Variant report

Variant	nsv963093
Chromosome Location	chr19:44850276-44876742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:327)
CpG islands
(count:490)
Chromatin interactive
region (count:11)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:44860835-44861069	HepG2	liver:	n/a	n/a
2	ATF1	chr19:44871198-44871556	K562	blood:	n/a	n/a
3	ATF1	chr19:44875907-44876237	K562	blood:	n/a	n/a
4	ATF1	chr19:44860821-44861048	K562	blood:	n/a	n/a
5	ATF1	chr19:44861728-44861911	K562	blood:	n/a	n/a
6	BACH1	chr19:44870602-44870694	K562	blood:	n/a	n/a
7	BCL3	chr19:44860537-44861188	A549	lung:	n/a	chr19:44860818-44860827
8	BRCA1	chr19:44860716-44861217	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr19:44875836-44876178	K562	blood:	n/a	n/a
10	CEBPB	chr19:44864800-44865045	HepG2	liver:	n/a	chr19:44864900-44864911
11	CEBPB	chr19:44864746-44865036	A549	lung:	n/a	chr19:44864900-44864911
12	CEBPB	chr19:44864820-44865058	IMR90	lung:	n/a	chr19:44864900-44864911
13	CEBPB	chr19:44861711-44861950	K562	blood:	n/a	n/a
14	CEBPB	chr19:44861600-44861952	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr19:44861742-44861936	A549	lung:	n/a	n/a
16	CEBPB	chr19:44861742-44861893	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:44861623-44861969	K562	blood:	n/a	n/a
18	CEBPB	chr19:44875737-44875827	HepG2	liver:	n/a	chr19:44875775-44875786
19	CHD2	chr19:44860650-44861175	Hela-S3	cervix:	n/a	chr19:44861149-44861156 chr19:44861153-44861160
20	CHD2	chr19:44860754-44861010	HepG2	liver:	n/a	n/a
21	CHD2	chr19:44860838-44860947	K562	blood:	n/a	n/a
22	CREB1	chr19:44860521-44861161	A549	lung:	n/a	n/a
23	CREB1	chr19:44860550-44861201	HepG2	liver:	n/a	n/a
24	CREB1	chr19:44860733-44861051	A549	lung:	n/a	n/a
25	CTCF	chr19:44859008-44859009	HepG2	liver:	n/a	n/a
26	CTCF	chr19:44875948-44875992	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:44876063-44876106	ProgFib	skin:	n/a	n/a
28	CTCF	chr19:44858960-44859110	RPTEC	kidney:	n/a	n/a
29	CTCF	chr19:44858943-44859097	MCF-7	breast:	n/a	n/a
30	CTCF	chr19:44858872-44859117	K562	blood:	n/a	n/a
31	CTCF	chr19:44858960-44859110	A549	lung:	n/a	n/a
32	CTCF	chr19:44858930-44859108	K562	blood:	n/a	n/a
33	CTCF	chr19:44861705-44861713	ProgFib	skin:	n/a	n/a
34	CTCF	chr19:44858976-44859018	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr19:44875945-44876018	A549	lung:	n/a	n/a
36	CTCF	chr19:44859040-44859190	BE2_C	brain:	n/a	n/a
37	CTCF	chr19:44858940-44859090	HepG2	liver:	n/a	n/a
38	CTCF	chr19:44876060-44876126	A549	lung:	n/a	n/a
39	CTCF	chr19:44858940-44859090	HEK293	kidney:	n/a	n/a
40	CTCF	chr19:44861000-44861150	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr19:44858940-44859090	K562	blood:	n/a	n/a
42	CTCF	chr19:44858900-44859050	K562	blood:	n/a	n/a
43	CTCF	chr19:44858951-44859070	NHEK	skin:	n/a	n/a
44	CTCF	chr19:44858855-44859104	A549	lung:	n/a	n/a
45	CTCF	chr19:44861639-44861659	ProgFib	skin:	n/a	n/a
46	CTCF	chr19:44870396-44870457	Lung_OC	lung:	n/a	n/a
47	CTCF	chr19:44860901-44860964	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr19:44850860-44851010	K562	blood:	n/a	n/a
49	CTCF	chr19:44860881-44860982	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr19:44858935-44859099	MCF-7	breast:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:44864843-44864893	CMK	blood:	n/a
2	chr19:44857751-44857801	HCT-116	colon:	n/a
3	chr19:44864843-44864893	CMK	blood:	n/a
4	chr19:44857751-44857801	HCT-116	colon:	n/a
5	chr19:44860658-44860708	HUVEC	blood vessel:	n/a
6	chr19:44857751-44857801	H1-hESC	embryonic stem cell:	embryo
7	chr19:44864843-44864893	A549	lung:	n/a
8	chr19:44861002-44861052	AG09319	gingival:	n/a
9	chr19:44861002-44861052	SK-N-SH_RA	brain:	n/a
10	chr19:44864843-44864893	Hela-S3	cervix:	n/a
11	chr19:44861241-44861291	GM12878	blood:	n/a
12	chr19:44857751-44857801	HRPEpiC	eye:	n/a
13	chr19:44858848-44858898	AG04450	lung:	fetal
14	chr19:44861002-44861052	Jurkat	blood:	n/a
15	chr19:44858848-44858898	AG10803	skin:	n/a
16	chr19:44861154-44861204	ProgFib	skin:	n/a
17	chr19:44860658-44860708	GM06990	blood:	n/a
18	chr19:44861154-44861204	PFSK-1	brain:	n/a
19	chr19:44860820-44860870	HIPEpiC	eye:	n/a
20	chr19:44861002-44861052	BJ	skin:	n/a
21	chr19:44864843-44864893	HCT-116	colon:	n/a
22	chr19:44857751-44857801	Hela-S3	cervix:	n/a
23	chr19:44858848-44858898	AoSMC	blood vessel:	n/a
24	chr19:44861241-44861291	LNCaP	prostate:	n/a
25	chr19:44858848-44858898	HEK293	kidney:	embryo
26	chr19:44861002-44861052	HEEpiC	esophagus:	n/a
27	chr19:44861154-44861204	H1-hESC	embryonic stem cell:	embryo
28	chr19:44857751-44857801	GM06990	blood:	n/a
29	chr19:44861154-44861204	GM06990	blood:	n/a
30	chr19:44861002-44861052	SKMC	muscle:	n/a
31	chr19:44860658-44860708	PANC-1	pancreas:	n/a
32	chr19:44858848-44858898	Hela-S3	cervix:	n/a
33	chr19:44858848-44858898	HEEpiC	esophagus:	n/a
34	chr19:44861241-44861291	HUVEC	blood vessel:	n/a
35	chr19:44861241-44861291	HRPEpiC	eye:	n/a
36	chr19:44861241-44861291	IMR90	lung:	fetal
37	chr19:44860658-44860708	AG10803	skin:	n/a
38	chr19:44861154-44861204	Caco-2	colon:	n/a
39	chr19:44861154-44861204	U87	brain:	n/a
40	chr19:44857751-44857801	A549	lung:	n/a
41	chr19:44861241-44861291	AG10803	skin:	n/a
42	chr19:44857751-44857801	PFSK-1	brain:	n/a
43	chr19:44861241-44861291	GM12892	blood:	n/a
44	chr19:44860658-44860708	NT2-D1	testis:	n/a
45	chr19:44858848-44858898	AG09319	gingival:	n/a
46	chr19:44860658-44860708	AG04449	skin:	fetal
47	chr19:44857751-44857801	U87	brain:	n/a
48	chr19:44864843-44864893	NHDF-neo	bronchial:	n/a
49	chr19:44857751-44857801	SAEC	small airway:	n/a
50	chr19:44861241-44861291	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:44860226..44861181-chr2:133104577..133105347,5	HCT-116	colon:
2	chr19:44852656..44854693-chr19:44860503..44863096,2	K562	blood:
3	chr19:44847055..44849987-chr19:44852679..44854366,2	MCF-7	breast:
4	chr19:44859033..44861169-chr2:133104533..133106354,2	K562	blood:
5	chr19:44858569..44859729-chr2:133105937..133107575,6	MCF-7	breast:
6	chr19:44860583..44861870-chr2:133104308..133105302,7	Hela-S3	cervix:
7	chr19:44716323..44716954-chr19:44860163..44860822,2	MCF-7	breast:
8	chr19:44860567..44861162-chr2:133104579..133105358,2	MCF-7	breast:
9	chr19:44858582..44859085-chr2:133106403..133107293,2	K562	blood:
10	chr19:44846057..44848981-chr19:44852585..44854533,2	MCF-7	breast:
11	chr19:44858590..44859395-chr2:133106608..133107319,5	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF233-1	chr19:44861854-44861914	NONHSAT066691
2	lnc-ZNF233-1	chr19:44863913-44863989	NONHSAT066691
3	lnc-ZNF233-1	chr19:44868665-44868848	NONHSAT066691
4	lnc-ZNF233-1	chr19:44868036-44868132	NONHSAT066691
5	lnc-ZNF233-1	chr19:44867724-44867898	NONHSAT066694
6	lnc-ZNF233-1	chr19:44865967-44867898	NONHSAT066691
7	lnc-ZNF233-1	chr19:44861873-44861914	ucscGeneNc_uc002omd_1
8	lnc-ZNF233-1	chr19:44865967-44867731	NONHSAT066692
9	lnc-ZNF233-1	chr19:44865967-44867898	ucscGeneNc_uc002omd_1
10	lnc-ZNF233-1	chr19:44861873-44861914	NONHSAT066692
11	lnc-ZNF233-1	chr19:44864478-44864688	NONHSAT066691

No data

Variant related genes	Relation type
ZNF112	TF binding region
ZNF112	CpG island
ENSG00000131115	chromatin interactions
ENSG00000062370	chromatin interactions
ENSG00000272769	chromatin interactions

Extended variants
information (count: 772 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:772 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71362683	chr19:44850314-44850315	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs546248558	chr19:44850406-44850407	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs564751635	chr19:44850434-44850435	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs147168623	chr19:44850542-44850543	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs2356881	chr19:44850553-44850554	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs560845310	chr19:44850563-44850564	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs533542269	chr19:44850582-44850583	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs186671061	chr19:44850600-44850601	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs7507180	chr19:44850608-44850609	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs2196187	chr19:44850621-44850622	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373825584	chr19:44850642-44850643	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs377689848	chr19:44850669-44850670	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs2196186	chr19:44850798-44850799	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191725677	chr19:44850807-44850808	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs10407844	chr19:44850929-44850930	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs548947962	chr19:44850944-44850945	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs2196185	chr19:44850977-44850978	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs148655304	chr19:44850979-44850980	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs576892918	chr19:44851018-44851019	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs183499841	chr19:44851066-44851067	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs537858597	chr19:44851075-44851076	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs570787516	chr19:44851086-44851087	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs76035817	chr19:44851088-44851089	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs142177705	chr19:44851176-44851177	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs554478909	chr19:44851210-44851211	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs540815920	chr19:44851252-44851253	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs562702988	chr19:44851289-44851290	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs187220809	chr19:44851291-44851292	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs574622923	chr19:44851349-44851350	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs556237737	chr19:44851374-44851375	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs386809649	chr19:44851396-44851397	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs8104642	chr19:44851398-44851399	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139190235	chr19:44851432-44851433	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs191215690	chr19:44851454-44851455	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs528738708	chr19:44851501-44851502	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs182260381	chr19:44851532-44851533	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs186920623	chr19:44851533-44851534	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs531124008	chr19:44851555-44851556	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs551213231	chr19:44851563-44851564	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs144170374	chr19:44851585-44851586	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs539444198	chr19:44851594-44851595	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs553090482	chr19:44851601-44851602	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs146545308	chr19:44851630-44851631	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs151128809	chr19:44851658-44851659	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs374957366	chr19:44851659-44851660	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs35763692	chr19:44851675-44851676	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs201473795	chr19:44851702-44851703	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs12982443	chr19:44851719-44851720	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs12982487	chr19:44851762-44851763	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs141230130	chr19:44851784-44851785	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44823200-44856200	ZNF genes & repeats	Liver	Liver
2	chr19:44828600-44851000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
3	chr19:44830800-44850400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:44837400-44851000	ZNF genes & repeats	Ovary	ovary
5	chr19:44840800-44860000	Weak transcription	NHDF-Ad	bronchial
6	chr19:44844200-44859600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr19:44844200-44859800	Weak transcription	Osteobl	bone
8	chr19:44844800-44851000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr19:44844800-44853000	Weak transcription	HSMMtube	muscle
10	chr19:44845000-44860000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr19:44845200-44860000	Weak transcription	HSMM	muscle
12	chr19:44845400-44859800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:44847000-44853200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:44847200-44850600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
15	chr19:44847400-44850400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:44847400-44851400	ZNF genes & repeats	Aorta	Aorta
17	chr19:44847400-44855200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr19:44847800-44855400	Weak transcription	Right Ventricle	heart
19	chr19:44848000-44850600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr19:44848000-44851800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr19:44848200-44852200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr19:44848200-44853400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr19:44848200-44854800	Weak transcription	Fetal Brain Male	brain
24	chr19:44848600-44851000	Enhancers	Brain Anterior Caudate	brain
25	chr19:44849000-44851000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr19:44849000-44851400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr19:44849000-44852200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr19:44849000-44852800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr19:44849200-44850400	ZNF genes & repeats	Left Ventricle	heart
30	chr19:44849200-44851000	Enhancers	Brain Germinal Matrix	brain
31	chr19:44849400-44850600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:44849600-44850400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr19:44849600-44859800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr19:44849800-44850400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr19:44850000-44850600	Active TSS	Brain Substantia Nigra	brain
36	chr19:44850000-44853400	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr19:44850200-44850400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr19:44850200-44850400	ZNF genes & repeats	Esophagus	oesophagus
39	chr19:44850200-44850400	Enhancers	Fetal Heart	heart
40	chr19:44850200-44850400	Enhancers	NH-A	brain
41	chr19:44850400-44850600	Weak transcription	Fetal Heart	heart
42	chr19:44850400-44850800	Weak transcription	A549	lung
43	chr19:44850400-44851400	Weak transcription	Esophagus	oesophagus
44	chr19:44850400-44851600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr19:44850400-44851600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr19:44850400-44860000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:44850400-44860200	Weak transcription	Left Ventricle	heart
48	chr19:44851400-44860400	Weak transcription	Aorta	Aorta
49	chr19:44851600-44852600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr19:44852000-44853600	ZNF genes & repeats	A549	lung

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