Variant report

Variant	nsv543942
Chromosome Location	chr19:21711611-21767567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:198)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:198 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21756597-21757002	K562	blood:	n/a	n/a
2	ATF1	chr19:21756594-21757067	K562	blood:	n/a	n/a
3	ATF3	chr19:21756520-21757045	K562	blood:	n/a	n/a
4	BHLHE40	chr19:21748929-21749238	K562	blood:	n/a	chr19:21749052-21749073 chr19:21749056-21749069
5	BHLHE40	chr19:21756673-21757583	K562	blood:	n/a	n/a
6	CBX3	chr19:21756514-21757083	K562	blood:	n/a	n/a
7	CEBPB	chr19:21750847-21750982	K562	blood:	n/a	n/a
8	CEBPB	chr19:21740957-21741100	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr19:21750808-21751049	K562	blood:	n/a	n/a
10	CEBPB	chr19:21756463-21757311	K562	blood:	n/a	n/a
11	CEBPB	chr19:21715858-21715920	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr19:21756680-21757218	K562	blood:	n/a	n/a
13	CEBPB	chr19:21756603-21757299	K562	blood:	n/a	n/a
14	CEBPB	chr19:21759510-21759606	K562	blood:	n/a	n/a
15	CEBPB	chr19:21715804-21716043	K562	blood:	n/a	n/a
16	CHD2	chr19:21752031-21752238	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr19:21756465-21757280	K562	blood:	n/a	n/a
18	CREB1	chr19:21756576-21757234	K562	blood:	n/a	n/a
19	CTCF	chr19:21742240-21742390	GM12870	blood:	n/a	n/a
20	CTCF	chr19:21722985-21723020	LNCaP	prostate:	n/a	n/a
21	CTCF	chr19:21753960-21754110	GM12865	blood:	n/a	n/a
22	CTCF	chr19:21764774-21764931	K562	blood:	n/a	n/a
23	CTCF	chr19:21764536-21764601	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr19:21732116-21732154	LNCaP	prostate:	n/a	n/a
25	CTCF	chr19:21764680-21764830	K562	blood:	n/a	n/a
26	CTCF	chr19:21712413-21712499	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr19:21730338-21730424	GM20000	blood:	n/a	n/a
28	CTCF	chr19:21757218-21757312	Lung_OC	lung:	n/a	n/a
29	CUX1	chr19:21759134-21759150	GM12878	blood:	n/a	n/a
30	CUX1	chr19:21728751-21728757	K562	blood:	n/a	n/a
31	CUX1	chr19:21756568-21756943	K562	blood:	n/a	n/a
32	E2F4	chr19:21750186-21750225	MCF10A-Er-Src	breast:	n/a	n/a
33	EGR1	chr19:21756687-21757036	K562	blood:	n/a	n/a
34	EGR1	chr19:21756699-21757045	K562	blood:	n/a	n/a
35	ELF1	chr19:21751794-21752441	MCF-7	breast:	n/a	n/a
36	ELF1	chr19:21751768-21752387	MCF-7	breast:	n/a	n/a
37	EP300	chr19:21728894-21728954	K562	blood:	n/a	n/a
38	EP300	chr19:21749022-21749165	K562	blood:	n/a	n/a
39	EP300	chr19:21762482-21762569	GM12878	blood:	n/a	n/a
40	EP300	chr19:21756584-21757170	K562	blood:	n/a	n/a
41	FOS	chr19:21748977-21749159	MCF10A-Er-Src	breast:	n/a	n/a
42	FOSL1	chr19:21756741-21757060	K562	blood:	n/a	chr19:21756822-21756833
43	FOSL1	chr19:21756681-21757013	K562	blood:	n/a	chr19:21756822-21756833
44	FOXA2	chr19:21750825-21751193	A549	lung:	n/a	n/a
45	GABPA	chr19:21751655-21752522	MCF-7	breast:	n/a	n/a
46	GABPA	chr19:21751741-21752336	MCF-7	breast:	n/a	n/a
47	HCFC1	chr19:21756670-21757018	K562	blood:	n/a	n/a
48	HEY1	chr19:21751841-21751988	HepG2	liver:	n/a	n/a
49	HEY1	chr19:21751803-21752127	HepG2	liver:	n/a	n/a
50	HEY1	chr19:21751817-21752053	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21767566-21767616	AG09319	gingival:	n/a
2	chr19:21767566-21767616	K562	blood:	n/a
3	chr19:21766543-21766593	MCF10A-Er-Src	breast:	n/a
4	chr19:21767566-21767616	SK-N-SH_RA	brain:	n/a
5	chr19:21766543-21766593	NT2-D1	testis:	n/a
6	chr19:21767566-21767616	U87	brain:	n/a
7	chr19:21766543-21766593	HRE	kidney:	n/a
8	chr19:21767566-21767616	SAEC	small airway:	n/a
9	chr19:21766543-21766593	PFSK-1	brain:	n/a
10	chr19:21767566-21767616	HEK293	kidney:	embryo
11	chr19:21767566-21767616	HCT-116	colon:	n/a
12	chr19:21766543-21766593	SK-N-MC	brain:	n/a
13	chr19:21767566-21767616	AG10803	skin:	n/a
14	chr19:21766543-21766593	SK-N-SH	brain:	n/a
15	chr19:21766543-21766593	HRPEpiC	eye:	n/a
16	chr19:21766543-21766593	HEEpiC	esophagus:	n/a
17	chr19:21767566-21767616	HL-60	blood:	n/a
18	chr19:21766543-21766593	HAEpiC	amniotic membrane:	n/a
19	chr19:21767566-21767616	AoSMC	blood vessel:	n/a
20	chr19:21766543-21766593	U87	brain:	n/a
21	chr19:21766543-21766593	GM12892	blood:	n/a
22	chr19:21766543-21766593	HepG2	liver:	n/a
23	chr19:21766543-21766593	GM12878	blood:	n/a
24	chr19:21766543-21766593	HEK293	kidney:	embryo
25	chr19:21766543-21766593	SKMC	muscle:	n/a
26	chr19:21767566-21767616	PANC-1	pancreas:	n/a
27	chr19:21767566-21767616	HNPCEpiC	eye:	n/a
28	chr19:21766543-21766593	K562	blood:	n/a
29	chr19:21766543-21766593	AoSMC	blood vessel:	n/a
30	chr19:21767566-21767616	HCPEpiC	choroid plexus:	n/a
31	chr19:21767566-21767616	AG09309	skin:	n/a
32	chr19:21766543-21766593	AG09319	gingival:	n/a
33	chr19:21767566-21767616	NT2-D1	testis:	n/a
34	chr19:21766543-21766593	ProgFib	skin:	n/a
35	chr19:21766543-21766593	AG10803	skin:	n/a
36	chr19:21767566-21767616	BJ	skin:	n/a
37	chr19:21767566-21767616	H1-hESC	embryonic stem cell:	embryo
38	chr19:21766543-21766593	ECC-1	luminal epithelium:	n/a
39	chr19:21767566-21767616	AG04449	skin:	fetal
40	chr19:21766543-21766593	BE2_C	brain:	n/a
41	chr19:21767566-21767616	MCF10A-Er-Src	breast:	n/a
42	chr19:21766543-21766593	GM06990	blood:	n/a
43	chr19:21766543-21766593	NH-A	brain:	n/a
44	chr19:21767566-21767616	HRCEpiC	kidney:	n/a
45	chr19:21766543-21766593	GM19239	blood:	n/a
46	chr19:21767566-21767616	GM12892	blood:	n/a
47	chr19:21766543-21766593	HCF	heart:	n/a
48	chr19:21766543-21766593	ovcar-3	ovarian:	n/a
49	chr19:21766543-21766593	HCPEpiC	choroid plexus:	n/a
50	chr19:21766543-21766593	PANC-1	pancreas:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
2	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
3	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
4	chr19:21687245..21689707-chr19:21740240..21743085,2	MCF-7	breast:
5	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF100-3	chr19:21747057-21747283	XLOC_013263
2	lnc-ZNF100-2	chr19:21754050-21754341	NONHSAT063727
3	lnc-ZNF100-3	chr19:21751906-21752048	XLOC_013263
4	lnc-ZNF100-2	chr19:21753624-21754341	ENSG00000268555.1
5	lnc-ZNF100-2	chr19:21753139-21754341	ENSG00000249473
6	lnc-ZNF100-3	chr19:21748631-21748673	XLOC_013263
7	lnc-ZNF100-3	chr19:21737442-21737754	ENSG00000268081.1
8	lnc-ZNF100-3	chr19:21751906-21752039	ENSG00000268081.1
9	lnc-ZNF100-2	chr19:21762538-21762616	NONHSAT063727
10	lnc-ZNF100-2	chr19:21752904-21754341	NONHSAT063726
11	lnc-ZNF100-3	chr19:21744136-21747283	XLOC_013263
12	lnc-ZNF100-8	chr19:21763358-21765406	NONHSAT063728

No data

Variant related genes	Relation type
ZNF429	TF binding region
ENSG00000268081	TF binding region
ZNF429	CpG island
ENSG00000268081	CpG island
ENSG00000197013	chromatin interactions

Extended variants
information (count: 3083 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:3083 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73926398	chr19:21711640-21711641	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs188803496	chr19:21711658-21711659	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs564057012	chr19:21711667-21711668	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs191899880	chr19:21711676-21711677	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs184241205	chr19:21711679-21711680	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs141042810	chr19:21711727-21711728	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs531459783	chr19:21711761-21711762	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs367563475	chr19:21711818-21711819	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs545224245	chr19:21711885-21711886	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs547875935	chr19:21711888-21711889	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs557288298	chr19:21711892-21711893	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs111449710	chr19:21711919-21711920	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs575855400	chr19:21711924-21711925	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs542955520	chr19:21711925-21711926	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs561722453	chr19:21711952-21711953	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs187569217	chr19:21711964-21711965	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs373154415	chr19:21711977-21711978	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs541114609	chr19:21712035-21712036	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs144890306	chr19:21712049-21712050	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs151302171	chr19:21712059-21712060	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs551564840	chr19:21712099-21712100	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs532587034	chr19:21712143-21712144	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs139333469	chr19:21712147-21712148	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs543025999	chr19:21712196-21712197	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549052981	chr19:21712218-21712219	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs150034261	chr19:21712252-21712253	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs551497406	chr19:21712328-21712329	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs553027248	chr19:21712330-21712331	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs571380009	chr19:21712356-21712357	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs191125623	chr19:21712398-21712399	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs150891896	chr19:21712413-21712414	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs75506979	chr19:21712415-21712416	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs57524066	chr19:21712416-21712417	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs144785712	chr19:21712423-21712424	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs397784908	chr19:21712424-21712425	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs77074124	chr19:21712442-21712443	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs370047895	chr19:21712460-21712461	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs373788851	chr19:21712488-21712489	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs575795769	chr19:21712510-21712511	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs536943907	chr19:21712536-21712537	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs368773099	chr19:21712561-21712562	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs183631992	chr19:21712573-21712574	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs528209656	chr19:21712671-21712672	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs541002104	chr19:21712676-21712677	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs375768405	chr19:21712686-21712687	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs559409502	chr19:21712721-21712722	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs577769665	chr19:21712722-21712723	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs78727132	chr19:21712726-21712727	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs563492572	chr19:21712727-21712728	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs530656288	chr19:21712728-21712729	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:41)

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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21699600-21720800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
2	chr19:21699600-21727600	ZNF genes & repeats	Liver	Liver
3	chr19:21701000-21733400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:21701600-21712600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr19:21701600-21720400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
6	chr19:21702400-21721400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr19:21702600-21713400	Weak transcription	Right Ventricle	heart
8	chr19:21702600-21713400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr19:21702600-21717200	Weak transcription	Psoas Muscle	Psoas
10	chr19:21702800-21713400	Weak transcription	Brain Angular Gyrus	brain
11	chr19:21702800-21717200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr19:21702800-21718600	Weak transcription	Colon Smooth Muscle	Colon
13	chr19:21702800-21718600	Weak transcription	Fetal Heart	heart
14	chr19:21703000-21713400	Weak transcription	Brain Anterior Caudate	brain
15	chr19:21704000-21714600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
16	chr19:21704000-21717200	Weak transcription	NHDF-Ad	bronchial
17	chr19:21704400-21714400	Strong transcription	Primary T cells from cord blood	blood
18	chr19:21705000-21714200	Weak transcription	Fetal Thymus	thymus
19	chr19:21705000-21718600	Weak transcription	HSMM	muscle
20	chr19:21705200-21713200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr19:21705200-21713600	Weak transcription	Brain Substantia Nigra	brain
22	chr19:21705400-21713400	Weak transcription	Brain Hippocampus Middle	brain
23	chr19:21705800-21713600	Weak transcription	Fetal Stomach	stomach
24	chr19:21706000-21713400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:21706000-21713400	Weak transcription	Fetal Kidney	kidney
26	chr19:21706000-21713400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr19:21706200-21713800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:21706400-21713600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr19:21706400-21714000	Weak transcription	Osteobl	bone
30	chr19:21706400-21717200	Weak transcription	K562	blood
31	chr19:21706600-21712000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr19:21706600-21713400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr19:21706600-21713400	Weak transcription	Thymus	Thymus
34	chr19:21706800-21713000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr19:21706800-21713400	Weak transcription	HSMMtube	muscle
36	chr19:21707000-21713000	Weak transcription	Fetal Lung	lung
37	chr19:21707000-21713400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr19:21707000-21713400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr19:21707000-21714000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr19:21707000-21719000	Weak transcription	Stomach Mucosa	stomach
41	chr19:21707200-21713400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr19:21707200-21713800	Weak transcription	Fetal Brain Male	brain
43	chr19:21708200-21716200	Strong transcription	Dnd41	blood
44	chr19:21708200-21717400	Strong transcription	Placenta	Placenta
45	chr19:21709000-21722800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:21709400-21712200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr19:21709600-21716800	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr19:21709600-21717200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr19:21709800-21712600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
50	chr19:21710000-21713400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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