Variant report

Variant	esv1816907
Chromosome Location	chr1:145310895-145379944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:246)
Chromatin interactive
region (count:6)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:145351628-145351787	GM12878	blood:	n/a	n/a
2	BATF	chr1:145368329-145368784	GM12878	blood:	n/a	n/a
3	BATF	chr1:145346898-145347057	GM12878	blood:	n/a	n/a
4	BATF	chr1:145323297-145323456	GM12878	blood:	n/a	n/a
5	BATF	chr1:145356362-145356521	GM12878	blood:	n/a	n/a
6	BATF	chr1:145337454-145337613	GM12878	blood:	n/a	n/a
7	BATF	chr1:145369080-145369247	GM12878	blood:	n/a	n/a
8	BATF	chr1:145362622-145362781	GM12878	blood:	n/a	n/a
9	BATF	chr1:145368315-145369169	GM12878	blood:	n/a	n/a
10	BATF	chr1:145310440-145310923	GM12878	blood:	n/a	chr1:145310669-145310677
11	BATF	chr1:145369205-145369460	GM12878	blood:	n/a	n/a
12	BATF	chr1:145342174-145342333	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:145368833-145369396	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:145368357-145368693	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:145371020-145371254	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:145372417-145372713	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:145371671-145371949	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:145368785-145368995	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:145368346-145368788	GM12878	blood:	n/a	n/a
20	CEBPB	chr1:145375617-145375817	HepG2	liver:	n/a	chr1:145375659-145375670
21	CEBPB	chr1:145379058-145379419	K562	blood:	n/a	n/a
22	CEBPD	chr1:145318153-145318499	K562	blood:	n/a	n/a
23	CEBPD	chr1:145327521-145327927	K562	blood:	n/a	n/a
24	CEBPD	chr1:145313384-145313734	K562	blood:	n/a	n/a
25	CEBPD	chr1:145336969-145337366	K562	blood:	n/a	n/a
26	CEBPD	chr1:145362124-145362505	K562	blood:	n/a	n/a
27	CEBPD	chr1:145355853-145356223	K562	blood:	n/a	n/a
28	CEBPD	chr1:145351134-145351473	K562	blood:	n/a	n/a
29	CEBPD	chr1:145366836-145367254	K562	blood:	n/a	n/a
30	CEBPD	chr1:145332252-145332648	K562	blood:	n/a	n/a
31	CEBPD	chr1:145341663-145342018	K562	blood:	n/a	n/a
32	CEBPD	chr1:145322721-145323135	K562	blood:	n/a	n/a
33	CTCF	chr1:145376480-145376630	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr1:145323600-145323750	GM12864	blood:	n/a	n/a
35	CTCF	chr1:145376500-145376650	AG04450	lung:	n/a	n/a
36	CTCF	chr1:145376480-145376630	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:145359126-145359191	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:145376540-145376690	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr1:145376460-145376610	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:145323540-145323690	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr1:145376480-145376630	HPF	lung:	n/a	n/a
42	CTCF	chr1:145323580-145323730	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:145323560-145323710	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr1:145323540-145323690	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr1:145376480-145376630	AG04450	lung:	n/a	n/a
46	CTCF	chr1:145376480-145376630	AG10803	skin:	n/a	n/a
47	CTCF	chr1:145376460-145376610	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr1:145336565-145336629	GM13976	blood:	n/a	n/a
49	CTCF	chr1:145376480-145376630	HCFaa	heart:	n/a	n/a
50	CTCF	chr1:145376460-145376610	Hela-S3	cervix:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145375603-145375653	BE2_C	brain:	n/a
2	chr1:145366524-145366574	U87	brain:	n/a
3	chr1:145375603-145375653	BE2_C	brain:	n/a
4	chr1:145366524-145366574	U87	brain:	n/a
5	chr1:145375603-145375653	ECC-1	luminal epithelium:	n/a
6	chr1:145366536-145366586	AG04450	lung:	fetal
7	chr1:145366524-145366574	NH-A	brain:	n/a
8	chr1:145375603-145375653	NHBE	bronchial:	n/a
9	chr1:145366524-145366574	NT2-D1	testis:	n/a
10	chr1:145366536-145366586	AG09319	gingival:	n/a
11	chr1:145375603-145375653	HAEpiC	amniotic membrane:	n/a
12	chr1:145366536-145366586	HNPCEpiC	eye:	n/a
13	chr1:145366524-145366574	HCPEpiC	choroid plexus:	n/a
14	chr1:145378947-145378997	PFSK-1	brain:	n/a
15	chr1:145366524-145366574	GM19239	blood:	n/a
16	chr1:145378947-145378997	Hela-S3	cervix:	n/a
17	chr1:145366524-145366574	GM12878	blood:	n/a
18	chr1:145378947-145378997	GM06990	blood:	n/a
19	chr1:145366524-145366574	SAEC	small airway:	n/a
20	chr1:145375603-145375653	HRCEpiC	kidney:	n/a
21	chr1:145366536-145366586	HEEpiC	esophagus:	n/a
22	chr1:145378947-145378997	HUVEC	blood vessel:	n/a
23	chr1:145378947-145378997	NH-A	brain:	n/a
24	chr1:145366524-145366574	HCM	heart:	n/a
25	chr1:145366524-145366574	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:145366524-145366574	MCF-7	breast:	n/a
27	chr1:145378947-145378997	SAEC	small airway:	n/a
28	chr1:145366536-145366586	RPTEC	kidney:	n/a
29	chr1:145378947-145378997	HIPEpiC	eye:	n/a
30	chr1:145366524-145366574	SK-N-SH_RA	brain:	n/a
31	chr1:145366536-145366586	IMR90	lung:	fetal
32	chr1:145378947-145378997	HMEC	breast:	n/a
33	chr1:145375603-145375653	IMR90	lung:	fetal
34	chr1:145366536-145366586	H1-hESC	embryonic stem cell:	embryo
35	chr1:145375603-145375653	GM12892	blood:	n/a
36	chr1:145366524-145366574	HNPCEpiC	eye:	n/a
37	chr1:145375603-145375653	GM12878	blood:	n/a
38	chr1:145366524-145366574	GM12891	blood:	n/a
39	chr1:145366536-145366586	ProgFib	skin:	n/a
40	chr1:145375603-145375653	NB4	blood:	n/a
41	chr1:145378947-145378997	HL-60	blood:	n/a
42	chr1:145378947-145378997	SK-N-SH_RA	brain:	n/a
43	chr1:145375603-145375653	MCF10A-Er-Src	breast:	n/a
44	chr1:145366536-145366586	Jurkat	blood:	n/a
45	chr1:145366524-145366574	ovcar-3	ovarian:	n/a
46	chr1:145378947-145378997	Jurkat	blood:	n/a
47	chr1:145375603-145375653	CMK	blood:	n/a
48	chr1:145366524-145366574	HUVEC	blood vessel:	n/a
49	chr1:145378947-145378997	PrEC	prostate:	n/a
50	chr1:145366524-145366574	HEK293	kidney:	embryo

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:145374045..145378813-chr1:145381593..145384779,5	MCF-7	breast:
2	chr1:17230015..17233047-chr1:145379825..145384079,5	K562	blood:
3	chr1:145379802..145384450-chr1:145513670..145517902,5	MCF-7	breast:
4	chr1:145379178..145384447-chr1:149221650..149226208,18	MCF-7	breast:
5	chr1:145379807..145384578-chr1:149221277..149226175,8	K562	blood:
6	chr1:145377352..145378949-chr1:145381369..145383840,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR3GL-2	chr1:145373054-145373507	ENSG00000227280.1
2	lnc-POLR3GL-2	chr1:145375343-145375554	ENSG00000227280.1
3	lnc-NOTCH2NL-2	chr1:145316512-145316684	NR_104217
4	lnc-POLR3GL-1	chr1:145372088-145373798	NONHSAT005886
5	lnc-NOTCH2NL-2	chr1:145319624-145319796	NR_104217
6	lnc-POLR3GL-1	chr1:145375583-145376447	NONHSAT005888
7	lnc-NOTCH2NL-2	chr1:145369718-145370303	NR_104217
8	lnc-POLR3GL-1	chr1:145376544-145376705	NONHSAT005888
9	lnc-NOTCH2NL-2	chr1:145317406-145317457	NR_104217
10	lnc-NOTCH2NL-2	chr1:145318936-145318987	NR_104217
11	lnc-POLR3GL-1	chr1:145376167-145376447	ENSG00000233396
12	lnc-POLR3GL-1	chr1:145376544-145376692	ENSG00000233396.3
13	lnc-POLR3GL-1	chr1:145377701-145377772	ENSG00000233396
14	lnc-POLR3GL-1	chr1:145377701-145377822	NONHSAT005894
15	lnc-POLR3GL-1	chr1:145377017-145377311	ENSG00000233396
16	lnc-POLR3GL-1	chr1:145375343-145375672	NONHSAT005887
17	lnc-NOTCH2NL-2	chr1:145368441-145369446	NR_104217
18	lnc-POLR3GL-1	chr1:145373054-145373507	NONHSAT005887
19	lnc-POLR3GL-1	chr1:145373296-145373507	ENSG00000233396.3
20	lnc-NOTCH2NL-2	chr1:145318054-145318226	NR_104217
21	lnc-NOTCH2NL-2	chr1:145311103-145311154	NR_104217
22	lnc-NOTCH2NL-2	chr1:145320511-145320619	NR_104217
23	lnc-POLR3GL-1	chr1:145377017-145377311	ENSG00000233396.3
24	lnc-POLR3GL-1	chr1:145377107-145377311	NONHSAT005894

No data

Variant related genes	Relation type
ENSG00000233396	TF binding region
RNVU1-6	TF binding region
ENSG00000233396	CpG island
RNVU1-6	CpG island
ENSG00000131779	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000211451	chromatin interactions
ENSG00000233396	chromatin interactions

Extended variants
information (count: 1770 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4084534	chr1:145310897-145310898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4084533	chr1:145310904-145310905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61816364	chr1:145310932-145310933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587691671	chr1:145310952-145310953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587747138	chr1:145310954-145310955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587624308	chr1:145310969-145310970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139987921	chr1:145310971-145310972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60660425	chr1:145310983-145310984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373281454	chr1:145310989-145310990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587703870	chr1:145310994-145310995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9424895	chr1:145311003-145311004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587757673	chr1:145311013-145311014	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587645535	chr1:145311030-145311031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372452648	chr1:145311071-145311072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs61816366	chr1:145311083-145311084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141899955	chr1:145311110-145311111	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs587688326	chr1:145311161-145311162	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9424896	chr1:145311176-145311177	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587762867	chr1:145311192-145311193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587650557	chr1:145311194-145311195	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587727661	chr1:145311202-145311203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587627290	chr1:145311222-145311223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587660224	chr1:145311224-145311225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587737623	chr1:145311227-145311228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7364450	chr1:145311230-145311231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587594087	chr1:145311244-145311245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61816367	chr1:145311249-145311250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7364460	chr1:145311278-145311279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9424897	chr1:145311290-145311291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28465046	chr1:145311292-145311293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4649547	chr1:145311380-145311381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368181254	chr1:145311381-145311382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371931916	chr1:145311387-145311388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7364467	chr1:145311401-145311402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587727264	chr1:145311404-145311405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587605748	chr1:145311421-145311422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61816391	chr1:145311423-145311424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372692313	chr1:145311432-145311433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587667585	chr1:145311434-145311435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587749080	chr1:145311435-145311436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587624358	chr1:145311451-145311452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587698216	chr1:145311459-145311460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587728092	chr1:145311478-145311479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2023308	chr1:145311486-145311487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587631957	chr1:145311490-145311491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587683233	chr1:145311522-145311523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587751177	chr1:145311534-145311535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28640909	chr1:145311539-145311540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587677084	chr1:145311547-145311548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56373283	chr1:145311548-145311549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:170)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	20808228	CNVD
Autism	22102821	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145277800-145323400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:145282000-145325400	Weak transcription	Fetal Brain Female	brain
3	chr1:145283000-145318600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:145283800-145311200	Weak transcription	Stomach Mucosa	stomach
5	chr1:145290800-145313800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:145290800-145323400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:145290800-145328000	Weak transcription	Small Intestine	intestine
8	chr1:145291000-145323400	Weak transcription	Brain Anterior Caudate	brain
9	chr1:145291000-145323600	Weak transcription	Brain Angular Gyrus	brain
10	chr1:145291000-145324000	Weak transcription	Brain Substantia Nigra	brain
11	chr1:145292800-145313000	Weak transcription	NHDF-Ad	bronchial
12	chr1:145293400-145313800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:145293400-145331400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:145293600-145311800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr1:145293800-145323400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:145293800-145332200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr1:145294000-145311000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr1:145294000-145323800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:145294600-145332200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:145297000-145323400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:145297000-145325000	Weak transcription	Left Ventricle	heart
22	chr1:145297000-145327600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr1:145297000-145328000	Weak transcription	Primary hematopoietic stem cells	blood
24	chr1:145297000-145328000	Weak transcription	Brain Hippocampus Middle	brain
25	chr1:145297000-145332600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr1:145297200-145332400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:145298000-145318200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:145298000-145325200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr1:145298200-145311400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:145298200-145316200	Weak transcription	NHEK	skin
31	chr1:145298200-145325400	Weak transcription	Right Ventricle	heart
32	chr1:145298800-145312800	Weak transcription	HMEC	breast
33	chr1:145298800-145313800	Weak transcription	NHLF	lung
34	chr1:145298800-145314600	Weak transcription	NH-A	brain
35	chr1:145298800-145318200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:145298800-145325400	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr1:145298800-145332400	Weak transcription	Colon Smooth Muscle	Colon
38	chr1:145304200-145311000	Weak transcription	HSMMtube	muscle
39	chr1:145304200-145331600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:145304200-145331600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:145304200-145333200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr1:145304400-145318200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:145304400-145323400	Weak transcription	Pancreas	Pancrea
44	chr1:145304400-145332400	Weak transcription	Gastric	stomach
45	chr1:145304600-145311400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:145304800-145311000	Weak transcription	Placenta	Placenta
47	chr1:145304800-145323600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr1:145304800-145325400	Weak transcription	Esophagus	oesophagus
49	chr1:145304800-145327600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr1:145304800-145332400	Weak transcription	Aorta	Aorta

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