Variant report

Variant	esv3328872
Chromosome Location	chr14:105326457-105329755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:105327370-105327623	GM19239	blood:	n/a	n/a
2	CTCF	chr14:105327713-105327773	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr14:105326678-105326680	GM19239	blood:	n/a	n/a
4	CTCF	chr14:105327624-105327633	GM12891	blood:	n/a	n/a
5	CTCF	chr14:105327667-105327672	GM12891	blood:	n/a	n/a
6	CTCF	chr14:105327741-105327743	GM12892	blood:	n/a	n/a
7	CTCF	chr14:105327420-105327570	GM12872	blood:	n/a	n/a
8	CTCF	chr14:105327322-105327357	Lung_OC	lung:	n/a	n/a
9	CTCF	chr14:105327643-105327652	GM19239	blood:	n/a	n/a
10	CTCF	chr14:105327744-105327836	GM12892	blood:	n/a	n/a
11	EGR1	chr14:105328418-105328753	GM12878	blood:	n/a	n/a
12	GABPA	chr14:105328361-105328511	Hela-S3	cervix:	n/a	n/a
13	HEY1	chr14:105328347-105328676	HepG2	liver:	n/a	n/a
14	HEY1	chr14:105328330-105328865	HepG2	liver:	n/a	n/a
15	IRF4	chr14:105328317-105328811	GM12878	blood:	n/a	n/a
16	JUND	chr14:105328351-105328537	HepG2	liver:	n/a	n/a
17	MYC	chr14:105327558-105327575	GM12878	blood:	n/a	n/a
18	MYC	chr14:105327613-105327666	MCF-7	breast:	n/a	n/a
19	MYC	chr14:105327758-105327863	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr14:105327669-105327672	MCF-7	breast:	n/a	n/a
21	MYC	chr14:105327589-105327737	GM12878	blood:	n/a	n/a
22	POLR2A	chr14:105328469-105328898	HepG2	liver:	n/a	n/a
23	POLR2A	chr14:105327478-105327703	MCF-7	breast:	n/a	n/a
24	POLR2A	chr14:105328501-105328742	HepG2	liver:	n/a	n/a
25	POLR2A	chr14:105328233-105329120	HepG2	liver:	n/a	n/a
26	POLR2A	chr14:105325013-105328346	HepG2	liver:	n/a	n/a
27	POLR2A	chr14:105328264-105328727	HepG2	liver:	n/a	n/a
28	POLR2A	chr14:105327133-105327981	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr14:105328322-105328433	K562	blood:	n/a	n/a
30	POLR2A	chr14:105327715-105327930	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr14:105328135-105328804	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr14:105327308-105327378	HepG2	liver:	n/a	n/a
33	POLR2A	chr14:105328022-105328772	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr14:105328264-105328729	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr14:105327395-105327417	K562	blood:	n/a	n/a
36	POLR2A	chr14:105327604-105327947	HepG2	liver:	n/a	n/a
37	POLR2A	chr14:105327127-105328857	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr14:105327518-105328721	HepG2	liver:	n/a	n/a
39	POLR2A	chr14:105329203-105329387	HepG2	liver:	n/a	n/a
40	POLR2A	chr14:105327693-105328224	HepG2	liver:	n/a	n/a
41	POLR2A	chr14:105328738-105329130	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:105328292-105328519	A549	lung:	n/a	n/a
43	POLR2A	chr14:105328604-105328721	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr14:105327421-105327540	K562	blood:	n/a	n/a
45	POLR2A	chr14:105328988-105329020	HepG2	liver:	n/a	n/a
46	POLR2A	chr14:105327626-105327655	HepG2	liver:	n/a	n/a
47	POLR2A	chr14:105327099-105328890	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr14:105328870-105328999	HepG2	liver:	n/a	n/a
49	POU2F2	chr14:105328308-105328770	GM12878	blood:	n/a	n/a
50	RCOR1	chr14:105326291-105326507	K562	blood:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105325199..105327039-chr14:105327761..105330678,2	K562	blood:
2	chr14:105322733..105324801-chr14:105327014..105329537,2	K562	blood:
3	chr14:105239791..105242217-chr14:105329726..105333005,4	MCF-7	breast:
4	chr14:105265888..105268831-chr14:105329056..105330600,3	MCF-7	breast:
5	chr14:105155136..105157307-chr14:105329558..105331716,2	MCF-7	breast:
6	chr14:105325199..105327039-chr14:105327761..105330678,2	K562	blood:
7	chr14:105287373..105290281-chr14:105329548..105332218,5	MCF-7	breast:
8	chr14:105265912..105268902-chr14:105329301..105333250,7	MCF-7	breast:
9	chr14:105277673..105279757-chr14:105329358..105331314,2	K562	blood:
10	chr14:105329238..105330750-chr14:105398198..105400578,2	MCF-7	breast:
11	chr14:105319643..105321546-chr14:105328371..105330492,2	K562	blood:
12	chr14:105308114..105313218-chr14:105327481..105332918,6	MCF-7	breast:

(count:24 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000258593	TF binding region
CEP170B	TF binding region
ENSG00000166428	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000203485	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000258811	chromatin interactions
ENSG00000142208	chromatin interactions

Extended variants
information (count: 136 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146073487	chr14:105326518-105326519	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs372053399	chr14:105326519-105326520	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs144379164	chr14:105326535-105326536	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs557682344	chr14:105326599-105326600	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs201390869	chr14:105326605-105326606	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs571291522	chr14:105326662-105326663	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs536774282	chr14:105326704-105326705	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs556523816	chr14:105326719-105326720	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs142028724	chr14:105326724-105326725	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs573342156	chr14:105326732-105326733	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs542114834	chr14:105326744-105326745	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs181130702	chr14:105326759-105326760	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs572661677	chr14:105326789-105326790	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs147779340	chr14:105326839-105326840	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs386781080	chr14:105326845-105326846	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs138797119	chr14:105326847-105326848	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs386781081	chr14:105326864-105326865	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs376641929	chr14:105326865-105326866	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs541580927	chr14:105326869-105326870	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs386781082	chr14:105326871-105326872	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs373335523	chr14:105326873-105326874	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs377070764	chr14:105326878-105326879	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs386781083	chr14:105326884-105326885	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs564548746	chr14:105326934-105326935	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs533486466	chr14:105327000-105327001	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs562314453	chr14:105327011-105327012	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs375310633	chr14:105327012-105327013	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs201974025	chr14:105327013-105327014	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs543899581	chr14:105327042-105327043	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs563678533	chr14:105327046-105327047	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs531355676	chr14:105327061-105327062	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs141864729	chr14:105327062-105327063	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs529354820	chr14:105327125-105327126	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs549391708	chr14:105327155-105327156	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs199771703	chr14:105327173-105327174	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs115468514	chr14:105327184-105327185	Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs72700143	chr14:105327201-105327202	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs201241141	chr14:105327215-105327216	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs138074208	chr14:105327253-105327254	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs202109310	chr14:105327305-105327306	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs571320527	chr14:105327331-105327332	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs536759382	chr14:105327334-105327335	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs186776727	chr14:105327336-105327337	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs567018367	chr14:105327363-105327364	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs535883175	chr14:105327409-105327410	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs377694250	chr14:105327426-105327427	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs191686441	chr14:105327512-105327513	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs61995981	chr14:105327524-105327525	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs534977409	chr14:105327551-105327552	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs558343993	chr14:105327607-105327608	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 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:101 , 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	chr14:105320200-105330400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr14:105321600-105329400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr14:105322800-105328600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:105322800-105329000	Weak transcription	Fetal Intestine Small	intestine
8	chr14:105323000-105328800	Weak transcription	HepG2	liver
9	chr14:105323200-105327200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr14:105323200-105328800	Weak transcription	NHEK	skin
11	chr14:105323800-105327400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:105323800-105327400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:105323800-105330200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:105324000-105328800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:105324000-105329600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr14:105324000-105330800	Weak transcription	Brain Substantia Nigra	brain
17	chr14:105324200-105329000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr14:105324600-105329000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr14:105325000-105330200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:105325800-105327800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr14:105325800-105329600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:105326200-105326600	ZNF genes & repeats	Pancreas	Pancrea
23	chr14:105326200-105328000	Enhancers	Gastric	stomach
24	chr14:105326600-105327200	Weak transcription	Pancreas	Pancrea
25	chr14:105327200-105327600	Enhancers	Esophagus	oesophagus
26	chr14:105327200-105328200	Genic enhancers	Pancreas	Pancrea
27	chr14:105327200-105329400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:105327400-105327600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr14:105327400-105327600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:105327400-105327600	ZNF genes & repeats	Fetal Kidney	kidney
31	chr14:105327400-105327600	ZNF genes & repeats	Lung	lung
32	chr14:105327400-105327800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:105327400-105328000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr14:105327600-105328000	Weak transcription	Lung	lung
35	chr14:105327600-105328600	Weak transcription	Fetal Kidney	kidney
36	chr14:105327600-105329400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr14:105327600-105329800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr14:105327600-105330200	Weak transcription	Esophagus	oesophagus
39	chr14:105327800-105328200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:105327800-105329600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr14:105327800-105329800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:105327800-105330200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr14:105327800-105330200	Weak transcription	Liver	Liver
44	chr14:105327800-105330200	Weak transcription	Hela-S3	cervix
45	chr14:105328000-105328200	Flanking Active TSS	Gastric	stomach
46	chr14:105328000-105328400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr14:105328000-105328800	Enhancers	Lung	lung
48	chr14:105328000-105329000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr14:105328200-105328600	Enhancers	Gastric	stomach
50	chr14:105328200-105329000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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