Variant report

Variant	esv1009469
Chromosome Location	chr19:53313866-53324346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:84)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:84 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:53319087-53319167	HepG2	liver:	n/a	chr19:53319119-53319130
2	E2F6	chr19:53324163-53324362	K562	blood:	n/a	n/a
3	ELF1	chr19:53324122-53325153	GM12878	blood:	n/a	chr19:53325007-53325019
4	HEY1	chr19:53323828-53324075	HepG2	liver:	n/a	n/a
5	HEY1	chr19:53323765-53324097	K562	blood:	n/a	n/a
6	HEY1	chr19:53322366-53322605	K562	blood:	n/a	n/a
7	HEY1	chr19:53323617-53325058	K562	blood:	n/a	n/a
8	IRF4	chr19:53324226-53324977	GM12878	blood:	n/a	n/a
9	MAX	chr19:53324046-53324376	K562	blood:	n/a	n/a
10	MXI1	chr19:53323964-53325421	SK-N-SH	brain:	n/a	n/a
11	MYC	chr19:53324303-53324306	MCF-7	breast:	n/a	n/a
12	MYC	chr19:53324311-53324462	MCF-7	breast:	n/a	n/a
13	MYC	chr19:53316188-53316245	Hela-S3	cervix:	n/a	n/a
14	MYC	chr19:53324296-53324493	MCF-7	breast:	n/a	n/a
15	NR2F2	chr19:53315495-53316027	K562	blood:	n/a	n/a
16	NR2F2	chr19:53315586-53315975	K562	blood:	n/a	n/a
17	PAX5	chr19:53323772-53324003	GM12878	blood:	n/a	n/a
18	PBX3	chr19:53323779-53323895	GM12878	blood:	n/a	n/a
19	POLR2A	chr19:53324114-53325097	GM12891	blood:	n/a	n/a
20	POLR2A	chr19:53323959-53323974	K562	blood:	n/a	n/a
21	POLR2A	chr19:53319262-53319450	ProgFib	skin:	n/a	n/a
22	POLR2A	chr19:53322197-53322581	GM12878	blood:	n/a	n/a
23	POLR2A	chr19:53323759-53323992	GM12878	blood:	n/a	n/a
24	POLR2A	chr19:53316815-53316836	MCF-7	breast:	n/a	n/a
25	POLR2A	chr19:53324262-53324479	MCF-7	breast:	n/a	n/a
26	POLR2A	chr19:53322223-53322672	GM12878	blood:	n/a	n/a
27	POLR2A	chr19:53324241-53324997	GM12892	blood:	n/a	n/a
28	POLR2A	chr19:53324208-53325176	PANC-1	pancreas:	n/a	n/a
29	POLR2A	chr19:53324215-53324490	HepG2	liver:	n/a	n/a
30	POLR2A	chr19:53316465-53316917	GM12878	blood:	n/a	n/a
31	POLR2A	chr19:53316009-53316213	MCF-7	breast:	n/a	n/a
32	POLR2A	chr19:53316535-53316878	K562	blood:	n/a	n/a
33	POLR2A	chr19:53324153-53325114	GM12892	blood:	n/a	n/a
34	POLR2A	chr19:53322394-53322553	K562	blood:	n/a	n/a
35	POLR2A	chr19:53316792-53316806	MCF-7	breast:	n/a	n/a
36	POLR2A	chr19:53321079-53321393	GM12878	blood:	n/a	n/a
37	POLR2A	chr19:53324155-53324160	K562	blood:	n/a	n/a
38	POLR2A	chr19:53320122-53320175	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr19:53324265-53324455	Gliobla	brain:	n/a	n/a
40	POLR2A	chr19:53317483-53317673	ProgFib	skin:	n/a	n/a
41	POLR2A	chr19:53324169-53325206	MCF-7	breast:	n/a	n/a
42	POLR2A	chr19:53324189-53324579	GM12878	blood:	n/a	n/a
43	POLR2A	chr19:53323783-53323927	MCF-7	breast:	n/a	n/a
44	POLR2A	chr19:53324172-53325119	SK-N-MC	brain:	n/a	n/a
45	POLR2A	chr19:53321724-53321860	HepG2	liver:	n/a	n/a
46	POLR2A	chr19:53322370-53322379	K562	blood:	n/a	n/a
47	POLR2A	chr19:53324095-53325136	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr19:53322983-53323395	GM12878	blood:	n/a	n/a
49	POLR2A	chr19:53324240-53324255	Gliobla	brain:	n/a	n/a
50	POLR2A	chr19:53324201-53324298	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53324198-53324248	Caco-2	colon:	n/a
2	chr19:53324278-53324328	HEEpiC	esophagus:	n/a
3	chr19:53324198-53324248	HepG2	liver:	n/a
4	chr19:53324198-53324248	GM12892	blood:	n/a
5	chr19:53324198-53324248	Hela-S3	cervix:	n/a
6	chr19:53324278-53324328	Caco-2	colon:	n/a
7	chr19:53324278-53324328	HPAEpiC	pulmonary alveolar:	n/a
8	chr19:53324278-53324328	ovcar-3	ovarian:	n/a
9	chr19:53324278-53324328	LNCaP	prostate:	n/a
10	chr19:53324278-53324328	HAEpiC	amniotic membrane:	n/a
11	chr19:53324278-53324328	T-47D	breast:	n/a
12	chr19:53324278-53324328	AG04450	lung:	fetal
13	chr19:53324278-53324328	U87	brain:	n/a
14	chr19:53324278-53324328	HMEC	breast:	n/a
15	chr19:53324198-53324248	BE2_C	brain:	n/a
16	chr19:53324278-53324328	ProgFib	skin:	n/a
17	chr19:53324278-53324328	Hela-S3	cervix:	n/a
18	chr19:53324198-53324248	HIPEpiC	eye:	n/a
19	chr19:53324198-53324248	HRE	kidney:	n/a
20	chr19:53324278-53324328	RPTEC	kidney:	n/a
21	chr19:53324278-53324328	A549	lung:	n/a
22	chr19:53324198-53324248	H1-hESC	embryonic stem cell:	embryo
23	chr19:53324198-53324248	NB4	blood:	n/a
24	chr19:53324198-53324248	GM12891	blood:	n/a
25	chr19:53324198-53324248	HMEC	breast:	n/a
26	chr19:53324198-53324248	K562	blood:	n/a
27	chr19:53324278-53324328	NT2-D1	testis:	n/a
28	chr19:53324278-53324328	GM12892	blood:	n/a
29	chr19:53324198-53324248	GM06990	blood:	n/a
30	chr19:53324278-53324328	GM06990	blood:	n/a
31	chr19:53324278-53324328	MCF10A-Er-Src	breast:	n/a
32	chr19:53324278-53324328	GM19239	blood:	n/a
33	chr19:53324198-53324248	ProgFib	skin:	n/a
34	chr19:53324278-53324328	NHBE	bronchial:	n/a
35	chr19:53324278-53324328	Hepatocyte	liver:	n/a
36	chr19:53324278-53324328	HRPEpiC	eye:	n/a
37	chr19:53324198-53324248	IMR90	lung:	fetal
38	chr19:53324198-53324248	PrEC	prostate:	n/a
39	chr19:53324278-53324328	HNPCEpiC	eye:	n/a
40	chr19:53324278-53324328	AG09309	skin:	n/a
41	chr19:53324278-53324328	NH-A	brain:	n/a
42	chr19:53324198-53324248	AG04449	skin:	fetal
43	chr19:53324198-53324248	LNCaP	prostate:	n/a
44	chr19:53324198-53324248	BJ	skin:	n/a
45	chr19:53324198-53324248	T-47D	breast:	n/a
46	chr19:53324198-53324248	NHDF-neo	bronchial:	n/a
47	chr19:53324278-53324328	Jurkat	blood:	n/a
48	chr19:53324278-53324328	IMR90	lung:	fetal
49	chr19:53324278-53324328	HUVEC	blood vessel:	n/a
50	chr19:53324198-53324248	GM19239	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
2	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-3	chr19:53321197-53321284	NONHSAT067588
2	lnc-ZNF468-3	chr19:53317537-53317679	NONHSAT067589
3	lnc-ZNF468-3	chr19:53321197-53321281	NONHSAT067589

No data

Variant related genes	Relation type
ZNF28	TF binding region
ZNF28	CpG island
ENSG00000204604	chromatin interactions
ENSG00000198538	chromatin interactions

Extended variants
information (count: 510 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:510 , 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	rs537110094	chr19:53313911-53313912	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555424903	chr19:53313914-53313915	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560698347	chr19:53313936-53313937	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111419953	chr19:53313946-53313947	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11454962	chr19:53314008-53314009	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs371578865	chr19:53314009-53314010	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs201866551	chr19:53314021-53314022	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs375621295	chr19:53314022-53314023	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs552986610	chr19:53314030-53314031	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs368878409	chr19:53314031-53314032	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs200898708	chr19:53314032-53314033	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs8101411	chr19:53314033-53314034	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs112245508	chr19:53314034-53314035	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs543487142	chr19:53314038-53314039	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs561778178	chr19:53314049-53314050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs529240186	chr19:53314057-53314058	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs200567176	chr19:53314066-53314067	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs548115483	chr19:53314068-53314069	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs187385486	chr19:53314070-53314071	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs4803000	chr19:53314072-53314073	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs551699175	chr19:53314083-53314084	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs4803001	chr19:53314092-53314093	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs537171409	chr19:53314093-53314094	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs549084740	chr19:53314094-53314095	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs57570517	chr19:53314098-53314099	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs538037515	chr19:53314115-53314116	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs561758193	chr19:53314119-53314120	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs529233873	chr19:53314127-53314128	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs531628905	chr19:53314133-53314134	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs59787081	chr19:53314155-53314156	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs373220758	chr19:53314198-53314199	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs61567227	chr19:53314225-53314226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192585539	chr19:53314317-53314318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10406336	chr19:53314355-53314356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552887899	chr19:53314398-53314399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28584987	chr19:53314414-53314415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538894657	chr19:53314428-53314429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556764105	chr19:53314433-53314434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575077286	chr19:53314451-53314452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543548537	chr19:53314457-53314458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112323468	chr19:53314474-53314475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574031361	chr19:53314475-53314476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113332816	chr19:53314504-53314505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541074835	chr19:53314509-53314510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371211338	chr19:53314558-53314559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533479392	chr19:53314562-53314563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137989305	chr19:53314602-53314603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545695421	chr19:53314625-53314626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563906890	chr19:53314833-53314834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531119004	chr19:53314848-53314849	Weak transcription	n/a	n/a	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
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53296200-53324000	Weak transcription	Fetal Brain Male	brain
2	chr19:53297400-53314000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
3	chr19:53299200-53314000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:53299200-53314000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr19:53299200-53314000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:53299200-53314000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:53299600-53314000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr19:53299600-53314000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
9	chr19:53299800-53314000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr19:53301000-53314000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr19:53301400-53314000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
12	chr19:53302000-53314000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
13	chr19:53302800-53314000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
14	chr19:53302800-53314000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:53303000-53314000	ZNF genes & repeats	Primary B cells from cord blood	blood
16	chr19:53303200-53314000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr19:53303200-53314000	ZNF genes & repeats	Lung	lung
18	chr19:53303400-53314000	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr19:53303600-53314000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr19:53304200-53314000	ZNF genes & repeats	Aorta	Aorta
21	chr19:53304400-53315600	Weak transcription	Fetal Heart	heart
22	chr19:53305200-53314000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
23	chr19:53305400-53314000	ZNF genes & repeats	Fetal Intestine Small	intestine
24	chr19:53306000-53324000	Weak transcription	Colon Smooth Muscle	Colon
25	chr19:53306400-53314000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr19:53306400-53314000	ZNF genes & repeats	Esophagus	oesophagus
27	chr19:53306600-53314000	Strong transcription	Fetal Muscle Trunk	muscle
28	chr19:53306600-53324000	Weak transcription	Psoas Muscle	Psoas
29	chr19:53307000-53314000	Strong transcription	Skeletal Muscle Male	skeletal muscle
30	chr19:53308000-53319600	Weak transcription	HUVEC	blood vessel
31	chr19:53308200-53314000	Strong transcription	Fetal Muscle Leg	muscle
32	chr19:53308200-53319200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr19:53308200-53320200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr19:53308200-53324000	Weak transcription	Fetal Kidney	kidney
35	chr19:53310200-53314000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
36	chr19:53310600-53314000	Strong transcription	Fetal Brain Female	brain
37	chr19:53311000-53323600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr19:53311200-53320200	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr19:53311400-53314000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr19:53311400-53317600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr19:53311400-53323600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr19:53311400-53324000	Weak transcription	NHDF-Ad	bronchial
43	chr19:53311600-53314000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr19:53311600-53317600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr19:53311800-53314000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr19:53311800-53314000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr19:53312200-53314000	Strong transcription	Brain Anterior Caudate	brain
48	chr19:53312400-53314000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr19:53312400-53314000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr19:53312400-53314000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood

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