Variant report

Variant	nsv1056122
Chromosome Location	chr19:43647978-43846382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3024)
CpG islands
(count:1282)
Chromatin interactive
region (count:17)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3024 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

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	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
3	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
4	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
7	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
8	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
9	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
10	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
11	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
12	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
13	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
15	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
16	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
18	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
22	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
23	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
24	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr19:43656390-43656701	K562	blood:	n/a	chr19:43656521-43656532
27	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
28	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43656366-43656852	IMR90	lung:	n/a	chr19:43656521-43656532
30	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
31	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
33	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
35	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr19:43656430-43656683	A549	lung:	n/a	chr19:43656521-43656532
38	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
43	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
48	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
49	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
50	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774893-43774943	NHBE	bronchial:	n/a
2	chr19:43774893-43774943	NHBE	bronchial:	n/a
3	chr19:43773649-43773699	HEK293	kidney:	embryo
4	chr19:43711249-43711299	HEEpiC	esophagus:	n/a
5	chr19:43710277-43710327	Hepatocyte	liver:	n/a
6	chr19:43774893-43774943	ProgFib	skin:	n/a
7	chr19:43774893-43774943	HAEpiC	amniotic membrane:	n/a
8	chr19:43690996-43691046	HEK293	kidney:	embryo
9	chr19:43774820-43774870	MCF10A-Er-Src	breast:	n/a
10	chr19:43709832-43709882	H1-hESC	embryonic stem cell:	embryo
11	chr19:43673501-43673551	Caco-2	colon:	n/a
12	chr19:43709654-43709704	HNPCEpiC	eye:	n/a
13	chr19:43691878-43691928	HNPCEpiC	eye:	n/a
14	chr19:43711064-43711114	GM19239	blood:	n/a
15	chr19:43709654-43709704	HCT-116	colon:	n/a
16	chr19:43709360-43709410	AoSMC	blood vessel:	n/a
17	chr19:43709360-43709410	HRPEpiC	eye:	n/a
18	chr19:43774982-43775032	Caco-2	colon:	n/a
19	chr19:43680072-43680122	SK-N-SH	brain:	n/a
20	chr19:43697480-43697530	NHDF-neo	bronchial:	n/a
21	chr19:43774982-43775032	HUVEC	blood vessel:	n/a
22	chr19:43774982-43775032	PrEC	prostate:	n/a
23	chr19:43711064-43711114	PrEC	prostate:	n/a
24	chr19:43691930-43691980	BJ	skin:	n/a
25	chr19:43774820-43774870	HCM	heart:	n/a
26	chr19:43709654-43709704	NHBE	bronchial:	n/a
27	chr19:43691930-43691980	PANC-1	pancreas:	n/a
28	chr19:43709754-43709804	HPAEpiC	pulmonary alveolar:	n/a
29	chr19:43709360-43709410	PFSK-1	brain:	n/a
30	chr19:43774921-43774971	AG10803	skin:	n/a
31	chr19:43710277-43710327	HepG2	liver:	n/a
32	chr19:43774820-43774870	SKMC	muscle:	n/a
33	chr19:43711249-43711299	HCM	heart:	n/a
34	chr19:43697480-43697530	ECC-1	luminal epithelium:	n/a
35	chr19:43773649-43773699	Hela-S3	cervix:	n/a
36	chr19:43711249-43711299	ProgFib	skin:	n/a
37	chr19:43709654-43709704	AG04450	lung:	fetal
38	chr19:43709832-43709882	HIPEpiC	eye:	n/a
39	chr19:43774893-43774943	SK-N-SH	brain:	n/a
40	chr19:43691878-43691928	Hela-S3	cervix:	n/a
41	chr19:43774893-43774943	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:43697480-43697530	MCF10A-Er-Src	breast:	n/a
43	chr19:43697480-43697530	K562	blood:	n/a
44	chr19:43697480-43697530	MCF-7	breast:	n/a
45	chr19:43691878-43691928	K562	blood:	n/a
46	chr19:43691878-43691928	HCM	heart:	n/a
47	chr19:43774982-43775032	SK-N-MC	brain:	n/a
48	chr19:43711249-43711299	HepG2	liver:	n/a
49	chr19:43709654-43709704	NB4	blood:	n/a
50	chr19:43774982-43775032	NT2-D1	testis:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
2	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
3	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
4	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
5	chr19:43835562..43838441-chr19:43843809..43845441,2	MCF-7	breast:
6	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
7	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
8	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
9	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
10	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
11	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
12	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
13	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
14	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
15	chr1:117602243..117602763-chr19:43822533..43823090,2	Hela-S3	cervix:
16	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
17	chr19:43820533..43821452-chr19:44166758..44167329,2	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
2	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
3	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
4	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
5	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
6	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
7	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
8	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
9	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
10	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
11	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
12	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
13	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
14	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
15	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
16	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
17	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
18	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
19	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
20	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
21	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
22	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
23	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+
24	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
25	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
26	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
27	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
28	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
29	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
30	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
31	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
32	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
33	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
34	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
35	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
36	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1

No data

Variant related genes	Relation type
ENSG00000231412	TF binding region
PSG5	TF binding region
CEACAMP4	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	TF binding region
CEACAMP11	TF binding region
ENSG00000227606	TF binding region
ENSG00000231412	CpG island
PSG5	CpG island
CEACAMP4	CpG island
CEACAMP10	CpG island
PSG9	CpG island
PSG4	CpG island
CEACAMP11	CpG island
ENSG00000227606	CpG island
ENSG00000243137	chromatin interactions
ENSG00000231412	chromatin interactions

Extended variants
information (count: 9250 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9250 , 50 per page) page: 1 2 3 4 5 6 7 ... 185

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2354278	chr19:43647978-43647979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548305752	chr19:43647980-43647981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575031410	chr19:43647984-43647985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4441378	chr19:43648006-43648007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs139463676	chr19:43648014-43648015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550571185	chr19:43648044-43648045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571079581	chr19:43648063-43648064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6509060	chr19:43648074-43648075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs371031818	chr19:43648100-43648101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553523397	chr19:43648112-43648113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112907351	chr19:43648114-43648115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373593522	chr19:43648164-43648165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144854463	chr19:43648249-43648250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111460020	chr19:43648264-43648265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534683515	chr19:43648276-43648277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554676255	chr19:43648295-43648296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574600222	chr19:43648324-43648325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs62112074	chr19:43648346-43648347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556683732	chr19:43648436-43648437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200002758	chr19:43648437-43648438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188847855	chr19:43648477-43648478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545817128	chr19:43648534-43648535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374595444	chr19:43648584-43648585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559479487	chr19:43648606-43648607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528245674	chr19:43648621-43648622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541641324	chr19:43648648-43648649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs193086057	chr19:43648695-43648696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530915310	chr19:43648762-43648763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550950538	chr19:43648766-43648767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570798839	chr19:43648772-43648773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140948891	chr19:43648777-43648778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547004717	chr19:43648796-43648797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567174412	chr19:43648806-43648807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536023164	chr19:43648814-43648815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549605047	chr19:43648816-43648817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10425900	chr19:43648818-43648819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537187801	chr19:43648823-43648824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2354277	chr19:43648838-43648839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs576794637	chr19:43648849-43648850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115761842	chr19:43648866-43648867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367867211	chr19:43648867-43648868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552960310	chr19:43648868-43648869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186582504	chr19:43648899-43648900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572814065	chr19:43648922-43648923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534578751	chr19:43648986-43648987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112036028	chr19:43648988-43648989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376420780	chr19:43649008-43649009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368870579	chr19:43649032-43649033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56151169	chr19:43649057-43649058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56203109	chr19:43649067-43649068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	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:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43636000-43651800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:43646000-43651800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:43646200-43649600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr19:43646600-43649600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr19:43646600-43652200	Weak transcription	Osteobl	bone
6	chr19:43646800-43652000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr19:43647000-43651800	Weak transcription	NHDF-Ad	bronchial
8	chr19:43649600-43650000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr19:43649600-43650000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr19:43650000-43652200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr19:43650800-43652200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr19:43650800-43654600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr19:43650800-43655400	Enhancers	NHEK	skin
14	chr19:43651400-43652200	Enhancers	Esophagus	oesophagus
15	chr19:43651400-43654400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr19:43651600-43654400	Enhancers	HMEC	breast
17	chr19:43651800-43652800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr19:43651800-43653000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:43651800-43653800	Enhancers	NHDF-Ad	bronchial
20	chr19:43652000-43652600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr19:43652000-43653000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr19:43652200-43653200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr19:43652200-43653200	Enhancers	Osteobl	bone
24	chr19:43652200-43655200	Weak transcription	Esophagus	oesophagus
25	chr19:43652400-43652800	Enhancers	Placenta Amnion	Placenta Amnion
26	chr19:43652600-43654400	Enhancers	NHLF	lung
27	chr19:43652800-43653600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr19:43653000-43654000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:43653200-43654200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr19:43653200-43656400	Weak transcription	Osteobl	bone
31	chr19:43653600-43654200	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr19:43653600-43654400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr19:43653800-43654200	Enhancers	Brain Cingulate Gyrus	brain
34	chr19:43653800-43654200	Weak transcription	NHDF-Ad	bronchial
35	chr19:43654000-43655000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:43654200-43654400	Enhancers	Muscle Satellite Cultured Cells	--
37	chr19:43654200-43654400	Enhancers	NHDF-Ad	bronchial
38	chr19:43654400-43656000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:43654400-43668200	Weak transcription	NHDF-Ad	bronchial
40	chr19:43654600-43655000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr19:43655000-43655400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr19:43655000-43655600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr19:43655200-43655600	Enhancers	Esophagus	oesophagus
44	chr19:43655400-43655600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr19:43655600-43656600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:43655600-43656800	Weak transcription	Esophagus	oesophagus
47	chr19:43655600-43665200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr19:43656000-43657000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr19:43656400-43656800	Enhancers	Osteobl	bone
50	chr19:43656600-43657000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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