HepG2	liver:	n/a
16	chr19:51505001-51505051	U87	brain:	n/a
17	chr19:51505507-51505557	HRPEpiC	eye:	n/a
18	chr19:51504823-51504873	K562	blood:	n/a
19	chr19:51499358-51499408	SK-N-MC	brain:	n/a
20	chr19:51502695-51502745	PFSK-1	brain:	n/a
21	chr19:51505507-51505557	HRE	kidney:	n/a
22	chr19:51506358-51506408	MCF10A-Er-Src	breast:	n/a
23	chr19:51506358-51506408	HPAEpiC	pulmonary alveolar:	n/a
24	chr19:51505001-51505051	ECC-1	luminal epithelium:	n/a
25	chr19:51502695-51502745	HL-60	blood:	n/a
26	chr19:51506273-51506323	SK-N-MC	brain:	n/a
27	chr19:51508927-51508977	HRPEpiC	eye:	n/a
28	chr19:51504234-51504284	GM06990	blood:	n/a
29	chr19:51505507-51505557	GM19239	blood:	n/a
30	chr19:51506888-51506938	ovcar-3	ovarian:	n/a
31	chr19:51506273-51506323	NHBE	bronchial:	n/a
32	chr19:51508927-51508977	CMK	blood:	n/a
33	chr19:51504516-51504566	Hepatocyte	liver:	n/a
34	chr19:51504516-51504566	HMEC	breast:	n/a
35	chr19:51505779-51505829	NB4	blood:	n/a
36	chr19:51506358-51506408	SK-N-MC	brain:	n/a
37	chr19:51505507-51505557	SK-N-SH_RA	brain:	n/a
38	chr19:51506358-51506408	MCF-7	breast:	n/a
39	chr19:51504234-51504284	IMR90	lung:	fetal
40	chr19:51504823-51504873	HCT-116	colon:	n/a
41	chr19:51504823-51504873	MCF10A-Er-Src	breast:	n/a
42	chr19:51505507-51505557	HMEC	breast:	n/a
43	chr19:51508927-51508977	HRCEpiC	kidney:	n/a
44	chr19:51506362-51506412	MCF10A-Er-Src	breast:	n/a
45	chr19:51506888-51506938	Hepatocyte	liver:	n/a
46	chr19:51506273-51506323	GM12892	blood:	n/a
47	chr19:51506888-51506938	HEEpiC	esophagus:	n/a
48	chr19:51506273-51506323	NT2-D1	testis:	n/a
49	chr19:51506273-51506323	HL-60	blood:	n/a
50	chr19:51505001-51505051	HPAEpiC	pulmonary alveolar:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51496140..51499135-chr19:51503262..51506454,3	MCF-7	breast:
2	chr19:51432897..51433716-chr19:51502734..51503640,2	MCF-7	breast:
3	chr19:51487899..51489635-chr19:51493828..51496214,2	MCF-7	breast:
4	chr19:51466266..51466970-chr19:51493872..51494430,2	MCF-7	breast:
5	chr19:51509564..51511935-chr19:51512603..51515013,2	K562	blood:
6	chr19:51465141..51466716-chr19:51492896..51495060,2	K562	blood:
7	chr19:51480632..51483251-chr19:51496429..51498251,2	K562	blood:
8	chr19:51482020..51484953-chr19:51487883..51489631,2	MCF-7	breast:
9	chr19:51487899..51489635-chr19:51493828..51496214,2	MCF-7	breast:
10	chr19:51465646..51468437-chr19:51495218..51498068,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLK2-5	chr19:51494205-51494336	ENSG00000267879.1
2	lnc-KLK9-1	chr19:51504354-51504431	NONHSAT067403
3	lnc-KLK9-1	chr19:51504788-51504859	NONHSAT067403
4	lnc-KLK9-1	chr19:51503641-51503974	NONHSAT067403

No data

Variant related genes	Relation type
KLK8	TF binding region
ENSG00000269741	TF binding region
KLK7	TF binding region
KLK8	CpG island
ENSG00000269741	CpG island
KLK7	CpG island
ENSG00000213022	chromatin interactions
ENSG00000167755	chromatin interactions
ENSG00000129455	chromatin interactions

Extended variants
information (count: 947 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:947 , 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	rs368401575	chr19:51488559-51488560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573999441	chr19:51488560-51488561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10402381	chr19:51488576-51488577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553243827	chr19:51488580-51488581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577854420	chr19:51488622-51488623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545177271	chr19:51488690-51488691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563650809	chr19:51488704-51488705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575656706	chr19:51488729-51488730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374962818	chr19:51488736-51488737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374502073	chr19:51488737-51488738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542663085	chr19:51488739-51488740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561286526	chr19:51488740-51488741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60729211	chr19:51488751-51488752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199532585	chr19:51488752-51488753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183653617	chr19:51488792-51488793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567312106	chr19:51488795-51488796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547752353	chr19:51488801-51488802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559670101	chr19:51488831-51488832	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs558194349	chr19:51488977-51488978	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149836616	chr19:51488983-51488984	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs145813120	chr19:51489001-51489002	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537104776	chr19:51489002-51489003	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs1722547	chr19:51489007-51489008	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546890627	chr19:51489008-51489009	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs118035941	chr19:51489022-51489023	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs571806029	chr19:51489023-51489024	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs553282581	chr19:51489024-51489025	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577885400	chr19:51489061-51489062	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs189093990	chr19:51489067-51489068	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs557487209	chr19:51489075-51489076	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs60165914	chr19:51489090-51489091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs59010718	chr19:51489123-51489124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs561356698	chr19:51489160-51489161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573308343	chr19:51489224-51489225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35387185	chr19:51489255-51489256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76030536	chr19:51489275-51489276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540608954	chr19:51489290-51489291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559701121	chr19:51489326-51489327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533223136	chr19:51489337-51489338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544879948	chr19:51489383-51489384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1701948	chr19:51489456-51489457	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs143224859	chr19:51489457-51489458	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs543780598	chr19:51489483-51489484	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549098473	chr19:51489487-51489488	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs146669300	chr19:51489496-51489497	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs557243407	chr19:51489506-51489507	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs35890431	chr19:51489538-51489539	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs575323118	chr19:51489582-51489583	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs192836345	chr19:51489597-51489598	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs546152102	chr19:51489615-51489616	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:139 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51487400-51494200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:51487600-51492800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:51487600-51493800	Weak transcription	HMEC	breast
4	chr19:51493400-51493600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr19:51493600-51495200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr19:51493800-51496800	Enhancers	HMEC	breast
7	chr19:51494000-51494600	Enhancers	Stomach Mucosa	stomach
8	chr19:51494200-51498000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr19:51494600-51495000	Weak transcription	Stomach Mucosa	stomach
10	chr19:51495000-51495400	Enhancers	Stomach Mucosa	stomach
11	chr19:51495000-51495600	Enhancers	NHEK	skin
12	chr19:51495000-51496600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr19:51495000-51496600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr19:51495200-51495400	Enhancers	Esophagus	oesophagus
15	chr19:51495200-51496400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr19:51495600-51496200	Flanking Active TSS	NHEK	skin
17	chr19:51496200-51496600	Enhancers	NHEK	skin
18	chr19:51496400-51499200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr19:51496600-51499200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr19:51496600-51502000	Weak transcription	NHEK	skin
21	chr19:51496600-51503000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr19:51496800-51497200	Weak transcription	HMEC	breast
23	chr19:51497200-51498000	Enhancers	HMEC	breast
24	chr19:51498000-51502200	Weak transcription	HMEC	breast
25	chr19:51498000-51503000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:51498600-51499400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:51499200-51500400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr19:51499200-51501600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr19:51499400-51499800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:51499800-51503200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr19:51500400-51502000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr19:51500800-51501000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
33	chr19:51501200-51501400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:51501600-51501800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:51501800-51502200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr19:51502000-51502200	Enhancers	NHEK	skin
37	chr19:51502000-51502400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:51502200-51502600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr19:51502200-51503200	Enhancers	HMEC	breast
40	chr19:51502200-51503400	Genic enhancers	NHEK	skin
41	chr19:51502400-51503400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr19:51502600-51503200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr19:51503000-51503400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr19:51503000-51503800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr19:51503200-51504200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:51503200-51506000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr19:51503200-51506000	Flanking Active TSS	HMEC	breast
48	chr19:51503400-51503600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
49	chr19:51503400-51506000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr19:51503400-51506000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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