Variant report

Variant	nsv961218
Chromosome Location	chr19:40365009-40412126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1079)
CpG islands
(count:1529)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1079 , 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	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40388564-40388584	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
4	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
5	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
8	BCL11A	chr19:40404210-40404647	GM12878	blood:	n/a	chr19:40404401-40404414
9	BCL3	chr19:40411970-40412242	GM12878	blood:	n/a	n/a
10	BCL3	chr19:40412032-40412240	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	chr19:40372310-40372375	K562	blood:	n/a	n/a
14	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
15	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:40404194-40404362	GM12878	blood:	n/a	n/a
17	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
18	CBX3	chr19:40404078-40404473	K562	blood:	n/a	n/a
19	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:40402571-40402768	K562	blood:	n/a	chr19:40402707-40402718
21	CEBPB	chr19:40402703-40402726	H1-hESC	embryonic stem cell:	n/a	chr19:40402707-40402718
22	CEBPB	chr19:40402564-40402888	HepG2	liver:	n/a	chr19:40402707-40402718
23	CEBPB	chr19:40402641-40402841	A549	lung:	n/a	chr19:40402707-40402718
24	CEBPB	chr19:40388532-40388555	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:40402580-40402849	IMR90	lung:	n/a	chr19:40402707-40402718
26	CHD2	chr19:40388541-40388748	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr19:40404120-40404312	GM12878	blood:	n/a	n/a
28	CTCF	chr19:40372280-40372430	HEK293	kidney:	n/a	n/a
29	CTCF	chr19:40372280-40372430	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr19:40404200-40404350	BJ	skin:	n/a	n/a
31	CTCF	chr19:40404240-40404390	Caco-2	colon:	n/a	n/a
32	CTCF	chr19:40388448-40388745	K562	blood:	n/a	n/a
33	CTCF	chr19:40404060-40404210	HCM	heart:	n/a	n/a
34	CTCF	chr19:40404220-40404370	GM12875	blood:	n/a	n/a
35	CTCF	chr19:40388500-40388650	AG04450	lung:	n/a	n/a
36	CTCF	chr19:40372280-40372430	NB4	blood:	n/a	n/a
37	CTCF	chr19:40404189-40404629	GM10248	blood:	n/a	n/a
38	CTCF	chr19:40404216-40404416	ProgFib	skin:	n/a	n/a
39	CTCF	chr19:40404260-40404410	NHLF	lung:	n/a	n/a
40	CTCF	chr19:40382398-40382766	K562	blood:	n/a	n/a
41	CTCF	chr19:40398082-40398446	K562	blood:	n/a	n/a
42	CTCF	chr19:40372541-40372625	GM13977	blood:	n/a	n/a
43	CTCF	chr19:40388491-40388735	GM13977	blood:	n/a	n/a
44	CTCF	chr19:40372236-40372444	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:40404220-40404370	Caco-2	colon:	n/a	n/a
46	CTCF	chr19:40404100-40404547	HepG2	liver:	n/a	n/a
47	CTCF	chr19:40388505-40388656	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr19:40403711-40404843	A549	lung:	n/a	n/a
49	CTCF	chr19:40404260-40404410	MCF-7	breast:	n/a	n/a
50	CTCF	chr19:40372260-40372410	NHEK	skin:	n/a	n/a

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40368830-40368880	HMEC	breast:	n/a
2	chr19:40388677-40388727	AoSMC	blood vessel:	n/a
3	chr19:40380319-40380369	U87	brain:	n/a
4	chr19:40393119-40393169	HRE	kidney:	n/a
5	chr19:40368830-40368880	HMEC	breast:	n/a
6	chr19:40388677-40388727	AoSMC	blood vessel:	n/a
7	chr19:40380319-40380369	U87	brain:	n/a
8	chr19:40393119-40393169	HRE	kidney:	n/a
9	chr19:40366088-40366138	K562	blood:	n/a
10	chr19:40393119-40393169	HRCEpiC	kidney:	n/a
11	chr19:40379680-40379730	GM12878	blood:	n/a
12	chr19:40380853-40380903	AG04450	lung:	fetal
13	chr19:40399454-40399504	HAEpiC	amniotic membrane:	n/a
14	chr19:40392568-40392618	BE2_C	brain:	n/a
15	chr19:40380853-40380903	HCM	heart:	n/a
16	chr19:40376883-40376933	NH-A	brain:	n/a
17	chr19:40366607-40366657	HUVEC	blood vessel:	n/a
18	chr19:40376883-40376933	HRPEpiC	eye:	n/a
19	chr19:40372977-40373027	HCPEpiC	choroid plexus:	n/a
20	chr19:40380319-40380369	AG09309	skin:	n/a
21	chr19:40380319-40380369	GM12891	blood:	n/a
22	chr19:40368363-40368413	AG10803	skin:	n/a
23	chr19:40375973-40376023	AoSMC	blood vessel:	n/a
24	chr19:40392568-40392618	HMEC	breast:	n/a
25	chr19:40396032-40396082	HAEpiC	amniotic membrane:	n/a
26	chr19:40372977-40373027	HEEpiC	esophagus:	n/a
27	chr19:40368830-40368880	HCF	heart:	n/a
28	chr19:40372977-40373027	PFSK-1	brain:	n/a
29	chr19:40408707-40408757	NB4	blood:	n/a
30	chr19:40368830-40368880	HRPEpiC	eye:	n/a
31	chr19:40366394-40366444	HRE	kidney:	n/a
32	chr19:40398384-40398434	NH-A	brain:	n/a
33	chr19:40411970-40412020	CMK	blood:	n/a
34	chr19:40380853-40380903	HPAEpiC	pulmonary alveolar:	n/a
35	chr19:40408707-40408757	GM12892	blood:	n/a
36	chr19:40399454-40399504	CMK	blood:	n/a
37	chr19:40379680-40379730	AG04449	skin:	fetal
38	chr19:40398384-40398434	IMR90	lung:	fetal
39	chr19:40393119-40393169	ECC-1	luminal epithelium:	n/a
40	chr19:40398384-40398434	PANC-1	pancreas:	n/a
41	chr19:40366607-40366657	HIPEpiC	eye:	n/a
42	chr19:40398384-40398434	ProgFib	skin:	n/a
43	chr19:40388677-40388727	AG09319	gingival:	n/a
44	chr19:40410325-40410375	HEEpiC	esophagus:	n/a
45	chr19:40377434-40377484	PANC-1	pancreas:	n/a
46	chr19:40408707-40408757	SK-N-SH_RA	brain:	n/a
47	chr19:40380319-40380369	HEEpiC	esophagus:	n/a
48	chr19:40368363-40368413	GM12878	blood:	n/a
49	chr19:40399454-40399504	RPTEC	kidney:	n/a
50	chr19:40368363-40368413	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
2	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
3	chr19:40403844..40404724-chr19:40476336..40477181,3	MCF-7	breast:
4	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: 2039 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2039 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544143073	chr19:40365010-40365011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569148384	chr19:40365033-40365034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576467045	chr19:40365050-40365051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537722587	chr19:40365067-40365068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576743674	chr19:40365083-40365084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150864681	chr19:40365111-40365112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558897599	chr19:40365170-40365171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529746056	chr19:40365198-40365199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547838319	chr19:40365231-40365232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545536996	chr19:40365289-40365290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111839625	chr19:40365296-40365297	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530613559	chr19:40365310-40365311	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116213619	chr19:40365375-40365376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570638422	chr19:40365416-40365417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528360055	chr19:40365435-40365436	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373097453	chr19:40365440-40365441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138275435	chr19:40365469-40365470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149624701	chr19:40365500-40365501	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193000036	chr19:40365506-40365507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370059483	chr19:40365507-40365508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554763495	chr19:40365516-40365517	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374021426	chr19:40365521-40365522	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114924653	chr19:40365523-40365524	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376341219	chr19:40365528-40365529	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576541285	chr19:40365529-40365530	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs398059728	chr19:40365538-40365539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559075717	chr19:40365631-40365632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544066668	chr19:40365718-40365719	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146090022	chr19:40365720-40365721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182468950	chr19:40365745-40365746	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562285904	chr19:40365763-40365764	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376565227	chr19:40365775-40365776	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140092108	chr19:40365780-40365781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574081997	chr19:40365792-40365793	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541951986	chr19:40365794-40365795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563213807	chr19:40365800-40365801	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs530766721	chr19:40365804-40365805	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs545694311	chr19:40365806-40365807	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs564245489	chr19:40365811-40365812	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs528398782	chr19:40365823-40365824	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs546907394	chr19:40365838-40365839	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs566126282	chr19:40365839-40365840	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs73930665	chr19:40365884-40365885	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs200745234	chr19:40366002-40366003	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs373504885	chr19:40366017-40366018	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs375885686	chr19:40366020-40366021	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs570069078	chr19:40366027-40366028	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs537526940	chr19:40366028-40366029	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs147737435	chr19:40366039-40366040	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs558890815	chr19:40366047-40366048	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
2	chr19:40350400-40372200	Weak transcription	Dnd41	blood
3	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
4	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
6	chr19:40353400-40366000	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr19:40354200-40370800	Weak transcription	Fetal Brain Female	brain
8	chr19:40354600-40372200	Weak transcription	HepG2	liver
9	chr19:40355200-40372200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr19:40355800-40367200	Strong transcription	Primary T cells from cord blood	blood
11	chr19:40356200-40365800	Strong transcription	Fetal Stomach	stomach
12	chr19:40358400-40372200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr19:40359800-40369600	Weak transcription	Fetal Muscle Leg	muscle
14	chr19:40360400-40367000	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr19:40360600-40366200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr19:40361000-40372200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr19:40361200-40366000	Weak transcription	Spleen	Spleen
18	chr19:40361200-40374000	Weak transcription	Pancreas	Pancrea
19	chr19:40361400-40365800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:40363400-40365800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr19:40364000-40366600	Weak transcription	Stomach Mucosa	stomach
22	chr19:40364400-40365600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:40364400-40366800	Weak transcription	Fetal Intestine Small	intestine
24	chr19:40364400-40372200	Weak transcription	Right Atrium	heart
25	chr19:40364400-40372400	Weak transcription	Gastric	stomach
26	chr19:40364600-40365800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:40364600-40366400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr19:40364600-40366600	Weak transcription	Fetal Muscle Trunk	muscle
29	chr19:40364600-40369200	Weak transcription	Colonic Mucosa	Colon
30	chr19:40364800-40366600	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr19:40365200-40366800	Enhancers	Placenta	Placenta
32	chr19:40365600-40365800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr19:40365800-40366000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:40365800-40366200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:40365800-40366600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr19:40365800-40372200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr19:40365800-40372600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr19:40366000-40366200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr19:40366000-40367000	Enhancers	Spleen	Spleen
40	chr19:40366000-40369000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr19:40366200-40366400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:40366200-40366400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:40366200-40367000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr19:40366200-40367000	Bivalent Enhancer	Fetal Stomach	stomach
45	chr19:40366200-40372800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr19:40366400-40366600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr19:40366400-40366600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr19:40366400-40367000	Enhancers	Fetal Heart	heart
49	chr19:40366400-40367200	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr19:40366600-40367000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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