Variant report

Variant	esv1817068
Chromosome Location	chr19:40357271-40400950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:1649)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
10	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
11	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
12	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
13	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
14	CEBPB	chr19:40388532-40388555	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
16	CHD2	chr19:40388541-40388748	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr19:40388448-40388745	K562	blood:	n/a	n/a
18	CTCF	chr19:40388484-40388694	GM12891	blood:	n/a	n/a
19	CTCF	chr19:40372210-40372497	GM13977	blood:	n/a	chr19:40372450-40372463
20	CTCF	chr19:40372260-40372410	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr19:40372249-40372463	HCT-116	colon:	n/a	chr19:40372450-40372463
22	CTCF	chr19:40388500-40388650	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr19:40388270-40388904	A549	lung:	n/a	n/a
24	CTCF	chr19:40388540-40388690	GM12869	blood:	n/a	n/a
25	CTCF	chr19:40372235-40372423	T-47D	breast:	n/a	n/a
26	CTCF	chr19:40388500-40388650	AG04449	skin:	n/a	n/a
27	CTCF	chr19:40388540-40388690	HFF	foreskin:	n/a	n/a
28	CTCF	chr19:40398384-40398389	GM20000	blood:	n/a	n/a
29	CTCF	chr19:40388540-40388690	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr19:40388500-40388650	GM06990	blood:	n/a	n/a
31	CTCF	chr19:40372260-40372410	K562	blood:	n/a	n/a
32	CTCF	chr19:40388501-40388671	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:40372260-40372410	HRE	kidney:	n/a	n/a
34	CTCF	chr19:40399202-40399254	GM10248	blood:	n/a	n/a
35	CTCF	chr19:40372203-40372550	LNCaP	prostate:	n/a	chr19:40372450-40372463
36	CTCF	chr19:40372248-40372468	Lung_OC	lung:	n/a	chr19:40372450-40372463
37	CTCF	chr19:40388500-40388650	NHLF	lung:	n/a	n/a
38	CTCF	chr19:40372280-40372430	GM12865	blood:	n/a	n/a
39	CTCF	chr19:40372600-40372750	HEK293	kidney:	n/a	n/a
40	CTCF	chr19:40371596-40371670	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr19:40388500-40388650	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr19:40388503-40388714	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr19:40388485-40388708	GM10248	blood:	n/a	n/a
44	CTCF	chr19:40388505-40388656	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr19:40388500-40388650	GM12874	blood:	n/a	n/a
46	CTCF	chr19:40388540-40388690	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr19:40372151-40372680	A549	lung:	n/a	chr19:40372450-40372463
48	CTCF	chr19:40388500-40388650	AG09319	gingival:	n/a	n/a
49	CTCF	chr19:40388540-40388690	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr19:40388500-40388650	HAc	cerebellar:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40366607-40366657	SK-N-MC	brain:	n/a
2	chr19:40360856-40360906	ovcar-3	ovarian:	n/a
3	chr19:40366607-40366657	SK-N-MC	brain:	n/a
4	chr19:40360856-40360906	ovcar-3	ovarian:	n/a
5	chr19:40363285-40363335	H1-hESC	embryonic stem cell:	embryo
6	chr19:40366088-40366138	U87	brain:	n/a
7	chr19:40359249-40359299	HMEC	breast:	n/a
8	chr19:40392568-40392618	IMR90	lung:	fetal
9	chr19:40376883-40376933	MCF10A-Er-Src	breast:	n/a
10	chr19:40359249-40359299	NH-A	brain:	n/a
11	chr19:40368363-40368413	SKMC	muscle:	n/a
12	chr19:40362773-40362823	HepG2	liver:	n/a
13	chr19:40360856-40360906	LNCaP	prostate:	n/a
14	chr19:40366394-40366444	AG10803	skin:	n/a
15	chr19:40366607-40366657	HAEpiC	amniotic membrane:	n/a
16	chr19:40388677-40388727	HRPEpiC	eye:	n/a
17	chr19:40368363-40368413	HCM	heart:	n/a
18	chr19:40372977-40373027	AG04450	lung:	fetal
19	chr19:40397977-40398027	K562	blood:	n/a
20	chr19:40359249-40359299	AG04449	skin:	fetal
21	chr19:40366607-40366657	SK-N-SH	brain:	n/a
22	chr19:40363285-40363335	Hepatocyte	liver:	n/a
23	chr19:40366394-40366444	HEEpiC	esophagus:	n/a
24	chr19:40362773-40362823	U87	brain:	n/a
25	chr19:40360856-40360906	HCT-116	colon:	n/a
26	chr19:40396538-40396588	GM06990	blood:	n/a
27	chr19:40391320-40391370	HCT-116	colon:	n/a
28	chr19:40397977-40398027	HIPEpiC	eye:	n/a
29	chr19:40396538-40396588	PANC-1	pancreas:	n/a
30	chr19:40366607-40366657	T-47D	breast:	n/a
31	chr19:40366088-40366138	Caco-2	colon:	n/a
32	chr19:40362773-40362823	HCF	heart:	n/a
33	chr19:40375973-40376023	MCF-7	breast:	n/a
34	chr19:40393119-40393169	MCF-7	breast:	n/a
35	chr19:40388677-40388727	HRCEpiC	kidney:	n/a
36	chr19:40366088-40366138	MCF10A-Er-Src	breast:	n/a
37	chr19:40368830-40368880	ovcar-3	ovarian:	n/a
38	chr19:40393119-40393169	ovcar-3	ovarian:	n/a
39	chr19:40364151-40364201	NB4	blood:	n/a
40	chr19:40366394-40366444	GM19239	blood:	n/a
41	chr19:40397977-40398027	HepG2	liver:	n/a
42	chr19:40366607-40366657	H1-hESC	embryonic stem cell:	embryo
43	chr19:40377434-40377484	BJ	skin:	n/a
44	chr19:40363285-40363335	GM12878	blood:	n/a
45	chr19:40366607-40366657	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:40397977-40398027	Hela-S3	cervix:	n/a
47	chr19:40396538-40396588	IMR90	lung:	fetal
48	chr19:40398384-40398434	HNPCEpiC	eye:	n/a
49	chr19:40380853-40380903	HPAEpiC	pulmonary alveolar:	n/a
50	chr19:40393119-40393169	GM19239	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
2	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
3	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
4	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
5	chr19:40337506..40339114-chr19:40356435..40358897,2	MCF-7	breast:
6	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
7	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: 1739 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1739 , 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	rs4436880	chr19:40357341-40357342	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117543378	chr19:40357358-40357359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2075097	chr19:40357360-40357361	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs368445716	chr19:40357387-40357388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs151192322	chr19:40357393-40357394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140253776	chr19:40357398-40357399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376799195	chr19:40357428-40357429	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs367675319	chr19:40357439-40357440	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs371919834	chr19:40357450-40357451	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs201323823	chr19:40357461-40357462	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs186617149	chr19:40357467-40357468	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs115392675	chr19:40357477-40357478	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs138776300	chr19:40357487-40357488	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs560527265	chr19:40357508-40357509	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs199798429	chr19:40357520-40357521	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs190665776	chr19:40357522-40357523	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs200500325	chr19:40357523-40357524	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs141970866	chr19:40357535-40357536	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs182861563	chr19:40357557-40357558	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs375256745	chr19:40357564-40357565	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs200691490	chr19:40357565-40357566	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs369249103	chr19:40357587-40357588	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs571193281	chr19:40357600-40357601	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145630356	chr19:40357619-40357620	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs202029040	chr19:40357636-40357637	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201695744	chr19:40357646-40357647	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553823334	chr19:40357653-40357654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201267637	chr19:40357655-40357656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75241092	chr19:40357663-40357664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149980020	chr19:40357670-40357671	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148773345	chr19:40357682-40357683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs759120	chr19:40357683-40357684	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562548497	chr19:40357723-40357724	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200520932	chr19:40357727-40357728	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370196020	chr19:40357728-40357729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373078489	chr19:40357738-40357739	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545210725	chr19:40357760-40357761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377488670	chr19:40357770-40357771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73554445	chr19:40357778-40357779	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs560272597	chr19:40357790-40357791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199505645	chr19:40357793-40357794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543228490	chr19:40357794-40357795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368236969	chr19:40357802-40357803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201520357	chr19:40357803-40357804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187009917	chr19:40357816-40357817	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs759121	chr19:40357824-40357825	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs111425931	chr19:40357855-40357856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374067041	chr19:40357873-40357874	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377087322	chr19:40357877-40357878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547205082	chr19:40357879-40357880	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40349800-40357400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
3	chr19:40350400-40372200	Weak transcription	Dnd41	blood
4	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
5	chr19:40351000-40361000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:40352000-40363200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr19:40352000-40364200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
10	chr19:40352600-40364000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr19:40352800-40360600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr19:40352800-40360600	Weak transcription	Spleen	Spleen
13	chr19:40353400-40366000	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr19:40353600-40360000	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr19:40354200-40370800	Weak transcription	Fetal Brain Female	brain
16	chr19:40354400-40362600	Weak transcription	Gastric	stomach
17	chr19:40354600-40362800	Weak transcription	Stomach Mucosa	stomach
18	chr19:40354600-40372200	Weak transcription	HepG2	liver
19	chr19:40355200-40372200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr19:40355800-40367200	Strong transcription	Primary T cells from cord blood	blood
21	chr19:40356000-40358800	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr19:40356000-40359000	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr19:40356200-40364400	Strong transcription	Fetal Intestine Small	intestine
24	chr19:40356200-40364600	Strong transcription	Colonic Mucosa	Colon
25	chr19:40356200-40365800	Strong transcription	Fetal Stomach	stomach
26	chr19:40356400-40358200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr19:40357000-40362600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr19:40357200-40358000	Strong transcription	Primary B cells from cord blood	blood
29	chr19:40357200-40358600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr19:40357200-40359800	Strong transcription	Fetal Muscle Leg	muscle
31	chr19:40357400-40357600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr19:40357400-40358400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr19:40357600-40358200	Enhancers	HMEC	breast
34	chr19:40357600-40358600	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr19:40358000-40364000	Weak transcription	Primary B cells from cord blood	blood
36	chr19:40358200-40360600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr19:40358400-40372200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:40358600-40360600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr19:40358600-40363800	Weak transcription	Right Atrium	heart
40	chr19:40358800-40360400	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr19:40359000-40360400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr19:40359800-40369600	Weak transcription	Fetal Muscle Leg	muscle
43	chr19:40360000-40361600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr19:40360400-40360600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr19:40360400-40363200	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr19:40360400-40367000	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr19:40360600-40360800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr19:40360600-40360800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr19:40360600-40360800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
50	chr19:40360600-40360800	Active TSS	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links