Variant report

Variant	esv3319158
Chromosome Location	chr19:53225543-53236310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53227580-53227746	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:53227189-53227366	K562	blood:	n/a	n/a
3	ARID3A	chr19:53228340-53228382	K562	blood:	n/a	n/a
4	ARID3A	chr19:53228598-53228749	K562	blood:	n/a	n/a
5	ATF1	chr19:53233027-53233245	K562	blood:	n/a	n/a
6	ATF1	chr19:53227069-53227523	K562	blood:	n/a	n/a
7	ATF3	chr19:53228814-53229132	K562	blood:	n/a	n/a
8	BCL3	chr19:53235753-53236010	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:53229503-53229523	K562	blood:	n/a	n/a
10	BHLHE40	chr19:53228364-53229160	K562	blood:	n/a	n/a
11	BHLHE40	chr19:53227179-53227448	K562	blood:	n/a	n/a
12	CBX3	chr19:53226892-53227577	K562	blood:	n/a	n/a
13	CBX3	chr19:53228183-53229250	K562	blood:	n/a	n/a
14	CCNT2	chr19:53228300-53228706	K562	blood:	n/a	n/a
15	CCNT2	chr19:53228944-53229189	K562	blood:	n/a	n/a
16	CEBPB	chr19:53232623-53232823	IMR90	lung:	n/a	n/a
17	CEBPB	chr19:53232598-53232808	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:53234585-53234747	HepG2	liver:	n/a	chr19:53234679-53234690
19	CEBPB	chr19:53234633-53234653	K562	blood:	n/a	n/a
20	CEBPB	chr19:53227084-53227394	K562	blood:	n/a	n/a
21	CEBPB	chr19:53232571-53232835	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr19:53225607-53225921	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:53225552-53226003	IMR90	lung:	n/a	n/a
24	CEBPD	chr19:53226938-53227607	K562	blood:	n/a	n/a
25	CEBPD	chr19:53227157-53227540	K562	blood:	n/a	n/a
26	CHD2	chr19:53228983-53229099	K562	blood:	n/a	n/a
27	CTCF	chr19:53227119-53227241	K562	blood:	n/a	n/a
28	CTCF	chr19:53232594-53232629	GM13976	blood:	n/a	n/a
29	CTCF	chr19:53227789-53227958	K562	blood:	n/a	n/a
30	CUX1	chr19:53226892-53227369	K562	blood:	n/a	n/a
31	CUX1	chr19:53228792-53228867	K562	blood:	n/a	n/a
32	E2F4	chr19:53225632-53225879	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F6	chr19:53228913-53229178	K562	blood:	n/a	chr19:53229068-53229078
34	E2F6	chr19:53227295-53227424	K562	blood:	n/a	n/a
35	E2F6	chr19:53228255-53229209	K562	blood:	n/a	chr19:53229068-53229078 chr19:53228656-53228668
36	E2F6	chr19:53228488-53228912	K562	blood:	n/a	chr19:53228656-53228668
37	E2F6	chr19:53228279-53229276	K562	blood:	n/a	chr19:53229068-53229078 chr19:53228656-53228668
38	ELF1	chr19:53228291-53229270	K562	blood:	n/a	chr19:53229136-53229148 chr19:53229007-53229018 chr19:53229008-53229017 chr19:53229007-53229018
39	ELF1	chr19:53228644-53229316	K562	blood:	n/a	chr19:53229136-53229148 chr19:53229007-53229018 chr19:53229008-53229017 chr19:53229007-53229018
40	ELK1	chr19:53228755-53229124	K562	blood:	n/a	n/a
41	EP300	chr19:53228712-53229145	K562	blood:	n/a	chr19:53229008-53229015
42	EP300	chr19:53225686-53225937	Hela-S3	cervix:	n/a	chr19:53225845-53225854
43	EP300	chr19:53228867-53229002	GM12878	blood:	n/a	n/a
44	EP300	chr19:53228231-53228368	K562	blood:	n/a	n/a
45	EP300	chr19:53227152-53227386	K562	blood:	n/a	n/a
46	EP300	chr19:53226858-53227812	K562	blood:	n/a	n/a
47	FOS	chr19:53225602-53225967	Hela-S3	cervix:	n/a	chr19:53225754-53225762 chr19:53225757-53225765 chr19:53225845-53225854 chr19:53225845-53225852 chr19:53225843-53225854
48	FOS	chr19:53225570-53226014	MCF10A-Er-Src	breast:	n/a	chr19:53225754-53225762 chr19:53225757-53225765 chr19:53225845-53225854 chr19:53225845-53225852 chr19:53225843-53225854
49	FOS	chr19:53225484-53225999	MCF10A-Er-Src	breast:	n/a	chr19:53225754-53225762 chr19:53225757-53225765 chr19:53225845-53225854 chr19:53225845-53225852 chr19:53225843-53225854
50	FOS	chr19:53225477-53226075	HUVEC	blood vessel:	n/a	chr19:53225754-53225762 chr19:53225757-53225765 chr19:53225845-53225854 chr19:53225845-53225852 chr19:53225843-53225854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53233245-53233295	Hepatocyte	liver:	n/a
2	chr19:53233245-53233295	Hepatocyte	liver:	n/a
3	chr19:53233368-53233418	MCF-7	breast:	n/a
4	chr19:53228974-53229024	AG09309	skin:	n/a
5	chr19:53228974-53229024	HCM	heart:	n/a
6	chr19:53234126-53234176	GM12891	blood:	n/a
7	chr19:53228974-53229024	CMK	blood:	n/a
8	chr19:53229096-53229146	ProgFib	skin:	n/a
9	chr19:53234126-53234176	HEK293	kidney:	embryo
10	chr19:53233245-53233295	HEEpiC	esophagus:	n/a
11	chr19:53233164-53233214	MCF10A-Er-Src	breast:	n/a
12	chr19:53229096-53229146	Caco-2	colon:	n/a
13	chr19:53233368-53233418	HUVEC	blood vessel:	n/a
14	chr19:53233368-53233418	T-47D	breast:	n/a
15	chr19:53233245-53233295	NHBE	bronchial:	n/a
16	chr19:53233164-53233214	IMR90	lung:	fetal
17	chr19:53234126-53234176	HepG2	liver:	n/a
18	chr19:53233245-53233295	SKMC	muscle:	n/a
19	chr19:53233368-53233418	NT2-D1	testis:	n/a
20	chr19:53228974-53229024	HCPEpiC	choroid plexus:	n/a
21	chr19:53228974-53229024	AG04450	lung:	fetal
22	chr19:53229096-53229146	HL-60	blood:	n/a
23	chr19:53233368-53233418	Hela-S3	cervix:	n/a
24	chr19:53233164-53233214	Jurkat	blood:	n/a
25	chr19:53233164-53233214	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:53233164-53233214	HUVEC	blood vessel:	n/a
27	chr19:53233368-53233418	Jurkat	blood:	n/a
28	chr19:53233083-53233133	AoSMC	blood vessel:	n/a
29	chr19:53233083-53233133	AG10803	skin:	n/a
30	chr19:53229096-53229146	PANC-1	pancreas:	n/a
31	chr19:53233245-53233295	HepG2	liver:	n/a
32	chr19:53233164-53233214	ProgFib	skin:	n/a
33	chr19:53233164-53233214	HRCEpiC	kidney:	n/a
34	chr19:53229766-53229816	NH-A	brain:	n/a
35	chr19:53233245-53233295	SK-N-SH	brain:	n/a
36	chr19:53229766-53229816	NHDF-neo	bronchial:	n/a
37	chr19:53228974-53229024	HRPEpiC	eye:	n/a
38	chr19:53233164-53233214	SK-N-SH_RA	brain:	n/a
39	chr19:53233245-53233295	HCPEpiC	choroid plexus:	n/a
40	chr19:53229766-53229816	HRPEpiC	eye:	n/a
41	chr19:53233368-53233418	ECC-1	luminal epithelium:	n/a
42	chr19:53234126-53234176	GM12878	blood:	n/a
43	chr19:53234126-53234176	PFSK-1	brain:	n/a
44	chr19:53233245-53233295	LNCaP	prostate:	n/a
45	chr19:53234126-53234176	BE2_C	brain:	n/a
46	chr19:53228974-53229024	BE2_C	brain:	n/a
47	chr19:53233083-53233133	AG09309	skin:	n/a
48	chr19:53233368-53233418	BJ	skin:	n/a
49	chr19:53234126-53234176	HUVEC	blood vessel:	n/a
50	chr19:53233368-53233418	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:53233250..53234773-chr19:53236233..53238057,2	K562	blood:
2	chr19:53227707..53230460-chr19:53236213..53239636,6	K562	blood:
3	chr19:53236244..53237950-chr19:53242142..53244901,2	K562	blood:
4	chr19:53226674..53228672-chr19:53232730..53234940,2	K562	blood:
5	chr19:53227642..53230112-chr19:53236849..53239461,2	K562	blood:
6	chr19:53226674..53228672-chr19:53232730..53234940,2	K562	blood:
7	chr19:53233250..53234773-chr19:53236233..53238057,2	K562	blood:
8	chr19:53227707..53230460-chr19:53236213..53239636,6	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF83-5	chr19:53226674-53227917	NONHSAT067581
2	lnc-ZNF83-5	chr19:53231983-53232084	NONHSAT067579
3	lnc-ZNF83-5	chr19:53233159-53233258	NONHSAT067580
4	lnc-ZNF83-5	chr19:53233159-53233258	NONHSAT067579
5	lnc-ZNF83-5	chr19:53231983-53232084	NONHSAT067580
6	lnc-ZNF83-5	chr19:53227124-53227242	NONHSAT067579

Variant related genes	Relation type
ZNF611	TF binding region
ZNF611	CpG island
ENSG00000213020	chromatin interactions

Extended variants
information (count: 635 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532093975	chr19:53225568-53225569	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565812650	chr19:53225592-53225593	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376884438	chr19:53225640-53225641	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559207018	chr19:53225643-53225644	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6509681	chr19:53225649-53225650	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs75804103	chr19:53225666-53225667	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115329274	chr19:53225681-53225682	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73576376	chr19:53225689-53225690	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs7258734	chr19:53225722-53225723	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183537668	chr19:53225753-53225754	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573975027	chr19:53225754-53225755	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73576380	chr19:53225773-53225774	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs113700253	chr19:53225776-53225777	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568909514	chr19:53225784-53225785	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553183304	chr19:53225785-53225786	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572538798	chr19:53225828-53225829	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188754809	chr19:53225840-53225841	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193181052	chr19:53225855-53225856	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531614556	chr19:53225947-53225948	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185097778	chr19:53225981-53225982	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562082284	chr19:53225983-53225984	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529537106	chr19:53225987-53225988	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111827602	chr19:53226004-53226005	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367915339	chr19:53226010-53226011	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7246970	chr19:53226023-53226024	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs531729664	chr19:53226031-53226032	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551208751	chr19:53226034-53226035	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113160154	chr19:53226102-53226103	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372056346	chr19:53226158-53226159	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397936249	chr19:53226177-53226178	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111557828	chr19:53226180-53226181	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113702340	chr19:53226248-53226249	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs58333113	chr19:53226253-53226254	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs148984664	chr19:53226268-53226269	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143801678	chr19:53226291-53226292	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577785153	chr19:53226292-53226293	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs56704961	chr19:53226295-53226296	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs188515759	chr19:53226296-53226297	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs58076588	chr19:53226319-53226320	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs535030205	chr19:53226343-53226344	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543454809	chr19:53226387-53226388	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59694757	chr19:53226436-53226437	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs574026270	chr19:53226454-53226455	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541339749	chr19:53226458-53226459	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192719495	chr19:53226461-53226462	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533364050	chr19:53226503-53226504	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs56217135	chr19:53226526-53226527	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551910086	chr19:53226531-53226532	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111614312	chr19:53226613-53226614	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73576389	chr19:53226642-53226643	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53206600-53227200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr19:53209400-53225800	Weak transcription	Hela-S3	cervix
3	chr19:53210200-53227000	Weak transcription	Fetal Heart	heart
4	chr19:53210400-53236600	Weak transcription	Psoas Muscle	Psoas
5	chr19:53210600-53237200	Weak transcription	NHDF-Ad	bronchial
6	chr19:53212200-53227000	Strong transcription	Fetal Stomach	stomach
7	chr19:53212400-53231000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr19:53212600-53226800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr19:53214800-53237200	Weak transcription	Stomach Mucosa	stomach
10	chr19:53215800-53237000	Weak transcription	Brain Angular Gyrus	brain
11	chr19:53216000-53230000	Weak transcription	HSMM	muscle
12	chr19:53216400-53230800	Weak transcription	Colon Smooth Muscle	Colon
13	chr19:53216600-53228200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr19:53216600-53228600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr19:53216600-53230600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr19:53216800-53236600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr19:53217400-53228000	Weak transcription	Aorta	Aorta
18	chr19:53217400-53230200	Weak transcription	Small Intestine	intestine
19	chr19:53217600-53229800	Weak transcription	Brain Substantia Nigra	brain
20	chr19:53218800-53226200	Weak transcription	Primary T cells from cord blood	blood
21	chr19:53218800-53226800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr19:53218800-53226800	Weak transcription	A549	lung
23	chr19:53218800-53228600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr19:53218800-53230000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr19:53219000-53227200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr19:53219000-53228400	Weak transcription	HSMMtube	muscle
27	chr19:53219200-53228600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr19:53219600-53230000	Weak transcription	Primary B cells from cord blood	blood
29	chr19:53220600-53231400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
30	chr19:53221000-53237400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr19:53222200-53227200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:53222400-53226000	Weak transcription	K562	blood
33	chr19:53222600-53225600	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr19:53223400-53225600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr19:53223400-53225600	ZNF genes & repeats	Thymus	Thymus
36	chr19:53223400-53232200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
37	chr19:53223600-53225800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:53223600-53225800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
39	chr19:53223600-53229600	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr19:53223800-53225600	Strong transcription	Fetal Muscle Trunk	muscle
41	chr19:53223800-53225600	ZNF genes & repeats	Fetal Thymus	thymus
42	chr19:53223800-53225800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr19:53223800-53226200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
44	chr19:53223800-53227000	ZNF genes & repeats	Dnd41	blood
45	chr19:53224000-53232400	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr19:53224200-53228600	Weak transcription	Left Ventricle	heart
47	chr19:53224200-53228600	Weak transcription	NHLF	lung
48	chr19:53224400-53226800	Weak transcription	Adipose Nuclei	Adipose
49	chr19:53224400-53226800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr19:53224400-53227000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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