Variant report

Variant	nsv1056850
Chromosome Location	chr19:36752663-36847486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:609)
CpG islands
(count:1403)
Chromatin interactive
region (count:0)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:36822690-36822768	K562	blood:	n/a	n/a
2	ATF1	chr19:36757608-36757618	K562	blood:	n/a	n/a
3	BACH1	chr19:36822319-36822665	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr19:36757499-36757673	K562	blood:	n/a	n/a
5	BHLHE40	chr19:36822590-36822698	K562	blood:	n/a	n/a
6	BHLHE40	chr19:36822480-36822814	GM12878	blood:	n/a	n/a
7	BRCA1	chr19:36762836-36763037	HepG2	liver:	n/a	n/a
8	CBX3	chr19:36787829-36788041	K562	blood:	n/a	n/a
9	CBX3	chr19:36768844-36769134	K562	blood:	n/a	n/a
10	CBX3	chr19:36762724-36763179	K562	blood:	n/a	n/a
11	CBX3	chr19:36785308-36785504	K562	blood:	n/a	n/a
12	CBX3	chr19:36789665-36790026	K562	blood:	n/a	n/a
13	CBX3	chr19:36782055-36782327	K562	blood:	n/a	n/a
14	CBX3	chr19:36796036-36796224	K562	blood:	n/a	n/a
15	CBX3	chr19:36795732-36796004	K562	blood:	n/a	n/a
16	CCNT2	chr19:36757335-36757662	K562	blood:	n/a	n/a
17	CEBPB	chr19:36830460-36830486	A549	lung:	n/a	n/a
18	CEBPB	chr19:36822504-36822774	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr19:36757408-36757715	K562	blood:	n/a	n/a
20	CHD1	chr19:36821511-36822557	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr19:36822518-36822932	GM12878	blood:	n/a	n/a
22	CHD2	chr19:36762837-36763034	HepG2	liver:	n/a	n/a
23	CHD2	chr19:36822351-36823045	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr19:36822377-36823060	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr19:36822370-36822951	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr19:36822540-36822690	AG04450	lung:	n/a	n/a
27	CTCF	chr19:36781989-36782277	K562	blood:	n/a	n/a
28	CTCF	chr19:36822500-36822650	HMEC	breast:	n/a	n/a
29	CTCF	chr19:36802017-36802247	H1-hESC	embryonic stem cell:	n/a	chr19:36802140-36802161 chr19:36802141-36802154 chr19:36802138-36802156
30	CTCF	chr19:36774392-36774650	K562	blood:	n/a	n/a
31	CTCF	chr19:36822460-36822610	HPF	lung:	n/a	n/a
32	CTCF	chr19:36806260-36806283	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:36822580-36822730	NHEK	skin:	n/a	n/a
34	CTCF	chr19:36822400-36822550	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr19:36822580-36822730	BE2_C	brain:	n/a	n/a
36	CTCF	chr19:36806229-36806346	NHEK	skin:	n/a	n/a
37	CTCF	chr19:36822480-36822630	AG10803	skin:	n/a	n/a
38	CTCF	chr19:36822460-36822610	HCFaa	heart:	n/a	n/a
39	CTCF	chr19:36794674-36794939	K562	blood:	n/a	n/a
40	CTCF	chr19:36822520-36822670	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr19:36792105-36792428	K562	blood:	n/a	n/a
42	CTCF	chr19:36797154-36797521	K562	blood:	n/a	n/a
43	CTCF	chr19:36822420-36822570	HEK293	kidney:	n/a	n/a
44	CTCF	chr19:36792132-36792443	K562	blood:	n/a	n/a
45	CTCF	chr19:36806159-36806371	LNCaP	prostate:	n/a	n/a
46	CTCF	chr19:36774379-36774800	K562	blood:	n/a	n/a
47	CTCF	chr19:36799747-36799943	K562	blood:	n/a	n/a
48	CTCF	chr19:36806194-36806324	MCF-7	breast:	n/a	n/a
49	CTCF	chr19:36806229-36806341	GM12878	blood:	n/a	n/a
50	CTCF	chr19:36822460-36822610	GM12870	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36822770-36822820	K562	blood:	n/a
2	chr19:36802391-36802441	LNCaP	prostate:	n/a
3	chr19:36822549-36822599	PrEC	prostate:	n/a
4	chr19:36799625-36799675	ProgFib	skin:	n/a
5	chr19:36758564-36758614	NH-A	brain:	n/a
6	chr19:36825565-36825615	HEEpiC	esophagus:	n/a
7	chr19:36825565-36825615	Caco-2	colon:	n/a
8	chr19:36758736-36758786	Jurkat	blood:	n/a
9	chr19:36764158-36764208	GM19239	blood:	n/a
10	chr19:36822564-36822614	NHDF-neo	bronchial:	n/a
11	chr19:36800845-36800895	PrEC	prostate:	n/a
12	chr19:36802391-36802441	AG09319	gingival:	n/a
13	chr19:36822311-36822361	HEK293	kidney:	embryo
14	chr19:36833695-36833745	Jurkat	blood:	n/a
15	chr19:36818607-36818657	SK-N-SH_RA	brain:	n/a
16	chr19:36763026-36763076	GM19239	blood:	n/a
17	chr19:36764158-36764208	HCF	heart:	n/a
18	chr19:36763026-36763076	NT2-D1	testis:	n/a
19	chr19:36822672-36822722	HCF	heart:	n/a
20	chr19:36827430-36827480	ProgFib	skin:	n/a
21	chr19:36827430-36827480	HRE	kidney:	n/a
22	chr19:36822564-36822614	HL-60	blood:	n/a
23	chr19:36801484-36801534	MCF10A-Er-Src	breast:	n/a
24	chr19:36802391-36802441	HUVEC	blood vessel:	n/a
25	chr19:36818607-36818657	NT2-D1	testis:	n/a
26	chr19:36827430-36827480	HPAEpiC	pulmonary alveolar:	n/a
27	chr19:36763026-36763076	GM12892	blood:	n/a
28	chr19:36794212-36794262	Hela-S3	cervix:	n/a
29	chr19:36763026-36763076	HRCEpiC	kidney:	n/a
30	chr19:36801484-36801534	HUVEC	blood vessel:	n/a
31	chr19:36822311-36822361	Jurkat	blood:	n/a
32	chr19:36822442-36822492	BJ	skin:	n/a
33	chr19:36795950-36796000	LNCaP	prostate:	n/a
34	chr19:36794212-36794262	MCF10A-Er-Src	breast:	n/a
35	chr19:36822770-36822820	GM12891	blood:	n/a
36	chr19:36827430-36827480	PFSK-1	brain:	n/a
37	chr19:36801484-36801534	HMEC	breast:	n/a
38	chr19:36794212-36794262	H1-hESC	embryonic stem cell:	embryo
39	chr19:36822564-36822614	H1-hESC	embryonic stem cell:	embryo
40	chr19:36801503-36801553	AG09319	gingival:	n/a
41	chr19:36764158-36764208	HRPEpiC	eye:	n/a
42	chr19:36795950-36796000	GM19239	blood:	n/a
43	chr19:36822672-36822722	ECC-1	luminal epithelium:	n/a
44	chr19:36800845-36800895	GM12892	blood:	n/a
45	chr19:36818607-36818657	PrEC	prostate:	n/a
46	chr19:36763026-36763076	U87	brain:	n/a
47	chr19:36764158-36764208	CMK	blood:	n/a
48	chr19:36822311-36822361	CMK	blood:	n/a
49	chr19:36799625-36799675	AG10803	skin:	n/a
50	chr19:36758736-36758786	HUVEC	blood vessel:	n/a

No data

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP14-1	chr19:36813032-36813127	ENSG00000232677
2	lnc-ZNF146-1	chr19:36811922-36812079	XLOC_013054
3	lnc-ZFP14-1	chr19:36822349-36822602	ENSG00000232677
4	lnc-ZNF146-1	chr19:36811922-36812260	XLOC_013054
5	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
6	lnc-ZFP14-1	chr19:36806859-36806972	NONHSAT065986
7	lnc-ZFP14-1	chr19:36803969-36806639	ENSG00000232677.2
8	lnc-ZNF146-1	chr19:36803424-36803570	ENSG00000267053.2
9	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
10	lnc-ZFP14-1	chr19:36804644-36804814	ENSG00000232677
11	lnc-ZNF146-1	chr19:36801260-36803564	ENSG00000267053.2
12	lnc-ZFP14-1	chr19:36806262-36806430	ENSG00000232677
13	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
14	lnc-ZFP14-1	chr19:36803622-36804224	NONHSAT065983
15	lnc-ZFP14-1	chr19:36803973-36804224	NONHSAT065986
16	lnc-ZFP14-1	chr19:36806478-36806972	ENSG00000232677.2
17	lnc-ZNF146-1	chr19:36802525-36802694	XLOC_013054
18	lnc-ZFP14-1	chr19:36812202-36812259	NONHSAT065992
19	lnc-ZFP14-1	chr19:36807080-36807229	NONHSAT065986
20	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677.2
21	lnc-ZNF146-1	chr19:36811922-36812194	XLOC_013054
22	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
23	lnc-ZNF146-1	chr19:36802083-36802290	XLOC_013054
24	lnc-ZFP14-1	chr19:36811026-36811662	NONHSAT065992
25	lnc-ZNF146-1	chr19:36802423-36802694	XLOC_013054
26	lnc-ZNF146-1	chr19:36802446-36802694	ENSG00000267053.2
27	lnc-ZFP14-1	chr19:36811507-36811662	ENSG00000232677
28	lnc-ZFP14-1	chr19:36813032-36813130	ENSG00000232677.2
29	lnc-ZNF146-1	chr19:36803410-36803537	XLOC_013054
30	lnc-ZNF146-1	chr19:36802245-36802694	NONHSAT065980
31	lnc-ZNF146-1	chr19:36801260-36803563	ENSG00000267053.2
32	lnc-ZFP14-1	chr19:36812895-36812933	NONHSAT065992
33	lnc-ZFP14-1	chr19:36813032-36813286	ENSG00000232677
34	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
35	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
36	lnc-ZNF146-1	chr19:36802245-36802694	XLOC_013054
37	lnc-ZFP14-1	chr19:36806859-36807236	NONHSAT065983
38	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
39	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
40	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
41	lnc-ZFP14-1	chr19:36813032-36813112	ENSG00000232677
42	lnc-ZNF146-1	chr19:36803424-36803570	NONHSAT065980
43	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
44	lnc-ZNF146-1	chr19:36803424-36803568	XLOC_013054
45	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677.2

No data

Variant related genes	Relation type
LINC00665	TF binding region
ENSG00000222730	TF binding region
ENSG00000267053	TF binding region
LINC00665	CpG island
ENSG00000222730	CpG island
ENSG00000267053	CpG island
SLC35F3	miRNA target sites
SLC35F5	miRNA target sites
SLC35D2	miRNA target sites

Extended variants
information (count: 2556 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2556 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73040148	chr19:36752667-36752668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62113154	chr19:36752691-36752692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146513551	chr19:36752708-36752709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554887533	chr19:36752709-36752710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112534612	chr19:36752755-36752756	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs543800419	chr19:36752761-36752762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10402614	chr19:36752806-36752807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs7507379	chr19:36752808-36752809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs670689	chr19:36752812-36752813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541571444	chr19:36752813-36752814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117723682	chr19:36752835-36752836	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs530359972	chr19:36752837-36752838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10410716	chr19:36752839-36752840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs75947264	chr19:36752841-36752842	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs10404252	chr19:36752842-36752843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs62113155	chr19:36752859-36752860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs181105087	chr19:36752877-36752878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10402836	chr19:36752910-36752911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185347139	chr19:36752955-36752956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565425979	chr19:36752982-36752983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536044603	chr19:36753013-36753014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188988613	chr19:36753035-36753036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569953119	chr19:36753072-36753073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374159703	chr19:36753086-36753087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138035133	chr19:36753125-36753126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577338758	chr19:36753135-36753136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181622372	chr19:36753139-36753140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143174968	chr19:36753142-36753143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574939057	chr19:36753145-36753146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187422213	chr19:36753167-36753168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563698169	chr19:36753180-36753181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4805166	chr19:36753218-36753219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577861430	chr19:36753245-36753246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545023451	chr19:36753279-36753280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs28794274	chr19:36753295-36753296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs28890289	chr19:36753297-36753298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs546945732	chr19:36753304-36753305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555931856	chr19:36753308-36753309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575710833	chr19:36753309-36753310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377661547	chr19:36753348-36753349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2918358	chr19:36753362-36753363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs544785569	chr19:36753385-36753386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552234760	chr19:36753386-36753387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144395547	chr19:36753402-36753403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148704347	chr19:36753417-36753418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553377020	chr19:36753424-36753425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142283295	chr19:36753441-36753442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34409006	chr19:36753458-36753459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557407431	chr19:36753481-36753482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192262378	chr19:36753503-36753504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Pleomorphic liposarcoma	18784837	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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1595 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36739600-36756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr19:36748800-36762800	Weak transcription	Right Atrium	heart
3	chr19:36749200-36762800	Weak transcription	Colon Smooth Muscle	Colon
4	chr19:36749200-36764800	Weak transcription	Brain Substantia Nigra	brain
5	chr19:36749400-36762600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr19:36749400-36764200	Weak transcription	Brain Angular Gyrus	brain
7	chr19:36749600-36757400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr19:36749600-36762600	Weak transcription	Brain Hippocampus Middle	brain
9	chr19:36749600-36763400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr19:36749800-36757600	Weak transcription	Brain Anterior Caudate	brain
11	chr19:36749800-36760000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr19:36756200-36756800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:36756600-36758800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
14	chr19:36756800-36757000	Flanking Active TSS	K562	blood
15	chr19:36756800-36757800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
16	chr19:36756800-36757800	Active TSS	Rectal Mucosa Donor 31	rectum
17	chr19:36756800-36758200	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr19:36756800-36758200	ZNF genes & repeats	Pancreas	Pancrea
19	chr19:36756800-36758400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:36757000-36757400	Active TSS	Psoas Muscle	Psoas
21	chr19:36757000-36757600	Active TSS	Right Ventricle	heart
22	chr19:36757000-36757800	Active TSS	Muscle Satellite Cultured Cells	--
23	chr19:36757000-36758000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr19:36757000-36758000	Active TSS	Left Ventricle	heart
25	chr19:36757000-36758200	Active TSS	K562	blood
26	chr19:36757000-36758600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
27	chr19:36757000-36758800	ZNF genes & repeats	Gastric	stomach
28	chr19:36757000-36759200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr19:36757000-36759400	ZNF genes & repeats	Placenta	Placenta
30	chr19:36757200-36759000	ZNF genes & repeats	Brain Germinal Matrix	brain
31	chr19:36757400-36757600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr19:36757400-36757800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr19:36757400-36762600	Weak transcription	Psoas Muscle	Psoas
34	chr19:36757600-36758800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
35	chr19:36757600-36759000	Strong transcription	Brain Anterior Caudate	brain
36	chr19:36757600-36762600	Weak transcription	Right Ventricle	heart
37	chr19:36757800-36762800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:36758000-36758200	ZNF genes & repeats	Lung	lung
39	chr19:36758000-36759200	ZNF genes & repeats	Fetal Brain Female	brain
40	chr19:36758000-36762800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr19:36758000-36762800	Weak transcription	Left Ventricle	heart
42	chr19:36758400-36758800	ZNF genes & repeats	Ovary	ovary
43	chr19:36758400-36759000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr19:36758400-36759000	ZNF genes & repeats	Liver	Liver
45	chr19:36758400-36762600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:36758400-36762800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr19:36758800-36759000	ZNF genes & repeats	Esophagus	oesophagus
48	chr19:36758800-36762600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr19:36758800-36762600	Weak transcription	Gastric	stomach
50	chr19:36758800-36762600	Weak transcription	Ovary	ovary

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