Variant report

Variant	nsv1066876
Chromosome Location	chr19:53123577-53157096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:569)
CpG islands
(count:733)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53141435-53141564	K562	blood:	n/a	n/a
2	ATF1	chr19:53150020-53150354	K562	blood:	n/a	n/a
3	ATF2	chr19:53141325-53141694	GM12878	blood:	n/a	n/a
4	BACH1	chr19:53141538-53141574	K562	blood:	n/a	n/a
5	BCL11A	chr19:53143129-53143365	GM12878	blood:	n/a	n/a
6	BCLAF1	chr19:53141115-53141672	GM12878	blood:	n/a	chr19:53141336-53141345
7	BCLAF1	chr19:53141256-53141655	GM12878	blood:	n/a	chr19:53141336-53141345
8	BHLHE40	chr19:53141339-53141678	K562	blood:	n/a	n/a
9	BHLHE40	chr19:53141335-53141727	GM12878	blood:	n/a	n/a
10	CBX3	chr19:53150111-53150413	K562	blood:	n/a	n/a
11	CBX3	chr19:53149990-53150565	HCT-116	colon:	n/a	n/a
12	CBX3	chr19:53150016-53150408	K562	blood:	n/a	n/a
13	CBX3	chr19:53150055-53150488	HCT-116	colon:	n/a	n/a
14	CBX3	chr19:53141151-53141942	K562	blood:	n/a	n/a
15	CCNT2	chr19:53141473-53141801	K562	blood:	n/a	chr19:53141683-53141692
16	CEBPB	chr19:53156509-53156709	HepG2	liver:	n/a	chr19:53156597-53156608
17	CEBPB	chr19:53149990-53150363	K562	blood:	n/a	n/a
18	CEBPB	chr19:53130295-53130394	K562	blood:	n/a	n/a
19	CEBPD	chr19:53141013-53141270	HepG2	liver:	n/a	n/a
20	CHD1	chr19:53141329-53141570	GM12878	blood:	n/a	n/a
21	CHD2	chr19:53141120-53141701	Hela-S3	cervix:	n/a	chr19:53141684-53141694 chr19:53141292-53141302
22	CHD2	chr19:53141130-53141717	GM12878	blood:	n/a	chr19:53141684-53141694 chr19:53141292-53141302
23	CTCF	chr19:53141300-53141450	BJ	skin:	n/a	n/a
24	CTCF	chr19:53125681-53125733	MCF-7	breast:	n/a	n/a
25	CTCF	chr19:53141101-53141103	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr19:53137958-53138037	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr19:53138700-53138740	GM13976	blood:	n/a	n/a
28	CTCF	chr19:53141201-53141269	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr19:53140420-53140570	Caco-2	colon:	n/a	n/a
30	CTCF	chr19:53125600-53125750	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr19:53125634-53125770	HepG2	liver:	n/a	n/a
32	CTCF	chr19:53141322-53141579	K562	blood:	n/a	n/a
33	CTCF	chr19:53125704-53125727	GM19238	blood:	n/a	n/a
34	CTCF	chr19:53125620-53125770	Caco-2	colon:	n/a	n/a
35	CTCF	chr19:53125528-53125891	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr19:53125620-53125770	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr19:53125709-53125807	GM13977	blood:	n/a	n/a
38	CTCF	chr19:53125580-53125730	NB4	blood:	n/a	n/a
39	CTCF	chr19:53125658-53125748	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr19:53125643-53125743	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr19:53141480-53141630	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr19:53125671-53125778	Lung_OC	lung:	n/a	n/a
43	CTCF	chr19:53125465-53125912	MCF-7	breast:	n/a	n/a
44	CTCF	chr19:53125620-53125770	HMEC	breast:	n/a	n/a
45	CTCF	chr19:53125680-53125834	IMR90	lung:	n/a	n/a
46	CTCF	chr19:53125690-53125740	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr19:53147885-53147940	GM13976	blood:	n/a	n/a
48	CTCF	chr19:53141196-53141199	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr19:53125680-53125830	SAEC	small airway:	n/a	n/a
50	CTCF	chr19:53125600-53125750	HMEC	breast:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53142146-53142196	ECC-1	luminal epithelium:	n/a
2	chr19:53142146-53142196	ECC-1	luminal epithelium:	n/a
3	chr19:53142304-53142354	HRPEpiC	eye:	n/a
4	chr19:53141778-53141828	HRCEpiC	kidney:	n/a
5	chr19:53144247-53144297	BJ	skin:	n/a
6	chr19:53142106-53142156	GM12892	blood:	n/a
7	chr19:53141745-53141795	PrEC	prostate:	n/a
8	chr19:53141394-53141444	BJ	skin:	n/a
9	chr19:53140973-53141023	GM12892	blood:	n/a
10	chr19:53141745-53141795	Hepatocyte	liver:	n/a
11	chr19:53142304-53142354	ovcar-3	ovarian:	n/a
12	chr19:53141620-53141670	NH-A	brain:	n/a
13	chr19:53141745-53141795	GM12878	blood:	n/a
14	chr19:53141745-53141795	HCT-116	colon:	n/a
15	chr19:53141394-53141444	HCT-116	colon:	n/a
16	chr19:53140973-53141023	MCF10A-Er-Src	breast:	n/a
17	chr19:53141793-53141843	HCM	heart:	n/a
18	chr19:53141394-53141444	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:53141620-53141670	HepG2	liver:	n/a
20	chr19:53139159-53139209	AG10803	skin:	n/a
21	chr19:53144247-53144297	NHDF-neo	bronchial:	n/a
22	chr19:53141372-53141422	BE2_C	brain:	n/a
23	chr19:53142304-53142354	GM12892	blood:	n/a
24	chr19:53142106-53142156	CMK	blood:	n/a
25	chr19:53141372-53141422	PFSK-1	brain:	n/a
26	chr19:53142106-53142156	HEK293	kidney:	embryo
27	chr19:53141394-53141444	AG04449	skin:	fetal
28	chr19:53144247-53144297	CMK	blood:	n/a
29	chr19:53142146-53142196	U87	brain:	n/a
30	chr19:53142304-53142354	HNPCEpiC	eye:	n/a
31	chr19:53141620-53141670	SK-N-SH_RA	brain:	n/a
32	chr19:53141793-53141843	HCPEpiC	choroid plexus:	n/a
33	chr19:53141620-53141670	AG04449	skin:	fetal
34	chr19:53141778-53141828	HAEpiC	amniotic membrane:	n/a
35	chr19:53141620-53141670	Hela-S3	cervix:	n/a
36	chr19:53144247-53144297	NHBE	bronchial:	n/a
37	chr19:53139159-53139209	MCF-7	breast:	n/a
38	chr19:53140973-53141023	HEEpiC	esophagus:	n/a
39	chr19:53141372-53141422	K562	blood:	n/a
40	chr19:53141394-53141444	HRPEpiC	eye:	n/a
41	chr19:53141620-53141670	HUVEC	blood vessel:	n/a
42	chr19:53142146-53142196	NB4	blood:	n/a
43	chr19:53141394-53141444	PrEC	prostate:	n/a
44	chr19:53141745-53141795	MCF10A-Er-Src	breast:	n/a
45	chr19:53139159-53139209	HRCEpiC	kidney:	n/a
46	chr19:53141372-53141422	MCF-7	breast:	n/a
47	chr19:53140973-53141023	CMK	blood:	n/a
48	chr19:53141778-53141828	GM19239	blood:	n/a
49	chr19:53141778-53141828	SKMC	muscle:	n/a
50	chr19:53141745-53141795	NHBE	bronchial:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53115087..53117490-chr19:53126115..53129040,2	K562	blood:
2	chr19:53149533..53152778-chr19:53154420..53157722,3	K562	blood:
3	chr19:53148354..53151033-chr19:53154176..53155920,2	K562	blood:
4	chr19:53148354..53151033-chr19:53154176..53155920,2	K562	blood:
5	chr19:53139623..53144311-chr19:53192220..53194807,4	MCF-7	breast:
6	chr19:53128911..53130963-chr19:53136725..53138232,2	K562	blood:
7	chr19:53124557..53126496-chr19:53127801..53130626,2	K562	blood:
8	chr19:53140133..53142689-chr19:53604558..53606639,2	MCF-7	breast:
9	chr19:53128911..53130963-chr19:53136725..53138232,2	K562	blood:
10	chr19:53141360..53143345-chr19:53143350..53145363,3	K562	blood:
11	chr19:53138548..53141148-chr19:53148838..53150932,2	K562	blood:
12	chr19:53143960..53145524-chr19:53164055..53166816,2	K562	blood:
13	chr19:53124557..53126496-chr19:53127801..53130626,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF611-1	chr19:53153690-53156537	ENSG00000269825.1

No data

Variant related genes	Relation type
ENSG00000269825	TF binding region
ZNF83	TF binding region
ENSG00000269825	CpG island
ZNF83	CpG island
ENSG00000269825	chromatin interactions
ENSG00000170949	chromatin interactions
ENSG00000167766	chromatin interactions

Extended variants
information (count: 1616 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62118483	chr19:53123612-53123613	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569319752	chr19:53123617-53123618	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542962405	chr19:53123679-53123680	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs116669870	chr19:53123693-53123694	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369690436	chr19:53123704-53123705	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs375227721	chr19:53123705-53123706	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs114463730	chr19:53123707-53123708	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs534903584	chr19:53123785-53123786	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs572557687	chr19:53123886-53123887	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550122581	chr19:53123896-53123897	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs138178499	chr19:53123937-53123938	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183744053	chr19:53123964-53123965	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs189190691	chr19:53124021-53124022	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143732867	chr19:53124037-53124038	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs193057512	chr19:53124068-53124069	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576790284	chr19:53124086-53124087	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs66599469	chr19:53124093-53124094	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs562096836	chr19:53124112-53124113	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112649627	chr19:53124128-53124129	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs562029327	chr19:53124134-53124135	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547679024	chr19:53124137-53124138	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556449243	chr19:53124139-53124140	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs559561651	chr19:53124151-53124152	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs533309307	chr19:53124160-53124161	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs551063745	chr19:53124182-53124183	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs569621823	chr19:53124189-53124190	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185573384	chr19:53124210-53124211	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs548738976	chr19:53124277-53124278	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs190038536	chr19:53124299-53124300	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs191906816	chr19:53124331-53124332	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs536586178	chr19:53124341-53124342	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs377114055	chr19:53124360-53124361	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs76719431	chr19:53124364-53124365	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs553297829	chr19:53124383-53124384	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs529390065	chr19:53124410-53124411	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs577924986	chr19:53124444-53124445	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs113559831	chr19:53124451-53124452	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558307379	chr19:53124507-53124508	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs576492739	chr19:53124518-53124519	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77468127	chr19:53124528-53124529	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs79914887	chr19:53124564-53124565	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559294609	chr19:53124578-53124579	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs183989842	chr19:53124585-53124586	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs138376671	chr19:53124604-53124605	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs559571993	chr19:53124625-53124626	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533199825	chr19:53124650-53124651	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs533369413	chr19:53124679-53124680	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375237616	chr19:53124687-53124688	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs74711382	chr19:53124763-53124764	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372553348	chr19:53124764-53124765	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1416 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53105800-53129000	Weak transcription	Hela-S3	cervix
2	chr19:53107000-53136600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:53112000-53131600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
4	chr19:53113800-53123800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:53115400-53123800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr19:53115400-53123800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr19:53115400-53131800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr19:53115600-53124600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr19:53115600-53130600	Strong transcription	Placenta	Placenta
10	chr19:53115600-53131200	Strong transcription	Dnd41	blood
11	chr19:53115600-53131400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr19:53116200-53124000	ZNF genes & repeats	GM12878-XiMat	blood
13	chr19:53116200-53131000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr19:53116400-53123600	Strong transcription	Stomach Smooth Muscle	stomach
15	chr19:53116400-53125000	Strong transcription	Brain Inferior Temporal Lobe	brain
16	chr19:53116400-53127000	Strong transcription	Fetal Muscle Trunk	muscle
17	chr19:53116400-53127000	Strong transcription	Ovary	ovary
18	chr19:53116800-53125000	Strong transcription	Fetal Muscle Leg	muscle
19	chr19:53117200-53127400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr19:53117800-53126800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
21	chr19:53117800-53131200	Strong transcription	Adipose Nuclei	Adipose
22	chr19:53117800-53140400	Weak transcription	Brain Substantia Nigra	brain
23	chr19:53117800-53140400	Weak transcription	Fetal Heart	heart
24	chr19:53118000-53123600	Weak transcription	Small Intestine	intestine
25	chr19:53118000-53128600	Weak transcription	Psoas Muscle	Psoas
26	chr19:53118000-53140400	Weak transcription	Right Ventricle	heart
27	chr19:53118600-53124200	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr19:53118600-53132800	Strong transcription	Fetal Stomach	stomach
29	chr19:53118800-53124600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr19:53119000-53124200	ZNF genes & repeats	Fetal Intestine Large	intestine
31	chr19:53119000-53125200	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr19:53119400-53125400	Weak transcription	Colon Smooth Muscle	Colon
33	chr19:53119600-53126000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr19:53119600-53126600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr19:53119600-53132800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr19:53119800-53128200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr19:53119800-53131200	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr19:53120000-53127200	Weak transcription	Fetal Lung	lung
39	chr19:53120200-53130000	Strong transcription	Aorta	Aorta
40	chr19:53120400-53129000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr19:53120400-53132000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr19:53120600-53123800	Strong transcription	K562	blood
43	chr19:53120600-53125400	Weak transcription	Colonic Mucosa	Colon
44	chr19:53120600-53127400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr19:53120600-53128600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr19:53120600-53129400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr19:53120600-53130600	Weak transcription	HUVEC	blood vessel
48	chr19:53120600-53132000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr19:53120600-53139800	Weak transcription	NHLF	lung
50	chr19:53120800-53123600	Weak transcription	Rectal Smooth Muscle	rectum

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