Variant report

Variant	esv3524144
Chromosome Location	chr19:53420493-53425635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:30)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:30 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA2	chr19:53423600-53423896	A549	lung:	n/a	n/a
2	GABPA	chr19:53423714-53423774	HepG2	liver:	n/a	n/a
3	HEY1	chr19:53425399-53426825	K562	blood:	n/a	n/a
4	NR2F2	chr19:53423539-53423804	K562	blood:	n/a	n/a
5	PAX5	chr19:53422436-53422659	GM12878	blood:	n/a	n/a
6	PAX5	chr19:53422427-53422738	GM12878	blood:	n/a	n/a
7	PAX5	chr19:53422424-53422626	GM12878	blood:	n/a	n/a
8	PAX5	chr19:53422456-53422686	GM12878	blood:	n/a	n/a
9	POLR2A	chr19:53424280-53424751	GM12878	blood:	n/a	n/a
10	POLR2A	chr19:53425600-53425637	MCF-7	breast:	n/a	n/a
11	POLR2A	chr19:53421656-53421811	HepG2	liver:	n/a	n/a
12	POLR2A	chr19:53425594-53425638	K562	blood:	n/a	n/a
13	POLR2A	chr19:53425541-53425725	GM12878	blood:	n/a	n/a
14	POLR2A	chr19:53425225-53425570	K562	blood:	n/a	n/a
15	POLR2A	chr19:53421328-53421725	K562	blood:	n/a	n/a
16	POLR2A	chr19:53424961-53425130	HepG2	liver:	n/a	n/a
17	POLR2A	chr19:53424986-53425201	GM12878	blood:	n/a	n/a
18	POLR2A	chr19:53425543-53425681	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr19:53425454-53426939	GM12892	blood:	n/a	n/a
20	POLR2A	chr19:53421267-53421287	K562	blood:	n/a	n/a
21	POLR2A	chr19:53420882-53420926	HepG2	liver:	n/a	n/a
22	POLR2A	chr19:53424300-53424366	K562	blood:	n/a	n/a
23	POLR2A	chr19:53425614-53426955	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr19:53421285-53421300	K562	blood:	n/a	n/a
25	POLR2A	chr19:53425455-53426135	GM12878	blood:	n/a	n/a
26	POLR2A	chr19:53425439-53426948	GM12878	blood:	n/a	n/a
27	POLR2A	chr19:53420953-53421091	HepG2	liver:	n/a	n/a
28	POLR2A	chr19:53425572-53425592	K562	blood:	n/a	n/a
29	POLR2A	chr19:53425536-53425605	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr19:53425517-53426947	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53424670-53424720	GM06990	blood:	n/a
2	chr19:53424670-53424720	AG09319	gingival:	n/a
3	chr19:53424670-53424720	AG10803	skin:	n/a
4	chr19:53424670-53424720	HEK293	kidney:	embryo
5	chr19:53424670-53424720	ProgFib	skin:	n/a
6	chr19:53424670-53424720	HMEC	breast:	n/a
7	chr19:53424670-53424720	A549	lung:	n/a
8	chr19:53424670-53424720	GM19239	blood:	n/a
9	chr19:53424670-53424720	NHBE	bronchial:	n/a
10	chr19:53424670-53424720	CMK	blood:	n/a
11	chr19:53424670-53424720	H1-hESC	embryonic stem cell:	embryo
12	chr19:53424670-53424720	HEEpiC	esophagus:	n/a
13	chr19:53424670-53424720	HL-60	blood:	n/a
14	chr19:53424670-53424720	PrEC	prostate:	n/a
15	chr19:53424670-53424720	SAEC	small airway:	n/a
16	chr19:53424670-53424720	HNPCEpiC	eye:	n/a
17	chr19:53424670-53424720	HAEpiC	amniotic membrane:	n/a
18	chr19:53424670-53424720	SK-N-SH_RA	brain:	n/a
19	chr19:53424670-53424720	HepG2	liver:	n/a
20	chr19:53424670-53424720	HUVEC	blood vessel:	n/a
21	chr19:53424670-53424720	Jurkat	blood:	n/a
22	chr19:53424670-53424720	Caco-2	colon:	n/a
23	chr19:53424670-53424720	SKMC	muscle:	n/a
24	chr19:53424670-53424720	NHDF-neo	bronchial:	n/a
25	chr19:53424670-53424720	K562	blood:	n/a
26	chr19:53424670-53424720	NT2-D1	testis:	n/a
27	chr19:53424670-53424720	NB4	blood:	n/a
28	chr19:53424670-53424720	PFSK-1	brain:	n/a
29	chr19:53424670-53424720	SK-N-MC	brain:	n/a
30	chr19:53424670-53424720	PANC-1	pancreas:	n/a
31	chr19:53424670-53424720	AG04449	skin:	fetal
32	chr19:53424670-53424720	U87	brain:	n/a
33	chr19:53424670-53424720	HCPEpiC	choroid plexus:	n/a
34	chr19:53424670-53424720	T-47D	breast:	n/a
35	chr19:53424670-53424720	GM12878	blood:	n/a
36	chr19:53424670-53424720	HIPEpiC	eye:	n/a
37	chr19:53424670-53424720	ECC-1	luminal epithelium:	n/a
38	chr19:53424670-53424720	HRE	kidney:	n/a
39	chr19:53424670-53424720	HCT-116	colon:	n/a
40	chr19:53424670-53424720	Hepatocyte	liver:	n/a
41	chr19:53424670-53424720	BJ	skin:	n/a
42	chr19:53424670-53424720	AG09309	skin:	n/a
43	chr19:53424670-53424720	IMR90	lung:	fetal
44	chr19:53424670-53424720	AG04450	lung:	fetal
45	chr19:53424670-53424720	RPTEC	kidney:	n/a
46	chr19:53424670-53424720	HCF	heart:	n/a
47	chr19:53424670-53424720	HRPEpiC	eye:	n/a
48	chr19:53424670-53424720	BE2_C	brain:	n/a
49	chr19:53424670-53424720	HPAEpiC	pulmonary alveolar:	n/a
50	chr19:53424670-53424720	NH-A	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53398338..53403121-chr19:53425170..53428184,6	K562	blood:
2	chr19:53419869..53422803-chr19:53423217..53426977,4	K562	blood:
3	chr19:53424791..53427731-chr19:53464365..53467863,4	K562	blood:
4	chr19:53399773..53402425-chr19:53424830..53427617,2	MCF-7	breast:
5	chr19:53424714..53426568-chr19:53443432..53446550,3	MCF-7	breast:
6	chr19:53398338..53401958-chr19:53425181..53428572,6	K562	blood:
7	chr19:53418400..53422745-chr19:53423096..53427800,7	K562	blood:
8	chr19:53419869..53422803-chr19:53423217..53426977,4	K562	blood:
9	chr19:53418400..53422745-chr19:53423096..53427800,7	K562	blood:
10	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269646	TF binding region
ZNF888	TF binding region
ENSG00000269646	CpG island
ZNF888	CpG island
ENSG00000221874	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000213801	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000213793	chromatin interactions

Extended variants
information (count: 213 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:213 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545098617	chr19:53420505-53420506	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs563798212	chr19:53420519-53420520	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs2016456	chr19:53420526-53420527	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs181336166	chr19:53420594-53420595	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560748518	chr19:53420658-53420659	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs3037968	chr19:53420663-53420664	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs58752402	chr19:53420664-53420665	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2870130	chr19:53420665-53420666	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs186068072	chr19:53420700-53420701	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs144705543	chr19:53420702-53420703	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs571487203	chr19:53420713-53420714	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs117158286	chr19:53420766-53420767	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs11669026	chr19:53420774-53420775	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs8111659	chr19:53420796-53420797	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs77090812	chr19:53420810-53420811	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11437452	chr19:53420812-53420813	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs71183855	chr19:53420813-53420814	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs377522037	chr19:53420828-53420829	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551014372	chr19:53420847-53420848	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs11669844	chr19:53420849-53420850	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567875535	chr19:53420863-53420864	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372024405	chr19:53420867-53420868	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535266768	chr19:53420881-53420882	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs147911288	chr19:53420889-53420890	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs539629428	chr19:53420908-53420909	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs553572394	chr19:53420910-53420911	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370712845	chr19:53420915-53420916	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs148663866	chr19:53420937-53420938	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs112355992	chr19:53420945-53420946	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs555241317	chr19:53420946-53420947	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs560718184	chr19:53420952-53420953	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142189089	chr19:53420985-53420986	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540067306	chr19:53420986-53420987	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs180743541	chr19:53420997-53420998	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs113109544	chr19:53421000-53421001	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs186508493	chr19:53421002-53421003	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs562348600	chr19:53421104-53421105	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529780569	chr19:53421163-53421164	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs371753216	chr19:53421175-53421176	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs10401262	chr19:53421196-53421197	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs566599218	chr19:53421211-53421212	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs190855517	chr19:53421227-53421228	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113678175	chr19:53421263-53421264	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs571868004	chr19:53421271-53421272	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs113000018	chr19:53421291-53421292	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs538963616	chr19:53421304-53421305	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557292859	chr19:53421344-53421345	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575254330	chr19:53421360-53421361	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs145203210	chr19:53421380-53421381	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs113543192	chr19:53421382-53421383	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Melanoma	20877625	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53401000-53425600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:53401400-53425600	Weak transcription	NHDF-Ad	bronchial
3	chr19:53401400-53425800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr19:53401600-53425600	Weak transcription	Brain Hippocampus Middle	brain
5	chr19:53401600-53425600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr19:53401600-53426000	Weak transcription	Brain Substantia Nigra	brain
7	chr19:53401800-53421200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr19:53401800-53425600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr19:53401800-53426000	Weak transcription	Brain Angular Gyrus	brain
10	chr19:53401800-53426000	Weak transcription	Right Ventricle	heart
11	chr19:53402000-53425800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr19:53402000-53425800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr19:53408800-53421400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:53409400-53420800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr19:53409600-53425600	Weak transcription	Fetal Kidney	kidney
16	chr19:53410000-53421400	Strong transcription	Rectal Mucosa Donor 31	rectum
17	chr19:53410400-53425400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:53410800-53425000	Weak transcription	Stomach Mucosa	stomach
19	chr19:53410800-53425000	Weak transcription	HepG2	liver
20	chr19:53410800-53425800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr19:53411400-53425600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr19:53411400-53425600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr19:53411400-53425600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr19:53411400-53425600	Weak transcription	HUVEC	blood vessel
25	chr19:53411400-53425800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr19:53411400-53425800	Weak transcription	Brain Anterior Caudate	brain
27	chr19:53411400-53426000	Weak transcription	HSMM	muscle
28	chr19:53411600-53420800	Weak transcription	Fetal Lung	lung
29	chr19:53411600-53425600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr19:53411600-53425800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr19:53411800-53425600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr19:53411800-53425600	Weak transcription	HMEC	breast
33	chr19:53412000-53422000	Strong transcription	Fetal Stomach	stomach
34	chr19:53412000-53426000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr19:53412200-53425800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr19:53412400-53425600	Weak transcription	Colonic Mucosa	Colon
37	chr19:53413400-53422200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr19:53413600-53425800	Weak transcription	Colon Smooth Muscle	Colon
39	chr19:53414400-53420600	Weak transcription	Gastric	stomach
40	chr19:53414600-53420800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr19:53414600-53425600	Weak transcription	Small Intestine	intestine
42	chr19:53415000-53421800	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr19:53415200-53421400	Strong transcription	Fetal Muscle Leg	muscle
44	chr19:53415400-53421600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr19:53415400-53422000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr19:53415600-53420800	Strong transcription	Placenta	Placenta
47	chr19:53415600-53421600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:53415600-53421800	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr19:53415600-53422000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr19:53415600-53422200	Strong transcription	Sigmoid Colon	Sigmoid Colon

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