Variant report

Variant	nsv1040612
Chromosome Location	chr14:21353099-21417022
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	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
3	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
5	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
6	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
10	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
11	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
12	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
13	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
15	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
16	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
17	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
18	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
19	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
20	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
21	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
22	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
23	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
24	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
25	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
26	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
27	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
28	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
29	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
30	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	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	chr14:21402440-21402590	GM12866	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
33	CTCF	chr14:21402420-21402570	WERI-Rb-1	eye:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
34	CTCF	chr14:21402440-21402590	GM12870	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
35	CTCF	chr14:21402392-21402645	GM12892	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
36	CTCF	chr14:21402460-21402569	Lung_OC	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
37	CTCF	chr14:21402313-21402630	A549	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
38	CTCF	chr14:21402440-21402590	WERI-Rb-1	eye:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
39	CTCF	chr14:21385976-21386064	GM13976	blood:	n/a	n/a
40	CTCF	chr14:21372680-21372830	NB4	blood:	n/a	n/a
41	CTCF	chr14:21402421-21402603	Hela-S3	cervix:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
42	CTCF	chr14:21372602-21372857	K562	blood:	n/a	n/a
43	CTCF	chr14:21402420-21402570	HUVEC	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
44	CTCF	chr14:21402387-21402658	H1-hESC	embryonic stem cell:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21402460-21402610	BE2_C	brain:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
46	CTCF	chr14:21402440-21402590	RPTEC	kidney:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21372680-21372830	GM12865	blood:	n/a	n/a
48	CTCF	chr14:21403520-21403670	HCT-116	colon:	n/a	n/a
49	CTCF	chr14:21412420-21412570	GM12872	blood:	n/a	n/a
50	CTCF	chr14:21372620-21372770	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21359295-21359345	HCT-116	colon:	n/a
2	chr14:21359295-21359345	HCT-116	colon:	n/a
3	chr14:21358233-21358283	AG09319	gingival:	n/a
4	chr14:21386453-21386503	AG09319	gingival:	n/a
5	chr14:21386453-21386503	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:21359943-21359993	HEK293	kidney:	embryo
7	chr14:21359943-21359993	NT2-D1	testis:	n/a
8	chr14:21358233-21358283	T-47D	breast:	n/a
9	chr14:21359295-21359345	HRE	kidney:	n/a
10	chr14:21359943-21359993	NB4	blood:	n/a
11	chr14:21386453-21386503	HRE	kidney:	n/a
12	chr14:21358099-21358149	H1-hESC	embryonic stem cell:	embryo
13	chr14:21358233-21358283	GM12892	blood:	n/a
14	chr14:21386453-21386503	SK-N-MC	brain:	n/a
15	chr14:21359737-21359787	AG09309	skin:	n/a
16	chr14:21358233-21358283	NT2-D1	testis:	n/a
17	chr14:21359295-21359345	PANC-1	pancreas:	n/a
18	chr14:21358099-21358149	MCF-7	breast:	n/a
19	chr14:21358233-21358283	Caco-2	colon:	n/a
20	chr14:21359737-21359787	NHBE	bronchial:	n/a
21	chr14:21359943-21359993	AG04450	lung:	fetal
22	chr14:21359295-21359345	HUVEC	blood vessel:	n/a
23	chr14:21358233-21358283	NH-A	brain:	n/a
24	chr14:21386453-21386503	SKMC	muscle:	n/a
25	chr14:21359295-21359345	A549	lung:	n/a
26	chr14:21359943-21359993	HEEpiC	esophagus:	n/a
27	chr14:21358233-21358283	BJ	skin:	n/a
28	chr14:21358099-21358149	HPAEpiC	pulmonary alveolar:	n/a
29	chr14:21359943-21359993	HCPEpiC	choroid plexus:	n/a
30	chr14:21358233-21358283	GM12878	blood:	n/a
31	chr14:21358099-21358149	GM12892	blood:	n/a
32	chr14:21358233-21358283	HUVEC	blood vessel:	n/a
33	chr14:21358233-21358283	NB4	blood:	n/a
34	chr14:21359737-21359787	Hela-S3	cervix:	n/a
35	chr14:21358233-21358283	HRPEpiC	eye:	n/a
36	chr14:21359737-21359787	RPTEC	kidney:	n/a
37	chr14:21359943-21359993	K562	blood:	n/a
38	chr14:21359737-21359787	HNPCEpiC	eye:	n/a
39	chr14:21359295-21359345	HCM	heart:	n/a
40	chr14:21359295-21359345	HCF	heart:	n/a
41	chr14:21386453-21386503	H1-hESC	embryonic stem cell:	embryo
42	chr14:21386453-21386503	HAEpiC	amniotic membrane:	n/a
43	chr14:21359737-21359787	SK-N-MC	brain:	n/a
44	chr14:21358099-21358149	AG04449	skin:	fetal
45	chr14:21359943-21359993	HL-60	blood:	n/a
46	chr14:21359295-21359345	HRPEpiC	eye:	n/a
47	chr14:21358099-21358149	SAEC	small airway:	n/a
48	chr14:21358099-21358149	NHDF-neo	bronchial:	n/a
49	chr14:21359295-21359345	H1-hESC	embryonic stem cell:	embryo
50	chr14:21359295-21359345	LNCaP	prostate:	n/a

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

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

Extended variants
information (count: 1915 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1915 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8009165	chr14:21353099-21353100	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537315812	chr14:21353102-21353103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551979339	chr14:21353133-21353134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568970474	chr14:21353147-21353148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537619293	chr14:21353193-21353194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2020174	chr14:21353200-21353201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558493068	chr14:21353228-21353229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554367784	chr14:21353267-21353268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376278661	chr14:21353449-21353450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2019381	chr14:21353450-21353451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576920670	chr14:21353460-21353461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533844933	chr14:21353466-21353467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554078112	chr14:21353499-21353500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372770348	chr14:21353514-21353515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577166215	chr14:21353538-21353539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1743060	chr14:21353551-21353552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556366507	chr14:21353610-21353611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576625728	chr14:21353619-21353620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542413450	chr14:21353663-21353664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562268764	chr14:21353734-21353735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527946379	chr14:21353740-21353741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541735465	chr14:21353751-21353752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564842710	chr14:21353752-21353753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370577636	chr14:21353802-21353803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531988156	chr14:21353804-21353805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139650618	chr14:21353831-21353832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142606231	chr14:21353832-21353833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187898821	chr14:21353839-21353840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574967417	chr14:21353852-21353853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544288404	chr14:21353923-21353924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191995259	chr14:21353977-21353978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570759655	chr14:21353978-21353979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539415381	chr14:21354107-21354108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537838993	chr14:21354230-21354231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556324392	chr14:21354249-21354250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556543620	chr14:21354253-21354254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576557643	chr14:21354259-21354260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150993146	chr14:21354331-21354332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555936553	chr14:21354332-21354333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375732923	chr14:21354337-21354338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140841330	chr14:21354374-21354375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564606925	chr14:21354385-21354386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149732748	chr14:21354447-21354448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185368101	chr14:21354453-21354454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189432386	chr14:21354472-21354473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1951418	chr14:21354496-21354497	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs547879385	chr14:21354497-21354498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567843942	chr14:21354609-21354610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370708721	chr14:21354619-21354620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71112529	chr14:21354636-21354637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	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:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21350000-21354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:21350200-21354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:21350200-21354200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:21352800-21353200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:21352800-21353400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr14:21352800-21355600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr14:21353400-21353800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr14:21353800-21355000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr14:21354000-21354200	Weak transcription	Thymus	Thymus
10	chr14:21354000-21355000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:21354200-21354400	Enhancers	Thymus	Thymus
12	chr14:21354200-21354800	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr14:21354200-21354800	Enhancers	Primary hematopoietic stem cells	blood
14	chr14:21354200-21355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:21354400-21357200	Weak transcription	Thymus	Thymus
16	chr14:21354800-21355800	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr14:21355000-21356000	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr14:21355200-21356200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:21355600-21356000	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr14:21355800-21358200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr14:21356000-21359200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:21356200-21356800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr14:21356200-21357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr14:21356800-21359400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:21357200-21357400	Enhancers	Thymus	Thymus
27	chr14:21358200-21358600	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr14:21358600-21359600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr14:21359200-21360400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr14:21359400-21359800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr14:21359600-21359800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr14:21359800-21360000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr14:21360000-21360200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr14:21360200-21360800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr14:21360400-21362400	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr14:21360800-21361200	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr14:21361200-21362200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr14:21362200-21363200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr14:21362200-21364600	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr14:21362400-21363400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr14:21363200-21363800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr14:21363400-21364200	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr14:21363800-21364600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr14:21364200-21364400	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr14:21364400-21364800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr14:21364600-21365600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr14:21364600-21365600	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr14:21364800-21365400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr14:21365400-21365600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:21365600-21372400	Weak transcription	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links