Variant report

Variant	nsv1057430
Chromosome Location	chr19:43663357-43838753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2915)
CpG islands
(count:1285)
Chromatin interactive
region (count:15)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2915 , 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	chr19:43779068-43779071	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	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
8	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
9	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
10	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
11	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
12	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
13	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
15	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
16	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
18	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
20	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	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	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
27	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
29	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
30	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
35	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
38	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
43	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
46	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
48	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
49	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
50	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43773649-43773699	HCT-116	colon:	n/a
2	chr19:43697480-43697530	MCF10A-Er-Src	breast:	n/a
3	chr19:43773649-43773699	AG04450	lung:	fetal
4	chr19:43690996-43691046	Caco-2	colon:	n/a
5	chr19:43773649-43773699	HCT-116	colon:	n/a
6	chr19:43697480-43697530	MCF10A-Er-Src	breast:	n/a
7	chr19:43773649-43773699	AG04450	lung:	fetal
8	chr19:43690996-43691046	Caco-2	colon:	n/a
9	chr19:43690622-43690672	HMEC	breast:	n/a
10	chr19:43709754-43709804	LNCaP	prostate:	n/a
11	chr19:43709360-43709410	AG04449	skin:	fetal
12	chr19:43774893-43774943	T-47D	breast:	n/a
13	chr19:43711249-43711299	AG09319	gingival:	n/a
14	chr19:43683698-43683748	SK-N-SH_RA	brain:	n/a
15	chr19:43680072-43680122	GM12892	blood:	n/a
16	chr19:43691930-43691980	ProgFib	skin:	n/a
17	chr19:43691878-43691928	HPAEpiC	pulmonary alveolar:	n/a
18	chr19:43690996-43691046	HCT-116	colon:	n/a
19	chr19:43769725-43769775	CMK	blood:	n/a
20	chr19:43711249-43711299	GM19239	blood:	n/a
21	chr19:43711064-43711114	GM06990	blood:	n/a
22	chr19:43774893-43774943	Hela-S3	cervix:	n/a
23	chr19:43711064-43711114	HNPCEpiC	eye:	n/a
24	chr19:43709654-43709704	BJ	skin:	n/a
25	chr19:43774820-43774870	CMK	blood:	n/a
26	chr19:43709832-43709882	ovcar-3	ovarian:	n/a
27	chr19:43709654-43709704	GM12878	blood:	n/a
28	chr19:43691878-43691928	Jurkat	blood:	n/a
29	chr19:43711249-43711299	H1-hESC	embryonic stem cell:	embryo
30	chr19:43709754-43709804	GM12891	blood:	n/a
31	chr19:43774982-43775032	RPTEC	kidney:	n/a
32	chr19:43690622-43690672	SKMC	muscle:	n/a
33	chr19:43774921-43774971	AG09319	gingival:	n/a
34	chr19:43709832-43709882	PrEC	prostate:	n/a
35	chr19:43709360-43709410	HRCEpiC	kidney:	n/a
36	chr19:43683698-43683748	GM12891	blood:	n/a
37	chr19:43709654-43709704	K562	blood:	n/a
38	chr19:43774893-43774943	GM12891	blood:	n/a
39	chr19:43691930-43691980	AG04450	lung:	fetal
40	chr19:43774982-43775032	BJ	skin:	n/a
41	chr19:43774820-43774870	AG04450	lung:	fetal
42	chr19:43774921-43774971	NB4	blood:	n/a
43	chr19:43711249-43711299	K562	blood:	n/a
44	chr19:43691878-43691928	GM19239	blood:	n/a
45	chr19:43673501-43673551	PANC-1	pancreas:	n/a
46	chr19:43709832-43709882	GM12892	blood:	n/a
47	chr19:43709654-43709704	ProgFib	skin:	n/a
48	chr19:43691930-43691980	SK-N-MC	brain:	n/a
49	chr19:43680072-43680122	GM12878	blood:	n/a
50	chr19:43710277-43710327	GM06990	blood:	n/a

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

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

(count:32 , 50 per page) page: 1

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

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
ENSG00000243137	chromatin interactions

Extended variants
information (count: 8143 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:8143 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571894762	chr19:43663373-43663374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534253875	chr19:43663382-43663383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554470965	chr19:43663390-43663391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78699563	chr19:43663508-43663509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542815292	chr19:43663539-43663540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555040033	chr19:43663608-43663609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142363445	chr19:43663622-43663623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543789758	chr19:43663662-43663663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566281399	chr19:43663681-43663682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563952111	chr19:43663703-43663704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187791386	chr19:43663711-43663712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540120720	chr19:43663725-43663726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200712228	chr19:43663742-43663743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376079155	chr19:43663758-43663759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529054171	chr19:43663761-43663762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192409431	chr19:43663811-43663812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562963694	chr19:43663845-43663846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183134062	chr19:43663873-43663874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551729973	chr19:43663891-43663892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143226158	chr19:43663908-43663909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188025458	chr19:43663923-43663924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547735003	chr19:43663942-43663943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34995907	chr19:43663960-43663961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146197710	chr19:43663967-43663968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562243046	chr19:43663970-43663971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536437869	chr19:43664055-43664056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372382239	chr19:43664057-43664058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148284507	chr19:43664076-43664077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141335317	chr19:43664100-43664101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562548341	chr19:43664116-43664117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557847716	chr19:43664153-43664154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112487193	chr19:43664167-43664168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs193020229	chr19:43664171-43664172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530258690	chr19:43664265-43664266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377000930	chr19:43664283-43664284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537484384	chr19:43664300-43664301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542831083	chr19:43664345-43664346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150365081	chr19:43664352-43664353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375589570	chr19:43664356-43664357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531558597	chr19:43664462-43664463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184494994	chr19:43664479-43664480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189201949	chr19:43664483-43664484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527681557	chr19:43664501-43664502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547809412	chr19:43664514-43664515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567603118	chr19:43664556-43664557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536576815	chr19:43664592-43664593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192448974	chr19:43664597-43664598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138035446	chr19:43664603-43664604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539230010	chr19:43664607-43664608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142532060	chr19:43664612-43664613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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

Chromatin state (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43654400-43668200	Weak transcription	NHDF-Ad	bronchial
2	chr19:43655600-43665200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:43662600-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:43662800-43663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr19:43662800-43663400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:43662800-43663600	Enhancers	A549	lung
7	chr19:43663000-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr19:43663000-43663600	Enhancers	NHEK	skin
9	chr19:43663200-43663400	Enhancers	HSMMtube	muscle
10	chr19:43663200-43663600	Enhancers	HMEC	breast
11	chr19:43663600-43666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr19:43663600-43666000	Weak transcription	HMEC	breast
13	chr19:43663600-43666000	Weak transcription	NHEK	skin
14	chr19:43663600-43668200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:43664000-43666200	Weak transcription	HSMMtube	muscle
16	chr19:43665200-43666000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr19:43665600-43666200	Enhancers	Placenta	Placenta
18	chr19:43666000-43666400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:43666000-43666800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr19:43666000-43667200	Enhancers	HMEC	breast
21	chr19:43666000-43668600	Enhancers	NHEK	skin
22	chr19:43666200-43666400	Enhancers	HSMMtube	muscle
23	chr19:43666200-43668200	Weak transcription	Placenta	Placenta
24	chr19:43666400-43666600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr19:43666400-43667800	Enhancers	A549	lung
26	chr19:43666400-43668200	Weak transcription	HSMMtube	muscle
27	chr19:43666600-43667800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr19:43666800-43668000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr19:43667000-43668600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr19:43667200-43668200	Weak transcription	HMEC	breast
31	chr19:43667600-43668800	Enhancers	Hela-S3	cervix
32	chr19:43667800-43668000	Flanking Active TSS	A549	lung
33	chr19:43667800-43669200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr19:43668000-43668600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:43668000-43668800	Enhancers	A549	lung
36	chr19:43668200-43668600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr19:43668200-43668600	Enhancers	Fetal Muscle Trunk	muscle
38	chr19:43668200-43668600	Enhancers	HMEC	breast
39	chr19:43668200-43669000	Enhancers	HSMMtube	muscle
40	chr19:43668200-43669400	Enhancers	NHDF-Ad	bronchial
41	chr19:43668200-43671000	Enhancers	Placenta	Placenta
42	chr19:43668400-43669000	Enhancers	Fetal Muscle Leg	muscle
43	chr19:43669400-43669800	Weak transcription	NHDF-Ad	bronchial
44	chr19:43669800-43670000	Enhancers	NHDF-Ad	bronchial
45	chr19:43670000-43685000	Weak transcription	NHDF-Ad	bronchial
46	chr19:43671000-43674600	Weak transcription	Placenta	Placenta
47	chr19:43674600-43674800	Genic enhancers	Placenta	Placenta
48	chr19:43674600-43675000	Enhancers	Fetal Muscle Leg	muscle
49	chr19:43674800-43678800	Weak transcription	Placenta	Placenta
50	chr19:43678800-43680400	Enhancers	Placenta	Placenta

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