Variant report

Variant	nsv580047
Chromosome Location	chr19:53506542-53557749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:427)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53518961-53519336	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:53510497-53510963	K562	blood:	n/a	n/a
3	BHLHE40	chr19:53510493-53510782	GM12878	blood:	n/a	n/a
4	BRCA1	chr19:53548078-53548353	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr19:53556503-53556768	K562	blood:	n/a	n/a
6	CEBPB	chr19:53514645-53514955	HepG2	liver:	n/a	chr19:53514790-53514801
7	CEBPB	chr19:53514709-53514946	Hela-S3	cervix:	n/a	chr19:53514790-53514801
8	CEBPB	chr19:53520162-53520365	MCF-7	breast:	n/a	n/a
9	CEBPB	chr19:53520072-53520352	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr19:53520052-53520352	K562	blood:	n/a	n/a
11	CEBPB	chr19:53514622-53514961	K562	blood:	n/a	chr19:53514790-53514801
12	CEBPB	chr19:53514683-53514869	A549	lung:	n/a	chr19:53514790-53514801
13	CEBPB	chr19:53520045-53520364	IMR90	lung:	n/a	n/a
14	CTCF	chr19:53523080-53523230	HMEC	breast:	n/a	n/a
15	CTCF	chr19:53523060-53523210	HVMF	connective:	n/a	n/a
16	CTCF	chr19:53523040-53523190	NHLF	lung:	n/a	n/a
17	CTCF	chr19:53523040-53523190	GM12873	blood:	n/a	n/a
18	CTCF	chr19:53522967-53523271	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr19:53523070-53523239	NHEK	skin:	n/a	n/a
20	CTCF	chr19:53523040-53523190	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr19:53523019-53523263	K562	blood:	n/a	n/a
22	CTCF	chr19:53517080-53517230	GM12866	blood:	n/a	n/a
23	CTCF	chr19:53523084-53523245	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr19:53522826-53523257	HCT-116	colon:	n/a	n/a
25	CTCF	chr19:53518162-53518286	GM20000	blood:	n/a	n/a
26	CTCF	chr19:53522940-53523090	HCT-116	colon:	n/a	n/a
27	CTCF	chr19:53523195-53523198	GM10266	blood:	n/a	n/a
28	CTCF	chr19:53523040-53523190	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr19:53523101-53523200	GM19239	blood:	n/a	n/a
30	CTCF	chr19:53523018-53523242	HepG2	liver:	n/a	n/a
31	CTCF	chr19:53547820-53547970	GM12875	blood:	n/a	n/a
32	CTCF	chr19:53523066-53523216	GM12891	blood:	n/a	n/a
33	CTCF	chr19:53523140-53523202	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:53523020-53523170	GM12874	blood:	n/a	n/a
35	CTCF	chr19:53522968-53523321	K562	blood:	n/a	n/a
36	CTCF	chr19:53523060-53523210	HCFaa	heart:	n/a	n/a
37	CTCF	chr19:53522989-53523273	K562	blood:	n/a	n/a
38	CTCF	chr19:53523092-53523198	GM19238	blood:	n/a	n/a
39	CTCF	chr19:53513738-53514155	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr19:53523000-53523150	NHEK	skin:	n/a	n/a
41	CTCF	chr19:53523056-53523245	Gliobla	brain:	n/a	n/a
42	CTCF	chr19:53523060-53523210	AG09309	skin:	n/a	n/a
43	CTCF	chr19:53513826-53514079	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr19:53523100-53523250	HCM	heart:	n/a	n/a
45	CTCF	chr19:53550349-53550463	GM10248	blood:	n/a	n/a
46	CTCF	chr19:53523020-53523170	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr19:53523060-53523210	HEK293	kidney:	n/a	n/a
48	CTCF	chr19:53523155-53523182	HepG2	liver:	n/a	n/a
49	CTCF	chr19:53541320-53541470	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr19:53523054-53523213	GM12892	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53557328-53557378	H1-hESC	embryonic stem cell:	embryo
2	chr19:53540902-53540952	HepG2	liver:	n/a
3	chr19:53540845-53540895	HUVEC	blood vessel:	n/a
4	chr19:53540902-53540952	HRE	kidney:	n/a
5	chr19:53557328-53557378	ovcar-3	ovarian:	n/a
6	chr19:53538687-53538737	HCF	heart:	n/a
7	chr19:53538883-53538933	CMK	blood:	n/a
8	chr19:53541186-53541236	NB4	blood:	n/a
9	chr19:53541287-53541337	AG09309	skin:	n/a
10	chr19:53538687-53538737	PFSK-1	brain:	n/a
11	chr19:53538883-53538933	PrEC	prostate:	n/a
12	chr19:53557328-53557378	HCPEpiC	choroid plexus:	n/a
13	chr19:53538883-53538933	Hela-S3	cervix:	n/a
14	chr19:53557328-53557378	AG09319	gingival:	n/a
15	chr19:53538883-53538933	SK-N-MC	brain:	n/a
16	chr19:53541287-53541337	T-47D	breast:	n/a
17	chr19:53540845-53540895	SKMC	muscle:	n/a
18	chr19:53538687-53538737	Hela-S3	cervix:	n/a
19	chr19:53541186-53541236	HUVEC	blood vessel:	n/a
20	chr19:53557328-53557378	HepG2	liver:	n/a
21	chr19:53538883-53538933	A549	lung:	n/a
22	chr19:53541287-53541337	CMK	blood:	n/a
23	chr19:53541287-53541337	HUVEC	blood vessel:	n/a
24	chr19:53557328-53557378	SAEC	small airway:	n/a
25	chr19:53538883-53538933	HRCEpiC	kidney:	n/a
26	chr19:53540845-53540895	CMK	blood:	n/a
27	chr19:53538883-53538933	BJ	skin:	n/a
28	chr19:53557328-53557378	HCM	heart:	n/a
29	chr19:53538883-53538933	SK-N-SH_RA	brain:	n/a
30	chr19:53541287-53541337	LNCaP	prostate:	n/a
31	chr19:53541186-53541236	CMK	blood:	n/a
32	chr19:53540845-53540895	PANC-1	pancreas:	n/a
33	chr19:53538687-53538737	IMR90	lung:	fetal
34	chr19:53540845-53540895	AG04449	skin:	fetal
35	chr19:53538883-53538933	Jurkat	blood:	n/a
36	chr19:53540902-53540952	AG09309	skin:	n/a
37	chr19:53557328-53557378	HUVEC	blood vessel:	n/a
38	chr19:53540902-53540952	HCPEpiC	choroid plexus:	n/a
39	chr19:53538687-53538737	HRCEpiC	kidney:	n/a
40	chr19:53557328-53557378	NB4	blood:	n/a
41	chr19:53541186-53541236	HEEpiC	esophagus:	n/a
42	chr19:53538687-53538737	GM12892	blood:	n/a
43	chr19:53541186-53541236	NH-A	brain:	n/a
44	chr19:53557328-53557378	RPTEC	kidney:	n/a
45	chr19:53540845-53540895	HEK293	kidney:	embryo
46	chr19:53538883-53538933	MCF10A-Er-Src	breast:	n/a
47	chr19:53540845-53540895	ECC-1	luminal epithelium:	n/a
48	chr19:53538687-53538737	HRE	kidney:	n/a
49	chr19:53541287-53541337	Jurkat	blood:	n/a
50	chr19:53540845-53540895	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53536567..53539141-chr19:53540653..53542425,2	K562	blood:
2	chr19:53557284..53559670-chr19:53575484..53577211,2	K562	blood:
3	chr19:53515874..53517968-chr19:53519511..53521544,2	K562	blood:
4	chr19:53514929..53517284-chr19:53527300..53529548,2	MCF-7	breast:
5	chr10:9353360..9353955-chr19:53525559..53526530,2	MCF-7	breast:
6	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:
7	chr19:53541069..53542606-chr19:53543581..53546044,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF160-1	chr19:53517584-53517806	ENSG00000251255
2	lnc-ZNF816-2	chr19:53540978-53541136	NONHSAT067613
3	lnc-ZNF160-1	chr19:53517843-53519833	ENSG00000251255

No data

Variant related genes	Relation type
ERVV-1	TF binding region
ENSG00000268282	TF binding region
ERVV-2	TF binding region
ENSG00000267943	TF binding region
ZNF702P	TF binding region
ERVV-1	CpG island
ENSG00000268282	CpG island
ERVV-2	CpG island
ENSG00000267943	CpG island
ZNF702P	CpG island
ENSG00000213020	chromatin interactions
ENSG00000269526	chromatin interactions
ENSG00000242779	chromatin interactions
RNF4	miRNA target sites
GPR107	miRNA target sites

Extended variants
information (count: 1955 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11670490	chr19:53506542-53506543	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs71361296	chr19:53506585-53506586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192822147	chr19:53506601-53506602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546710399	chr19:53506626-53506627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557159110	chr19:53506627-53506628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538717123	chr19:53506640-53506641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527719645	chr19:53506655-53506656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146017114	chr19:53506678-53506679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575612557	chr19:53506729-53506730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16984293	chr19:53506732-53506733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs75645744	chr19:53506754-53506755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1650941	chr19:53506797-53506798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183277143	chr19:53506799-53506800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117242933	chr19:53506807-53506808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576936634	chr19:53506810-53506811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1661914	chr19:53506834-53506835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138767028	chr19:53506842-53506843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141135398	chr19:53506856-53506857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542891855	chr19:53506905-53506906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561610714	chr19:53506914-53506915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113405145	chr19:53506945-53506946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528808752	chr19:53506953-53506954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150712769	chr19:53507005-53507006	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1661913	chr19:53507033-53507034	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1661912	chr19:53507064-53507065	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200732046	chr19:53507069-53507070	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187860311	chr19:53507092-53507093	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372005037	chr19:53507095-53507096	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569059234	chr19:53507100-53507101	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191481504	chr19:53507116-53507117	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538752761	chr19:53507128-53507129	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566737919	chr19:53507133-53507134	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183719608	chr19:53507150-53507151	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189645147	chr19:53507165-53507166	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371236866	chr19:53507185-53507186	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192497488	chr19:53507202-53507203	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs11671598	chr19:53507205-53507206	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs556283937	chr19:53507218-53507219	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs574617917	chr19:53507220-53507221	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs543182955	chr19:53507234-53507235	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs554834926	chr19:53507241-53507242	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs73068756	chr19:53507242-53507243	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1661911	chr19:53507245-53507246	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs1661910	chr19:53507265-53507266	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs1650940	chr19:53507299-53507300	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs544243432	chr19:53507319-53507320	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs563528501	chr19:53507333-53507334	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs371899647	chr19:53507340-53507341	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs117648425	chr19:53507388-53507389	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs11882069	chr19:53507401-53507402	Bivalent Enhancer Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

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
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
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53497600-53509800	Weak transcription	Right Atrium	heart
2	chr19:53498000-53510400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:53499200-53507200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:53503200-53507000	Weak transcription	Placenta	Placenta
5	chr19:53506000-53509800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr19:53506200-53507200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr19:53507000-53507600	Active TSS	Brain Germinal Matrix	brain
8	chr19:53507000-53510400	Enhancers	Placenta	Placenta
9	chr19:53507200-53507400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr19:53507200-53507400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr19:53507200-53507600	Active TSS	Brain Anterior Caudate	brain
12	chr19:53507200-53507600	Active TSS	Fetal Brain Female	brain
13	chr19:53507200-53507600	Enhancers	K562	blood
14	chr19:53507200-53507800	Active TSS	Brain Substantia Nigra	brain
15	chr19:53507200-53508400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:53507400-53507600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr19:53507400-53507600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr19:53507400-53507800	Enhancers	Fetal Heart	heart
19	chr19:53507600-53509600	Weak transcription	K562	blood
20	chr19:53507800-53508000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:53507800-53508400	ZNF genes & repeats	Gastric	stomach
22	chr19:53508000-53513200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr19:53508400-53509600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr19:53509600-53509800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr19:53509600-53509800	Enhancers	K562	blood
26	chr19:53509800-53510200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:53509800-53510200	Weak transcription	K562	blood
28	chr19:53510200-53510400	Enhancers	K562	blood
29	chr19:53510200-53511000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr19:53510400-53510800	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr19:53510400-53511000	Enhancers	Placenta Amnion	Placenta Amnion
32	chr19:53510400-53511200	Enhancers	Dnd41	blood
33	chr19:53510400-53511200	Flanking Active TSS	K562	blood
34	chr19:53510400-53511400	Flanking Active TSS	Placenta	Placenta
35	chr19:53510600-53511600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr19:53510800-53511200	Weak transcription	Right Ventricle	heart
37	chr19:53511000-53511200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
38	chr19:53511000-53511800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:53511200-53511400	Enhancers	Right Ventricle	heart
40	chr19:53511200-53511800	Bivalent Enhancer	K562	blood
41	chr19:53511200-53512600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr19:53511400-53511800	Active TSS	Placenta	Placenta
43	chr19:53511400-53512000	Weak transcription	Right Ventricle	heart
44	chr19:53511600-53512200	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr19:53511800-53512000	Flanking Active TSS	Placenta	Placenta
46	chr19:53511800-53512400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr19:53512000-53512200	Active TSS	Placenta	Placenta
48	chr19:53512200-53512400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr19:53512200-53512400	Flanking Active TSS	Placenta	Placenta
50	chr19:53512200-53512400	Enhancers	Right Ventricle	heart

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