Variant report

Variant	esv3404701
Chromosome Location	chr19:52986895-53035152
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:751)
CpG islands
(count:1342)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53030907-53031004	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:53030319-53030487	K562	blood:	n/a	n/a
3	ATF1	chr19:53030283-53031114	K562	blood:	n/a	n/a
4	ATF2	chr19:53030208-53030710	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:53030243-53030702	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:53030186-53030755	GM12878	blood:	n/a	n/a
7	ATF2	chr19:53030190-53030680	GM12878	blood:	n/a	n/a
8	ATF3	chr19:53030291-53030590	K562	blood:	n/a	n/a
9	ATF3	chr19:53030298-53030700	K562	blood:	n/a	n/a
10	BACH1	chr19:53030537-53030601	K562	blood:	n/a	n/a
11	BATF	chr19:53021956-53022186	GM12878	blood:	n/a	chr19:53022128-53022138 chr19:53022124-53022134
12	BATF	chr19:53030276-53030547	GM12878	blood:	n/a	n/a
13	BATF	chr19:53004948-53005213	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
14	BATF	chr19:53004998-53005244	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
15	BCL11A	chr19:53028616-53028797	GM12878	blood:	n/a	n/a
16	BCLAF1	chr19:53030266-53030752	GM12878	blood:	n/a	chr19:53030409-53030422
17	BHLHE40	chr19:53030331-53031440	K562	blood:	n/a	n/a
18	BRCA1	chr19:52996530-52996612	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:53030788-53031097	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr19:53030524-53030612	GM12878	blood:	n/a	n/a
21	CBX3	chr19:53030053-53031085	K562	blood:	n/a	n/a
22	CBX3	chr19:53030255-53030758	K562	blood:	n/a	n/a
23	CCNT2	chr19:53030418-53030847	K562	blood:	n/a	n/a
24	CEBPB	chr19:53024161-53024462	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:53030801-53031107	K562	blood:	n/a	n/a
26	CEBPB	chr19:53011938-53012138	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:53023382-53023686	HepG2	liver:	n/a	chr19:53023522-53023533
28	CEBPB	chr19:52991963-52992022	H1-hESC	embryonic stem cell:	n/a	chr19:52991987-52991998
29	CEBPB	chr19:53011963-53012116	K562	blood:	n/a	n/a
30	CEBPB	chr19:53011918-53012150	A549	lung:	n/a	n/a
31	CEBPB	chr19:53030405-53030582	K562	blood:	n/a	n/a
32	CEBPB	chr19:52993321-52993417	HepG2	liver:	n/a	chr19:52993340-52993349 chr19:52993338-52993351 chr19:52993338-52993349 chr19:52993340-52993349 chr19:52993339-52993350 chr19:52993340-52993349 chr19:52993340-52993349
33	CEBPB	chr19:53030839-53031138	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:53030333-53031155	IMR90	lung:	n/a	n/a
35	CEBPB	chr19:53023353-53023673	K562	blood:	n/a	chr19:53023522-53023533
36	CEBPB	chr19:52991868-52992035	HepG2	liver:	n/a	chr19:52991987-52991998
37	CEBPB	chr19:53030600-53031145	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:53023422-53023684	H1-hESC	embryonic stem cell:	n/a	chr19:53023522-53023533
39	CEBPB	chr19:53030268-53030737	GM12878	blood:	n/a	n/a
40	CEBPB	chr19:53023339-53023693	K562	blood:	n/a	chr19:53023522-53023533
41	CEBPB	chr19:52996555-52996636	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPD	chr19:53030856-53031116	HepG2	liver:	n/a	n/a
43	CHD1	chr19:53030984-53031204	GM12878	blood:	n/a	n/a
44	CHD2	chr19:53031443-53031545	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr19:53030349-53030741	K562	blood:	n/a	n/a
46	CHD2	chr19:53030358-53031168	Hela-S3	cervix:	n/a	chr19:53030873-53030883 chr19:53030825-53030835
47	CHD2	chr19:52996409-52996675	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr19:53030964-53031146	K562	blood:	n/a	n/a
49	CHD2	chr19:53030912-53031013	HepG2	liver:	n/a	n/a
50	CHD2	chr19:52995873-52996149	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52996548-52996598	NHDF-neo	bronchial:	n/a
2	chr19:53030736-53030786	NHDF-neo	bronchial:	n/a
3	chr19:52996083-52996133	AG09309	skin:	n/a
4	chr19:53030958-53031008	SK-N-SH	brain:	n/a
5	chr19:53034554-53034604	GM12891	blood:	n/a
6	chr19:53030774-53030824	IMR90	lung:	fetal
7	chr19:53031511-53031561	HCPEpiC	choroid plexus:	n/a
8	chr19:53031138-53031188	AG10803	skin:	n/a
9	chr19:52996352-52996402	AG09309	skin:	n/a
10	chr19:52996352-52996402	NH-A	brain:	n/a
11	chr19:52999520-52999570	GM12891	blood:	n/a
12	chr19:53018151-53018201	HEK293	kidney:	embryo
13	chr19:53028694-53028744	NB4	blood:	n/a
14	chr19:52992415-52992465	RPTEC	kidney:	n/a
15	chr19:53030489-53030539	RPTEC	kidney:	n/a
16	chr19:53018151-53018201	HCT-116	colon:	n/a
17	chr19:53030780-53030830	BE2_C	brain:	n/a
18	chr19:52999520-52999570	HL-60	blood:	n/a
19	chr19:52996617-52996667	Hepatocyte	liver:	n/a
20	chr19:53030774-53030824	AG04449	skin:	fetal
21	chr19:53030736-53030786	Hepatocyte	liver:	n/a
22	chr19:53030996-53031046	NH-A	brain:	n/a
23	chr19:53030605-53030655	PFSK-1	brain:	n/a
24	chr19:52996617-52996667	AG09319	gingival:	n/a
25	chr19:53030996-53031046	NB4	blood:	n/a
26	chr19:52992415-52992465	HEEpiC	esophagus:	n/a
27	chr19:52992415-52992465	NB4	blood:	n/a
28	chr19:53018151-53018201	BE2_C	brain:	n/a
29	chr19:52995647-52995697	ECC-1	luminal epithelium:	n/a
30	chr19:53030705-53030755	U87	brain:	n/a
31	chr19:52995647-52995697	ProgFib	skin:	n/a
32	chr19:53030705-53030755	SK-N-MC	brain:	n/a
33	chr19:53030711-53030761	AG04449	skin:	fetal
34	chr19:53031138-53031188	HRPEpiC	eye:	n/a
35	chr19:52992415-52992465	U87	brain:	n/a
36	chr19:52996548-52996598	U87	brain:	n/a
37	chr19:53031333-53031383	PrEC	prostate:	n/a
38	chr19:53030705-53030755	K562	blood:	n/a
39	chr19:52999520-52999570	HNPCEpiC	eye:	n/a
40	chr19:52995647-52995697	HRE	kidney:	n/a
41	chr19:52996617-52996667	NB4	blood:	n/a
42	chr19:53030711-53030761	BJ	skin:	n/a
43	chr19:53030605-53030655	NH-A	brain:	n/a
44	chr19:52996083-52996133	BJ	skin:	n/a
45	chr19:52992415-52992465	NT2-D1	testis:	n/a
46	chr19:53031333-53031383	ovcar-3	ovarian:	n/a
47	chr19:53030958-53031008	AG09309	skin:	n/a
48	chr19:53034554-53034604	BJ	skin:	n/a
49	chr19:53018151-53018201	CMK	blood:	n/a
50	chr19:52992415-52992465	MCF-7	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53029450..53032188-chr19:53072538..53074123,2	K562	blood:
2	chr19:53029127..53032188-chr19:53072538..53075129,3	K562	blood:
3	chr19:53029459..53032258-chr19:53036873..53039549,6	MCF-7	breast:
4	chr19:53024234..53025826-chr19:53029049..53030597,2	MCF-7	breast:
5	chr19:53031656..53034156-chr19:53037494..53039065,2	MCF-7	breast:
6	chr19:53024234..53025826-chr19:53029049..53030597,2	MCF-7	breast:
7	chr19:53025941..53027882-chr19:53028687..53031111,3	MCF-7	breast:
8	chr19:52641251..52643352-chr19:52987033..52989760,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF83-7	chr19:53015428-53015595	ENSG00000269349.1
2	lnc-ZNF83-7	chr19:53014535-53015246	ENSG00000269349.1

No data

Variant related genes	Relation type
ENSG00000269349	TF binding region
ZNF808	TF binding region
ZNF578	TF binding region
ENSG00000269349	CpG island
ZNF808	CpG island
ZNF578	CpG island
ENSG00000204611	chromatin interactions
ENSG00000167562	chromatin interactions
ENSG00000198482	chromatin interactions

Extended variants
information (count: 2576 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2576 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150748022	chr19:52986901-52986902	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs529606676	chr19:52986907-52986908	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs191493296	chr19:52986917-52986918	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs73934539	chr19:52986944-52986945	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs4802962	chr19:52986955-52986956	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs73934540	chr19:52986958-52986959	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs139334733	chr19:52986973-52986974	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs551475465	chr19:52986984-52986985	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs112953766	chr19:52987033-52987034	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370987597	chr19:52987038-52987039	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569798630	chr19:52987043-52987044	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537030670	chr19:52987044-52987045	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553521046	chr19:52987049-52987050	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555445140	chr19:52987058-52987059	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10775555	chr19:52987067-52987068	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs199505610	chr19:52987135-52987136	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150033100	chr19:52987141-52987142	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs80277552	chr19:52987145-52987146	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77646350	chr19:52987154-52987155	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376616085	chr19:52987164-52987165	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200087962	chr19:52987170-52987171	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146414350	chr19:52987198-52987199	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs59065375	chr19:52987202-52987203	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs1673916	chr19:52987223-52987224	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577727042	chr19:52987235-52987236	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10853851	chr19:52987236-52987237	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs141000640	chr19:52987247-52987248	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576162229	chr19:52987265-52987266	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534217121	chr19:52987296-52987297	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371574305	chr19:52987366-52987367	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373805385	chr19:52987398-52987399	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543409647	chr19:52987407-52987408	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111754552	chr19:52987416-52987417	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535958154	chr19:52987426-52987427	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs58067500	chr19:52987449-52987450	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143683750	chr19:52987458-52987459	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541329626	chr19:52987473-52987474	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs78751766	chr19:52987498-52987499	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570929970	chr19:52987506-52987507	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533344423	chr19:52987519-52987520	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552039840	chr19:52987522-52987523	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs538140462	chr19:52987529-52987530	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375860220	chr19:52987541-52987542	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs76787899	chr19:52987543-52987544	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530668285	chr19:52987551-52987552	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs75481827	chr19:52987565-52987566	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141013423	chr19:52987577-52987578	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148248164	chr19:52987609-52987610	Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534624531	chr19:52987613-52987614	Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7249798	chr19:52987624-52987625	Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
Adrenocortical carcinoma	18281524	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52957800-52990400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
2	chr19:52963400-52987600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr19:52967800-52990600	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr19:52985200-52987800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:52985400-52987400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr19:52985600-52987400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:52985800-52987000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:52986200-52987200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:52987000-52987400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr19:52987000-52988000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr19:52987000-52990200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr19:52987200-52987400	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr19:52987400-52987600	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr19:52987400-52987600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr19:52987400-52987800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr19:52987600-52987800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr19:52987600-52987800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr19:52987800-52988400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr19:52987800-52988400	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr19:52987800-52988400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr19:52988000-52988400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr19:52988200-52988600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr19:52988400-52988600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr19:52988400-52988800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr19:52988400-52988800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr19:52988400-52989000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr19:52988400-52989200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr19:52988600-52988800	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr19:52988600-52989000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr19:52988600-52989200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr19:52988800-52989000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr19:52988800-52989200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr19:52988800-52989800	Enhancers	Placenta	Placenta
34	chr19:52989000-52989200	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr19:52989000-52989800	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr19:52989000-52990000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr19:52989000-52991400	ZNF genes & repeats	Liver	Liver
38	chr19:52989200-52989400	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr19:52989200-52989600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr19:52989200-52989800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr19:52989200-52990800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr19:52989400-52989600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr19:52989400-52989800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:52989600-52989800	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr19:52989600-52990200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr19:52989800-52990200	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr19:52989800-52990400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:52989800-52990600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:52989800-52990800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr19:52989800-52990800	ZNF genes & repeats	Stomach Smooth Muscle	stomach

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