Variant report

Variant	nsv1061582
Chromosome Location	chr19:43660795-43817862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2360)
CpG islands
(count:1283)
Chromatin interactive
region (count:7)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2360 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

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	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
5	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
6	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
7	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
8	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
9	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
11	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
12	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
13	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
14	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
16	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
17	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
19	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
21	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
22	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
23	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
25	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
31	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
32	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
33	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
36	CHD1	chr19:43778774-43779172	IMR90	lung:	n/a	n/a
37	CHD2	chr19:43790318-43790669	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr19:43769435-43769730	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr19:43742429-43742602	K562	blood:	n/a	chr19:43742523-43742532
40	CTCF	chr19:43702850-43703058	GM12878	blood:	n/a	chr19:43703001-43703014 chr19:43702998-43703016 chr19:43703000-43703021 chr19:43703001-43703014 chr19:43702999-43703015
41	CTCF	chr19:43683940-43684090	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr19:43795443-43795509	NHEK	skin:	n/a	n/a
43	CTCF	chr19:43733520-43733670	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr19:43702917-43703095	Pancreas_OC	pancreas:	n/a	chr19:43703001-43703014 chr19:43702998-43703016 chr19:43703000-43703021 chr19:43703001-43703014 chr19:43702999-43703015
45	CTCF	chr19:43778962-43779171	GM12892	blood:	n/a	n/a
46	CTCF	chr19:43733395-43733780	A549	lung:	n/a	n/a
47	CTCF	chr19:43775420-43775570	HPF	lung:	n/a	chr19:43775423-43775439 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437
48	CTCF	chr19:43778987-43779172	GM10248	blood:	n/a	n/a
49	CTCF	chr19:43683900-43684050	HepG2	liver:	n/a	n/a
50	CTCF	chr19:43695940-43696090	NB4	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	chr19:43774982-43775032	CMK	blood:	n/a
2	chr19:43774982-43775032	AG09319	gingival:	n/a
3	chr19:43774982-43775032	CMK	blood:	n/a
4	chr19:43774982-43775032	AG09319	gingival:	n/a
5	chr19:43774820-43774870	ovcar-3	ovarian:	n/a
6	chr19:43691930-43691980	LNCaP	prostate:	n/a
7	chr19:43690996-43691046	HUVEC	blood vessel:	n/a
8	chr19:43673501-43673551	GM06990	blood:	n/a
9	chr19:43697480-43697530	HEK293	kidney:	embryo
10	chr19:43680072-43680122	GM19239	blood:	n/a
11	chr19:43691878-43691928	K562	blood:	n/a
12	chr19:43691878-43691928	Hepatocyte	liver:	n/a
13	chr19:43709832-43709882	SKMC	muscle:	n/a
14	chr19:43673501-43673551	HepG2	liver:	n/a
15	chr19:43690622-43690672	RPTEC	kidney:	n/a
16	chr19:43690996-43691046	SK-N-SH_RA	brain:	n/a
17	chr19:43709754-43709804	GM19239	blood:	n/a
18	chr19:43690996-43691046	A549	lung:	n/a
19	chr19:43774893-43774943	ECC-1	luminal epithelium:	n/a
20	chr19:43697480-43697530	HRE	kidney:	n/a
21	chr19:43709754-43709804	HIPEpiC	eye:	n/a
22	chr19:43673501-43673551	SK-N-SH_RA	brain:	n/a
23	chr19:43709360-43709410	HUVEC	blood vessel:	n/a
24	chr19:43709832-43709882	K562	blood:	n/a
25	chr19:43673501-43673551	NHDF-neo	bronchial:	n/a
26	chr19:43769725-43769775	HIPEpiC	eye:	n/a
27	chr19:43697480-43697530	AoSMC	blood vessel:	n/a
28	chr19:43769725-43769775	SKMC	muscle:	n/a
29	chr19:43774921-43774971	GM19239	blood:	n/a
30	chr19:43774982-43775032	SK-N-MC	brain:	n/a
31	chr19:43709832-43709882	MCF-7	breast:	n/a
32	chr19:43709754-43709804	ECC-1	luminal epithelium:	n/a
33	chr19:43709360-43709410	HepG2	liver:	n/a
34	chr19:43690622-43690672	NB4	blood:	n/a
35	chr19:43711249-43711299	PANC-1	pancreas:	n/a
36	chr19:43710277-43710327	GM19239	blood:	n/a
37	chr19:43709832-43709882	PANC-1	pancreas:	n/a
38	chr19:43709654-43709704	H1-hESC	embryonic stem cell:	embryo
39	chr19:43769725-43769775	U87	brain:	n/a
40	chr19:43709360-43709410	MCF-7	breast:	n/a
41	chr19:43709754-43709804	AoSMC	blood vessel:	n/a
42	chr19:43773649-43773699	HNPCEpiC	eye:	n/a
43	chr19:43691878-43691928	HRPEpiC	eye:	n/a
44	chr19:43697480-43697530	HNPCEpiC	eye:	n/a
45	chr19:43691878-43691928	HCT-116	colon:	n/a
46	chr19:43774982-43775032	HNPCEpiC	eye:	n/a
47	chr19:43690996-43691046	HCM	heart:	n/a
48	chr19:43690996-43691046	MCF-7	breast:	n/a
49	chr19:43769725-43769775	AG09319	gingival:	n/a
50	chr19:43774820-43774870	AG04449	skin:	fetal

(count:7 , 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	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
4	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
5	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
6	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
7	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 7346 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:7346 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568610637	chr19:43660800-43660801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189717733	chr19:43660815-43660816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549859656	chr19:43660841-43660842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138306008	chr19:43660878-43660879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1971667	chr19:43660906-43660907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs180913380	chr19:43660907-43660908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185492262	chr19:43660910-43660911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143804434	chr19:43660912-43660913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191378575	chr19:43660915-43660916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147223005	chr19:43660968-43660969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543224215	chr19:43660991-43660992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1971668	chr19:43661016-43661017	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs576972043	chr19:43661053-43661054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183138436	chr19:43661161-43661162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144004960	chr19:43661171-43661172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56154631	chr19:43661177-43661178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188572258	chr19:43661197-43661198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149304511	chr19:43661232-43661233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191664823	chr19:43661239-43661240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562377773	chr19:43661257-43661258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183906007	chr19:43661272-43661273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187785576	chr19:43661289-43661290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191090542	chr19:43661305-43661306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182200692	chr19:43661308-43661309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116937711	chr19:43661311-43661312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565644392	chr19:43661317-43661318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186807856	chr19:43661322-43661323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548426539	chr19:43661324-43661325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568019447	chr19:43661325-43661326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371958246	chr19:43661339-43661340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536845800	chr19:43661342-43661343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9789329	chr19:43661420-43661421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs148439489	chr19:43661468-43661469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539951975	chr19:43661529-43661530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34831581	chr19:43661550-43661551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565610045	chr19:43661584-43661585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553207319	chr19:43661623-43661624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192887289	chr19:43661650-43661651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541860629	chr19:43661671-43661672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144046041	chr19:43661672-43661673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576046131	chr19:43661677-43661678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56407641	chr19:43661684-43661685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs564695158	chr19:43661704-43661705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533380323	chr19:43661707-43661708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs55670621	chr19:43661790-43661791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs2190839	chr19:43661803-43661804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184891118	chr19:43661809-43661810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2190840	chr19:43661882-43661883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547830750	chr19:43661909-43661910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200425381	chr19:43661917-43661918	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:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr19:43662800-43663200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr19:43662800-43663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr19:43662800-43663400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr19:43662800-43663600	Enhancers	A549	lung
8	chr19:43663000-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr19:43663000-43663600	Enhancers	NHEK	skin
10	chr19:43663200-43663400	Enhancers	HSMMtube	muscle
11	chr19:43663200-43663600	Enhancers	HMEC	breast
12	chr19:43663600-43666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:43663600-43666000	Weak transcription	HMEC	breast
14	chr19:43663600-43666000	Weak transcription	NHEK	skin
15	chr19:43663600-43668200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr19:43664000-43666200	Weak transcription	HSMMtube	muscle
17	chr19:43665200-43666000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr19:43665600-43666200	Enhancers	Placenta	Placenta
19	chr19:43666000-43666400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr19:43666000-43666800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr19:43666000-43667200	Enhancers	HMEC	breast
22	chr19:43666000-43668600	Enhancers	NHEK	skin
23	chr19:43666200-43666400	Enhancers	HSMMtube	muscle
24	chr19:43666200-43668200	Weak transcription	Placenta	Placenta
25	chr19:43666400-43666600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr19:43666400-43667800	Enhancers	A549	lung
27	chr19:43666400-43668200	Weak transcription	HSMMtube	muscle
28	chr19:43666600-43667800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:43666800-43668000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:43667000-43668600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr19:43667200-43668200	Weak transcription	HMEC	breast
32	chr19:43667600-43668800	Enhancers	Hela-S3	cervix
33	chr19:43667800-43668000	Flanking Active TSS	A549	lung
34	chr19:43667800-43669200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr19:43668000-43668600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr19:43668000-43668800	Enhancers	A549	lung
37	chr19:43668200-43668600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr19:43668200-43668600	Enhancers	Fetal Muscle Trunk	muscle
39	chr19:43668200-43668600	Enhancers	HMEC	breast
40	chr19:43668200-43669000	Enhancers	HSMMtube	muscle
41	chr19:43668200-43669400	Enhancers	NHDF-Ad	bronchial
42	chr19:43668200-43671000	Enhancers	Placenta	Placenta
43	chr19:43668400-43669000	Enhancers	Fetal Muscle Leg	muscle
44	chr19:43669400-43669800	Weak transcription	NHDF-Ad	bronchial
45	chr19:43669800-43670000	Enhancers	NHDF-Ad	bronchial
46	chr19:43670000-43685000	Weak transcription	NHDF-Ad	bronchial
47	chr19:43671000-43674600	Weak transcription	Placenta	Placenta
48	chr19:43674600-43674800	Genic enhancers	Placenta	Placenta
49	chr19:43674600-43675000	Enhancers	Fetal Muscle Leg	muscle
50	chr19:43674800-43678800	Weak transcription	Placenta	Placenta

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