Variant report

Variant	esv1850151
Chromosome Location	chr19:43674470-43840095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2872)
CpG islands
(count:1222)
Chromatin interactive
region (count:15)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2872 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

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	chr19:43822401-43822627	K562	blood:	n/a	n/a
5	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
8	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
9	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
10	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
11	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
12	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
13	BATF	chr19:43692397-43692675	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	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	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	chr19:43685962-43686735	A549	lung:	n/a	n/a
25	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a
26	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43829661-43830104	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	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
31	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
35	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
37	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
39	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
42	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
43	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
45	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774921-43774971	SK-N-SH	brain:	n/a
2	chr19:43710277-43710327	HMEC	breast:	n/a
3	chr19:43774921-43774971	SK-N-SH	brain:	n/a
4	chr19:43710277-43710327	HMEC	breast:	n/a
5	chr19:43774893-43774943	NB4	blood:	n/a
6	chr19:43774982-43775032	U87	brain:	n/a
7	chr19:43709754-43709804	HNPCEpiC	eye:	n/a
8	chr19:43690996-43691046	RPTEC	kidney:	n/a
9	chr19:43774820-43774870	HRCEpiC	kidney:	n/a
10	chr19:43683698-43683748	HNPCEpiC	eye:	n/a
11	chr19:43690622-43690672	HIPEpiC	eye:	n/a
12	chr19:43690996-43691046	PFSK-1	brain:	n/a
13	chr19:43774820-43774870	HEK293	kidney:	embryo
14	chr19:43710277-43710327	SK-N-MC	brain:	n/a
15	chr19:43710277-43710327	SK-N-SH_RA	brain:	n/a
16	chr19:43690622-43690672	AG10803	skin:	n/a
17	chr19:43710277-43710327	HEEpiC	esophagus:	n/a
18	chr19:43690996-43691046	HCM	heart:	n/a
19	chr19:43683698-43683748	Jurkat	blood:	n/a
20	chr19:43711249-43711299	HIPEpiC	eye:	n/a
21	chr19:43774893-43774943	HEK293	kidney:	embryo
22	chr19:43709654-43709704	HCPEpiC	choroid plexus:	n/a
23	chr19:43691878-43691928	AG04450	lung:	fetal
24	chr19:43683698-43683748	GM06990	blood:	n/a
25	chr19:43773649-43773699	K562	blood:	n/a
26	chr19:43697480-43697530	AG10803	skin:	n/a
27	chr19:43709654-43709704	HEEpiC	esophagus:	n/a
28	chr19:43774982-43775032	HEEpiC	esophagus:	n/a
29	chr19:43683698-43683748	NT2-D1	testis:	n/a
30	chr19:43774982-43775032	AG09309	skin:	n/a
31	chr19:43769725-43769775	HCT-116	colon:	n/a
32	chr19:43774921-43774971	AoSMC	blood vessel:	n/a
33	chr19:43690996-43691046	SKMC	muscle:	n/a
34	chr19:43683698-43683748	A549	lung:	n/a
35	chr19:43709754-43709804	ProgFib	skin:	n/a
36	chr19:43691930-43691980	HNPCEpiC	eye:	n/a
37	chr19:43711064-43711114	HepG2	liver:	n/a
38	chr19:43709360-43709410	T-47D	breast:	n/a
39	chr19:43774921-43774971	PFSK-1	brain:	n/a
40	chr19:43773649-43773699	H1-hESC	embryonic stem cell:	embryo
41	chr19:43691878-43691928	MCF10A-Er-Src	breast:	n/a
42	chr19:43680072-43680122	HepG2	liver:	n/a
43	chr19:43691930-43691980	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:43683698-43683748	AoSMC	blood vessel:	n/a
45	chr19:43774893-43774943	HUVEC	blood vessel:	n/a
46	chr19:43774921-43774971	AG09309	skin:	n/a
47	chr19:43709832-43709882	HMEC	breast:	n/a
48	chr19:43683698-43683748	AG09309	skin:	n/a
49	chr19:43709654-43709704	AG10803	skin:	n/a
50	chr19:43711064-43711114	PrEC	prostate:	n/a

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

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

(count:29 , 50 per page) page: 1

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

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: 7527 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7527 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149569511	chr19:43674471-43674472	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs533409425	chr19:43674483-43674484	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs79783895	chr19:43674485-43674486	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs547301540	chr19:43674542-43674543	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs567186269	chr19:43674543-43674544	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs535649897	chr19:43674545-43674546	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs111459823	chr19:43674559-43674560	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs115038468	chr19:43674562-43674563	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs536706481	chr19:43674564-43674565	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs191352784	chr19:43674584-43674585	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs542324470	chr19:43674588-43674589	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs576427072	chr19:43674590-43674591	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs114120969	chr19:43674633-43674634	Enhancers Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs552978420	chr19:43674679-43674680	Enhancers Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs138974310	chr19:43674681-43674682	Enhancers Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs541782861	chr19:43674699-43674700	Enhancers Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs372753496	chr19:43674702-43674703	Enhancers Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs182772078	chr19:43674703-43674704	Enhancers Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs530736501	chr19:43674724-43674725	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544673430	chr19:43674775-43674776	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564607948	chr19:43674781-43674782	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533346137	chr19:43674790-43674791	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546997597	chr19:43674859-43674860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187427347	chr19:43674906-43674907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9676931	chr19:43674920-43674921	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs73934964	chr19:43674937-43674938	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs192231286	chr19:43674958-43674959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139688037	chr19:43674964-43674965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555271843	chr19:43674974-43674975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375516190	chr19:43674997-43674998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570247449	chr19:43675009-43675010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368522690	chr19:43675029-43675030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs56195628	chr19:43675065-43675066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572767667	chr19:43675090-43675091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138655772	chr19:43675156-43675157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202192470	chr19:43675159-43675160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371517721	chr19:43675161-43675162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555380279	chr19:43675203-43675204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575498345	chr19:43675212-43675213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142598672	chr19:43675247-43675248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564547777	chr19:43675251-43675252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150545387	chr19:43675293-43675294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115051332	chr19:43675300-43675301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560451133	chr19:43675342-43675343	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs566873128	chr19:43675376-43675377	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs184763047	chr19:43675377-43675378	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201756705	chr19:43675379-43675380	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs529280642	chr19:43675394-43675395	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs139504843	chr19:43675400-43675401	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs562890612	chr19:43675433-43675434	Weak transcription	TF binding region	1 gene(s)	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:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43670000-43685000	Weak transcription	NHDF-Ad	bronchial
2	chr19:43671000-43674600	Weak transcription	Placenta	Placenta
3	chr19:43674600-43674800	Genic enhancers	Placenta	Placenta
4	chr19:43674600-43675000	Enhancers	Fetal Muscle Leg	muscle
5	chr19:43674800-43678800	Weak transcription	Placenta	Placenta
6	chr19:43678800-43680400	Enhancers	Placenta	Placenta
7	chr19:43680400-43681600	Weak transcription	Placenta	Placenta
8	chr19:43681600-43682200	Strong transcription	Placenta	Placenta
9	chr19:43681800-43683800	Enhancers	Liver	Liver
10	chr19:43682200-43682400	Genic enhancers	Placenta	Placenta
11	chr19:43682400-43683800	Enhancers	Placenta	Placenta
12	chr19:43683800-43685200	Weak transcription	Placenta	Placenta
13	chr19:43684000-43684200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr19:43684000-43684200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:43684000-43684200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr19:43684000-43684200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr19:43684000-43684200	Enhancers	A549	lung
18	chr19:43684000-43684200	Enhancers	Hela-S3	cervix
19	chr19:43684000-43684200	Enhancers	NHEK	skin
20	chr19:43684000-43684200	Enhancers	NHLF	lung
21	chr19:43684000-43684200	Enhancers	Osteobl	bone
22	chr19:43684000-43688400	Enhancers	HMEC	breast
23	chr19:43684200-43684800	Weak transcription	NHEK	skin
24	chr19:43684200-43685200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr19:43684200-43685200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:43684200-43685200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:43684200-43685200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr19:43684200-43685200	Weak transcription	A549	lung
29	chr19:43684200-43685200	Weak transcription	NHLF	lung
30	chr19:43684200-43685200	Weak transcription	Osteobl	bone
31	chr19:43684600-43685200	Weak transcription	Hela-S3	cervix
32	chr19:43684800-43685800	Enhancers	NHEK	skin
33	chr19:43685000-43685400	Genic enhancers	NHDF-Ad	bronchial
34	chr19:43685000-43686400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr19:43685000-43686600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr19:43685200-43685400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr19:43685200-43685400	Flanking Active TSS	Placenta	Placenta
38	chr19:43685200-43686000	Enhancers	A549	lung
39	chr19:43685200-43686200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr19:43685200-43686200	Enhancers	NH-A	brain
41	chr19:43685200-43686400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr19:43685200-43686600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr19:43685200-43686600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr19:43685200-43686600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr19:43685200-43686600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr19:43685200-43686800	Enhancers	NHLF	lung
47	chr19:43685200-43688000	Enhancers	Hela-S3	cervix
48	chr19:43685200-43688200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr19:43685200-43688200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr19:43685200-43691000	Enhancers	Osteobl	bone

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