Variant report

Variant	esv1805104
Chromosome Location	chr19:53090157-53100585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:53099899-53100273	HepG2	liver:	n/a	n/a
2	CEBPB	chr19:53099901-53100188	A549	lung:	n/a	n/a
3	CTCF	chr19:53094027-53094221	K562	blood:	n/a	n/a
4	CTCF	chr19:53095520-53095670	GM12867	blood:	n/a	n/a
5	CTCF	chr19:53095700-53095850	HCPEpiC	choroid plexus:	n/a	chr19:53095743-53095752
6	CTCF	chr19:53094080-53094230	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr19:53094102-53094191	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr19:53095620-53095770	SK-N-SH_RA	brain:	n/a	chr19:53095743-53095752
9	CTCF	chr19:53094111-53094235	NHEK	skin:	n/a	n/a
10	CTCF	chr19:53094022-53094435	MCF-7	breast:	n/a	n/a
11	CTCF	chr19:53094088-53094196	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr19:53095620-53095770	AoAF	blood vessel:	n/a	chr19:53095743-53095752
13	CTCF	chr19:53095700-53095850	HPAF	blood vessel:	n/a	chr19:53095743-53095752
14	CTCF	chr19:53095660-53095810	HRE	kidney:	n/a	chr19:53095743-53095752
15	CTCF	chr19:53094095-53094206	HepG2	liver:	n/a	n/a
16	CTCF	chr19:53094126-53094225	ProgFib	skin:	n/a	n/a
17	CTCF	chr19:53095680-53095830	GM12874	blood:	n/a	chr19:53095743-53095752
18	CTCF	chr19:53094040-53094190	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr19:53095760-53095910	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr19:53094020-53094170	AG09309	skin:	n/a	n/a
21	CTCF	chr19:53094120-53094220	Lung_OC	lung:	n/a	n/a
22	CTCF	chr19:53091576-53091671	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr19:53095620-53095770	GM12878	blood:	n/a	chr19:53095743-53095752
24	CTCF	chr19:53095640-53095790	GM12875	blood:	n/a	chr19:53095743-53095752
25	CTCF	chr19:53094040-53094190	RPTEC	kidney:	n/a	n/a
26	CTCF	chr19:53094080-53094230	HEK293	kidney:	n/a	n/a
27	CTCF	chr19:53094086-53094209	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr19:53095640-53095790	GM12872	blood:	n/a	chr19:53095743-53095752
29	CTCF	chr19:53095742-53095771	K562	blood:	n/a	chr19:53095743-53095752
30	CTCF	chr19:53093989-53094322	GM12878	blood:	n/a	n/a
31	CTCF	chr19:53094000-53094150	GM12873	blood:	n/a	n/a
32	CTCF	chr19:53095580-53095730	HAc	cerebellar:	n/a	n/a
33	CTCF	chr19:53094134-53094208	Gliobla	brain:	n/a	n/a
34	CTCF	chr19:53095760-53095910	K562	blood:	n/a	n/a
35	CTCF	chr19:53095720-53095870	HCT-116	colon:	n/a	chr19:53095743-53095752
36	CTCF	chr19:53094010-53094256	LNCaP	prostate:	n/a	n/a
37	CTCF	chr19:53094020-53094170	GM06990	blood:	n/a	n/a
38	CTCF	chr19:53094040-53094190	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr19:53095660-53095810	GM12873	blood:	n/a	chr19:53095743-53095752
40	CTCF	chr19:53094040-53094190	NB4	blood:	n/a	n/a
41	CTCF	chr19:53094060-53094210	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr19:53095720-53095870	HCPEpiC	choroid plexus:	n/a	chr19:53095743-53095752
43	CTCF	chr19:53095667-53095816	K562	blood:	n/a	chr19:53095743-53095752
44	CTCF	chr19:53094060-53094210	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr19:53095680-53095830	HPAF	blood vessel:	n/a	chr19:53095743-53095752
46	CTCF	chr19:53094020-53094170	HCT-116	colon:	n/a	n/a
47	CTCF	chr19:53095620-53095770	RPTEC	kidney:	n/a	chr19:53095743-53095752
48	CTCF	chr19:53094040-53094190	HEK293	kidney:	n/a	n/a
49	CTCF	chr19:53094060-53094210	NHEK	skin:	n/a	n/a
50	CTCF	chr19:53094080-53094230	HFF	foreskin:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53098945-53098995	IMR90	lung:	fetal
2	chr19:53099757-53099807	SAEC	small airway:	n/a
3	chr19:53098945-53098995	K562	blood:	n/a
4	chr19:53099796-53099846	HL-60	blood:	n/a
5	chr19:53099796-53099846	SAEC	small airway:	n/a
6	chr19:53099757-53099807	NB4	blood:	n/a
7	chr19:53092499-53092549	AG09319	gingival:	n/a
8	chr19:53098913-53098963	HEEpiC	esophagus:	n/a
9	chr19:53098945-53098995	HEK293	kidney:	embryo
10	chr19:53099796-53099846	HMEC	breast:	n/a
11	chr19:53098913-53098963	ovcar-3	ovarian:	n/a
12	chr19:53098945-53098995	AG09319	gingival:	n/a
13	chr19:53098945-53098995	NH-A	brain:	n/a
14	chr19:53099796-53099846	ECC-1	luminal epithelium:	n/a
15	chr19:53099796-53099846	AG09309	skin:	n/a
16	chr19:53099796-53099846	HEEpiC	esophagus:	n/a
17	chr19:53092499-53092549	GM12892	blood:	n/a
18	chr19:53098913-53098963	AG04449	skin:	fetal
19	chr19:53098913-53098963	AG04450	lung:	fetal
20	chr19:53092499-53092549	SK-N-SH	brain:	n/a
21	chr19:53099757-53099807	NHDF-neo	bronchial:	n/a
22	chr19:53099757-53099807	HEK293	kidney:	embryo
23	chr19:53099757-53099807	HCT-116	colon:	n/a
24	chr19:53098913-53098963	HCPEpiC	choroid plexus:	n/a
25	chr19:53099757-53099807	HEEpiC	esophagus:	n/a
26	chr19:53098945-53098995	HMEC	breast:	n/a
27	chr19:53099757-53099807	ECC-1	luminal epithelium:	n/a
28	chr19:53099757-53099807	HCF	heart:	n/a
29	chr19:53098913-53098963	HUVEC	blood vessel:	n/a
30	chr19:53099757-53099807	PANC-1	pancreas:	n/a
31	chr19:53098913-53098963	SK-N-SH_RA	brain:	n/a
32	chr19:53092499-53092549	HRCEpiC	kidney:	n/a
33	chr19:53099757-53099807	SKMC	muscle:	n/a
34	chr19:53099757-53099807	CMK	blood:	n/a
35	chr19:53092499-53092549	U87	brain:	n/a
36	chr19:53099757-53099807	HAEpiC	amniotic membrane:	n/a
37	chr19:53098945-53098995	HRCEpiC	kidney:	n/a
38	chr19:53092499-53092549	GM19239	blood:	n/a
39	chr19:53092499-53092549	HRE	kidney:	n/a
40	chr19:53099796-53099846	SKMC	muscle:	n/a
41	chr19:53098913-53098963	CMK	blood:	n/a
42	chr19:53098913-53098963	PrEC	prostate:	n/a
43	chr19:53099757-53099807	Jurkat	blood:	n/a
44	chr19:53099796-53099846	AG10803	skin:	n/a
45	chr19:53099796-53099846	BJ	skin:	n/a
46	chr19:53098945-53098995	SK-N-SH	brain:	n/a
47	chr19:53099796-53099846	HNPCEpiC	eye:	n/a
48	chr19:53099796-53099846	HRPEpiC	eye:	n/a
49	chr19:53099796-53099846	RPTEC	kidney:	n/a
50	chr19:53099757-53099807	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53085553..53087688-chr19:53089270..53091312,2	MCF-7	breast:
2	chr19:53073369..53074894-chr19:53098457..53100751,2	MCF-7	breast:
3	chr19:53087080..53089827-chr19:53090383..53092275,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF701-1	chr19:53095291-53095481	NONHSAT067565
2	lnc-ZNF701-1	chr19:53098870-53100598	NONHSAT067565
3	lnc-ZNF701-1	chr19:53099127-53099642	NONHSAT067567
4	lnc-ZNF701-1	chr19:53099792-53099841	NONHSAT067568
5	lnc-ZNF701-1	chr19:53100112-53100660	NONHSAT067567
6	lnc-ZNF701-1	chr19:53099657-53099709	NONHSAT067568
7	lnc-ZNF701-1	chr19:53095355-53095481	NONHSAT067564
8	lnc-ZNF701-1	chr19:53100112-53100176	NONHSAT067568
9	lnc-ZNF701-1	chr19:53099890-53100056	NONHSAT067567
10	lnc-ZNF701-1	chr19:53098870-53098941	NONHSAT067564
11	lnc-ZNF701-1	chr19:53091758-53091866	NONHSAT067564
12	lnc-ZNF701-1	chr19:53099127-53099572	NONHSAT067566
13	lnc-ZNF701-1	chr19:53099657-53099709	NONHSAT067566
14	lnc-ZNF701-1	chr19:53099937-53100823	NONHSAT067569
15	lnc-ZNF701-1	chr19:53100261-53100564	NONHSAT067568
16	lnc-ZNF701-1	chr19:53099127-53099572	NONHSAT067568
17	lnc-ZNF701-1	chr19:53099792-53100056	NONHSAT067566
18	lnc-ZNF701-1	chr19:53100006-53100056	NONHSAT067568
19	lnc-ZNF701-1	chr19:53100112-53100660	NONHSAT067566

No data

Variant related genes	Relation type
ZNF137P	TF binding region
ENSG00000268886	TF binding region
ZNF137P	CpG island
ENSG00000268886	CpG island
ENSG00000167562	chromatin interactions
ENSG00000268886	chromatin interactions

Extended variants
information (count: 504 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10402786	chr19:53090157-53090158	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs114817561	chr19:53090175-53090176	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs569842661	chr19:53090200-53090201	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs574583304	chr19:53090202-53090203	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs115486419	chr19:53090206-53090207	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs572375067	chr19:53090237-53090238	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs117427904	chr19:53090255-53090256	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs564322133	chr19:53090256-53090257	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs112174560	chr19:53090286-53090287	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs189212393	chr19:53090290-53090291	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs377505989	chr19:53090323-53090324	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs138121089	chr19:53090324-53090325	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs563954221	chr19:53090334-53090335	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs3339	chr19:53090335-53090336	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs530123160	chr19:53090338-53090339	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs3338	chr19:53090349-53090350	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs193064980	chr19:53090359-53090360	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs527997753	chr19:53090375-53090376	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs116133511	chr19:53090385-53090386	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs571105822	chr19:53090415-53090416	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114769087	chr19:53090424-53090425	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56342819	chr19:53090425-53090426	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534591868	chr19:53090433-53090434	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs59202222	chr19:53090537-53090538	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568172212	chr19:53090556-53090557	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs28680562	chr19:53090602-53090603	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553825797	chr19:53090607-53090608	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs548353159	chr19:53090618-53090619	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539404193	chr19:53090688-53090689	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs185386440	chr19:53090715-53090716	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs111820666	chr19:53090766-53090767	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576281833	chr19:53090780-53090781	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543292348	chr19:53090801-53090802	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114997970	chr19:53090820-53090821	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577187612	chr19:53090913-53090914	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189033969	chr19:53090914-53090915	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541889976	chr19:53090919-53090920	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs560127369	chr19:53090940-53090941	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147217514	chr19:53090951-53090952	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs552541206	chr19:53090959-53090960	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564669720	chr19:53091007-53091008	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531993404	chr19:53091085-53091086	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs138966968	chr19:53091088-53091089	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs56360583	chr19:53091094-53091095	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568642460	chr19:53091118-53091119	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374703226	chr19:53091141-53091142	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374220654	chr19:53091156-53091157	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368082402	chr19:53091161-53091162	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368303431	chr19:53091179-53091180	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149236593	chr19:53091193-53091194	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53074600-53103600	Weak transcription	Fetal Brain Male	brain
2	chr19:53075400-53092200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr19:53075400-53092400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr19:53075400-53092400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
5	chr19:53076400-53096000	Strong transcription	Dnd41	blood
6	chr19:53079200-53092200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr19:53079400-53090400	ZNF genes & repeats	Liver	Liver
8	chr19:53079400-53092200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
9	chr19:53079400-53094200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr19:53079400-53096000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
11	chr19:53079600-53091800	ZNF genes & repeats	Thymus	Thymus
12	chr19:53079800-53091000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr19:53081600-53090200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
14	chr19:53083200-53091000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:53083400-53090400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
16	chr19:53083400-53091000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:53083600-53090400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr19:53083600-53090800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
19	chr19:53083600-53092400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr19:53083800-53092400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
21	chr19:53084600-53091200	ZNF genes & repeats	Colonic Mucosa	Colon
22	chr19:53085400-53091200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr19:53087200-53091000	ZNF genes & repeats	Spleen	Spleen
24	chr19:53087400-53091000	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr19:53087400-53091000	ZNF genes & repeats	Fetal Thymus	thymus
26	chr19:53087400-53095200	Weak transcription	Brain Anterior Caudate	brain
27	chr19:53087400-53103600	Weak transcription	Brain Substantia Nigra	brain
28	chr19:53087600-53090400	ZNF genes & repeats	Gastric	stomach
29	chr19:53087600-53091600	Weak transcription	Fetal Lung	lung
30	chr19:53087600-53095000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr19:53087600-53095400	Weak transcription	Fetal Kidney	kidney
32	chr19:53087600-53095400	Weak transcription	NHLF	lung
33	chr19:53087600-53099000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr19:53087600-53099000	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr19:53087600-53099000	Weak transcription	NHDF-Ad	bronchial
36	chr19:53087600-53099400	Weak transcription	Brain Angular Gyrus	brain
37	chr19:53087600-53103600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:53087800-53090800	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr19:53087800-53092200	Weak transcription	Brain Hippocampus Middle	brain
40	chr19:53087800-53095200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr19:53087800-53095200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr19:53087800-53095200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr19:53087800-53095400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr19:53087800-53095400	Weak transcription	K562	blood
45	chr19:53087800-53098800	Weak transcription	HSMMtube	muscle
46	chr19:53088200-53099000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr19:53088400-53090800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr19:53088400-53092800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr19:53088400-53097600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr19:53088400-53099000	Weak transcription	HUVEC	blood vessel

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