Variant report

Variant	esv3376048
Chromosome Location	chr19:41969544-42022873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:401)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41985894-41986022	K562	blood:	n/a	n/a
2	ARID3A	chr19:41969568-41969577	HepG2	liver:	n/a	n/a
3	ATF1	chr19:41985515-41985820	K562	blood:	n/a	n/a
4	ATF3	chr19:42007044-42007229	K562	blood:	n/a	n/a
5	BACH1	chr19:41985825-41985834	K562	blood:	n/a	n/a
6	BACH1	chr19:42016903-42017186	K562	blood:	n/a	n/a
7	BATF	chr19:41969389-41969829	GM12878	blood:	n/a	n/a
8	BATF	chr19:41969506-41969785	GM12878	blood:	n/a	n/a
9	BATF	chr19:42007315-42007464	GM12878	blood:	n/a	n/a
10	BATF	chr19:42022723-42023153	GM12878	blood:	n/a	n/a
11	BCL11A	chr19:41969464-41969856	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:41969539-41969773	GM12878	blood:	n/a	n/a
13	BCL3	chr19:42016667-42016907	GM12878	blood:	n/a	n/a
14	BCL3	chr19:42016314-42016648	GM12878	blood:	n/a	n/a
15	BCL3	chr19:42016218-42016628	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:41969578-41969860	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:41985631-41985823	K562	blood:	n/a	n/a
18	BHLHE40	chr19:41986254-41986585	K562	blood:	n/a	n/a
19	BHLHE40	chr19:42007430-42007554	K562	blood:	n/a	n/a
20	CBX3	chr19:42007176-42007860	HCT-116	colon:	n/a	n/a
21	CBX3	chr19:41985547-41986099	K562	blood:	n/a	n/a
22	CEBPB	chr19:41992465-41992478	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr19:42022680-42022977	A549	lung:	n/a	chr19:42022803-42022814
24	CEBPB	chr19:42022705-42022860	HepG2	liver:	n/a	chr19:42022803-42022814
25	CEBPB	chr19:41969353-41969755	HepG2	liver:	n/a	chr19:41969517-41969528
26	CEBPB	chr19:41969468-41969606	HepG2	liver:	n/a	chr19:41969517-41969528
27	CEBPB	chr19:41969387-41969721	HepG2	liver:	n/a	chr19:41969517-41969528
28	CEBPB	chr19:41992919-41993068	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:41992986-41993092	IMR90	lung:	n/a	chr19:41993068-41993079
30	CEBPB	chr19:41992947-41993198	A549	lung:	n/a	chr19:41993068-41993079
31	CEBPB	chr19:41969487-41969587	IMR90	lung:	n/a	chr19:41969517-41969528
32	CEBPB	chr19:42022644-42023024	HepG2	liver:	n/a	chr19:42022803-42022814
33	CEBPB	chr19:41969385-41969602	K562	blood:	n/a	chr19:41969517-41969528
34	CEBPB	chr19:41992290-41992562	HepG2	liver:	n/a	n/a
35	CEBPB	chr19:41969394-41969671	K562	blood:	n/a	chr19:41969517-41969528
36	CEBPB	chr19:41969409-41969618	A549	lung:	n/a	chr19:41969517-41969528
37	CEBPB	chr19:41992260-41992553	A549	lung:	n/a	n/a
38	CEBPB	chr19:42022693-42022893	IMR90	lung:	n/a	chr19:42022803-42022814
39	CEBPB	chr19:41969489-41969670	Hela-S3	cervix:	n/a	chr19:41969517-41969528
40	CEBPB	chr19:42022763-42022875	Hela-S3	cervix:	n/a	chr19:42022803-42022814
41	CEBPB	chr19:42022688-42022956	K562	blood:	n/a	chr19:42022803-42022814
42	CEBPB	chr19:41992890-41993261	HepG2	liver:	n/a	chr19:41993068-41993079
43	CTCF	chr19:42022865-42022999	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr19:41969697-41969814	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr19:41984200-41984350	A549	lung:	n/a	chr19:41984245-41984254 chr19:41984245-41984258
46	CTCF	chr19:42012093-42012154	GM10248	blood:	n/a	chr19:42012118-42012131
47	CTCF	chr19:41984380-41984530	GM06990	blood:	n/a	n/a
48	CTCF	chr19:41969900-41970047	A549	lung:	n/a	n/a
49	CTCF	chr19:41969929-41970001	MCF-7	breast:	n/a	n/a
50	CTCF	chr19:42021680-42021830	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42007378-42007428	PrEC	prostate:	n/a
2	chr19:42007378-42007428	GM12891	blood:	n/a
3	chr19:42007378-42007428	PFSK-1	brain:	n/a
4	chr19:42007378-42007428	Caco-2	colon:	n/a
5	chr19:42007378-42007428	PANC-1	pancreas:	n/a
6	chr19:42007378-42007428	HL-60	blood:	n/a
7	chr19:42007378-42007428	NHDF-neo	bronchial:	n/a
8	chr19:42007378-42007428	RPTEC	kidney:	n/a
9	chr19:42007378-42007428	Jurkat	blood:	n/a
10	chr19:42007378-42007428	HUVEC	blood vessel:	n/a
11	chr19:42007378-42007428	CMK	blood:	n/a
12	chr19:42007378-42007428	HMEC	breast:	n/a
13	chr19:42007378-42007428	NHBE	bronchial:	n/a
14	chr19:42007378-42007428	U87	brain:	n/a
15	chr19:42007378-42007428	NH-A	brain:	n/a
16	chr19:42007378-42007428	H1-hESC	embryonic stem cell:	embryo
17	chr19:42007378-42007428	GM12892	blood:	n/a
18	chr19:42007378-42007428	SAEC	small airway:	n/a
19	chr19:42007378-42007428	ECC-1	luminal epithelium:	n/a
20	chr19:42007378-42007428	NB4	blood:	n/a
21	chr19:42007378-42007428	HNPCEpiC	eye:	n/a
22	chr19:42007378-42007428	BJ	skin:	n/a
23	chr19:42007378-42007428	HCF	heart:	n/a
24	chr19:42007378-42007428	MCF-7	breast:	n/a
25	chr19:42007378-42007428	HCPEpiC	choroid plexus:	n/a
26	chr19:42007378-42007428	BE2_C	brain:	n/a
27	chr19:42007378-42007428	AG09309	skin:	n/a
28	chr19:42007378-42007428	GM06990	blood:	n/a
29	chr19:42007378-42007428	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:42007378-42007428	K562	blood:	n/a
31	chr19:42007378-42007428	HRE	kidney:	n/a
32	chr19:42007378-42007428	AG04449	skin:	fetal
33	chr19:42007378-42007428	HIPEpiC	eye:	n/a
34	chr19:42007378-42007428	HAEpiC	amniotic membrane:	n/a
35	chr19:42007378-42007428	HepG2	liver:	n/a
36	chr19:42007378-42007428	AoSMC	blood vessel:	n/a
37	chr19:42007378-42007428	HRCEpiC	kidney:	n/a
38	chr19:42007378-42007428	HEEpiC	esophagus:	n/a
39	chr19:42007378-42007428	ProgFib	skin:	n/a
40	chr19:42007378-42007428	HCM	heart:	n/a
41	chr19:42007378-42007428	GM12878	blood:	n/a
42	chr19:42007378-42007428	SK-N-MC	brain:	n/a
43	chr19:42007378-42007428	AG10803	skin:	n/a
44	chr19:42007378-42007428	LNCaP	prostate:	n/a
45	chr19:42007378-42007428	HEK293	kidney:	embryo
46	chr19:42007378-42007428	T-47D	breast:	n/a
47	chr19:42007378-42007428	MCF10A-Er-Src	breast:	n/a
48	chr19:42007378-42007428	NT2-D1	testis:	n/a
49	chr19:42007378-42007428	HRPEpiC	eye:	n/a
50	chr19:42007378-42007428	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:41979781..41981328-chr19:41984407..41987088,2	K562	blood:
2	chr19:41944061..41946977-chr19:42000429..42002001,2	K562	blood:
3	chr19:41970790..41973417-chr19:42039173..42040939,2	K562	blood:
4	chr19:41944280..41946189-chr19:42004239..42006678,2	K562	blood:
5	chr19:41945911..41947481-chr19:41988789..41990689,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000249527
2	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000267107.2
3	lnc-ATP5SL-1	chr19:41980371-41980444	ENSG00000267107.2
4	lnc-ATP5SL-1	chr19:41984451-41985192	NONHSAT066458
5	lnc-ATP5SL-1	chr19:42000448-42001335	ENSG00000267107.2
6	lnc-ATP5SL-1	chr19:42001210-42001335	NONHSAT066451
7	lnc-ATP5SL-1	chr19:41984989-41985049	ENSG00000267107.2
8	lnc-ATP5SL-1	chr19:42001210-42001335	NONHSAT066458
9	lnc-ATP5SL-1	chr19:42000448-42001335	ENSG00000249527
10	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000249527
11	lnc-ATP5SL-1	chr19:41984989-41985192	NONHSAT066451
12	lnc-ATP5SL-1	chr19:41984989-41985192	NONHSAT066453
13	lnc-ATP5SL-1	chr19:42006494-42006545	NONHSAT066458
14	lnc-ATP5SL-1	chr19:42006494-42006540	NONHSAT066451
15	lnc-ATP5SL-1	chr19:42006494-42006559	ENSG00000249527
16	lnc-ATP5SL-1	chr19:42001210-42001338	NONHSAT066459
17	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000249527
18	lnc-ATP5SL-1	chr19:41984989-41985049	ENSG00000267107.2
19	lnc-ATP5SL-1	chr19:41985040-41985192	NONHSAT066459
20	lnc-ATP5SL-1	chr19:41984451-41985192	NONHSAT066457
21	lnc-ATP5SL-1	chr19:42001210-42001335	ENSG00000267107.2
22	lnc-ATP5SL-1	chr19:42006494-42006539	ENSG00000267107.2
23	lnc-ATP5SL-1	chr19:42006494-42006538	NONHSAT066457
24	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000267107.2
25	lnc-ATP5SL-1	chr19:41984989-41985051	ENSG00000267107.2
26	lnc-ATP5SL-1	chr19:42006494-42006554	NONHSAT066453
27	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000249527

No data

Variant related genes	Relation type
ENSG00000267107	TF binding region
ENSG00000268034	TF binding region
ENSG00000267107	CpG island
ENSG00000268034	CpG island
ENSG00000105341	chromatin interactions
ENSG00000267107	chromatin interactions
TMED7	miRNA target sites
EZH2	miRNA target sites
SPTBN1	miRNA target sites
CNN3	miRNA target sites
PRSS21	miRNA target sites
CHST11	miRNA target sites

Extended variants
information (count: 1709 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587720503	chr19:41969555-41969556	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370907161	chr19:41969559-41969560	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182852934	chr19:41969560-41969561	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372833276	chr19:41969622-41969623	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs10406791	chr19:41969678-41969679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs587601880	chr19:41969686-41969687	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs587668174	chr19:41969705-41969706	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs187519591	chr19:41969706-41969707	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs145698519	chr19:41969708-41969709	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs148939319	chr19:41969790-41969791	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs587772975	chr19:41969814-41969815	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587754172	chr19:41969837-41969838	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377055751	chr19:41969857-41969858	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12459980	chr19:41969858-41969859	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs587683155	chr19:41969866-41969867	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73049161	chr19:41969867-41969868	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111603372	chr19:41969870-41969871	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114383587	chr19:41969881-41969882	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587686122	chr19:41969885-41969886	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191104638	chr19:41969890-41969891	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587636837	chr19:41969895-41969896	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374063993	chr19:41969920-41969921	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587753623	chr19:41969941-41969942	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112407865	chr19:41969942-41969943	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371117588	chr19:41969955-41969956	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376175415	chr19:41969968-41969969	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587611947	chr19:41969971-41969972	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368214873	chr19:41969972-41969973	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150997718	chr19:41969973-41969974	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587617067	chr19:41969975-41969976	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78519520	chr19:41969991-41969992	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35589190	chr19:41969992-41969993	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372758514	chr19:41969993-41969994	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73049162	chr19:41970010-41970011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187815406	chr19:41970023-41970024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587652044	chr19:41970024-41970025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587673809	chr19:41970117-41970118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587724215	chr19:41970121-41970122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587630037	chr19:41970132-41970133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587680926	chr19:41970146-41970147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75870800	chr19:41970147-41970148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192341366	chr19:41970155-41970156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370874522	chr19:41970178-41970179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587753441	chr19:41970179-41970180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141123128	chr19:41970183-41970184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373910692	chr19:41970184-41970185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144738806	chr19:41970201-41970202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73931499	chr19:41970204-41970205	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs185134418	chr19:41970223-41970224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587617000	chr19:41970230-41970231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	18511947	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41968400-41970800	Enhancers	Primary B cells from peripheral blood	blood
2	chr19:41968400-41982200	Weak transcription	HUVEC	blood vessel
3	chr19:41969000-41970600	Enhancers	Primary B cells from cord blood	blood
4	chr19:41969200-41969600	Flanking Active TSS	GM12878-XiMat	blood
5	chr19:41969200-41969600	Enhancers	HepG2	liver
6	chr19:41969200-41969800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr19:41969200-41970200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr19:41969400-41969600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
9	chr19:41969400-41969600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr19:41969600-41969800	Enhancers	GM12878-XiMat	blood
11	chr19:41969800-41970000	Flanking Active TSS	GM12878-XiMat	blood
12	chr19:41969800-41970200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr19:41970000-41970200	Enhancers	Lung	lung
14	chr19:41970000-41970600	Enhancers	GM12878-XiMat	blood
15	chr19:41973000-41973600	Bivalent/Poised TSS	A549	lung
16	chr19:41976600-41976800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr19:41976600-41976800	Enhancers	Spleen	Spleen
18	chr19:41976800-41978800	Weak transcription	Spleen	Spleen
19	chr19:41978800-41979600	Enhancers	Spleen	Spleen
20	chr19:41979600-41982200	Weak transcription	Spleen	Spleen
21	chr19:41982200-41982400	Enhancers	Spleen	Spleen
22	chr19:41982200-41982800	Enhancers	GM12878-XiMat	blood
23	chr19:41982200-41983200	Enhancers	Primary B cells from peripheral blood	blood
24	chr19:41982200-41983400	Enhancers	HUVEC	blood vessel
25	chr19:41982400-41982800	Weak transcription	Spleen	Spleen
26	chr19:41982400-41983800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr19:41982800-41983000	Enhancers	Left Ventricle	heart
28	chr19:41982800-41983000	Enhancers	Right Atrium	heart
29	chr19:41982800-41983000	Enhancers	Spleen	Spleen
30	chr19:41982800-41983000	Flanking Active TSS	GM12878-XiMat	blood
31	chr19:41982800-41983600	Enhancers	Lung	lung
32	chr19:41983000-41983600	Genic enhancers	Left Ventricle	heart
33	chr19:41983000-41984000	Weak transcription	Right Atrium	heart
34	chr19:41983000-41986400	Weak transcription	Spleen	Spleen
35	chr19:41983400-41984000	Enhancers	Fetal Muscle Leg	muscle
36	chr19:41983400-41986400	Flanking Active TSS	HUVEC	blood vessel
37	chr19:41983600-41984200	Enhancers	Left Ventricle	heart
38	chr19:41983600-41985200	Active TSS	Lung	lung
39	chr19:41983800-41984600	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
40	chr19:41983800-41985000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr19:41984000-41984200	Bivalent Enhancer	Adipose Nuclei	Adipose
42	chr19:41984000-41984200	Weak transcription	Fetal Muscle Leg	muscle
43	chr19:41984000-41984200	Enhancers	Right Atrium	heart
44	chr19:41984200-41984400	Bivalent/Poised TSS	Fetal Stomach	stomach
45	chr19:41984200-41984400	Flanking Active TSS	Left Ventricle	heart
46	chr19:41984200-41984800	Bivalent/Poised TSS	Right Ventricle	heart
47	chr19:41984200-41985000	Active TSS	Fetal Muscle Leg	muscle
48	chr19:41984200-41985600	Active TSS	Right Atrium	heart
49	chr19:41984200-41986400	Active TSS	Ovary	ovary
50	chr19:41984400-41984600	Active TSS	Adipose Nuclei	Adipose

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