Variant report

Variant	nsv580057
Chromosome Location	chr19:53522100-53566629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:854)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:53558916-53559216	K562	blood:	n/a	n/a
2	ATF3	chr19:53558902-53559223	K562	blood:	n/a	n/a
3	BHLHE40	chr19:53558384-53558600	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	chr19:53563457-53563536	A549	lung:	n/a	chr19:53563503-53563514
7	CEBPB	chr19:53563196-53563210	HepG2	liver:	n/a	n/a
8	CEBPB	chr19:53563501-53563543	K562	blood:	n/a	chr19:53563503-53563514
9	CEBPB	chr19:53563520-53563530	HepG2	liver:	n/a	n/a
10	CEBPB	chr19:53559033-53559111	K562	blood:	n/a	n/a
11	CTBP2	chr19:53561350-53561890	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr19:53523060-53523210	HEK293	kidney:	n/a	n/a
13	CTCF	chr19:53522961-53523288	T-47D	breast:	n/a	n/a
14	CTCF	chr19:53523000-53523150	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr19:53523060-53523210	GM12867	blood:	n/a	n/a
16	CTCF	chr19:53523020-53523170	RPTEC	kidney:	n/a	n/a
17	CTCF	chr19:53523066-53523216	GM12891	blood:	n/a	n/a
18	CTCF	chr19:53523080-53523230	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr19:53522935-53523279	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr19:53523155-53523191	LNCaP	prostate:	n/a	n/a
21	CTCF	chr19:53523073-53523220	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:53523020-53523170	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr19:53523100-53523250	GM12866	blood:	n/a	n/a
24	CTCF	chr19:53522940-53523090	HCT-116	colon:	n/a	n/a
25	CTCF	chr19:53523040-53523190	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr19:53523195-53523198	GM10266	blood:	n/a	n/a
27	CTCF	chr19:53523080-53523230	K562	blood:	n/a	n/a
28	CTCF	chr19:53550380-53550387	GM20000	blood:	n/a	n/a
29	CTCF	chr19:53523000-53523150	NHEK	skin:	n/a	n/a
30	CTCF	chr19:53523060-53523210	AG09309	skin:	n/a	n/a
31	CTCF	chr19:53523080-53523230	GM12873	blood:	n/a	n/a
32	CTCF	chr19:53523481-53523551	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr19:53541320-53541470	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr19:53531550-53531621	Lung_OC	lung:	n/a	n/a
35	CTCF	chr19:53523040-53523190	NHLF	lung:	n/a	n/a
36	CTCF	chr19:53523116-53523172	GM12878	blood:	n/a	n/a
37	CTCF	chr19:53523020-53523170	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr19:53523100-53523250	HCT-116	colon:	n/a	n/a
39	CTCF	chr19:53523000-53523150	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr19:53523084-53523245	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr19:53522968-53523321	K562	blood:	n/a	n/a
42	CTCF	chr19:53523114-53523192	GM10266	blood:	n/a	n/a
43	CTCF	chr19:53523141-53523173	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr19:53523019-53523263	K562	blood:	n/a	n/a
45	CTCF	chr19:53554569-53554639	Lung_OC	lung:	n/a	n/a
46	CTCF	chr19:53523060-53523210	WI-38	lung:	n/a	n/a
47	CTCF	chr19:53523040-53523190	GM12873	blood:	n/a	n/a
48	CTCF	chr19:53547820-53547970	GM12875	blood:	n/a	n/a
49	CTCF	chr19:53523100-53523250	SAEC	small airway:	n/a	n/a
50	CTCF	chr19:53522981-53523241	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53561386-53561436	GM12891	blood:	n/a
2	chr19:53561441-53561491	BJ	skin:	n/a
3	chr19:53540902-53540952	HMEC	breast:	n/a
4	chr19:53564251-53564301	ovcar-3	ovarian:	n/a
5	chr19:53540902-53540952	Jurkat	blood:	n/a
6	chr19:53540902-53540952	GM06990	blood:	n/a
7	chr19:53541186-53541236	Jurkat	blood:	n/a
8	chr19:53538687-53538737	HUVEC	blood vessel:	n/a
9	chr19:53540845-53540895	HRE	kidney:	n/a
10	chr19:53538883-53538933	NH-A	brain:	n/a
11	chr19:53561973-53562023	AG04450	lung:	fetal
12	chr19:53540902-53540952	HEK293	kidney:	embryo
13	chr19:53538883-53538933	AG04449	skin:	fetal
14	chr19:53538687-53538737	CMK	blood:	n/a
15	chr19:53559508-53559558	GM06990	blood:	n/a
16	chr19:53561811-53561861	GM12891	blood:	n/a
17	chr19:53561441-53561491	HepG2	liver:	n/a
18	chr19:53540902-53540952	SK-N-MC	brain:	n/a
19	chr19:53561811-53561861	HIPEpiC	eye:	n/a
20	chr19:53564251-53564301	AG09319	gingival:	n/a
21	chr19:53540902-53540952	NHDF-neo	bronchial:	n/a
22	chr19:53557328-53557378	HCT-116	colon:	n/a
23	chr19:53538687-53538737	HIPEpiC	eye:	n/a
24	chr19:53561973-53562023	MCF-7	breast:	n/a
25	chr19:53564251-53564301	Jurkat	blood:	n/a
26	chr19:53540902-53540952	NB4	blood:	n/a
27	chr19:53564251-53564301	U87	brain:	n/a
28	chr19:53561811-53561861	BE2_C	brain:	n/a
29	chr19:53561563-53561613	Hepatocyte	liver:	n/a
30	chr19:53561973-53562023	AoSMC	blood vessel:	n/a
31	chr19:53559508-53559558	CMK	blood:	n/a
32	chr19:53538687-53538737	MCF10A-Er-Src	breast:	n/a
33	chr19:53561973-53562023	AG09309	skin:	n/a
34	chr19:53557328-53557378	ProgFib	skin:	n/a
35	chr19:53541186-53541236	Hela-S3	cervix:	n/a
36	chr19:53564251-53564301	NHBE	bronchial:	n/a
37	chr19:53540902-53540952	AG04450	lung:	fetal
38	chr19:53564251-53564301	HCF	heart:	n/a
39	chr19:53561811-53561861	HRPEpiC	eye:	n/a
40	chr19:53538687-53538737	Jurkat	blood:	n/a
41	chr19:53538883-53538933	AoSMC	blood vessel:	n/a
42	chr19:53541287-53541337	AoSMC	blood vessel:	n/a
43	chr19:53564251-53564301	NH-A	brain:	n/a
44	chr19:53541186-53541236	HRE	kidney:	n/a
45	chr19:53541186-53541236	ECC-1	luminal epithelium:	n/a
46	chr19:53561811-53561861	LNCaP	prostate:	n/a
47	chr19:53559508-53559558	Jurkat	blood:	n/a
48	chr19:53540845-53540895	SK-N-SH	brain:	n/a
49	chr19:53538883-53538933	AG09319	gingival:	n/a
50	chr19:53561973-53562023	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53557284..53559670-chr19:53575484..53577211,2	K562	blood:
2	chr19:53536567..53539141-chr19:53540653..53542425,2	K562	blood:
3	chr19:53565063..53566659-chr19:53568054..53569781,2	MCF-7	breast:
4	chr10:9353360..9353955-chr19:53525559..53526530,2	MCF-7	breast:
5	chr19:53191910..53193662-chr19:53562323..53563875,2	K562	blood:
6	chr19:53514929..53517284-chr19:53527300..53529548,2	MCF-7	breast:
7	chr19:53541069..53542606-chr19:53543581..53546044,2	K562	blood:
8	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF816-2	chr19:53540978-53541136	NONHSAT067613

No data

Variant related genes	Relation type
ERVV-2	TF binding region
ZNF702P	TF binding region
ERVV-2	CpG island
ZNF702P	CpG island
ENSG00000269526	chromatin interactions
ENSG00000213020	chromatin interactions
ENSG00000242779	chromatin interactions

Extended variants
information (count: 1693 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1693 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7508346	chr19:53522618-53522619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189406186	chr19:53522634-53522635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553925402	chr19:53522648-53522649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113777171	chr19:53522745-53522746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559441533	chr19:53522756-53522757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533412186	chr19:53522758-53522759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116422159	chr19:53522770-53522771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570166791	chr19:53522802-53522803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530598806	chr19:53522819-53522820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143090952	chr19:53522820-53522821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144226530	chr19:53522829-53522830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534567777	chr19:53522853-53522854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539573336	chr19:53522869-53522870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199928235	chr19:53522884-53522885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571144583	chr19:53522885-53522886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78001800	chr19:53522890-53522891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556757489	chr19:53522935-53522936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142344573	chr19:53522966-53522967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79978070	chr19:53523014-53523015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115271911	chr19:53523051-53523052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368486017	chr19:53523057-53523058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369467124	chr19:53523063-53523064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574288585	chr19:53523088-53523089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150852660	chr19:53523123-53523124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560035615	chr19:53523145-53523146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181690429	chr19:53523234-53523235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545415223	chr19:53523241-53523242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563555984	chr19:53523318-53523319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115237156	chr19:53523336-53523337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186086384	chr19:53523350-53523351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372259744	chr19:53523390-53523391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558080071	chr19:53527305-53527306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376049181	chr19:53527313-53527314	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543048468	chr19:53527339-53527340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554958617	chr19:53527340-53527341	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143927609	chr19:53527367-53527368	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541123333	chr19:53527398-53527399	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189783571	chr19:53527423-53527424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147400475	chr19:53527426-53527427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546175018	chr19:53527481-53527482	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564795511	chr19:53527493-53527494	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373354790	chr19:53527546-53527547	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531719360	chr19:53527556-53527557	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540299014	chr19:53527586-53527587	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550173359	chr19:53527633-53527634	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577975842	chr19:53527653-53527654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568470703	chr19:53527696-53527697	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570626594	chr19:53527709-53527710	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529330665	chr19:53527877-53527878	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112783707	chr19:53527904-53527905	Enhancers	Chromatin interactive region	1 gene(s)	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53522600-53523400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr19:53527800-53528000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:53528000-53538600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:53529400-53530000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr19:53529600-53529800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr19:53530000-53540400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:53531000-53531200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr19:53531000-53531800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr19:53531200-53532000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr19:53531600-53532200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr19:53531600-53532200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr19:53531800-53532000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr19:53531800-53532200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr19:53531800-53532400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr19:53532000-53532200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:53532000-53532800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:53532200-53539600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr19:53532800-53533000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:53536200-53536400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr19:53536400-53536600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:53536400-53539600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr19:53536600-53536800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:53536600-53539800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr19:53536800-53538600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr19:53537000-53538400	Weak transcription	Fetal Kidney	kidney
26	chr19:53537800-53538800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:53538400-53538800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr19:53538400-53540400	Enhancers	Placenta	Placenta
29	chr19:53538600-53538800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:53538600-53538800	ZNF genes & repeats	Fetal Kidney	kidney
31	chr19:53538800-53539200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr19:53538800-53539600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:53538800-53539600	Weak transcription	Fetal Kidney	kidney
34	chr19:53539200-53539400	Enhancers	Placenta Amnion	Placenta Amnion
35	chr19:53539400-53540600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr19:53539600-53539800	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
37	chr19:53539600-53540000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:53539600-53540000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr19:53539600-53540200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr19:53539600-53541400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:53539600-53541400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
42	chr19:53539800-53540000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr19:53539800-53540200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr19:53539800-53540400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr19:53539800-53541200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
46	chr19:53539800-53541400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr19:53539800-53541600	Active TSS	Fetal Kidney	kidney
48	chr19:53539800-53542200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
49	chr19:53540000-53540200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr19:53540000-53540600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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