Variant report

Variant	nsv1056104
Chromosome Location	chr19:52127030-52154905
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:734)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	ATF1	chr19:52154746-52155090	K562	blood:	n/a	n/a
3	ATF2	chr19:52154376-52154835	GM12878	blood:	n/a	n/a
4	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
5	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
6	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
7	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
8	BCL3	chr19:52131621-52132296	GM12878	blood:	n/a	n/a
9	BCL3	chr19:52131741-52132214	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
11	BHLHE40	chr19:52154406-52154749	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
13	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
14	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
15	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
16	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
17	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
18	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
19	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
20	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
21	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
22	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
23	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
24	CEBPB	chr19:52131571-52131646	K562	blood:	n/a	n/a
25	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
26	CTCF	chr19:52140720-52140870	HepG2	liver:	n/a	n/a
27	CTCF	chr19:52140760-52140910	SAEC	small airway:	n/a	n/a
28	CTCF	chr19:52140740-52140890	AG10803	skin:	n/a	n/a
29	CTCF	chr19:52131833-52132132	GM19239	blood:	n/a	n/a
30	CTCF	chr19:52140760-52140910	HMEC	breast:	n/a	n/a
31	CTCF	chr19:52140683-52140962	HepG2	liver:	n/a	n/a
32	CTCF	chr19:52131560-52131710	GM12875	blood:	n/a	chr19:52131602-52131611
33	CTCF	chr19:52140820-52140970	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr19:52140596-52140952	K562	blood:	n/a	n/a
35	CTCF	chr19:52140740-52140890	K562	blood:	n/a	n/a
36	CTCF	chr19:52140740-52140890	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr19:52140640-52140790	WI-38	lung:	n/a	n/a
38	CTCF	chr19:52140740-52140890	SAEC	small airway:	n/a	n/a
39	CTCF	chr19:52140740-52140890	GM12864	blood:	n/a	n/a
40	CTCF	chr19:52140740-52140890	NHLF	lung:	n/a	n/a
41	CTCF	chr19:52140760-52140910	GM06990	blood:	n/a	n/a
42	CTCF	chr19:52140740-52140890	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr19:52140747-52140939	Gliobla	brain:	n/a	n/a
44	CTCF	chr19:52149807-52149816	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:52140760-52140910	AG04450	lung:	n/a	n/a
46	CTCF	chr19:52140765-52140908	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr19:52140800-52140950	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr19:52140720-52140870	BE2_C	brain:	n/a	n/a
49	CTCF	chr19:52140760-52140910	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr19:52140760-52140929	MCF-7	breast:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52140097-52140147	SKMC	muscle:	n/a
2	chr19:52134296-52134346	PFSK-1	brain:	n/a
3	chr19:52140097-52140147	SKMC	muscle:	n/a
4	chr19:52134296-52134346	PFSK-1	brain:	n/a
5	chr19:52150230-52150280	HAEpiC	amniotic membrane:	n/a
6	chr19:52133837-52133887	NHBE	bronchial:	n/a
7	chr19:52150634-52150684	GM12878	blood:	n/a
8	chr19:52150547-52150597	Hepatocyte	liver:	n/a
9	chr19:52150634-52150684	HMEC	breast:	n/a
10	chr19:52134289-52134339	U87	brain:	n/a
11	chr19:52148354-52148404	GM12878	blood:	n/a
12	chr19:52131310-52131360	HAEpiC	amniotic membrane:	n/a
13	chr19:52150230-52150280	HEK293	kidney:	embryo
14	chr19:52133837-52133887	CMK	blood:	n/a
15	chr19:52150230-52150280	HEEpiC	esophagus:	n/a
16	chr19:52146598-52146648	BE2_C	brain:	n/a
17	chr19:52131310-52131360	ProgFib	skin:	n/a
18	chr19:52150634-52150684	HRCEpiC	kidney:	n/a
19	chr19:52150547-52150597	NHBE	bronchial:	n/a
20	chr19:52134393-52134443	U87	brain:	n/a
21	chr19:52133837-52133887	GM12891	blood:	n/a
22	chr19:52134393-52134443	HCM	heart:	n/a
23	chr19:52148354-52148404	HRCEpiC	kidney:	n/a
24	chr19:52134289-52134339	Hela-S3	cervix:	n/a
25	chr19:52131310-52131360	AG09319	gingival:	n/a
26	chr19:52148354-52148404	HNPCEpiC	eye:	n/a
27	chr19:52140097-52140147	SK-N-SH	brain:	n/a
28	chr19:52131310-52131360	Caco-2	colon:	n/a
29	chr19:52150230-52150280	K562	blood:	n/a
30	chr19:52146598-52146648	Jurkat	blood:	n/a
31	chr19:52134393-52134443	Jurkat	blood:	n/a
32	chr19:52140097-52140147	NT2-D1	testis:	n/a
33	chr19:52146598-52146648	HEK293	kidney:	embryo
34	chr19:52131310-52131360	AG04450	lung:	fetal
35	chr19:52150634-52150684	BE2_C	brain:	n/a
36	chr19:52140097-52140147	AG09319	gingival:	n/a
37	chr19:52131310-52131360	NHDF-neo	bronchial:	n/a
38	chr19:52134289-52134339	SK-N-SH	brain:	n/a
39	chr19:52134296-52134346	RPTEC	kidney:	n/a
40	chr19:52134289-52134339	SK-N-SH_RA	brain:	n/a
41	chr19:52131310-52131360	U87	brain:	n/a
42	chr19:52140097-52140147	HPAEpiC	pulmonary alveolar:	n/a
43	chr19:52148354-52148404	NT2-D1	testis:	n/a
44	chr19:52134393-52134443	AG04450	lung:	fetal
45	chr19:52134289-52134339	CMK	blood:	n/a
46	chr19:52134296-52134346	SAEC	small airway:	n/a
47	chr19:52131310-52131360	HCT-116	colon:	n/a
48	chr19:52140097-52140147	ovcar-3	ovarian:	n/a
49	chr19:52150547-52150597	CMK	blood:	n/a
50	chr19:52133837-52133887	GM12878	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
2	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
3	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
4	chr19:51620285..51621823-chr19:52126371..52128453,2	K562	blood:
5	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
6	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
7	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
8	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
9	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
10	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
11	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
12	chr19:51965493..51967976-chr19:52153295..52156025,2	K562	blood:
13	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
14	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
15	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
16	chr19:51873847..51875580-chr19:52152831..52155624,2	K562	blood:
17	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
18	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF175-5	chr19:52152115-52152863	NONHSAT067458
2	lnc-SIGLEC14-1	chr19:52133552-52133919	ENSG00000258669.1
3	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1
4	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
ENSG00000268500	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
ENSG00000268500	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000244071	chromatin interactions
ENSG00000213822	chromatin interactions
ENSG00000105366	chromatin interactions

Extended variants
information (count: 1174 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11084095	chr19:52127030-52127031	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577375670	chr19:52127039-52127040	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192988382	chr19:52127052-52127053	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4801882	chr19:52127053-52127054	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs7251977	chr19:52127059-52127060	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76116566	chr19:52127082-52127083	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4802831	chr19:52127134-52127135	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs560670435	chr19:52127149-52127150	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527258009	chr19:52127163-52127164	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543594079	chr19:52127211-52127212	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184736011	chr19:52127244-52127245	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189561836	chr19:52127315-52127316	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568429646	chr19:52127325-52127326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537521486	chr19:52127337-52127338	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549470993	chr19:52127361-52127362	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567876460	chr19:52127362-52127363	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148939000	chr19:52127366-52127367	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35811046	chr19:52127434-52127435	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372301264	chr19:52127477-52127478	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554010612	chr19:52127480-52127481	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147036077	chr19:52127507-52127508	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563383238	chr19:52127522-52127523	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529869943	chr19:52127603-52127604	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537555760	chr19:52127633-52127634	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374191359	chr19:52127694-52127695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558962383	chr19:52127725-52127726	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10414149	chr19:52127744-52127745	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
28	rs10414347	chr19:52127777-52127778	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs563010766	chr19:52127788-52127789	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574972726	chr19:52127816-52127817	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542087408	chr19:52127838-52127839	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180809995	chr19:52127849-52127850	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527945793	chr19:52127874-52127875	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546110965	chr19:52127896-52127897	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186493368	chr19:52127903-52127904	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138574388	chr19:52127948-52127949	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6509558	chr19:52127949-52127950	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs567840189	chr19:52127950-52127951	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529066015	chr19:52127967-52127968	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547239864	chr19:52128001-52128002	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144080278	chr19:52128050-52128051	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189366444	chr19:52128066-52128067	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558092508	chr19:52128084-52128085	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113117608	chr19:52128115-52128116	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538289176	chr19:52128159-52128160	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556673227	chr19:52128166-52128167	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577045414	chr19:52128174-52128175	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537908504	chr19:52128181-52128182	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556008965	chr19:52128185-52128186	Strong transcription Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139267979	chr19:52128203-52128204	Strong transcription Transcr. at gene 5' and 3' Weak 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:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52116600-52130200	Weak transcription	Spleen	Spleen
2	chr19:52119400-52128200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr19:52124200-52130800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:52125000-52128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr19:52125200-52130800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:52125800-52129200	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr19:52125800-52129800	Strong transcription	Primary B cells from peripheral blood	blood
9	chr19:52126000-52129200	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr19:52126200-52128200	Weak transcription	Primary B cells from cord blood	blood
11	chr19:52126600-52129800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr19:52126800-52127800	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr19:52127000-52127200	Enhancers	GM12878-XiMat	blood
14	chr19:52127200-52129800	Weak transcription	GM12878-XiMat	blood
15	chr19:52127800-52132400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
16	chr19:52128200-52128400	Strong transcription	Primary B cells from cord blood	blood
17	chr19:52128200-52128800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:52128200-52131000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr19:52128400-52128600	Genic enhancers	Primary B cells from cord blood	blood
20	chr19:52128600-52129200	Strong transcription	Primary B cells from cord blood	blood
21	chr19:52128800-52133800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:52129200-52129600	Genic enhancers	Primary B cells from cord blood	blood
23	chr19:52129200-52130400	Genic enhancers	Monocytes-CD14+_RO01746	blood
24	chr19:52129200-52131400	Genic enhancers	Primary monocytes fromperipheralblood	blood
25	chr19:52129600-52130200	Enhancers	Primary B cells from cord blood	blood
26	chr19:52129800-52130600	Enhancers	GM12878-XiMat	blood
27	chr19:52129800-52132400	Genic enhancers	Primary B cells from peripheral blood	blood
28	chr19:52129800-52132400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr19:52130200-52130600	Active TSS	Primary B cells from cord blood	blood
30	chr19:52130200-52131400	Strong transcription	Spleen	Spleen
31	chr19:52130200-52132400	Weak transcription	Right Atrium	heart
32	chr19:52130400-52132400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
33	chr19:52130400-52132600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr19:52130600-52131000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:52130600-52131400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:52130600-52131400	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr19:52130600-52131800	Weak transcription	GM12878-XiMat	blood
38	chr19:52130800-52131400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr19:52130800-52132400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr19:52130800-52133200	Weak transcription	Gastric	stomach
41	chr19:52131000-52133800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:52131000-52134000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr19:52131400-52131600	Active TSS	Primary B cells from cord blood	blood
44	chr19:52131400-52131800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr19:52131400-52132200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr19:52131400-52132200	ZNF genes & repeats	Spleen	Spleen
47	chr19:52131400-52132400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr19:52131400-52132600	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
49	chr19:52131600-52132200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr19:52131600-52132200	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood

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