Variant report

Variant	nsv912335
Chromosome Location	chr19:53331914-53374032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:671)
Chromatin interactive
region (count:13)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 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	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
3	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
4	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
5	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
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	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
10	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
12	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
13	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
14	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
15	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
16	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
17	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
18	CTCF	chr19:53361020-53361170	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr19:53360774-53361155	K562	blood:	n/a	chr19:53360990-53361003
20	CTCF	chr19:53360771-53361087	Spleen_OC	spleen:	n/a	chr19:53360990-53361003
21	CTCF	chr19:53361020-53361170	AG10803	skin:	n/a	n/a
22	CTCF	chr19:53360980-53361130	HMEC	breast:	n/a	chr19:53360990-53361003
23	CTCF	chr19:53360794-53360918	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr19:53360855-53360873	NHEK	skin:	n/a	n/a
25	CTCF	chr19:53360919-53361045	GM19240	blood:	n/a	chr19:53360990-53361003
26	CTCF	chr19:53360980-53361130	GM12866	blood:	n/a	chr19:53360990-53361003
27	CTCF	chr19:53361060-53361210	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr19:53343023-53343127	GM20000	blood:	n/a	n/a
29	CTCF	chr19:53361000-53361150	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr19:53360828-53360986	GM19239	blood:	n/a	n/a
31	CTCF	chr19:53360980-53361130	HCT-116	colon:	n/a	chr19:53360990-53361003
32	CTCF	chr19:53361000-53361150	GM12865	blood:	n/a	n/a
33	CTCF	chr19:53352092-53352147	GM13976	blood:	n/a	n/a
34	CTCF	chr19:53346656-53346707	GM13976	blood:	n/a	n/a
35	CTCF	chr19:53360909-53361007	LNCaP	prostate:	n/a	chr19:53360990-53361003
36	CTCF	chr19:53360920-53361070	HMEC	breast:	n/a	chr19:53360990-53361003
37	CTCF	chr19:53361020-53361170	HMF	breast:	n/a	n/a
38	CTCF	chr19:53361000-53361150	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr19:53360843-53361069	GM12878	blood:	n/a	chr19:53360990-53361003
40	CTCF	chr19:53360980-53361130	SK-N-SH_RA	brain:	n/a	chr19:53360990-53361003
41	CTCF	chr19:53360980-53361130	BE2_C	brain:	n/a	chr19:53360990-53361003
42	CTCF	chr19:53361000-53361150	HVMF	connective:	n/a	n/a
43	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr19:53360924-53361043	Kidney_OC	kidney:	n/a	chr19:53360990-53361003
45	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
46	CTCF	chr19:53360960-53361110	GM12869	blood:	n/a	chr19:53360990-53361003
47	CTCF	chr19:53360927-53361017	Hela-S3	cervix:	n/a	chr19:53360990-53361003
48	CTCF	chr19:53360907-53360918	GM19240	blood:	n/a	n/a
49	CTCF	chr19:53361000-53361150	GM12870	blood:	n/a	n/a
50	CTCF	chr19:53361000-53361150	HBMEC	blood vessel:	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	chr19:53360728-53360778	AG04450	lung:	fetal
2	chr19:53357134-53357184	HNPCEpiC	eye:	n/a
3	chr19:53357134-53357184	SK-N-SH_RA	brain:	n/a
4	chr19:53344366-53344416	MCF10A-Er-Src	breast:	n/a
5	chr19:53362925-53362975	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:53359733-53359783	Hepatocyte	liver:	n/a
7	chr19:53357134-53357184	Hepatocyte	liver:	n/a
8	chr19:53361448-53361498	MCF10A-Er-Src	breast:	n/a
9	chr19:53360728-53360778	HRE	kidney:	n/a
10	chr19:53361448-53361498	Hela-S3	cervix:	n/a
11	chr19:53363482-53363532	BE2_C	brain:	n/a
12	chr19:53362925-53362975	HRCEpiC	kidney:	n/a
13	chr19:53361066-53361116	A549	lung:	n/a
14	chr19:53363482-53363532	NT2-D1	testis:	n/a
15	chr19:53344366-53344416	HCF	heart:	n/a
16	chr19:53360213-53360263	CMK	blood:	n/a
17	chr19:53361448-53361498	K562	blood:	n/a
18	chr19:53360213-53360263	HCPEpiC	choroid plexus:	n/a
19	chr19:53361164-53361214	SK-N-SH	brain:	n/a
20	chr19:53357134-53357184	HEEpiC	esophagus:	n/a
21	chr19:53344366-53344416	K562	blood:	n/a
22	chr19:53342580-53342630	MCF10A-Er-Src	breast:	n/a
23	chr19:53357134-53357184	NHDF-neo	bronchial:	n/a
24	chr19:53361448-53361498	IMR90	lung:	fetal
25	chr19:53363482-53363532	T-47D	breast:	n/a
26	chr19:53360213-53360263	HEEpiC	esophagus:	n/a
27	chr19:53360728-53360778	NH-A	brain:	n/a
28	chr19:53359733-53359783	RPTEC	kidney:	n/a
29	chr19:53363482-53363532	SK-N-SH	brain:	n/a
30	chr19:53360728-53360778	GM19239	blood:	n/a
31	chr19:53357134-53357184	GM12891	blood:	n/a
32	chr19:53361066-53361116	NB4	blood:	n/a
33	chr19:53342580-53342630	HCF	heart:	n/a
34	chr19:53363482-53363532	HepG2	liver:	n/a
35	chr19:53361448-53361498	HEEpiC	esophagus:	n/a
36	chr19:53359733-53359783	SK-N-SH_RA	brain:	n/a
37	chr19:53363482-53363532	PFSK-1	brain:	n/a
38	chr19:53357134-53357184	AG04449	skin:	fetal
39	chr19:53360213-53360263	GM19239	blood:	n/a
40	chr19:53360213-53360263	Hela-S3	cervix:	n/a
41	chr19:53342580-53342630	AG09309	skin:	n/a
42	chr19:53344366-53344416	AG09319	gingival:	n/a
43	chr19:53344366-53344416	AG09309	skin:	n/a
44	chr19:53362925-53362975	GM12878	blood:	n/a
45	chr19:53361448-53361498	HRE	kidney:	n/a
46	chr19:53360728-53360778	LNCaP	prostate:	n/a
47	chr19:53360213-53360263	NT2-D1	testis:	n/a
48	chr19:53361066-53361116	NHDF-neo	bronchial:	n/a
49	chr19:53362925-53362975	HL-60	blood:	n/a
50	chr19:53361066-53361116	RPTEC	kidney:	n/a

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

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

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
2	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
3	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
4	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
5	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
6	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
7	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
8	lnc-ZNF320-3	chr19:53367043-53367412	NONHSAT067591
9	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
10	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
11	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
12	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
13	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
14	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
15	lnc-ZNF468-2	chr19:53365060-53366119	NONHSAT067590
16	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
17	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
18	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585
19	lnc-ZNF320-3	chr19:53367175-53367412	NONHSAT067592
20	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
21	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301

No data

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

Extended variants
information (count: 2391 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2391 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10423685	chr19:53331914-53331915	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191060727	chr19:53331970-53331971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548305282	chr19:53332024-53332025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10423923	chr19:53332039-53332040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs183327253	chr19:53332041-53332042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558533298	chr19:53332044-53332045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112148797	chr19:53332065-53332066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570729600	chr19:53332081-53332082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538187352	chr19:53332088-53332089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547607179	chr19:53332099-53332100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116045911	chr19:53332116-53332117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541921699	chr19:53332120-53332121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553926146	chr19:53332125-53332126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573321255	chr19:53332136-53332137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187681463	chr19:53332141-53332142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565390432	chr19:53332192-53332193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147532968	chr19:53332196-53332197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12982789	chr19:53332199-53332200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12980994	chr19:53332202-53332203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs12980987	chr19:53332233-53332234	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs34044502	chr19:53332246-53332247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548245265	chr19:53332252-53332253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374996466	chr19:53332259-53332260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7257943	chr19:53332266-53332267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374485733	chr19:53332270-53332271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374325379	chr19:53332274-53332275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552344401	chr19:53332289-53332290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12609688	chr19:53332329-53332330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191502524	chr19:53332336-53332337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57311698	chr19:53332345-53332346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12983300	chr19:53332358-53332359	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs535458355	chr19:53332361-53332362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553545423	chr19:53332364-53332365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572109243	chr19:53332374-53332375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539201331	chr19:53332397-53332398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559092350	chr19:53332401-53332402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368214904	chr19:53332412-53332413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544475589	chr19:53332419-53332420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12981503	chr19:53332425-53332426	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs143633009	chr19:53332434-53332435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12983526	chr19:53332436-53332437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372022385	chr19:53332437-53332438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12983537	chr19:53332452-53332453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149269860	chr19:53332461-53332462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146145568	chr19:53332466-53332467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79743891	chr19:53332480-53332481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369212403	chr19:53332487-53332488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374807791	chr19:53332492-53332493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541826608	chr19:53332591-53332592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144985952	chr19:53332617-53332618	Weak transcription	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:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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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