Variant report

Variant	esv1827409
Chromosome Location	chr19:52133064-52150859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:672)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 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	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
4	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
5	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
7	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
8	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
9	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
10	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
11	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
12	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
13	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
14	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
15	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
16	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
17	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
18	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
19	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
20	CTCF	chr19:52141072-52141194	K562	blood:	n/a	n/a
21	CTCF	chr19:52140740-52140890	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr19:52140720-52140870	HCT-116	colon:	n/a	n/a
23	CTCF	chr19:52140760-52140910	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr19:52140740-52140890	AG10803	skin:	n/a	n/a
25	CTCF	chr19:52140720-52140870	AG04449	skin:	n/a	n/a
26	CTCF	chr19:52140680-52140830	GM12878	blood:	n/a	n/a
27	CTCF	chr19:52140808-52140906	NHEK	skin:	n/a	n/a
28	CTCF	chr19:52141080-52141230	A549	lung:	n/a	n/a
29	CTCF	chr19:52141060-52141210	HCM	heart:	n/a	n/a
30	CTCF	chr19:52140763-52140899	GM20000	blood:	n/a	n/a
31	CTCF	chr19:52140740-52140890	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:52140740-52140890	HCM	heart:	n/a	n/a
33	CTCF	chr19:52140713-52140931	GM12878	blood:	n/a	n/a
34	CTCF	chr19:52140780-52140930	HRE	kidney:	n/a	n/a
35	CTCF	chr19:52140656-52140963	IMR90	lung:	n/a	n/a
36	CTCF	chr19:52140797-52140906	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:52140800-52140950	GM12872	blood:	n/a	n/a
38	CTCF	chr19:52140713-52140866	A549	lung:	n/a	n/a
39	CTCF	chr19:52140720-52140870	GM12872	blood:	n/a	n/a
40	CTCF	chr19:52140720-52140870	NHEK	skin:	n/a	n/a
41	CTCF	chr19:52140760-52140910	AG04450	lung:	n/a	n/a
42	CTCF	chr19:52140680-52140830	Caco-2	colon:	n/a	n/a
43	CTCF	chr19:52150047-52150052	GM19239	blood:	n/a	n/a
44	CTCF	chr19:52140780-52140930	HCM	heart:	n/a	n/a
45	CTCF	chr19:52140800-52140950	BJ	skin:	n/a	n/a
46	CTCF	chr19:52140747-52140939	Gliobla	brain:	n/a	n/a
47	CTCF	chr19:52140754-52140946	ProgFib	skin:	n/a	n/a
48	CTCF	chr19:52149807-52149816	MCF-7	breast:	n/a	n/a
49	CTCF	chr19:52140740-52140890	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr19:52140753-52140920	GM13977	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52146598-52146648	AG04450	lung:	fetal
2	chr19:52146598-52146648	AG04450	lung:	fetal
3	chr19:52134393-52134443	BE2_C	brain:	n/a
4	chr19:52146598-52146648	T-47D	breast:	n/a
5	chr19:52150230-52150280	HIPEpiC	eye:	n/a
6	chr19:52134289-52134339	HEK293	kidney:	embryo
7	chr19:52134393-52134443	PrEC	prostate:	n/a
8	chr19:52134296-52134346	A549	lung:	n/a
9	chr19:52150230-52150280	NH-A	brain:	n/a
10	chr19:52150547-52150597	IMR90	lung:	fetal
11	chr19:52134393-52134443	HCT-116	colon:	n/a
12	chr19:52150233-52150283	HRCEpiC	kidney:	n/a
13	chr19:52134289-52134339	BJ	skin:	n/a
14	chr19:52150230-52150280	SK-N-SH	brain:	n/a
15	chr19:52150634-52150684	HRPEpiC	eye:	n/a
16	chr19:52134296-52134346	AG09309	skin:	n/a
17	chr19:52134393-52134443	Hepatocyte	liver:	n/a
18	chr19:52150547-52150597	BE2_C	brain:	n/a
19	chr19:52134296-52134346	Hela-S3	cervix:	n/a
20	chr19:52134393-52134443	BJ	skin:	n/a
21	chr19:52150233-52150283	NH-A	brain:	n/a
22	chr19:52150547-52150597	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:52134289-52134339	CMK	blood:	n/a
24	chr19:52134393-52134443	HCPEpiC	choroid plexus:	n/a
25	chr19:52133837-52133887	SK-N-SH	brain:	n/a
26	chr19:52134289-52134339	PrEC	prostate:	n/a
27	chr19:52134289-52134339	A549	lung:	n/a
28	chr19:52146598-52146648	AG04449	skin:	fetal
29	chr19:52148354-52148404	K562	blood:	n/a
30	chr19:52146598-52146648	HIPEpiC	eye:	n/a
31	chr19:52134393-52134443	T-47D	breast:	n/a
32	chr19:52134289-52134339	AG09309	skin:	n/a
33	chr19:52140097-52140147	SKMC	muscle:	n/a
34	chr19:52133837-52133887	ProgFib	skin:	n/a
35	chr19:52148354-52148404	NB4	blood:	n/a
36	chr19:52150547-52150597	NHBE	bronchial:	n/a
37	chr19:52148354-52148404	HCT-116	colon:	n/a
38	chr19:52134289-52134339	AG04449	skin:	fetal
39	chr19:52150634-52150684	SK-N-SH	brain:	n/a
40	chr19:52134296-52134346	GM19239	blood:	n/a
41	chr19:52134393-52134443	MCF10A-Er-Src	breast:	n/a
42	chr19:52148354-52148404	LNCaP	prostate:	n/a
43	chr19:52150547-52150597	HRE	kidney:	n/a
44	chr19:52148354-52148404	BE2_C	brain:	n/a
45	chr19:52133837-52133887	BJ	skin:	n/a
46	chr19:52134393-52134443	NHBE	bronchial:	n/a
47	chr19:52134289-52134339	PANC-1	pancreas:	n/a
48	chr19:52134289-52134339	SAEC	small airway:	n/a
49	chr19:52134393-52134443	ECC-1	luminal epithelium:	n/a
50	chr19:52150634-52150684	AG04450	lung:	fetal

(count:12 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIGLEC14-1	chr19:52133552-52133919	ENSG00000258669.1
2	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1
3	lnc-SIGLEC14-1	chr19:52148730-52148798	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
ENSG00000213822	chromatin interactions
ENSG00000244071	chromatin interactions
ENSG00000105366	chromatin interactions

Extended variants
information (count: 591 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117156027	chr19:52133070-52133071	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375317816	chr19:52133075-52133076	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200820951	chr19:52133088-52133089	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201954824	chr19:52133098-52133099	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559592597	chr19:52133162-52133163	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533236117	chr19:52133168-52133169	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377628577	chr19:52133182-52133183	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs199864224	chr19:52133191-52133192	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570741509	chr19:52133206-52133207	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374509897	chr19:52133213-52133214	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550003561	chr19:52133236-52133237	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376860084	chr19:52133241-52133242	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201664362	chr19:52133270-52133271	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535585442	chr19:52133278-52133279	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1973019	chr19:52133292-52133293	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373602892	chr19:52133322-52133323	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539707737	chr19:52133477-52133478	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565805733	chr19:52133503-52133504	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558062338	chr19:52133505-52133506	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575947372	chr19:52133506-52133507	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543449315	chr19:52133555-52133556	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs561541263	chr19:52133598-52133599	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs573637066	chr19:52133606-52133607	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs201309818	chr19:52133627-52133628	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs541149646	chr19:52133682-52133683	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs559556158	chr19:52133713-52133714	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs533198086	chr19:52133718-52133719	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs62115014	chr19:52133734-52133735	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs143752060	chr19:52133768-52133769	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs200603828	chr19:52133785-52133786	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs182054731	chr19:52133797-52133798	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs2864140	chr19:52133799-52133800	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs73934260	chr19:52133809-52133810	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs529317874	chr19:52133811-52133812	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs3961257	chr19:52133812-52133813	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs547017066	chr19:52133861-52133862	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs8107979	chr19:52133863-52133864	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs186431035	chr19:52133905-52133906	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs539693765	chr19:52133908-52133909	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs76992492	chr19:52133927-52133928	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570291283	chr19:52133947-52133948	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75983937	chr19:52133982-52133983	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555315947	chr19:52134001-52134002	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs74176145	chr19:52134195-52134196	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs190354362	chr19:52134256-52134257	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146204540	chr19:52134271-52134272	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145465138	chr19:52134334-52134335	Enhancers Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs569509212	chr19:52134335-52134336	Enhancers Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs11667857	chr19:52134345-52134346	Enhancers Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs577908687	chr19:52134347-52134348	Enhancers Active TSS 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:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr19:52128800-52133800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:52130800-52133200	Weak transcription	Gastric	stomach
4	chr19:52131000-52133800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:52131000-52134000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:52132400-52133600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr19:52132600-52133600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr19:52132600-52133800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr19:52132600-52133800	Weak transcription	Primary B cells from cord blood	blood
10	chr19:52132600-52133800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr19:52132600-52134600	Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr19:52132800-52133800	Active TSS	Primary monocytes fromperipheralblood	blood
13	chr19:52132800-52133800	Active TSS	Monocytes-CD14+_RO01746	blood
14	chr19:52133000-52133400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr19:52133400-52133600	Enhancers	Primary B cells from peripheral blood	blood
16	chr19:52133600-52133800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:52133600-52134000	Enhancers	Primary hematopoietic stem cells	blood
18	chr19:52133600-52134000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:52133600-52134200	Flanking Active TSS	Primary B cells from peripheral blood	blood
20	chr19:52133800-52134000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr19:52133800-52134000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr19:52133800-52134200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr19:52133800-52134200	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr19:52133800-52134200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr19:52133800-52134200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr19:52133800-52134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr19:52133800-52134600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:52133800-52135200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr19:52133800-52136200	Enhancers	Placenta	Placenta
30	chr19:52134000-52134200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr19:52134200-52134400	Enhancers	Primary B cells from cord blood	blood
32	chr19:52134200-52134600	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr19:52134200-52134600	Enhancers	Primary B cells from peripheral blood	blood
34	chr19:52134200-52134600	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr19:52134200-52140200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:52134200-52144400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr19:52134400-52138000	Weak transcription	Primary B cells from cord blood	blood
38	chr19:52134600-52137800	Weak transcription	Primary B cells from peripheral blood	blood
39	chr19:52134600-52139400	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr19:52134600-52139400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr19:52135200-52140000	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr19:52135400-52135600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
43	chr19:52137800-52141200	Enhancers	Primary B cells from peripheral blood	blood
44	chr19:52138000-52140600	Enhancers	Primary B cells from cord blood	blood
45	chr19:52139400-52141200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr19:52139400-52141400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr19:52139600-52140800	Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr19:52140000-52140200	Enhancers	Placenta Amnion	Placenta Amnion
49	chr19:52140200-52140600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr19:52141200-52142400	Weak transcription	Primary B cells from peripheral blood	blood

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