Variant report

Variant	esv3693159
Chromosome Location	chr14:21358155-21421088
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	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
2	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
3	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
5	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
6	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
7	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
8	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
9	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
10	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
11	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
13	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
15	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
17	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
18	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
19	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
20	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
21	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
22	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
23	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
24	CEBPB	chr14:21387197-21387553	H1-hESC	embryonic stem cell:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
25	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
26	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
27	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
28	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
29	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
31	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
32	CTCF	chr14:21402422-21402574	LNCaP	prostate:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
33	CTCF	chr14:21402409-21402590	MCF-7	breast:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
34	CTCF	chr14:21402400-21402550	K562	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
35	CTCF	chr14:21402343-21402658	H1-hESC	embryonic stem cell:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
36	CTCF	chr14:21402420-21402570	NHLF	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
37	CTCF	chr14:21402387-21402608	SK-N-SH_RA	brain:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
38	CTCF	chr14:21402420-21402570	HUVEC	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
39	CTCF	chr14:21402440-21402590	GM12864	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
40	CTCF	chr14:21402260-21402410	AG04450	lung:	n/a	n/a
41	CTCF	chr14:21403520-21403670	HCT-116	colon:	n/a	n/a
42	CTCF	chr14:21402480-21402630	HCM	heart:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
43	CTCF	chr14:21402320-21402470	HAc	cerebellar:	n/a	n/a
44	CTCF	chr14:21412260-21412410	MCF-7	breast:	n/a	chr14:21412306-21412314
45	CTCF	chr14:21372521-21372923	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr14:21402460-21402610	GM12874	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21402360-21402510	GM12865	blood:	n/a	n/a
48	CTCF	chr14:21372620-21372770	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr14:21402460-21402610	AoAF	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21372521-21372908	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21358233-21358283	AG09309	skin:	n/a
2	chr14:21386453-21386503	BJ	skin:	n/a
3	chr14:21358233-21358283	RPTEC	kidney:	n/a
4	chr14:21359737-21359787	SK-N-MC	brain:	n/a
5	chr14:21386453-21386503	H1-hESC	embryonic stem cell:	embryo
6	chr14:21359737-21359787	HCPEpiC	choroid plexus:	n/a
7	chr14:21359943-21359993	ECC-1	luminal epithelium:	n/a
8	chr14:21386453-21386503	HCT-116	colon:	n/a
9	chr14:21358233-21358283	ECC-1	luminal epithelium:	n/a
10	chr14:21359737-21359787	HIPEpiC	eye:	n/a
11	chr14:21358233-21358283	Jurkat	blood:	n/a
12	chr14:21386453-21386503	LNCaP	prostate:	n/a
13	chr14:21386453-21386503	HRCEpiC	kidney:	n/a
14	chr14:21359943-21359993	A549	lung:	n/a
15	chr14:21386453-21386503	Jurkat	blood:	n/a
16	chr14:21386453-21386503	Hela-S3	cervix:	n/a
17	chr14:21358233-21358283	AG09319	gingival:	n/a
18	chr14:21359295-21359345	SAEC	small airway:	n/a
19	chr14:21359295-21359345	BJ	skin:	n/a
20	chr14:21359943-21359993	Caco-2	colon:	n/a
21	chr14:21359295-21359345	HCPEpiC	choroid plexus:	n/a
22	chr14:21359943-21359993	CMK	blood:	n/a
23	chr14:21358233-21358283	HIPEpiC	eye:	n/a
24	chr14:21358233-21358283	HCT-116	colon:	n/a
25	chr14:21358233-21358283	AoSMC	blood vessel:	n/a
26	chr14:21386453-21386503	SK-N-SH_RA	brain:	n/a
27	chr14:21358233-21358283	SKMC	muscle:	n/a
28	chr14:21358233-21358283	GM12891	blood:	n/a
29	chr14:21386453-21386503	AG09309	skin:	n/a
30	chr14:21358233-21358283	IMR90	lung:	fetal
31	chr14:21359295-21359345	HCM	heart:	n/a
32	chr14:21386453-21386503	HUVEC	blood vessel:	n/a
33	chr14:21386453-21386503	GM12892	blood:	n/a
34	chr14:21386453-21386503	PFSK-1	brain:	n/a
35	chr14:21359295-21359345	ECC-1	luminal epithelium:	n/a
36	chr14:21359737-21359787	HL-60	blood:	n/a
37	chr14:21358233-21358283	U87	brain:	n/a
38	chr14:21359737-21359787	HRE	kidney:	n/a
39	chr14:21358233-21358283	HRE	kidney:	n/a
40	chr14:21359295-21359345	GM12891	blood:	n/a
41	chr14:21358233-21358283	NHBE	bronchial:	n/a
42	chr14:21358233-21358283	PrEC	prostate:	n/a
43	chr14:21359295-21359345	HCT-116	colon:	n/a
44	chr14:21359943-21359993	BE2_C	brain:	n/a
45	chr14:21358233-21358283	H1-hESC	embryonic stem cell:	embryo
46	chr14:21359737-21359787	RPTEC	kidney:	n/a
47	chr14:21359737-21359787	HRCEpiC	kidney:	n/a
48	chr14:21359295-21359345	HRPEpiC	eye:	n/a
49	chr14:21386453-21386503	NT2-D1	testis:	n/a
50	chr14:21359295-21359345	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASE2-1	chr14:21418698-21418708	NONHSAT035618
2	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
3	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
4	lnc-RNASE2-1	chr14:21419045-21419476	NONHSAT035618
5	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
6	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
7	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
8	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
RNASE3	TF binding region
ENSG00000258918	TF binding region
RNASE2	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island
RNASE2	CpG island

Extended variants
information (count: 1878 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1878 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28525131	chr14:21358155-21358156	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559196993	chr14:21358164-21358165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149189886	chr14:21358188-21358189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563083375	chr14:21358212-21358213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143367850	chr14:21358233-21358234	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs183263194	chr14:21358279-21358280	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs562394008	chr14:21358311-21358312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529642031	chr14:21358312-21358313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546590195	chr14:21358371-21358372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370880413	chr14:21358405-21358406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139004485	chr14:21358414-21358415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186513196	chr14:21358417-21358418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551910575	chr14:21358439-21358440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142283974	chr14:21358464-21358465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145904137	chr14:21358467-21358468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34627055	chr14:21358487-21358488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189657603	chr14:21358490-21358491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568361815	chr14:21358493-21358494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182295829	chr14:21358509-21358510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563441432	chr14:21358610-21358611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375276864	chr14:21358619-21358620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138171691	chr14:21358628-21358629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs57987846	chr14:21358638-21358639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577228595	chr14:21358676-21358677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539933052	chr14:21358688-21358689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530509698	chr14:21358711-21358712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556740561	chr14:21358737-21358738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576686682	chr14:21358767-21358768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542476813	chr14:21358768-21358769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562210283	chr14:21358798-21358799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141844353	chr14:21358888-21358889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570326448	chr14:21358889-21358890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187633717	chr14:21358914-21358915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117413508	chr14:21358929-21358930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114516193	chr14:21358932-21358933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112635084	chr14:21358954-21358955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs3216677	chr14:21359008-21359009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397701594	chr14:21359015-21359016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201098992	chr14:21359016-21359017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192560566	chr14:21359039-21359040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551835516	chr14:21359068-21359069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568354171	chr14:21359069-21359070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562279804	chr14:21359127-21359128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150638511	chr14:21359154-21359155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183256768	chr14:21359185-21359186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568218077	chr14:21359227-21359228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs534103750	chr14:21359231-21359232	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs28435898	chr14:21359234-21359235	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570824109	chr14:21359243-21359244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs35201704	chr14:21359253-21359254	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21355800-21358200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr14:21356000-21359200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr14:21356800-21359400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:21358200-21358600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:21358600-21359600	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr14:21359200-21360400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr14:21359400-21359800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr14:21359600-21359800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr14:21359800-21360000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr14:21360000-21360200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr14:21360200-21360800	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr14:21360400-21362400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr14:21360800-21361200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr14:21361200-21362200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr14:21362200-21363200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr14:21362200-21364600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:21362400-21363400	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr14:21363200-21363800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr14:21363400-21364200	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr14:21363800-21364600	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr14:21364200-21364400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr14:21364400-21364800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr14:21364600-21365600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr14:21364600-21365600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr14:21364800-21365400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr14:21365400-21365600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr14:21365600-21372400	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr14:21370400-21370600	Enhancers	Gastric	stomach
30	chr14:21371800-21373000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr14:21371800-21375600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr14:21372400-21372600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr14:21372400-21372800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr14:21372400-21373000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr14:21372400-21373000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr14:21372400-21373200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr14:21372400-21373200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr14:21372400-21373200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr14:21372400-21373200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr14:21372600-21373000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr14:21372600-21373000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr14:21372600-21373000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr14:21372600-21374600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr14:21372600-21374800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr14:21372800-21373200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr14:21373000-21373400	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr14:21373400-21374000	Enhancers	Primary B cells from cord blood	blood
48	chr14:21373400-21374800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr14:21374800-21375400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:21378800-21379000	Flanking Active TSS	HepG2	liver

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