Variant report

Variant	esv1809448
Chromosome Location	chr19:43547103-43799223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3374)
CpG islands
(count:1649)
Chromatin interactive
region (count:3)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3374 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

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	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
5	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
6	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
7	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
8	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
9	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
10	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
11	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
12	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
13	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
14	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
15	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
16	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
18	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
21	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
22	CEBPB	chr19:43573042-43573317	HepG2	liver:	n/a	chr19:43573163-43573174
23	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:43562867-43563067	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43562984-43563042	A549	lung:	n/a	n/a
27	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43590049-43590324	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43560474-43560633	A549	lung:	n/a	chr19:43560568-43560581 chr19:43560568-43560579 chr19:43560568-43560581
30	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43564423-43564649	IMR90	lung:	n/a	n/a
33	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:43562801-43563050	IMR90	lung:	n/a	n/a
35	CEBPB	chr19:43634604-43634632	HepG2	liver:	n/a	chr19:43634618-43634629 chr19:43634616-43634629 chr19:43634616-43634629 chr19:43634616-43634627
36	CEBPB	chr19:43562943-43563108	MCF-7	breast:	n/a	n/a
37	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:43564424-43564703	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
41	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43582058-43582378	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:43656430-43656683	A549	lung:	n/a	chr19:43656521-43656532
44	CEBPB	chr19:43588559-43588762	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:43656349-43656822	Hela-S3	cervix:	n/a	chr19:43656521-43656532
47	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a
48	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
49	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
50	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774982-43775032	Hepatocyte	liver:	n/a
2	chr19:43588055-43588105	HRE	kidney:	n/a
3	chr19:43774982-43775032	Hepatocyte	liver:	n/a
4	chr19:43588055-43588105	HRE	kidney:	n/a
5	chr19:43709360-43709410	Caco-2	colon:	n/a
6	chr19:43683698-43683748	HRCEpiC	kidney:	n/a
7	chr19:43769725-43769775	H1-hESC	embryonic stem cell:	embryo
8	chr19:43683698-43683748	K562	blood:	n/a
9	chr19:43569592-43569642	NHBE	bronchial:	n/a
10	chr19:43683698-43683748	HCPEpiC	choroid plexus:	n/a
11	chr19:43710277-43710327	PrEC	prostate:	n/a
12	chr19:43710277-43710327	HCM	heart:	n/a
13	chr19:43691930-43691980	HCT-116	colon:	n/a
14	chr19:43691878-43691928	H1-hESC	embryonic stem cell:	embryo
15	chr19:43691930-43691980	HIPEpiC	eye:	n/a
16	chr19:43697480-43697530	GM19239	blood:	n/a
17	chr19:43683698-43683748	AG09309	skin:	n/a
18	chr19:43569592-43569642	U87	brain:	n/a
19	chr19:43673501-43673551	NHBE	bronchial:	n/a
20	chr19:43683698-43683748	MCF10A-Er-Src	breast:	n/a
21	chr19:43690622-43690672	HNPCEpiC	eye:	n/a
22	chr19:43587500-43587550	HRCEpiC	kidney:	n/a
23	chr19:43587500-43587550	Caco-2	colon:	n/a
24	chr19:43569592-43569642	GM19239	blood:	n/a
25	chr19:43711064-43711114	SAEC	small airway:	n/a
26	chr19:43683698-43683748	IMR90	lung:	fetal
27	chr19:43711249-43711299	AG10803	skin:	n/a
28	chr19:43680072-43680122	HEK293	kidney:	embryo
29	chr19:43580600-43580650	Hepatocyte	liver:	n/a
30	chr19:43690622-43690672	GM06990	blood:	n/a
31	chr19:43774893-43774943	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:43691878-43691928	AG04450	lung:	fetal
33	chr19:43588055-43588105	Hepatocyte	liver:	n/a
34	chr19:43774921-43774971	SK-N-MC	brain:	n/a
35	chr19:43709832-43709882	HCT-116	colon:	n/a
36	chr19:43580600-43580650	AG04450	lung:	fetal
37	chr19:43673501-43673551	IMR90	lung:	fetal
38	chr19:43690996-43691046	AoSMC	blood vessel:	n/a
39	chr19:43690622-43690672	U87	brain:	n/a
40	chr19:43580600-43580650	HEEpiC	esophagus:	n/a
41	chr19:43691878-43691928	GM19239	blood:	n/a
42	chr19:43709832-43709882	HAEpiC	amniotic membrane:	n/a
43	chr19:43580600-43580650	NB4	blood:	n/a
44	chr19:43709832-43709882	SK-N-SH_RA	brain:	n/a
45	chr19:43588055-43588105	GM12891	blood:	n/a
46	chr19:43587500-43587550	A549	lung:	n/a
47	chr19:43588025-43588075	HRPEpiC	eye:	n/a
48	chr19:43691878-43691928	A549	lung:	n/a
49	chr19:43691930-43691980	SK-N-MC	brain:	n/a
50	chr19:43690622-43690672	SKMC	muscle:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
2	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
3	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
2	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
3	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
4	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
5	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
6	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
7	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
8	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
9	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
10	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
11	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
12	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
13	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
14	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
15	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
16	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
17	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
18	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
19	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
20	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
21	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
22	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
23	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
24	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
25	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
26	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
27	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
28	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
29	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
30	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
31	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
32	lnc-PSG2-1	chr19:43586658-43586820	NONHSAT066581
33	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
34	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
35	lnc-PSG2-2	chr19:43575923-43576106	NONHSAT066580
36	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
37	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
38	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
39	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591

No data

Variant related genes	Relation type
PSG4	TF binding region
CEACAMP9	TF binding region
CEACAMP8	TF binding region
CEACAMP11	TF binding region
PSG2	TF binding region
ENSG00000227606	TF binding region
PSG5	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	CpG island
CEACAMP9	CpG island
CEACAMP8	CpG island
CEACAMP11	CpG island
PSG2	CpG island
ENSG00000227606	CpG island
PSG5	CpG island
CEACAMP10	CpG island
PSG9	CpG island
ENSG00000243137	chromatin interactions

Extended variants
information (count: 12992 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:12992 , 50 per page) page: 1 2 3 4 5 6 7 ... 260

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539057498	chr19:43547166-43547167	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs552971349	chr19:43547175-43547176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs62110998	chr19:43547188-43547189	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs144446990	chr19:43547221-43547222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs561837220	chr19:43547222-43547223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs12462178	chr19:43547240-43547241	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs142481505	chr19:43547253-43547254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs376749069	chr19:43547279-43547280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs56099400	chr19:43548587-43548588	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs7257136	chr19:43548593-43548594	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs192263435	chr19:43553800-43553801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117433584	chr19:43553805-43553806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140292875	chr19:43553808-43553809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113305820	chr19:43553827-43553828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10426137	chr19:43553873-43553874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150942936	chr19:43553875-43553876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116201122	chr19:43553889-43553890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547615107	chr19:43553890-43553891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371590601	chr19:43553891-43553892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs55892446	chr19:43553895-43553896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545933281	chr19:43553902-43553903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559885462	chr19:43553904-43553905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140682189	chr19:43553925-43553926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533086364	chr19:43553977-43553978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551071523	chr19:43554017-43554018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2079283	chr19:43554029-43554030	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs562084981	chr19:43554049-43554050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531075578	chr19:43554104-43554105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372002408	chr19:43554112-43554113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184648764	chr19:43554119-43554120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116893463	chr19:43554135-43554136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536672430	chr19:43554136-43554137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549619944	chr19:43554146-43554147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533562393	chr19:43554147-43554148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117480110	chr19:43554149-43554150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189434178	chr19:43554176-43554177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565415656	chr19:43554182-43554183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114817503	chr19:43554210-43554211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1812034	chr19:43554213-43554214	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs150492040	chr19:43554224-43554225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371264853	chr19:43554238-43554239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61048842	chr19:43554245-43554246	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs184407781	chr19:43554252-43554253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114307294	chr19:43554296-43554297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138553567	chr19:43554301-43554302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189685181	chr19:43554318-43554319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542366734	chr19:43554324-43554325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs59201715	chr19:43554326-43554327	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575605570	chr19:43554332-43554333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553198921	chr19:43554351-43554352	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Ependymoma	20639864	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
early-passage human iPS cells	21368824	CNVD
Primary Severe Spermatogenic Failure	20378930	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43553800-43554200	Enhancers	NHEK	skin
2	chr19:43554000-43554400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:43562600-43563400	Enhancers	Placenta	Placenta
4	chr19:43562800-43563000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr19:43562800-43563000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr19:43562800-43564400	Enhancers	NHEK	skin
7	chr19:43562800-43564800	Enhancers	A549	lung
8	chr19:43562800-43565400	Enhancers	HMEC	breast
9	chr19:43563000-43563200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr19:43563200-43563800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr19:43563200-43564000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr19:43563200-43564600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:43563200-43566000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr19:43563400-43564600	Weak transcription	Placenta	Placenta
15	chr19:43563800-43565000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:43564000-43564800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr19:43564000-43565600	Enhancers	NHDF-Ad	bronchial
18	chr19:43564000-43566200	Enhancers	HSMMtube	muscle
19	chr19:43564400-43565400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr19:43564600-43565000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr19:43564600-43565600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr19:43564600-43565600	Enhancers	Placenta	Placenta
23	chr19:43565200-43565600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr19:43565600-43569600	Weak transcription	NHDF-Ad	bronchial
25	chr19:43565600-43571200	Weak transcription	Placenta	Placenta
26	chr19:43569600-43570200	Enhancers	NHDF-Ad	bronchial
27	chr19:43571200-43571600	Enhancers	Placenta	Placenta
28	chr19:43571600-43575600	Weak transcription	Placenta	Placenta
29	chr19:43575600-43577000	Genic enhancers	Placenta	Placenta
30	chr19:43577000-43579200	Weak transcription	Placenta	Placenta
31	chr19:43579200-43581000	Enhancers	Placenta	Placenta
32	chr19:43579200-43581600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr19:43579400-43579600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr19:43579600-43581800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr19:43581000-43582000	Weak transcription	Placenta	Placenta
36	chr19:43581600-43582200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr19:43581600-43582400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr19:43581600-43582600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr19:43581600-43582800	Enhancers	NHLF	lung
40	chr19:43581600-43583200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr19:43581600-43584000	Enhancers	HMEC	breast
42	chr19:43581600-43584400	Enhancers	Osteobl	bone
43	chr19:43581600-43584600	Enhancers	NHDF-Ad	bronchial
44	chr19:43581800-43582600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:43581800-43582800	Enhancers	HSMMtube	muscle
46	chr19:43581800-43584000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr19:43582000-43582400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr19:43582000-43582400	Enhancers	Placenta	Placenta
49	chr19:43582000-43582600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr19:43582000-43582600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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