Variant report

Variant	esv2760514
Chromosome Location	chr19:21746688-21766892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:141)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:141 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21756597-21757002	K562	blood:	n/a	n/a
2	ATF1	chr19:21756594-21757067	K562	blood:	n/a	n/a
3	ATF3	chr19:21756520-21757045	K562	blood:	n/a	n/a
4	BHLHE40	chr19:21756673-21757583	K562	blood:	n/a	n/a
5	BHLHE40	chr19:21748929-21749238	K562	blood:	n/a	chr19:21749052-21749073 chr19:21749056-21749069
6	CBX3	chr19:21756514-21757083	K562	blood:	n/a	n/a
7	CEBPB	chr19:21756680-21757218	K562	blood:	n/a	n/a
8	CEBPB	chr19:21756603-21757299	K562	blood:	n/a	n/a
9	CEBPB	chr19:21750808-21751049	K562	blood:	n/a	n/a
10	CEBPB	chr19:21759510-21759606	K562	blood:	n/a	n/a
11	CEBPB	chr19:21756463-21757311	K562	blood:	n/a	n/a
12	CEBPB	chr19:21750847-21750982	K562	blood:	n/a	n/a
13	CHD2	chr19:21752031-21752238	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr19:21756576-21757234	K562	blood:	n/a	n/a
15	CREB1	chr19:21756465-21757280	K562	blood:	n/a	n/a
16	CTCF	chr19:21764774-21764931	K562	blood:	n/a	n/a
17	CTCF	chr19:21764680-21764830	K562	blood:	n/a	n/a
18	CTCF	chr19:21764536-21764601	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr19:21757218-21757312	Lung_OC	lung:	n/a	n/a
20	CTCF	chr19:21753960-21754110	GM12865	blood:	n/a	n/a
21	CUX1	chr19:21756568-21756943	K562	blood:	n/a	n/a
22	CUX1	chr19:21759134-21759150	GM12878	blood:	n/a	n/a
23	E2F4	chr19:21750186-21750225	MCF10A-Er-Src	breast:	n/a	n/a
24	EGR1	chr19:21756699-21757045	K562	blood:	n/a	n/a
25	EGR1	chr19:21756687-21757036	K562	blood:	n/a	n/a
26	ELF1	chr19:21751794-21752441	MCF-7	breast:	n/a	n/a
27	ELF1	chr19:21751768-21752387	MCF-7	breast:	n/a	n/a
28	EP300	chr19:21749022-21749165	K562	blood:	n/a	n/a
29	EP300	chr19:21756584-21757170	K562	blood:	n/a	n/a
30	EP300	chr19:21762482-21762569	GM12878	blood:	n/a	n/a
31	FOS	chr19:21748977-21749159	MCF10A-Er-Src	breast:	n/a	n/a
32	FOSL1	chr19:21756741-21757060	K562	blood:	n/a	chr19:21756822-21756833
33	FOSL1	chr19:21756681-21757013	K562	blood:	n/a	chr19:21756822-21756833
34	FOXA2	chr19:21750825-21751193	A549	lung:	n/a	n/a
35	GABPA	chr19:21751741-21752336	MCF-7	breast:	n/a	n/a
36	GABPA	chr19:21751655-21752522	MCF-7	breast:	n/a	n/a
37	HCFC1	chr19:21756670-21757018	K562	blood:	n/a	n/a
38	HEY1	chr19:21751803-21752127	HepG2	liver:	n/a	n/a
39	HEY1	chr19:21751782-21752096	K562	blood:	n/a	n/a
40	HEY1	chr19:21751817-21752053	K562	blood:	n/a	n/a
41	HEY1	chr19:21751841-21751988	HepG2	liver:	n/a	n/a
42	IRF1	chr19:21757706-21757716	K562	blood:	n/a	n/a
43	IRF1	chr19:21756643-21757004	K562	blood:	n/a	n/a
44	JUN	chr19:21756636-21757082	K562	blood:	n/a	n/a
45	JUN	chr19:21756402-21757858	K562	blood:	n/a	chr19:21757615-21757628
46	JUN	chr19:21756642-21756999	K562	blood:	n/a	n/a
47	JUN	chr19:21755367-21755523	HepG2	liver:	n/a	chr19:21755447-21755460
48	JUN	chr19:21756645-21757073	K562	blood:	n/a	n/a
49	JUN	chr19:21757506-21757726	HepG2	liver:	n/a	chr19:21757615-21757628
50	JUN	chr19:21756654-21756875	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21766543-21766593	MCF10A-Er-Src	breast:	n/a
2	chr19:21766543-21766593	Hela-S3	cervix:	n/a
3	chr19:21766543-21766593	GM06990	blood:	n/a
4	chr19:21766543-21766593	Jurkat	blood:	n/a
5	chr19:21766543-21766593	GM12878	blood:	n/a
6	chr19:21766543-21766593	HL-60	blood:	n/a
7	chr19:21766543-21766593	AG10803	skin:	n/a
8	chr19:21766543-21766593	SK-N-SH_RA	brain:	n/a
9	chr19:21766543-21766593	T-47D	breast:	n/a
10	chr19:21766543-21766593	HAEpiC	amniotic membrane:	n/a
11	chr19:21766543-21766593	HRPEpiC	eye:	n/a
12	chr19:21766543-21766593	RPTEC	kidney:	n/a
13	chr19:21766543-21766593	MCF-7	breast:	n/a
14	chr19:21766543-21766593	SAEC	small airway:	n/a
15	chr19:21766543-21766593	AG04449	skin:	fetal
16	chr19:21766543-21766593	HRCEpiC	kidney:	n/a
17	chr19:21766543-21766593	Hepatocyte	liver:	n/a
18	chr19:21766543-21766593	Caco-2	colon:	n/a
19	chr19:21766543-21766593	HCM	heart:	n/a
20	chr19:21766543-21766593	ProgFib	skin:	n/a
21	chr19:21766543-21766593	CMK	blood:	n/a
22	chr19:21766543-21766593	HIPEpiC	eye:	n/a
23	chr19:21766543-21766593	NT2-D1	testis:	n/a
24	chr19:21766543-21766593	K562	blood:	n/a
25	chr19:21766543-21766593	AG09319	gingival:	n/a
26	chr19:21766543-21766593	SK-N-SH	brain:	n/a
27	chr19:21766543-21766593	A549	lung:	n/a
28	chr19:21766543-21766593	NHBE	bronchial:	n/a
29	chr19:21766543-21766593	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:21766543-21766593	HUVEC	blood vessel:	n/a
31	chr19:21766543-21766593	HEEpiC	esophagus:	n/a
32	chr19:21766543-21766593	HepG2	liver:	n/a
33	chr19:21766543-21766593	GM12891	blood:	n/a
34	chr19:21766543-21766593	NHDF-neo	bronchial:	n/a
35	chr19:21766543-21766593	ovcar-3	ovarian:	n/a
36	chr19:21766543-21766593	AoSMC	blood vessel:	n/a
37	chr19:21766543-21766593	PANC-1	pancreas:	n/a
38	chr19:21766543-21766593	H1-hESC	embryonic stem cell:	embryo
39	chr19:21766543-21766593	BJ	skin:	n/a
40	chr19:21766543-21766593	BE2_C	brain:	n/a
41	chr19:21766543-21766593	IMR90	lung:	fetal
42	chr19:21766543-21766593	U87	brain:	n/a
43	chr19:21766543-21766593	AG04450	lung:	fetal
44	chr19:21766543-21766593	SKMC	muscle:	n/a
45	chr19:21766543-21766593	AG09309	skin:	n/a
46	chr19:21766543-21766593	NB4	blood:	n/a
47	chr19:21766543-21766593	HCF	heart:	n/a
48	chr19:21766543-21766593	GM19239	blood:	n/a
49	chr19:21766543-21766593	GM12892	blood:	n/a
50	chr19:21766543-21766593	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
2	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
3	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
4	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF100-2	chr19:21754050-21754341	NONHSAT063727
2	lnc-ZNF100-3	chr19:21744136-21747283	XLOC_013263
3	lnc-ZNF100-2	chr19:21753139-21754341	ENSG00000249473
4	lnc-ZNF100-3	chr19:21748631-21748673	XLOC_013263
5	lnc-ZNF100-2	chr19:21753624-21754341	ENSG00000268555.1
6	lnc-ZNF100-2	chr19:21752904-21754341	NONHSAT063726
7	lnc-ZNF100-3	chr19:21751906-21752039	ENSG00000268081.1
8	lnc-ZNF100-8	chr19:21763358-21765406	NONHSAT063728
9	lnc-ZNF100-3	chr19:21747057-21747283	XLOC_013263
10	lnc-ZNF100-3	chr19:21751906-21752048	XLOC_013263
11	lnc-ZNF100-2	chr19:21762538-21762616	NONHSAT063727

No data

Variant related genes	Relation type
ENSG00000268081	TF binding region
ENSG00000268081	CpG island

Extended variants
information (count: 1306 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:1306 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371380854	chr19:21746709-21746710	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs73023898	chr19:21746723-21746724	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs73929311	chr19:21746747-21746748	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs533094379	chr19:21746748-21746749	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs73023899	chr19:21746755-21746756	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs539064106	chr19:21746765-21746766	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs80331924	chr19:21746786-21746787	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs73023902	chr19:21746798-21746799	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs200762608	chr19:21746808-21746809	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs112965467	chr19:21746815-21746816	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs202172475	chr19:21746837-21746838	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs200837344	chr19:21746846-21746847	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs201577246	chr19:21746870-21746871	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs199935914	chr19:21746876-21746877	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs75280480	chr19:21746935-21746936	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs572792978	chr19:21746965-21746966	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs201311904	chr19:21746967-21746968	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs142457126	chr19:21746972-21746973	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs530642442	chr19:21746988-21746989	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs139740465	chr19:21747008-21747009	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs567561023	chr19:21747023-21747024	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs534700064	chr19:21747051-21747052	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs553380201	chr19:21747056-21747057	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs571629657	chr19:21747057-21747058	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs539168463	chr19:21747117-21747118	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs185588690	chr19:21747145-21747146	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs566313726	chr19:21747146-21747147	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs575878593	chr19:21747166-21747167	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs190302769	chr19:21747173-21747174	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs182972605	chr19:21747178-21747179	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs187606573	chr19:21747207-21747208	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs535116608	chr19:21747214-21747215	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs540665013	chr19:21747228-21747229	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs145254667	chr19:21747229-21747230	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs191946845	chr19:21747243-21747244	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs558015906	chr19:21747286-21747287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74975845	chr19:21747299-21747300	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544677995	chr19:21747327-21747328	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563049534	chr19:21747337-21747338	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs202155396	chr19:21747347-21747348	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147605833	chr19:21747410-21747411	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548806706	chr19:21747417-21747418	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200837388	chr19:21747425-21747426	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184222399	chr19:21747440-21747441	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202215505	chr19:21747465-21747466	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200159021	chr19:21747519-21747520	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559431052	chr19:21747532-21747533	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77334718	chr19:21747533-21747534	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188824014	chr19:21747534-21747535	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148190591	chr19:21747558-21747559	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:38)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
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
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21737200-21747200	ZNF genes & repeats	Fetal Intestine Small	intestine
2	chr19:21738000-21749400	Weak transcription	Left Ventricle	heart
3	chr19:21738000-21751400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr19:21738600-21751600	Weak transcription	Osteobl	bone
5	chr19:21739400-21751200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr19:21740600-21750600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr19:21742800-21750600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:21743200-21750400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr19:21743600-21751600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr19:21744200-21747000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
11	chr19:21744800-21747600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr19:21744800-21750600	Weak transcription	Colonic Mucosa	Colon
13	chr19:21744800-21750600	Weak transcription	Fetal Kidney	kidney
14	chr19:21745000-21750600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr19:21745200-21749400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr19:21745800-21746800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr19:21745800-21747200	Strong transcription	Fetal Stomach	stomach
18	chr19:21745800-21748000	Strong transcription	Dnd41	blood
19	chr19:21746000-21746800	ZNF genes & repeats	Liver	Liver
20	chr19:21746000-21746800	Strong transcription	Fetal Lung	lung
21	chr19:21746000-21746800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
22	chr19:21746000-21747000	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr19:21746000-21747600	Strong transcription	Primary T cells from cord blood	blood
24	chr19:21746200-21746800	Strong transcription	Primary B cells from peripheral blood	blood
25	chr19:21746200-21746800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
26	chr19:21746200-21747000	ZNF genes & repeats	Thymus	Thymus
27	chr19:21746400-21747000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr19:21746400-21747000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
29	chr19:21746400-21747000	Strong transcription	Fetal Intestine Large	intestine
30	chr19:21746600-21746800	Strong transcription	Ovary	ovary
31	chr19:21746600-21747000	Weak transcription	NHDF-Ad	bronchial
32	chr19:21746600-21747200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr19:21746600-21748200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr19:21746600-21748400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr19:21746600-21749000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr19:21746600-21749200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr19:21746600-21749200	Weak transcription	Adipose Nuclei	Adipose
38	chr19:21746600-21750600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:21746600-21751200	Weak transcription	Stomach Smooth Muscle	stomach
40	chr19:21746600-21751600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr19:21746600-21751600	Weak transcription	Fetal Brain Male	brain
42	chr19:21746800-21750200	Weak transcription	Ovary	ovary
43	chr19:21746800-21750400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr19:21746800-21750600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr19:21746800-21750800	Weak transcription	Fetal Lung	lung
46	chr19:21747000-21747200	Genic enhancers	Fetal Intestine Large	intestine
47	chr19:21747000-21750200	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr19:21747000-21750200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr19:21747000-21750400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr19:21747200-21747400	Weak transcription	Fetal Intestine Large	intestine

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