Variant report

Variant	nsv911474
Chromosome Location	chr19:23943243-24082673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1067)
CpG islands
(count:675)
Chromatin interactive
region (count:14)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1067 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:23946565-23946828	K562	blood:	n/a	n/a
2	ARID3A	chr19:23953533-23953728	K562	blood:	n/a	n/a
3	ATF1	chr19:24006791-24007164	K562	blood:	n/a	n/a
4	ATF1	chr19:23958138-23958329	K562	blood:	n/a	n/a
5	BACH1	chr19:24000521-24000697	K562	blood:	n/a	n/a
6	BATF	chr19:23967036-23967332	GM12878	blood:	n/a	n/a
7	BATF	chr19:23955417-23955716	GM12878	blood:	n/a	n/a
8	BATF	chr19:23955472-23955714	GM12878	blood:	n/a	n/a
9	BATF	chr19:23967080-23967345	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:23945754-23945986	K562	blood:	n/a	n/a
11	BHLHE40	chr19:23943218-23943418	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:24006925-24007160	K562	blood:	n/a	n/a
13	BHLHE40	chr19:23968376-23968383	K562	blood:	n/a	n/a
14	CBX3	chr19:24006670-24007006	K562	blood:	n/a	n/a
15	CBX3	chr19:24006626-24007181	K562	blood:	n/a	n/a
16	CBX3	chr19:23945432-23946054	K562	blood:	n/a	n/a
17	CCNT2	chr19:23945563-23946451	K562	blood:	n/a	n/a
18	CEBPB	chr19:23956978-23957871	A549	lung:	n/a	n/a
19	CEBPB	chr19:23962499-23962745	IMR90	lung:	n/a	n/a
20	CEBPB	chr19:24007084-24007141	K562	blood:	n/a	n/a
21	CEBPB	chr19:23954195-23954412	HepG2	liver:	n/a	n/a
22	CEBPB	chr19:23961586-23961803	K562	blood:	n/a	n/a
23	CEBPB	chr19:23954779-23955040	A549	lung:	n/a	n/a
24	CEBPB	chr19:23952624-23952715	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:23951625-23951915	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:23971312-23971526	HepG2	liver:	n/a	chr19:23971380-23971391
27	CEBPB	chr19:23964650-23965334	A549	lung:	n/a	n/a
28	CEBPB	chr19:23945825-23946100	MCF-7	breast:	n/a	n/a
29	CEBPB	chr19:24048053-24048211	A549	lung:	n/a	n/a
30	CEBPB	chr19:23966086-23966642	K562	blood:	n/a	chr19:23966205-23966216 chr19:23966237-23966248
31	CEBPB	chr19:24004841-24005271	MCF-7	breast:	n/a	n/a
32	CEBPB	chr19:23962419-23962766	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:23965636-23965845	IMR90	lung:	n/a	chr19:23965729-23965740
34	CEBPB	chr19:23969813-23970335	MCF-7	breast:	n/a	n/a
35	CEBPB	chr19:24072664-24072864	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:23959151-23959571	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:23959197-23959542	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:23969400-23969658	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:23959786-23960810	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:24065481-24065571	HepG2	liver:	n/a	n/a
41	CEBPB	chr19:23945549-23946148	K562	blood:	n/a	n/a
42	CEBPB	chr19:23964661-23965311	HepG2	liver:	n/a	n/a
43	CEBPB	chr19:24005510-24006011	MCF-7	breast:	n/a	n/a
44	CEBPB	chr19:23952594-23952832	K562	blood:	n/a	n/a
45	CEBPB	chr19:23966087-23966409	IMR90	lung:	n/a	chr19:23966205-23966216 chr19:23966237-23966248
46	CEBPB	chr19:24000487-24000738	K562	blood:	n/a	n/a
47	CEBPB	chr19:23965616-23965852	A549	lung:	n/a	chr19:23965729-23965740
48	CEBPB	chr19:23992206-23992260	K562	blood:	n/a	n/a
49	CEBPB	chr19:23959200-23959410	K562	blood:	n/a	n/a
50	CEBPB	chr19:24072689-24072942	A549	lung:	n/a	n/a

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23945203-23945253	U87	brain:	n/a
2	chr19:23945722-23945772	HL-60	blood:	n/a
3	chr19:23944615-23944665	CMK	blood:	n/a
4	chr19:23945996-23946046	NHBE	bronchial:	n/a
5	chr19:23945203-23945253	U87	brain:	n/a
6	chr19:23945722-23945772	HL-60	blood:	n/a
7	chr19:23944615-23944665	CMK	blood:	n/a
8	chr19:23945996-23946046	NHBE	bronchial:	n/a
9	chr19:23945659-23945709	Jurkat	blood:	n/a
10	chr19:23945641-23945691	SAEC	small airway:	n/a
11	chr19:23945903-23945953	Hepatocyte	liver:	n/a
12	chr19:23945743-23945793	AG04449	skin:	fetal
13	chr19:23946205-23946255	ovcar-3	ovarian:	n/a
14	chr19:23945203-23945253	PFSK-1	brain:	n/a
15	chr19:23945659-23945709	GM12892	blood:	n/a
16	chr19:23945472-23945522	AoSMC	blood vessel:	n/a
17	chr19:23945472-23945522	SK-N-SH	brain:	n/a
18	chr19:23945722-23945772	NHDF-neo	bronchial:	n/a
19	chr19:23945743-23945793	K562	blood:	n/a
20	chr19:23945743-23945793	HPAEpiC	pulmonary alveolar:	n/a
21	chr19:23945722-23945772	IMR90	lung:	fetal
22	chr19:23945996-23946046	SK-N-SH_RA	brain:	n/a
23	chr19:23945743-23945793	GM12891	blood:	n/a
24	chr19:23945996-23946046	SAEC	small airway:	n/a
25	chr19:23945641-23945691	RPTEC	kidney:	n/a
26	chr19:23945203-23945253	Hela-S3	cervix:	n/a
27	chr19:23945472-23945522	IMR90	lung:	fetal
28	chr19:23945903-23945953	AG09309	skin:	n/a
29	chr19:23945472-23945522	PANC-1	pancreas:	n/a
30	chr19:23945641-23945691	H1-hESC	embryonic stem cell:	embryo
31	chr19:23944615-23944665	ECC-1	luminal epithelium:	n/a
32	chr19:23945641-23945691	NH-A	brain:	n/a
33	chr19:23945641-23945691	U87	brain:	n/a
34	chr19:23945641-23945691	HUVEC	blood vessel:	n/a
35	chr19:23945472-23945522	A549	lung:	n/a
36	chr19:23945761-23945811	BE2_C	brain:	n/a
37	chr19:23945472-23945522	ECC-1	luminal epithelium:	n/a
38	chr19:23945659-23945709	HCPEpiC	choroid plexus:	n/a
39	chr19:23945659-23945709	AoSMC	blood vessel:	n/a
40	chr19:23945472-23945522	GM06990	blood:	n/a
41	chr19:23945761-23945811	Hepatocyte	liver:	n/a
42	chr19:23946205-23946255	HMEC	breast:	n/a
43	chr19:23945641-23945691	HIPEpiC	eye:	n/a
44	chr19:23945996-23946046	U87	brain:	n/a
45	chr19:23945722-23945772	HEEpiC	esophagus:	n/a
46	chr19:23945641-23945691	SKMC	muscle:	n/a
47	chr19:23945472-23945522	AG10803	skin:	n/a
48	chr19:23945996-23946046	CMK	blood:	n/a
49	chr19:23945903-23945953	HL-60	blood:	n/a
50	chr19:23945641-23945691	SK-N-MC	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:24000616..24002168-chr19:24002694..24005183,2	MCF-7	breast:
2	chr19:23990207..23992454-chr19:24002314..24004892,2	K562	blood:
3	chr19:23946413..23950001-chr19:23953368..23955533,3	K562	blood:
4	chr19:23956310..23957870-chr19:23960230..23962213,2	K562	blood:
5	chr19:23944623..23946640-chr19:23952768..23956450,3	MCF-7	breast:
6	chr19:23946413..23950001-chr19:23953368..23955533,3	K562	blood:
7	chr19:24000616..24002168-chr19:24002694..24005183,2	MCF-7	breast:
8	chr19:23990207..23992454-chr19:24002314..24004892,2	K562	blood:
9	chr19:24046219..24048369-chr19:24050993..24053040,2	MCF-7	breast:
10	chr19:23956310..23957870-chr19:23960230..23962213,2	K562	blood:
11	chr19:23947709..23949776-chr19:23958415..23961237,2	K562	blood:
12	chr19:23947709..23949776-chr19:23958415..23961237,2	K562	blood:
13	chr19:24046219..24048369-chr19:24050993..24053040,2	MCF-7	breast:
14	chr19:23940633..23942866-chr19:23945047..23947463,3	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPSAP58-3	chr19:24051557-24054170	NONHSAT063941
2	lnc-RPSAP58-2	chr19:23945814-23945936	NONHSAT063934
3	lnc-RPSAP58-2	chr19:23964883-23965301	NONHSAT063935
4	lnc-ZNF681-3	chr19:23981726-23982279	NONHSAT063937
5	lnc-RPSAP58-2	chr19:23990628-23990741	NONHSAT063935
6	lnc-RPSAP58-2	chr19:24014399-24014998	NONHSAT063934
7	lnc-RPSAP58-2	chr19:23991521-23991616	NONHSAT063933
8	lnc-ZNF726-1	chr19:23969947-23970608	ENSG00000250795
9	lnc-ZNF726-1	chr19:23968384-23969193	ENSG00000250795
10	lnc-RPSAP58-2	chr19:24014399-24014998	NONHSAT063933
11	lnc-RPSAP58-2	chr19:23991521-23992317	NONHSAT063935
12	lnc-RPSAP58-3	chr19:24051517-24052736	NONHSAT063942
13	lnc-ZNF726-1	chr19:23969576-23969850	ENSG00000250795
14	lnc-RPSAP58-2	chr19:23990628-23990741	NONHSAT063933
15	lnc-RPSAP58-3	chr19:24047842-24047979	NONHSAT063941
16	lnc-RPSAP58-3	chr19:24053508-24054170	NONHSAT063942
17	lnc-RPSAP58-2	chr19:23945746-23945936	NONHSAT063933

No data

Variant related genes	Relation type
ENSG00000269662	TF binding region
ENSG00000267924	TF binding region
ZNF681	TF binding region
ENSG00000233836	TF binding region
RPSAP58	TF binding region
ENSG00000269662	CpG island
ENSG00000267924	CpG island
ZNF681	CpG island
ENSG00000233836	CpG island
RPSAP58	CpG island
ENSG00000196172	chromatin interactions
ENSG00000205246	chromatin interactions
ENSG00000233836	chromatin interactions
NOTCH2	miRNA target sites
TIAL1	miRNA target sites
GATA6	miRNA target sites

Extended variants
information (count: 6309 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:6309 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4530290	chr19:23943243-23943244	Weak transcription Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563412745	chr19:23943324-23943325	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs530385441	chr19:23943362-23943363	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs548967329	chr19:23943368-23943369	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs567958918	chr19:23943424-23943425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72086579	chr19:23943451-23943452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201928342	chr19:23943467-23943468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200001940	chr19:23943468-23943469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150519323	chr19:23943469-23943470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7507436	chr19:23943471-23943472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11329521	chr19:23943472-23943473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7249193	chr19:23943473-23943474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377137795	chr19:23943474-23943475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4517910	chr19:23943488-23943489	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs188164371	chr19:23943503-23943504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547949349	chr19:23943536-23943537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192011778	chr19:23943562-23943563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs36046070	chr19:23943693-23943694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539258514	chr19:23943697-23943698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62118631	chr19:23943716-23943717	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs569341278	chr19:23943740-23943741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536203195	chr19:23943760-23943761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140295220	chr19:23943811-23943812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372085043	chr19:23943812-23943813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139519150	chr19:23943816-23943817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56122715	chr19:23943819-23943820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111863013	chr19:23943820-23943821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113113139	chr19:23943821-23943822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56069620	chr19:23943830-23943831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199508490	chr19:23943832-23943833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146145392	chr19:23943844-23943845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139446350	chr19:23943845-23943846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs56087805	chr19:23943851-23943852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369051712	chr19:23943852-23943853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573585578	chr19:23943854-23943855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71309646	chr19:23943855-23943856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs55762003	chr19:23943867-23943868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200628071	chr19:23943880-23943881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143553360	chr19:23943890-23943891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs56074018	chr19:23943891-23943892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113359144	chr19:23943902-23943903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397740588	chr19:23943905-23943906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62118633	chr19:23943942-23943943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566165917	chr19:23943949-23943950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202182101	chr19:23943955-23943956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146244433	chr19:23943968-23943969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139367994	chr19:23944017-23944018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12979066	chr19:23944072-23944073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs144145312	chr19:23944078-23944079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372575353	chr19:23944097-23944098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23941800-23945000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:23941800-23945000	Weak transcription	Aorta	Aorta
3	chr19:23941800-23945000	Weak transcription	Esophagus	oesophagus
4	chr19:23941800-23945000	Weak transcription	Placenta	Placenta
5	chr19:23941800-23945000	Weak transcription	Pancreas	Pancrea
6	chr19:23941800-23945200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr19:23941800-23945200	Weak transcription	Spleen	Spleen
8	chr19:23941800-23945400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr19:23941800-23945600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:23941800-23945600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr19:23942000-23944400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr19:23942000-23945000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr19:23942000-23945000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr19:23942000-23945000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr19:23942000-23945200	Weak transcription	Adipose Nuclei	Adipose
16	chr19:23942000-23945200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr19:23942000-23945200	Weak transcription	Brain Substantia Nigra	brain
18	chr19:23942000-23945200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr19:23942000-23945200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr19:23942000-23945400	Weak transcription	Fetal Kidney	kidney
21	chr19:23942000-23945400	Weak transcription	HSMMtube	muscle
22	chr19:23942200-23943400	Enhancers	Primary B cells from peripheral blood	blood
23	chr19:23942200-23943400	Enhancers	Primary T cells from cord blood	blood
24	chr19:23942200-23943400	Enhancers	Primary T cells fromperipheralblood	blood
25	chr19:23942200-23943400	Enhancers	Dnd41	blood
26	chr19:23942200-23945000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr19:23942200-23945000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr19:23942200-23945000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr19:23942200-23945000	Weak transcription	Fetal Stomach	stomach
30	chr19:23942200-23945200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:23942200-23945200	Weak transcription	Primary B cells from cord blood	blood
32	chr19:23942200-23945200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr19:23942200-23945200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr19:23942200-23945200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr19:23942200-23945200	Weak transcription	Brain Angular Gyrus	brain
36	chr19:23942200-23945200	Weak transcription	Brain Hippocampus Middle	brain
37	chr19:23942200-23945200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:23942200-23945200	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr19:23942200-23945200	Weak transcription	Right Ventricle	heart
40	chr19:23942200-23945200	Weak transcription	Stomach Smooth Muscle	stomach
41	chr19:23942200-23945400	Weak transcription	Brain Germinal Matrix	brain
42	chr19:23942200-23945400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr19:23942200-23945400	Weak transcription	Fetal Brain Male	brain
44	chr19:23942200-23945400	Weak transcription	Fetal Thymus	thymus
45	chr19:23942200-23945400	Weak transcription	Left Ventricle	heart
46	chr19:23942200-23945400	Weak transcription	K562	blood
47	chr19:23942200-23945600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr19:23942200-23945600	Weak transcription	Gastric	stomach
49	chr19:23942200-23945600	Weak transcription	Lung	lung
50	chr19:23942200-23945800	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links