Variant report

Variant	nsv580358
Chromosome Location	chr19:56851001-56869794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:518)
CpG islands
(count:184)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:56859692-56859938	K562	blood:	n/a	n/a
2	ARID3A	chr19:56861841-56862087	K562	blood:	n/a	n/a
3	ARID3A	chr19:56866390-56867520	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:56858731-56858932	K562	blood:	n/a	n/a
5	ARID3A	chr19:56861841-56862098	HepG2	liver:	n/a	n/a
6	ATF1	chr19:56858697-56859141	K562	blood:	n/a	n/a
7	ATF1	chr19:56861870-56862141	K562	blood:	n/a	n/a
8	BACH1	chr19:56868468-56868645	K562	blood:	n/a	n/a
9	BCL3	chr19:56851135-56851431	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:56857346-56857437	K562	blood:	n/a	n/a
11	BHLHE40	chr19:56861839-56862108	GM12878	blood:	n/a	n/a
12	CBX3	chr19:56861759-56862199	K562	blood:	n/a	n/a
13	CBX3	chr19:56868338-56868616	K562	blood:	n/a	n/a
14	CBX3	chr19:56868281-56868662	K562	blood:	n/a	n/a
15	CBX3	chr19:56859647-56860104	K562	blood:	n/a	n/a
16	CCNT2	chr19:56858664-56858991	K562	blood:	n/a	n/a
17	CEBPB	chr19:56856774-56856854	K562	blood:	n/a	n/a
18	CEBPB	chr19:56858595-56858976	K562	blood:	n/a	n/a
19	CEBPB	chr19:56861856-56862111	MCF-7	breast:	n/a	n/a
20	CEBPB	chr19:56856656-56856990	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:56866960-56867199	HepG2	liver:	n/a	n/a
22	CEBPB	chr19:56858760-56859421	K562	blood:	n/a	n/a
23	CEBPB	chr19:56864074-56864274	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:56867598-56867926	HepG2	liver:	n/a	chr19:56867757-56867768
25	CEBPB	chr19:56861866-56862166	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:56861840-56862188	K562	blood:	n/a	n/a
27	CEBPB	chr19:56868669-56868820	HepG2	liver:	n/a	n/a
28	CEBPD	chr19:56858477-56858925	K562	blood:	n/a	n/a
29	CEBPD	chr19:56858504-56858989	K562	blood:	n/a	n/a
30	CTCF	chr19:56861881-56862161	K562	blood:	n/a	chr19:56862006-56862024 chr19:56862001-56862022 chr19:56862007-56862023
31	CTCF	chr19:56859816-56859905	MCF-7	breast:	n/a	n/a
32	CTCF	chr19:56859720-56859870	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr19:56861960-56862110	K562	blood:	n/a	chr19:56862006-56862024 chr19:56862001-56862022 chr19:56862007-56862023
34	CTCF	chr19:56859720-56859870	K562	blood:	n/a	n/a
35	CTCF	chr19:56861940-56862090	GM12801	blood:	n/a	chr19:56862006-56862024 chr19:56862001-56862022 chr19:56862007-56862023
36	CTCF	chr19:56859740-56859890	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr19:56859740-56859890	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr19:56859614-56860013	K562	blood:	n/a	n/a
39	CTCF	chr19:56859680-56859830	HAc	cerebellar:	n/a	n/a
40	CTCF	chr19:56859700-56859850	GM12870	blood:	n/a	n/a
41	CTCF	chr19:56862000-56862150	Hela-S3	cervix:	n/a	chr19:56862006-56862024 chr19:56862001-56862022 chr19:56862007-56862023
42	CTCF	chr19:56859800-56859950	HEK293	kidney:	n/a	n/a
43	CTCF	chr19:56859500-56859650	GM12865	blood:	n/a	n/a
44	CTCF	chr19:56859740-56859890	GM12864	blood:	n/a	n/a
45	CTCF	chr19:56861940-56862090	WERI-Rb-1	eye:	n/a	chr19:56862006-56862024 chr19:56862001-56862022 chr19:56862007-56862023
46	CTCF	chr19:56859740-56859890	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr19:56859436-56860251	A549	lung:	n/a	n/a
48	CTCF	chr19:56862277-56862403	GM19238	blood:	n/a	n/a
49	CTCF	chr19:56861936-56862114	Fibrobl	skin:	n/a	chr19:56862006-56862024 chr19:56862001-56862022 chr19:56862007-56862023
50	CTCF	chr19:56859570-56859950	A549	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56851220-56851270	GM12878	blood:	n/a
2	chr19:56851220-56851270	GM12878	blood:	n/a
3	chr19:56852136-56852186	RPTEC	kidney:	n/a
4	chr19:56854907-56854957	GM12892	blood:	n/a
5	chr19:56852136-56852186	MCF10A-Er-Src	breast:	n/a
6	chr19:56851220-56851270	HCF	heart:	n/a
7	chr19:56851220-56851270	HepG2	liver:	n/a
8	chr19:56854907-56854957	T-47D	breast:	n/a
9	chr19:56851220-56851270	T-47D	breast:	n/a
10	chr19:56851220-56851270	NHBE	bronchial:	n/a
11	chr19:56854907-56854957	AG10803	skin:	n/a
12	chr19:56854907-56854957	GM06990	blood:	n/a
13	chr19:56854907-56854957	Jurkat	blood:	n/a
14	chr19:56852136-56852186	SK-N-SH_RA	brain:	n/a
15	chr19:56851220-56851270	PANC-1	pancreas:	n/a
16	chr19:56851220-56851270	PFSK-1	brain:	n/a
17	chr19:56851220-56851270	SK-N-SH	brain:	n/a
18	chr19:56854907-56854957	HRCEpiC	kidney:	n/a
19	chr19:56854907-56854957	MCF10A-Er-Src	breast:	n/a
20	chr19:56854907-56854957	NHDF-neo	bronchial:	n/a
21	chr19:56852136-56852186	SKMC	muscle:	n/a
22	chr19:56854907-56854957	AG04450	lung:	fetal
23	chr19:56851220-56851270	NT2-D1	testis:	n/a
24	chr19:56854907-56854957	PANC-1	pancreas:	n/a
25	chr19:56854907-56854957	K562	blood:	n/a
26	chr19:56852136-56852186	MCF-7	breast:	n/a
27	chr19:56854907-56854957	HAEpiC	amniotic membrane:	n/a
28	chr19:56852136-56852186	AG09309	skin:	n/a
29	chr19:56854907-56854957	AoSMC	blood vessel:	n/a
30	chr19:56851220-56851270	AG04450	lung:	fetal
31	chr19:56852136-56852186	HepG2	liver:	n/a
32	chr19:56851220-56851270	ProgFib	skin:	n/a
33	chr19:56852136-56852186	T-47D	breast:	n/a
34	chr19:56851220-56851270	GM12891	blood:	n/a
35	chr19:56852136-56852186	HUVEC	blood vessel:	n/a
36	chr19:56854907-56854957	ProgFib	skin:	n/a
37	chr19:56854907-56854957	NHBE	bronchial:	n/a
38	chr19:56854907-56854957	GM12891	blood:	n/a
39	chr19:56851220-56851270	HRCEpiC	kidney:	n/a
40	chr19:56854907-56854957	BE2_C	brain:	n/a
41	chr19:56854907-56854957	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:56851220-56851270	ovcar-3	ovarian:	n/a
43	chr19:56851220-56851270	AG04449	skin:	fetal
44	chr19:56851220-56851270	Hepatocyte	liver:	n/a
45	chr19:56854907-56854957	AG04449	skin:	fetal
46	chr19:56851220-56851270	AoSMC	blood vessel:	n/a
47	chr19:56852136-56852186	GM19239	blood:	n/a
48	chr19:56854907-56854957	AG09319	gingival:	n/a
49	chr19:56851220-56851270	SKMC	muscle:	n/a
50	chr19:56851220-56851270	U87	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56861231..56864651-chr19:56864910..56868187,3	K562	blood:
2	chr19:56825650..56827475-chr19:56859296..56861906,3	K562	blood:
3	chr19:56861231..56863974-chr19:56864374..56866865,3	K562	blood:
4	chr19:56587879..56588429-chr19:56861518..56862050,2	MCF-7	breast:
5	chr19:56861231..56863974-chr19:56864374..56866865,3	K562	blood:
6	chr19:56821792..56823459-chr19:56860076..56862047,2	K562	blood:
7	chr19:56861231..56864651-chr19:56864910..56868187,3	K562	blood:
8	chr19:56821112..56821613-chr19:56861782..56862434,2	K562	blood:
9	chr19:56668300..56669866-chr19:56860009..56861949,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF583-5	chr19:56852155-56852609	NONHSAT068099
2	lnc-ZSCAN5A-3	chr19:56858450-56859552	ENSG00000267429.1
3	lnc-ZSCAN5A-3	chr19:56859115-56859550	NONHSAT068109
4	lnc-ZSCAN5A-3	chr19:56865862-56866010	ENSG00000267606.1
5	lnc-ZNF583-5	chr19:56852155-56852656	ENSG00000267549.1
6	lnc-ZNF583-5	chr19:56852155-56852374	ENSG00000267549.1

No data

Variant related genes	Relation type
ENSG00000267429	TF binding region
ENSG00000266932	TF binding region
ENSG00000267145	TF binding region
ENSG00000267429	CpG island
ENSG00000266932	CpG island
ENSG00000267145	CpG island
ENSG00000167685	chromatin interactions
ENSG00000267549	chromatin interactions
ENSG00000131848	chromatin interactions

Extended variants
information (count: 683 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112423468	chr19:56851018-56851019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569682517	chr19:56851026-56851027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34939841	chr19:56851032-56851033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12978936	chr19:56851043-56851044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113625429	chr19:56851052-56851053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536137502	chr19:56851060-56851061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs71333213	chr19:56851066-56851067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10407754	chr19:56851077-56851078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572596002	chr19:56851094-56851095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71333214	chr19:56851100-56851101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8103436	chr19:56851111-56851112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71333215	chr19:56851134-56851135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558338142	chr19:56851142-56851143	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs578014336	chr19:56851143-56851144	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs34270390	chr19:56851145-56851146	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543525857	chr19:56851160-56851161	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs542309171	chr19:56851163-56851164	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs34259704	chr19:56851168-56851169	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573724932	chr19:56851177-56851178	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs35397317	chr19:56851179-56851180	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs143377837	chr19:56851187-56851188	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs561876363	chr19:56851196-56851197	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs35831358	chr19:56851202-56851203	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs540823412	chr19:56851203-56851204	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564326323	chr19:56851216-56851217	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532852118	chr19:56851221-56851222	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs372517406	chr19:56851222-56851223	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs565103822	chr19:56851237-56851238	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs143345977	chr19:56851262-56851263	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs192739034	chr19:56851280-56851281	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs549688643	chr19:56851317-56851318	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs8103677	chr19:56851322-56851323	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs184779453	chr19:56851352-56851353	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs558036272	chr19:56851369-56851370	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs571845648	chr19:56851418-56851419	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs190001266	chr19:56851495-56851496	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs369517907	chr19:56851523-56851524	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs373965935	chr19:56851525-56851526	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs557082880	chr19:56851542-56851543	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs115428873	chr19:56851576-56851577	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs191990656	chr19:56851629-56851630	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs553337212	chr19:56851638-56851639	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs572217580	chr19:56851690-56851691	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs79588341	chr19:56851719-56851720	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs564108269	chr19:56851720-56851721	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs147509101	chr19:56851724-56851725	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs543539878	chr19:56851734-56851735	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs563414051	chr19:56851762-56851763	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs184496983	chr19:56851765-56851766	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs529006274	chr19:56851766-56851767	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56850400-56851600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr19:56851200-56852000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
3	chr19:56851600-56852000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr19:56852000-56854000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr19:56854000-56854200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:56854000-56855000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr19:56854200-56854800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:56854200-56863200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr19:56854800-56855000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr19:56854800-56857600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:56855000-56870200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr19:56855200-56855800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr19:56855800-56856600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr19:56856600-56857800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr19:56856600-56857800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr19:56856600-56859600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr19:56856800-56857600	Enhancers	K562	blood
18	chr19:56857000-56857200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr19:56857000-56857800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr19:56857200-56858000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr19:56857400-56857800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr19:56857400-56857800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr19:56857600-56858000	Flanking Active TSS	K562	blood
24	chr19:56857600-56859200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr19:56857600-56859600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:56857800-56859200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr19:56857800-56859200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr19:56857800-56859200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr19:56857800-56859400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr19:56858000-56858400	Enhancers	K562	blood
31	chr19:56858000-56859200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr19:56858400-56859400	Flanking Active TSS	K562	blood
33	chr19:56859200-56859400	ZNF genes & repeats	Ovary	ovary
34	chr19:56859200-56859600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr19:56859200-56859800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr19:56859200-56859800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr19:56859200-56859800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr19:56859200-56860000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr19:56859400-56859800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr19:56859400-56860000	Enhancers	K562	blood
41	chr19:56859400-56872800	Weak transcription	Ovary	ovary
42	chr19:56859600-56859800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr19:56859600-56862400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr19:56859600-56862400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr19:56860000-56862800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr19:56861600-56862000	Enhancers	Colon Smooth Muscle	Colon
47	chr19:56861800-56862000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr19:56862000-56868400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:56862400-56863000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr19:56862400-56863400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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