Variant report

Variant	esv3404070
Chromosome Location	chr14:105323807-105329505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:105327713-105327773	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr14:105327420-105327570	GM12872	blood:	n/a	n/a
3	CTCF	chr14:105327667-105327672	GM12891	blood:	n/a	n/a
4	CTCF	chr14:105327744-105327836	GM12892	blood:	n/a	n/a
5	CTCF	chr14:105327643-105327652	GM19239	blood:	n/a	n/a
6	CTCF	chr14:105327741-105327743	GM12892	blood:	n/a	n/a
7	CTCF	chr14:105327370-105327623	GM19239	blood:	n/a	n/a
8	CTCF	chr14:105327322-105327357	Lung_OC	lung:	n/a	n/a
9	CTCF	chr14:105326678-105326680	GM19239	blood:	n/a	n/a
10	CTCF	chr14:105327624-105327633	GM12891	blood:	n/a	n/a
11	EGR1	chr14:105328418-105328753	GM12878	blood:	n/a	n/a
12	FOXP2	chr14:105323748-105323993	SK-N-MC	brain:	n/a	n/a
13	GABPA	chr14:105328361-105328511	Hela-S3	cervix:	n/a	n/a
14	GTF2F1	chr14:105323496-105323810	H1-hESC	embryonic stem cell:	n/a	n/a
15	HEY1	chr14:105328330-105328865	HepG2	liver:	n/a	n/a
16	HEY1	chr14:105328347-105328676	HepG2	liver:	n/a	n/a
17	IRF4	chr14:105328317-105328811	GM12878	blood:	n/a	n/a
18	JUND	chr14:105328351-105328537	HepG2	liver:	n/a	n/a
19	MYC	chr14:105327758-105327863	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr14:105327558-105327575	GM12878	blood:	n/a	n/a
21	MYC	chr14:105327589-105327737	GM12878	blood:	n/a	n/a
22	MYC	chr14:105326201-105326214	HUVEC	blood vessel:	n/a	n/a
23	MYC	chr14:105325204-105325437	H1-hESC	embryonic stem cell:	n/a	n/a
24	MYC	chr14:105327613-105327666	MCF-7	breast:	n/a	n/a
25	MYC	chr14:105327669-105327672	MCF-7	breast:	n/a	n/a
26	POLR2A	chr14:105327604-105327947	HepG2	liver:	n/a	n/a
27	POLR2A	chr14:105325976-105326378	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr14:105328264-105328729	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr14:105328988-105329020	HepG2	liver:	n/a	n/a
30	POLR2A	chr14:105327693-105328224	HepG2	liver:	n/a	n/a
31	POLR2A	chr14:105328135-105328804	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr14:105328469-105328898	HepG2	liver:	n/a	n/a
33	POLR2A	chr14:105328501-105328742	HepG2	liver:	n/a	n/a
34	POLR2A	chr14:105328264-105328727	HepG2	liver:	n/a	n/a
35	POLR2A	chr14:105325013-105328346	HepG2	liver:	n/a	n/a
36	POLR2A	chr14:105323738-105324184	SK-N-MC	brain:	n/a	n/a
37	POLR2A	chr14:105327715-105327930	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr14:105324531-105324822	HepG2	liver:	n/a	n/a
39	POLR2A	chr14:105324111-105324453	HepG2	liver:	n/a	n/a
40	POLR2A	chr14:105327308-105327378	HepG2	liver:	n/a	n/a
41	POLR2A	chr14:105328322-105328433	K562	blood:	n/a	n/a
42	POLR2A	chr14:105327099-105328890	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr14:105327478-105327703	MCF-7	breast:	n/a	n/a
44	POLR2A	chr14:105327133-105327981	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr14:105327421-105327540	K562	blood:	n/a	n/a
46	POLR2A	chr14:105327127-105328857	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr14:105322971-105323918	HepG2	liver:	n/a	n/a
48	POLR2A	chr14:105327395-105327417	K562	blood:	n/a	n/a
49	POLR2A	chr14:105328738-105329130	HepG2	liver:	n/a	n/a
50	POLR2A	chr14:105328604-105328721	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr14:105325199..105327039-chr14:105327761..105330678,2	K562	blood:
2	chr14:105325199..105327039-chr14:105327761..105330678,2	K562	blood:
3	chr14:105265888..105268831-chr14:105329056..105330600,3	MCF-7	breast:
4	chr14:105265912..105268902-chr14:105329301..105333250,7	MCF-7	breast:
5	chr14:105277673..105279757-chr14:105329358..105331314,2	K562	blood:
6	chr14:105322733..105324801-chr14:105327014..105329537,2	K562	blood:
7	chr14:105329238..105330750-chr14:105398198..105400578,2	MCF-7	breast:
8	chr14:105322733..105324801-chr14:105327014..105329537,2	K562	blood:
9	chr14:105308114..105313218-chr14:105327481..105332918,6	MCF-7	breast:
10	chr14:105264903..105267195-chr14:105323456..105325361,2	MCF-7	breast:
11	chr14:105319643..105321546-chr14:105328371..105330492,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKT1-1	chr14:105327909-105329049	NONHSAT040292
2	lnc-AKT1-1	chr14:105328010-105328919	NONHSAT040298
3	lnc-AKT1-1	chr14:105328126-105328768	NONHSAT040300
4	lnc-AKT1-1	chr14:105325379-105325618	ENSG00000258593.1
5	lnc-AKT1-1	chr14:105328672-105329100	NONHSAT040301
6	lnc-AKT1-1	chr14:105327493-105328919	NONHSAT040297
7	lnc-AKT1-1	chr14:105325778-105325789	NONHSAT040295
8	lnc-AKT1-1	chr14:105327785-105327843	NONHSAT040291
9	lnc-AKT1-1	chr14:105327506-105327765	NONHSAT040294
10	lnc-AKT1-1	chr14:105324129-105325173	ENSG00000258593.2
11	lnc-AKT1-1	chr14:105324129-105325113	ENSG00000258593.1
12	lnc-AKT1-1	chr14:105325098-105325205	NONHSAT040291
13	lnc-AKT1-1	chr14:105327063-105327687	NONHSAT040292
14	lnc-AKT1-1	chr14:105327063-105329049	NONHSAT040293
15	lnc-AKT1-1	chr14:105327188-105327362	NONHSAT040297
16	lnc-AKT1-1	chr14:105327564-105329057	NONHSAT040295
17	lnc-AKT1-1	chr14:105325769-105326662	NONHSAT040294
18	lnc-AKT1-1	chr14:105327063-105327427	NONHSAT040294
19	lnc-AKT1-1	chr14:105327922-105328954	NONHSAT040291
20	lnc-AKT1-1	chr14:105325183-105325493	NONHSAT040292
21	lnc-AKT1-1	chr14:105327335-105327765	NONHSAT040300
22	lnc-KIAA0284-3	chr14:105327183-105327694	NONHSAT040296
23	lnc-AKT1-1	chr14:105327314-105327973	NONHSAT040299
24	lnc-AKT1-1	chr14:105325942-105326662	NONHSAT040293
25	lnc-AKT1-1	chr14:105325981-105326662	NONHSAT040292
26	lnc-KIAA0284-3	chr14:105328548-105329057	NONHSAT040296
27	lnc-AKT1-1	chr14:105328529-105328626	NONHSAT040299
28	lnc-AKT1-1	chr14:105327188-105327882	NONHSAT040298
29	lnc-AKT1-1	chr14:105325183-105325493	NONHSAT040293
30	lnc-AKT1-1	chr14:105327974-105329049	NONHSAT040294
31	lnc-AKT1-1	chr14:105328195-105328281	NONHSAT040301

No data

Variant related genes	Relation type
ENSG00000258593	TF binding region
CEP170B	TF binding region
ENSG00000166428	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000258811	chromatin interactions

Extended variants
information (count: 218 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:218 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568217082	chr14:105323824-105323825	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs533891592	chr14:105323874-105323875	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs117062957	chr14:105323889-105323890	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs79091350	chr14:105323908-105323909	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375553592	chr14:105323913-105323914	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185207186	chr14:105323921-105323922	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149221980	chr14:105323970-105323971	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560393746	chr14:105324017-105324018	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112424674	chr14:105324064-105324065	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142435217	chr14:105324082-105324083	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190051534	chr14:105324113-105324114	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182207509	chr14:105324120-105324121	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561721294	chr14:105324161-105324162	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs540423137	chr14:105324167-105324168	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs572182190	chr14:105324218-105324219	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs11846387	chr14:105324299-105324300	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564134275	chr14:105324362-105324363	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs545963085	chr14:105324402-105324403	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs34344799	chr14:105324484-105324485	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560353333	chr14:105324493-105324494	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs562935938	chr14:105324502-105324503	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs531742998	chr14:105324504-105324505	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs116500307	chr14:105324508-105324509	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs140548864	chr14:105324512-105324513	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs534048774	chr14:105324513-105324514	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs185554039	chr14:105324535-105324536	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs11847346	chr14:105324537-105324538	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs539343754	chr14:105324568-105324569	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs188295222	chr14:105324569-105324570	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs576409503	chr14:105324587-105324588	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs535606691	chr14:105324658-105324659	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs555618555	chr14:105324661-105324662	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs572147013	chr14:105324716-105324717	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs528464224	chr14:105324724-105324725	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs180764001	chr14:105324752-105324753	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs377489205	chr14:105324780-105324781	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs558034317	chr14:105324781-105324782	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs2028417	chr14:105324800-105324801	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs138302948	chr14:105324856-105324857	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs567626681	chr14:105324877-105324878	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs185660531	chr14:105324884-105324885	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs543679979	chr14:105324903-105324904	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs531898586	chr14:105324919-105324920	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs144191572	chr14:105324946-105324947	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs548345966	chr14:105325042-105325043	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs561973548	chr14:105325065-105325066	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs71423205	chr14:105325090-105325091	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs71421888	chr14:105325091-105325092	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs71454486	chr14:105325115-105325116	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs530106147	chr14:105325119-105325120	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
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
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105311000-105330600	Weak transcription	Right Atrium	heart
2	chr14:105312600-105329000	Weak transcription	HMEC	breast
3	chr14:105313200-105327600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:105318800-105326200	Weak transcription	Pancreas	Pancrea
5	chr14:105319000-105325800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:105320200-105330400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:105321600-105329400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr14:105322800-105328600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:105322800-105329000	Weak transcription	Fetal Intestine Small	intestine
10	chr14:105323000-105324000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr14:105323000-105324000	Enhancers	Brain Angular Gyrus	brain
12	chr14:105323000-105328800	Weak transcription	HepG2	liver
13	chr14:105323200-105324200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr14:105323200-105327200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:105323200-105328800	Weak transcription	NHEK	skin
16	chr14:105323400-105324000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:105323400-105324000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr14:105323400-105324000	Enhancers	Brain Anterior Caudate	brain
19	chr14:105323600-105324000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr14:105323600-105324000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:105323600-105324000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:105323600-105324200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr14:105323800-105324000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:105323800-105324000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:105323800-105324000	Active TSS	Brain Hippocampus Middle	brain
26	chr14:105323800-105324000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
27	chr14:105323800-105324000	Enhancers	Brain Substantia Nigra	brain
28	chr14:105323800-105325000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:105323800-105326200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:105323800-105327400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:105323800-105327400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:105323800-105330200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr14:105324000-105328800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:105324000-105329600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr14:105324000-105330800	Weak transcription	Brain Substantia Nigra	brain
36	chr14:105324200-105329000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr14:105324600-105329000	Weak transcription	Duodenum Mucosa	Duodenum
38	chr14:105325000-105330200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:105325200-105325400	Enhancers	Spleen	Spleen
40	chr14:105325800-105327800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
41	chr14:105325800-105329600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:105326200-105326600	ZNF genes & repeats	Pancreas	Pancrea
43	chr14:105326200-105328000	Enhancers	Gastric	stomach
44	chr14:105326600-105327200	Weak transcription	Pancreas	Pancrea
45	chr14:105327200-105327600	Enhancers	Esophagus	oesophagus
46	chr14:105327200-105328200	Genic enhancers	Pancreas	Pancrea
47	chr14:105327200-105329400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:105327400-105327600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
49	chr14:105327400-105327600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr14:105327400-105327600	ZNF genes & repeats	Fetal Kidney	kidney

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