Variant report

Variant	esv1846009
Chromosome Location	chr19:40353983-40410533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1127)
CpG islands
(count:1769)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40388564-40388584	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
4	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
5	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr19:40404210-40404647	GM12878	blood:	n/a	chr19:40404401-40404414
8	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
9	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
10	BHLHE40	chr19:40404194-40404362	GM12878	blood:	n/a	n/a
11	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
12	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
13	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
15	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
16	CBX3	chr19:40404078-40404473	K562	blood:	n/a	n/a
17	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
18	CEBPB	chr19:40388532-40388555	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:40354800-40355128	K562	blood:	n/a	n/a
20	CEBPB	chr19:40402703-40402726	H1-hESC	embryonic stem cell:	n/a	chr19:40402707-40402718
21	CEBPB	chr19:40402564-40402888	HepG2	liver:	n/a	chr19:40402707-40402718
22	CEBPB	chr19:40402580-40402849	IMR90	lung:	n/a	chr19:40402707-40402718
23	CEBPB	chr19:40354824-40355043	K562	blood:	n/a	n/a
24	CEBPB	chr19:40354817-40355067	K562	blood:	n/a	n/a
25	CEBPB	chr19:40402571-40402768	K562	blood:	n/a	chr19:40402707-40402718
26	CEBPB	chr19:40354870-40355111	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:40402641-40402841	A549	lung:	n/a	chr19:40402707-40402718
28	CEBPB	chr19:40354843-40355101	A549	lung:	n/a	n/a
29	CHD2	chr19:40404120-40404312	GM12878	blood:	n/a	n/a
30	CHD2	chr19:40388541-40388748	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr19:40404240-40404390	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr19:40404260-40404410	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr19:40388500-40388650	HEK293	kidney:	n/a	n/a
34	CTCF	chr19:40388500-40388650	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr19:40372260-40372410	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr19:40404200-40404416	T-47D	breast:	n/a	n/a
37	CTCF	chr19:40388481-40388696	GM19240	blood:	n/a	n/a
38	CTCF	chr19:40372260-40372410	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr19:40404080-40404230	HCM	heart:	n/a	n/a
40	CTCF	chr19:40388520-40388670	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr19:40372260-40372410	AG04450	lung:	n/a	n/a
42	CTCF	chr19:40372280-40372430	GM06990	blood:	n/a	n/a
43	CTCF	chr19:40404220-40404370	HMF	breast:	n/a	n/a
44	CTCF	chr19:40408540-40408690	HepG2	liver:	n/a	n/a
45	CTCF	chr19:40372280-40372430	GM12866	blood:	n/a	n/a
46	CTCF	chr19:40404175-40404434	ECC-1	luminal epithelium:	n/a	n/a
47	CTCF	chr19:40388500-40388650	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr19:40388540-40388690	GM12865	blood:	n/a	n/a
49	CTCF	chr19:40404060-40404210	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr19:40388460-40388610	GM12869	blood:	n/a	n/a

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40396032-40396082	Caco-2	colon:	n/a
2	chr19:40368363-40368413	RPTEC	kidney:	n/a
3	chr19:40364151-40364201	Jurkat	blood:	n/a
4	chr19:40362773-40362823	K562	blood:	n/a
5	chr19:40396032-40396082	IMR90	lung:	fetal
6	chr19:40408707-40408757	PFSK-1	brain:	n/a
7	chr19:40376883-40376933	HCM	heart:	n/a
8	chr19:40375973-40376023	BE2_C	brain:	n/a
9	chr19:40410325-40410375	GM19239	blood:	n/a
10	chr19:40366394-40366444	HIPEpiC	eye:	n/a
11	chr19:40376883-40376933	Hela-S3	cervix:	n/a
12	chr19:40379680-40379730	Caco-2	colon:	n/a
13	chr19:40363285-40363335	U87	brain:	n/a
14	chr19:40368363-40368413	HCT-116	colon:	n/a
15	chr19:40408707-40408757	HepG2	liver:	n/a
16	chr19:40377434-40377484	HepG2	liver:	n/a
17	chr19:40398384-40398434	GM19239	blood:	n/a
18	chr19:40396538-40396588	H1-hESC	embryonic stem cell:	embryo
19	chr19:40364151-40364201	ProgFib	skin:	n/a
20	chr19:40380319-40380369	AG09309	skin:	n/a
21	chr19:40393119-40393169	RPTEC	kidney:	n/a
22	chr19:40366394-40366444	MCF10A-Er-Src	breast:	n/a
23	chr19:40363285-40363335	HCPEpiC	choroid plexus:	n/a
24	chr19:40372977-40373027	ECC-1	luminal epithelium:	n/a
25	chr19:40359249-40359299	SK-N-SH_RA	brain:	n/a
26	chr19:40363285-40363335	AG04450	lung:	fetal
27	chr19:40372977-40373027	HCM	heart:	n/a
28	chr19:40380319-40380369	NHDF-neo	bronchial:	n/a
29	chr19:40368363-40368413	U87	brain:	n/a
30	chr19:40368363-40368413	HL-60	blood:	n/a
31	chr19:40393119-40393169	H1-hESC	embryonic stem cell:	embryo
32	chr19:40380319-40380369	NHBE	bronchial:	n/a
33	chr19:40399454-40399504	AG10803	skin:	n/a
34	chr19:40364151-40364201	HUVEC	blood vessel:	n/a
35	chr19:40397977-40398027	SAEC	small airway:	n/a
36	chr19:40368830-40368880	RPTEC	kidney:	n/a
37	chr19:40408707-40408757	A549	lung:	n/a
38	chr19:40388677-40388727	CMK	blood:	n/a
39	chr19:40379680-40379730	HepG2	liver:	n/a
40	chr19:40372977-40373027	HIPEpiC	eye:	n/a
41	chr19:40362928-40362978	NHDF-neo	bronchial:	n/a
42	chr19:40396032-40396082	SK-N-SH_RA	brain:	n/a
43	chr19:40372977-40373027	IMR90	lung:	fetal
44	chr19:40396032-40396082	NHBE	bronchial:	n/a
45	chr19:40397977-40398027	U87	brain:	n/a
46	chr19:40380853-40380903	A549	lung:	n/a
47	chr19:40392568-40392618	ovcar-3	ovarian:	n/a
48	chr19:40362773-40362823	SK-N-SH_RA	brain:	n/a
49	chr19:40380853-40380903	PFSK-1	brain:	n/a
50	chr19:40388677-40388727	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:40337506..40339114-chr19:40356435..40358897,2	MCF-7	breast:
2	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
3	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
4	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
5	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
6	chr19:40337126..40339206-chr19:40352976..40355937,2	K562	blood:
7	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
8	chr19:40403844..40404724-chr19:40476336..40477181,3	MCF-7	breast:
9	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
10	chr19:40333922..40335627-chr19:40352940..40355252,2	K562	blood:
11	chr19:40371880..40372846-chr19:40476486..40477439,2	MCF-7	breast:

No data

Variant related genes	Relation type
FCGBP	TF binding region
FCGBP	CpG island
ENSG00000013275	chromatin interactions

Extended variants
information (count: 2450 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2450 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1053716	chr19:40354019-40354020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570208270	chr19:40354026-40354027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2405	chr19:40354067-40354068	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs373711667	chr19:40354085-40354086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367890414	chr19:40354108-40354109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371759371	chr19:40354124-40354125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202103012	chr19:40354128-40354129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112096457	chr19:40354147-40354148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374865085	chr19:40354148-40354149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568135849	chr19:40354164-40354165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372528999	chr19:40354165-40354166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73554429	chr19:40354178-40354179	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs557255128	chr19:40354212-40354213	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs570106133	chr19:40354214-40354215	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs369922574	chr19:40354216-40354217	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs187681545	chr19:40354252-40354253	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs374994567	chr19:40354255-40354256	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs200288664	chr19:40354258-40354259	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs201081922	chr19:40354260-40354261	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs35722884	chr19:40354263-40354264	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs112547840	chr19:40354268-40354269	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs369912208	chr19:40354272-40354273	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs372806560	chr19:40354278-40354279	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs199845989	chr19:40354279-40354280	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs199709546	chr19:40354280-40354281	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs192220048	chr19:40354299-40354300	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs549346109	chr19:40354302-40354303	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs35431483	chr19:40354309-40354310	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs373276034	chr19:40354310-40354311	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs376346474	chr19:40354335-40354336	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs556429522	chr19:40354340-40354341	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs148404215	chr19:40354341-40354342	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs372988668	chr19:40354359-40354360	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs183703176	chr19:40354383-40354384	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs376090141	chr19:40354411-40354412	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574888232	chr19:40354420-40354421	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370519737	chr19:40354447-40354448	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145000879	chr19:40354448-40354449	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147646179	chr19:40354469-40354470	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542126929	chr19:40354475-40354476	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150214514	chr19:40354477-40354478	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373955201	chr19:40354482-40354483	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75112544	chr19:40354485-40354486	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201901608	chr19:40354498-40354499	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35682720	chr19:40354506-40354507	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146042671	chr19:40354518-40354519	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545369839	chr19:40354520-40354521	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114573010	chr19:40354535-40354536	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528213544	chr19:40354539-40354540	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368138714	chr19:40354542-40354543	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Lung cancer	21569311	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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40349400-40354400	Weak transcription	Colonic Mucosa	Colon
2	chr19:40349800-40356000	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr19:40349800-40357400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
5	chr19:40350400-40372200	Weak transcription	Dnd41	blood
6	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
7	chr19:40351000-40361000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr19:40351600-40357200	Weak transcription	Primary B cells from cord blood	blood
9	chr19:40352000-40357000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr19:40352000-40357200	Weak transcription	Fetal Muscle Leg	muscle
11	chr19:40352000-40363200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr19:40352000-40364200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr19:40352200-40356400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
16	chr19:40352600-40364000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr19:40352800-40360600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:40352800-40360600	Weak transcription	Spleen	Spleen
19	chr19:40353200-40354200	Weak transcription	Gastric	stomach
20	chr19:40353400-40354600	Strong transcription	Fetal Intestine Small	intestine
21	chr19:40353400-40354600	Strong transcription	Stomach Mucosa	stomach
22	chr19:40353400-40354800	Strong transcription	Fetal Stomach	stomach
23	chr19:40353400-40366000	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr19:40353600-40355000	Strong transcription	Primary T cells from cord blood	blood
25	chr19:40353600-40360000	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr19:40353800-40354600	Strong transcription	Sigmoid Colon	Sigmoid Colon
27	chr19:40354200-40354400	ZNF genes & repeats	Gastric	stomach
28	chr19:40354200-40370800	Weak transcription	Fetal Brain Female	brain
29	chr19:40354400-40354600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:40354400-40354600	Strong transcription	Colonic Mucosa	Colon
31	chr19:40354400-40354800	Enhancers	A549	lung
32	chr19:40354400-40355400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr19:40354400-40362600	Weak transcription	Gastric	stomach
34	chr19:40354600-40356000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr19:40354600-40356200	Weak transcription	Colonic Mucosa	Colon
36	chr19:40354600-40356200	Weak transcription	Fetal Intestine Small	intestine
37	chr19:40354600-40357200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr19:40354600-40362800	Weak transcription	Stomach Mucosa	stomach
39	chr19:40354600-40372200	Weak transcription	HepG2	liver
40	chr19:40354800-40356200	Weak transcription	Fetal Stomach	stomach
41	chr19:40355000-40355800	Weak transcription	Primary T cells from cord blood	blood
42	chr19:40355200-40372200	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr19:40355800-40367200	Strong transcription	Primary T cells from cord blood	blood
44	chr19:40356000-40358800	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr19:40356000-40359000	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr19:40356200-40364400	Strong transcription	Fetal Intestine Small	intestine
47	chr19:40356200-40364600	Strong transcription	Colonic Mucosa	Colon
48	chr19:40356200-40365800	Strong transcription	Fetal Stomach	stomach
49	chr19:40356400-40358200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr19:40357000-40362600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood

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