Variant report

Variant	esv2754667
Chromosome Location	chr19:43559330-43819404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3553)
CpG islands
(count:1649)
Chromatin interactive
region (count:8)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3553 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

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	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
5	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
6	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
7	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
8	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
9	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
10	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
11	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
12	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
13	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
14	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
15	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
16	BHLHE40	chr19:43582147-43582203	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	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
20	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
22	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
23	CEBPB	chr19:43656448-43656689	HepG2	liver:	n/a	chr19:43656521-43656532
24	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43624758-43624915	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a
28	CEBPB	chr19:43562867-43563067	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:43656349-43656822	Hela-S3	cervix:	n/a	chr19:43656521-43656532
31	CEBPB	chr19:43618826-43619087	IMR90	lung:	n/a	n/a
32	CEBPB	chr19:43656366-43656852	IMR90	lung:	n/a	chr19:43656521-43656532
33	CEBPB	chr19:43634604-43634632	HepG2	liver:	n/a	chr19:43634618-43634629 chr19:43634616-43634629 chr19:43634616-43634629 chr19:43634616-43634627
34	CEBPB	chr19:43573042-43573317	HepG2	liver:	n/a	chr19:43573163-43573174
35	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
36	CEBPB	chr19:43582033-43582419	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:43562943-43563108	MCF-7	breast:	n/a	n/a
38	CEBPB	chr19:43564423-43564649	IMR90	lung:	n/a	n/a
39	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
41	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:43562984-43563042	A549	lung:	n/a	n/a
47	CEBPB	chr19:43564424-43564703	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:43590049-43590324	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
50	CEBPB	chr19:43656390-43656701	K562	blood:	n/a	chr19:43656521-43656532

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43588069-43588119	SAEC	small airway:	n/a
2	chr19:43709754-43709804	AG04449	skin:	fetal
3	chr19:43588069-43588119	SAEC	small airway:	n/a
4	chr19:43709754-43709804	AG04449	skin:	fetal
5	chr19:43710277-43710327	GM06990	blood:	n/a
6	chr19:43569592-43569642	Hela-S3	cervix:	n/a
7	chr19:43580600-43580650	GM06990	blood:	n/a
8	chr19:43711249-43711299	SK-N-SH	brain:	n/a
9	chr19:43709654-43709704	HIPEpiC	eye:	n/a
10	chr19:43711249-43711299	AG09319	gingival:	n/a
11	chr19:43711249-43711299	Jurkat	blood:	n/a
12	chr19:43711249-43711299	HRCEpiC	kidney:	n/a
13	chr19:43690996-43691046	LNCaP	prostate:	n/a
14	chr19:43774921-43774971	NH-A	brain:	n/a
15	chr19:43774982-43775032	PANC-1	pancreas:	n/a
16	chr19:43774982-43775032	AG09309	skin:	n/a
17	chr19:43691878-43691928	HepG2	liver:	n/a
18	chr19:43580600-43580650	ECC-1	luminal epithelium:	n/a
19	chr19:43580600-43580650	HCPEpiC	choroid plexus:	n/a
20	chr19:43774982-43775032	PrEC	prostate:	n/a
21	chr19:43709360-43709410	SAEC	small airway:	n/a
22	chr19:43690996-43691046	CMK	blood:	n/a
23	chr19:43709654-43709704	K562	blood:	n/a
24	chr19:43769725-43769775	SK-N-MC	brain:	n/a
25	chr19:43774893-43774943	GM06990	blood:	n/a
26	chr19:43774921-43774971	HCT-116	colon:	n/a
27	chr19:43680072-43680122	MCF10A-Er-Src	breast:	n/a
28	chr19:43711064-43711114	HMEC	breast:	n/a
29	chr19:43769725-43769775	Hela-S3	cervix:	n/a
30	chr19:43588069-43588119	AG10803	skin:	n/a
31	chr19:43774820-43774870	BJ	skin:	n/a
32	chr19:43680072-43680122	BJ	skin:	n/a
33	chr19:43710277-43710327	GM12892	blood:	n/a
34	chr19:43690996-43691046	NHBE	bronchial:	n/a
35	chr19:43711064-43711114	GM06990	blood:	n/a
36	chr19:43588025-43588075	U87	brain:	n/a
37	chr19:43711064-43711114	AG04450	lung:	fetal
38	chr19:43569592-43569642	PANC-1	pancreas:	n/a
39	chr19:43691878-43691928	HNPCEpiC	eye:	n/a
40	chr19:43569592-43569642	AG04449	skin:	fetal
41	chr19:43587500-43587550	AG09319	gingival:	n/a
42	chr19:43683698-43683748	T-47D	breast:	n/a
43	chr19:43680072-43680122	AG09309	skin:	n/a
44	chr19:43587500-43587550	NHBE	bronchial:	n/a
45	chr19:43690996-43691046	HAEpiC	amniotic membrane:	n/a
46	chr19:43680072-43680122	NB4	blood:	n/a
47	chr19:43711064-43711114	HEEpiC	esophagus:	n/a
48	chr19:43774982-43775032	HCF	heart:	n/a
49	chr19:43709832-43709882	NHDF-neo	bronchial:	n/a
50	chr19:43774921-43774971	PrEC	prostate:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
2	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
3	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
4	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
5	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
6	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
7	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
8	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
2	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
3	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
4	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
5	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
6	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
7	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
8	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
9	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
10	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
11	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
12	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
13	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
14	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
15	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
16	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
17	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
18	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
19	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
20	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
21	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
22	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
23	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
24	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
25	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
26	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
27	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
28	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
29	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
30	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
31	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
32	lnc-PSG2-1	chr19:43586658-43586820	NONHSAT066581
33	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
34	lnc-PSG2-2	chr19:43575923-43576106	NONHSAT066580
35	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
36	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
37	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
38	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
39	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
40	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
41	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591

No data

Variant related genes	Relation type
PSG4	TF binding region
CEACAMP9	TF binding region
CEACAMP11	TF binding region
PSG2	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
CEACAMP9	CpG island
CEACAMP11	CpG island
PSG2	CpG island
ENSG00000227606	CpG island
PSG5	CpG island
CEACAMP4	CpG island
CEACAMP10	CpG island
PSG9	CpG island
ENSG00000243137	chromatin interactions

Extended variants
information (count: 13561 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:13561 , 50 per page) page: 1 2 3 4 5 6 7 ... 272

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557487629	chr19:43562636-43562637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188378100	chr19:43562641-43562642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546200859	chr19:43562680-43562681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192849086	chr19:43562694-43562695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573453010	chr19:43562699-43562700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542169895	chr19:43562702-43562703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4369784	chr19:43562716-43562717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562446398	chr19:43562720-43562721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2354812	chr19:43562750-43562751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs544430824	chr19:43562752-43562753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563031146	chr19:43562760-43562761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185345312	chr19:43562802-43562803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552125118	chr19:43562807-43562808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565544607	chr19:43562819-43562820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7259852	chr19:43562848-43562849	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs28637091	chr19:43562856-43562857	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142498087	chr19:43562875-43562876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146832812	chr19:43562900-43562901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368240520	chr19:43562907-43562908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35612538	chr19:43562923-43562924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537217910	chr19:43562938-43562939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368162255	chr19:43563013-43563014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs58860528	chr19:43563015-43563016	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs564621614	chr19:43563031-43563032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190224023	chr19:43563074-43563075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368084664	chr19:43563090-43563091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553292498	chr19:43563148-43563149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115092185	chr19:43563156-43563157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181884900	chr19:43563177-43563178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555618961	chr19:43563203-43563204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184864129	chr19:43563209-43563210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7260273	chr19:43563224-43563225	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7260376	chr19:43563238-43563239	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs370084380	chr19:43563239-43563240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372427549	chr19:43563273-43563274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545588122	chr19:43563280-43563281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559438451	chr19:43563282-43563283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376753835	chr19:43563283-43563284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548194019	chr19:43563288-43563289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561948056	chr19:43563297-43563298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28519535	chr19:43563320-43563321	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550766434	chr19:43563339-43563340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369454103	chr19:43563355-43563356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373671926	chr19:43563362-43563363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188108142	chr19:43563380-43563381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377529908	chr19:43563402-43563403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529971633	chr19:43563409-43563410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369293581	chr19:43563416-43563417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539662214	chr19:43563427-43563428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180964291	chr19:43563429-43563430	Enhancers Weak transcription	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:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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

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