Variant report

Variant	esv1846813
Chromosome Location	chr19:52119490-52158241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:579)
CpG islands
(count:732)
Chromatin interactive
region (count:25)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	ATF1	chr19:52124551-52124727	K562	blood:	n/a	n/a
4	ATF2	chr19:52124388-52124859	GM12878	blood:	n/a	n/a
5	ATF2	chr19:52154376-52154835	GM12878	blood:	n/a	n/a
6	BATF	chr19:52124396-52124758	GM12878	blood:	n/a	n/a
7	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
8	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
9	BCL11A	chr19:52124445-52124855	GM12878	blood:	n/a	n/a
10	BCL11A	chr19:52124451-52124734	GM12878	blood:	n/a	n/a
11	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
13	BCL3	chr19:52131741-52132214	GM12878	blood:	n/a	n/a
14	BCL3	chr19:52131621-52132296	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	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
19	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
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	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
23	CBX3	chr19:52157924-52158374	K562	blood:	n/a	n/a
24	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
25	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
26	CBX3	chr19:52157930-52158454	K562	blood:	n/a	n/a
27	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
28	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
29	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
30	CEBPB	chr19:52119469-52119692	HepG2	liver:	n/a	chr19:52119654-52119665 chr19:52119563-52119576
31	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
32	CEBPB	chr19:52119481-52119697	A549	lung:	n/a	chr19:52119654-52119665 chr19:52119563-52119576
33	CEBPB	chr19:52131571-52131646	K562	blood:	n/a	n/a
34	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
35	CEBPB	chr19:52119395-52119727	MCF-7	breast:	n/a	chr19:52119654-52119665 chr19:52119563-52119576
36	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
37	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
38	CTCF	chr19:52140720-52140870	BE2_C	brain:	n/a	n/a
39	CTCF	chr19:52140760-52140910	GM12872	blood:	n/a	n/a
40	CTCF	chr19:52140442-52141373	A549	lung:	n/a	n/a
41	CTCF	chr19:52149807-52149816	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:52132045-52132087	MCF-7	breast:	n/a	n/a
43	CTCF	chr19:52140686-52140970	K562	blood:	n/a	n/a
44	CTCF	chr19:52140763-52140899	GM20000	blood:	n/a	n/a
45	CTCF	chr19:52140723-52140918	A549	lung:	n/a	n/a
46	CTCF	chr19:52140760-52140910	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr19:52140720-52140870	AG04449	skin:	n/a	n/a
48	CTCF	chr19:52141020-52141170	K562	blood:	n/a	n/a
49	CTCF	chr19:52154452-52154497	GM13976	blood:	n/a	chr19:52154471-52154492
50	CTCF	chr19:52158180-52158330	Hela-S3	cervix:	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	chr19:52150230-52150280	NHDF-neo	bronchial:	n/a
2	chr19:52140097-52140147	CMK	blood:	n/a
3	chr19:52150547-52150597	HCPEpiC	choroid plexus:	n/a
4	chr19:52150547-52150597	H1-hESC	embryonic stem cell:	embryo
5	chr19:52148354-52148404	AG10803	skin:	n/a
6	chr19:52150547-52150597	SK-N-SH	brain:	n/a
7	chr19:52148354-52148404	NB4	blood:	n/a
8	chr19:52150547-52150597	Hela-S3	cervix:	n/a
9	chr19:52150230-52150280	HCM	heart:	n/a
10	chr19:52134289-52134339	HCPEpiC	choroid plexus:	n/a
11	chr19:52146598-52146648	BE2_C	brain:	n/a
12	chr19:52131310-52131360	Caco-2	colon:	n/a
13	chr19:52134296-52134346	ovcar-3	ovarian:	n/a
14	chr19:52134296-52134346	HEK293	kidney:	embryo
15	chr19:52150233-52150283	AG09309	skin:	n/a
16	chr19:52150230-52150280	GM19239	blood:	n/a
17	chr19:52134393-52134443	CMK	blood:	n/a
18	chr19:52134393-52134443	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:52150634-52150684	HepG2	liver:	n/a
20	chr19:52134393-52134443	RPTEC	kidney:	n/a
21	chr19:52150230-52150280	HEEpiC	esophagus:	n/a
22	chr19:52140097-52140147	HNPCEpiC	eye:	n/a
23	chr19:52150233-52150283	AoSMC	blood vessel:	n/a
24	chr19:52150233-52150283	SK-N-SH_RA	brain:	n/a
25	chr19:52131310-52131360	HEK293	kidney:	embryo
26	chr19:52131310-52131360	HRPEpiC	eye:	n/a
27	chr19:52150230-52150280	PANC-1	pancreas:	n/a
28	chr19:52150230-52150280	AG10803	skin:	n/a
29	chr19:52146598-52146648	H1-hESC	embryonic stem cell:	embryo
30	chr19:52140097-52140147	AG09309	skin:	n/a
31	chr19:52150547-52150597	HRCEpiC	kidney:	n/a
32	chr19:52150547-52150597	AG10803	skin:	n/a
33	chr19:52146598-52146648	ovcar-3	ovarian:	n/a
34	chr19:52150547-52150597	NB4	blood:	n/a
35	chr19:52150230-52150280	PrEC	prostate:	n/a
36	chr19:52131310-52131360	ovcar-3	ovarian:	n/a
37	chr19:52150634-52150684	CMK	blood:	n/a
38	chr19:52131310-52131360	LNCaP	prostate:	n/a
39	chr19:52134289-52134339	HRPEpiC	eye:	n/a
40	chr19:52150547-52150597	BJ	skin:	n/a
41	chr19:52150230-52150280	Caco-2	colon:	n/a
42	chr19:52131310-52131360	ECC-1	luminal epithelium:	n/a
43	chr19:52131310-52131360	HNPCEpiC	eye:	n/a
44	chr19:52146598-52146648	HCPEpiC	choroid plexus:	n/a
45	chr19:52150634-52150684	Hepatocyte	liver:	n/a
46	chr19:52133837-52133887	LNCaP	prostate:	n/a
47	chr19:52150547-52150597	HAEpiC	amniotic membrane:	n/a
48	chr19:52134289-52134339	CMK	blood:	n/a
49	chr19:52150547-52150597	GM06990	blood:	n/a
50	chr19:52150233-52150283	RPTEC	kidney:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
2	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
3	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
4	chr19:52118220..52120065-chr19:52121660..52123490,2	K562	blood:
5	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
6	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
7	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
8	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
9	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
10	chr19:52110556..52111829-chr19:52157738..52158676,7	MCF-7	breast:
11	chr19:51873847..51875580-chr19:52152831..52155624,2	K562	blood:
12	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
13	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
14	chr19:52050819..52052546-chr19:52117300..52119490,2	K562	blood:
15	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
16	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
17	chr19:51620285..51621823-chr19:52126371..52128453,2	K562	blood:
18	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
19	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
20	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
21	chr19:52118220..52120065-chr19:52121660..52123490,2	K562	blood:
22	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:
23	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
24	chr19:51965493..51967976-chr19:52153295..52156025,2	K562	blood:
25	chr19:52107187..52109556-chr19:52121301..52123809,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF175-4	chr19:52124389-52124954	NONHSAT067457
2	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1
3	lnc-ZNF175-5	chr19:52152115-52152863	NONHSAT067458
4	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1
5	lnc-SIGLEC14-1	chr19:52133552-52133919	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
ENSG00000105501	chromatin interactions
ENSG00000105366	chromatin interactions
ENSG00000213822	chromatin interactions
ENSG00000244071	chromatin interactions

Extended variants
information (count: 1537 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1537 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557774614	chr19:52119492-52119493	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs150927502	chr19:52119519-52119520	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs11084094	chr19:52119546-52119547	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs139445453	chr19:52119585-52119586	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572084543	chr19:52119602-52119603	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs542360458	chr19:52119612-52119613	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs560708673	chr19:52119707-52119708	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs149751199	chr19:52119728-52119729	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552798297	chr19:52119733-52119734	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372611542	chr19:52119751-52119752	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553087887	chr19:52119759-52119760	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531205592	chr19:52119816-52119817	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs62114989	chr19:52119839-52119840	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs79731559	chr19:52119874-52119875	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146742020	chr19:52119918-52119919	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547090040	chr19:52119970-52119971	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34511943	chr19:52120037-52120038	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35475969	chr19:52120070-52120071	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs36079430	chr19:52120079-52120080	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140362980	chr19:52120112-52120113	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34974873	chr19:52120159-52120160	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10426413	chr19:52120172-52120173	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386389214	chr19:52120183-52120184	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs71187696	chr19:52120184-52120185	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558028837	chr19:52120222-52120223	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576285384	chr19:52120225-52120226	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538225968	chr19:52120232-52120233	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556862062	chr19:52120240-52120241	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145449133	chr19:52120301-52120302	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574908419	chr19:52120319-52120320	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534676714	chr19:52120322-52120323	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181481353	chr19:52120328-52120329	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184039609	chr19:52120333-52120334	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188434481	chr19:52120335-52120336	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373169895	chr19:52120338-52120339	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572593833	chr19:52120349-52120350	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546130186	chr19:52120365-52120366	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554706941	chr19:52120369-52120370	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560763798	chr19:52120376-52120377	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs564781721	chr19:52120381-52120382	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs34984145	chr19:52120410-52120411	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs34056987	chr19:52120508-52120509	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539953785	chr19:52120518-52120519	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs11880807	chr19:52120522-52120523	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs113917424	chr19:52120523-52120524	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs528864708	chr19:52120604-52120605	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs149160426	chr19:52120611-52120612	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565684216	chr19:52120688-52120689	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180870189	chr19:52120754-52120755	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551320813	chr19:52120769-52120770	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:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52114200-52122200	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr19:52116200-52123400	Weak transcription	Primary B cells from cord blood	blood
3	chr19:52116600-52130200	Weak transcription	Spleen	Spleen
4	chr19:52117800-52123000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr19:52118600-52120600	Enhancers	Placenta	Placenta
6	chr19:52118800-52119600	Genic enhancers	Primary monocytes fromperipheralblood	blood
7	chr19:52118800-52121400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr19:52119000-52119600	Enhancers	GM12878-XiMat	blood
9	chr19:52119000-52119600	Genic enhancers	Monocytes-CD14+_RO01746	blood
10	chr19:52119200-52121600	Strong transcription	Primary B cells from peripheral blood	blood
11	chr19:52119400-52128200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr19:52119600-52122800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr19:52119600-52123000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr19:52119600-52123600	Weak transcription	GM12878-XiMat	blood
15	chr19:52120600-52121600	Weak transcription	Placenta	Placenta
16	chr19:52121600-52121800	Enhancers	Placenta	Placenta
17	chr19:52121600-52123800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr19:52122200-52122400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
19	chr19:52122400-52125800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr19:52122800-52123400	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr19:52123000-52123800	Genic enhancers	Monocytes-CD14+_RO01746	blood
22	chr19:52123000-52126000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr19:52123400-52123800	Genic enhancers	Primary monocytes fromperipheralblood	blood
24	chr19:52123400-52125600	Enhancers	Primary B cells from cord blood	blood
25	chr19:52123600-52124600	Enhancers	GM12878-XiMat	blood
26	chr19:52123600-52125200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr19:52123800-52124000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr19:52123800-52124800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr19:52123800-52125000	Enhancers	Primary B cells from peripheral blood	blood
30	chr19:52123800-52125000	Enhancers	Primary hematopoietic stem cells	blood
31	chr19:52123800-52125600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr19:52124000-52124200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr19:52124000-52125000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr19:52124200-52130800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr19:52124600-52125000	Flanking Active TSS	GM12878-XiMat	blood
36	chr19:52124800-52125000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr19:52125000-52125200	Enhancers	GM12878-XiMat	blood
38	chr19:52125000-52125600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr19:52125000-52125800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr19:52125000-52128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr19:52125200-52127000	Weak transcription	GM12878-XiMat	blood
43	chr19:52125200-52130800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr19:52125600-52125800	Genic enhancers	Primary monocytes fromperipheralblood	blood
45	chr19:52125600-52126000	Weak transcription	Primary B cells from cord blood	blood
46	chr19:52125600-52126000	Genic enhancers	Monocytes-CD14+_RO01746	blood
47	chr19:52125800-52126800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
48	chr19:52125800-52129200	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr19:52125800-52129800	Strong transcription	Primary B cells from peripheral blood	blood
50	chr19:52126000-52126200	Enhancers	Primary B cells from cord blood	blood

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