Variant report

Variant	esv3496949
Chromosome Location	chr19:52125665-52135420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:307)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
2	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
3	BCL3	chr19:52131621-52132296	GM12878	blood:	n/a	n/a
4	BCL3	chr19:52131741-52132214	GM12878	blood:	n/a	n/a
5	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
6	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
7	CEBPB	chr19:52131571-52131646	K562	blood:	n/a	n/a
8	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
9	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
10	CTCF	chr19:52131585-52131650	GM13977	blood:	n/a	chr19:52131602-52131611
11	CTCF	chr19:52131520-52131670	K562	blood:	n/a	chr19:52131602-52131611
12	CTCF	chr19:52131928-52131975	GM19238	blood:	n/a	n/a
13	CTCF	chr19:52131480-52131630	GM12869	blood:	n/a	chr19:52131602-52131611
14	CTCF	chr19:52131597-52131612	GM12891	blood:	n/a	chr19:52131602-52131611
15	CTCF	chr19:52131833-52132132	GM19239	blood:	n/a	n/a
16	CTCF	chr19:52131560-52131710	GM12875	blood:	n/a	chr19:52131602-52131611
17	CTCF	chr19:52132045-52132087	MCF-7	breast:	n/a	n/a
18	CTCF	chr19:52131507-52131690	K562	blood:	n/a	chr19:52131602-52131611
19	CTCF	chr19:52131571-52131635	MCF-7	breast:	n/a	chr19:52131602-52131611
20	EBF1	chr19:52133515-52133788	GM12878	blood:	n/a	n/a
21	EP300	chr19:52135351-52135776	T-47D	breast:	n/a	n/a
22	EP300	chr19:52133518-52133832	GM12878	blood:	n/a	n/a
23	EP300	chr19:52135364-52135721	T-47D	breast:	n/a	n/a
24	EP300	chr19:52135403-52135811	MCF-7	breast:	n/a	n/a
25	FOXM1	chr19:52135197-52135879	MCF-7	breast:	n/a	n/a
26	GATA3	chr19:52135389-52135772	MCF-7	breast:	n/a	n/a
27	GATA3	chr19:52135282-52135842	T-47D	breast:	n/a	n/a
28	GATA3	chr19:52135337-52135755	T-47D	breast:	n/a	n/a
29	GATA3	chr19:52135382-52135756	MCF-7	breast:	n/a	n/a
30	GATA3	chr19:52135167-52135933	MCF-7	breast:	n/a	n/a
31	GATA3	chr19:52135200-52135820	MCF-7	breast:	n/a	n/a
32	HDAC2	chr19:52135316-52135876	MCF-7	breast:	n/a	n/a
33	HDAC2	chr19:52135288-52135791	MCF-7	breast:	n/a	n/a
34	IRF4	chr19:52133517-52133792	GM12878	blood:	n/a	n/a
35	JUND	chr19:52135374-52135915	MCF-7	breast:	n/a	n/a
36	JUND	chr19:52135257-52135865	T-47D	breast:	n/a	n/a
37	MAX	chr19:52131482-52132107	NB4	blood:	n/a	chr19:52131932-52131942
38	MAX	chr19:52133716-52133845	NB4	blood:	n/a	chr19:52133763-52133773
39	MAX	chr19:52130710-52130960	NB4	blood:	n/a	n/a
40	MYC	chr19:52131098-52131169	NB4	blood:	n/a	n/a
41	MYC	chr19:52133483-52133517	MCF-7	breast:	n/a	n/a
42	MYC	chr19:52131900-52131907	GM12878	blood:	n/a	n/a
43	MYC	chr19:52131445-52131772	NB4	blood:	n/a	n/a
44	MYC	chr19:52133523-52133571	MCF-7	breast:	n/a	n/a
45	MYC	chr19:52131912-52132025	GM12878	blood:	n/a	chr19:52131932-52131942
46	MYC	chr19:52133428-52133473	MCF-7	breast:	n/a	n/a
47	MYC	chr19:52133158-52133445	H1-hESC	embryonic stem cell:	n/a	n/a
48	MYC	chr19:52133395-52133400	MCF-7	breast:	n/a	n/a
49	NFATC1	chr19:52131680-52132265	GM12878	blood:	n/a	n/a
50	NFATC1	chr19:52131712-52132131	GM12878	blood:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52133837-52133887	HL-60	blood:	n/a
2	chr19:52134393-52134443	HRCEpiC	kidney:	n/a
3	chr19:52133837-52133887	HL-60	blood:	n/a
4	chr19:52134393-52134443	HRCEpiC	kidney:	n/a
5	chr19:52131310-52131360	PANC-1	pancreas:	n/a
6	chr19:52134393-52134443	HCF	heart:	n/a
7	chr19:52134289-52134339	SK-N-SH	brain:	n/a
8	chr19:52134296-52134346	T-47D	breast:	n/a
9	chr19:52134393-52134443	HepG2	liver:	n/a
10	chr19:52134296-52134346	ovcar-3	ovarian:	n/a
11	chr19:52131310-52131360	T-47D	breast:	n/a
12	chr19:52134393-52134443	CMK	blood:	n/a
13	chr19:52134296-52134346	GM06990	blood:	n/a
14	chr19:52134289-52134339	HRE	kidney:	n/a
15	chr19:52134393-52134443	HPAEpiC	pulmonary alveolar:	n/a
16	chr19:52134393-52134443	SK-N-MC	brain:	n/a
17	chr19:52133837-52133887	SK-N-MC	brain:	n/a
18	chr19:52134393-52134443	RPTEC	kidney:	n/a
19	chr19:52134296-52134346	HepG2	liver:	n/a
20	chr19:52134289-52134339	HCT-116	colon:	n/a
21	chr19:52134289-52134339	NB4	blood:	n/a
22	chr19:52133837-52133887	T-47D	breast:	n/a
23	chr19:52134289-52134339	MCF10A-Er-Src	breast:	n/a
24	chr19:52134296-52134346	HCF	heart:	n/a
25	chr19:52134296-52134346	Jurkat	blood:	n/a
26	chr19:52133837-52133887	PFSK-1	brain:	n/a
27	chr19:52134289-52134339	MCF-7	breast:	n/a
28	chr19:52134296-52134346	Caco-2	colon:	n/a
29	chr19:52131310-52131360	HRCEpiC	kidney:	n/a
30	chr19:52134289-52134339	ovcar-3	ovarian:	n/a
31	chr19:52131310-52131360	IMR90	lung:	fetal
32	chr19:52133837-52133887	SK-N-SH_RA	brain:	n/a
33	chr19:52134393-52134443	HNPCEpiC	eye:	n/a
34	chr19:52133837-52133887	HepG2	liver:	n/a
35	chr19:52134296-52134346	AG09319	gingival:	n/a
36	chr19:52133837-52133887	Hepatocyte	liver:	n/a
37	chr19:52131310-52131360	HL-60	blood:	n/a
38	chr19:52134393-52134443	HCT-116	colon:	n/a
39	chr19:52131310-52131360	HCF	heart:	n/a
40	chr19:52131310-52131360	AG04450	lung:	fetal
41	chr19:52133837-52133887	AoSMC	blood vessel:	n/a
42	chr19:52134296-52134346	NB4	blood:	n/a
43	chr19:52134289-52134339	HCF	heart:	n/a
44	chr19:52134393-52134443	U87	brain:	n/a
45	chr19:52134289-52134339	SK-N-MC	brain:	n/a
46	chr19:52133837-52133887	HCF	heart:	n/a
47	chr19:52134296-52134346	A549	lung:	n/a
48	chr19:52131310-52131360	HRE	kidney:	n/a
49	chr19:52133837-52133887	HNPCEpiC	eye:	n/a
50	chr19:52134289-52134339	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:51620285..51621823-chr19:52126371..52128453,2	K562	blood:
2	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
3	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
4	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
5	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
6	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:

(count:2 , 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	chr19:52133552-52133919	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC5	TF binding region
SIGLEC5	CpG island
ENSG00000244071	chromatin interactions
ENSG00000105501	chromatin interactions

Extended variants
information (count: 480 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532792616	chr19:52125667-52125668	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551289889	chr19:52125671-52125672	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs8113092	chr19:52125672-52125673	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs536236301	chr19:52125681-52125682	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs60718062	chr19:52125720-52125721	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554513874	chr19:52125726-52125727	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs398035002	chr19:52125730-52125731	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35814965	chr19:52125832-52125833	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144114538	chr19:52125842-52125843	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs533837879	chr19:52125860-52125861	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73050882	chr19:52125869-52125870	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370493275	chr19:52125922-52125923	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576618726	chr19:52125923-52125924	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs77841713	chr19:52125947-52125948	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574506501	chr19:52126231-52126232	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574426954	chr19:52126235-52126236	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs4802830	chr19:52126262-52126263	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs561308639	chr19:52126281-52126282	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146490279	chr19:52126312-52126313	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540684845	chr19:52126314-52126315	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565280022	chr19:52126331-52126332	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532727345	chr19:52126447-52126448	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75309079	chr19:52126477-52126478	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75290748	chr19:52126478-52126479	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs80306567	chr19:52126479-52126480	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551228503	chr19:52126480-52126481	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs113981661	chr19:52126579-52126580	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140813503	chr19:52126594-52126595	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548602100	chr19:52126625-52126626	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188581698	chr19:52126761-52126762	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150219603	chr19:52126799-52126800	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528815974	chr19:52126814-52126815	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570241633	chr19:52126823-52126824	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540224899	chr19:52126827-52126828	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145738554	chr19:52126878-52126879	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574315969	chr19:52126903-52126904	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532940967	chr19:52126922-52126923	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535695290	chr19:52126936-52126937	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367697905	chr19:52126979-52126980	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553793746	chr19:52127002-52127003	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573185043	chr19:52127013-52127014	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540294401	chr19:52127019-52127020	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11084095	chr19:52127030-52127031	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs577375670	chr19:52127039-52127040	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192988382	chr19:52127052-52127053	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4801882	chr19:52127053-52127054	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs7251977	chr19:52127059-52127060	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76116566	chr19:52127082-52127083	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4802831	chr19:52127134-52127135	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs560670435	chr19:52127149-52127150	Strong transcription Weak transcription Enhancers	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:116 , 50 per page) page: 1 2 3

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	chr19:52122400-52125800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr19:52123000-52126000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr19:52124200-52130800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr19:52125000-52125800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr19:52125000-52128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr19:52125200-52127000	Weak transcription	GM12878-XiMat	blood
10	chr19:52125200-52130800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:52125600-52125800	Genic enhancers	Primary monocytes fromperipheralblood	blood
12	chr19:52125600-52126000	Weak transcription	Primary B cells from cord blood	blood
13	chr19:52125600-52126000	Genic enhancers	Monocytes-CD14+_RO01746	blood
14	chr19:52125800-52126800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
15	chr19:52125800-52129200	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr19:52125800-52129800	Strong transcription	Primary B cells from peripheral blood	blood
17	chr19:52126000-52126200	Enhancers	Primary B cells from cord blood	blood
18	chr19:52126000-52126600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr19:52126000-52129200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr19:52126200-52128200	Weak transcription	Primary B cells from cord blood	blood
21	chr19:52126600-52129800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr19:52126800-52127800	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr19:52127000-52127200	Enhancers	GM12878-XiMat	blood
24	chr19:52127200-52129800	Weak transcription	GM12878-XiMat	blood
25	chr19:52127800-52132400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
26	chr19:52128200-52128400	Strong transcription	Primary B cells from cord blood	blood
27	chr19:52128200-52128800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr19:52128200-52131000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr19:52128400-52128600	Genic enhancers	Primary B cells from cord blood	blood
30	chr19:52128600-52129200	Strong transcription	Primary B cells from cord blood	blood
31	chr19:52128800-52133800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr19:52129200-52129600	Genic enhancers	Primary B cells from cord blood	blood
33	chr19:52129200-52130400	Genic enhancers	Monocytes-CD14+_RO01746	blood
34	chr19:52129200-52131400	Genic enhancers	Primary monocytes fromperipheralblood	blood
35	chr19:52129600-52130200	Enhancers	Primary B cells from cord blood	blood
36	chr19:52129800-52130600	Enhancers	GM12878-XiMat	blood
37	chr19:52129800-52132400	Genic enhancers	Primary B cells from peripheral blood	blood
38	chr19:52129800-52132400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr19:52130200-52130600	Active TSS	Primary B cells from cord blood	blood
40	chr19:52130200-52131400	Strong transcription	Spleen	Spleen
41	chr19:52130200-52132400	Weak transcription	Right Atrium	heart
42	chr19:52130400-52132400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
43	chr19:52130400-52132600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr19:52130600-52131000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr19:52130600-52131400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:52130600-52131400	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr19:52130600-52131800	Weak transcription	GM12878-XiMat	blood
48	chr19:52130800-52131400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr19:52130800-52132400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr19:52130800-52133200	Weak transcription	Gastric	stomach

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