Variant report

Variant	esv1800828
Chromosome Location	chr14:104343852-104351500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:104345731-104347463	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:104347732-104348043	HepG2	liver:	n/a	n/a
3	BACH1	chr14:104349871-104350089	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:104346415-104346682	HepG2	liver:	n/a	n/a
5	BHLHE40	chr14:104345769-104348105	HepG2	liver:	n/a	n/a
6	BHLHE40	chr14:104346450-104346698	A549	lung:	n/a	n/a
7	BHLHE40	chr14:104346404-104346918	HepG2	liver:	n/a	n/a
8	BRCA1	chr14:104346610-104346954	HepG2	liver:	n/a	n/a
9	BRCA1	chr14:104347700-104347836	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:104345886-104346995	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:104347441-104347848	HepG2	liver:	n/a	n/a
12	CEBPD	chr14:104347533-104348183	HepG2	liver:	n/a	n/a
13	CEBPD	chr14:104346767-104347340	HepG2	liver:	n/a	n/a
14	CEBPD	chr14:104345976-104346543	HepG2	liver:	n/a	n/a
15	CHD2	chr14:104346405-104346600	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr14:104346387-104346611	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr14:104346194-104346827	HepG2	liver:	n/a	n/a
18	CTCF	chr14:104347640-104347790	HepG2	liver:	n/a	chr14:104347669-104347682
19	CTCF	chr14:104347760-104347855	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:104347797-104347819	GM12892	blood:	n/a	n/a
21	CTCF	chr14:104347660-104347810	BE2_C	brain:	n/a	chr14:104347669-104347682
22	CTCF	chr14:104349120-104349270	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr14:104346280-104346570	HEEpiC	esophagus:	n/a	chr14:104346333-104346341
24	CTCF	chr14:104349080-104349230	HepG2	liver:	n/a	n/a
25	CTCF	chr14:104346540-104346690	AG10803	skin:	n/a	n/a
26	CTCF	chr14:104347778-104347826	MCF-7	breast:	n/a	n/a
27	CTCF	chr14:104345940-104346090	GM12878	blood:	n/a	n/a
28	CTCF	chr14:104347754-104347847	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr14:104346520-104346670	BJ	skin:	n/a	n/a
30	CTCF	chr14:104347760-104347910	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr14:104347726-104347850	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr14:104349020-104349170	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr14:104347745-104347867	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:104347759-104347842	MCF-7	breast:	n/a	n/a
35	E2F6	chr14:104346503-104347236	A549	lung:	n/a	n/a
36	EBF1	chr14:104346779-104347001	GM12878	blood:	n/a	n/a
37	ELF1	chr14:104346334-104346623	A549	lung:	n/a	n/a
38	ELF1	chr14:104346247-104346579	HepG2	liver:	n/a	n/a
39	ELF1	chr14:104346078-104346623	HepG2	liver:	n/a	n/a
40	EP300	chr14:104346240-104346665	T-47D	breast:	n/a	n/a
41	EP300	chr14:104348759-104349133	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr14:104347715-104347977	HepG2	liver:	n/a	n/a
43	EP300	chr14:104345947-104346948	ECC-1	luminal epithelium:	n/a	chr14:104346185-104346192
44	EP300	chr14:104345824-104347102	HepG2	liver:	n/a	chr14:104346185-104346192
45	EP300	chr14:104346179-104346734	T-47D	breast:	n/a	chr14:104346185-104346192
46	EP300	chr14:104346046-104346812	A549	lung:	n/a	chr14:104346185-104346192
47	EP300	chr14:104345926-104347277	HepG2	liver:	n/a	chr14:104346185-104346192
48	EP300	chr14:104346056-104346808	HepG2	liver:	n/a	chr14:104346185-104346192
49	ESR1	chr14:104346244-104346670	T-47D	breast:	n/a	n/a
50	ESR1	chr14:104346250-104346669	T-47D	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104345945-104345995	SK-N-SH_RA	brain:	n/a
2	chr14:104346591-104346641	GM06990	blood:	n/a
3	chr14:104345945-104345995	HNPCEpiC	eye:	n/a
4	chr14:104346591-104346641	MCF10A-Er-Src	breast:	n/a
5	chr14:104346241-104346291	A549	lung:	n/a
6	chr14:104346241-104346291	HAEpiC	amniotic membrane:	n/a
7	chr14:104346241-104346291	MCF-7	breast:	n/a
8	chr14:104346591-104346641	HCM	heart:	n/a
9	chr14:104345945-104345995	SKMC	muscle:	n/a
10	chr14:104345945-104345995	NB4	blood:	n/a
11	chr14:104345945-104345995	SAEC	small airway:	n/a
12	chr14:104346241-104346291	U87	brain:	n/a
13	chr14:104345945-104345995	HEK293	kidney:	embryo
14	chr14:104345945-104345995	AG04449	skin:	fetal
15	chr14:104345945-104345995	SK-N-MC	brain:	n/a
16	chr14:104345945-104345995	Hela-S3	cervix:	n/a
17	chr14:104345945-104345995	HRCEpiC	kidney:	n/a
18	chr14:104346241-104346291	HMEC	breast:	n/a
19	chr14:104346241-104346291	PrEC	prostate:	n/a
20	chr14:104346241-104346291	HRPEpiC	eye:	n/a
21	chr14:104345945-104345995	IMR90	lung:	fetal
22	chr14:104346591-104346641	HMEC	breast:	n/a
23	chr14:104346241-104346291	PFSK-1	brain:	n/a
24	chr14:104346241-104346291	NB4	blood:	n/a
25	chr14:104345945-104345995	AG10803	skin:	n/a
26	chr14:104346241-104346291	AoSMC	blood vessel:	n/a
27	chr14:104345945-104345995	SK-N-SH	brain:	n/a
28	chr14:104346241-104346291	CMK	blood:	n/a
29	chr14:104346591-104346641	IMR90	lung:	fetal
30	chr14:104346241-104346291	HNPCEpiC	eye:	n/a
31	chr14:104345945-104345995	ProgFib	skin:	n/a
32	chr14:104345945-104345995	LNCaP	prostate:	n/a
33	chr14:104345945-104345995	MCF-7	breast:	n/a
34	chr14:104346241-104346291	BJ	skin:	n/a
35	chr14:104345945-104345995	U87	brain:	n/a
36	chr14:104346591-104346641	HL-60	blood:	n/a
37	chr14:104346591-104346641	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:104346241-104346291	HCT-116	colon:	n/a
39	chr14:104346591-104346641	NH-A	brain:	n/a
40	chr14:104345945-104345995	GM12878	blood:	n/a
41	chr14:104346241-104346291	SAEC	small airway:	n/a
42	chr14:104346591-104346641	HNPCEpiC	eye:	n/a
43	chr14:104346591-104346641	SKMC	muscle:	n/a
44	chr14:104346241-104346291	PANC-1	pancreas:	n/a
45	chr14:104346591-104346641	HRPEpiC	eye:	n/a
46	chr14:104346241-104346291	SKMC	muscle:	n/a
47	chr14:104346241-104346291	HL-60	blood:	n/a
48	chr14:104345945-104345995	NHDF-neo	bronchial:	n/a
49	chr14:104346591-104346641	SK-N-MC	brain:	n/a
50	chr14:104346591-104346641	HEEpiC	esophagus:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104343466..104345327-chr14:104362441..104364606,2	K562	blood:
2	chr14:104181031..104183384-chr14:104347626..104349344,2	MCF-7	breast:
3	chr14:104320594..104323018-chr14:104349310..104351645,2	MCF-7	breast:
4	chr14:104348645..104351214-chr14:104375295..104378157,2	MCF-7	breast:
5	chr14:104340678..104342509-chr14:104346127..104348373,2	MCF-7	breast:
6	chr14:104348563..104351528-chr14:104352651..104356401,4	K562	blood:
7	chr14:104342467..104345187-chr14:104355394..104358113,2	MCF-7	breast:
8	chr14:104348563..104350260-chr14:104352651..104354424,2	K562	blood:
9	chr14:104343585..104349004-chr14:104350289..104354893,7	MCF-7	breast:
10	chr14:104312778..104315212-chr14:104344720..104347233,3	MCF-7	breast:
11	chr14:104347054..104348741-chr14:104350069..104352618,2	K562	blood:
12	chr14:104005381..104007221-chr14:104349678..104351959,2	K562	blood:
13	chr14:104348661..104350567-chr14:104371429..104374100,2	MCF-7	breast:
14	chr14:104320208..104324271-chr14:104346660..104350133,4	MCF-7	breast:
15	chr14:104347054..104348741-chr14:104350069..104352618,2	K562	blood:
16	chr14:104159610..104160117-chr14:104349177..104349684,2	MCF-7	breast:
17	chr14:104336130..104339253-chr14:104343612..104346035,4	MCF-7	breast:
18	chr14:104319613..104324063-chr14:104346589..104349290,5	MCF-7	breast:
19	chr14:104335008..104337928-chr14:104351341..104353510,3	MCF-7	breast:
20	chr14:104351018..104353647-chr14:104363104..104364953,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2134A5.2.1-2	chr14:104345741-104346670	XLOC_010945
2	lnc-PPP1R13B-1	chr14:104345681-104345793	ENSG00000258534
3	lnc-PPP1R13B-1	chr14:104345681-104346641	NONHSAT040223
4	lnc-CTD-2134A5.2.1-2	chr14:104343732-104343932	XLOC_010945
5	lnc-PPP1R13B-1	chr14:104346301-104346448	ENSG00000258534
6	lnc-PPP1R13B-1	chr14:104345681-104346641	NONHSAT040224

No data

Variant related genes	Relation type
ENSG00000258534	TF binding region
ENSG00000258534	CpG island
ENSG00000126215	chromatin interactions
ENSG00000258534	chromatin interactions
ENSG00000258735	chromatin interactions
ENSG00000100711	chromatin interactions
ENSG00000258914	chromatin interactions
ENSG00000088808	chromatin interactions
PPP3CA	miRNA target sites
PPP2R5C	miRNA target sites

Extended variants
information (count: 318 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12432225	chr14:104343852-104343853	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568575595	chr14:104343925-104343926	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534328697	chr14:104343943-104343944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538012982	chr14:104343971-104343972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115129143	chr14:104344012-104344013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117230797	chr14:104344015-104344016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192828165	chr14:104344017-104344018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553491901	chr14:104344109-104344110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556196971	chr14:104344142-104344143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569604315	chr14:104344173-104344174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143224356	chr14:104344196-104344197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554986498	chr14:104344207-104344208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369918047	chr14:104344254-104344255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376160152	chr14:104344263-104344264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35125081	chr14:104344305-104344306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540758477	chr14:104344319-104344320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553933110	chr14:104344328-104344329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10135270	chr14:104344341-104344342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs10135198	chr14:104344391-104344392	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559004020	chr14:104344410-104344411	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs145552077	chr14:104344431-104344432	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs531691483	chr14:104344442-104344443	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs542233946	chr14:104344444-104344445	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs562109847	chr14:104344514-104344515	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs138073943	chr14:104344544-104344545	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs575869783	chr14:104344545-104344546	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs142535712	chr14:104344551-104344552	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs570623817	chr14:104344580-104344581	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs199731159	chr14:104344593-104344594	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533000542	chr14:104344611-104344612	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372213537	chr14:104344632-104344633	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs550000836	chr14:104344673-104344674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185761881	chr14:104344691-104344692	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs535791379	chr14:104344712-104344713	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs77913665	chr14:104344722-104344723	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189423975	chr14:104344723-104344724	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs116677596	chr14:104344726-104344727	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs145979050	chr14:104344732-104344733	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs79593551	chr14:104344736-104344737	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546091386	chr14:104344750-104344751	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs556756319	chr14:104344773-104344774	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs181824794	chr14:104344878-104344879	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374785299	chr14:104344881-104344882	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs72712843	chr14:104344883-104344884	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs527699035	chr14:104344894-104344895	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539986631	chr14:104344895-104344896	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs541506369	chr14:104344945-104344946	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs12889842	chr14:104344947-104344948	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs532216000	chr14:104344959-104344960	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs78903115	chr14:104345018-104345019	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104339200-104344400	Weak transcription	HepG2	liver
2	chr14:104339200-104345600	Weak transcription	A549	lung
3	chr14:104339200-104345800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr14:104339200-104346200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr14:104339200-104346200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr14:104339400-104345400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr14:104339400-104345600	Weak transcription	Fetal Muscle Leg	muscle
8	chr14:104339400-104345800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr14:104339400-104345800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr14:104339400-104345800	Weak transcription	Colonic Mucosa	Colon
11	chr14:104339400-104345800	Weak transcription	Right Ventricle	heart
12	chr14:104339400-104346000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:104339400-104346000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:104339400-104346000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:104339400-104346000	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr14:104339400-104346000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr14:104339400-104346000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr14:104339400-104346000	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr14:104339600-104346000	Weak transcription	Primary T cells from cord blood	blood
20	chr14:104340000-104345600	Weak transcription	Fetal Intestine Large	intestine
21	chr14:104340000-104345800	Weak transcription	Left Ventricle	heart
22	chr14:104340200-104344600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr14:104340200-104345600	Weak transcription	Fetal Intestine Small	intestine
24	chr14:104340200-104346000	Weak transcription	Placenta	Placenta
25	chr14:104340200-104346000	Weak transcription	Fetal Stomach	stomach
26	chr14:104340200-104346200	Weak transcription	Fetal Thymus	thymus
27	chr14:104341400-104346400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr14:104341600-104344800	Weak transcription	Liver	Liver
29	chr14:104341600-104345000	Weak transcription	Stomach Mucosa	stomach
30	chr14:104341600-104345200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr14:104341600-104345400	Weak transcription	Pancreas	Pancrea
32	chr14:104341600-104345800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr14:104341600-104345800	Weak transcription	Esophagus	oesophagus
34	chr14:104341600-104346000	Weak transcription	Lung	lung
35	chr14:104341600-104346000	Weak transcription	Spleen	Spleen
36	chr14:104341600-104346000	Weak transcription	GM12878-XiMat	blood
37	chr14:104341600-104346200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr14:104341600-104346800	Weak transcription	Gastric	stomach
39	chr14:104342800-104344200	Enhancers	Duodenum Mucosa	Duodenum
40	chr14:104343400-104344000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr14:104343600-104344000	Enhancers	Primary hematopoietic stem cells	blood
42	chr14:104343600-104344000	Enhancers	Fetal Lung	lung
43	chr14:104343600-104345800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr14:104343800-104344000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:104343800-104345600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr14:104344000-104345000	Weak transcription	Fetal Lung	lung
47	chr14:104344000-104345600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr14:104344000-104346000	Weak transcription	Primary hematopoietic stem cells	blood
49	chr14:104344200-104345000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr14:104344400-104344600	Active TSS	HepG2	liver

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