Variant report

Variant	nsv1060712
Chromosome Location	chr19:53327378-53364138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:671)
Chromatin interactive
region (count:13)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 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	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
3	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
4	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
5	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
6	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
7	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
8	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
9	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
10	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr19:53328995-53329384	K562	blood:	n/a	n/a
12	CEBPB	chr19:53329163-53329370	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
14	CEBPB	chr19:53329098-53329325	K562	blood:	n/a	n/a
15	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
16	CEBPB	chr19:53329092-53329271	MCF-7	breast:	n/a	n/a
17	CEBPB	chr19:53329012-53329572	K562	blood:	n/a	n/a
18	CEBPB	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
19	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
20	CEBPD	chr19:53329085-53329417	K562	blood:	n/a	n/a
21	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
22	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
23	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
24	CTCF	chr19:53361000-53361150	GM12865	blood:	n/a	n/a
25	CTCF	chr19:53360859-53361107	Lung_OC	lung:	n/a	chr19:53360990-53361003
26	CTCF	chr19:53328417-53328457	K562	blood:	n/a	n/a
27	CTCF	chr19:53361000-53361150	HVMF	connective:	n/a	n/a
28	CTCF	chr19:53361020-53361170	HCM	heart:	n/a	n/a
29	CTCF	chr19:53361020-53361170	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr19:53360940-53361025	GM12892	blood:	n/a	chr19:53360990-53361003
31	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:53360980-53361130	GM12866	blood:	n/a	chr19:53360990-53361003
33	CTCF	chr19:53360980-53361130	SK-N-SH_RA	brain:	n/a	chr19:53360990-53361003
34	CTCF	chr19:53360774-53361155	K562	blood:	n/a	chr19:53360990-53361003
35	CTCF	chr19:53360980-53361130	HCT-116	colon:	n/a	chr19:53360990-53361003
36	CTCF	chr19:53361020-53361170	BJ	skin:	n/a	n/a
37	CTCF	chr19:53360835-53361022	GM19238	blood:	n/a	chr19:53360990-53361003
38	CTCF	chr19:53360980-53361130	HCM	heart:	n/a	chr19:53360990-53361003
39	CTCF	chr19:53361020-53361170	AG09309	skin:	n/a	n/a
40	CTCF	chr19:53361020-53361170	AG10803	skin:	n/a	n/a
41	CTCF	chr19:53360901-53361081	K562	blood:	n/a	chr19:53360990-53361003
42	CTCF	chr19:53361000-53361150	GM12870	blood:	n/a	n/a
43	CTCF	chr19:53360771-53361087	Spleen_OC	spleen:	n/a	chr19:53360990-53361003
44	CTCF	chr19:53361040-53361190	HAc	cerebellar:	n/a	n/a
45	CTCF	chr19:53352092-53352147	GM13976	blood:	n/a	n/a
46	CTCF	chr19:53360980-53361130	BE2_C	brain:	n/a	chr19:53360990-53361003
47	CTCF	chr19:53361060-53361210	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
49	CTCF	chr19:53360855-53360873	NHEK	skin:	n/a	n/a
50	CTCF	chr19:53328020-53328170	HCPEpiC	choroid plexus:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53357134-53357184	AG04450	lung:	fetal
2	chr19:53344366-53344416	AG09319	gingival:	n/a
3	chr19:53361448-53361498	GM12892	blood:	n/a
4	chr19:53363482-53363532	HUVEC	blood vessel:	n/a
5	chr19:53363482-53363532	GM12878	blood:	n/a
6	chr19:53363482-53363532	HRPEpiC	eye:	n/a
7	chr19:53360728-53360778	GM12878	blood:	n/a
8	chr19:53344366-53344416	HUVEC	blood vessel:	n/a
9	chr19:53360728-53360778	CMK	blood:	n/a
10	chr19:53360213-53360263	Hela-S3	cervix:	n/a
11	chr19:53342580-53342630	HRCEpiC	kidney:	n/a
12	chr19:53363482-53363532	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:53362925-53362975	HCT-116	colon:	n/a
14	chr19:53361448-53361498	GM06990	blood:	n/a
15	chr19:53359733-53359783	HepG2	liver:	n/a
16	chr19:53357134-53357184	GM12878	blood:	n/a
17	chr19:53357134-53357184	A549	lung:	n/a
18	chr19:53360728-53360778	A549	lung:	n/a
19	chr19:53359733-53359783	AG04450	lung:	fetal
20	chr19:53361164-53361214	HepG2	liver:	n/a
21	chr19:53362925-53362975	BE2_C	brain:	n/a
22	chr19:53363482-53363532	PrEC	prostate:	n/a
23	chr19:53360728-53360778	BJ	skin:	n/a
24	chr19:53357134-53357184	MCF-7	breast:	n/a
25	chr19:53344366-53344416	GM19239	blood:	n/a
26	chr19:53361066-53361116	NHDF-neo	bronchial:	n/a
27	chr19:53360213-53360263	BE2_C	brain:	n/a
28	chr19:53363482-53363532	PFSK-1	brain:	n/a
29	chr19:53361448-53361498	Caco-2	colon:	n/a
30	chr19:53357134-53357184	PANC-1	pancreas:	n/a
31	chr19:53363482-53363532	HCF	heart:	n/a
32	chr19:53360213-53360263	ProgFib	skin:	n/a
33	chr19:53361066-53361116	AG10803	skin:	n/a
34	chr19:53362925-53362975	HRPEpiC	eye:	n/a
35	chr19:53357134-53357184	AoSMC	blood vessel:	n/a
36	chr19:53360213-53360263	HPAEpiC	pulmonary alveolar:	n/a
37	chr19:53360728-53360778	Hepatocyte	liver:	n/a
38	chr19:53359733-53359783	HRCEpiC	kidney:	n/a
39	chr19:53363482-53363532	PANC-1	pancreas:	n/a
40	chr19:53361164-53361214	Hela-S3	cervix:	n/a
41	chr19:53360728-53360778	T-47D	breast:	n/a
42	chr19:53344366-53344416	BE2_C	brain:	n/a
43	chr19:53359733-53359783	LNCaP	prostate:	n/a
44	chr19:53360728-53360778	H1-hESC	embryonic stem cell:	embryo
45	chr19:53360728-53360778	SK-N-SH_RA	brain:	n/a
46	chr19:53342580-53342630	SK-N-MC	brain:	n/a
47	chr19:53344366-53344416	HRPEpiC	eye:	n/a
48	chr19:53362925-53362975	HEK293	kidney:	embryo
49	chr19:53361448-53361498	GM12878	blood:	n/a
50	chr19:53361066-53361116	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
2	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
3	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
4	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
5	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:
6	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
7	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
8	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
9	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
10	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
11	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
12	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
13	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
2	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
3	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
4	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
5	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
6	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
7	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
8	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
9	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
10	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
11	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
12	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
13	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585
14	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
15	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
16	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
17	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
18	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301

No data

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

Extended variants
information (count: 2074 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2074 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567712509	chr19:53327418-53327419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114231749	chr19:53327432-53327433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199515977	chr19:53327434-53327435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141605970	chr19:53327440-53327441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79975732	chr19:53327514-53327515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111624725	chr19:53327537-53327538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545895166	chr19:53327613-53327614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557858072	chr19:53327725-53327726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112374610	chr19:53327743-53327744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544802906	chr19:53327758-53327759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13313712	chr19:53327760-53327761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530325401	chr19:53327802-53327803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571292111	chr19:53327841-53327842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542159011	chr19:53327844-53327845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190119754	chr19:53327850-53327851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527707909	chr19:53327871-53327872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111354365	chr19:53327888-53327889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182807675	chr19:53327916-53327917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376384086	chr19:53327998-53327999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552361102	chr19:53328067-53328068	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs570940172	chr19:53328195-53328196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556280120	chr19:53328212-53328213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574655356	chr19:53328226-53328227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113899243	chr19:53328264-53328265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571589889	chr19:53328309-53328310	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs549948919	chr19:53328335-53328336	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs568306346	chr19:53328345-53328346	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs535736083	chr19:53328359-53328360	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554140243	chr19:53328369-53328370	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs565653136	chr19:53328372-53328373	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs539436813	chr19:53328375-53328376	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs557529749	chr19:53328387-53328388	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186273225	chr19:53328413-53328414	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373707646	chr19:53328446-53328447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs75963828	chr19:53328454-53328455	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111638803	chr19:53328523-53328524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs144487579	chr19:53328536-53328537	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184180443	chr19:53328543-53328544	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533966647	chr19:53328739-53328740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553823655	chr19:53328746-53328747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148436776	chr19:53328770-53328771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141944113	chr19:53328789-53328790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546187847	chr19:53328808-53328809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564374947	chr19:53328809-53328810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554235643	chr19:53328862-53328863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs8111889	chr19:53328909-53328910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187947718	chr19:53328910-53328911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150677898	chr19:53328922-53328923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192419476	chr19:53328934-53328935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565992339	chr19:53328945-53328946	Weak transcription	n/a	n/a	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1049 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53325200-53333400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:53333400-53333600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:53333400-53333600	Weak transcription	Placenta	Placenta
4	chr19:53333400-53334600	Enhancers	HepG2	liver
5	chr19:53333600-53333800	Enhancers	Placenta	Placenta
6	chr19:53333600-53345000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:53333800-53339000	Weak transcription	Placenta	Placenta
8	chr19:53335000-53338000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:53335000-53342800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr19:53336400-53337400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr19:53336400-53337400	Enhancers	Dnd41	blood
12	chr19:53336600-53336800	Enhancers	K562	blood
13	chr19:53336800-53339000	Weak transcription	K562	blood
14	chr19:53337000-53337200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:53337000-53340800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:53337000-53340800	Weak transcription	Ovary	ovary
17	chr19:53337200-53337800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr19:53337200-53338200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:53337400-53338000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr19:53337400-53340600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr19:53337400-53340600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr19:53337400-53340600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:53337400-53340800	Weak transcription	Brain Hippocampus Middle	brain
24	chr19:53337400-53340800	Weak transcription	Fetal Brain Female	brain
25	chr19:53337400-53340800	Weak transcription	Dnd41	blood
26	chr19:53337600-53337800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr19:53337600-53338000	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
28	chr19:53337600-53342200	Weak transcription	Brain Germinal Matrix	brain
29	chr19:53337600-53342200	Weak transcription	Fetal Stomach	stomach
30	chr19:53337800-53338000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr19:53337800-53338000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr19:53337800-53338000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr19:53337800-53338000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr19:53337800-53338800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr19:53337800-53341400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr19:53337800-53342200	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr19:53337800-53342400	Weak transcription	Right Ventricle	heart
38	chr19:53338000-53338200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr19:53338000-53340800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr19:53338000-53341400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr19:53338000-53342400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr19:53338000-53342600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr19:53338000-53343400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr19:53338200-53339000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:53338200-53340600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr19:53338200-53341400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr19:53338200-53342600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr19:53338600-53339200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr19:53338800-53342200	Weak transcription	Fetal Muscle Trunk	muscle
50	chr19:53338800-53342600	Weak transcription	Brain Substantia Nigra	brain

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