Variant report

Variant	nsv1061385
Chromosome Location	chr19:43642540-43846382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3032)
CpG islands
(count:1286)
Chromatin interactive
region (count:17)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3032 , 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	chr19:43822401-43822627	K562	blood:	n/a	n/a
6	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
8	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
9	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
10	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
11	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
12	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
13	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
15	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
16	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
18	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
20	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	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	chr19:43759754-43759856	K562	blood:	n/a	n/a
25	CEBPB	chr19:43656430-43656683	A549	lung:	n/a	chr19:43656521-43656532
26	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
29	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
31	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
32	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
36	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
38	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
42	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
44	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43656349-43656822	Hela-S3	cervix:	n/a	chr19:43656521-43656532
48	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
50	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43690622-43690672	H1-hESC	embryonic stem cell:	embryo
2	chr19:43709754-43709804	Hepatocyte	liver:	n/a
3	chr19:43773649-43773699	SK-N-SH	brain:	n/a
4	chr19:43680072-43680122	AG09319	gingival:	n/a
5	chr19:43710277-43710327	AG04450	lung:	fetal
6	chr19:43690622-43690672	H1-hESC	embryonic stem cell:	embryo
7	chr19:43709754-43709804	Hepatocyte	liver:	n/a
8	chr19:43773649-43773699	SK-N-SH	brain:	n/a
9	chr19:43680072-43680122	AG09319	gingival:	n/a
10	chr19:43710277-43710327	AG04450	lung:	fetal
11	chr19:43711249-43711299	HL-60	blood:	n/a
12	chr19:43673501-43673551	PANC-1	pancreas:	n/a
13	chr19:43769725-43769775	HRE	kidney:	n/a
14	chr19:43691930-43691980	K562	blood:	n/a
15	chr19:43773649-43773699	LNCaP	prostate:	n/a
16	chr19:43711064-43711114	H1-hESC	embryonic stem cell:	embryo
17	chr19:43697480-43697530	HEEpiC	esophagus:	n/a
18	chr19:43774921-43774971	SK-N-MC	brain:	n/a
19	chr19:43774820-43774870	AG10803	skin:	n/a
20	chr19:43774893-43774943	HEEpiC	esophagus:	n/a
21	chr19:43690996-43691046	H1-hESC	embryonic stem cell:	embryo
22	chr19:43774893-43774943	HMEC	breast:	n/a
23	chr19:43690622-43690672	HMEC	breast:	n/a
24	chr19:43690622-43690672	A549	lung:	n/a
25	chr19:43680072-43680122	IMR90	lung:	fetal
26	chr19:43709832-43709882	HCM	heart:	n/a
27	chr19:43773649-43773699	HCPEpiC	choroid plexus:	n/a
28	chr19:43690622-43690672	GM06990	blood:	n/a
29	chr19:43711249-43711299	AG04450	lung:	fetal
30	chr19:43673501-43673551	HAEpiC	amniotic membrane:	n/a
31	chr19:43673501-43673551	GM06990	blood:	n/a
32	chr19:43711249-43711299	MCF-7	breast:	n/a
33	chr19:43709360-43709410	RPTEC	kidney:	n/a
34	chr19:43709360-43709410	HCT-116	colon:	n/a
35	chr19:43709832-43709882	ProgFib	skin:	n/a
36	chr19:43773649-43773699	A549	lung:	n/a
37	chr19:43709832-43709882	BJ	skin:	n/a
38	chr19:43773649-43773699	HCF	heart:	n/a
39	chr19:43709360-43709410	HCPEpiC	choroid plexus:	n/a
40	chr19:43711064-43711114	HCM	heart:	n/a
41	chr19:43774982-43775032	ECC-1	luminal epithelium:	n/a
42	chr19:43709360-43709410	NT2-D1	testis:	n/a
43	chr19:43774893-43774943	HNPCEpiC	eye:	n/a
44	chr19:43683698-43683748	HCPEpiC	choroid plexus:	n/a
45	chr19:43683698-43683748	GM12891	blood:	n/a
46	chr19:43709754-43709804	PANC-1	pancreas:	n/a
47	chr19:43709832-43709882	HCPEpiC	choroid plexus:	n/a
48	chr19:43774921-43774971	RPTEC	kidney:	n/a
49	chr19:43709754-43709804	HNPCEpiC	eye:	n/a
50	chr19:43709654-43709704	HPAEpiC	pulmonary alveolar:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 9541 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9541 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200757581	chr19:43642547-43642548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539119191	chr19:43642567-43642568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146665396	chr19:43642588-43642589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577400913	chr19:43642594-43642595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73564155	chr19:43642596-43642597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541031757	chr19:43642646-43642647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141471295	chr19:43642658-43642659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574984254	chr19:43642664-43642665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190370843	chr19:43642706-43642707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3925330	chr19:43642832-43642833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs532598018	chr19:43642857-43642858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149854545	chr19:43642888-43642889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113169092	chr19:43642934-43642935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145841981	chr19:43642938-43642939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182922154	chr19:43642940-43642941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547032976	chr19:43642971-43642972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186077383	chr19:43642980-43642981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529937461	chr19:43642986-43642987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148986735	chr19:43642994-43642995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116597497	chr19:43643037-43643038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538807204	chr19:43643089-43643090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558800292	chr19:43643132-43643133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369753697	chr19:43643144-43643145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143754915	chr19:43643153-43643154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202197388	chr19:43643157-43643158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190881443	chr19:43643167-43643168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554661139	chr19:43643292-43643293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35623923	chr19:43643319-43643320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563164604	chr19:43643338-43643339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574813779	chr19:43643377-43643378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2078350	chr19:43643378-43643379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs557800612	chr19:43643385-43643386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549074126	chr19:43643396-43643397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557207392	chr19:43643398-43643399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372192716	chr19:43643410-43643411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376566241	chr19:43643413-43643414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138418211	chr19:43643429-43643430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559902049	chr19:43643431-43643432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571594352	chr19:43643501-43643502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371931867	chr19:43643502-43643503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184066464	chr19:43643578-43643579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142428637	chr19:43643580-43643581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35561656	chr19:43643607-43643608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34949453	chr19:43643613-43643614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560707242	chr19:43643620-43643621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529721011	chr19:43643662-43643663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549824465	chr19:43643741-43643742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569931343	chr19:43643756-43643757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532457175	chr19:43643819-43643820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552352229	chr19:43643820-43643821	Weak transcription	n/a	n/a	Overlapped CNVs	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:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43636000-43651800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:43637400-43645600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:43645200-43645800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr19:43645400-43646600	Enhancers	Osteobl	bone
5	chr19:43645400-43646800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:43645600-43646000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr19:43645600-43646200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr19:43645600-43646600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr19:43645600-43647000	Enhancers	NHDF-Ad	bronchial
10	chr19:43646000-43651800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr19:43646200-43649600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr19:43646600-43649600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr19:43646600-43652200	Weak transcription	Osteobl	bone
14	chr19:43646800-43652000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr19:43647000-43651800	Weak transcription	NHDF-Ad	bronchial
16	chr19:43649600-43650000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr19:43649600-43650000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr19:43650000-43652200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr19:43650800-43652200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr19:43650800-43654600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:43650800-43655400	Enhancers	NHEK	skin
22	chr19:43651400-43652200	Enhancers	Esophagus	oesophagus
23	chr19:43651400-43654400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr19:43651600-43654400	Enhancers	HMEC	breast
25	chr19:43651800-43652800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:43651800-43653000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr19:43651800-43653800	Enhancers	NHDF-Ad	bronchial
28	chr19:43652000-43652600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr19:43652000-43653000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr19:43652200-43653200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr19:43652200-43653200	Enhancers	Osteobl	bone
32	chr19:43652200-43655200	Weak transcription	Esophagus	oesophagus
33	chr19:43652400-43652800	Enhancers	Placenta Amnion	Placenta Amnion
34	chr19:43652600-43654400	Enhancers	NHLF	lung
35	chr19:43652800-43653600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:43653000-43654000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr19:43653200-43654200	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr19:43653200-43656400	Weak transcription	Osteobl	bone
39	chr19:43653600-43654200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr19:43653600-43654400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:43653800-43654200	Enhancers	Brain Cingulate Gyrus	brain
42	chr19:43653800-43654200	Weak transcription	NHDF-Ad	bronchial
43	chr19:43654000-43655000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr19:43654200-43654400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr19:43654200-43654400	Enhancers	NHDF-Ad	bronchial
46	chr19:43654400-43656000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr19:43654400-43668200	Weak transcription	NHDF-Ad	bronchial
48	chr19:43654600-43655000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr19:43655000-43655400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr19:43655000-43655600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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