Variant report

Variant	nsv580346
Chromosome Location	chr19:56246520-56369314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:591)
CpG islands
(count:1771)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:591 , 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	ATF3	chr19:56320795-56321061	K562	blood:	n/a	n/a
2	ATF3	chr19:56320785-56321060	GM12878	blood:	n/a	n/a
3	BHLHE40	chr19:56320784-56321089	HepG2	liver:	n/a	n/a
4	BHLHE40	chr19:56320723-56321185	K562	blood:	n/a	n/a
5	CBX3	chr19:56320575-56321158	K562	blood:	n/a	n/a
6	CBX3	chr19:56320742-56321100	K562	blood:	n/a	n/a
7	CBX3	chr19:56347744-56348093	K562	blood:	n/a	n/a
8	CEBPB	chr19:56313719-56313987	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr19:56306160-56306187	Hela-S3	cervix:	n/a	chr19:56306161-56306174 chr19:56306161-56306172
10	CEBPB	chr19:56341872-56342423	HCT-116	colon:	n/a	n/a
11	CEBPB	chr19:56341826-56342415	HCT-116	colon:	n/a	n/a
12	CEBPB	chr19:56303064-56303264	K562	blood:	n/a	chr19:56303175-56303186 chr19:56303172-56303189
13	CEBPB	chr19:56306047-56306327	HepG2	liver:	n/a	chr19:56306161-56306174 chr19:56306161-56306172
14	CEBPB	chr19:56252761-56252952	K562	blood:	n/a	chr19:56252917-56252928
15	CEBPB	chr19:56342114-56342249	K562	blood:	n/a	n/a
16	CEBPB	chr19:56342021-56342353	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:56303142-56303233	A549	lung:	n/a	chr19:56303175-56303186 chr19:56303172-56303189
18	CEBPB	chr19:56309941-56309963	HepG2	liver:	n/a	chr19:56309945-56309956
19	CEBPB	chr19:56267971-56268186	K562	blood:	n/a	chr19:56268130-56268143
20	CEBPB	chr19:56252893-56252942	HepG2	liver:	n/a	chr19:56252917-56252928
21	CEBPB	chr19:56303101-56303314	HepG2	liver:	n/a	chr19:56303175-56303186 chr19:56303172-56303189
22	CEBPB	chr19:56268023-56268280	A549	lung:	n/a	chr19:56268130-56268143
23	CEBPB	chr19:56252920-56252934	A549	lung:	n/a	n/a
24	CEBPB	chr19:56268125-56268161	Hela-S3	cervix:	n/a	chr19:56268130-56268143
25	CEBPB	chr19:56342129-56342342	K562	blood:	n/a	n/a
26	CEBPB	chr19:56258745-56258858	HepG2	liver:	n/a	chr19:56258809-56258820
27	CEBPB	chr19:56342078-56342348	HepG2	liver:	n/a	n/a
28	CEBPB	chr19:56320804-56321149	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:56344099-56344348	A549	lung:	n/a	n/a
30	CEBPB	chr19:56277973-56278182	K562	blood:	n/a	chr19:56278128-56278141
31	CREB1	chr19:56320773-56321071	A549	lung:	n/a	n/a
32	CREB1	chr19:56368555-56368853	GM12878	blood:	n/a	n/a
33	CTCF	chr19:56322960-56323110	HCT-116	colon:	n/a	n/a
34	CTCF	chr19:56359283-56359341	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:56321100-56321250	RPTEC	kidney:	n/a	n/a
36	CTCF	chr19:56320907-56321142	IMR90	lung:	n/a	n/a
37	CTCF	chr19:56320800-56320950	GM12801	blood:	n/a	n/a
38	CTCF	chr19:56320920-56321070	SAEC	small airway:	n/a	n/a
39	CTCF	chr19:56320980-56321130	GM12873	blood:	n/a	n/a
40	CTCF	chr19:56320860-56321010	NHLF	lung:	n/a	n/a
41	CTCF	chr19:56320880-56321030	BJ	skin:	n/a	n/a
42	CTCF	chr19:56320833-56321195	A549	lung:	n/a	n/a
43	CTCF	chr19:56289040-56289190	SK-N-SH_RA	brain:	n/a	chr19:56289124-56289137 chr19:56289121-56289139
44	CTCF	chr19:56321300-56321450	HEK293	kidney:	n/a	n/a
45	CTCF	chr19:56282862-56282960	GM13976	blood:	n/a	n/a
46	CTCF	chr19:56321280-56321430	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr19:56289000-56289150	GM12873	blood:	n/a	chr19:56289124-56289137 chr19:56289121-56289139
48	CTCF	chr19:56321000-56321150	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr19:56288905-56289243	K562	blood:	n/a	chr19:56289124-56289137 chr19:56289121-56289139
50	CTCF	chr19:56289028-56289145	GM12891	blood:	n/a	chr19:56289124-56289137 chr19:56289121-56289139

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56348889-56348939	HEEpiC	esophagus:	n/a
2	chr19:56250127-56250177	HCPEpiC	choroid plexus:	n/a
3	chr19:56348889-56348939	HEEpiC	esophagus:	n/a
4	chr19:56250127-56250177	HCPEpiC	choroid plexus:	n/a
5	chr19:56250127-56250177	H1-hESC	embryonic stem cell:	embryo
6	chr19:56342665-56342715	NT2-D1	testis:	n/a
7	chr19:56363105-56363155	HUVEC	blood vessel:	n/a
8	chr19:56321115-56321165	T-47D	breast:	n/a
9	chr19:56321115-56321165	NHDF-neo	bronchial:	n/a
10	chr19:56346628-56346678	HepG2	liver:	n/a
11	chr19:56349119-56349169	SAEC	small airway:	n/a
12	chr19:56249891-56249941	SAEC	small airway:	n/a
13	chr19:56348889-56348939	U87	brain:	n/a
14	chr19:56249743-56249793	NB4	blood:	n/a
15	chr19:56249891-56249941	HNPCEpiC	eye:	n/a
16	chr19:56347771-56347821	PFSK-1	brain:	n/a
17	chr19:56363105-56363155	HCT-116	colon:	n/a
18	chr19:56367316-56367366	PANC-1	pancreas:	n/a
19	chr19:56342665-56342715	ProgFib	skin:	n/a
20	chr19:56361716-56361766	HEK293	kidney:	embryo
21	chr19:56347847-56347897	A549	lung:	n/a
22	chr19:56367830-56367880	AG04449	skin:	fetal
23	chr19:56347847-56347897	ProgFib	skin:	n/a
24	chr19:56367316-56367366	NH-A	brain:	n/a
25	chr19:56342665-56342715	NHDF-neo	bronchial:	n/a
26	chr19:56346628-56346678	NHDF-neo	bronchial:	n/a
27	chr19:56348889-56348939	SK-N-SH	brain:	n/a
28	chr19:56367316-56367366	NHDF-neo	bronchial:	n/a
29	chr19:56347847-56347897	AG04450	lung:	fetal
30	chr19:56348889-56348939	MCF10A-Er-Src	breast:	n/a
31	chr19:56348889-56348939	NB4	blood:	n/a
32	chr19:56347870-56347920	MCF10A-Er-Src	breast:	n/a
33	chr19:56269246-56269296	SKMC	muscle:	n/a
34	chr19:56367830-56367880	NB4	blood:	n/a
35	chr19:56346743-56346793	HL-60	blood:	n/a
36	chr19:56349119-56349169	T-47D	breast:	n/a
37	chr19:56346743-56346793	RPTEC	kidney:	n/a
38	chr19:56348742-56348792	HCM	heart:	n/a
39	chr19:56249291-56249341	HCM	heart:	n/a
40	chr19:56347722-56347772	T-47D	breast:	n/a
41	chr19:56367830-56367880	NHDF-neo	bronchial:	n/a
42	chr19:56321115-56321165	CMK	blood:	n/a
43	chr19:56250652-56250702	HRE	kidney:	n/a
44	chr19:56367316-56367366	CMK	blood:	n/a
45	chr19:56348742-56348792	HEK293	kidney:	embryo
46	chr19:56349119-56349169	GM19239	blood:	n/a
47	chr19:56250127-56250177	AG10803	skin:	n/a
48	chr19:56363105-56363155	AG04450	lung:	fetal
49	chr19:56364183-56364233	Jurkat	blood:	n/a
50	chr19:56349119-56349169	MCF-7	breast:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56288962..56289563-chr19:56320651..56321410,3	MCF-7	breast:
2	chr19:56321292..56324216-chr19:56328648..56330959,2	K562	blood:
3	chr19:56311206..56314019-chr19:56318458..56321376,2	K562	blood:
4	chr19:56320256..56321150-chr19:56577550..56578288,2	K562	blood:
5	chr19:56271991..56273573-chr19:56281048..56283702,2	K562	blood:
6	chr19:56015535..56016051-chr19:56320998..56321733,2	K562	blood:
7	chr19:56252523..56255492-chr19:56257324..56260762,3	K562	blood:
8	chr19:56154646..56157469-chr19:56320244..56322064,2	K562	blood:
9	chr19:56230205..56232527-chr19:56319829..56322446,2	K562	blood:
10	chr19:56311206..56314019-chr19:56318458..56321376,2	K562	blood:
11	chr19:56252523..56255492-chr19:56257324..56260762,3	K562	blood:
12	chr19:56164701..56165323-chr19:56320540..56321426,2	MCF-7	breast:
13	chr19:56294175..56296046-chr19:56307232..56309273,2	MCF-7	breast:
14	chr19:56288962..56289563-chr19:56320651..56321410,3	MCF-7	breast:
15	chr19:56327095..56328748-chr19:56329446..56331884,2	K562	blood:
16	chr19:56271991..56273573-chr19:56281048..56283702,2	K562	blood:
17	chr19:56143497..56144412-chr19:56320540..56321434,5	K562	blood:
18	chr17:41464575..41466240-chr19:56288867..56290367,2	K562	blood:
19	chr19:56294175..56296046-chr19:56307232..56309273,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFPL4A-1	chr19:56248651-56248966	NONHSAT068080

No data

Variant related genes	Relation type
RFPL4AL1	TF binding region
RN7SKP109	TF binding region
RFPL4AP1	TF binding region
NLRP11	TF binding region
NLRP4	TF binding region
RFPL4A	TF binding region
NLRP9	TF binding region
RFPL4AL1	CpG island
RN7SKP109	CpG island
RFPL4AP1	CpG island
NLRP11	CpG island
NLRP4	CpG island
RFPL4A	CpG island
NLRP9	CpG island
ENSG00000179873	chromatin interactions
ENSG00000267522	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 3052 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3052 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558175237	chr19:56248468-56248469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs541862989	chr19:56248469-56248470	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs184929950	chr19:56248472-56248473	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs189787871	chr19:56248518-56248519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573838900	chr19:56248526-56248527	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs571287225	chr19:56248560-56248561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs538831580	chr19:56248561-56248562	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs371550588	chr19:56248606-56248607	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs532179882	chr19:56248654-56248655	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs555098156	chr19:56248692-56248693	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs571920789	chr19:56248700-56248701	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs114683555	chr19:56248711-56248712	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs368454091	chr19:56248724-56248725	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs182439669	chr19:56248750-56248751	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs532919896	chr19:56248770-56248771	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs543084352	chr19:56248774-56248775	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs34736097	chr19:56248775-56248776	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs10403433	chr19:56248780-56248781	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs550574399	chr19:56248799-56248800	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs10402884	chr19:56248807-56248808	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs549101197	chr19:56248820-56248821	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs8103725	chr19:56248837-56248838	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs115268376	chr19:56248839-56248840	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs112172984	chr19:56248888-56248889	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs370767891	chr19:56249743-56249744	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs141752595	chr19:56249744-56249745	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs559472872	chr19:56249750-56249751	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs201668498	chr19:56249783-56249784	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs189047566	chr19:56249891-56249892	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs565298299	chr19:56249892-56249893	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs10417652	chr19:56249933-56249934	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150560665	chr19:56250170-56250171	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs117513746	chr19:56250653-56250654	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs566316870	chr19:56250699-56250700	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs77318755	chr19:56252193-56252194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs35905323	chr19:56252200-56252201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs190241095	chr19:56252246-56252247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs79822914	chr19:56252270-56252271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs541170870	chr19:56252295-56252296	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs560253045	chr19:56252297-56252298	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532222103	chr19:56252303-56252304	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs11668316	chr19:56252305-56252306	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs562470377	chr19:56252324-56252325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs531190083	chr19:56252351-56252352	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs577135187	chr19:56252789-56252790	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs181739804	chr19:56252790-56252791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs113382229	chr19:56252792-56252793	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs368067786	chr19:56252797-56252798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558823753	chr19:56252806-56252807	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs570490194	chr19:56252833-56252834	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Breast cancer	20409316	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56264400-56265000	Enhancers	Liver	Liver
2	chr19:56264800-56265600	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr19:56265000-56265400	Flanking Active TSS	Liver	Liver
4	chr19:56265000-56266000	Enhancers	Pancreas	Pancrea
5	chr19:56265400-56265600	Enhancers	Liver	Liver
6	chr19:56265400-56265800	Enhancers	Gastric	stomach
7	chr19:56265600-56265800	Flanking Active TSS	Liver	Liver
8	chr19:56265800-56268200	Weak transcription	Liver	Liver
9	chr19:56266000-56266800	Weak transcription	Pancreas	Pancrea
10	chr19:56266800-56267000	Enhancers	Pancreas	Pancrea
11	chr19:56267000-56268200	Weak transcription	Pancreas	Pancrea
12	chr19:56268000-56269800	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr19:56268200-56268400	ZNF genes & repeats	Liver	Liver
14	chr19:56268200-56268400	Enhancers	Pancreas	Pancrea
15	chr19:56268400-56272600	Weak transcription	Liver	Liver
16	chr19:56269800-56270200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr19:56270200-56271800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr19:56272600-56272800	Active TSS	Liver	Liver
19	chr19:56277000-56279600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr19:56278000-56278200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
21	chr19:56279600-56280000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr19:56280000-56281800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr19:56281200-56281800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr19:56293200-56293400	Enhancers	Hela-S3	cervix
25	chr19:56295400-56295600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
26	chr19:56300600-56304000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr19:56306200-56310800	Weak transcription	Pancreas	Pancrea
28	chr19:56307400-56313400	Weak transcription	Liver	Liver
29	chr19:56312000-56313000	Enhancers	GM12878-XiMat	blood
30	chr19:56312800-56313200	Active TSS	Brain Substantia Nigra	brain
31	chr19:56312800-56313400	Enhancers	Primary B cells from peripheral blood	blood
32	chr19:56313000-56313400	Flanking Active TSS	GM12878-XiMat	blood
33	chr19:56313000-56313400	Enhancers	Hela-S3	cervix
34	chr19:56313200-56315600	Weak transcription	Brain Substantia Nigra	brain
35	chr19:56313400-56314200	Enhancers	Liver	Liver
36	chr19:56313800-56314000	Enhancers	Hela-S3	cervix
37	chr19:56315600-56316000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
38	chr19:56315600-56316200	ZNF genes & repeats	Brain Substantia Nigra	brain
39	chr19:56316200-56320800	Weak transcription	Brain Substantia Nigra	brain
40	chr19:56318800-56319800	Weak transcription	Liver	Liver
41	chr19:56319800-56320600	Enhancers	Liver	Liver
42	chr19:56320200-56321000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr19:56320400-56320600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr19:56320400-56321000	ZNF genes & repeats	A549	lung
45	chr19:56320400-56321200	Enhancers	GM12878-XiMat	blood
46	chr19:56320600-56320800	Active TSS	Adipose Nuclei	Adipose
47	chr19:56320600-56320800	Flanking Active TSS	Hela-S3	cervix
48	chr19:56320600-56321000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr19:56320600-56321000	Flanking Active TSS	Liver	Liver
50	chr19:56320600-56321000	Active TSS	Duodenum Mucosa	Duodenum

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