Variant report

Variant	nsv1063723
Chromosome Location	chr19:43669018-43846382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2911)
CpG islands
(count:1283)
Chromatin interactive
region (count:17)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2911 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
2	ATF1	chr19:43779068-43779071	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	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
8	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
9	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
10	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
11	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
12	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
13	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
15	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
16	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
18	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
21	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
23	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
24	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
31	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
32	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
34	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
37	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
39	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a
41	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
44	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
45	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
46	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
50	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43691878-43691928	HRPEpiC	eye:	n/a
2	chr19:43709754-43709804	GM12878	blood:	n/a
3	chr19:43691878-43691928	HRPEpiC	eye:	n/a
4	chr19:43709754-43709804	GM12878	blood:	n/a
5	chr19:43774820-43774870	HepG2	liver:	n/a
6	chr19:43709754-43709804	BJ	skin:	n/a
7	chr19:43680072-43680122	ProgFib	skin:	n/a
8	chr19:43690996-43691046	T-47D	breast:	n/a
9	chr19:43709360-43709410	AG04450	lung:	fetal
10	chr19:43691930-43691980	HNPCEpiC	eye:	n/a
11	chr19:43691878-43691928	MCF-7	breast:	n/a
12	chr19:43774921-43774971	PFSK-1	brain:	n/a
13	chr19:43711064-43711114	Caco-2	colon:	n/a
14	chr19:43773649-43773699	HepG2	liver:	n/a
15	chr19:43710277-43710327	Caco-2	colon:	n/a
16	chr19:43709360-43709410	GM19239	blood:	n/a
17	chr19:43709360-43709410	HCT-116	colon:	n/a
18	chr19:43711249-43711299	HIPEpiC	eye:	n/a
19	chr19:43711249-43711299	HCT-116	colon:	n/a
20	chr19:43691878-43691928	ovcar-3	ovarian:	n/a
21	chr19:43709832-43709882	Caco-2	colon:	n/a
22	chr19:43773649-43773699	SK-N-SH_RA	brain:	n/a
23	chr19:43774820-43774870	U87	brain:	n/a
24	chr19:43673501-43673551	CMK	blood:	n/a
25	chr19:43774982-43775032	ECC-1	luminal epithelium:	n/a
26	chr19:43697480-43697530	MCF-7	breast:	n/a
27	chr19:43710277-43710327	PFSK-1	brain:	n/a
28	chr19:43711249-43711299	U87	brain:	n/a
29	chr19:43711064-43711114	AG09319	gingival:	n/a
30	chr19:43709754-43709804	HCT-116	colon:	n/a
31	chr19:43769725-43769775	K562	blood:	n/a
32	chr19:43680072-43680122	RPTEC	kidney:	n/a
33	chr19:43774820-43774870	NT2-D1	testis:	n/a
34	chr19:43690622-43690672	GM06990	blood:	n/a
35	chr19:43673501-43673551	HCT-116	colon:	n/a
36	chr19:43683698-43683748	AG09309	skin:	n/a
37	chr19:43691930-43691980	SKMC	muscle:	n/a
38	chr19:43691878-43691928	GM06990	blood:	n/a
39	chr19:43709754-43709804	T-47D	breast:	n/a
40	chr19:43680072-43680122	AG09309	skin:	n/a
41	chr19:43691878-43691928	RPTEC	kidney:	n/a
42	chr19:43683698-43683748	AG04450	lung:	fetal
43	chr19:43709360-43709410	NH-A	brain:	n/a
44	chr19:43774921-43774971	NHBE	bronchial:	n/a
45	chr19:43774820-43774870	GM12892	blood:	n/a
46	chr19:43709360-43709410	PrEC	prostate:	n/a
47	chr19:43774982-43775032	SK-N-MC	brain:	n/a
48	chr19:43774921-43774971	Jurkat	blood:	n/a
49	chr19:43690622-43690672	A549	lung:	n/a
50	chr19:43709832-43709882	RPTEC	kidney:	n/a

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

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

(count:31 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 8161 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8161 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186571210	chr19:43669018-43669019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377246958	chr19:43669023-43669024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554105403	chr19:43669024-43669025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117812857	chr19:43669031-43669032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142843552	chr19:43669032-43669033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556353774	chr19:43669040-43669041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576181582	chr19:43669047-43669048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374137101	chr19:43669060-43669061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567755930	chr19:43669068-43669069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535741085	chr19:43669083-43669084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146544367	chr19:43669085-43669086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs62112088	chr19:43669110-43669111	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541065119	chr19:43669113-43669114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372793746	chr19:43669129-43669130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143489875	chr19:43669146-43669147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550228898	chr19:43669149-43669150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191343218	chr19:43669164-43669165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532605538	chr19:43669177-43669178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551411281	chr19:43669204-43669205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs59300109	chr19:43669228-43669229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146747577	chr19:43669244-43669245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35607352	chr19:43669246-43669247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374590910	chr19:43669261-43669262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140333353	chr19:43669262-43669263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567547875	chr19:43669311-43669312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183836929	chr19:43669319-43669320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs8108484	chr19:43669320-43669321	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188563000	chr19:43669369-43669370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181357671	chr19:43669373-43669374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558614471	chr19:43669388-43669389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576413316	chr19:43669390-43669391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201236882	chr19:43669399-43669400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368576706	chr19:43669400-43669401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560917210	chr19:43669401-43669402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574754908	chr19:43669402-43669403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185102358	chr19:43669417-43669418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563832126	chr19:43669419-43669420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532738349	chr19:43669423-43669424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552537195	chr19:43669439-43669440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4802156	chr19:43669453-43669454	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs527413376	chr19:43669456-43669457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112902538	chr19:43669461-43669462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567239040	chr19:43669475-43669476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190345321	chr19:43669488-43669489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550044127	chr19:43669489-43669490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375697030	chr19:43669490-43669491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569890524	chr19:43669564-43669565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11668113	chr19:43669591-43669592	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181985961	chr19:43669623-43669624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370905336	chr19:43669642-43669643	Enhancers 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:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43667800-43669200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr19:43668200-43669400	Enhancers	NHDF-Ad	bronchial
3	chr19:43668200-43671000	Enhancers	Placenta	Placenta
4	chr19:43669400-43669800	Weak transcription	NHDF-Ad	bronchial
5	chr19:43669800-43670000	Enhancers	NHDF-Ad	bronchial
6	chr19:43670000-43685000	Weak transcription	NHDF-Ad	bronchial
7	chr19:43671000-43674600	Weak transcription	Placenta	Placenta
8	chr19:43674600-43674800	Genic enhancers	Placenta	Placenta
9	chr19:43674600-43675000	Enhancers	Fetal Muscle Leg	muscle
10	chr19:43674800-43678800	Weak transcription	Placenta	Placenta
11	chr19:43678800-43680400	Enhancers	Placenta	Placenta
12	chr19:43680400-43681600	Weak transcription	Placenta	Placenta
13	chr19:43681600-43682200	Strong transcription	Placenta	Placenta
14	chr19:43681800-43683800	Enhancers	Liver	Liver
15	chr19:43682200-43682400	Genic enhancers	Placenta	Placenta
16	chr19:43682400-43683800	Enhancers	Placenta	Placenta
17	chr19:43683800-43685200	Weak transcription	Placenta	Placenta
18	chr19:43684000-43684200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:43684000-43684200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:43684000-43684200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:43684000-43684200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:43684000-43684200	Enhancers	A549	lung
23	chr19:43684000-43684200	Enhancers	Hela-S3	cervix
24	chr19:43684000-43684200	Enhancers	NHEK	skin
25	chr19:43684000-43684200	Enhancers	NHLF	lung
26	chr19:43684000-43684200	Enhancers	Osteobl	bone
27	chr19:43684000-43688400	Enhancers	HMEC	breast
28	chr19:43684200-43684800	Weak transcription	NHEK	skin
29	chr19:43684200-43685200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr19:43684200-43685200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr19:43684200-43685200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:43684200-43685200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr19:43684200-43685200	Weak transcription	A549	lung
34	chr19:43684200-43685200	Weak transcription	NHLF	lung
35	chr19:43684200-43685200	Weak transcription	Osteobl	bone
36	chr19:43684600-43685200	Weak transcription	Hela-S3	cervix
37	chr19:43684800-43685800	Enhancers	NHEK	skin
38	chr19:43685000-43685400	Genic enhancers	NHDF-Ad	bronchial
39	chr19:43685000-43686400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr19:43685000-43686600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:43685200-43685400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr19:43685200-43685400	Flanking Active TSS	Placenta	Placenta
43	chr19:43685200-43686000	Enhancers	A549	lung
44	chr19:43685200-43686200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:43685200-43686200	Enhancers	NH-A	brain
46	chr19:43685200-43686400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:43685200-43686600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr19:43685200-43686600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr19:43685200-43686600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:43685200-43686600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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