Variant report

Variant	nsv458725
Chromosome Location	chr19:52123549-52155449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:732)
Chromatin interactive
region (count:20)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr19:52124551-52124727	K562	blood:	n/a	n/a
3	ATF1	chr19:52154746-52155090	K562	blood:	n/a	n/a
4	ATF2	chr19:52154376-52154835	GM12878	blood:	n/a	n/a
5	ATF2	chr19:52124388-52124859	GM12878	blood:	n/a	n/a
6	BATF	chr19:52124396-52124758	GM12878	blood:	n/a	n/a
7	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
8	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
9	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
10	BCL11A	chr19:52124445-52124855	GM12878	blood:	n/a	n/a
11	BCL11A	chr19:52124451-52124734	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
13	BCL3	chr19:52131621-52132296	GM12878	blood:	n/a	n/a
14	BCL3	chr19:52131741-52132214	GM12878	blood:	n/a	n/a
15	BCLAF1	chr19:52124371-52124835	GM12878	blood:	n/a	n/a
16	BCLAF1	chr19:52124469-52124839	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:52154406-52154749	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
19	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
20	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
21	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
22	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
23	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
24	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
25	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
26	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
27	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
28	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
29	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
30	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
31	CEBPB	chr19:52131571-52131646	K562	blood:	n/a	n/a
32	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:52140780-52140930	HPF	lung:	n/a	n/a
34	CTCF	chr19:52140760-52140910	HMEC	breast:	n/a	n/a
35	CTCF	chr19:52140700-52140850	K562	blood:	n/a	n/a
36	CTCF	chr19:52140780-52140930	GM12874	blood:	n/a	n/a
37	CTCF	chr19:52141103-52141138	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr19:52140720-52140870	NHEK	skin:	n/a	n/a
39	CTCF	chr19:52140780-52140930	HCM	heart:	n/a	n/a
40	CTCF	chr19:52140720-52140870	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr19:52140808-52140906	NHEK	skin:	n/a	n/a
42	CTCF	chr19:52140680-52140830	GM12878	blood:	n/a	n/a
43	CTCF	chr19:52140740-52140890	HCFaa	heart:	n/a	n/a
44	CTCF	chr19:52140740-52140890	GM12874	blood:	n/a	n/a
45	CTCF	chr19:52140760-52140910	GM12875	blood:	n/a	n/a
46	CTCF	chr19:52140754-52140946	ProgFib	skin:	n/a	n/a
47	CTCF	chr19:52140740-52140890	GM12873	blood:	n/a	n/a
48	CTCF	chr19:52140760-52140910	AG04450	lung:	n/a	n/a
49	CTCF	chr19:52140740-52140890	HCM	heart:	n/a	n/a
50	CTCF	chr19:52140713-52140931	GM12878	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52134393-52134443	K562	blood:	n/a
2	chr19:52146598-52146648	NB4	blood:	n/a
3	chr19:52146598-52146648	HL-60	blood:	n/a
4	chr19:52131310-52131360	Jurkat	blood:	n/a
5	chr19:52150634-52150684	HIPEpiC	eye:	n/a
6	chr19:52140097-52140147	AG09319	gingival:	n/a
7	chr19:52134296-52134346	AG04449	skin:	fetal
8	chr19:52134393-52134443	AG04450	lung:	fetal
9	chr19:52150230-52150280	AG10803	skin:	n/a
10	chr19:52150233-52150283	HCF	heart:	n/a
11	chr19:52133837-52133887	ECC-1	luminal epithelium:	n/a
12	chr19:52150230-52150280	ovcar-3	ovarian:	n/a
13	chr19:52148354-52148404	CMK	blood:	n/a
14	chr19:52150233-52150283	Hepatocyte	liver:	n/a
15	chr19:52150230-52150280	HUVEC	blood vessel:	n/a
16	chr19:52150233-52150283	GM12892	blood:	n/a
17	chr19:52133837-52133887	HRCEpiC	kidney:	n/a
18	chr19:52148354-52148404	T-47D	breast:	n/a
19	chr19:52150634-52150684	LNCaP	prostate:	n/a
20	chr19:52146598-52146648	NT2-D1	testis:	n/a
21	chr19:52150634-52150684	NH-A	brain:	n/a
22	chr19:52150233-52150283	NHBE	bronchial:	n/a
23	chr19:52134393-52134443	HEK293	kidney:	embryo
24	chr19:52134393-52134443	HCF	heart:	n/a
25	chr19:52150547-52150597	SK-N-SH	brain:	n/a
26	chr19:52133837-52133887	NHDF-neo	bronchial:	n/a
27	chr19:52140097-52140147	HCPEpiC	choroid plexus:	n/a
28	chr19:52146598-52146648	PANC-1	pancreas:	n/a
29	chr19:52134393-52134443	SK-N-SH_RA	brain:	n/a
30	chr19:52146598-52146648	ovcar-3	ovarian:	n/a
31	chr19:52148354-52148404	HCF	heart:	n/a
32	chr19:52146598-52146648	ProgFib	skin:	n/a
33	chr19:52133837-52133887	Hepatocyte	liver:	n/a
34	chr19:52146598-52146648	HCPEpiC	choroid plexus:	n/a
35	chr19:52140097-52140147	HCF	heart:	n/a
36	chr19:52133837-52133887	MCF-7	breast:	n/a
37	chr19:52150547-52150597	K562	blood:	n/a
38	chr19:52134289-52134339	SK-N-MC	brain:	n/a
39	chr19:52150233-52150283	RPTEC	kidney:	n/a
40	chr19:52146598-52146648	HepG2	liver:	n/a
41	chr19:52148354-52148404	HRCEpiC	kidney:	n/a
42	chr19:52150634-52150684	AG09309	skin:	n/a
43	chr19:52131310-52131360	NB4	blood:	n/a
44	chr19:52133837-52133887	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:52150230-52150280	LNCaP	prostate:	n/a
46	chr19:52148354-52148404	AG04450	lung:	fetal
47	chr19:52131310-52131360	AG04450	lung:	fetal
48	chr19:52133837-52133887	GM06990	blood:	n/a
49	chr19:52150547-52150597	HNPCEpiC	eye:	n/a
50	chr19:52150547-52150597	RPTEC	kidney:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
2	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
3	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
4	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
5	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
6	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
7	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
8	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
9	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:
10	chr19:51620285..51621823-chr19:52126371..52128453,2	K562	blood:
11	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
12	chr19:51965493..51967976-chr19:52153295..52156025,2	K562	blood:
13	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
14	chr19:52107187..52109556-chr19:52121301..52123809,2	K562	blood:
15	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
16	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
17	chr19:51873847..51875580-chr19:52152831..52155624,2	K562	blood:
18	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
19	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
20	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:

(count:5 , 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-ZNF175-4	chr19:52124389-52124954	NONHSAT067457
4	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1
5	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
RPL9P33	TF binding region
ENSG00000268500	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
RPL9P33	CpG island
ENSG00000268500	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000244071	chromatin interactions
ENSG00000105366	chromatin interactions
ENSG00000105501	chromatin interactions
ENSG00000213822	chromatin interactions

Extended variants
information (count: 1287 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2053924	chr19:52123549-52123550	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528502041	chr19:52123640-52123641	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185802994	chr19:52123654-52123655	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148586539	chr19:52123659-52123660	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113593490	chr19:52123670-52123671	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546621020	chr19:52123697-52123698	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2053925	chr19:52123716-52123717	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs7251908	chr19:52123744-52123745	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs143937367	chr19:52123819-52123820	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11672302	chr19:52123932-52123933	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187600553	chr19:52123941-52123942	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377647580	chr19:52124098-52124099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199928458	chr19:52124150-52124151	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561004038	chr19:52124289-52124290	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs572946422	chr19:52124294-52124295	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs55825878	chr19:52124312-52124313	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs1868950	chr19:52124326-52124327	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs557554090	chr19:52124365-52124366	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs536504218	chr19:52124366-52124367	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs550481445	chr19:52124395-52124396	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs563295139	chr19:52124475-52124476	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs530823429	chr19:52124508-52124509	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs549058500	chr19:52124515-52124516	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs567795332	chr19:52124521-52124522	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs148612704	chr19:52124547-52124548	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs547208842	chr19:52124584-52124585	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs1530878	chr19:52124643-52124644	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs539312908	chr19:52124700-52124701	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs557693363	chr19:52124777-52124778	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs568859758	chr19:52124848-52124849	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs62114991	chr19:52124869-52124870	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs533744585	chr19:52125002-52125003	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572925164	chr19:52125004-52125005	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552494305	chr19:52125022-52125023	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs145630891	chr19:52125035-52125036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564399608	chr19:52125036-52125037	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539967821	chr19:52125045-52125046	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558690024	chr19:52125108-52125109	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558617961	chr19:52125155-52125156	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192180252	chr19:52125173-52125174	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs35831168	chr19:52125231-52125232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546486093	chr19:52125236-52125237	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544059772	chr19:52125290-52125291	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs111677744	chr19:52125295-52125296	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563031884	chr19:52125325-52125326	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577001276	chr19:52125353-52125354	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs562484637	chr19:52125407-52125408	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530813292	chr19:52125408-52125409	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544367415	chr19:52125412-52125413	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs542641401	chr19:52125414-52125415	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	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:301 , 50 per page) page: 1 2 3 4 5 6 7

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	chr19:52119600-52123600	Weak transcription	GM12878-XiMat	blood
4	chr19:52121600-52123800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr19:52122400-52125800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr19:52123000-52123800	Genic enhancers	Monocytes-CD14+_RO01746	blood
7	chr19:52123000-52126000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr19:52123400-52123800	Genic enhancers	Primary monocytes fromperipheralblood	blood
9	chr19:52123400-52125600	Enhancers	Primary B cells from cord blood	blood
10	chr19:52123600-52124600	Enhancers	GM12878-XiMat	blood
11	chr19:52123600-52125200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:52123800-52124000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr19:52123800-52124800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr19:52123800-52125000	Enhancers	Primary B cells from peripheral blood	blood
15	chr19:52123800-52125000	Enhancers	Primary hematopoietic stem cells	blood
16	chr19:52123800-52125600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr19:52124000-52124200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:52124000-52125000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:52124200-52130800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr19:52124600-52125000	Flanking Active TSS	GM12878-XiMat	blood
21	chr19:52124800-52125000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr19:52125000-52125200	Enhancers	GM12878-XiMat	blood
23	chr19:52125000-52125600	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr19:52125000-52125800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr19:52125000-52128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr19:52125200-52127000	Weak transcription	GM12878-XiMat	blood
28	chr19:52125200-52130800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:52125600-52125800	Genic enhancers	Primary monocytes fromperipheralblood	blood
30	chr19:52125600-52126000	Weak transcription	Primary B cells from cord blood	blood
31	chr19:52125600-52126000	Genic enhancers	Monocytes-CD14+_RO01746	blood
32	chr19:52125800-52126800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
33	chr19:52125800-52129200	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr19:52125800-52129800	Strong transcription	Primary B cells from peripheral blood	blood
35	chr19:52126000-52126200	Enhancers	Primary B cells from cord blood	blood
36	chr19:52126000-52126600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr19:52126000-52129200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr19:52126200-52128200	Weak transcription	Primary B cells from cord blood	blood
39	chr19:52126600-52129800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr19:52126800-52127800	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr19:52127000-52127200	Enhancers	GM12878-XiMat	blood
42	chr19:52127200-52129800	Weak transcription	GM12878-XiMat	blood
43	chr19:52127800-52132400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
44	chr19:52128200-52128400	Strong transcription	Primary B cells from cord blood	blood
45	chr19:52128200-52128800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:52128200-52131000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr19:52128400-52128600	Genic enhancers	Primary B cells from cord blood	blood
48	chr19:52128600-52129200	Strong transcription	Primary B cells from cord blood	blood
49	chr19:52128800-52133800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr19:52129200-52129600	Genic enhancers	Primary B cells from cord blood	blood

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