Variant report

Variant	esv3412133
Chromosome Location	chr19:52907745-52935907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:366)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:52927611-52927688	GM10248	blood:	n/a	n/a
2	CTCF	chr19:52922700-52922797	GM13976	blood:	n/a	n/a
3	CUX1	chr19:52913956-52914001	GM12878	blood:	n/a	n/a
4	E2F6	chr19:52932315-52932507	K562	blood:	n/a	chr19:52932429-52932446 chr19:52932432-52932439 chr19:52932432-52932443 chr19:52932429-52932446 chr19:52932433-52932447 chr19:52932432-52932439 chr19:52932431-52932440 chr19:52932432-52932439 chr19:52932431-52932442 chr19:52932432-52932440 chr19:52932431-52932441 chr19:52932432-52932440
5	ELF1	chr19:52932156-52932587	K562	blood:	n/a	chr19:52932400-52932413 chr19:52932361-52932373 chr19:52932403-52932412 chr19:52932402-52932413
6	ELF1	chr19:52932161-52932605	K562	blood:	n/a	chr19:52932400-52932413 chr19:52932361-52932373 chr19:52932403-52932412 chr19:52932402-52932413 chr19:52932588-52932600
7	GABPA	chr19:52932259-52932534	K562	blood:	n/a	n/a
8	GATA2	chr19:52923635-52923876	K562	blood:	n/a	n/a
9	GATA3	chr19:52913479-52913820	T-47D	breast:	n/a	n/a
10	JUN	chr19:52920447-52920494	H1-hESC	embryonic stem cell:	n/a	n/a
11	KAP1	chr19:52918786-52919534	HEK293	kidney:	n/a	n/a
12	MAFF	chr19:52921167-52921364	HepG2	liver:	n/a	chr19:52921226-52921244
13	MAFK	chr19:52932263-52932303	K562	blood:	n/a	chr19:52932294-52932303
14	MAFK	chr19:52921107-52921374	IMR90	lung:	n/a	chr19:52921227-52921242
15	MAFK	chr19:52921068-52921404	HepG2	liver:	n/a	chr19:52921227-52921242
16	MAFK	chr19:52921091-52921361	HepG2	liver:	n/a	chr19:52921227-52921242
17	MYC	chr19:52912594-52912668	MCF-7	breast:	n/a	n/a
18	POLR2A	chr19:52920622-52920863	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr19:52921847-52921872	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr19:52927642-52927663	MCF-7	breast:	n/a	n/a
21	POLR2A	chr19:52919331-52919489	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr19:52908275-52908437	GM12878	blood:	n/a	n/a
23	POLR2A	chr19:52914678-52914774	GM12878	blood:	n/a	n/a
24	POLR2A	chr19:52920242-52920353	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr19:52926697-52926834	MCF-7	breast:	n/a	n/a
26	POLR2A	chr19:52920989-52921009	ProgFib	skin:	n/a	n/a
27	POLR2A	chr19:52923674-52923885	K562	blood:	n/a	n/a
28	POLR2A	chr19:52912605-52912680	MCF-7	breast:	n/a	n/a
29	POLR2A	chr19:52927669-52927699	MCF-7	breast:	n/a	n/a
30	POLR2A	chr19:52921661-52921686	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr19:52932321-52932574	K562	blood:	n/a	n/a
32	SETDB1	chr19:52918694-52920108	U2OS	brain:	n/a	n/a
33	STAT3	chr19:52916602-52916678	MCF10A-Er-Src	breast:	n/a	n/a
34	TAL1	chr19:52923679-52923950	K562	blood:	n/a	n/a
35	TEAD4	chr19:52923663-52923964	K562	blood:	n/a	n/a
36	TEAD4	chr19:52923688-52923887	K562	blood:	n/a	n/a
37	ZNF274	chr19:52918939-52919341	H1-hESC	embryonic stem cell:	n/a	n/a
38	ZNF274	chr19:52918740-52919498	NT2-D1	testis:	n/a	n/a
39	ZNF274	chr19:52919106-52919485	GM08714	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52934393-52934443	HRPEpiC	eye:	n/a
2	chr19:52933429-52933479	AG09309	skin:	n/a
3	chr19:52934466-52934516	NHDF-neo	bronchial:	n/a
4	chr19:52934393-52934443	AG10803	skin:	n/a
5	chr19:52933695-52933745	HIPEpiC	eye:	n/a
6	chr19:52934466-52934516	HCM	heart:	n/a
7	chr19:52934981-52935031	GM12892	blood:	n/a
8	chr19:52934393-52934443	AG09309	skin:	n/a
9	chr19:52934981-52935031	NHBE	bronchial:	n/a
10	chr19:52933429-52933479	AG09319	gingival:	n/a
11	chr19:52933429-52933479	K562	blood:	n/a
12	chr19:52934393-52934443	HCM	heart:	n/a
13	chr19:52934466-52934516	T-47D	breast:	n/a
14	chr19:52921300-52921350	AG04449	skin:	fetal
15	chr19:52934466-52934516	AG09319	gingival:	n/a
16	chr19:52934466-52934516	GM19239	blood:	n/a
17	chr19:52934393-52934443	AG09319	gingival:	n/a
18	chr19:52934466-52934516	SKMC	muscle:	n/a
19	chr19:52934393-52934443	CMK	blood:	n/a
20	chr19:52934981-52935031	SKMC	muscle:	n/a
21	chr19:52933695-52933745	GM12891	blood:	n/a
22	chr19:52934981-52935031	HEK293	kidney:	embryo
23	chr19:52934981-52935031	HRPEpiC	eye:	n/a
24	chr19:52934981-52935031	Caco-2	colon:	n/a
25	chr19:52921300-52921350	LNCaP	prostate:	n/a
26	chr19:52934466-52934516	U87	brain:	n/a
27	chr19:52934393-52934443	HIPEpiC	eye:	n/a
28	chr19:52921300-52921350	ECC-1	luminal epithelium:	n/a
29	chr19:52921300-52921350	HUVEC	blood vessel:	n/a
30	chr19:52933695-52933745	PANC-1	pancreas:	n/a
31	chr19:52934393-52934443	AoSMC	blood vessel:	n/a
32	chr19:52921300-52921350	Caco-2	colon:	n/a
33	chr19:52933695-52933745	Hepatocyte	liver:	n/a
34	chr19:52934393-52934443	BJ	skin:	n/a
35	chr19:52921300-52921350	HCF	heart:	n/a
36	chr19:52933695-52933745	GM19239	blood:	n/a
37	chr19:52934981-52935031	NH-A	brain:	n/a
38	chr19:52934393-52934443	HEEpiC	esophagus:	n/a
39	chr19:52934393-52934443	PFSK-1	brain:	n/a
40	chr19:52934466-52934516	NH-A	brain:	n/a
41	chr19:52934981-52935031	AG09319	gingival:	n/a
42	chr19:52934393-52934443	Caco-2	colon:	n/a
43	chr19:52934393-52934443	Hela-S3	cervix:	n/a
44	chr19:52934393-52934443	HRE	kidney:	n/a
45	chr19:52933695-52933745	NH-A	brain:	n/a
46	chr19:52933429-52933479	IMR90	lung:	fetal
47	chr19:52934466-52934516	AG09309	skin:	n/a
48	chr19:52934981-52935031	H1-hESC	embryonic stem cell:	embryo
49	chr19:52933429-52933479	H1-hESC	embryonic stem cell:	embryo
50	chr19:52921300-52921350	AG10803	skin:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52908988..52911904-chr19:52916328..52918022,2	K562	blood:
2	chr19:52903104..52905523-chr19:52907320..52908934,2	K562	blood:
3	chr19:52908988..52911904-chr19:52916328..52918022,2	K562	blood:
4	chr19:52918097..52920312-chr19:52920533..52923080,2	MCF-7	breast:
5	chr19:52918301..52920285-chr19:52922376..52925176,2	K562	blood:
6	chr19:52901728..52903647-chr19:52912630..52914410,2	MCF-7	breast:
7	chr19:52918301..52920285-chr19:52922376..52925176,2	K562	blood:
8	chr19:52918097..52920312-chr19:52920533..52923080,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF534-2	chr19:52918377-52918606	NONHSAT067551
2	lnc-ZNF534-2	chr19:52914625-52917621	NONHSAT067551
3	lnc-ZNF534-2	chr19:52918192-52918292	NONHSAT067551
4	lnc-ZNF83-8	chr19:52929116-52929455	NONHSAT067553

No data

Variant related genes	Relation type
ZNF528	TF binding region
ZNF534	TF binding region
DPPA5P1	TF binding region
ZNF528	CpG island
ZNF534	CpG island
DPPA5P1	CpG island
ENSG00000167555	chromatin interactions

Extended variants
information (count: 1370 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566659664	chr19:52907757-52907758	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115224238	chr19:52907779-52907780	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558508386	chr19:52907814-52907815	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs578140235	chr19:52907815-52907816	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545544245	chr19:52907828-52907829	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376712691	chr19:52907835-52907836	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577702796	chr19:52907848-52907849	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542677290	chr19:52907885-52907886	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201480206	chr19:52907886-52907887	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140599561	chr19:52907937-52907938	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555420241	chr19:52907950-52907951	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111608834	chr19:52907964-52907965	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375755064	chr19:52908117-52908118	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565367715	chr19:52908133-52908134	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369057929	chr19:52908164-52908165	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373838240	chr19:52908180-52908181	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs113364183	chr19:52908208-52908209	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568634864	chr19:52908234-52908235	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529599637	chr19:52908250-52908251	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544160968	chr19:52908297-52908298	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547889888	chr19:52908343-52908344	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566747759	chr19:52908389-52908390	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563750656	chr19:52908416-52908417	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573751220	chr19:52908431-52908432	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs370946440	chr19:52908458-52908459	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs11666879	chr19:52908481-52908482	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs552324227	chr19:52908483-52908484	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570692449	chr19:52908487-52908488	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116669745	chr19:52908498-52908499	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149144967	chr19:52908514-52908515	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186703643	chr19:52908515-52908516	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191166608	chr19:52908562-52908563	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114646522	chr19:52908575-52908576	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs183559386	chr19:52908586-52908587	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs57295520	chr19:52908604-52908605	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542737583	chr19:52908629-52908630	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530730784	chr19:52908701-52908702	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11084158	chr19:52908742-52908743	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs544402918	chr19:52908745-52908746	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562201116	chr19:52908773-52908774	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371437035	chr19:52908776-52908777	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140961573	chr19:52908779-52908780	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548167662	chr19:52908790-52908791	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371055947	chr19:52908793-52908794	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12459721	chr19:52908802-52908803	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs527569922	chr19:52908818-52908819	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552154878	chr19:52908844-52908845	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570783644	chr19:52908855-52908856	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537992750	chr19:52908875-52908876	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113070908	chr19:52908906-52908907	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Adrenocortical carcinoma	18281524	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
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52901800-52912600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:52902000-52908000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr19:52902000-52908800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr19:52902000-52913800	Weak transcription	Fetal Heart	heart
5	chr19:52902200-52908800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:52902200-52909200	Strong transcription	Placenta	Placenta
7	chr19:52902200-52909800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:52902200-52913800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr19:52902200-52917400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr19:52902200-52919200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:52902400-52910400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr19:52902400-52913400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr19:52902400-52913400	Strong transcription	Fetal Muscle Trunk	muscle
14	chr19:52902400-52917600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr19:52902600-52908200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr19:52902600-52910400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
17	chr19:52902600-52913000	Strong transcription	Fetal Stomach	stomach
18	chr19:52902600-52913600	Strong transcription	Stomach Smooth Muscle	stomach
19	chr19:52902600-52914000	ZNF genes & repeats	Lung	lung
20	chr19:52902600-52917600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr19:52902600-52918200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
22	chr19:52902800-52912800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr19:52902800-52913400	Strong transcription	Brain Inferior Temporal Lobe	brain
24	chr19:52902800-52914000	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr19:52902800-52914200	Strong transcription	Brain Anterior Caudate	brain
26	chr19:52902800-52914200	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr19:52902800-52915600	Strong transcription	HSMMtube	muscle
28	chr19:52902800-52924200	ZNF genes & repeats	Liver	Liver
29	chr19:52903000-52911800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
30	chr19:52903000-52913000	Strong transcription	Fetal Muscle Leg	muscle
31	chr19:52903000-52913600	Strong transcription	Brain Cingulate Gyrus	brain
32	chr19:52903000-52913600	Strong transcription	Brain Hippocampus Middle	brain
33	chr19:52903000-52914000	ZNF genes & repeats	Ovary	ovary
34	chr19:52903000-52916200	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr19:52903200-52907800	ZNF genes & repeats	Esophagus	oesophagus
36	chr19:52903200-52908400	Strong transcription	Left Ventricle	heart
37	chr19:52903200-52911800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr19:52903200-52916800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
39	chr19:52903400-52912600	Strong transcription	Dnd41	blood
40	chr19:52903600-52912200	Strong transcription	Fetal Lung	lung
41	chr19:52903600-52912600	Strong transcription	Rectal Smooth Muscle	rectum
42	chr19:52903800-52909200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr19:52903800-52910600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr19:52904200-52914000	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr19:52904200-52917200	Strong transcription	Brain Germinal Matrix	brain
46	chr19:52904200-52917600	Strong transcription	Right Ventricle	heart
47	chr19:52904400-52910600	Strong transcription	NH-A	brain
48	chr19:52904400-52913400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr19:52904400-52916200	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr19:52904400-52916200	Strong transcription	Brain Angular Gyrus	brain

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