Variant report

Variant	nsv534996
Chromosome Location	chr1:72477436-72700903
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	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72503489-72503650	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
5	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
6	BHLHE40	chr1:72563429-72563467	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72519630-72519642	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:72663464-72663828	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
9	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
10	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:72568547-72568841	A549	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
13	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
14	CEBPB	chr1:72568541-72568867	HepG2	liver:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
15	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:72568532-72568868	IMR90	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
17	CEBPB	chr1:72588186-72588499	IMR90	lung:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
18	CEBPB	chr1:72649995-72650046	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:72700804-72701056	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:72503347-72503641	HepG2	liver:	n/a	chr1:72503460-72503471 chr1:72503459-72503472
21	CEBPB	chr1:72490316-72490600	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:72588279-72588474	HepG2	liver:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
23	CEBPB	chr1:72656927-72657197	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:72568659-72568859	K562	blood:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
25	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
26	CTCF	chr1:72503480-72503769	HUVEC	blood vessel:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
27	CTCF	chr1:72503540-72503690	GM12867	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
28	CTCF	chr1:72652520-72652670	HPF	lung:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
29	CTCF	chr1:72503580-72503730	HCM	heart:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
30	CTCF	chr1:72652380-72652530	HAc	cerebellar:	n/a	n/a
31	CTCF	chr1:72503520-72503670	HBMEC	blood vessel:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
32	CTCF	chr1:72600909-72601198	K562	blood:	n/a	n/a
33	CTCF	chr1:72503580-72503730	Hela-S3	cervix:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
34	CTCF	chr1:72503560-72503710	AG04450	lung:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
35	CTCF	chr1:72503560-72503710	GM12872	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
36	CTCF	chr1:72652500-72652650	BJ	skin:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
37	CTCF	chr1:72503534-72503673	SK-N-SH_RA	brain:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
38	CTCF	chr1:72652500-72652650	HMEC	breast:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
39	CTCF	chr1:72503540-72503690	GM12864	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
40	CTCF	chr1:72503540-72503690	NB4	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
41	CTCF	chr1:72503520-72503670	WI-38	lung:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
42	CTCF	chr1:72652520-72652670	NHEK	skin:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
43	CTCF	chr1:72652504-72652665	HepG2	liver:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
44	CTCF	chr1:72652520-72652670	AG04450	lung:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
45	CTCF	chr1:72652500-72652650	AG09319	gingival:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
46	CTCF	chr1:72503560-72503710	NHDF-neo	bronchial:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
47	CTCF	chr1:72503540-72503690	HEK293	kidney:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
48	CTCF	chr1:72503550-72503707	GM13976	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
49	CTCF	chr1:72503600-72503750	HUVEC	blood vessel:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
50	CTCF	chr1:72543887-72543977	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72566690-72566740	BE2_C	brain:	n/a
2	chr1:72566690-72566740	BE2_C	brain:	n/a
3	chr1:72500866-72500916	LNCaP	prostate:	n/a
4	chr1:72566690-72566740	HEEpiC	esophagus:	n/a
5	chr1:72500866-72500916	IMR90	lung:	fetal
6	chr1:72500866-72500916	BE2_C	brain:	n/a
7	chr1:72500866-72500916	PANC-1	pancreas:	n/a
8	chr1:72566690-72566740	Hepatocyte	liver:	n/a
9	chr1:72566690-72566740	MCF-7	breast:	n/a
10	chr1:72566690-72566740	HIPEpiC	eye:	n/a
11	chr1:72500866-72500916	GM06990	blood:	n/a
12	chr1:72566690-72566740	NH-A	brain:	n/a
13	chr1:72566690-72566740	NHBE	bronchial:	n/a
14	chr1:72566690-72566740	HMEC	breast:	n/a
15	chr1:72566690-72566740	Caco-2	colon:	n/a
16	chr1:72500866-72500916	U87	brain:	n/a
17	chr1:72500866-72500916	RPTEC	kidney:	n/a
18	chr1:72566690-72566740	MCF10A-Er-Src	breast:	n/a
19	chr1:72500866-72500916	HCPEpiC	choroid plexus:	n/a
20	chr1:72566690-72566740	SKMC	muscle:	n/a
21	chr1:72566690-72566740	AG04450	lung:	fetal
22	chr1:72566690-72566740	GM12892	blood:	n/a
23	chr1:72566690-72566740	SK-N-SH	brain:	n/a
24	chr1:72566690-72566740	PrEC	prostate:	n/a
25	chr1:72500866-72500916	HRCEpiC	kidney:	n/a
26	chr1:72500866-72500916	AG09319	gingival:	n/a
27	chr1:72500866-72500916	SKMC	muscle:	n/a
28	chr1:72500866-72500916	MCF-7	breast:	n/a
29	chr1:72566690-72566740	SK-N-MC	brain:	n/a
30	chr1:72500866-72500916	ECC-1	luminal epithelium:	n/a
31	chr1:72566690-72566740	K562	blood:	n/a
32	chr1:72566690-72566740	Hela-S3	cervix:	n/a
33	chr1:72500866-72500916	HRPEpiC	eye:	n/a
34	chr1:72500866-72500916	NH-A	brain:	n/a
35	chr1:72566690-72566740	PFSK-1	brain:	n/a
36	chr1:72566690-72566740	NB4	blood:	n/a
37	chr1:72500866-72500916	AG09309	skin:	n/a
38	chr1:72500866-72500916	H1-hESC	embryonic stem cell:	embryo
39	chr1:72566690-72566740	HCF	heart:	n/a
40	chr1:72500866-72500916	Caco-2	colon:	n/a
41	chr1:72500866-72500916	T-47D	breast:	n/a
42	chr1:72500866-72500916	HMEC	breast:	n/a
43	chr1:72566690-72566740	HAEpiC	amniotic membrane:	n/a
44	chr1:72566690-72566740	ovcar-3	ovarian:	n/a
45	chr1:72500866-72500916	HL-60	blood:	n/a
46	chr1:72566690-72566740	AG04449	skin:	fetal
47	chr1:72566690-72566740	HRPEpiC	eye:	n/a
48	chr1:72500866-72500916	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:72500866-72500916	GM12891	blood:	n/a
50	chr1:72500866-72500916	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:71559221..71560259-chr1:72503170..72503778,3	MCF-7	breast:
2	chr1:72487764..72489951-chr1:72495667..72497783,2	K562	blood:
3	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
4	chr1:72472788..72474801-chr1:72492789..72495541,2	K562	blood:
5	chr1:72483188..72484849-chr1:72487728..72489377,2	K562	blood:
6	chr1:72053665..72054637-chr1:72503102..72503767,2	MCF-7	breast:
7	chr1:72495707..72498590-chr1:72500903..72503366,2	K562	blood:
8	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
9	chr1:72488016..72488819-chr1:72503014..72503883,2	K562	blood:
10	chr1:72495707..72498590-chr1:72500903..72503366,2	K562	blood:
11	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
12	chr1:72483188..72484849-chr1:72487728..72489377,2	K562	blood:
13	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
14	chr1:72488016..72488819-chr1:72503014..72503883,2	K562	blood:
15	chr1:72487764..72489951-chr1:72495667..72497783,2	K562	blood:

Variant related genes	Relation type
NEGR1	TF binding region
NEGR1	CpG island

Extended variants
information (count: 6250 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:6250 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529220430	chr1:72477456-72477457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376277956	chr1:72477470-72477471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191680628	chr1:72477474-72477475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375701997	chr1:72477509-72477510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4650127	chr1:72477520-72477521	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs531293399	chr1:72477529-72477530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113724573	chr1:72477554-72477555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570956032	chr1:72477582-72477583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138074189	chr1:72477628-72477629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553164276	chr1:72477653-72477654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566792902	chr1:72477654-72477655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79477710	chr1:72477681-72477682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149116829	chr1:72477790-72477791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565760311	chr1:72477794-72477795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116294354	chr1:72477828-72477829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7546373	chr1:72477903-72477904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1948060	chr1:72477916-72477917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs12567329	chr1:72477924-72477925	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540394447	chr1:72477985-72477986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375212249	chr1:72477988-72477989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571147856	chr1:72478015-72478016	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538328806	chr1:72478066-72478067	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529182577	chr1:72478085-72478086	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542980557	chr1:72478097-72478098	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562336708	chr1:72478098-72478099	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12565657	chr1:72478099-72478100	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551097937	chr1:72478112-72478113	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1948061	chr1:72478126-72478127	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527403632	chr1:72478188-72478189	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs3102916	chr1:72478194-72478195	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs187411948	chr1:72478223-72478224	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574275921	chr1:72478281-72478282	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144738953	chr1:72478303-72478304	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138677910	chr1:72478336-72478337	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56876687	chr1:72478347-72478348	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs375555820	chr1:72478391-72478392	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141997375	chr1:72478404-72478405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557884983	chr1:72478422-72478423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578024909	chr1:72478481-72478482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147632951	chr1:72478499-72478500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368168942	chr1:72478500-72478501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191944653	chr1:72478501-72478502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12724549	chr1:72478511-72478512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374179258	chr1:72478515-72478516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185645441	chr1:72478524-72478525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375131531	chr1:72478525-72478526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370957723	chr1:72478526-72478527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573925925	chr1:72478529-72478530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199507503	chr1:72478541-72478542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200932551	chr1:72478543-72478544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cancer	21272361	CNVD
Obesity	21131291	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72473000-72478000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:72475400-72478400	Enhancers	Fetal Heart	heart
3	chr1:72475800-72486400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:72476000-72478000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:72476200-72488800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:72476400-72482400	Weak transcription	Left Ventricle	heart
7	chr1:72477200-72478200	Enhancers	HSMMtube	muscle
8	chr1:72477400-72477600	Enhancers	HSMM	muscle
9	chr1:72477400-72477800	Weak transcription	Brain Anterior Caudate	brain
10	chr1:72477400-72478200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:72477800-72478200	Enhancers	Brain Anterior Caudate	brain
12	chr1:72478000-72478200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:72478000-72478400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:72478200-72478400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:72478400-72479400	Weak transcription	Fetal Heart	heart
16	chr1:72479400-72480200	Enhancers	Fetal Heart	heart
17	chr1:72482200-72482400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr1:72482600-72484000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr1:72484000-72484800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr1:72484200-72484600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:72484200-72484800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:72484200-72484800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:72484200-72484800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr1:72484200-72484800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr1:72484200-72485000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:72484400-72484600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:72484400-72484600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:72484400-72484800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:72484400-72484800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:72484600-72485200	Enhancers	Brain Angular Gyrus	brain
31	chr1:72484600-72489600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:72484800-72488200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:72484800-72488400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr1:72484800-72488600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr1:72484800-72488600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr1:72484800-72488600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:72484800-72490200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:72485000-72488400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr1:72488200-72488600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:72488400-72488600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:72488400-72488600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr1:72488400-72488600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:72488400-72490800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr1:72488600-72488800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:72488600-72488800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:72488600-72489000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:72488600-72489000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr1:72488600-72489000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr1:72488600-72489000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr1:72488600-72489400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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