Variant report

Variant	nsv1067101
Chromosome Location	chr19:36901010-36956251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:36927570-36927771	K562	blood:	n/a	n/a
2	ATF3	chr19:36911828-36912112	K562	blood:	n/a	n/a
3	BACH1	chr19:36909044-36909727	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr19:36908971-36909895	A549	lung:	n/a	chr19:36909719-36909732 chr19:36909735-36909748
5	BHLHE40	chr19:36909422-36909440	K562	blood:	n/a	n/a
6	BHLHE40	chr19:36908569-36908892	GM12878	blood:	n/a	n/a
7	BHLHE40	chr19:36909284-36909624	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:36908676-36908833	K562	blood:	n/a	n/a
9	CCNT2	chr19:36909379-36909794	K562	blood:	n/a	n/a
10	CEBPB	chr19:36911378-36911546	HepG2	liver:	n/a	chr19:36911403-36911414
11	CEBPD	chr19:36909390-36909667	HepG2	liver:	n/a	n/a
12	CHD1	chr19:36909072-36909157	GM12878	blood:	n/a	n/a
13	CHD2	chr19:36909336-36909689	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr19:36927539-36927776	HepG2	liver:	n/a	n/a
15	CREB1	chr19:36927503-36927869	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr19:36909025-36909766	A549	lung:	n/a	n/a
17	CREB1	chr19:36927452-36927753	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr19:36908996-36909752	GM12878	blood:	n/a	n/a
19	CREB1	chr19:36908976-36909834	HepG2	liver:	n/a	n/a
20	CTCF	chr19:36909100-36909250	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr19:36927520-36927670	Caco-2	colon:	n/a	n/a
22	CTCF	chr19:36909800-36909950	HPF	lung:	n/a	n/a
23	CTCF	chr19:36909758-36909843	GM12892	blood:	n/a	n/a
24	CTCF	chr19:36912180-36912330	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr19:36909680-36909830	GM06990	blood:	n/a	n/a
26	CTCF	chr19:36931230-36931270	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:36912289-36912429	H1-hESC	embryonic stem cell:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
28	CTCF	chr19:36909360-36909510	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr19:36909756-36909769	Fibrobl	skin:	n/a	n/a
30	CTCF	chr19:36912220-36912370	BJ	skin:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
31	CTCF	chr19:36909680-36909830	GM12871	blood:	n/a	n/a
32	CTCF	chr19:36909688-36909691	GM19239	blood:	n/a	n/a
33	CTCF	chr19:36905140-36905290	A549	lung:	n/a	n/a
34	CTCF	chr19:36909780-36909930	BJ	skin:	n/a	n/a
35	CTCF	chr19:36912240-36912390	AG04449	skin:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
36	CTCF	chr19:36909680-36909830	GM12873	blood:	n/a	n/a
37	CTCF	chr19:36909800-36909950	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr19:36912260-36912410	BJ	skin:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
39	CTCF	chr19:36909680-36909830	AG04449	skin:	n/a	n/a
40	CTCF	chr19:36912240-36912390	HMEC	breast:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
41	CTCF	chr19:36912240-36912390	HRE	kidney:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
42	CTCF	chr19:36912220-36912370	HRPEpiC	eye:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
43	CTCF	chr19:36909498-36909668	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr19:36912240-36912390	AG09309	skin:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
45	CTCF	chr19:36912200-36912350	HVMF	connective:	n/a	chr19:36912337-36912346 chr19:36912339-36912349
46	CTCF	chr19:36912220-36912370	HPF	lung:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
47	CTCF	chr19:36912280-36912430	HCFaa	heart:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
48	CTCF	chr19:36909815-36909854	GM12878	blood:	n/a	n/a
49	CTCF	chr19:36909821-36909876	GM12878	blood:	n/a	n/a
50	CTCF	chr19:36912260-36912410	SK-N-SH_RA	brain:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36909418-36909468	AG09309	skin:	n/a
2	chr19:36910116-36910166	HCT-116	colon:	n/a
3	chr19:36909418-36909468	PANC-1	pancreas:	n/a
4	chr19:36909418-36909468	IMR90	lung:	fetal
5	chr19:36912702-36912752	HRE	kidney:	n/a
6	chr19:36909606-36909656	AG04450	lung:	fetal
7	chr19:36913451-36913501	IMR90	lung:	fetal
8	chr19:36911014-36911064	K562	blood:	n/a
9	chr19:36909413-36909463	SK-N-SH_RA	brain:	n/a
10	chr19:36912880-36912930	PrEC	prostate:	n/a
11	chr19:36912880-36912930	K562	blood:	n/a
12	chr19:36910144-36910194	PANC-1	pancreas:	n/a
13	chr19:36912880-36912930	AG04450	lung:	fetal
14	chr19:36909418-36909468	SKMC	muscle:	n/a
15	chr19:36913451-36913501	MCF10A-Er-Src	breast:	n/a
16	chr19:36909413-36909463	MCF10A-Er-Src	breast:	n/a
17	chr19:36911014-36911064	PFSK-1	brain:	n/a
18	chr19:36909326-36909376	HRCEpiC	kidney:	n/a
19	chr19:36909606-36909656	A549	lung:	n/a
20	chr19:36909418-36909468	GM19239	blood:	n/a
21	chr19:36906819-36906869	AG04450	lung:	fetal
22	chr19:36909326-36909376	AG04450	lung:	fetal
23	chr19:36909326-36909376	Jurkat	blood:	n/a
24	chr19:36913451-36913501	GM12891	blood:	n/a
25	chr19:36915447-36915497	Jurkat	blood:	n/a
26	chr19:36910116-36910166	BJ	skin:	n/a
27	chr19:36906819-36906869	GM12891	blood:	n/a
28	chr19:36906819-36906869	HUVEC	blood vessel:	n/a
29	chr19:36909326-36909376	RPTEC	kidney:	n/a
30	chr19:36912880-36912930	HRCEpiC	kidney:	n/a
31	chr19:36937832-36937882	Hepatocyte	liver:	n/a
32	chr19:36910144-36910194	HRE	kidney:	n/a
33	chr19:36909606-36909656	Jurkat	blood:	n/a
34	chr19:36909913-36909963	HL-60	blood:	n/a
35	chr19:36912880-36912930	BJ	skin:	n/a
36	chr19:36912880-36912930	GM12878	blood:	n/a
37	chr19:36909413-36909463	GM12891	blood:	n/a
38	chr19:36912702-36912752	HEEpiC	esophagus:	n/a
39	chr19:36909606-36909656	PANC-1	pancreas:	n/a
40	chr19:36910116-36910166	PFSK-1	brain:	n/a
41	chr19:36915447-36915497	PFSK-1	brain:	n/a
42	chr19:36909418-36909468	HRE	kidney:	n/a
43	chr19:36911014-36911064	SK-N-MC	brain:	n/a
44	chr19:36910116-36910166	MCF10A-Er-Src	breast:	n/a
45	chr19:36909326-36909376	H1-hESC	embryonic stem cell:	embryo
46	chr19:36909418-36909468	Hepatocyte	liver:	n/a
47	chr19:36912880-36912930	PANC-1	pancreas:	n/a
48	chr19:36909831-36909881	ECC-1	luminal epithelium:	n/a
49	chr19:36911014-36911064	U87	brain:	n/a
50	chr19:36937832-36937882	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:36921260..36923762-chr19:37063794..37066625,2	K562	blood:
2	chr19:36944101..36946636-chr19:36951837..36953729,2	K562	blood:
3	chr19:36924487..36927399-chr19:37259800..37262103,2	K562	blood:
4	chr19:36884346..36886585-chr19:36904076..36906046,2	MCF-7	breast:
5	chr19:36895506..36897062-chr19:36899280..36901611,2	K562	blood:
6	chr19:36909374..36910931-chr19:36934594..36936776,2	K562	blood:
7	chr19:36944101..36946636-chr19:36951837..36953729,2	K562	blood:
8	chr19:36952422..36955146-chr19:36978594..36981025,2	K562	blood:
9	chr19:36940091..36943076-chr19:37061156..37065481,3	K562	blood:

Variant related genes	Relation type
ZNF566	TF binding region
ENSG00000267142	TF binding region
ZFP82	TF binding region
ZNF566	CpG island
ENSG00000267142	CpG island
ZFP82	CpG island
ENSG00000186020	chromatin interactions
ENSG00000186017	chromatin interactions
ENSG00000181007	chromatin interactions
ENSG00000233527	chromatin interactions
ENSG00000267309	chromatin interactions

Extended variants
information (count: 1456 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1456 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2271844	chr19:36901010-36901011	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79886957	chr19:36901021-36901022	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530626616	chr19:36901039-36901040	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141842793	chr19:36901061-36901062	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182150448	chr19:36901077-36901078	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188094593	chr19:36901121-36901122	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371881139	chr19:36901139-36901140	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191519005	chr19:36901176-36901177	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566709005	chr19:36901246-36901247	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527487724	chr19:36901252-36901253	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549294907	chr19:36901253-36901254	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567202029	chr19:36901291-36901292	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10660107	chr19:36901333-36901334	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141959407	chr19:36901335-36901336	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34819087	chr19:36901336-36901337	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7254481	chr19:36901337-36901338	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77430304	chr19:36901339-36901340	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537720206	chr19:36901344-36901345	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372944303	chr19:36901349-36901350	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs58703752	chr19:36901352-36901353	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369516359	chr19:36901353-36901354	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs200444469	chr19:36901355-36901356	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571260998	chr19:36901367-36901368	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs7259288	chr19:36901416-36901417	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs539169793	chr19:36901438-36901439	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182840717	chr19:36901459-36901460	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571133546	chr19:36901467-36901468	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538008029	chr19:36901468-36901469	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542830499	chr19:36901498-36901499	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555171224	chr19:36901552-36901553	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113181501	chr19:36901562-36901563	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544086971	chr19:36901570-36901571	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369055261	chr19:36901572-36901573	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562473569	chr19:36901580-36901581	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376471446	chr19:36901616-36901617	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201249390	chr19:36901625-36901626	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145778120	chr19:36901627-36901628	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201905921	chr19:36901636-36901637	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111763572	chr19:36901642-36901643	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188705373	chr19:36901645-36901646	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529240634	chr19:36901654-36901655	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527511239	chr19:36901655-36901656	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142640231	chr19:36901700-36901701	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556842676	chr19:36901701-36901702	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567089458	chr19:36901741-36901742	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568963414	chr19:36901753-36901754	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545032823	chr19:36901794-36901795	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191957341	chr19:36901821-36901822	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571347489	chr19:36901833-36901834	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538640274	chr19:36901857-36901858	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Pleomorphic liposarcoma	18784837	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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1460 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36880400-36904600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr19:36882200-36908800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:36882400-36907600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:36882600-36904200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:36883000-36905200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
6	chr19:36885600-36908000	Weak transcription	K562	blood
7	chr19:36888400-36901200	Strong transcription	Brain Hippocampus Middle	brain
8	chr19:36889800-36908200	Weak transcription	HepG2	liver
9	chr19:36890400-36901400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr19:36891000-36904800	Strong transcription	Dnd41	blood
11	chr19:36891200-36901400	ZNF genes & repeats	A549	lung
12	chr19:36891800-36908200	Weak transcription	Fetal Heart	heart
13	chr19:36891800-36908200	Weak transcription	Hela-S3	cervix
14	chr19:36892400-36901400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr19:36892400-36901600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr19:36894400-36901200	Strong transcription	Primary B cells from peripheral blood	blood
17	chr19:36894400-36901400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr19:36894400-36901600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
19	chr19:36894400-36902600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr19:36894600-36901200	Strong transcription	NHDF-Ad	bronchial
21	chr19:36894800-36901200	Strong transcription	Colon Smooth Muscle	Colon
22	chr19:36895000-36901200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr19:36895000-36901400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr19:36895000-36901400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:36895000-36908200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr19:36895200-36901200	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr19:36895400-36901800	Strong transcription	Left Ventricle	heart
28	chr19:36895600-36901400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr19:36895600-36901400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr19:36896400-36901800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr19:36896600-36908200	Weak transcription	Right Ventricle	heart
32	chr19:36896600-36908400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:36897200-36908200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr19:36897800-36901200	ZNF genes & repeats	GM12878-XiMat	blood
35	chr19:36898200-36901400	Strong transcription	Placenta	Placenta
36	chr19:36898400-36901200	Strong transcription	H9 Cell Line	embryonic stem cell
37	chr19:36898400-36901200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
38	chr19:36898400-36901200	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr19:36898400-36901200	Strong transcription	Pancreatic Islets	Pancreatic Islet
40	chr19:36898400-36901200	ZNF genes & repeats	Thymus	Thymus
41	chr19:36898400-36901400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
42	chr19:36898400-36901400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr19:36898400-36901400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:36898400-36901600	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
45	chr19:36898400-36901800	ZNF genes & repeats	Primary T cells from cord blood	blood
46	chr19:36898400-36901800	ZNF genes & repeats	Fetal Brain Female	brain
47	chr19:36898400-36902400	ZNF genes & repeats	Ovary	ovary
48	chr19:36898400-36904400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
49	chr19:36898400-36904600	ZNF genes & repeats	Primary B cells from cord blood	blood
50	chr19:36898400-36904600	ZNF genes & repeats	Liver	Liver

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