Variant report

Variant	nsv945913
Chromosome Location	chr1:45308885-45310435
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	BACH1	chr1:45308671-45309035	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr1:45308761-45309098	GM12878	blood:	n/a	chr1:45308838-45308851 chr1:45309014-45309027 chr1:45309015-45309028 chr1:45308839-45308848 chr1:45308841-45308854
3	CCNT2	chr1:45308627-45309218	K562	blood:	n/a	chr1:45309053-45309062
4	CHD2	chr1:45308962-45309187	H1-hESC	embryonic stem cell:	n/a	chr1:45309054-45309064
5	CREB1	chr1:45308672-45309230	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr1:45308435-45309406	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr1:45308880-45309030	BJ	skin:	n/a	n/a
8	CTCF	chr1:45308920-45309070	BJ	skin:	n/a	chr1:45309047-45309060
9	CTCF	chr1:45308860-45309010	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr1:45308780-45308930	AG09319	gingival:	n/a	n/a
11	CTCF	chr1:45308920-45309070	HUVEC	blood vessel:	n/a	chr1:45309047-45309060
12	CTCF	chr1:45308840-45308990	AG04449	skin:	n/a	n/a
13	E2F6	chr1:45308598-45309021	K562	blood:	n/a	chr1:45308842-45308852 chr1:45308804-45308814 chr1:45308618-45308627
14	E2F6	chr1:45309036-45309159	K562	blood:	n/a	chr1:45309097-45309109 chr1:45309089-45309098 chr1:45309053-45309062 chr1:45309058-45309070
15	EGR1	chr1:45308541-45308908	K562	blood:	n/a	chr1:45308617-45308627 chr1:45308627-45308640 chr1:45308622-45308631
16	EGR1	chr1:45308662-45308987	ECC-1	luminal epithelium:	n/a	chr1:45308920-45308944 chr1:45308962-45308972
17	EGR1	chr1:45308510-45309077	K562	blood:	n/a	chr1:45308617-45308627 chr1:45308627-45308640 chr1:45308622-45308631 chr1:45309053-45309063 chr1:45308920-45308944 chr1:45308962-45308972
18	ELF1	chr1:45308846-45309170	K562	blood:	n/a	n/a
19	EP300	chr1:45308551-45309297	ECC-1	luminal epithelium:	n/a	chr1:45309044-45309060 chr1:45308791-45308807
20	EP300	chr1:45308950-45309199	SK-N-SH_RA	brain:	n/a	chr1:45309044-45309060
21	EP300	chr1:45308858-45309161	H1-hESC	embryonic stem cell:	n/a	chr1:45309044-45309060
22	FOSL2	chr1:45308730-45309168	HepG2	liver:	n/a	chr1:45309057-45309066 chr1:45308981-45308990
23	GTF2F1	chr1:45309115-45309210	H1-hESC	embryonic stem cell:	n/a	n/a
24	HDAC2	chr1:45308863-45309098	K562	blood:	n/a	n/a
25	HDAC2	chr1:45308625-45308914	HepG2	liver:	n/a	n/a
26	HDAC2	chr1:45308598-45309045	H1-hESC	embryonic stem cell:	n/a	n/a
27	HEY1	chr1:45308710-45308985	K562	blood:	n/a	n/a
28	HMGN3	chr1:45308465-45309173	K562	blood:	n/a	n/a
29	JUND	chr1:45308893-45309080	K562	blood:	n/a	chr1:45309057-45309066 chr1:45308981-45308990
30	JUND	chr1:45309007-45309206	H1-hESC	embryonic stem cell:	n/a	chr1:45309057-45309066
31	JUND	chr1:45308951-45309146	H1-hESC	embryonic stem cell:	n/a	chr1:45309057-45309066 chr1:45308981-45308990
32	KAP1	chr1:45308846-45309395	HEK293	kidney:	n/a	n/a
33	MAX	chr1:45308160-45309229	K562	blood:	n/a	chr1:45309127-45309137
34	MAX	chr1:45308756-45309088	K562	blood:	n/a	n/a
35	MAX	chr1:45308592-45309218	HepG2	liver:	n/a	chr1:45309127-45309137
36	MAX	chr1:45308604-45308997	ECC-1	luminal epithelium:	n/a	n/a
37	MAX	chr1:45308838-45309271	H1-hESC	embryonic stem cell:	n/a	chr1:45309127-45309137
38	MAX	chr1:45308607-45309334	ECC-1	luminal epithelium:	n/a	chr1:45309127-45309137
39	MAX	chr1:45308778-45309006	K562	blood:	n/a	n/a
40	MAX	chr1:45308777-45309203	H1-hESC	embryonic stem cell:	n/a	chr1:45309127-45309137
41	MAX	chr1:45308674-45309141	SK-N-SH	brain:	n/a	chr1:45309127-45309137
42	MAZ	chr1:45308302-45309299	IMR90	lung:	n/a	chr1:45309127-45309137
43	MAZ	chr1:45308336-45309259	K562	blood:	n/a	chr1:45309127-45309137
44	MAZ	chr1:45308901-45309241	GM12878	blood:	n/a	chr1:45309127-45309137
45	MAZ	chr1:45308830-45309271	HepG2	liver:	n/a	chr1:45309127-45309137
46	MTA3	chr1:45308647-45309000	GM12878	blood:	n/a	n/a
47	MXI1	chr1:45308947-45309197	H1-hESC	embryonic stem cell:	n/a	n/a
48	MXI1	chr1:45308757-45309199	HepG2	liver:	n/a	n/a
49	MXI1	chr1:45308141-45309564	SK-N-SH	brain:	n/a	n/a
50	MYC	chr1:45308831-45309063	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45308976-45309026	PFSK-1	brain:	n/a
2	chr1:45309425-45309475	SKMC	muscle:	n/a
3	chr1:45309425-45309475	GM12878	blood:	n/a
4	chr1:45308976-45309026	HRPEpiC	eye:	n/a
5	chr1:45309425-45309475	A549	lung:	n/a
6	chr1:45309425-45309475	GM06990	blood:	n/a
7	chr1:45309425-45309475	H1-hESC	embryonic stem cell:	embryo
8	chr1:45309425-45309475	ECC-1	luminal epithelium:	n/a
9	chr1:45309425-45309475	HIPEpiC	eye:	n/a
10	chr1:45309379-45309429	AoSMC	blood vessel:	n/a
11	chr1:45308976-45309026	GM12878	blood:	n/a
12	chr1:45309379-45309429	AG04450	lung:	fetal
13	chr1:45308976-45309026	AoSMC	blood vessel:	n/a
14	chr1:45309379-45309429	GM12878	blood:	n/a
15	chr1:45309155-45309205	HCT-116	colon:	n/a
16	chr1:45309155-45309205	AG04450	lung:	fetal
17	chr1:45309425-45309475	HepG2	liver:	n/a
18	chr1:45309425-45309475	HRE	kidney:	n/a
19	chr1:45309379-45309429	HUVEC	blood vessel:	n/a
20	chr1:45309425-45309475	ovcar-3	ovarian:	n/a
21	chr1:45309379-45309429	H1-hESC	embryonic stem cell:	embryo
22	chr1:45308976-45309026	HL-60	blood:	n/a
23	chr1:45308976-45309026	PANC-1	pancreas:	n/a
24	chr1:45308976-45309026	HAEpiC	amniotic membrane:	n/a
25	chr1:45309155-45309205	HCPEpiC	choroid plexus:	n/a
26	chr1:45308976-45309026	Hela-S3	cervix:	n/a
27	chr1:45309425-45309475	AG09309	skin:	n/a
28	chr1:45309379-45309429	HCPEpiC	choroid plexus:	n/a
29	chr1:45308976-45309026	ProgFib	skin:	n/a
30	chr1:45308976-45309026	SK-N-MC	brain:	n/a
31	chr1:45308976-45309026	Hepatocyte	liver:	n/a
32	chr1:45308976-45309026	ECC-1	luminal epithelium:	n/a
33	chr1:45309155-45309205	AG09309	skin:	n/a
34	chr1:45308976-45309026	K562	blood:	n/a
35	chr1:45308976-45309026	AG10803	skin:	n/a
36	chr1:45309155-45309205	MCF10A-Er-Src	breast:	n/a
37	chr1:45308976-45309026	HCPEpiC	choroid plexus:	n/a
38	chr1:45309155-45309205	IMR90	lung:	fetal
39	chr1:45308976-45309026	HIPEpiC	eye:	n/a
40	chr1:45309155-45309205	LNCaP	prostate:	n/a
41	chr1:45308976-45309026	SAEC	small airway:	n/a
42	chr1:45308976-45309026	U87	brain:	n/a
43	chr1:45309379-45309429	SKMC	muscle:	n/a
44	chr1:45309379-45309429	HEEpiC	esophagus:	n/a
45	chr1:45309379-45309429	PANC-1	pancreas:	n/a
46	chr1:45308976-45309026	AG04450	lung:	fetal
47	chr1:45309155-45309205	HL-60	blood:	n/a
48	chr1:45309379-45309429	MCF-7	breast:	n/a
49	chr1:45309379-45309429	HL-60	blood:	n/a
50	chr1:45309155-45309205	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:45185746..45188870-chr1:45307191..45310438,4	K562	blood:
2	chr1:45307699..45310286-chr1:45986112..45988725,2	K562	blood:
3	chr1:45224240..45226290-chr1:45308445..45310205,2	K562	blood:
4	chr1:45306981..45310503-chr1:45474976..45481200,7	K562	blood:
5	chr1:45305082..45310090-chr1:45475264..45482808,8	K562	blood:
6	chr1:45195257..45196854-chr1:45307118..45309179,2	K562	blood:
7	chr1:45194535..45197095-chr1:45307118..45309179,4	K562	blood:

Variant related genes	Relation type
ENSG00000226499	TF binding region
PTCH2	TF binding region
ENSG00000226499	CpG island
PTCH2	CpG island
ENSG00000142945	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000126088	chromatin interactions
ENSG00000126107	chromatin interactions

Extended variants
information (count: 53 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:53 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11573536	chr1:45308911-45308912	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs555208212	chr1:45308912-45308913	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs568529571	chr1:45308926-45308927	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs537562073	chr1:45308928-45308929	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs532331058	chr1:45309026-45309027	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs371641104	chr1:45309029-45309030	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs370682709	chr1:45309089-45309090	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs369031071	chr1:45309144-45309145	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs139332078	chr1:45309196-45309197	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs553188087	chr1:45309223-45309224	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs377020768	chr1:45309232-45309233	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs552126419	chr1:45309244-45309245	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs573065380	chr1:45309341-45309342	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs541976041	chr1:45309357-45309358	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs561567683	chr1:45309379-45309380	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs530646543	chr1:45309402-45309403	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs12118515	chr1:45309449-45309450	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537577932	chr1:45309450-45309451	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs554259744	chr1:45309486-45309487	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs563878849	chr1:45309530-45309531	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs567678477	chr1:45309532-45309533	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs567770993	chr1:45309541-45309542	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs369183063	chr1:45309542-45309543	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs538326008	chr1:45309546-45309547	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs371118142	chr1:45309554-45309555	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs71040512	chr1:45309555-45309556	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs186438837	chr1:45309631-45309632	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs546281014	chr1:45309728-45309729	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs190853638	chr1:45309773-45309774	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs528796466	chr1:45309793-45309794	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs35429559	chr1:45309830-45309831	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs548769757	chr1:45309872-45309873	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs183478807	chr1:45309953-45309954	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs537684471	chr1:45309971-45309972	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs146034442	chr1:45309989-45309990	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs12119410	chr1:45310037-45310038	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs573500026	chr1:45310052-45310053	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs570862019	chr1:45310069-45310070	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs67433620	chr1:45310073-45310074	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs398049245	chr1:45310074-45310075	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs57743504	chr1:45310091-45310092	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs539781693	chr1:45310131-45310132	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs553109390	chr1:45310179-45310180	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs559225311	chr1:45310218-45310219	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs12408818	chr1:45310234-45310235	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs527418282	chr1:45310251-45310252	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs555277897	chr1:45310335-45310336	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575085602	chr1:45310337-45310338	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs188530107	chr1:45310338-45310339	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs149984712	chr1:45310352-45310353	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
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
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
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	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
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45307600-45309400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:45307600-45309400	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr1:45307800-45309200	Active TSS	Fetal Stomach	stomach
4	chr1:45307800-45309200	Active TSS	Ovary	ovary
5	chr1:45307800-45309400	Active TSS	Fetal Kidney	kidney
6	chr1:45308000-45309200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:45308000-45309200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:45308000-45309400	Active TSS	Brain Cingulate Gyrus	brain
9	chr1:45308200-45309000	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr1:45308200-45309000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
11	chr1:45308200-45309000	Enhancers	Lung	lung
12	chr1:45308200-45309200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:45308200-45309200	Active TSS	Primary T cells from cord blood	blood
14	chr1:45308200-45309400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:45308200-45309400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:45308200-45309400	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr1:45308200-45309400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:45308200-45309400	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr1:45308200-45309400	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr1:45308200-45309400	Active TSS	NHLF	lung
21	chr1:45308200-45309600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr1:45308400-45309000	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr1:45308400-45309000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
24	chr1:45308400-45309000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
25	chr1:45308400-45309000	Flanking Active TSS	Colonic Mucosa	Colon
26	chr1:45308400-45309000	Flanking Active TSS	Esophagus	oesophagus
27	chr1:45308400-45309000	Active TSS	Psoas Muscle	Psoas
28	chr1:45308400-45309000	Flanking Active TSS	Spleen	Spleen
29	chr1:45308400-45309000	Flanking Active TSS	HUVEC	blood vessel
30	chr1:45308400-45309200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr1:45308400-45309200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:45308400-45309200	Active TSS	Aorta	Aorta
33	chr1:45308400-45309200	Active TSS	Left Ventricle	heart
34	chr1:45308400-45309200	Active TSS	HMEC	breast
35	chr1:45308400-45309400	Active TSS	H9 Cell Line	embryonic stem cell
36	chr1:45308400-45309400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr1:45308400-45309400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr1:45308400-45309400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
39	chr1:45308400-45309400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:45308400-45309400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr1:45308400-45309400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:45308400-45309400	Active TSS	Brain Angular Gyrus	brain
43	chr1:45308400-45309400	Active TSS	Colon Smooth Muscle	Colon
44	chr1:45308400-45309400	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr1:45308400-45309400	Active TSS	Fetal Intestine Large	intestine
46	chr1:45308400-45309400	Active TSS	Rectal Smooth Muscle	rectum
47	chr1:45308400-45309400	Active TSS	Right Atrium	heart
48	chr1:45308400-45309400	Active TSS	A549	lung
49	chr1:45308400-45309600	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr1:45308400-45309600	Enhancers	Fetal Heart	heart

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