Variant report

Variant	nsv519533
Chromosome Location	chr19:19789528-19831544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr19:19823445-19823679	K562	blood:	n/a	n/a
2	CBX3	chr19:19822080-19822914	K562	blood:	n/a	n/a
3	CBX3	chr19:19830634-19830946	K562	blood:	n/a	n/a
4	CBX3	chr19:19823175-19823828	K562	blood:	n/a	n/a
5	CBX3	chr19:19822096-19823012	K562	blood:	n/a	n/a
6	CEBPB	chr19:19805122-19805433	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr19:19807817-19808052	HepG2	liver:	n/a	n/a
8	CEBPB	chr19:19815694-19816114	HepG2	liver:	n/a	n/a
9	CTCF	chr19:19807284-19807461	GM12878	blood:	n/a	n/a
10	CTCF	chr19:19807340-19807490	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr19:19807202-19807570	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr19:19795243-19795291	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr19:19806554-19806589	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr19:19807226-19807524	K562	blood:	n/a	n/a
15	CTCF	chr19:19807394-19807467	HepG2	liver:	n/a	n/a
16	CTCF	chr19:19807320-19807470	NB4	blood:	n/a	n/a
17	CTCF	chr19:19807248-19807511	K562	blood:	n/a	n/a
18	CTCF	chr19:19807318-19807444	K562	blood:	n/a	n/a
19	CTCF	chr19:19825774-19825835	GM20000	blood:	n/a	n/a
20	CTCF	chr19:19798078-19798116	ProgFib	skin:	n/a	n/a
21	CTCF	chr19:19827330-19827349	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:19807244-19807473	HepG2	liver:	n/a	n/a
23	CTCF	chr19:19811497-19811582	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr19:19822520-19822670	BE2_C	brain:	n/a	n/a
25	CTCF	chr19:19807323-19807509	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr19:19807249-19807451	HepG2	liver:	n/a	n/a
27	CTCF	chr19:19822421-19822500	GM20000	blood:	n/a	n/a
28	CTCF	chr19:19807356-19807366	HepG2	liver:	n/a	n/a
29	CTCF	chr19:19807270-19807567	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr19:19807225-19807559	K562	blood:	n/a	n/a
31	CTCF	chr19:19807253-19807521	K562	blood:	n/a	n/a
32	CTCF	chr19:19807300-19807450	K562	blood:	n/a	n/a
33	E2F6	chr19:19791415-19791526	K562	blood:	n/a	n/a
34	ELF1	chr19:19815696-19815860	HepG2	liver:	n/a	n/a
35	ELF1	chr19:19818260-19818695	GM12878	blood:	n/a	n/a
36	ELF1	chr19:19817883-19818152	GM12878	blood:	n/a	n/a
37	EP300	chr19:19828960-19828964	GM12878	blood:	n/a	n/a
38	FOS	chr19:19790939-19790963	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr19:19818438-19818828	HepG2	liver:	n/a	chr19:19818641-19818655
40	FOSL2	chr19:19820288-19820558	HepG2	liver:	n/a	n/a
41	GATA2	chr19:19826236-19826645	K562	blood:	n/a	n/a
42	GATA3	chr19:19822743-19823458	A549	lung:	n/a	n/a
43	GTF2F1	chr19:19822290-19822307	Hela-S3	cervix:	n/a	n/a
44	HDAC2	chr19:19802606-19802802	K562	blood:	n/a	n/a
45	HNF4A	chr19:19815677-19815994	HepG2	liver:	n/a	chr19:19815824-19815839
46	HNF4A	chr19:19815674-19815977	HepG2	liver:	n/a	chr19:19815824-19815839
47	JUN	chr19:19807844-19807981	HepG2	liver:	n/a	chr19:19807884-19807897 chr19:19807912-19807925
48	JUN	chr19:19822749-19822795	K562	blood:	n/a	n/a
49	JUND	chr19:19807852-19808065	HepG2	liver:	n/a	n/a
50	KAP1	chr19:19820901-19823946	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19822024-19822074	Caco-2	colon:	n/a
2	chr19:19822024-19822074	Caco-2	colon:	n/a
3	chr19:19822024-19822074	Hepatocyte	liver:	n/a
4	chr19:19822024-19822074	NT2-D1	testis:	n/a
5	chr19:19822024-19822074	NHDF-neo	bronchial:	n/a
6	chr19:19822024-19822074	SK-N-SH	brain:	n/a
7	chr19:19822024-19822074	AoSMC	blood vessel:	n/a
8	chr19:19822024-19822074	HRE	kidney:	n/a
9	chr19:19822024-19822074	BE2_C	brain:	n/a
10	chr19:19822024-19822074	HRCEpiC	kidney:	n/a
11	chr19:19822024-19822074	Jurkat	blood:	n/a
12	chr19:19822024-19822074	ovcar-3	ovarian:	n/a
13	chr19:19822024-19822074	NHBE	bronchial:	n/a
14	chr19:19822024-19822074	HPAEpiC	pulmonary alveolar:	n/a
15	chr19:19822024-19822074	HUVEC	blood vessel:	n/a
16	chr19:19822024-19822074	HAEpiC	amniotic membrane:	n/a
17	chr19:19822024-19822074	IMR90	lung:	fetal
18	chr19:19822024-19822074	HNPCEpiC	eye:	n/a
19	chr19:19822024-19822074	AG09319	gingival:	n/a
20	chr19:19822024-19822074	SK-N-SH_RA	brain:	n/a
21	chr19:19822024-19822074	PFSK-1	brain:	n/a
22	chr19:19822024-19822074	HCM	heart:	n/a
23	chr19:19822024-19822074	H1-hESC	embryonic stem cell:	embryo
24	chr19:19822024-19822074	HMEC	breast:	n/a
25	chr19:19822024-19822074	MCF10A-Er-Src	breast:	n/a
26	chr19:19822024-19822074	AG04449	skin:	fetal
27	chr19:19822024-19822074	GM12878	blood:	n/a
28	chr19:19822024-19822074	CMK	blood:	n/a
29	chr19:19822024-19822074	HL-60	blood:	n/a
30	chr19:19822024-19822074	AG09309	skin:	n/a
31	chr19:19822024-19822074	AG04450	lung:	fetal
32	chr19:19822024-19822074	HCPEpiC	choroid plexus:	n/a
33	chr19:19822024-19822074	GM12891	blood:	n/a
34	chr19:19822024-19822074	GM12892	blood:	n/a
35	chr19:19822024-19822074	MCF-7	breast:	n/a
36	chr19:19822024-19822074	HCF	heart:	n/a
37	chr19:19822024-19822074	PrEC	prostate:	n/a
38	chr19:19822024-19822074	Hela-S3	cervix:	n/a
39	chr19:19822024-19822074	SKMC	muscle:	n/a
40	chr19:19822024-19822074	AG10803	skin:	n/a
41	chr19:19822024-19822074	SAEC	small airway:	n/a
42	chr19:19822024-19822074	HRPEpiC	eye:	n/a
43	chr19:19822024-19822074	LNCaP	prostate:	n/a
44	chr19:19822024-19822074	HEK293	kidney:	embryo
45	chr19:19822024-19822074	NB4	blood:	n/a
46	chr19:19822024-19822074	A549	lung:	n/a
47	chr19:19822024-19822074	ProgFib	skin:	n/a
48	chr19:19822024-19822074	HEEpiC	esophagus:	n/a
49	chr19:19822024-19822074	T-47D	breast:	n/a
50	chr19:19822024-19822074	GM19239	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19779580..19781317-chr19:19788331..19791225,2	MCF-7	breast:
2	chr19:19809682..19811235-chr19:19811521..19813836,2	K562	blood:
3	chr19:19814568..19817544-chr19:19975321..19978730,3	MCF-7	breast:
4	chr19:19825299..19827793-chr19:19827916..19829892,2	K562	blood:
5	chr19:19784981..19786975-chr19:19793453..19795583,2	K562	blood:
6	chr19:19825299..19827793-chr19:19827916..19829892,2	K562	blood:
7	chr19:19772412..19775307-chr19:19800186..19802110,2	K562	blood:
8	chr19:19828998..19830532-chr19:20011609..20013262,2	MCF-7	breast:
9	chr19:19814581..19818356-chr19:19819384..19821651,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF101-4	chr19:19821997-19822576	NONHSAT063083
2	lnc-ZNF101-4	chr19:19822661-19822691	NONHSAT063083
3	lnc-ZNF101-3	chr19:19793892-19794318	NONHSAT063080
4	lnc-ZNF101-3	chr19:19792103-19792278	NONHSAT063080

No data

Variant related genes	Relation type
ENSG00000270402	TF binding region
ENSG00000271283	TF binding region
ZNF101	TF binding region
ENSG00000270402	CpG island
ENSG00000271283	CpG island
ZNF101	CpG island
ENSG00000256771	chromatin interactions
ENSG00000271283	chromatin interactions
ENSG00000184635	chromatin interactions
ENSG00000105726	chromatin interactions
ENSG00000181896	chromatin interactions
ENSG00000270402	chromatin interactions
ENSG00000267268	chromatin interactions

Extended variants
information (count: 1668 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2304130	chr19:19789528-19789529	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs537586270	chr19:19789550-19789551	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557852144	chr19:19789559-19789560	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149677520	chr19:19789579-19789580	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375298165	chr19:19789584-19789585	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375905793	chr19:19789618-19789619	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367853335	chr19:19789622-19789623	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377519320	chr19:19789628-19789629	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370371254	chr19:19789632-19789633	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184133452	chr19:19789662-19789663	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371065947	chr19:19789665-19789666	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76764681	chr19:19789670-19789671	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553447063	chr19:19789675-19789676	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574022609	chr19:19789683-19789684	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34291041	chr19:19789685-19789686	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112443831	chr19:19789792-19789793	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542939281	chr19:19789806-19789807	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs556420188	chr19:19789876-19789877	ZNF genes & repeats Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576288209	chr19:19789916-19789917	ZNF genes & repeats Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572352801	chr19:19789937-19789938	ZNF genes & repeats Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs374714677	chr19:19789961-19789962	ZNF genes & repeats Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs199509604	chr19:19789971-19789972	ZNF genes & repeats Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs375840501	chr19:19790016-19790017	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540664407	chr19:19790026-19790027	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs56203750	chr19:19790042-19790043	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368647046	chr19:19790045-19790046	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs146664542	chr19:19790062-19790063	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs137966424	chr19:19790114-19790115	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs267605378	chr19:19790134-19790135	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201804406	chr19:19790135-19790136	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs61742977	chr19:19790136-19790137	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs143536186	chr19:19790145-19790146	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149078805	chr19:19790146-19790147	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs4808209	chr19:19790159-19790160	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs181251469	chr19:19790169-19790170	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs59327775	chr19:19790178-19790179	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs140983546	chr19:19790183-19790184	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375316779	chr19:19790184-19790185	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200536821	chr19:19790195-19790196	ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs146451992	chr19:19790214-19790215	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs138984536	chr19:19790235-19790236	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs33967144	chr19:19790255-19790256	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs201852500	chr19:19790260-19790261	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs147527039	chr19:19790273-19790274	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs374050913	chr19:19790289-19790290	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377049955	chr19:19790298-19790299	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs558462983	chr19:19790321-19790322	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201056707	chr19:19790348-19790349	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs578082766	chr19:19790367-19790368	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs138381823	chr19:19790374-19790375	ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	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
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19780200-19789800	Weak transcription	Fetal Brain Male	brain
2	chr19:19780200-19790000	Weak transcription	Fetal Heart	heart
3	chr19:19780600-19790000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr19:19780600-19795000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:19780800-19789800	Weak transcription	Psoas Muscle	Psoas
6	chr19:19780800-19790000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr19:19780800-19795000	ZNF genes & repeats	Fetal Thymus	thymus
8	chr19:19780800-19795000	ZNF genes & repeats	Thymus	Thymus
9	chr19:19781000-19789600	Weak transcription	Fetal Brain Female	brain
10	chr19:19781000-19789800	Weak transcription	Brain Substantia Nigra	brain
11	chr19:19781000-19792600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr19:19781200-19789800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr19:19781200-19790000	Weak transcription	Colon Smooth Muscle	Colon
14	chr19:19781200-19795800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr19:19781400-19790000	Weak transcription	Right Ventricle	heart
16	chr19:19781400-19792800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
17	chr19:19781400-19793000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
18	chr19:19781400-19793400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr19:19781600-19795000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
20	chr19:19781800-19794400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
21	chr19:19782000-19795000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:19782000-19795600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
23	chr19:19782000-19798200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr19:19782200-19789800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr19:19782200-19789800	Weak transcription	Brain Germinal Matrix	brain
26	chr19:19782600-19793800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:19782800-19795000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
28	chr19:19783000-19791200	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
29	chr19:19783000-19791600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
30	chr19:19783000-19792200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
31	chr19:19783000-19793400	ZNF genes & repeats	Primary B cells from cord blood	blood
32	chr19:19783000-19795000	ZNF genes & repeats	Primary T cells from cord blood	blood
33	chr19:19783200-19789800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr19:19783400-19795000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
35	chr19:19783600-19790200	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr19:19784800-19789800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr19:19784800-19792600	ZNF genes & repeats	GM12878-XiMat	blood
38	chr19:19784800-19792800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
39	chr19:19785000-19791200	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
40	chr19:19785000-19792200	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
41	chr19:19785000-19792600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr19:19785000-19792600	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
43	chr19:19785000-19792600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
44	chr19:19785000-19792600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr19:19785000-19794000	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr19:19785200-19792600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr19:19785200-19792600	ZNF genes & repeats	Liver	Liver
48	chr19:19785200-19793400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr19:19785600-19792200	ZNF genes & repeats	Fetal Intestine Large	intestine
50	chr19:19785800-19792600	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon

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