Variant report

Variant	nsv1061849
Chromosome Location	chr19:53508419-53556812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:368)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 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	BACH1	chr19:53518961-53519336	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:53510493-53510782	GM12878	blood:	n/a	n/a
3	BHLHE40	chr19:53510497-53510963	K562	blood:	n/a	n/a
4	BRCA1	chr19:53548078-53548353	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr19:53556503-53556768	K562	blood:	n/a	n/a
6	CEBPB	chr19:53520072-53520352	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr19:53520045-53520364	IMR90	lung:	n/a	n/a
8	CEBPB	chr19:53520052-53520352	K562	blood:	n/a	n/a
9	CEBPB	chr19:53514709-53514946	Hela-S3	cervix:	n/a	chr19:53514790-53514801
10	CEBPB	chr19:53514683-53514869	A549	lung:	n/a	chr19:53514790-53514801
11	CEBPB	chr19:53520162-53520365	MCF-7	breast:	n/a	n/a
12	CEBPB	chr19:53514645-53514955	HepG2	liver:	n/a	chr19:53514790-53514801
13	CEBPB	chr19:53514622-53514961	K562	blood:	n/a	chr19:53514790-53514801
14	CTCF	chr19:53523080-53523230	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr19:53523141-53523173	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr19:53523060-53523210	HL-60	blood:	n/a	n/a
17	CTCF	chr19:53522863-53523276	K562	blood:	n/a	n/a
18	CTCF	chr19:53523073-53523220	MCF-7	breast:	n/a	n/a
19	CTCF	chr19:53523100-53523250	HCM	heart:	n/a	n/a
20	CTCF	chr19:53523070-53523239	NHEK	skin:	n/a	n/a
21	CTCF	chr19:53518162-53518286	GM20000	blood:	n/a	n/a
22	CTCF	chr19:53523114-53523192	GM10266	blood:	n/a	n/a
23	CTCF	chr19:53513788-53514075	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr19:53523481-53523551	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr19:53522860-53523010	K562	blood:	n/a	n/a
26	CTCF	chr19:53522935-53523279	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr19:53513826-53514079	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr19:53523000-53523150	HVMF	connective:	n/a	n/a
29	CTCF	chr19:53523000-53523150	HEK293	kidney:	n/a	n/a
30	CTCF	chr19:53523020-53523170	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr19:53523066-53523216	GM12891	blood:	n/a	n/a
32	CTCF	chr19:53523018-53523242	HepG2	liver:	n/a	n/a
33	CTCF	chr19:53523040-53523190	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr19:53523040-53523190	GM12873	blood:	n/a	n/a
35	CTCF	chr19:53523113-53523185	ProgFib	skin:	n/a	n/a
36	CTCF	chr19:53523080-53523230	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr19:53547820-53547970	GM12875	blood:	n/a	n/a
38	CTCF	chr19:53523080-53523230	K562	blood:	n/a	n/a
39	CTCF	chr19:53523080-53523230	GM12874	blood:	n/a	n/a
40	CTCF	chr19:53522968-53523321	K562	blood:	n/a	n/a
41	CTCF	chr19:53523116-53523172	GM12878	blood:	n/a	n/a
42	CTCF	chr19:53523040-53523190	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr19:53523040-53523190	BJ	skin:	n/a	n/a
44	CTCF	chr19:53522996-53523308	GM12878	blood:	n/a	n/a
45	CTCF	chr19:53517968-53518032	K562	blood:	n/a	n/a
46	CTCF	chr19:53523060-53523210	WI-38	lung:	n/a	n/a
47	CTCF	chr19:53523195-53523198	GM10266	blood:	n/a	n/a
48	CTCF	chr19:53522993-53523208	HepG2	liver:	n/a	n/a
49	CTCF	chr19:53523155-53523182	HepG2	liver:	n/a	n/a
50	CTCF	chr19:53523080-53523230	NHEK	skin:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53538883-53538933	NHDF-neo	bronchial:	n/a
2	chr19:53540845-53540895	MCF-7	breast:	n/a
3	chr19:53538883-53538933	NHDF-neo	bronchial:	n/a
4	chr19:53540845-53540895	MCF-7	breast:	n/a
5	chr19:53538883-53538933	AG10803	skin:	n/a
6	chr19:53538687-53538737	ECC-1	luminal epithelium:	n/a
7	chr19:53540845-53540895	GM12878	blood:	n/a
8	chr19:53538687-53538737	SK-N-SH_RA	brain:	n/a
9	chr19:53538883-53538933	HRCEpiC	kidney:	n/a
10	chr19:53541287-53541337	LNCaP	prostate:	n/a
11	chr19:53538687-53538737	PrEC	prostate:	n/a
12	chr19:53538687-53538737	IMR90	lung:	fetal
13	chr19:53540902-53540952	PFSK-1	brain:	n/a
14	chr19:53541287-53541337	AG04450	lung:	fetal
15	chr19:53541287-53541337	NT2-D1	testis:	n/a
16	chr19:53541287-53541337	PANC-1	pancreas:	n/a
17	chr19:53540902-53540952	ECC-1	luminal epithelium:	n/a
18	chr19:53538883-53538933	GM12892	blood:	n/a
19	chr19:53540902-53540952	AG10803	skin:	n/a
20	chr19:53538687-53538737	HL-60	blood:	n/a
21	chr19:53540902-53540952	HCT-116	colon:	n/a
22	chr19:53541287-53541337	PFSK-1	brain:	n/a
23	chr19:53541186-53541236	NT2-D1	testis:	n/a
24	chr19:53540845-53540895	HepG2	liver:	n/a
25	chr19:53538883-53538933	Hela-S3	cervix:	n/a
26	chr19:53541186-53541236	BE2_C	brain:	n/a
27	chr19:53540902-53540952	HMEC	breast:	n/a
28	chr19:53540902-53540952	SK-N-SH	brain:	n/a
29	chr19:53538687-53538737	SAEC	small airway:	n/a
30	chr19:53538687-53538737	HEEpiC	esophagus:	n/a
31	chr19:53541186-53541236	HCT-116	colon:	n/a
32	chr19:53540845-53540895	SK-N-MC	brain:	n/a
33	chr19:53538883-53538933	HRPEpiC	eye:	n/a
34	chr19:53541186-53541236	HRCEpiC	kidney:	n/a
35	chr19:53540845-53540895	ovcar-3	ovarian:	n/a
36	chr19:53541287-53541337	NHBE	bronchial:	n/a
37	chr19:53540902-53540952	GM12891	blood:	n/a
38	chr19:53538687-53538737	GM12892	blood:	n/a
39	chr19:53540845-53540895	HCT-116	colon:	n/a
40	chr19:53538687-53538737	SKMC	muscle:	n/a
41	chr19:53541186-53541236	PANC-1	pancreas:	n/a
42	chr19:53541186-53541236	MCF-7	breast:	n/a
43	chr19:53540845-53540895	AG10803	skin:	n/a
44	chr19:53538687-53538737	HEK293	kidney:	embryo
45	chr19:53541287-53541337	HEEpiC	esophagus:	n/a
46	chr19:53538687-53538737	K562	blood:	n/a
47	chr19:53540845-53540895	NH-A	brain:	n/a
48	chr19:53538687-53538737	AG10803	skin:	n/a
49	chr19:53541287-53541337	HAEpiC	amniotic membrane:	n/a
50	chr19:53540845-53540895	SAEC	small airway:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:
2	chr19:53536567..53539141-chr19:53540653..53542425,2	K562	blood:
3	chr10:9353360..9353955-chr19:53525559..53526530,2	MCF-7	breast:
4	chr19:53515874..53517968-chr19:53519511..53521544,2	K562	blood:
5	chr19:53514929..53517284-chr19:53527300..53529548,2	MCF-7	breast:
6	chr19:53541069..53542606-chr19:53543581..53546044,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF160-1	chr19:53517584-53517806	ENSG00000251255
2	lnc-ZNF160-1	chr19:53517843-53519833	ENSG00000251255
3	lnc-ZNF816-2	chr19:53540978-53541136	NONHSAT067613

No data

Variant related genes	Relation type
ENSG00000267943	TF binding region
ERVV-1	TF binding region
ERVV-2	TF binding region
ZNF702P	TF binding region
ENSG00000267943	CpG island
ERVV-1	CpG island
ERVV-2	CpG island
ZNF702P	CpG island
ENSG00000269526	chromatin interactions
ENSG00000242779	chromatin interactions
ENSG00000213020	chromatin interactions
GPR107	miRNA target sites
RNF4	miRNA target sites

Extended variants
information (count: 1801 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570672284	chr19:53508420-53508421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538053905	chr19:53508427-53508428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114645809	chr19:53508451-53508452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374067712	chr19:53508462-53508463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535458726	chr19:53508468-53508469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554108702	chr19:53508469-53508470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200710880	chr19:53508475-53508476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186621753	chr19:53508485-53508486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188488005	chr19:53508493-53508494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1650936	chr19:53508512-53508513	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs543680459	chr19:53508533-53508534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561821791	chr19:53508544-53508545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1650935	chr19:53508558-53508559	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs36056588	chr19:53508581-53508582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201307911	chr19:53508582-53508583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528745658	chr19:53508584-53508585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532006206	chr19:53508592-53508593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1661907	chr19:53508610-53508611	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs527399976	chr19:53508658-53508659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180951247	chr19:53508676-53508677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550376182	chr19:53508690-53508691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1052353	chr19:53508714-53508715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1140734	chr19:53508745-53508746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1132299	chr19:53508746-53508747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532642712	chr19:53508747-53508748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536111492	chr19:53508757-53508758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565131316	chr19:53508766-53508767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566015229	chr19:53508767-53508768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539887170	chr19:53508787-53508788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs367700960	chr19:53508809-53508810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185060057	chr19:53508836-53508837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543621387	chr19:53508871-53508872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11665696	chr19:53508978-53508979	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573772608	chr19:53508988-53508989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551078589	chr19:53509001-53509002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559390781	chr19:53509006-53509007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146818770	chr19:53509021-53509022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200553236	chr19:53509084-53509085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376611106	chr19:53509097-53509098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60918402	chr19:53509184-53509185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111591573	chr19:53509212-53509213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530493005	chr19:53509286-53509287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191044003	chr19:53509299-53509300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547543963	chr19:53509338-53509339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369644633	chr19:53509348-53509349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs8100426	chr19:53509349-53509350	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs566765918	chr19:53509353-53509354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529464577	chr19:53509355-53509356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548063333	chr19:53509356-53509357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566415650	chr19:53509386-53509387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53497600-53509800	Weak transcription	Right Atrium	heart
2	chr19:53498000-53510400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:53506000-53509800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr19:53507000-53510400	Enhancers	Placenta	Placenta
5	chr19:53507600-53509600	Weak transcription	K562	blood
6	chr19:53508000-53513200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:53508400-53509600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr19:53509600-53509800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr19:53509600-53509800	Enhancers	K562	blood
10	chr19:53509800-53510200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr19:53509800-53510200	Weak transcription	K562	blood
12	chr19:53510200-53510400	Enhancers	K562	blood
13	chr19:53510200-53511000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr19:53510400-53510800	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr19:53510400-53511000	Enhancers	Placenta Amnion	Placenta Amnion
16	chr19:53510400-53511200	Enhancers	Dnd41	blood
17	chr19:53510400-53511200	Flanking Active TSS	K562	blood
18	chr19:53510400-53511400	Flanking Active TSS	Placenta	Placenta
19	chr19:53510600-53511600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr19:53510800-53511200	Weak transcription	Right Ventricle	heart
21	chr19:53511000-53511200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
22	chr19:53511000-53511800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:53511200-53511400	Enhancers	Right Ventricle	heart
24	chr19:53511200-53511800	Bivalent Enhancer	K562	blood
25	chr19:53511200-53512600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr19:53511400-53511800	Active TSS	Placenta	Placenta
27	chr19:53511400-53512000	Weak transcription	Right Ventricle	heart
28	chr19:53511600-53512200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr19:53511800-53512000	Flanking Active TSS	Placenta	Placenta
30	chr19:53511800-53512400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr19:53512000-53512200	Active TSS	Placenta	Placenta
32	chr19:53512200-53512400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:53512200-53512400	Flanking Active TSS	Placenta	Placenta
34	chr19:53512200-53512400	Enhancers	Right Ventricle	heart
35	chr19:53512400-53512600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr19:53512400-53513000	Enhancers	Placenta	Placenta
37	chr19:53512400-53513200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr19:53512400-53513400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr19:53512600-53514200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:53512600-53518800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:53513000-53513800	Genic enhancers	Placenta	Placenta
42	chr19:53513200-53513400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr19:53513200-53513600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr19:53513400-53514000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr19:53513400-53514200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr19:53513600-53513800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr19:53513800-53514000	Flanking Active TSS	Placenta	Placenta
48	chr19:53513800-53514200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr19:53514000-53514200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr19:53514000-53516600	Enhancers	Placenta	Placenta

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