Variant report

Variant	esv3371264
Chromosome Location	chr19:52129189-52148980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:489)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52140651-52140961	K562	blood:	n/a	n/a
2	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
3	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
4	BCL3	chr19:52131621-52132296	GM12878	blood:	n/a	n/a
5	BCL3	chr19:52131741-52132214	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
7	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
8	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
9	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
10	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
11	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
12	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
13	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
14	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
15	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
16	CEBPB	chr19:52131571-52131646	K562	blood:	n/a	n/a
17	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
18	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
19	CTCF	chr19:52141040-52141190	GM12866	blood:	n/a	n/a
20	CTCF	chr19:52140760-52140910	AG04449	skin:	n/a	n/a
21	CTCF	chr19:52140760-52140910	GM12873	blood:	n/a	n/a
22	CTCF	chr19:52140740-52140890	SAEC	small airway:	n/a	n/a
23	CTCF	chr19:52140720-52140870	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr19:52140760-52140910	HMEC	breast:	n/a	n/a
25	CTCF	chr19:52140840-52140990	A549	lung:	n/a	n/a
26	CTCF	chr19:52140760-52140910	GM12864	blood:	n/a	n/a
27	CTCF	chr19:52131507-52131690	K562	blood:	n/a	chr19:52131602-52131611
28	CTCF	chr19:52140683-52140962	HepG2	liver:	n/a	n/a
29	CTCF	chr19:52131585-52131650	GM13977	blood:	n/a	chr19:52131602-52131611
30	CTCF	chr19:52140780-52140930	BE2_C	brain:	n/a	n/a
31	CTCF	chr19:52140760-52140910	GM12865	blood:	n/a	n/a
32	CTCF	chr19:52140880-52141030	WI-38	lung:	n/a	n/a
33	CTCF	chr19:52140753-52140920	GM13977	blood:	n/a	n/a
34	CTCF	chr19:52140780-52140930	HPF	lung:	n/a	n/a
35	CTCF	chr19:52140740-52140890	NHLF	lung:	n/a	n/a
36	CTCF	chr19:52131560-52131710	GM12875	blood:	n/a	chr19:52131602-52131611
37	CTCF	chr19:52140720-52140870	BE2_C	brain:	n/a	n/a
38	CTCF	chr19:52140740-52140890	GM12873	blood:	n/a	n/a
39	CTCF	chr19:52140720-52140870	NHEK	skin:	n/a	n/a
40	CTCF	chr19:52144876-52144972	LNCaP	prostate:	n/a	n/a
41	CTCF	chr19:52140760-52140910	GM06990	blood:	n/a	n/a
42	CTCF	chr19:52140740-52140890	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr19:52140720-52140870	GM12865	blood:	n/a	n/a
44	CTCF	chr19:52140680-52140830	AG04450	lung:	n/a	n/a
45	CTCF	chr19:52140740-52140890	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr19:52140641-52140958	A549	lung:	n/a	n/a
47	CTCF	chr19:52140680-52140830	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:52140220-52140370	GM12871	blood:	n/a	n/a
49	CTCF	chr19:52140721-52140931	HepG2	liver:	n/a	n/a
50	CTCF	chr19:52140740-52140890	GM06990	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52134296-52134346	Caco-2	colon:	n/a
2	chr19:52134296-52134346	Caco-2	colon:	n/a
3	chr19:52146598-52146648	NB4	blood:	n/a
4	chr19:52140097-52140147	HRE	kidney:	n/a
5	chr19:52140097-52140147	GM19239	blood:	n/a
6	chr19:52131310-52131360	HIPEpiC	eye:	n/a
7	chr19:52134289-52134339	AG09309	skin:	n/a
8	chr19:52134289-52134339	HEK293	kidney:	embryo
9	chr19:52140097-52140147	Jurkat	blood:	n/a
10	chr19:52134393-52134443	Hepatocyte	liver:	n/a
11	chr19:52131310-52131360	GM19239	blood:	n/a
12	chr19:52134393-52134443	MCF10A-Er-Src	breast:	n/a
13	chr19:52146598-52146648	NT2-D1	testis:	n/a
14	chr19:52134296-52134346	HPAEpiC	pulmonary alveolar:	n/a
15	chr19:52131310-52131360	SK-N-SH_RA	brain:	n/a
16	chr19:52140097-52140147	SK-N-MC	brain:	n/a
17	chr19:52148354-52148404	HMEC	breast:	n/a
18	chr19:52148354-52148404	Caco-2	colon:	n/a
19	chr19:52131310-52131360	HL-60	blood:	n/a
20	chr19:52146598-52146648	HUVEC	blood vessel:	n/a
21	chr19:52131310-52131360	Jurkat	blood:	n/a
22	chr19:52131310-52131360	HCF	heart:	n/a
23	chr19:52133837-52133887	CMK	blood:	n/a
24	chr19:52140097-52140147	NH-A	brain:	n/a
25	chr19:52134289-52134339	AG09319	gingival:	n/a
26	chr19:52146598-52146648	GM12891	blood:	n/a
27	chr19:52146598-52146648	SK-N-SH_RA	brain:	n/a
28	chr19:52133837-52133887	NHBE	bronchial:	n/a
29	chr19:52134296-52134346	HEEpiC	esophagus:	n/a
30	chr19:52134289-52134339	GM12892	blood:	n/a
31	chr19:52133837-52133887	HRPEpiC	eye:	n/a
32	chr19:52134296-52134346	ProgFib	skin:	n/a
33	chr19:52148354-52148404	HRCEpiC	kidney:	n/a
34	chr19:52134296-52134346	HUVEC	blood vessel:	n/a
35	chr19:52131310-52131360	AG04449	skin:	fetal
36	chr19:52146598-52146648	HepG2	liver:	n/a
37	chr19:52148354-52148404	NHDF-neo	bronchial:	n/a
38	chr19:52133837-52133887	HL-60	blood:	n/a
39	chr19:52131310-52131360	HCM	heart:	n/a
40	chr19:52133837-52133887	AG09309	skin:	n/a
41	chr19:52134289-52134339	IMR90	lung:	fetal
42	chr19:52133837-52133887	SK-N-SH_RA	brain:	n/a
43	chr19:52133837-52133887	SAEC	small airway:	n/a
44	chr19:52133837-52133887	SK-N-SH	brain:	n/a
45	chr19:52134393-52134443	AG09309	skin:	n/a
46	chr19:52134289-52134339	HRE	kidney:	n/a
47	chr19:52134296-52134346	NHDF-neo	bronchial:	n/a
48	chr19:52148354-52148404	HL-60	blood:	n/a
49	chr19:52131310-52131360	Caco-2	colon:	n/a
50	chr19:52131310-52131360	HRE	kidney:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
2	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:
3	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
4	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
5	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
6	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
7	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
8	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
9	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
10	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
11	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
12	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
13	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
14	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1
2	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1
3	lnc-SIGLEC14-1	chr19:52133552-52133919	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000105366	chromatin interactions
ENSG00000244071	chromatin interactions
ENSG00000213822	chromatin interactions

Extended variants
information (count: 780 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539557907	chr19:52129223-52129224	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200690110	chr19:52129243-52129244	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149252288	chr19:52129246-52129247	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369568422	chr19:52129248-52129249	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372894396	chr19:52129253-52129254	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146177723	chr19:52129268-52129269	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527535281	chr19:52129285-52129286	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139056611	chr19:52129290-52129291	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368962435	chr19:52129291-52129292	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150210009	chr19:52129301-52129302	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76711639	chr19:52129326-52129327	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559167909	chr19:52129358-52129359	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377570353	chr19:52129377-52129378	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375088094	chr19:52129383-52129384	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370729941	chr19:52129404-52129405	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371468771	chr19:52129418-52129419	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545147085	chr19:52129420-52129421	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563427887	chr19:52129447-52129448	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530736216	chr19:52129453-52129454	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548998635	chr19:52129476-52129477	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561284524	chr19:52129477-52129478	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529252864	chr19:52129488-52129489	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372837439	chr19:52129507-52129508	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547807839	chr19:52129555-52129556	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74576825	chr19:52129586-52129587	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539499380	chr19:52129587-52129588	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551467608	chr19:52129597-52129598	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117456649	chr19:52129640-52129641	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570436336	chr19:52129642-52129643	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183456323	chr19:52129660-52129661	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371269678	chr19:52129669-52129670	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535023522	chr19:52129675-52129676	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552906078	chr19:52129738-52129739	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78139985	chr19:52129749-52129750	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537821857	chr19:52129750-52129751	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186270978	chr19:52129753-52129754	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557136389	chr19:52129766-52129767	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191085175	chr19:52129792-52129793	Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375857706	chr19:52129827-52129828	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542838248	chr19:52129828-52129829	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561012857	chr19:52129844-52129845	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528357388	chr19:52129872-52129873	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4801883	chr19:52129903-52129904	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4801884	chr19:52129904-52129905	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182108379	chr19:52130026-52130027	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75214204	chr19:52130121-52130122	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75511196	chr19:52130122-52130123	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147859411	chr19:52130148-52130149	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs67056047	chr19:52130149-52130150	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58875618	chr19:52130167-52130168	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52116600-52130200	Weak transcription	Spleen	Spleen
2	chr19:52124200-52130800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr19:52125200-52130800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr19:52125800-52129200	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr19:52125800-52129800	Strong transcription	Primary B cells from peripheral blood	blood
7	chr19:52126000-52129200	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr19:52126600-52129800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr19:52127200-52129800	Weak transcription	GM12878-XiMat	blood
10	chr19:52127800-52132400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
11	chr19:52128200-52131000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr19:52128600-52129200	Strong transcription	Primary B cells from cord blood	blood
13	chr19:52128800-52133800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:52129200-52129600	Genic enhancers	Primary B cells from cord blood	blood
15	chr19:52129200-52130400	Genic enhancers	Monocytes-CD14+_RO01746	blood
16	chr19:52129200-52131400	Genic enhancers	Primary monocytes fromperipheralblood	blood
17	chr19:52129600-52130200	Enhancers	Primary B cells from cord blood	blood
18	chr19:52129800-52130600	Enhancers	GM12878-XiMat	blood
19	chr19:52129800-52132400	Genic enhancers	Primary B cells from peripheral blood	blood
20	chr19:52129800-52132400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr19:52130200-52130600	Active TSS	Primary B cells from cord blood	blood
22	chr19:52130200-52131400	Strong transcription	Spleen	Spleen
23	chr19:52130200-52132400	Weak transcription	Right Atrium	heart
24	chr19:52130400-52132400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
25	chr19:52130400-52132600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr19:52130600-52131000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:52130600-52131400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr19:52130600-52131400	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr19:52130600-52131800	Weak transcription	GM12878-XiMat	blood
30	chr19:52130800-52131400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr19:52130800-52132400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:52130800-52133200	Weak transcription	Gastric	stomach
33	chr19:52131000-52133800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr19:52131000-52134000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:52131400-52131600	Active TSS	Primary B cells from cord blood	blood
36	chr19:52131400-52131800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:52131400-52132200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
38	chr19:52131400-52132200	ZNF genes & repeats	Spleen	Spleen
39	chr19:52131400-52132400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr19:52131400-52132600	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
41	chr19:52131600-52132200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr19:52131600-52132200	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
43	chr19:52131800-52132000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
44	chr19:52131800-52132200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr19:52131800-52132200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:52131800-52132200	Bivalent Enhancer	Adipose Nuclei	Adipose
47	chr19:52131800-52132200	Bivalent/Poised TSS	Fetal Lung	lung
48	chr19:52131800-52132200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
49	chr19:52131800-52132200	Enhancers	GM12878-XiMat	blood
50	chr19:52132000-52132200	Bivalent/Poised TSS	Primary T cells from cord blood	blood

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