Variant report

Variant	esv1822309
Chromosome Location	chr1:145302482-145378841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:145304748-145305052	GM12878	blood:	n/a	n/a
2	BATF	chr1:145310436-145310883	GM12878	blood:	n/a	chr1:145310669-145310677
3	BATF	chr1:145368329-145368784	GM12878	blood:	n/a	n/a
4	BATF	chr1:145351628-145351787	GM12878	blood:	n/a	n/a
5	BATF	chr1:145346898-145347057	GM12878	blood:	n/a	n/a
6	BATF	chr1:145368315-145369169	GM12878	blood:	n/a	n/a
7	BATF	chr1:145369080-145369247	GM12878	blood:	n/a	n/a
8	BATF	chr1:145337454-145337613	GM12878	blood:	n/a	n/a
9	BATF	chr1:145304760-145305106	GM12878	blood:	n/a	n/a
10	BATF	chr1:145310440-145310923	GM12878	blood:	n/a	chr1:145310669-145310677
11	BATF	chr1:145342174-145342333	GM12878	blood:	n/a	n/a
12	BATF	chr1:145369205-145369460	GM12878	blood:	n/a	n/a
13	BATF	chr1:145356362-145356521	GM12878	blood:	n/a	n/a
14	BATF	chr1:145323297-145323456	GM12878	blood:	n/a	n/a
15	BATF	chr1:145362622-145362781	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:145371671-145371949	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:145368833-145369396	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:145310496-145310688	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:145368785-145368995	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:145372417-145372713	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:145304809-145304968	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:145368357-145368693	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:145371020-145371254	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:145368346-145368788	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:145310475-145310707	GM12878	blood:	n/a	n/a
26	CEBPB	chr1:145375617-145375817	HepG2	liver:	n/a	chr1:145375659-145375670
27	CEBPD	chr1:145355853-145356223	K562	blood:	n/a	n/a
28	CEBPD	chr1:145322721-145323135	K562	blood:	n/a	n/a
29	CEBPD	chr1:145327521-145327927	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	chr1:145336969-145337366	K562	blood:	n/a	n/a
33	CEBPD	chr1:145351134-145351473	K562	blood:	n/a	n/a
34	CEBPD	chr1:145318153-145318499	K562	blood:	n/a	n/a
35	CEBPD	chr1:145362124-145362505	K562	blood:	n/a	n/a
36	CEBPD	chr1:145366836-145367254	K562	blood:	n/a	n/a
37	CEBPD	chr1:145313384-145313734	K562	blood:	n/a	n/a
38	CTCF	chr1:145376480-145376630	AG10803	skin:	n/a	n/a
39	CTCF	chr1:145376480-145376630	AG04449	skin:	n/a	n/a
40	CTCF	chr1:145368485-145368682	K562	blood:	n/a	n/a
41	CTCF	chr1:145359126-145359191	LNCaP	prostate:	n/a	n/a
42	CTCF	chr1:145323580-145323730	GM12872	blood:	n/a	n/a
43	CTCF	chr1:145335669-145335724	GM10248	blood:	n/a	n/a
44	CTCF	chr1:145376480-145376630	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr1:145323580-145323730	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:145323580-145323730	HMEC	breast:	n/a	n/a
47	CTCF	chr1:145376500-145376650	HVMF	connective:	n/a	n/a
48	CTCF	chr1:145323540-145323690	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr1:145323580-145323730	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr1:145376500-145376650	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145366536-145366586	SK-N-MC	brain:	n/a
2	chr1:145366524-145366574	NHDF-neo	bronchial:	n/a
3	chr1:145302551-145302601	GM12891	blood:	n/a
4	chr1:145302551-145302601	AG10803	skin:	n/a
5	chr1:145366524-145366574	RPTEC	kidney:	n/a
6	chr1:145366536-145366586	SK-N-SH	brain:	n/a
7	chr1:145366524-145366574	PrEC	prostate:	n/a
8	chr1:145366524-145366574	NHBE	bronchial:	n/a
9	chr1:145366524-145366574	AG09309	skin:	n/a
10	chr1:145366524-145366574	HUVEC	blood vessel:	n/a
11	chr1:145375603-145375653	BJ	skin:	n/a
12	chr1:145366536-145366586	AG09319	gingival:	n/a
13	chr1:145366536-145366586	U87	brain:	n/a
14	chr1:145375603-145375653	ECC-1	luminal epithelium:	n/a
15	chr1:145366524-145366574	HepG2	liver:	n/a
16	chr1:145366524-145366574	HMEC	breast:	n/a
17	chr1:145302551-145302601	SAEC	small airway:	n/a
18	chr1:145366524-145366574	HL-60	blood:	n/a
19	chr1:145302551-145302601	CMK	blood:	n/a
20	chr1:145366524-145366574	AoSMC	blood vessel:	n/a
21	chr1:145366536-145366586	HIPEpiC	eye:	n/a
22	chr1:145302551-145302601	IMR90	lung:	fetal
23	chr1:145375603-145375653	NT2-D1	testis:	n/a
24	chr1:145366536-145366586	AG10803	skin:	n/a
25	chr1:145366536-145366586	HRCEpiC	kidney:	n/a
26	chr1:145375603-145375653	NB4	blood:	n/a
27	chr1:145302551-145302601	PrEC	prostate:	n/a
28	chr1:145366524-145366574	AG04450	lung:	fetal
29	chr1:145366536-145366586	K562	blood:	n/a
30	chr1:145302551-145302601	GM12878	blood:	n/a
31	chr1:145302551-145302601	HCF	heart:	n/a
32	chr1:145366536-145366586	RPTEC	kidney:	n/a
33	chr1:145366536-145366586	IMR90	lung:	fetal
34	chr1:145375603-145375653	HL-60	blood:	n/a
35	chr1:145302551-145302601	HRCEpiC	kidney:	n/a
36	chr1:145302551-145302601	BE2_C	brain:	n/a
37	chr1:145375603-145375653	ProgFib	skin:	n/a
38	chr1:145366536-145366586	HL-60	blood:	n/a
39	chr1:145366536-145366586	Hela-S3	cervix:	n/a
40	chr1:145366536-145366586	MCF10A-Er-Src	breast:	n/a
41	chr1:145366524-145366574	HEK293	kidney:	embryo
42	chr1:145375603-145375653	AG09309	skin:	n/a
43	chr1:145375603-145375653	Jurkat	blood:	n/a
44	chr1:145302551-145302601	MCF-7	breast:	n/a
45	chr1:145366536-145366586	ECC-1	luminal epithelium:	n/a
46	chr1:145302551-145302601	H1-hESC	embryonic stem cell:	embryo
47	chr1:145302551-145302601	HRPEpiC	eye:	n/a
48	chr1:145302551-145302601	NHDF-neo	bronchial:	n/a
49	chr1:145302551-145302601	HEK293	kidney:	embryo
50	chr1:145375603-145375653	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:145377352..145378949-chr1:145381369..145383840,2	K562	blood:
2	chr1:145374045..145378813-chr1:145381593..145384779,5	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR3GL-1	chr1:145375343-145375672	NONHSAT005887
2	lnc-NOTCH2NL-2	chr1:145305945-145305996	NR_104217
3	lnc-POLR3GL-1	chr1:145377107-145377311	NONHSAT005894
4	lnc-NOTCH2NL-2	chr1:145303910-145303982	NR_104217
5	lnc-POLR3GL-1	chr1:145376544-145376705	NONHSAT005888
6	lnc-POLR3GL-1	chr1:145375583-145376447	NONHSAT005888
7	lnc-NOTCH2NL-2	chr1:145318054-145318226	NR_104217
8	lnc-NOTCH2NL-2	chr1:145309900-145310063	NR_104217
9	lnc-NOTCH2NL-2	chr1:145302649-145302868	NR_104217
10	lnc-NOTCH2NL-2	chr1:145317406-145317457	NR_104217
11	lnc-NOTCH2NL-2	chr1:145369718-145370303	NR_104217
12	lnc-POLR3GL-1	chr1:145372088-145373798	NONHSAT005886
13	lnc-POLR3GL-1	chr1:145373296-145373507	ENSG00000233396.3
14	lnc-POLR3GL-2	chr1:145375343-145375554	ENSG00000227280.1
15	lnc-NOTCH2NL-2	chr1:145319624-145319796	NR_104217
16	lnc-NOTCH2NL-2	chr1:145311103-145311154	NR_104217
17	lnc-POLR3GL-1	chr1:145377701-145377772	ENSG00000233396
18	lnc-POLR3GL-1	chr1:145373054-145373507	NONHSAT005887
19	lnc-NOTCH2NL-2	chr1:145316512-145316684	NR_104217
20	lnc-NOTCH2NL-2	chr1:145320511-145320619	NR_104217
21	lnc-POLR3GL-2	chr1:145373054-145373507	ENSG00000227280.1
22	lnc-POLR3GL-1	chr1:145377017-145377311	ENSG00000233396.3
23	lnc-NOTCH2NL-2	chr1:145368441-145369446	NR_104217
24	lnc-POLR3GL-1	chr1:145376167-145376447	ENSG00000233396
25	lnc-POLR3GL-1	chr1:145376544-145376692	ENSG00000233396.3
26	lnc-POLR3GL-1	chr1:145377701-145377822	NONHSAT005894
27	lnc-NOTCH2NL-2	chr1:145318936-145318987	NR_104217
28	lnc-NOTCH2NL-2	chr1:145304447-145304652	NR_104217
29	lnc-POLR3GL-1	chr1:145377017-145377311	ENSG00000233396

No data

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

Extended variants
information (count: 2012 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:2012 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61814644	chr1:145302505-145302506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587745371	chr1:145302534-145302535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185101955	chr1:145302548-145302549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187856635	chr1:145302552-145302553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587734677	chr1:145302557-145302558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201994470	chr1:145302562-145302563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200475393	chr1:145302581-145302582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368693522	chr1:145302601-145302602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201611932	chr1:145302621-145302622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587618219	chr1:145302641-145302642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199528759	chr1:145302642-145302643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200948811	chr1:145302647-145302648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113140328	chr1:145302670-145302671	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs200242621	chr1:145302676-145302677	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs201507635	chr1:145302685-145302686	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs587628031	chr1:145302695-145302696	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs199751510	chr1:145302696-145302697	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs376664024	chr1:145302700-145302701	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs3926769	chr1:145302704-145302705	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs9424867	chr1:145302714-145302715	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs587656023	chr1:145302716-145302717	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs376449217	chr1:145302745-145302746	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs587713446	chr1:145302762-145302763	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs376014420	chr1:145302775-145302776	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs587773151	chr1:145302783-145302784	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs587678489	chr1:145302792-145302793	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs182724392	chr1:145302793-145302794	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs587606960	chr1:145302820-145302821	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs587642491	chr1:145302832-145302833	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs587717888	chr1:145302858-145302859	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs587600091	chr1:145302867-145302868	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs4068056	chr1:145302901-145302902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587677425	chr1:145302909-145302910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587720493	chr1:145302930-145302931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201726140	chr1:145302940-145302941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs67070475	chr1:145302941-145302942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201911329	chr1:145302942-145302943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587597363	chr1:145302998-145302999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587667611	chr1:145302999-145303000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377156096	chr1:145303008-145303009	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587620584	chr1:145303010-145303011	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370410575	chr1:145303020-145303021	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587658698	chr1:145303031-145303032	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374855817	chr1:145303040-145303041	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368223748	chr1:145303073-145303074	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4068057	chr1:145303082-145303083	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376088396	chr1:145303099-145303100	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368654294	chr1:145303114-145303115	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587723748	chr1:145303132-145303133	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201378438	chr1:145303148-145303149	Weak transcription Strong transcription Genic enhancers	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:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145277600-145305400	Weak transcription	HepG2	liver
2	chr1:145277800-145323400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:145282000-145325400	Weak transcription	Fetal Brain Female	brain
4	chr1:145283000-145318600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:145283800-145311200	Weak transcription	Stomach Mucosa	stomach
6	chr1:145286800-145304000	Weak transcription	K562	blood
7	chr1:145290800-145303800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:145290800-145313800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:145290800-145323400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:145290800-145328000	Weak transcription	Small Intestine	intestine
11	chr1:145291000-145323400	Weak transcription	Brain Anterior Caudate	brain
12	chr1:145291000-145323600	Weak transcription	Brain Angular Gyrus	brain
13	chr1:145291000-145324000	Weak transcription	Brain Substantia Nigra	brain
14	chr1:145292800-145304400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:145292800-145313000	Weak transcription	NHDF-Ad	bronchial
16	chr1:145293000-145303800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:145293000-145310000	Weak transcription	Dnd41	blood
18	chr1:145293400-145310000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:145293400-145313800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:145293400-145331400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr1:145293600-145311800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr1:145293800-145303800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr1:145293800-145323400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr1:145293800-145332200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr1:145294000-145303800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:145294000-145306400	Weak transcription	Fetal Heart	heart
27	chr1:145294000-145311000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr1:145294000-145323800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr1:145294600-145304400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:145294600-145332200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr1:145297000-145303600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr1:145297000-145303800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:145297000-145303800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:145297000-145303800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr1:145297000-145303800	Weak transcription	Fetal Intestine Large	intestine
36	chr1:145297000-145303800	Weak transcription	Fetal Lung	lung
37	chr1:145297000-145303800	Weak transcription	Gastric	stomach
38	chr1:145297000-145303800	Weak transcription	HUVEC	blood vessel
39	chr1:145297000-145310000	Weak transcription	Rectal Smooth Muscle	rectum
40	chr1:145297000-145323400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:145297000-145325000	Weak transcription	Left Ventricle	heart
42	chr1:145297000-145327600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:145297000-145328000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr1:145297000-145328000	Weak transcription	Brain Hippocampus Middle	brain
45	chr1:145297000-145332600	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr1:145297200-145332400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:145298000-145303800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr1:145298000-145310000	Weak transcription	Colonic Mucosa	Colon
49	chr1:145298000-145318200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr1:145298000-145325200	Weak transcription	Placenta Amnion	Placenta Amnion

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