Variant report

Variant	nsv482472
Chromosome Location	chr19:43777147-43934334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:1954)
Chromatin interactive
region (count:24)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
2	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
3	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
6	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
7	BHLHE40	chr19:43858417-43858453	K562	blood:	n/a	n/a
8	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
9	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
10	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
11	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr19:43917630-43917850	K562	blood:	n/a	n/a
14	CBX3	chr19:43917535-43917884	K562	blood:	n/a	n/a
15	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
16	CEBPB	chr19:43896514-43896714	K562	blood:	n/a	n/a
17	CEBPB	chr19:43896574-43896768	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
19	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:43926858-43927126	Hela-S3	cervix:	n/a	chr19:43926999-43927010
21	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
23	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:43926815-43927157	K562	blood:	n/a	chr19:43926999-43927010
25	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43926853-43927151	HepG2	liver:	n/a	chr19:43926999-43927010
28	CEBPB	chr19:43928885-43929232	HepG2	liver:	n/a	chr19:43929097-43929108
29	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
30	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
31	CEBPB	chr19:43896414-43896759	IMR90	lung:	n/a	n/a
32	CEBPB	chr19:43848801-43848963	K562	blood:	n/a	n/a
33	CEBPB	chr19:43896450-43896720	A549	lung:	n/a	n/a
34	CEBPB	chr19:43848780-43848968	A549	lung:	n/a	n/a
35	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43926854-43927175	IMR90	lung:	n/a	chr19:43926999-43927010
37	CEBPB	chr19:43916687-43916887	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:43848766-43848967	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:43896505-43896663	HepG2	liver:	n/a	n/a
41	CEBPB	chr19:43848755-43848998	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43931758-43932062	HepG2	liver:	n/a	chr19:43931836-43931847 chr19:43931836-43931847
43	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr19:43928890-43929216	A549	lung:	n/a	chr19:43929097-43929108
46	CEBPB	chr19:43876631-43876918	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:43920752-43920932	K562	blood:	n/a	n/a
48	CEBPB	chr19:43928882-43929119	IMR90	lung:	n/a	chr19:43929097-43929108
49	CEBPB	chr19:43928874-43929095	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43919028-43919078	SAEC	small airway:	n/a
2	chr19:43912227-43912277	Caco-2	colon:	n/a
3	chr19:43919028-43919078	SAEC	small airway:	n/a
4	chr19:43912227-43912277	Caco-2	colon:	n/a
5	chr19:43919028-43919078	AG04449	skin:	fetal
6	chr19:43912227-43912277	HIPEpiC	eye:	n/a
7	chr19:43918868-43918918	T-47D	breast:	n/a
8	chr19:43922723-43922773	HepG2	liver:	n/a
9	chr19:43922723-43922773	SK-N-SH	brain:	n/a
10	chr19:43908315-43908365	HMEC	breast:	n/a
11	chr19:43851787-43851837	A549	lung:	n/a
12	chr19:43918882-43918932	ProgFib	skin:	n/a
13	chr19:43918943-43918993	NHBE	bronchial:	n/a
14	chr19:43891866-43891916	PFSK-1	brain:	n/a
15	chr19:43911682-43911732	NB4	blood:	n/a
16	chr19:43918868-43918918	PrEC	prostate:	n/a
17	chr19:43918868-43918918	HRE	kidney:	n/a
18	chr19:43891281-43891331	IMR90	lung:	fetal
19	chr19:43922723-43922773	NH-A	brain:	n/a
20	chr19:43892826-43892876	HepG2	liver:	n/a
21	chr19:43892826-43892876	HEEpiC	esophagus:	n/a
22	chr19:43851787-43851837	HepG2	liver:	n/a
23	chr19:43911682-43911732	HRPEpiC	eye:	n/a
24	chr19:43891866-43891916	T-47D	breast:	n/a
25	chr19:43919003-43919053	K562	blood:	n/a
26	chr19:43919536-43919586	GM12892	blood:	n/a
27	chr19:43856594-43856644	NHDF-neo	bronchial:	n/a
28	chr19:43922723-43922773	GM06990	blood:	n/a
29	chr19:43866487-43866537	AoSMC	blood vessel:	n/a
30	chr19:43866487-43866537	A549	lung:	n/a
31	chr19:43851787-43851837	CMK	blood:	n/a
32	chr19:43916594-43916644	NB4	blood:	n/a
33	chr19:43858174-43858224	GM19239	blood:	n/a
34	chr19:43892826-43892876	HCM	heart:	n/a
35	chr19:43891281-43891331	A549	lung:	n/a
36	chr19:43858174-43858224	HNPCEpiC	eye:	n/a
37	chr19:43892826-43892876	NHDF-neo	bronchial:	n/a
38	chr19:43858174-43858224	HUVEC	blood vessel:	n/a
39	chr19:43919039-43919089	HCM	heart:	n/a
40	chr19:43918408-43918458	HCM	heart:	n/a
41	chr19:43918882-43918932	HEEpiC	esophagus:	n/a
42	chr19:43856746-43856796	HL-60	blood:	n/a
43	chr19:43891281-43891331	PrEC	prostate:	n/a
44	chr19:43919536-43919586	NT2-D1	testis:	n/a
45	chr19:43919039-43919089	PFSK-1	brain:	n/a
46	chr19:43918868-43918918	ProgFib	skin:	n/a
47	chr19:43856746-43856796	HCF	heart:	n/a
48	chr19:43922332-43922382	AG09309	skin:	n/a
49	chr19:43851787-43851837	IMR90	lung:	fetal
50	chr19:43918974-43919024	PFSK-1	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43909136..43910754-chr19:43912460..43914552,2	MCF-7	breast:
2	chr19:43835562..43838441-chr19:43843809..43845441,2	MCF-7	breast:
3	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
4	chr17:42852520..42853209-chr19:43915333..43915833,2	HCT-116	colon:
5	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
6	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
7	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
8	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
9	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
10	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
11	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
12	chr19:43820533..43821452-chr19:44166758..44167329,2	K562	blood:
13	chr19:43928435..43931381-chr19:43932773..43935782,3	K562	blood:
14	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
15	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
16	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
17	chr19:43857729..43859549-chr19:43967499..43969532,2	MCF-7	breast:
18	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
19	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
20	chr19:43928535..43930747-chr19:43966422..43969412,2	MCF-7	breast:
21	chr19:43928435..43931381-chr19:43932773..43935782,3	K562	blood:
22	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
23	chr1:117602243..117602763-chr19:43822533..43823090,2	Hela-S3	cervix:
24	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TEX101-2	chr19:43893587-43893979	expReg_chr19_6146_+
2	lnc-TEX101-1	chr19:43895826-43896306	expReg_chr19_6147_+
3	lnc-AC005392.1-1	chr19:43872546-43872658	NONHSAT066597
4	lnc-AC005392.1-1	chr19:43866622-43866779	ENSG00000272396.1
5	lnc-AC005392.1-1	chr19:43872981-43873122	ENSG00000272396.1
6	lnc-AC005392.1-1	chr19:43864837-43864995	ENSG00000272396.1
7	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
8	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
9	lnc-AC005392.1-1	chr19:43872981-43873227	NONHSAT066597
10	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
11	lnc-CD177-2	chr19:43853208-43853700	NONHSAT066596
12	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
13	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+

No data

Variant related genes	Relation type
CD177	TF binding region
CD177P1	TF binding region
ENSG00000231412	TF binding region
ENSG00000272396	TF binding region
CEACAMP11	TF binding region
CEACAMP4	TF binding region
TEX101	TF binding region
PSG9	TF binding region
CD177	CpG island
CD177P1	CpG island
ENSG00000231412	CpG island
ENSG00000272396	CpG island
CEACAMP11	CpG island
CEACAMP4	CpG island
TEX101	CpG island
PSG9	CpG island
ENSG00000073670	chromatin interactions
ENSG00000131126	chromatin interactions
ENSG00000231412	chromatin interactions
ENSG00000124466	chromatin interactions

Extended variants
information (count: 6086 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6086 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187169784	chr19:43777148-43777149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138334058	chr19:43777154-43777155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550404336	chr19:43777199-43777200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528912467	chr19:43777250-43777251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10405953	chr19:43777253-43777254	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191843490	chr19:43777254-43777255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552967130	chr19:43777263-43777264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369350014	chr19:43777274-43777275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566108795	chr19:43777294-43777295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183539480	chr19:43777300-43777301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555202380	chr19:43777331-43777332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530448154	chr19:43777337-43777338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73553925	chr19:43777351-43777352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557659965	chr19:43777352-43777353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578075184	chr19:43777361-43777362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540352103	chr19:43777388-43777389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35571250	chr19:43777389-43777390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75012652	chr19:43777391-43777392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560496982	chr19:43777472-43777473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200600533	chr19:43777475-43777476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369263454	chr19:43777476-43777477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372547009	chr19:43777483-43777484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543351130	chr19:43777486-43777487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148344715	chr19:43777503-43777504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533358015	chr19:43777530-43777531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10406606	chr19:43777536-43777537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs147480625	chr19:43777537-43777538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11670608	chr19:43777571-43777572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143836384	chr19:43777582-43777583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150604401	chr19:43777586-43777587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566140926	chr19:43777599-43777600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188985693	chr19:43777629-43777630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548567919	chr19:43777633-43777634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568854335	chr19:43777634-43777635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373459305	chr19:43777659-43777660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555465322	chr19:43777667-43777668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60735100	chr19:43777668-43777669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs62115918	chr19:43777690-43777691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs193111728	chr19:43777703-43777704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554264838	chr19:43777716-43777717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370490331	chr19:43777718-43777719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183675773	chr19:43777806-43777807	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373610284	chr19:43777827-43777828	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs186802985	chr19:43777861-43777862	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs562859747	chr19:43777870-43777871	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576707256	chr19:43777904-43777905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191643075	chr19:43777907-43777908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565496569	chr19:43777939-43777940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184135733	chr19:43777940-43777941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546292290	chr19:43777941-43777942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	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	21858162	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
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43772000-43778800	Weak transcription	NHDF-Ad	bronchial
2	chr19:43772200-43785200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:43774400-43784800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr19:43778600-43779000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr19:43778800-43779000	Enhancers	NHDF-Ad	bronchial
6	chr19:43788800-43789800	Enhancers	Hela-S3	cervix
7	chr19:43789800-43790000	Flanking Active TSS	Hela-S3	cervix
8	chr19:43790000-43790200	Enhancers	Hela-S3	cervix
9	chr19:43790200-43790800	Flanking Active TSS	Hela-S3	cervix
10	chr19:43790400-43790600	Enhancers	Colon Smooth Muscle	Colon
11	chr19:43790800-43791000	Enhancers	Hela-S3	cervix
12	chr19:43791000-43791200	Flanking Active TSS	Hela-S3	cervix
13	chr19:43791200-43792200	Enhancers	Hela-S3	cervix
14	chr19:43794000-43795800	ZNF genes & repeats	Adipose Nuclei	Adipose
15	chr19:43794200-43795400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
16	chr19:43794800-43795800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr19:43795000-43795400	Active TSS	Fetal Heart	heart
18	chr19:43795400-43795600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
19	chr19:43803800-43805800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:43804200-43804800	Enhancers	HMEC	breast
21	chr19:43804200-43805600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:43804400-43805600	Enhancers	NHEK	skin
23	chr19:43804400-43806000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr19:43804800-43810200	Weak transcription	HMEC	breast
25	chr19:43805600-43809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr19:43805600-43810200	Weak transcription	NHEK	skin
27	chr19:43805800-43810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr19:43806000-43809600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr19:43809600-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:43809800-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr19:43809800-43811200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr19:43810000-43811000	Enhancers	NHDF-Ad	bronchial
33	chr19:43810000-43811200	Enhancers	Hela-S3	cervix
34	chr19:43810200-43810400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr19:43810200-43810600	Enhancers	NHEK	skin
36	chr19:43810200-43810800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr19:43810200-43810800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr19:43810200-43810800	Enhancers	HMEC	breast
39	chr19:43810200-43811200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr19:43810400-43810600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:43810600-43811400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr19:43810800-43811200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr19:43811000-43812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:43811200-43814400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr19:43811200-43815800	Weak transcription	Hela-S3	cervix
46	chr19:43812000-43812800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr19:43814000-43815200	Enhancers	NHEK	skin
48	chr19:43814200-43814800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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