Variant report

Variant	nsv518134
Chromosome Location	chr19:51750238-51765953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:51763490-51763571	K562	blood:	n/a	n/a
2	ATF1	chr19:51762606-51762965	K562	blood:	n/a	n/a
3	ATF1	chr19:51761509-51761788	K562	blood:	n/a	n/a
4	ATF2	chr19:51754581-51755015	GM12878	blood:	n/a	n/a
5	BATF	chr19:51754691-51755046	GM12878	blood:	n/a	chr19:51754839-51754850
6	BATF	chr19:51754605-51755151	GM12878	blood:	n/a	chr19:51754839-51754850
7	BCL11A	chr19:51754668-51755111	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:51754830-51754937	GM12878	blood:	n/a	n/a
9	CEBPB	chr19:51760842-51760975	K562	blood:	n/a	n/a
10	CTCF	chr19:51762760-51762910	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr19:51762740-51762890	K562	blood:	n/a	n/a
12	CTCF	chr19:51762720-51762870	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr19:51762720-51762870	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr19:51762691-51762923	ProgFib	skin:	n/a	n/a
15	CTCF	chr19:51762567-51763005	K562	blood:	n/a	n/a
16	CTCF	chr19:51762612-51762870	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr19:51763020-51763170	GM12870	blood:	n/a	n/a
18	CTCF	chr19:51762740-51762890	GM12864	blood:	n/a	n/a
19	CTCF	chr19:51762704-51762908	MCF-7	breast:	n/a	n/a
20	CTCF	chr19:51762060-51762210	HEK293	kidney:	n/a	n/a
21	CTCF	chr19:51762600-51762750	HAc	cerebellar:	n/a	n/a
22	CTCF	chr19:51763100-51763250	GM12874	blood:	n/a	n/a
23	CTCF	chr19:51762651-51762901	HepG2	liver:	n/a	n/a
24	CTCF	chr19:51762640-51762790	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr19:51762665-51762952	MCF-7	breast:	n/a	n/a
26	CTCF	chr19:51762698-51762916	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:51762720-51762870	AG04450	lung:	n/a	n/a
28	CTCF	chr19:51762671-51762939	A549	lung:	n/a	n/a
29	CTCF	chr19:51762705-51762915	MCF-7	breast:	n/a	n/a
30	CTCF	chr19:51762700-51762850	GM12870	blood:	n/a	n/a
31	CTCF	chr19:51762720-51762870	HPF	lung:	n/a	n/a
32	CTCF	chr19:51762740-51762890	HMEC	breast:	n/a	n/a
33	CTCF	chr19:51762669-51762949	Gliobla	brain:	n/a	n/a
34	CTCF	chr19:51762683-51762911	A549	lung:	n/a	n/a
35	CTCF	chr19:51762680-51762830	WI-38	lung:	n/a	n/a
36	CTCF	chr19:51762720-51762870	BJ	skin:	n/a	n/a
37	CTCF	chr19:51762606-51762915	K562	blood:	n/a	n/a
38	CTCF	chr19:51762720-51762870	HMEC	breast:	n/a	n/a
39	CTCF	chr19:51762720-51762870	GM12864	blood:	n/a	n/a
40	CTCF	chr19:51762673-51762895	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr19:51762720-51762870	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr19:51762740-51762890	GM12871	blood:	n/a	n/a
43	CTCF	chr19:51762667-51762928	LNCaP	prostate:	n/a	n/a
44	CTCF	chr19:51762720-51762870	GM12878	blood:	n/a	n/a
45	CTCF	chr19:51762720-51762870	GM12873	blood:	n/a	n/a
46	CTCF	chr19:51762740-51762890	GM12868	blood:	n/a	n/a
47	CTCF	chr19:51762678-51762925	GM13977	blood:	n/a	n/a
48	CTCF	chr19:51762720-51762870	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr19:51762720-51762870	HEK293	kidney:	n/a	n/a
50	CTCF	chr19:51762659-51762946	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51762753-51762803	H1-hESC	embryonic stem cell:	embryo
2	chr19:51761116-51761166	HCM	heart:	n/a
3	chr19:51762753-51762803	PFSK-1	brain:	n/a
4	chr19:51762753-51762803	HEK293	kidney:	embryo
5	chr19:51761116-51761166	ProgFib	skin:	n/a
6	chr19:51762753-51762803	HRCEpiC	kidney:	n/a
7	chr19:51761116-51761166	HMEC	breast:	n/a
8	chr19:51762753-51762803	HCM	heart:	n/a
9	chr19:51761116-51761166	PANC-1	pancreas:	n/a
10	chr19:51761116-51761166	AG09309	skin:	n/a
11	chr19:51762753-51762803	NH-A	brain:	n/a
12	chr19:51762753-51762803	HCT-116	colon:	n/a
13	chr19:51761116-51761166	HCPEpiC	choroid plexus:	n/a
14	chr19:51761116-51761166	SK-N-SH	brain:	n/a
15	chr19:51761116-51761166	HAEpiC	amniotic membrane:	n/a
16	chr19:51761116-51761166	SK-N-SH_RA	brain:	n/a
17	chr19:51762753-51762803	HUVEC	blood vessel:	n/a
18	chr19:51762753-51762803	K562	blood:	n/a
19	chr19:51761116-51761166	MCF-7	breast:	n/a
20	chr19:51762753-51762803	HRPEpiC	eye:	n/a
21	chr19:51761116-51761166	GM12891	blood:	n/a
22	chr19:51761116-51761166	HUVEC	blood vessel:	n/a
23	chr19:51761116-51761166	HEEpiC	esophagus:	n/a
24	chr19:51762753-51762803	GM06990	blood:	n/a
25	chr19:51762753-51762803	CMK	blood:	n/a
26	chr19:51762753-51762803	IMR90	lung:	fetal
27	chr19:51762753-51762803	GM12891	blood:	n/a
28	chr19:51761116-51761166	Jurkat	blood:	n/a
29	chr19:51762753-51762803	HIPEpiC	eye:	n/a
30	chr19:51761116-51761166	HNPCEpiC	eye:	n/a
31	chr19:51762753-51762803	Caco-2	colon:	n/a
32	chr19:51762753-51762803	HMEC	breast:	n/a
33	chr19:51762753-51762803	GM12892	blood:	n/a
34	chr19:51761116-51761166	Hepatocyte	liver:	n/a
35	chr19:51762753-51762803	HCPEpiC	choroid plexus:	n/a
36	chr19:51762753-51762803	HCF	heart:	n/a
37	chr19:51761116-51761166	HRCEpiC	kidney:	n/a
38	chr19:51761116-51761166	H1-hESC	embryonic stem cell:	embryo
39	chr19:51761116-51761166	SAEC	small airway:	n/a
40	chr19:51762753-51762803	LNCaP	prostate:	n/a
41	chr19:51762753-51762803	HepG2	liver:	n/a
42	chr19:51762753-51762803	AoSMC	blood vessel:	n/a
43	chr19:51762753-51762803	AG04450	lung:	fetal
44	chr19:51762753-51762803	HAEpiC	amniotic membrane:	n/a
45	chr19:51761116-51761166	Hela-S3	cervix:	n/a
46	chr19:51761116-51761166	GM06990	blood:	n/a
47	chr19:51762753-51762803	MCF-7	breast:	n/a
48	chr19:51762753-51762803	HL-60	blood:	n/a
49	chr19:51761116-51761166	HCF	heart:	n/a
50	chr19:51761116-51761166	IMR90	lung:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51661493..51662394-chr19:51762311..51762910,6	MCF-7	breast:
2	chr19:51661431..51662712-chr19:51761692..51763149,12	K562	blood:
3	chr19:51747857..51749540-chr19:51750009..51752859,2	K562	blood:
4	chr19:51600353..51600887-chr19:51762311..51762872,2	K562	blood:
5	chr19:51763432..51765236-chr19:51768339..51771020,2	K562	blood:
6	chr19:51762812..51764543-chr19:51765982..51768235,3	K562	blood:
7	chr19:51661388..51662622-chr19:51761876..51763512,12	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C19orf75-1	chr19:51754332-51754799	NONHSAT067424
2	lnc-C19orf75-1	chr19:51754503-51754799	NONHSAT067426
3	lnc-C19orf75-1	chr19:51759188-51759286	NONHSAT067426
4	lnc-VSIG10L-1	chr19:51754485-51754788	ENSG00000268595.1

No data

Variant related genes	Relation type
SIGLECL1	TF binding region
SIGLECL1	CpG island
ENSG00000179213	chromatin interactions

Extended variants
information (count: 617 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11084062	chr19:51750238-51750239	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543236484	chr19:51750262-51750263	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs561876453	chr19:51750369-51750370	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs568621828	chr19:51750381-51750382	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs541434856	chr19:51750454-51750455	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs568477580	chr19:51750489-51750490	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs541113228	chr19:51750499-51750500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs559135467	chr19:51750506-51750507	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs115467503	chr19:51750510-51750511	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs368885146	chr19:51750522-51750523	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs551359196	chr19:51750523-51750524	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs191041848	chr19:51750551-51750552	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs531181064	chr19:51750612-51750613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371914839	chr19:51750656-51750657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537590516	chr19:51750657-51750658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35110842	chr19:51750680-51750681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs397717136	chr19:51750691-51750692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183174593	chr19:51750700-51750701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12461282	chr19:51750757-51750758	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368468362	chr19:51750761-51750762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538664889	chr19:51750802-51750803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556909100	chr19:51750831-51750832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575935448	chr19:51750847-51750848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536907235	chr19:51750848-51750849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111301369	chr19:51750863-51750864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs273648	chr19:51750879-51750880	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs140849439	chr19:51750886-51750887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540799126	chr19:51750919-51750920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559385662	chr19:51750955-51750956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187464602	chr19:51750968-51750969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150135301	chr19:51750973-51750974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11084063	chr19:51751123-51751124	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs546111285	chr19:51751216-51751217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557803389	chr19:51751219-51751220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193058167	chr19:51751236-51751237	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs35931165	chr19:51751285-51751286	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs368671729	chr19:51751315-51751316	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs113903697	chr19:51751372-51751373	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549646561	chr19:51751373-51751374	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561350056	chr19:51751381-51751382	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs57490406	chr19:51751417-51751418	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs183078952	chr19:51751425-51751426	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201627505	chr19:51751437-51751438	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs74197505	chr19:51751439-51751440	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs79854485	chr19:51751440-51751441	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs72509605	chr19:51751441-51751442	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571428988	chr19:51751458-51751459	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs538700927	chr19:51751477-51751478	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs550571399	chr19:51751497-51751498	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568904736	chr19:51751544-51751545	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51745400-51753200	Enhancers	Primary hematopoietic stem cells	blood
2	chr19:51745800-51754000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr19:51746400-51750600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:51748800-51750600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr19:51748800-51750800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr19:51749200-51750600	Enhancers	Fetal Kidney	kidney
7	chr19:51749400-51753400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:51749800-51751400	Weak transcription	Fetal Thymus	thymus
9	chr19:51749800-51753400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr19:51749800-51753400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:51750600-51754000	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr19:51751400-51752800	Enhancers	Fetal Thymus	thymus
13	chr19:51751600-51752200	Enhancers	GM12878-XiMat	blood
14	chr19:51751600-51752400	Enhancers	Thymus	Thymus
15	chr19:51753200-51756400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr19:51753400-51754200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr19:51753400-51755600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:51753400-51755600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:51754000-51755800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr19:51754200-51754600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
21	chr19:51754200-51754800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:51754600-51754800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr19:51754600-51755600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr19:51755600-51757400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr19:51755600-51757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:51755600-51757600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr19:51755800-51757400	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr19:51756000-51757600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr19:51756200-51757600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr19:51756400-51757000	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr19:51756400-51757400	Enhancers	Primary hematopoietic stem cells	blood
32	chr19:51757400-51759400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr19:51757400-51759400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr19:51757400-51759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr19:51757400-51761000	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr19:51757600-51758800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr19:51757600-51759400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr19:51757600-51761200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr19:51758800-51759400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr19:51759400-51761400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr19:51759400-51761400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:51759400-51762800	Enhancers	Primary hematopoietic stem cells	blood
43	chr19:51759400-51762800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr19:51759600-51761600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr19:51761000-51761600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr19:51761000-51761800	Enhancers	K562	blood
47	chr19:51761000-51762200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr19:51761200-51762400	Enhancers	Fetal Thymus	thymus
49	chr19:51761200-51762800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr19:51761400-51762000	Enhancers	GM12878-XiMat	blood

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