Variant report

Variant	nsv578946
Chromosome Location	chr19:21014403-21151796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:539)
CpG islands
(count:612)
Chromatin interactive
region (count:6)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:21147595-21147600	K562	blood:	n/a	n/a
2	BACH1	chr19:21106073-21106302	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr19:21032838-21032997	GM12878	blood:	n/a	chr19:21032899-21032910 chr19:21032904-21032914
4	BATF	chr19:21032836-21033000	GM12878	blood:	n/a	chr19:21032899-21032910 chr19:21032904-21032914
5	BCLAF1	chr19:21106064-21106734	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:21106054-21106146	GM12878	blood:	n/a	n/a
7	BRCA1	chr19:21106099-21106247	GM12878	blood:	n/a	n/a
8	CEBPB	chr19:21151165-21151573	IMR90	lung:	n/a	n/a
9	CEBPB	chr19:21150477-21150759	A549	lung:	n/a	n/a
10	CEBPB	chr19:21150502-21150834	HepG2	liver:	n/a	n/a
11	CEBPB	chr19:21113246-21113536	HepG2	liver:	n/a	chr19:21113372-21113383
12	CEBPB	chr19:21113225-21113528	IMR90	lung:	n/a	chr19:21113372-21113383
13	CEBPB	chr19:21150575-21150785	IMR90	lung:	n/a	n/a
14	CEBPB	chr19:21151071-21151772	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:21129511-21129516	HepG2	liver:	n/a	n/a
16	CEBPB	chr19:21113313-21113547	A549	lung:	n/a	chr19:21113372-21113383
17	CEBPB	chr19:21106059-21106307	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr19:21151053-21151339	A549	lung:	n/a	n/a
19	CEBPB	chr19:21111223-21111588	IMR90	lung:	n/a	n/a
20	CHD1	chr19:21041146-21041568	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr19:21106153-21106576	GM12878	blood:	n/a	n/a
22	CHD1	chr19:21106057-21106479	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr19:21105781-21106264	GM12878	blood:	n/a	n/a
24	CHD2	chr19:21105828-21106276	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr19:21147780-21147930	WERI-Rb-1	eye:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
26	CTCF	chr19:21147766-21147905	K562	blood:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
27	CTCF	chr19:21105876-21105885	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr19:21147772-21147941	Fibrobl	skin:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
29	CTCF	chr19:21106340-21106490	AG04449	skin:	n/a	chr19:21106358-21106379
30	CTCF	chr19:21147780-21147930	HepG2	liver:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
31	CTCF	chr19:21106380-21106530	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:21124105-21124181	GM10266	blood:	n/a	n/a
33	CTCF	chr19:21147761-21147932	K562	blood:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
34	CTCF	chr19:21147800-21147919	GM19238	blood:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
35	CTCF	chr19:21147768-21147975	H1-hESC	embryonic stem cell:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
36	CTCF	chr19:21022916-21022919	Medullo	brain:	n/a	n/a
37	CTCF	chr19:21061680-21061830	GM12866	blood:	n/a	n/a
38	CTCF	chr19:21106401-21106438	MCF-7	breast:	n/a	n/a
39	CTCF	chr19:21032872-21032964	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr19:21105371-21105401	MCF-7	breast:	n/a	n/a
41	CTCF	chr19:21147880-21148030	NHEK	skin:	n/a	n/a
42	CTCF	chr19:21147851-21147913	GM13976	blood:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
43	CTCF	chr19:21106360-21106510	NHEK	skin:	n/a	n/a
44	CTCF	chr19:21147760-21147910	NHEK	skin:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
45	CTCF	chr19:21106360-21106510	AG09309	skin:	n/a	n/a
46	CTCF	chr19:21096180-21096330	GM12867	blood:	n/a	n/a
47	CTCF	chr19:21147760-21147910	HPAF	blood vessel:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
48	CTCF	chr19:21147840-21147990	GM12873	blood:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
49	CTCF	chr19:21147800-21147950	K562	blood:	n/a	chr19:21147851-21147869 chr19:21147853-21147866
50	CTCF	chr19:21106320-21106470	HVMF	connective:	n/a	chr19:21106358-21106379

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21106002-21106052	HCT-116	colon:	n/a
2	chr19:21105452-21105502	AoSMC	blood vessel:	n/a
3	chr19:21106002-21106052	HCT-116	colon:	n/a
4	chr19:21105452-21105502	AoSMC	blood vessel:	n/a
5	chr19:21106043-21106093	Hepatocyte	liver:	n/a
6	chr19:21106027-21106077	SK-N-SH_RA	brain:	n/a
7	chr19:21105452-21105502	T-47D	breast:	n/a
8	chr19:21106053-21106103	ovcar-3	ovarian:	n/a
9	chr19:21106053-21106103	AG09309	skin:	n/a
10	chr19:21105452-21105502	HIPEpiC	eye:	n/a
11	chr19:21105303-21105353	Caco-2	colon:	n/a
12	chr19:21106053-21106103	H1-hESC	embryonic stem cell:	embryo
13	chr19:21106120-21106170	AG04450	lung:	fetal
14	chr19:21105303-21105353	HCF	heart:	n/a
15	chr19:21106027-21106077	SK-N-MC	brain:	n/a
16	chr19:21105452-21105502	Jurkat	blood:	n/a
17	chr19:21106370-21106420	Hepatocyte	liver:	n/a
18	chr19:21106016-21106066	BE2_C	brain:	n/a
19	chr19:21106043-21106093	AoSMC	blood vessel:	n/a
20	chr19:21106036-21106086	RPTEC	kidney:	n/a
21	chr19:21106027-21106077	HCT-116	colon:	n/a
22	chr19:21106036-21106086	Hepatocyte	liver:	n/a
23	chr19:21106002-21106052	AoSMC	blood vessel:	n/a
24	chr19:21106043-21106093	Caco-2	colon:	n/a
25	chr19:21105303-21105353	GM12891	blood:	n/a
26	chr19:21105303-21105353	HCT-116	colon:	n/a
27	chr19:21106120-21106170	IMR90	lung:	fetal
28	chr19:21105452-21105502	HEEpiC	esophagus:	n/a
29	chr19:21106002-21106052	ProgFib	skin:	n/a
30	chr19:21105452-21105502	AG09319	gingival:	n/a
31	chr19:21106002-21106052	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:21106120-21106170	SKMC	muscle:	n/a
33	chr19:21106053-21106103	PrEC	prostate:	n/a
34	chr19:21105452-21105502	PrEC	prostate:	n/a
35	chr19:21106027-21106077	GM19239	blood:	n/a
36	chr19:21106053-21106103	HCF	heart:	n/a
37	chr19:21106016-21106066	RPTEC	kidney:	n/a
38	chr19:21106370-21106420	U87	brain:	n/a
39	chr19:21106053-21106103	GM12892	blood:	n/a
40	chr19:21106027-21106077	HL-60	blood:	n/a
41	chr19:21106370-21106420	HAEpiC	amniotic membrane:	n/a
42	chr19:21106043-21106093	HCM	heart:	n/a
43	chr19:21106120-21106170	CMK	blood:	n/a
44	chr19:21106002-21106052	ECC-1	luminal epithelium:	n/a
45	chr19:21105303-21105353	Jurkat	blood:	n/a
46	chr19:21106002-21106052	AG09319	gingival:	n/a
47	chr19:21106036-21106086	HIPEpiC	eye:	n/a
48	chr19:21105303-21105353	HCM	heart:	n/a
49	chr19:21106043-21106093	K562	blood:	n/a
50	chr19:21106120-21106170	BE2_C	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21086946..21088802-chr19:21210415..21213328,2	MCF-7	breast:
2	chr19:21124387..21126595-chr19:21129898..21132890,2	MCF-7	breast:
3	chr19:21051172..21052986-chr19:21053944..21056414,2	MCF-7	breast:
4	chr19:21051172..21052986-chr19:21053944..21056414,2	MCF-7	breast:
5	chr19:21124387..21126595-chr19:21129898..21132890,2	MCF-7	breast:
6	chr19:21097861..21100856-chr19:21103633..21106940,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF85-4	chr19:21106059-21106222	NR_045830
2	lnc-ZNF626-4	chr19:21022210-21022336	NONHSAT063675
3	lnc-ZNF626-4	chr19:21030087-21030223	NONHSAT063675
4	lnc-ZNF85-4	chr19:21125607-21126783	NR_045830
5	lnc-ZNF626-5	chr19:21149318-21149428	NONHSAT063678
6	lnc-ZNF626-4	chr19:21021321-21021373	NONHSAT063675
7	lnc-ZNF85-4	chr19:21116830-21116956	NR_045830
8	lnc-ZNF85-4	chr19:21117755-21117853	NR_045830

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF85	hsa-miR-26b-5p	chr19:21126672-21126693

Variant related genes	Relation type
ENSG00000269147	TF binding region
ENSG00000269373	TF binding region
ZNF85	TF binding region
ENSG00000268326	TF binding region
KRT18P40	TF binding region
ENSG00000269147	CpG island
ENSG00000269373	CpG island
ZNF85	CpG island
ENSG00000268326	CpG island
KRT18P40	CpG island
ENSG00000105750	chromatin interactions
OAZ1	miRNA target sites

Extended variants
information (count: 5173 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:5173 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12104173	chr19:21014403-21014404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560106345	chr19:21014431-21014432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573386424	chr19:21014440-21014441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566751306	chr19:21014446-21014447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs430169	chr19:21014527-21014528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs555537929	chr19:21014553-21014554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562140048	chr19:21014565-21014566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs365590	chr19:21014575-21014576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs551098094	chr19:21014596-21014597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187957420	chr19:21014623-21014624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533477258	chr19:21014624-21014625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547133918	chr19:21014677-21014678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545935092	chr19:21014721-21014722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567101326	chr19:21014783-21014784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11881868	chr19:21014804-21014805	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs366654	chr19:21014848-21014849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs569385712	chr19:21014867-21014868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34823305	chr19:21014874-21014875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538194460	chr19:21014909-21014910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3867194	chr19:21014930-21014931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs577836463	chr19:21014932-21014933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3867195	chr19:21014960-21014961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141101551	chr19:21014980-21014981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573545551	chr19:21014990-21014991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs431157	chr19:21014999-21015000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs189977310	chr19:21015005-21015006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575734852	chr19:21015016-21015017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367380	chr19:21015017-21015018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs444905	chr19:21015036-21015037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs62125655	chr19:21015096-21015097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547028802	chr19:21015116-21015117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560662066	chr19:21015122-21015123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs3867196	chr19:21015133-21015134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs443899	chr19:21015169-21015170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs569347074	chr19:21015211-21015212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537971009	chr19:21015227-21015228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182559635	chr19:21015241-21015242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571581346	chr19:21015242-21015243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187215757	chr19:21015251-21015252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144849301	chr19:21015254-21015255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79874520	chr19:21015257-21015258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553691775	chr19:21015260-21015261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117387335	chr19:21015300-21015301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs118179307	chr19:21015314-21015315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547328493	chr19:21015381-21015382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112818288	chr19:21015409-21015410	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs138661792	chr19:21015410-21015411	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs192294780	chr19:21015417-21015418	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs558501070	chr19:21015436-21015437	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs571989338	chr19:21015454-21015455	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	20967226	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1108 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21009200-21021600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:21015400-21015800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr19:21016400-21017800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
4	chr19:21019000-21020000	ZNF genes & repeats	Adipose Nuclei	Adipose
5	chr19:21019200-21020000	ZNF genes & repeats	Ovary	ovary
6	chr19:21019200-21020200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
7	chr19:21019400-21024800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr19:21019600-21020200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr19:21020000-21021600	Weak transcription	Ovary	ovary
10	chr19:21020800-21024200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:21021000-21021400	ZNF genes & repeats	Fetal Brain Female	brain
12	chr19:21021600-21021800	ZNF genes & repeats	Ovary	ovary
13	chr19:21022400-21024000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
14	chr19:21022600-21023400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr19:21022600-21024000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr19:21022800-21024000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:21023000-21023200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr19:21023000-21023600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
19	chr19:21029800-21031000	ZNF genes & repeats	Adipose Nuclei	Adipose
20	chr19:21035200-21036000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
21	chr19:21040600-21040800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr19:21040800-21041200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
23	chr19:21040800-21042000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
24	chr19:21041200-21042000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr19:21042200-21042600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr19:21043200-21043400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:21043400-21045600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr19:21044200-21044400	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr19:21045600-21046000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:21049400-21071800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
31	chr19:21049800-21052800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
32	chr19:21052200-21063600	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr19:21052600-21052800	ZNF genes & repeats	Aorta	Aorta
34	chr19:21052600-21053200	Active TSS	Fetal Heart	heart
35	chr19:21052600-21053200	ZNF genes & repeats	Spleen	Spleen
36	chr19:21057200-21058200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
37	chr19:21063400-21075600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
38	chr19:21069600-21069800	ZNF genes & repeats	Fetal Brain Female	brain
39	chr19:21073000-21073600	Active TSS	Fetal Heart	heart
40	chr19:21073800-21075600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
41	chr19:21075000-21075400	ZNF genes & repeats	Adipose Nuclei	Adipose
42	chr19:21075600-21078800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr19:21078800-21081200	ZNF genes & repeats	Adipose Nuclei	Adipose
44	chr19:21078800-21082600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
45	chr19:21081800-21082800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
46	chr19:21085800-21086200	ZNF genes & repeats	Pancreas	Pancrea
47	chr19:21086600-21087800	ZNF genes & repeats	Fetal Brain Male	brain
48	chr19:21087800-21095400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
49	chr19:21089400-21090200	ZNF genes & repeats	Pancreas	Pancrea
50	chr19:21089600-21090000	ZNF genes & repeats	Fetal Heart	heart

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