Variant report

Variant	esv3374137
Chromosome Location	chr14:104870956-104894273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr14:104873436-104873767	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
2	BATF	chr14:104873533-104873737	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
3	BATF	chr14:104882766-104882975	GM12878	blood:	n/a	chr14:104882870-104882881
4	BHLHE40	chr14:104891140-104891268	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:104891142-104891342	K562	blood:	n/a	n/a
6	CREB1	chr14:104886313-104886828	GM12878	blood:	n/a	n/a
7	CREB1	chr14:104886256-104886838	GM12878	blood:	n/a	n/a
8	CTCF	chr14:104888440-104888590	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr14:104887154-104887218	GM20000	blood:	n/a	n/a
10	CTCF	chr14:104874198-104874278	GM10248	blood:	n/a	n/a
11	CTCF	chr14:104888520-104888670	BE2_C	brain:	n/a	n/a
12	CTCF	chr14:104886281-104886430	GM12878	blood:	n/a	n/a
13	CTCF	chr14:104888460-104888610	SK-N-SH_RA	brain:	n/a	n/a
14	CUX1	chr14:104884304-104884504	GM12878	blood:	n/a	n/a
15	EBF1	chr14:104886495-104886811	GM12878	blood:	n/a	n/a
16	ELF1	chr14:104871218-104871553	GM12878	blood:	n/a	n/a
17	FOXM1	chr14:104886318-104886800	GM12878	blood:	n/a	n/a
18	IKZF1	chr14:104882695-104882880	GM12878	blood:	n/a	n/a
19	MAX	chr14:104891071-104891360	K562	blood:	n/a	chr14:104891166-104891176 chr14:104891168-104891177 chr14:104891268-104891278 chr14:104891167-104891178 chr14:104891168-104891178 chr14:104891270-104891277 chr14:104891169-104891176 chr14:104891342-104891352 chr14:104891166-104891181 chr14:104891164-104891179
20	MAX	chr14:104871231-104871379	K562	blood:	n/a	n/a
21	MAX	chr14:104891083-104891338	NB4	blood:	n/a	chr14:104891166-104891176 chr14:104891168-104891177 chr14:104891268-104891278 chr14:104891167-104891178 chr14:104891168-104891178 chr14:104891270-104891277 chr14:104891169-104891176 chr14:104891166-104891181 chr14:104891164-104891179
22	MAX	chr14:104890991-104891519	ECC-1	luminal epithelium:	n/a	chr14:104891166-104891176 chr14:104891168-104891177 chr14:104891268-104891278 chr14:104891167-104891178 chr14:104891168-104891178 chr14:104891270-104891277 chr14:104891169-104891176 chr14:104891342-104891352 chr14:104891166-104891181 chr14:104891164-104891179
23	MAX	chr14:104891102-104891497	ECC-1	luminal epithelium:	n/a	chr14:104891166-104891176 chr14:104891168-104891177 chr14:104891268-104891278 chr14:104891167-104891178 chr14:104891168-104891178 chr14:104891270-104891277 chr14:104891169-104891176 chr14:104891342-104891352 chr14:104891166-104891181 chr14:104891164-104891179
24	MAX	chr14:104891027-104891370	H1-hESC	embryonic stem cell:	n/a	chr14:104891166-104891176 chr14:104891168-104891177 chr14:104891268-104891278 chr14:104891167-104891178 chr14:104891168-104891178 chr14:104891270-104891277 chr14:104891169-104891176 chr14:104891342-104891352 chr14:104891166-104891181 chr14:104891164-104891179
25	MAZ	chr14:104891282-104891292	K562	blood:	n/a	n/a
26	MEF2A	chr14:104886335-104886839	GM12878	blood:	n/a	n/a
27	MXI1	chr14:104890635-104891648	SK-N-SH	brain:	n/a	chr14:104891015-104891024 chr14:104891268-104891277 chr14:104891169-104891178 chr14:104891412-104891421
28	MYC	chr14:104871315-104871333	H1-hESC	embryonic stem cell:	n/a	n/a
29	MYC	chr14:104871147-104871345	K562	blood:	n/a	n/a
30	MYC	chr14:104871337-104871411	H1-hESC	embryonic stem cell:	n/a	n/a
31	MYC	chr14:104891178-104891193	NB4	blood:	n/a	n/a
32	NFIC	chr14:104886261-104886848	GM12878	blood:	n/a	n/a
33	PAX5	chr14:104873887-104874101	GM12878	blood:	n/a	n/a
34	PML	chr14:104886215-104886936	GM12878	blood:	n/a	n/a
35	POLR2A	chr14:104887927-104887935	MCF-7	breast:	n/a	n/a
36	POLR2A	chr14:104886975-104887045	MCF-7	breast:	n/a	n/a
37	POLR2A	chr14:104889260-104889318	MCF-7	breast:	n/a	n/a
38	POLR2A	chr14:104886238-104886549	GM12892	blood:	n/a	n/a
39	POLR2A	chr14:104886344-104886500	ProgFib	skin:	n/a	n/a
40	POLR2A	chr14:104892380-104892417	MCF-7	breast:	n/a	n/a
41	POLR2A	chr14:104886232-104886698	GM12892	blood:	n/a	n/a
42	POLR2A	chr14:104887955-104887960	MCF-7	breast:	n/a	n/a
43	RELA	chr14:104886281-104886888	GM18505	blood:	n/a	n/a
44	RELA	chr14:104886257-104886833	GM12878	blood:	n/a	n/a
45	RELA	chr14:104886340-104886847	GM12892	blood:	n/a	n/a
46	RFX5	chr14:104872508-104872618	K562	blood:	n/a	n/a
47	RUNX3	chr14:104882669-104883081	GM12878	blood:	n/a	n/a
48	RUNX3	chr14:104886275-104886830	GM12878	blood:	n/a	n/a
49	RUNX3	chr14:104882714-104883020	GM12878	blood:	n/a	n/a
50	SETDB1	chr14:104875394-104875850	U2OS	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104889005-104889055	K562	blood:	n/a
2	chr14:104889116-104889166	NB4	blood:	n/a
3	chr14:104889005-104889055	SK-N-MC	brain:	n/a
4	chr14:104889116-104889166	MCF10A-Er-Src	breast:	n/a
5	chr14:104889116-104889166	Hepatocyte	liver:	n/a
6	chr14:104893636-104893686	BE2_C	brain:	n/a
7	chr14:104888911-104888961	ovcar-3	ovarian:	n/a
8	chr14:104889005-104889055	HRCEpiC	kidney:	n/a
9	chr14:104893636-104893686	HCF	heart:	n/a
10	chr14:104888911-104888961	GM12891	blood:	n/a
11	chr14:104889116-104889166	SK-N-SH	brain:	n/a
12	chr14:104888911-104888961	SK-N-MC	brain:	n/a
13	chr14:104893636-104893686	HRE	kidney:	n/a
14	chr14:104893636-104893686	HIPEpiC	eye:	n/a
15	chr14:104889116-104889166	HRE	kidney:	n/a
16	chr14:104888911-104888961	HepG2	liver:	n/a
17	chr14:104889116-104889166	HEK293	kidney:	embryo
18	chr14:104893636-104893686	HEEpiC	esophagus:	n/a
19	chr14:104888911-104888961	A549	lung:	n/a
20	chr14:104888911-104888961	HAEpiC	amniotic membrane:	n/a
21	chr14:104889116-104889166	Hela-S3	cervix:	n/a
22	chr14:104893636-104893686	MCF10A-Er-Src	breast:	n/a
23	chr14:104893636-104893686	GM12878	blood:	n/a
24	chr14:104893636-104893686	SK-N-MC	brain:	n/a
25	chr14:104889005-104889055	H1-hESC	embryonic stem cell:	embryo
26	chr14:104889116-104889166	LNCaP	prostate:	n/a
27	chr14:104893636-104893686	A549	lung:	n/a
28	chr14:104888911-104888961	ECC-1	luminal epithelium:	n/a
29	chr14:104889005-104889055	PANC-1	pancreas:	n/a
30	chr14:104888911-104888961	GM12878	blood:	n/a
31	chr14:104888911-104888961	SK-N-SH	brain:	n/a
32	chr14:104893636-104893686	HCT-116	colon:	n/a
33	chr14:104888911-104888961	Jurkat	blood:	n/a
34	chr14:104889005-104889055	HCM	heart:	n/a
35	chr14:104889116-104889166	SAEC	small airway:	n/a
36	chr14:104889116-104889166	NHBE	bronchial:	n/a
37	chr14:104888911-104888961	LNCaP	prostate:	n/a
38	chr14:104893636-104893686	T-47D	breast:	n/a
39	chr14:104889005-104889055	RPTEC	kidney:	n/a
40	chr14:104888911-104888961	H1-hESC	embryonic stem cell:	embryo
41	chr14:104888911-104888961	Hela-S3	cervix:	n/a
42	chr14:104889116-104889166	U87	brain:	n/a
43	chr14:104889116-104889166	GM12891	blood:	n/a
44	chr14:104893636-104893686	Hepatocyte	liver:	n/a
45	chr14:104889005-104889055	HCPEpiC	choroid plexus:	n/a
46	chr14:104888911-104888961	GM19239	blood:	n/a
47	chr14:104889116-104889166	AG04450	lung:	fetal
48	chr14:104893636-104893686	SK-N-SH	brain:	n/a
49	chr14:104889005-104889055	SAEC	small airway:	n/a
50	chr14:104893636-104893686	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
2	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
3	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
4	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
5	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
6	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-684P	TF binding region
RNU6-684P	CpG island

Extended variants
information (count: 600 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527439469	chr14:104871008-104871009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150426940	chr14:104871014-104871015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570755192	chr14:104871025-104871026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183685225	chr14:104871045-104871046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188977061	chr14:104871065-104871066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377659884	chr14:104871078-104871079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138180071	chr14:104871125-104871126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535201576	chr14:104871145-104871146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553208243	chr14:104871202-104871203	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199917114	chr14:104871207-104871208	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs11621786	chr14:104871220-104871221	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370551990	chr14:104871262-104871263	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs181398474	chr14:104871337-104871338	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149550031	chr14:104871365-104871366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs577108391	chr14:104871369-104871370	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs539707965	chr14:104871374-104871375	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs556301356	chr14:104871400-104871401	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs143189615	chr14:104871416-104871417	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541967057	chr14:104871417-104871418	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs562202643	chr14:104871423-104871424	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572193037	chr14:104871429-104871430	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541204656	chr14:104871491-104871492	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs71419841	chr14:104871566-104871567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377380850	chr14:104871590-104871591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11626143	chr14:104871611-104871612	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs533289124	chr14:104871671-104871672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550053212	chr14:104871673-104871674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572686208	chr14:104871676-104871677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370346973	chr14:104871683-104871684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76179995	chr14:104871684-104871685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138893415	chr14:104871697-104871698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375454393	chr14:104871768-104871769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577989613	chr14:104871802-104871803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546193522	chr14:104871806-104871807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543447736	chr14:104871831-104871832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184704951	chr14:104871841-104871842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534159073	chr14:104871863-104871864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4619321	chr14:104871866-104871867	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs528287851	chr14:104871883-104871884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539744695	chr14:104871913-104871914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556772953	chr14:104871921-104871922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114094348	chr14:104871926-104871927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546427024	chr14:104871934-104871935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555607164	chr14:104872004-104872005	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs190418852	chr14:104872048-104872049	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs371539773	chr14:104872049-104872050	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs541510340	chr14:104872094-104872095	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs181528324	chr14:104872103-104872104	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs186539824	chr14:104872113-104872114	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs4343210	chr14:104872144-104872145	Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104866600-104871600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:104869400-104871400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:104869400-104872200	Enhancers	Lung	lung
4	chr14:104870000-104872000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:104871600-104871800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:104872000-104872200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
7	chr14:104872000-104872200	Enhancers	Left Ventricle	heart
8	chr14:104872000-104872400	Enhancers	Adipose Nuclei	Adipose
9	chr14:104872000-104872400	Enhancers	Fetal Brain Male	brain
10	chr14:104872000-104873400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:104872200-104872600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr14:104872200-104875200	Weak transcription	Left Ventricle	heart
13	chr14:104872400-104873400	Weak transcription	Fetal Brain Male	brain
14	chr14:104873400-104873600	Enhancers	Fetal Brain Male	brain
15	chr14:104874600-104874800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr14:104875200-104875400	ZNF genes & repeats	Left Ventricle	heart
17	chr14:104875600-104875800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
18	chr14:104885000-104885600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr14:104885200-104885600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr14:104885200-104885800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr14:104885400-104885800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:104885400-104886400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr14:104885600-104886600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr14:104885800-104886200	Active TSS	Brain Germinal Matrix	brain
25	chr14:104885800-104886200	Enhancers	GM12878-XiMat	blood
26	chr14:104885800-104891200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:104886200-104886600	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr14:104886200-104886800	Flanking Active TSS	GM12878-XiMat	blood
29	chr14:104886200-104887200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:104886200-104887200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr14:104886200-104892800	Enhancers	Fetal Brain Male	brain
32	chr14:104886400-104886800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr14:104886400-104886800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr14:104886400-104886800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr14:104886600-104886800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:104886600-104886800	Enhancers	Fetal Muscle Leg	muscle
37	chr14:104886600-104887200	Enhancers	Fetal Lung	lung
38	chr14:104886600-104887200	Enhancers	Ovary	ovary
39	chr14:104886600-104894200	Enhancers	Brain Germinal Matrix	brain
40	chr14:104886800-104887000	Enhancers	Brain Cingulate Gyrus	brain
41	chr14:104886800-104887000	Enhancers	Fetal Stomach	stomach
42	chr14:104886800-104887200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:104886800-104887400	Enhancers	Fetal Muscle Trunk	muscle
44	chr14:104886800-104887600	Enhancers	GM12878-XiMat	blood
45	chr14:104886800-104887800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr14:104886800-104892600	Enhancers	Fetal Brain Female	brain
47	chr14:104887000-104890800	Weak transcription	Brain Cingulate Gyrus	brain
48	chr14:104887200-104888000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr14:104887200-104888000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr14:104887200-104890200	Weak transcription	Ovary	ovary

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