Variant report

Variant	nsv579834
Chromosome Location	chr19:43765830-43845593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1421)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1421 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

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	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
6	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
7	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
9	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
10	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
14	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
15	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
16	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
22	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
23	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
24	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
25	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
28	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
30	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPD	chr19:43818150-43818430	K562	blood:	n/a	n/a
33	CHD1	chr19:43778774-43779172	IMR90	lung:	n/a	n/a
34	CHD2	chr19:43820096-43820344	K562	blood:	n/a	n/a
35	CHD2	chr19:43820019-43820330	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr19:43790318-43790669	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr19:43833232-43833538	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr19:43820875-43821218	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr19:43769435-43769730	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr19:43809940-43810090	SK-N-SH_RA	brain:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
41	CTCF	chr19:43837380-43837530	HCT-116	colon:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
42	CTCF	chr19:43809939-43810026	Gliobla	brain:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
43	CTCF	chr19:43820901-43821199	MCF-7	breast:	n/a	n/a
44	CTCF	chr19:43775420-43775570	HepG2	liver:	n/a	chr19:43775423-43775439 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437
45	CTCF	chr19:43820820-43821110	GM12872	blood:	n/a	n/a
46	CTCF	chr19:43778972-43779169	GM12891	blood:	n/a	n/a
47	CTCF	chr19:43837360-43837510	Caco-2	colon:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
48	CTCF	chr19:43820960-43821110	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr19:43837320-43837470	HFF-Myc	foreskin:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
50	CTCF	chr19:43775380-43775530	NB4	blood:	n/a	chr19:43775423-43775439 chr19:43775417-43775438 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774820-43774870	SKMC	muscle:	n/a
2	chr19:43769725-43769775	HIPEpiC	eye:	n/a
3	chr19:43774982-43775032	Hepatocyte	liver:	n/a
4	chr19:43774820-43774870	HIPEpiC	eye:	n/a
5	chr19:43774982-43775032	PANC-1	pancreas:	n/a
6	chr19:43773649-43773699	AG04450	lung:	fetal
7	chr19:43773649-43773699	NHBE	bronchial:	n/a
8	chr19:43774921-43774971	HEEpiC	esophagus:	n/a
9	chr19:43769725-43769775	K562	blood:	n/a
10	chr19:43774921-43774971	GM12878	blood:	n/a
11	chr19:43774820-43774870	AG04450	lung:	fetal
12	chr19:43769725-43769775	H1-hESC	embryonic stem cell:	embryo
13	chr19:43774982-43775032	PFSK-1	brain:	n/a
14	chr19:43774893-43774943	SAEC	small airway:	n/a
15	chr19:43774893-43774943	HRE	kidney:	n/a
16	chr19:43769725-43769775	PrEC	prostate:	n/a
17	chr19:43773649-43773699	GM19239	blood:	n/a
18	chr19:43774921-43774971	T-47D	breast:	n/a
19	chr19:43774982-43775032	K562	blood:	n/a
20	chr19:43774893-43774943	HL-60	blood:	n/a
21	chr19:43774893-43774943	ovcar-3	ovarian:	n/a
22	chr19:43774921-43774971	ovcar-3	ovarian:	n/a
23	chr19:43769725-43769775	SK-N-MC	brain:	n/a
24	chr19:43774893-43774943	NT2-D1	testis:	n/a
25	chr19:43773649-43773699	AG09309	skin:	n/a
26	chr19:43774982-43775032	GM19239	blood:	n/a
27	chr19:43774982-43775032	AG10803	skin:	n/a
28	chr19:43773649-43773699	BJ	skin:	n/a
29	chr19:43774893-43774943	Hepatocyte	liver:	n/a
30	chr19:43774893-43774943	HPAEpiC	pulmonary alveolar:	n/a
31	chr19:43769725-43769775	HepG2	liver:	n/a
32	chr19:43774893-43774943	IMR90	lung:	fetal
33	chr19:43774893-43774943	Caco-2	colon:	n/a
34	chr19:43774820-43774870	HCF	heart:	n/a
35	chr19:43769725-43769775	HAEpiC	amniotic membrane:	n/a
36	chr19:43774820-43774870	AG09319	gingival:	n/a
37	chr19:43774982-43775032	SK-N-SH	brain:	n/a
38	chr19:43774921-43774971	HRPEpiC	eye:	n/a
39	chr19:43773649-43773699	Caco-2	colon:	n/a
40	chr19:43774893-43774943	SK-N-SH_RA	brain:	n/a
41	chr19:43774820-43774870	AG04449	skin:	fetal
42	chr19:43773649-43773699	HCT-116	colon:	n/a
43	chr19:43774982-43775032	HNPCEpiC	eye:	n/a
44	chr19:43774893-43774943	MCF-7	breast:	n/a
45	chr19:43774820-43774870	AoSMC	blood vessel:	n/a
46	chr19:43769725-43769775	GM12891	blood:	n/a
47	chr19:43769725-43769775	HRE	kidney:	n/a
48	chr19:43774982-43775032	HRE	kidney:	n/a
49	chr19:43774893-43774943	NHBE	bronchial:	n/a
50	chr19:43774820-43774870	SK-N-SH	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
2	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
3	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
4	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
5	chr19:43820533..43821452-chr19:44166758..44167329,2	K562	blood:
6	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
7	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
8	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
9	chr19:43835562..43838441-chr19:43843809..43845441,2	MCF-7	breast:
10	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
11	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
12	chr1:117602243..117602763-chr19:43822533..43823090,2	Hela-S3	cervix:
13	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
14	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
15	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
2	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
3	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+
4	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
5	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594

No data

Variant related genes	Relation type
ENSG00000231412	TF binding region
CEACAMP4	TF binding region
PSG9	TF binding region
CEACAMP11	TF binding region
ENSG00000231412	CpG island
CEACAMP4	CpG island
PSG9	CpG island
CEACAMP11	CpG island
ENSG00000231412	chromatin interactions

Extended variants
information (count: 3508 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3508 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2074924	chr19:43765830-43765831	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530101403	chr19:43765834-43765835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185913740	chr19:43765860-43765861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564005979	chr19:43765869-43765870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532739864	chr19:43765876-43765877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552824795	chr19:43765885-43765886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566174398	chr19:43765892-43765893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535196736	chr19:43765913-43765914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56778279	chr19:43765938-43765939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs202030512	chr19:43765953-43765954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370730360	chr19:43765976-43765977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566986004	chr19:43765977-43765978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535851367	chr19:43765981-43765982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368574819	chr19:43765982-43765983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372374176	chr19:43766001-43766002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190735378	chr19:43766002-43766003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146026908	chr19:43766003-43766004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372741250	chr19:43766004-43766005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182343176	chr19:43766011-43766012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143780806	chr19:43766012-43766013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376174131	chr19:43766036-43766037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147736357	chr19:43766041-43766042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561377120	chr19:43766042-43766043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574939024	chr19:43766043-43766044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115363320	chr19:43766044-43766045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369317952	chr19:43766062-43766063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374080524	chr19:43766063-43766064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139045153	chr19:43766081-43766082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10417534	chr19:43766082-43766083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs150423600	chr19:43766087-43766088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138237862	chr19:43766088-43766089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552620945	chr19:43766089-43766090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149501197	chr19:43766095-43766096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146007230	chr19:43766097-43766098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548331593	chr19:43766104-43766105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561846842	chr19:43766108-43766109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568316162	chr19:43766111-43766112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139948336	chr19:43766112-43766113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143377407	chr19:43766113-43766114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141864275	chr19:43766128-43766129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146285613	chr19:43766132-43766133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139088828	chr19:43766133-43766134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142524489	chr19:43766156-43766157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371224482	chr19:43766164-43766165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373945115	chr19:43766171-43766172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149244305	chr19:43766182-43766183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187446101	chr19:43766188-43766189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150952802	chr19:43766196-43766197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146712977	chr19:43766202-43766203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201627278	chr19:43766211-43766212	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43765600-43766200	Weak transcription	Placenta	Placenta
2	chr19:43766200-43767200	Enhancers	Placenta	Placenta
3	chr19:43767000-43767200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr19:43767200-43767600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr19:43767200-43767600	Enhancers	HMEC	breast
6	chr19:43767200-43767800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr19:43767200-43768000	Weak transcription	Placenta	Placenta
8	chr19:43767200-43772000	Enhancers	NHDF-Ad	bronchial
9	chr19:43767600-43768000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr19:43767600-43768000	Weak transcription	HMEC	breast
11	chr19:43767800-43770400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr19:43768000-43768200	Active TSS	Placenta	Placenta
13	chr19:43768000-43769800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr19:43768000-43770200	Enhancers	A549	lung
15	chr19:43768000-43771600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr19:43768000-43771600	Enhancers	HMEC	breast
17	chr19:43768200-43768400	Flanking Active TSS	Placenta	Placenta
18	chr19:43768200-43769800	Enhancers	NHEK	skin
19	chr19:43768200-43771200	Enhancers	NH-A	brain
20	chr19:43768200-43771400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr19:43768200-43771600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr19:43768200-43771600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr19:43768200-43771600	Enhancers	Osteobl	bone
24	chr19:43768200-43772000	Enhancers	Hela-S3	cervix
25	chr19:43768200-43772200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:43768400-43768800	Enhancers	Placenta	Placenta
27	chr19:43768800-43769200	Flanking Active TSS	Placenta	Placenta
28	chr19:43768800-43769400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr19:43768800-43771400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr19:43769000-43769200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:43769000-43769200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr19:43769000-43770400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr19:43769000-43771600	Enhancers	NHLF	lung
34	chr19:43769200-43770000	Active TSS	Placenta	Placenta
35	chr19:43769400-43770200	Enhancers	Fetal Intestine Large	intestine
36	chr19:43769400-43770600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr19:43769800-43770000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr19:43769800-43770000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr19:43769800-43770200	Enhancers	HSMM	muscle
40	chr19:43769800-43770200	Flanking Active TSS	NHEK	skin
41	chr19:43770000-43770400	Flanking Active TSS	Placenta	Placenta
42	chr19:43770000-43770800	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr19:43770200-43770600	Weak transcription	A549	lung
44	chr19:43770200-43772000	Enhancers	NHEK	skin
45	chr19:43770400-43770800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr19:43770400-43771000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr19:43770400-43773200	Active TSS	Placenta	Placenta
48	chr19:43770600-43771400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr19:43770600-43771400	Enhancers	A549	lung
50	chr19:43770800-43771000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast

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