Variant report

Variant	nsv946389
Chromosome Location	chr1:151987731-151995842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:179)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:179 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:151994928-151995032	K562	blood:	n/a	n/a
2	CTCF	chr1:151991140-151991290	HUVEC	blood vessel:	n/a	n/a
3	CTCF	chr1:151991140-151991290	HBMEC	blood vessel:	n/a	n/a
4	CTCF	chr1:151991140-151991290	HPAF	blood vessel:	n/a	n/a
5	CTCF	chr1:151991140-151991290	HCFaa	heart:	n/a	n/a
6	CTCF	chr1:151991100-151991250	MCF-7	breast:	n/a	n/a
7	CTCF	chr1:151991140-151991290	GM06990	blood:	n/a	n/a
8	CTCF	chr1:151991080-151991230	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr1:151991140-151991290	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr1:151991140-151991290	GM12865	blood:	n/a	n/a
11	CTCF	chr1:151990920-151991070	NHLF	lung:	n/a	n/a
12	CTCF	chr1:151990880-151991030	K562	blood:	n/a	n/a
13	CTCF	chr1:151991145-151991233	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:151991120-151991270	AG09309	skin:	n/a	n/a
15	CTCF	chr1:151991140-151991307	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr1:151991180-151991330	HVMF	connective:	n/a	n/a
17	CTCF	chr1:151991140-151991290	HAc	cerebellar:	n/a	n/a
18	CTCF	chr1:151991140-151991290	HRE	kidney:	n/a	n/a
19	CTCF	chr1:151991120-151991270	HAc	cerebellar:	n/a	n/a
20	CTCF	chr1:151991133-151991254	Lung_OC	lung:	n/a	n/a
21	CTCF	chr1:151991120-151991270	GM12869	blood:	n/a	n/a
22	CTCF	chr1:151991140-151991290	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr1:151991127-151991299	Fibrobl	skin:	n/a	n/a
24	CTCF	chr1:151991160-151991310	SAEC	small airway:	n/a	n/a
25	CTCF	chr1:151991137-151991237	GM19238	blood:	n/a	n/a
26	CTCF	chr1:151991160-151991310	BJ	skin:	n/a	n/a
27	CTCF	chr1:151991111-151991377	GM12878	blood:	n/a	n/a
28	CTCF	chr1:151991140-151991290	K562	blood:	n/a	n/a
29	CTCF	chr1:151990895-151991416	A549	lung:	n/a	n/a
30	CTCF	chr1:151991160-151991310	K562	blood:	n/a	n/a
31	CTCF	chr1:151991160-151991310	HVMF	connective:	n/a	n/a
32	CTCF	chr1:151991180-151991330	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:151991160-151991310	AG04450	lung:	n/a	n/a
34	CTCF	chr1:151991140-151991290	GM12864	blood:	n/a	n/a
35	CTCF	chr1:151991165-151991268	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:151991193-151991218	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:151991123-151991294	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:151991136-151991254	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr1:151991220-151991370	GM12866	blood:	n/a	n/a
40	CTCF	chr1:151991120-151991270	BJ	skin:	n/a	n/a
41	CTCF	chr1:151991140-151991290	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr1:151991220-151991370	GM12865	blood:	n/a	n/a
43	CTCF	chr1:151991180-151991330	GM12868	blood:	n/a	n/a
44	CTCF	chr1:151991105-151991292	HepG2	liver:	n/a	n/a
45	CTCF	chr1:151991136-151991248	GM12892	blood:	n/a	n/a
46	CTCF	chr1:151991160-151991310	GM12875	blood:	n/a	n/a
47	CTCF	chr1:151991021-151991258	A549	lung:	n/a	n/a
48	CTCF	chr1:151990820-151990970	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:151991120-151991270	GM12878	blood:	n/a	n/a
50	CTCF	chr1:151991160-151991310	AoAF	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151988500-151988550	HAEpiC	amniotic membrane:	n/a
2	chr1:151988500-151988550	PFSK-1	brain:	n/a
3	chr1:151988500-151988550	GM12878	blood:	n/a
4	chr1:151988500-151988550	AG09319	gingival:	n/a
5	chr1:151988500-151988550	U87	brain:	n/a
6	chr1:151988500-151988550	HL-60	blood:	n/a
7	chr1:151988500-151988550	SK-N-MC	brain:	n/a
8	chr1:151988500-151988550	T-47D	breast:	n/a
9	chr1:151988500-151988550	HRE	kidney:	n/a
10	chr1:151988500-151988550	AG04450	lung:	fetal
11	chr1:151988500-151988550	NHBE	bronchial:	n/a
12	chr1:151988500-151988550	SK-N-SH	brain:	n/a
13	chr1:151988500-151988550	NT2-D1	testis:	n/a
14	chr1:151988500-151988550	HRPEpiC	eye:	n/a
15	chr1:151988500-151988550	HNPCEpiC	eye:	n/a
16	chr1:151988500-151988550	NHDF-neo	bronchial:	n/a
17	chr1:151988500-151988550	MCF10A-Er-Src	breast:	n/a
18	chr1:151988500-151988550	HRCEpiC	kidney:	n/a
19	chr1:151988500-151988550	HCT-116	colon:	n/a
20	chr1:151988500-151988550	NB4	blood:	n/a
21	chr1:151988500-151988550	GM06990	blood:	n/a
22	chr1:151988500-151988550	HIPEpiC	eye:	n/a
23	chr1:151988500-151988550	AG10803	skin:	n/a
24	chr1:151988500-151988550	PrEC	prostate:	n/a
25	chr1:151988500-151988550	ovcar-3	ovarian:	n/a
26	chr1:151988500-151988550	ProgFib	skin:	n/a
27	chr1:151988500-151988550	SKMC	muscle:	n/a
28	chr1:151988500-151988550	H1-hESC	embryonic stem cell:	embryo
29	chr1:151988500-151988550	GM12891	blood:	n/a
30	chr1:151988500-151988550	AG04449	skin:	fetal
31	chr1:151988500-151988550	PANC-1	pancreas:	n/a
32	chr1:151988500-151988550	Caco-2	colon:	n/a
33	chr1:151988500-151988550	HMEC	breast:	n/a
34	chr1:151988500-151988550	IMR90	lung:	fetal
35	chr1:151988500-151988550	HCF	heart:	n/a
36	chr1:151988500-151988550	HEK293	kidney:	embryo
37	chr1:151988500-151988550	HEEpiC	esophagus:	n/a
38	chr1:151988500-151988550	BJ	skin:	n/a
39	chr1:151988500-151988550	HepG2	liver:	n/a
40	chr1:151988500-151988550	CMK	blood:	n/a
41	chr1:151988500-151988550	Hepatocyte	liver:	n/a
42	chr1:151988500-151988550	AG09309	skin:	n/a
43	chr1:151988500-151988550	HCPEpiC	choroid plexus:	n/a
44	chr1:151988500-151988550	GM12892	blood:	n/a
45	chr1:151988500-151988550	HUVEC	blood vessel:	n/a
46	chr1:151988500-151988550	ECC-1	luminal epithelium:	n/a
47	chr1:151988500-151988550	Hela-S3	cervix:	n/a
48	chr1:151988500-151988550	AoSMC	blood vessel:	n/a
49	chr1:151988500-151988550	SK-N-SH_RA	brain:	n/a
50	chr1:151988500-151988550	K562	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:16934476..16935083-chr1:151995159..151995686,2	MCF-7	breast:
2	chr1:151958520..151979218-chr1:151992734..152014750,97	MCF-7	breast:
3	chr1:151986485..151988607-chr1:151992304..151995986,3	K562	blood:
4	chr1:151989267..151989972-chr1:152007766..152008625,2	MCF-7	breast:
5	chr1:151986485..151988607-chr1:151992304..151995986,3	K562	blood:
6	chr1:151857351..151860092-chr1:151985508..151987866,2	MCF-7	breast:
7	chr1:151972758..151974972-chr1:151986628..151989448,2	K562	blood:
8	chr1:151978814..151981429-chr1:151985476..151987794,2	K562	blood:
9	chr1:151880783..151882439-chr1:151984923..151987759,2	MCF-7	breast:
10	chr1:151880725..151882299-chr1:151990398..151992995,2	MCF-7	breast:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OAZ3-3	chr1:151991103-151991313	NONHSAT139905
2	lnc-OAZ3-3	chr1:151994078-151994228	NONHSAT006458
3	lnc-OAZ3-3	chr1:151994078-151994228	NONHSAT139905
4	lnc-OAZ3-3	chr1:151990754-151991004	NONHSAT139905
5	lnc-OAZ3-3	chr1:151988151-151988208	ENSG00000229021.2
6	lnc-OAZ3-3	chr1:151992713-151992812	NONHSAT006460
7	lnc-OAZ3-3	chr1:151988482-151988551	ENSG00000229021.2
8	lnc-OAZ3-3	chr1:151992713-151992815	NONHSAT006458
9	lnc-OAZ3-3	chr1:151992713-151992815	NONHSAT006459
10	lnc-OAZ3-3	chr1:151994078-151994228	NONHSAT006459
11	lnc-OAZ3-3	chr1:151989376-151991004	ENSG00000229021.2
12	lnc-OAZ3-3	chr1:151994912-151994984	NONHSAT006460
13	lnc-S100A11-1	chr1:151993641-151993854	NONHSAT006461
14	lnc-S100A11-1	chr1:151992728-151992810	NONHSAT006461
15	lnc-OAZ3-3	chr1:151994913-151994985	NONHSAT139905
16	lnc-OAZ3-3	chr1:151992713-151992815	ENSG00000229021.2
17	lnc-OAZ3-3	chr1:151991103-151991313	NONHSAT006459
18	lnc-OAZ3-3	chr1:151993640-151993856	NONHSAT006460
19	lnc-OAZ3-3	chr1:151994913-151994985	NONHSAT006459
20	lnc-OAZ3-3	chr1:151994078-151994228	ENSG00000229021.2
21	lnc-OAZ3-3	chr1:151988482-151988551	NONHSAT006459
22	lnc-OAZ3-3	chr1:151993646-151993860	NONHSAT139905
23	lnc-OAZ3-3	chr1:151991103-151991313	ENSG00000229021.2
24	lnc-OAZ3-3	chr1:151992713-151992815	NONHSAT139905
25	lnc-OAZ3-3	chr1:151988126-151988208	NONHSAT006459
26	lnc-OAZ3-3	chr1:151993646-151993860	NONHSAT006459
27	lnc-OAZ3-3	chr1:151989376-151989405	NONHSAT006459
28	lnc-OAZ3-3	chr1:151993646-151993860	ENSG00000229021.2
29	lnc-OAZ3-3	chr1:151993646-151993860	NONHSAT006458
30	lnc-OAZ3-3	chr1:151991138-151991315	NONHSAT006460
31	lnc-OAZ3-3	chr1:151994913-151994985	NONHSAT006458
32	lnc-OAZ3-3	chr1:151989376-151989405	NONHSAT006458
33	lnc-OAZ3-3	chr1:151988482-151988551	NONHSAT006458
34	lnc-OAZ3-3	chr1:151994913-151994985	ENSG00000229021.2
35	lnc-OAZ3-3	chr1:151991103-151991313	NONHSAT006458

No data

Variant related genes	Relation type
ENSG00000240667	TF binding region
ENSG00000240667	CpG island
ENSG00000197747	chromatin interactions
ENSG00000229021	chromatin interactions
ENSG00000159445	chromatin interactions

Extended variants
information (count: 315 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376860420	chr1:151987741-151987742	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191040513	chr1:151987773-151987774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568441317	chr1:151987807-151987808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368345549	chr1:151987858-151987859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546302594	chr1:151987882-151987883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183205045	chr1:151987901-151987902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372067672	chr1:151987974-151987975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556997231	chr1:151987978-151987979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150871338	chr1:151988006-151988007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539218061	chr1:151988014-151988015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs959945	chr1:151988019-151988020	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs368145561	chr1:151988025-151988026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572736098	chr1:151988041-151988042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375730133	chr1:151988064-151988065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542103003	chr1:151988077-151988078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115815995	chr1:151988086-151988087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554030097	chr1:151988091-151988092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538629186	chr1:151988123-151988124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs80217309	chr1:151988135-151988136	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs16833782	chr1:151988141-151988142	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs374771684	chr1:151988165-151988166	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs533073031	chr1:151988206-151988207	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs540361739	chr1:151988267-151988268	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs76686800	chr1:151988292-151988293	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575167346	chr1:151988312-151988313	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs187106269	chr1:151988413-151988414	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs537390491	chr1:151988433-151988434	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs149585647	chr1:151988437-151988438	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs79112301	chr1:151988485-151988486	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs144257606	chr1:151988488-151988489	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs140666812	chr1:151988491-151988492	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs570578578	chr1:151988529-151988530	Enhancers Weak transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs189696551	chr1:151988541-151988542	Enhancers Weak transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs539531237	chr1:151988551-151988552	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs553096729	chr1:151988563-151988564	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574317507	chr1:151988573-151988574	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs566648104	chr1:151988580-151988581	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs535300000	chr1:151988587-151988588	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs115451581	chr1:151988590-151988591	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs575468706	chr1:151988608-151988609	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs576933352	chr1:151988645-151988646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs79977249	chr1:151988664-151988665	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs145303111	chr1:151988695-151988696	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs182235145	chr1:151988769-151988770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560331419	chr1:151988783-151988784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528647862	chr1:151988833-151988834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542063192	chr1:151988887-151988888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562379014	chr1:151988888-151988889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147210651	chr1:151988972-151988973	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs550898294	chr1:151988994-151988995	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
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
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
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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151976800-151993600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:151986200-151989800	Enhancers	HMEC	breast
3	chr1:151986400-151988200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:151986600-151987800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:151986600-151988000	Weak transcription	NHEK	skin
6	chr1:151986600-151996200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:151986800-151988000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:151986800-151990000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:151986800-152007400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:151987400-151990000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:151987600-151988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:151987600-151988600	Enhancers	HSMMtube	muscle
13	chr1:151987600-151989800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:151987800-151989800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:151988000-151988600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:151988000-151989800	Enhancers	NHEK	skin
17	chr1:151988200-151988600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr1:151988400-151988600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:151988400-151988600	Enhancers	Fetal Muscle Leg	muscle
20	chr1:151988600-151992400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:151988600-152002600	Weak transcription	Fetal Muscle Leg	muscle
22	chr1:151988600-152004000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr1:151989800-151994000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:151989800-151994000	Weak transcription	HMEC	breast
25	chr1:151989800-151994400	Weak transcription	NHEK	skin
26	chr1:151989800-151994800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:151990000-151990200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr1:151990000-151993200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:151992400-151993400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:151992600-151992800	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:151993200-151994000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:151993200-151994200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:151993400-151993800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:151993400-152003000	Weak transcription	Fetal Intestine Small	intestine
35	chr1:151993600-151993800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:151993600-151993800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr1:151993600-151994400	Enhancers	Esophagus	oesophagus
38	chr1:151993800-151994000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:151993800-151994200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:151993800-151994200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:151993800-151994600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr1:151993800-151996000	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr1:151994000-151994400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr1:151994000-151995000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:151994000-151996000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:151994000-151996200	Enhancers	HMEC	breast
47	chr1:151994000-152002400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:151994200-151996200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr1:151994200-151996400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr1:151994200-151997800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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