Variant report

Variant	esv3412499
Chromosome Location	chr19:53353085-53391958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:612)
Chromatin interactive
region (count:12)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53360719-53361014	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
3	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
4	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
5	BHLHE40	chr19:53376302-53376339	K562	blood:	n/a	n/a
6	CBX3	chr19:53383913-53384365	K562	blood:	n/a	n/a
7	CBX3	chr19:53376216-53376620	K562	blood:	n/a	n/a
8	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
9	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
10	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
11	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
13	CEBPD	chr19:53376161-53376655	K562	blood:	n/a	n/a
14	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
15	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
16	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
17	CTCF	chr19:53384676-53384683	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
19	CTCF	chr19:53360924-53361043	Kidney_OC	kidney:	n/a	chr19:53360990-53361003
20	CTCF	chr19:53361020-53361170	GM12875	blood:	n/a	n/a
21	CTCF	chr19:53360927-53361017	Hela-S3	cervix:	n/a	chr19:53360990-53361003
22	CTCF	chr19:53382813-53382847	GM13977	blood:	n/a	n/a
23	CTCF	chr19:53361020-53361170	HCM	heart:	n/a	n/a
24	CTCF	chr19:53360901-53361081	K562	blood:	n/a	chr19:53360990-53361003
25	CTCF	chr19:53361000-53361150	HVMF	connective:	n/a	n/a
26	CTCF	chr19:53361040-53361190	HAc	cerebellar:	n/a	n/a
27	CTCF	chr19:53360940-53361025	GM12892	blood:	n/a	chr19:53360990-53361003
28	CTCF	chr19:53361020-53361170	HRE	kidney:	n/a	n/a
29	CTCF	chr19:53360771-53361087	Spleen_OC	spleen:	n/a	chr19:53360990-53361003
30	CTCF	chr19:53361040-53361190	GM12873	blood:	n/a	n/a
31	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:53361040-53361190	GM12865	blood:	n/a	n/a
33	CTCF	chr19:53361000-53361150	GM12865	blood:	n/a	n/a
34	CTCF	chr19:53360794-53360918	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr19:53360828-53360986	GM19239	blood:	n/a	n/a
36	CTCF	chr19:53360919-53361045	GM19240	blood:	n/a	chr19:53360990-53361003
37	CTCF	chr19:53361020-53361170	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr19:53360835-53361022	GM19238	blood:	n/a	chr19:53360990-53361003
39	CTCF	chr19:53360909-53361007	LNCaP	prostate:	n/a	chr19:53360990-53361003
40	CTCF	chr19:53360920-53361070	HMEC	breast:	n/a	chr19:53360990-53361003
41	CTCF	chr19:53360843-53361097	K562	blood:	n/a	chr19:53360990-53361003
42	CTCF	chr19:53391416-53391462	GM20000	blood:	n/a	n/a
43	CTCF	chr19:53360980-53361130	BE2_C	brain:	n/a	chr19:53360990-53361003
44	CTCF	chr19:53360855-53360873	NHEK	skin:	n/a	n/a
45	CTCF	chr19:53360980-53361130	HCT-116	colon:	n/a	chr19:53360990-53361003
46	CTCF	chr19:53360987-53361008	GM19239	blood:	n/a	chr19:53360990-53361003
47	CTCF	chr19:53361000-53361150	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr19:53361000-53361150	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr19:53361020-53361170	BJ	skin:	n/a	n/a
50	CTCF	chr19:53361020-53361170	GM12871	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53383549-53383599	SKMC	muscle:	n/a
2	chr19:53357134-53357184	PFSK-1	brain:	n/a
3	chr19:53383549-53383599	SKMC	muscle:	n/a
4	chr19:53357134-53357184	PFSK-1	brain:	n/a
5	chr19:53361164-53361214	Jurkat	blood:	n/a
6	chr19:53360213-53360263	U87	brain:	n/a
7	chr19:53383549-53383599	AG04449	skin:	fetal
8	chr19:53383549-53383599	IMR90	lung:	fetal
9	chr19:53360728-53360778	BE2_C	brain:	n/a
10	chr19:53361164-53361214	HRPEpiC	eye:	n/a
11	chr19:53362925-53362975	SAEC	small airway:	n/a
12	chr19:53361066-53361116	PFSK-1	brain:	n/a
13	chr19:53383549-53383599	HPAEpiC	pulmonary alveolar:	n/a
14	chr19:53357134-53357184	NHDF-neo	bronchial:	n/a
15	chr19:53361448-53361498	U87	brain:	n/a
16	chr19:53359733-53359783	GM12892	blood:	n/a
17	chr19:53361448-53361498	Caco-2	colon:	n/a
18	chr19:53360728-53360778	HIPEpiC	eye:	n/a
19	chr19:53359733-53359783	ProgFib	skin:	n/a
20	chr19:53363482-53363532	ECC-1	luminal epithelium:	n/a
21	chr19:53360728-53360778	RPTEC	kidney:	n/a
22	chr19:53383549-53383599	HCPEpiC	choroid plexus:	n/a
23	chr19:53359733-53359783	NHBE	bronchial:	n/a
24	chr19:53361448-53361498	LNCaP	prostate:	n/a
25	chr19:53383549-53383599	SAEC	small airway:	n/a
26	chr19:53360728-53360778	SKMC	muscle:	n/a
27	chr19:53361164-53361214	LNCaP	prostate:	n/a
28	chr19:53362925-53362975	HCF	heart:	n/a
29	chr19:53360213-53360263	NB4	blood:	n/a
30	chr19:53357134-53357184	K562	blood:	n/a
31	chr19:53362925-53362975	HCT-116	colon:	n/a
32	chr19:53361164-53361214	NH-A	brain:	n/a
33	chr19:53359733-53359783	HL-60	blood:	n/a
34	chr19:53363482-53363532	AoSMC	blood vessel:	n/a
35	chr19:53383549-53383599	AG09309	skin:	n/a
36	chr19:53361448-53361498	HRPEpiC	eye:	n/a
37	chr19:53361448-53361498	H1-hESC	embryonic stem cell:	embryo
38	chr19:53360213-53360263	PrEC	prostate:	n/a
39	chr19:53360213-53360263	RPTEC	kidney:	n/a
40	chr19:53361448-53361498	HEK293	kidney:	embryo
41	chr19:53362925-53362975	T-47D	breast:	n/a
42	chr19:53361164-53361214	HEK293	kidney:	embryo
43	chr19:53361164-53361214	AG04449	skin:	fetal
44	chr19:53361164-53361214	Hela-S3	cervix:	n/a
45	chr19:53357134-53357184	Caco-2	colon:	n/a
46	chr19:53362925-53362975	HUVEC	blood vessel:	n/a
47	chr19:53360213-53360263	HEK293	kidney:	embryo
48	chr19:53361164-53361214	AG04450	lung:	fetal
49	chr19:53359733-53359783	HMEC	breast:	n/a
50	chr19:53360728-53360778	HRPEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
2	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
3	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
4	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:
5	chr19:53377771..53379611-chr19:53399736..53401870,2	K562	blood:
6	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:
7	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
8	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
9	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
10	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
11	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
12	chr19:53390480..53393412-chr19:53415932..53418277,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-2	chr19:53365060-53366119	NONHSAT067590
2	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067591
3	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
4	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
5	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
6	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
7	lnc-ZNF320-3	chr19:53382704-53382886	NONHSAT067592
8	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067592
9	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
10	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
11	lnc-ZNF320-1	chr19:53379431-53379838	NONHSAT067593
12	lnc-ZNF320-3	chr19:53377411-53377490	NONHSAT067591
13	lnc-ZNF320-3	chr19:53367043-53367412	NONHSAT067591
14	lnc-ZNF320-3	chr19:53367175-53367412	NONHSAT067592
15	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
16	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
17	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF320	hsa-miR-192-5p	chr19:53381440-53381461

Variant related genes	Relation type
ENSG00000268225	TF binding region
ZNF320	TF binding region
ZNF28	TF binding region
ZNF468	TF binding region
ENSG00000268225	CpG island
ZNF320	CpG island
ZNF28	CpG island
ZNF468	CpG island
ENSG00000269646	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000198538	chromatin interactions

Extended variants
information (count: 1997 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548267339	chr19:53353110-53353111	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs187126789	chr19:53353113-53353114	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs148817726	chr19:53353120-53353121	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs58424417	chr19:53353141-53353142	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs571585356	chr19:53353149-53353150	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs10421456	chr19:53353151-53353152	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs556902872	chr19:53353169-53353170	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs11672777	chr19:53353230-53353231	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs3960272	chr19:53353234-53353235	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556742689	chr19:53353277-53353278	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs555045595	chr19:53353288-53353289	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs372146177	chr19:53353308-53353309	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs114915307	chr19:53353342-53353343	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs540409365	chr19:53353385-53353386	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs114646206	chr19:53353396-53353397	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs143469775	chr19:53353459-53353460	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs544536392	chr19:53353464-53353465	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs530461919	chr19:53353471-53353472	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150954493	chr19:53353485-53353486	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs56167334	chr19:53353495-53353496	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs570277231	chr19:53353504-53353505	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs201863485	chr19:53353577-53353578	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs142072185	chr19:53353578-53353579	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs146660563	chr19:53353580-53353581	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs139263902	chr19:53353582-53353583	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs181614796	chr19:53353598-53353599	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs28715134	chr19:53353601-53353602	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs28579478	chr19:53353602-53353603	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs7257628	chr19:53353636-53353637	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7257653	chr19:53353700-53353701	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536042691	chr19:53353718-53353719	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs185690202	chr19:53353721-53353722	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs554701968	chr19:53353726-53353727	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190153100	chr19:53353732-53353733	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs182504858	chr19:53353740-53353741	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7257841	chr19:53353742-53353743	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs573071552	chr19:53353747-53353748	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs376363604	chr19:53353778-53353779	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs111982805	chr19:53353784-53353785	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs577123383	chr19:53353807-53353808	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs552557918	chr19:53353832-53353833	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs540493725	chr19:53353847-53353848	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs113820231	chr19:53353848-53353849	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs558551394	chr19:53353869-53353870	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs186278326	chr19:53353879-53353880	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs559557003	chr19:53353880-53353881	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs111405711	chr19:53353881-53353882	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs113598785	chr19:53353891-53353892	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs556485521	chr19:53353902-53353903	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs574675779	chr19:53353918-53353919	Weak transcription Strong transcription ZNF genes & repeats	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
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53338800-53355000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:53339000-53357600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr19:53339000-53357800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
4	chr19:53339000-53359200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
5	chr19:53340600-53355000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
6	chr19:53340800-53355000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
7	chr19:53340800-53355000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:53340800-53357400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr19:53340800-53357800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
10	chr19:53341200-53353800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr19:53342200-53353200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
12	chr19:53342200-53355000	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
13	chr19:53342200-53357600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr19:53342400-53357800	ZNF genes & repeats	Liver	Liver
15	chr19:53343200-53359200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
16	chr19:53344000-53358000	ZNF genes & repeats	Lung	lung
17	chr19:53345400-53360200	Weak transcription	Fetal Heart	heart
18	chr19:53345400-53360200	Weak transcription	Hela-S3	cervix
19	chr19:53345800-53360400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr19:53346000-53355000	Strong transcription	Brain Inferior Temporal Lobe	brain
21	chr19:53346200-53353200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr19:53346200-53355000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:53346200-53357800	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr19:53346200-53357800	Strong transcription	Fetal Stomach	stomach
25	chr19:53346400-53355000	Strong transcription	Fetal Muscle Trunk	muscle
26	chr19:53346400-53357800	Strong transcription	Fetal Muscle Leg	muscle
27	chr19:53346400-53360400	Weak transcription	Fetal Brain Male	brain
28	chr19:53347200-53353200	Strong transcription	Brain Angular Gyrus	brain
29	chr19:53347200-53356400	Strong transcription	Placenta	Placenta
30	chr19:53347600-53357600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr19:53347600-53360000	Weak transcription	HMEC	breast
32	chr19:53347800-53355000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
33	chr19:53347800-53357600	Strong transcription	Stomach Smooth Muscle	stomach
34	chr19:53348000-53354800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
35	chr19:53348000-53355600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:53348000-53359200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr19:53348000-53359200	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr19:53348000-53360200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr19:53348200-53355000	Strong transcription	Left Ventricle	heart
40	chr19:53348200-53357600	Strong transcription	Adipose Nuclei	Adipose
41	chr19:53348200-53358200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr19:53348400-53353400	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr19:53348400-53355000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr19:53348400-53355000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr19:53348600-53353400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr19:53348600-53354400	Strong transcription	Fetal Thymus	thymus
47	chr19:53348600-53357600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr19:53348600-53358800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr19:53348600-53360200	Weak transcription	Stomach Mucosa	stomach
50	chr19:53349200-53356800	Weak transcription	Fetal Kidney	kidney

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