Variant report

Variant	esv3354291
Chromosome Location	chr1:95580964-95585362
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	chr1:95584322-95584937	K562	blood:	n/a	n/a
2	ARID3A	chr1:95581929-95582635	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:95582283-95582696	K562	blood:	n/a	n/a
4	ARID3A	chr1:95581075-95581712	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:95581076-95581651	K562	blood:	n/a	n/a
6	ATF2	chr1:95582241-95582637	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr1:95581222-95581665	K562	blood:	n/a	n/a
8	BACH1	chr1:95582140-95583091	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:95583325-95583787	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr1:95582280-95583563	K562	blood:	n/a	chr1:95583129-95583145 chr1:95583132-95583148 chr1:95582635-95582651
11	BHLHE40	chr1:95584362-95584610	K562	blood:	n/a	n/a
12	BRCA1	chr1:95583691-95583837	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:95582222-95582906	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:95582232-95582878	K562	blood:	n/a	n/a
15	CBX3	chr1:95581186-95581634	K562	blood:	n/a	n/a
16	CBX3	chr1:95581133-95581732	K562	blood:	n/a	n/a
17	CCNT2	chr1:95581094-95581627	K562	blood:	n/a	n/a
18	CCNT2	chr1:95582301-95583768	K562	blood:	n/a	chr1:95583655-95583664 chr1:95583192-95583201
19	CEBPB	chr1:95581261-95581822	A549	lung:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
20	CEBPB	chr1:95582228-95582576	K562	blood:	n/a	n/a
21	CEBPB	chr1:95581400-95581628	H1-hESC	embryonic stem cell:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
22	CEBPB	chr1:95581248-95581767	HepG2	liver:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
23	CEBPB	chr1:95581290-95581743	ECC-1	luminal epithelium:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
24	CEBPB	chr1:95581269-95581758	MCF-7	breast:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
25	CEBPB	chr1:95581334-95581702	IMR90	lung:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
26	CEBPB	chr1:95581335-95581702	A549	lung:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
27	CEBPB	chr1:95581058-95581867	K562	blood:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
28	CEBPB	chr1:95581321-95581716	HepG2	liver:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
29	CEBPB	chr1:95581333-95581722	ECC-1	luminal epithelium:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
30	CEBPB	chr1:95581304-95581680	K562	blood:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
31	CEBPB	chr1:95581350-95581619	HepG2	liver:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
32	CEBPB	chr1:95581189-95581696	HCT-116	colon:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
33	CEBPB	chr1:95582359-95582807	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:95581326-95581647	MCF-7	breast:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
35	CEBPB	chr1:95581021-95581886	K562	blood:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
36	CEBPB	chr1:95581305-95581721	HepG2	liver:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
37	CEBPB	chr1:95582299-95582813	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:95581327-95581703	Hela-S3	cervix:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
39	CEBPB	chr1:95581303-95581727	A549	lung:	n/a	chr1:95581482-95581493 chr1:95581481-95581494
40	CEBPD	chr1:95580991-95581750	K562	blood:	n/a	chr1:95581481-95581492
41	CEBPD	chr1:95582810-95583185	HepG2	liver:	n/a	n/a
42	CEBPD	chr1:95581377-95581641	HepG2	liver:	n/a	chr1:95581481-95581492
43	CEBPD	chr1:95581314-95581663	HepG2	liver:	n/a	chr1:95581481-95581492
44	CEBPD	chr1:95581091-95581812	K562	blood:	n/a	chr1:95581481-95581492
45	CHD1	chr1:95583386-95583581	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr1:95582499-95582680	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr1:95583460-95583703	HepG2	liver:	n/a	n/a
48	CHD2	chr1:95582251-95583700	Hela-S3	cervix:	n/a	chr1:95583227-95583237
49	CHD2	chr1:95582417-95582486	GM12878	blood:	n/a	n/a
50	CHD2	chr1:95582359-95582985	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95582329-95582379	ECC-1	luminal epithelium:	n/a
2	chr1:95582492-95582542	MCF10A-Er-Src	breast:	n/a
3	chr1:95582329-95582379	ECC-1	luminal epithelium:	n/a
4	chr1:95582492-95582542	MCF10A-Er-Src	breast:	n/a
5	chr1:95582825-95582875	LNCaP	prostate:	n/a
6	chr1:95582416-95582466	HIPEpiC	eye:	n/a
7	chr1:95582416-95582466	Jurkat	blood:	n/a
8	chr1:95583571-95583621	SAEC	small airway:	n/a
9	chr1:95583571-95583621	NH-A	brain:	n/a
10	chr1:95583073-95583123	HCT-116	colon:	n/a
11	chr1:95582666-95582716	GM12892	blood:	n/a
12	chr1:95582822-95582872	HCM	heart:	n/a
13	chr1:95581952-95582002	Caco-2	colon:	n/a
14	chr1:95582825-95582875	NH-A	brain:	n/a
15	chr1:95582416-95582466	MCF10A-Er-Src	breast:	n/a
16	chr1:95582751-95582801	GM06990	blood:	n/a
17	chr1:95582756-95582806	ovcar-3	ovarian:	n/a
18	chr1:95582751-95582801	HEEpiC	esophagus:	n/a
19	chr1:95583571-95583621	HRCEpiC	kidney:	n/a
20	chr1:95581952-95582002	GM06990	blood:	n/a
21	chr1:95583073-95583123	H1-hESC	embryonic stem cell:	embryo
22	chr1:95582416-95582466	AG04449	skin:	fetal
23	chr1:95582492-95582542	IMR90	lung:	fetal
24	chr1:95583636-95583686	Jurkat	blood:	n/a
25	chr1:95583518-95583568	HCM	heart:	n/a
26	chr1:95582647-95582697	AG09319	gingival:	n/a
27	chr1:95582329-95582379	HCF	heart:	n/a
28	chr1:95582751-95582801	GM12891	blood:	n/a
29	chr1:95582756-95582806	IMR90	lung:	fetal
30	chr1:95584445-95584495	HepG2	liver:	n/a
31	chr1:95582416-95582466	RPTEC	kidney:	n/a
32	chr1:95582751-95582801	Jurkat	blood:	n/a
33	chr1:95583571-95583621	SK-N-SH_RA	brain:	n/a
34	chr1:95582825-95582875	IMR90	lung:	fetal
35	chr1:95582751-95582801	GM12892	blood:	n/a
36	chr1:95584445-95584495	A549	lung:	n/a
37	chr1:95582789-95582839	Hepatocyte	liver:	n/a
38	chr1:95582756-95582806	CMK	blood:	n/a
39	chr1:95581952-95582002	NHBE	bronchial:	n/a
40	chr1:95582492-95582542	HL-60	blood:	n/a
41	chr1:95582666-95582716	HRCEpiC	kidney:	n/a
42	chr1:95583073-95583123	HRE	kidney:	n/a
43	chr1:95583518-95583568	AG04450	lung:	fetal
44	chr1:95583571-95583621	HEEpiC	esophagus:	n/a
45	chr1:95581952-95582002	HUVEC	blood vessel:	n/a
46	chr1:95582756-95582806	NT2-D1	testis:	n/a
47	chr1:95582751-95582801	ovcar-3	ovarian:	n/a
48	chr1:95584445-95584495	GM12892	blood:	n/a
49	chr1:95582416-95582466	NT2-D1	testis:	n/a
50	chr1:95583073-95583123	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:95577752..95581790-chr1:95581855..95584357,3	MCF-7	breast:
2	chr1:94946963..94948709-chr1:95581027..95583387,2	K562	blood:
3	chr1:95582616..95585939-chr1:95698259..95700506,4	K562	blood:
4	chr1:95579611..95582560-chr1:95641374..95643709,2	K562	blood:
5	chr1:95581571..95584597-chr1:95698513..95700535,3	MCF-7	breast:
6	chr1:95581745..95584156-chr1:95699309..95702187,2	MCF-7	breast:
7	chr1:95537896..95540428-chr1:95580653..95582591,2	MCF-7	breast:
8	chr1:95000799..95003612-chr1:95583736..95585676,2	K562	blood:
9	chr1:95582782..95583689-chr1:167189292..167190213,2	Hela-S3	cervix:
10	chr1:95582556..95585358-chr1:95698094..95701319,5	K562	blood:
11	chr1:95582496..95583191-chr1:95699224..95700072,2	K562	blood:
12	chr1:95537109..95538703-chr1:95581704..95583330,2	MCF-7	breast:
13	chr1:95549935..95550783-chr1:95583898..95584460,2	K562	blood:
14	chr1:95580754..95585035-chr1:95586074..95591340,6	K562	blood:

Variant related genes	Relation type
TMEM56	TF binding region
TMEM56-RWDD3	TF binding region
ENSG00000231992	TF binding region
TMEM56	CpG island
TMEM56-RWDD3	CpG island
ENSG00000231992	CpG island
ENSG00000206679	chromatin interactions
ENSG00000122481	chromatin interactions
ENSG00000226026	chromatin interactions
ENSG00000117528	chromatin interactions
ENSG00000152078	chromatin interactions
ENSG00000272205	chromatin interactions
ENSG00000117525	chromatin interactions
ENSG00000143190	chromatin interactions
ENSG00000172339	chromatin interactions
ENSG00000271092	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567507205	chr1:95581008-95581009	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs554761027	chr1:95581011-95581012	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs150061747	chr1:95581046-95581047	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs145345580	chr1:95581112-95581113	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs530347435	chr1:95581132-95581133	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs557060227	chr1:95581145-95581146	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs576808273	chr1:95581158-95581159	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs372030484	chr1:95581173-95581174	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs545832422	chr1:95581179-95581180	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs149202367	chr1:95581249-95581250	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs528785272	chr1:95581262-95581263	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs550196268	chr1:95581284-95581285	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs542016273	chr1:95581325-95581326	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs143252344	chr1:95581342-95581343	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs4245670	chr1:95581348-95581349	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs146702901	chr1:95581398-95581399	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs4489612	chr1:95581429-95581430	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs370150322	chr1:95581453-95581454	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs558964327	chr1:95581461-95581462	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs181885282	chr1:95581469-95581470	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs114325285	chr1:95581508-95581509	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs565798271	chr1:95581523-95581524	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs140297874	chr1:95581549-95581550	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs4344373	chr1:95581600-95581601	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568221683	chr1:95581654-95581655	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs536878911	chr1:95581673-95581674	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs150932308	chr1:95581692-95581693	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs576970066	chr1:95581693-95581694	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs140881414	chr1:95581701-95581702	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs4326672	chr1:95581713-95581714	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs573422895	chr1:95581772-95581773	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs375250088	chr1:95581861-95581862	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs562278549	chr1:95581867-95581868	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs150178493	chr1:95581931-95581932	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs544867141	chr1:95581939-95581940	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs563327595	chr1:95581940-95581941	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs185328027	chr1:95581987-95581988	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs552170706	chr1:95582135-95582136	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs553361920	chr1:95582141-95582142	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs559319169	chr1:95582159-95582160	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs61773101	chr1:95582202-95582203	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188500870	chr1:95582300-95582301	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs568302062	chr1:95582327-95582328	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs556888431	chr1:95582344-95582345	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs79980300	chr1:95582348-95582349	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs78209808	chr1:95582350-95582351	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs570572102	chr1:95582474-95582475	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs539559997	chr1:95582494-95582495	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs553219854	chr1:95582515-95582516	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs573175025	chr1:95582523-95582524	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
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
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD

Chromatin state (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95578000-95581000	Enhancers	K562	blood
2	chr1:95580800-95581600	Enhancers	Liver	Liver
3	chr1:95580800-95581600	Enhancers	HepG2	liver
4	chr1:95581000-95582200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr1:95581000-95582400	Flanking Active TSS	K562	blood
6	chr1:95581200-95581600	Enhancers	HMEC	breast
7	chr1:95581200-95582000	Enhancers	Fetal Heart	heart
8	chr1:95581200-95582000	Enhancers	Hela-S3	cervix
9	chr1:95581200-95582200	Enhancers	Brain Anterior Caudate	brain
10	chr1:95581200-95582200	Enhancers	Fetal Intestine Large	intestine
11	chr1:95581200-95582200	Enhancers	Fetal Intestine Small	intestine
12	chr1:95581400-95581600	Bivalent Enhancer	Primary B cells from cord blood	blood
13	chr1:95581400-95581600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
14	chr1:95581400-95581600	Enhancers	Esophagus	oesophagus
15	chr1:95581400-95581600	Enhancers	Right Ventricle	heart
16	chr1:95581400-95581800	Enhancers	A549	lung
17	chr1:95581600-95582000	Enhancers	Brain Cingulate Gyrus	brain
18	chr1:95581600-95582000	Weak transcription	HMEC	breast
19	chr1:95581600-95582200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:95581600-95582200	Enhancers	Placenta	Placenta
21	chr1:95581600-95582400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:95581600-95582400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
23	chr1:95581600-95582400	Weak transcription	Esophagus	oesophagus
24	chr1:95581600-95582400	Flanking Active TSS	HepG2	liver
25	chr1:95581600-95582800	Flanking Active TSS	Liver	Liver
26	chr1:95581800-95582000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:95581800-95582000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr1:95581800-95582200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr1:95581800-95582200	Flanking Active TSS	A549	lung
30	chr1:95582000-95582200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr1:95582000-95582200	Enhancers	Adipose Nuclei	Adipose
32	chr1:95582000-95582200	Enhancers	Brain Hippocampus Middle	brain
33	chr1:95582000-95582200	Enhancers	Brain Substantia Nigra	brain
34	chr1:95582000-95582200	Enhancers	Colon Smooth Muscle	Colon
35	chr1:95582000-95582200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr1:95582000-95582200	Enhancers	Stomach Mucosa	stomach
37	chr1:95582000-95582400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr1:95582000-95582400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr1:95582000-95582400	Flanking Active TSS	Fetal Heart	heart
40	chr1:95582000-95582400	Flanking Active TSS	Hela-S3	cervix
41	chr1:95582000-95582400	Enhancers	HMEC	breast
42	chr1:95582000-95583400	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr1:95582000-95583600	Active TSS	Stomach Smooth Muscle	stomach
44	chr1:95582000-95584200	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr1:95582000-95584800	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr1:95582200-95582400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:95582200-95582400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:95582200-95582400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:95582200-95582400	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:95582200-95582400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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