Variant report

Variant	nsv530661
Chromosome Location	chr14:47754197-47937396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:366)
Chromatin interactive
region (count:5)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:47872730-47872904	K562	blood:	n/a	n/a
2	BACH1	chr14:47858719-47859063	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:47840011-47840068	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:47827183-47827600	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:47804741-47804747	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr14:47911508-47911781	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:47758514-47758816	IMR90	lung:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
8	CEBPB	chr14:47804079-47804205	HepG2	liver:	n/a	chr14:47804143-47804160 chr14:47804146-47804157
9	CEBPB	chr14:47758513-47758743	A549	lung:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
10	CEBPB	chr14:47758740-47758766	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:47834961-47835168	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:47773674-47773940	HepG2	liver:	n/a	chr14:47773834-47773847 chr14:47773812-47773823
13	CEBPB	chr14:47898243-47898500	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:47927791-47928068	HepG2	liver:	n/a	chr14:47927927-47927938
15	CEBPB	chr14:47758518-47758817	HepG2	liver:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
16	CEBPB	chr14:47815640-47815914	HepG2	liver:	n/a	chr14:47815797-47815808
17	CEBPB	chr14:47815725-47815829	H1-hESC	embryonic stem cell:	n/a	chr14:47815797-47815808
18	CEBPB	chr14:47927810-47928060	A549	lung:	n/a	chr14:47927927-47927938
19	CEBPB	chr14:47769492-47769763	IMR90	lung:	n/a	n/a
20	CEBPB	chr14:47859186-47859218	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:47911347-47911849	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:47911556-47911635	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr14:47911596-47911650	GM12891	blood:	n/a	n/a
24	CTCF	chr14:47911525-47911710	NHEK	skin:	n/a	n/a
25	CTCF	chr14:47802060-47802210	BE2_C	brain:	n/a	n/a
26	CTCF	chr14:47911440-47911590	HAc	cerebellar:	n/a	n/a
27	CTCF	chr14:47911521-47911620	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr14:47802302-47802392	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr14:47802325-47802402	Medullo	brain:	n/a	n/a
30	CTCF	chr14:47911520-47911670	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr14:47846841-47846916	GM13977	blood:	n/a	n/a
32	CTCF	chr14:47802300-47802450	GM12878	blood:	n/a	n/a
33	CTCF	chr14:47887537-47887607	GM13976	blood:	n/a	n/a
34	CTCF	chr14:47802040-47802190	RPTEC	kidney:	n/a	n/a
35	CTCF	chr14:47911500-47911650	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr14:47802240-47802390	HCT-116	colon:	n/a	n/a
37	CTCF	chr14:47802200-47802350	HMF	breast:	n/a	n/a
38	CTCF	chr14:47802220-47802370	NHEK	skin:	n/a	n/a
39	CTCF	chr14:47911430-47911687	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr14:47890349-47890390	GM13976	blood:	n/a	n/a
41	CTCF	chr14:47911560-47911710	SAEC	small airway:	n/a	n/a
42	CTCF	chr14:47873703-47873764	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr14:47911460-47911610	GM12873	blood:	n/a	n/a
44	CTCF	chr14:47911520-47911670	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr14:47911578-47911654	GM19238	blood:	n/a	n/a
46	CTCF	chr14:47911523-47911709	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:47911500-47911650	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr14:47911540-47911690	HEK293	kidney:	n/a	n/a
49	CTCF	chr14:47802180-47802330	HL-60	blood:	n/a	n/a
50	CTCF	chr14:47792653-47792780	GM10248	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47769981-47770031	ovcar-3	ovarian:	n/a
2	chr14:47769981-47770031	BE2_C	brain:	n/a
3	chr14:47859275-47859325	HRPEpiC	eye:	n/a
4	chr14:47908980-47909030	AG09319	gingival:	n/a
5	chr14:47812515-47812565	MCF-7	breast:	n/a
6	chr14:47872288-47872338	GM12892	blood:	n/a
7	chr14:47812515-47812565	HIPEpiC	eye:	n/a
8	chr14:47812515-47812565	SK-N-SH_RA	brain:	n/a
9	chr14:47872288-47872338	HRE	kidney:	n/a
10	chr14:47769981-47770031	HRCEpiC	kidney:	n/a
11	chr14:47908980-47909030	PFSK-1	brain:	n/a
12	chr14:47859275-47859325	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:47859275-47859325	HEK293	kidney:	embryo
14	chr14:47812515-47812565	Caco-2	colon:	n/a
15	chr14:47872288-47872338	SAEC	small airway:	n/a
16	chr14:47908980-47909030	Hela-S3	cervix:	n/a
17	chr14:47812515-47812565	NHDF-neo	bronchial:	n/a
18	chr14:47769981-47770031	PFSK-1	brain:	n/a
19	chr14:47908980-47909030	SK-N-SH	brain:	n/a
20	chr14:47834520-47834570	ProgFib	skin:	n/a
21	chr14:47812515-47812565	HCPEpiC	choroid plexus:	n/a
22	chr14:47834520-47834570	GM12891	blood:	n/a
23	chr14:47769981-47770031	Caco-2	colon:	n/a
24	chr14:47812515-47812565	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:47769981-47770031	MCF-7	breast:	n/a
26	chr14:47859275-47859325	H1-hESC	embryonic stem cell:	embryo
27	chr14:47812515-47812565	H1-hESC	embryonic stem cell:	embryo
28	chr14:47769981-47770031	T-47D	breast:	n/a
29	chr14:47834520-47834570	T-47D	breast:	n/a
30	chr14:47769981-47770031	HNPCEpiC	eye:	n/a
31	chr14:47812515-47812565	AG04450	lung:	fetal
32	chr14:47872288-47872338	H1-hESC	embryonic stem cell:	embryo
33	chr14:47859275-47859325	HIPEpiC	eye:	n/a
34	chr14:47834520-47834570	HPAEpiC	pulmonary alveolar:	n/a
35	chr14:47834520-47834570	BE2_C	brain:	n/a
36	chr14:47872288-47872338	K562	blood:	n/a
37	chr14:47769981-47770031	AG09319	gingival:	n/a
38	chr14:47872288-47872338	SK-N-SH	brain:	n/a
39	chr14:47872288-47872338	ovcar-3	ovarian:	n/a
40	chr14:47769981-47770031	HepG2	liver:	n/a
41	chr14:47834520-47834570	MCF-7	breast:	n/a
42	chr14:47812515-47812565	BE2_C	brain:	n/a
43	chr14:47908980-47909030	AG09309	skin:	n/a
44	chr14:47834520-47834570	NB4	blood:	n/a
45	chr14:47812515-47812565	PFSK-1	brain:	n/a
46	chr14:47859275-47859325	GM12891	blood:	n/a
47	chr14:47872288-47872338	Hela-S3	cervix:	n/a
48	chr14:47872288-47872338	LNCaP	prostate:	n/a
49	chr14:47872288-47872338	U87	brain:	n/a
50	chr14:47769981-47770031	SAEC	small airway:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:47825822..47827429-chr14:47839476..47841080,2	K562	blood:
2	chr14:47910964..47912035-chr14:48008060..48009032,5	MCF-7	breast:
3	chr14:47825822..47827429-chr14:47839476..47841080,2	K562	blood:
4	chr14:47811604..47813341-chr14:47823132..47825953,2	K562	blood:
5	chr14:47911217..47911884-chr14:48008112..48009013,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL10L-3	chr14:47774384-47774574	l_980_chr14:47772660-47799743_76bGuttman_hES
2	lnc-RPL10L-3	chr14:47798814-47799743	l_980_chr14:47772660-47799743_76bGuttman_hES
3	lnc-RPL10L-3	chr14:47812301-47812319	NONHSAT036687
4	lnc-FANCM-12	chr14:47765169-47765272	l_979_chr14:47733075-47748994_testes
5	lnc-RPL10L-3	chr14:47768550-47768742	NONHSAT036687
6	lnc-RPL10L-3	chr14:47770614-47770753	NONHSAT036687
7	lnc-RPL10L-3	chr14:47774434-47774526	NONHSAT036687
8	lnc-RPL10L-3	chr14:47772661-47773179	l_980_chr14:47772660-47799743_76bGuttman_hES
9	lnc-FANCM-12	chr14:47766804-47767153	l_979_chr14:47733075-47748994_testes
10	lnc-RPL10L-3	chr14:47775280-47775345	NONHSAT036687

No data

Variant related genes	Relation type
MDGA2	TF binding region
RPS15AP3	TF binding region
MDGA2	CpG island
RPS15AP3	CpG island
ENSG00000139915	chromatin interactions

Extended variants
information (count: 4332 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4332 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569970696	chr14:47755657-47755658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78017699	chr14:47755673-47755674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555496638	chr14:47755676-47755677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139399490	chr14:47755677-47755678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190071252	chr14:47755721-47755722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558325180	chr14:47755773-47755774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529732086	chr14:47764813-47764814	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs546317812	chr14:47764823-47764824	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs560391880	chr14:47764828-47764829	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs200892485	chr14:47764829-47764830	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs372963746	chr14:47764833-47764834	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs376182786	chr14:47764846-47764847	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs184604658	chr14:47764854-47764855	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs10132633	chr14:47764882-47764883	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566251286	chr14:47764918-47764919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs10144713	chr14:47764940-47764941	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189345859	chr14:47764942-47764943	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs552120032	chr14:47764943-47764944	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs376215963	chr14:47764945-47764946	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs10135002	chr14:47764968-47764969	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182003280	chr14:47764978-47764979	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs7152122	chr14:47765012-47765013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368764214	chr14:47765026-47765027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184331513	chr14:47765086-47765087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200288813	chr14:47765131-47765132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143119375	chr14:47765134-47765135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201352698	chr14:47765135-47765136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534190658	chr14:47765137-47765138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573405631	chr14:47765139-47765140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554281373	chr14:47765141-47765142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577433038	chr14:47765153-47765154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144233973	chr14:47765165-47765166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373552195	chr14:47765180-47765181	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs200886627	chr14:47765182-47765183	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs79447366	chr14:47765183-47765184	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs576670783	chr14:47765225-47765226	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs7152633	chr14:47765274-47765275	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7151248	chr14:47765348-47765349	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs529613355	chr14:47765368-47765369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539856274	chr14:47765438-47765439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77471249	chr14:47765444-47765445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79249829	chr14:47765445-47765446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552344365	chr14:47765479-47765480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79982186	chr14:47765491-47765492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531539775	chr14:47765497-47765498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189557444	chr14:47765514-47765515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568388860	chr14:47765544-47765545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534150398	chr14:47765589-47765590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554244435	chr14:47765603-47765604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79339708	chr14:47765624-47765625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastric cancer	18160780	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47755600-47755800	Enhancers	Brain Anterior Caudate	brain
2	chr14:47764800-47765000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:47765000-47773800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:47765200-47766000	Enhancers	Brain Germinal Matrix	brain
5	chr14:47765600-47766200	Enhancers	Brain Substantia Nigra	brain
6	chr14:47765800-47766400	Enhancers	Brain Cingulate Gyrus	brain
7	chr14:47766000-47766200	Enhancers	Brain Angular Gyrus	brain
8	chr14:47766200-47766800	Weak transcription	Brain Angular Gyrus	brain
9	chr14:47766800-47767000	Enhancers	Brain Angular Gyrus	brain
10	chr14:47767000-47770800	Weak transcription	Brain Angular Gyrus	brain
11	chr14:47769600-47770800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:47769800-47770800	Enhancers	NH-A	brain
13	chr14:47770000-47770400	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr14:47770000-47771000	Enhancers	Fetal Heart	heart
15	chr14:47770400-47771200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:47770600-47771000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:47773800-47774000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr14:47774000-47774400	Enhancers	Brain Hippocampus Middle	brain
19	chr14:47774000-47776200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:47778000-47778200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr14:47790000-47790800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:47790400-47790800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr14:47790600-47791000	Enhancers	Brain Germinal Matrix	brain
24	chr14:47790600-47791200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr14:47791200-47792000	Enhancers	Fetal Lung	lung
26	chr14:47795800-47797400	Enhancers	Fetal Brain Male	brain
27	chr14:47796400-47797600	Enhancers	Fetal Brain Female	brain
28	chr14:47797400-47804000	Weak transcription	Fetal Brain Male	brain
29	chr14:47797600-47798600	Weak transcription	Fetal Brain Female	brain
30	chr14:47798600-47798800	Enhancers	Fetal Brain Female	brain
31	chr14:47800600-47802000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr14:47800800-47801600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:47801000-47801600	Enhancers	Brain Cingulate Gyrus	brain
34	chr14:47801000-47801600	Enhancers	Fetal Lung	lung
35	chr14:47801200-47802200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr14:47801400-47801800	Enhancers	Adipose Nuclei	Adipose
37	chr14:47801400-47801800	Enhancers	Brain Angular Gyrus	brain
38	chr14:47801400-47801800	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr14:47801400-47802200	Enhancers	Brain Anterior Caudate	brain
40	chr14:47801400-47802400	Enhancers	Brain Hippocampus Middle	brain
41	chr14:47801600-47802200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr14:47801600-47812000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr14:47802200-47802400	Enhancers	Brain Cingulate Gyrus	brain
44	chr14:47804000-47804600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr14:47804000-47804800	Enhancers	Fetal Brain Male	brain
46	chr14:47804800-47813000	Weak transcription	Fetal Brain Male	brain
47	chr14:47810400-47810600	Enhancers	Brain Substantia Nigra	brain
48	chr14:47810600-47812400	Weak transcription	Brain Substantia Nigra	brain
49	chr14:47812200-47812400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr14:47812200-47812600	Enhancers	HUES48 Cell Line	embryonic stem cell

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