Variant report

Variant	nsv1063208
Chromosome Location	chr19:36743461-36847486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:627)
CpG islands
(count:1712)
Chromatin interactive
region (count:1)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:627 , 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	chr19:36822590-36822698	K562	blood:	n/a	n/a
5	BHLHE40	chr19:36757499-36757673	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	chr19:36782055-36782327	K562	blood:	n/a	n/a
9	CBX3	chr19:36796036-36796224	K562	blood:	n/a	n/a
10	CBX3	chr19:36795732-36796004	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	chr19:36768844-36769134	K562	blood:	n/a	n/a
14	CBX3	chr19:36762724-36763179	K562	blood:	n/a	n/a
15	CBX3	chr19:36787829-36788041	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	chr19:36757408-36757715	K562	blood:	n/a	n/a
19	CEBPB	chr19:36822504-36822774	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr19:36821511-36822557	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr19:36822351-36823045	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr19:36822518-36822932	GM12878	blood:	n/a	n/a
23	CHD2	chr19:36762837-36763034	HepG2	liver:	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	chr19:36806229-36806346	NHEK	skin:	n/a	n/a
27	CTCF	chr19:36762880-36763030	GM12873	blood:	n/a	n/a
28	CTCF	chr19:36817200-36817236	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr19:36762860-36763010	HEK293	kidney:	n/a	n/a
30	CTCF	chr19:36806229-36806341	GM12878	blood:	n/a	n/a
31	CTCF	chr19:36769382-36769596	K562	blood:	n/a	n/a
32	CTCF	chr19:36806185-36806275	GM13977	blood:	n/a	n/a
33	CTCF	chr19:36757707-36757802	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr19:36822520-36822670	GM12873	blood:	n/a	n/a
35	CTCF	chr19:36822475-36822648	GM19238	blood:	n/a	n/a
36	CTCF	chr19:36789628-36789877	K562	blood:	n/a	n/a
37	CTCF	chr19:36822516-36822545	Fibrobl	skin:	n/a	n/a
38	CTCF	chr19:36764243-36764639	K562	blood:	n/a	n/a
39	CTCF	chr19:36822460-36822610	HPF	lung:	n/a	n/a
40	CTCF	chr19:36806748-36806813	GM13976	blood:	n/a	n/a
41	CTCF	chr19:36771880-36772177	K562	blood:	n/a	n/a
42	CTCF	chr19:36806187-36806321	Medullo	brain:	n/a	n/a
43	CTCF	chr19:36822583-36822628	GM12878	blood:	n/a	n/a
44	CTCF	chr19:36792105-36792428	K562	blood:	n/a	n/a
45	CTCF	chr19:36759169-36759486	K562	blood:	n/a	n/a
46	CTCF	chr19:36806159-36806371	LNCaP	prostate:	n/a	n/a
47	CTCF	chr19:36802038-36802155	K562	blood:	n/a	chr19:36802141-36802154
48	CTCF	chr19:36802017-36802247	H1-hESC	embryonic stem cell:	n/a	chr19:36802140-36802161 chr19:36802141-36802154 chr19:36802138-36802156
49	CTCF	chr19:36779440-36779728	K562	blood:	n/a	n/a
50	CTCF	chr19:36781989-36782277	K562	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36800845-36800895	AG04449	skin:	fetal
2	chr19:36822442-36822492	Hepatocyte	liver:	n/a
3	chr19:36801408-36801458	GM06990	blood:	n/a
4	chr19:36794212-36794262	NH-A	brain:	n/a
5	chr19:36800845-36800895	AG04449	skin:	fetal
6	chr19:36822442-36822492	Hepatocyte	liver:	n/a
7	chr19:36801408-36801458	GM06990	blood:	n/a
8	chr19:36794212-36794262	NH-A	brain:	n/a
9	chr19:36763026-36763076	ECC-1	luminal epithelium:	n/a
10	chr19:36758736-36758786	SAEC	small airway:	n/a
11	chr19:36794212-36794262	HEK293	kidney:	embryo
12	chr19:36822549-36822599	NB4	blood:	n/a
13	chr19:36795950-36796000	HCM	heart:	n/a
14	chr19:36822672-36822722	SK-N-MC	brain:	n/a
15	chr19:36833695-36833745	AG09309	skin:	n/a
16	chr19:36744465-36744515	GM12878	blood:	n/a
17	chr19:36822564-36822614	HNPCEpiC	eye:	n/a
18	chr19:36822564-36822614	SK-N-SH	brain:	n/a
19	chr19:36822564-36822614	U87	brain:	n/a
20	chr19:36827430-36827480	H1-hESC	embryonic stem cell:	embryo
21	chr19:36764158-36764208	HRPEpiC	eye:	n/a
22	chr19:36794212-36794262	AG09319	gingival:	n/a
23	chr19:36763026-36763076	SKMC	muscle:	n/a
24	chr19:36801503-36801553	GM19239	blood:	n/a
25	chr19:36746737-36746787	GM12891	blood:	n/a
26	chr19:36764158-36764208	Caco-2	colon:	n/a
27	chr19:36800845-36800895	HIPEpiC	eye:	n/a
28	chr19:36749224-36749274	GM06990	blood:	n/a
29	chr19:36822564-36822614	Hepatocyte	liver:	n/a
30	chr19:36825565-36825615	RPTEC	kidney:	n/a
31	chr19:36800845-36800895	H1-hESC	embryonic stem cell:	embryo
32	chr19:36749224-36749274	Jurkat	blood:	n/a
33	chr19:36800845-36800895	HCF	heart:	n/a
34	chr19:36802391-36802441	AG10803	skin:	n/a
35	chr19:36822564-36822614	HIPEpiC	eye:	n/a
36	chr19:36794212-36794262	Hela-S3	cervix:	n/a
37	chr19:36746845-36746895	T-47D	breast:	n/a
38	chr19:36818607-36818657	CMK	blood:	n/a
39	chr19:36833695-36833745	HRPEpiC	eye:	n/a
40	chr19:36800845-36800895	T-47D	breast:	n/a
41	chr19:36822672-36822722	GM12878	blood:	n/a
42	chr19:36822311-36822361	GM12878	blood:	n/a
43	chr19:36758736-36758786	HAEpiC	amniotic membrane:	n/a
44	chr19:36822442-36822492	HCM	heart:	n/a
45	chr19:36799625-36799675	HCF	heart:	n/a
46	chr19:36822672-36822722	HL-60	blood:	n/a
47	chr19:36822549-36822599	HUVEC	blood vessel:	n/a
48	chr19:36758736-36758786	T-47D	breast:	n/a
49	chr19:36799625-36799675	CMK	blood:	n/a
50	chr19:36744465-36744515	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:36740128..36741923-chr19:36743583..36745191,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP14-1	chr19:36811507-36811662	ENSG00000232677
2	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
3	lnc-ZFP14-1	chr19:36806262-36806430	ENSG00000232677
4	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677.2
5	lnc-ZNF146-1	chr19:36811922-36812260	XLOC_013054
6	lnc-ZFP14-1	chr19:36812895-36812933	NONHSAT065992
7	lnc-ZFP14-1	chr19:36806859-36807236	NONHSAT065983
8	lnc-ZNF146-1	chr19:36801260-36803564	ENSG00000267053.2
9	lnc-ZFP14-1	chr19:36813032-36813127	ENSG00000232677
10	lnc-ZFP14-1	chr19:36813032-36813112	ENSG00000232677
11	lnc-ZNF146-1	chr19:36802245-36802694	NONHSAT065980
12	lnc-ZFP14-1	chr19:36812202-36812259	NONHSAT065992
13	lnc-ZNF146-1	chr19:36803424-36803568	XLOC_013054
14	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
15	lnc-ZFP14-1	chr19:36803969-36806639	ENSG00000232677.2
16	lnc-ZNF146-1	chr19:36803424-36803570	NONHSAT065980
17	lnc-ZNF146-1	chr19:36802423-36802694	XLOC_013054
18	lnc-ZNF146-1	chr19:36802245-36802694	XLOC_013054
19	lnc-ZNF146-1	chr19:36802446-36802694	ENSG00000267053.2
20	lnc-ZFP14-1	chr19:36806478-36806972	ENSG00000232677.2
21	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
22	lnc-ZFP14-1	chr19:36813032-36813286	ENSG00000232677
23	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
24	lnc-ZFP14-1	chr19:36813032-36813130	ENSG00000232677.2
25	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
26	lnc-ZFP14-1	chr19:36806859-36806972	NONHSAT065986
27	lnc-ZNF146-1	chr19:36803424-36803570	ENSG00000267053.2
28	lnc-ZNF146-1	chr19:36811922-36812079	XLOC_013054
29	lnc-ZFP14-1	chr19:36822349-36822602	ENSG00000232677
30	lnc-ZFP14-1	chr19:36804644-36804814	ENSG00000232677
31	lnc-ZNF146-1	chr19:36802083-36802290	XLOC_013054
32	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
33	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
34	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
35	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
36	lnc-ZNF146-1	chr19:36803410-36803537	XLOC_013054
37	lnc-ZNF146-1	chr19:36802525-36802694	XLOC_013054
38	lnc-ZFP14-1	chr19:36807080-36807229	NONHSAT065986
39	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
40	lnc-ZFP14-1	chr19:36811026-36811662	NONHSAT065992
41	lnc-ZFP14-1	chr19:36803622-36804224	NONHSAT065983
42	lnc-ZNF146-1	chr19:36801260-36803563	ENSG00000267053.2
43	lnc-ZFP14-1	chr19:36803973-36804224	NONHSAT065986
44	lnc-ZNF146-1	chr19:36811922-36812194	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
SLC35D2	miRNA target sites
SLC35F5	miRNA target sites

Extended variants
information (count: 3023 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3023 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147423096	chr19:36743499-36743500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185707086	chr19:36743501-36743502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368621000	chr19:36743528-36743529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375226126	chr19:36743556-36743557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543189591	chr19:36743558-36743559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564880437	chr19:36743560-36743561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191011428	chr19:36743580-36743581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537664847	chr19:36743611-36743612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541072935	chr19:36743680-36743681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79101114	chr19:36743690-36743691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4806302	chr19:36743712-36743713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201179825	chr19:36743818-36743819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147716133	chr19:36743833-36743834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71171427	chr19:36743844-36743845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202216289	chr19:36743846-36743847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149047166	chr19:36743848-36743849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs71354130	chr19:36743933-36743934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548700528	chr19:36743938-36743939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563752128	chr19:36743956-36743957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2918328	chr19:36743999-36744000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs540987985	chr19:36744017-36744018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151249781	chr19:36744019-36744020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183730444	chr19:36744020-36744021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2972528	chr19:36744021-36744022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs535277862	chr19:36744075-36744076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547100449	chr19:36744090-36744091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371081216	chr19:36744096-36744097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565635950	chr19:36744103-36744104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535855898	chr19:36744105-36744106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554271751	chr19:36744159-36744160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144906949	chr19:36744202-36744203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376307056	chr19:36744209-36744210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76348853	chr19:36744218-36744219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143311751	chr19:36744300-36744301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191748128	chr19:36744310-36744311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35405244	chr19:36744327-36744328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559373845	chr19:36744390-36744391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183405328	chr19:36744391-36744392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146697798	chr19:36744425-36744426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563813866	chr19:36744430-36744431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369248539	chr19:36744444-36744445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187729509	chr19:36744446-36744447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552809276	chr19:36744454-36744455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564642902	chr19:36744465-36744466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141335495	chr19:36744500-36744501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145117894	chr19:36744600-36744601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568637781	chr19:36744604-36744605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546053637	chr19:36744616-36744617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547770712	chr19:36744626-36744627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569418220	chr19:36744682-36744683	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:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36730400-36748400	Weak transcription	HSMMtube	muscle
2	chr19:36736200-36746200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr19:36737400-36747800	Weak transcription	Brain Anterior Caudate	brain
4	chr19:36737400-36747800	Weak transcription	Brain Substantia Nigra	brain
5	chr19:36737400-36748000	Weak transcription	Ovary	ovary
6	chr19:36737600-36745400	Weak transcription	Pancreas	Pancrea
7	chr19:36737600-36746000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr19:36737600-36746200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr19:36737600-36747800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr19:36737600-36747800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr19:36737600-36747800	Weak transcription	Brain Hippocampus Middle	brain
12	chr19:36738000-36747800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr19:36739200-36746200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:36739200-36746800	Weak transcription	Colon Smooth Muscle	Colon
15	chr19:36739400-36745400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr19:36739600-36745200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr19:36739600-36756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr19:36742200-36746200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr19:36743000-36746000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr19:36744800-36748000	ZNF genes & repeats	Fetal Brain Female	brain
21	chr19:36745000-36745400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr19:36745200-36746000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:36745200-36746800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr19:36745400-36746000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:36745400-36748000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
26	chr19:36745400-36749200	ZNF genes & repeats	Pancreas	Pancrea
27	chr19:36745600-36746400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
28	chr19:36745800-36750600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
29	chr19:36746000-36746200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr19:36746000-36746400	ZNF genes & repeats	Brain Germinal Matrix	brain
31	chr19:36746000-36746800	Strong transcription	Stomach Smooth Muscle	stomach
32	chr19:36746000-36747200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:36746000-36747200	ZNF genes & repeats	Aorta	Aorta
34	chr19:36746000-36747200	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr19:36746000-36747200	ZNF genes & repeats	Gastric	stomach
36	chr19:36746200-36746400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr19:36746200-36746400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:36746200-36746600	Weak transcription	Fetal Lung	lung
39	chr19:36746200-36746800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr19:36746200-36747400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr19:36746200-36747400	ZNF genes & repeats	Lung	lung
42	chr19:36746200-36748200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
43	chr19:36746200-36748800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr19:36746200-36749400	ZNF genes & repeats	Fetal Stomach	stomach
45	chr19:36746400-36747200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chr19:36746400-36747800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr19:36746400-36747800	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr19:36746400-36748800	ZNF genes & repeats	Spleen	Spleen
49	chr19:36746800-36747800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr19:36746800-36747800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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