Variant report

Variant	nsv5276
Chromosome Location	chr1:247028364-247073098
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:61)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:247046289-247046346	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:247072726-247072877	HepG2	liver:	n/a	n/a
3	ATF2	chr1:247056556-247057142	GM12878	blood:	n/a	n/a
4	ATF2	chr1:247056455-247056990	GM12878	blood:	n/a	n/a
5	ATF3	chr1:247072642-247072955	K562	blood:	n/a	n/a
6	BATF	chr1:247056508-247056852	GM12878	blood:	n/a	n/a
7	BATF	chr1:247038587-247038975	GM12878	blood:	n/a	chr1:247038791-247038802
8	BATF	chr1:247038655-247039017	GM12878	blood:	n/a	chr1:247038791-247038802
9	CEBPB	chr1:247035337-247035635	HepG2	liver:	n/a	chr1:247035460-247035473 chr1:247035462-247035471 chr1:247035462-247035471 chr1:247035462-247035471
10	CEBPB	chr1:247072569-247072920	HepG2	liver:	n/a	chr1:247072747-247072758
11	CEBPB	chr1:247060624-247060993	IMR90	lung:	n/a	chr1:247060801-247060812
12	CEBPB	chr1:247072538-247072945	K562	blood:	n/a	chr1:247072747-247072758
13	CEBPB	chr1:247052386-247052699	A549	lung:	n/a	chr1:247052529-247052540
14	CEBPB	chr1:247060631-247060993	K562	blood:	n/a	chr1:247060801-247060812
15	CEBPB	chr1:247072514-247072971	K562	blood:	n/a	chr1:247072747-247072758
16	CEBPB	chr1:247060623-247060989	HepG2	liver:	n/a	chr1:247060801-247060812
17	CEBPB	chr1:247060629-247060980	Hela-S3	cervix:	n/a	chr1:247060801-247060812
18	CEBPB	chr1:247072685-247072783	H1-hESC	embryonic stem cell:	n/a	chr1:247072747-247072758
19	CEBPB	chr1:247072564-247072959	ECC-1	luminal epithelium:	n/a	chr1:247072747-247072758
20	CEBPB	chr1:247060728-247060834	HepG2	liver:	n/a	chr1:247060801-247060812
21	CEBPB	chr1:247070163-247070497	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:247035313-247035627	K562	blood:	n/a	chr1:247035460-247035473 chr1:247035462-247035471 chr1:247035462-247035471 chr1:247035462-247035471
23	CEBPB	chr1:247060627-247060990	A549	lung:	n/a	chr1:247060801-247060812
24	CEBPB	chr1:247072590-247072863	K562	blood:	n/a	chr1:247072747-247072758
25	CEBPB	chr1:247052395-247052595	HepG2	liver:	n/a	chr1:247052529-247052540
26	CEBPB	chr1:247035299-247035620	IMR90	lung:	n/a	chr1:247035460-247035473 chr1:247035462-247035471 chr1:247035462-247035471 chr1:247035462-247035471
27	CEBPB	chr1:247072564-247072926	A549	lung:	n/a	chr1:247072747-247072758
28	CEBPB	chr1:247039001-247039290	A549	lung:	n/a	n/a
29	CEBPB	chr1:247038452-247039314	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:247072539-247073329	Hela-S3	cervix:	n/a	chr1:247072747-247072758
31	CEBPB	chr1:247072571-247072930	ECC-1	luminal epithelium:	n/a	chr1:247072747-247072758
32	CHD2	chr1:247038870-247039087	GM12878	blood:	n/a	n/a
33	CTCF	chr1:247070940-247071090	AG04450	lung:	n/a	n/a
34	CTCF	chr1:247070873-247071096	GM12878	blood:	n/a	n/a
35	CTCF	chr1:247070917-247071059	GM13976	blood:	n/a	n/a
36	CTCF	chr1:247070900-247071050	HMEC	breast:	n/a	n/a
37	CTCF	chr1:247070900-247071050	GM06990	blood:	n/a	n/a
38	CTCF	chr1:247070920-247071070	HMF	breast:	n/a	n/a
39	CTCF	chr1:247070920-247071070	HCFaa	heart:	n/a	n/a
40	CTCF	chr1:247038740-247038890	HMF	breast:	n/a	n/a
41	CTCF	chr1:247038860-247039010	AG04450	lung:	n/a	n/a
42	CTCF	chr1:247038509-247038513	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:247070852-247071086	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr1:247070860-247071010	WI-38	lung:	n/a	n/a
45	CTCF	chr1:247061140-247061290	HL-60	blood:	n/a	n/a
46	CTCF	chr1:247070940-247071090	GM12875	blood:	n/a	n/a
47	CTCF	chr1:247070980-247071130	HCM	heart:	n/a	n/a
48	CTCF	chr1:247070940-247071090	Caco-2	colon:	n/a	n/a
49	CTCF	chr1:247051155-247051255	GM12878	blood:	n/a	chr1:247051172-247051193 chr1:247051170-247051188
50	CTCF	chr1:247070940-247071090	GM06990	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247037632-247037682	HNPCEpiC	eye:	n/a
2	chr1:247037632-247037682	HepG2	liver:	n/a
3	chr1:247037632-247037682	HMEC	breast:	n/a
4	chr1:247037632-247037682	AG09309	skin:	n/a
5	chr1:247037632-247037682	RPTEC	kidney:	n/a
6	chr1:247037632-247037682	AG04449	skin:	fetal
7	chr1:247037632-247037682	GM06990	blood:	n/a
8	chr1:247037632-247037682	PrEC	prostate:	n/a
9	chr1:247037632-247037682	Caco-2	colon:	n/a
10	chr1:247037632-247037682	NT2-D1	testis:	n/a
11	chr1:247037632-247037682	AG09319	gingival:	n/a
12	chr1:247037632-247037682	LNCaP	prostate:	n/a
13	chr1:247037632-247037682	HCF	heart:	n/a
14	chr1:247037632-247037682	HRPEpiC	eye:	n/a
15	chr1:247037632-247037682	T-47D	breast:	n/a
16	chr1:247037632-247037682	PFSK-1	brain:	n/a
17	chr1:247037632-247037682	HEK293	kidney:	embryo
18	chr1:247037632-247037682	NH-A	brain:	n/a
19	chr1:247037632-247037682	BE2_C	brain:	n/a
20	chr1:247037632-247037682	U87	brain:	n/a
21	chr1:247037632-247037682	HCM	heart:	n/a
22	chr1:247037632-247037682	IMR90	lung:	fetal
23	chr1:247037632-247037682	HIPEpiC	eye:	n/a
24	chr1:247037632-247037682	NB4	blood:	n/a
25	chr1:247037632-247037682	HL-60	blood:	n/a
26	chr1:247037632-247037682	AoSMC	blood vessel:	n/a
27	chr1:247037632-247037682	NHBE	bronchial:	n/a
28	chr1:247037632-247037682	BJ	skin:	n/a
29	chr1:247037632-247037682	MCF-7	breast:	n/a
30	chr1:247037632-247037682	GM12891	blood:	n/a
31	chr1:247037632-247037682	ovcar-3	ovarian:	n/a
32	chr1:247037632-247037682	SKMC	muscle:	n/a
33	chr1:247037632-247037682	GM19239	blood:	n/a
34	chr1:247037632-247037682	MCF10A-Er-Src	breast:	n/a
35	chr1:247037632-247037682	SK-N-SH_RA	brain:	n/a
36	chr1:247037632-247037682	GM12878	blood:	n/a
37	chr1:247037632-247037682	HRE	kidney:	n/a
38	chr1:247037632-247037682	Jurkat	blood:	n/a
39	chr1:247037632-247037682	HUVEC	blood vessel:	n/a
40	chr1:247037632-247037682	SK-N-MC	brain:	n/a
41	chr1:247037632-247037682	CMK	blood:	n/a
42	chr1:247037632-247037682	NHDF-neo	bronchial:	n/a
43	chr1:247037632-247037682	H1-hESC	embryonic stem cell:	embryo
44	chr1:247037632-247037682	Hepatocyte	liver:	n/a
45	chr1:247037632-247037682	HRCEpiC	kidney:	n/a
46	chr1:247037632-247037682	HCT-116	colon:	n/a
47	chr1:247037632-247037682	HCPEpiC	choroid plexus:	n/a
48	chr1:247037632-247037682	AG10803	skin:	n/a
49	chr1:247037632-247037682	SK-N-SH	brain:	n/a
50	chr1:247037632-247037682	A549	lung:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:247056985..247059643-chr1:247065954..247067972,2	K562	blood:
2	chr1:246996938..246999359-chr1:247044207..247046740,2	K562	blood:
3	chr1:247056985..247059643-chr1:247065954..247067972,2	K562	blood:
4	chr1:247064912..247069833-chr1:247070224..247074924,6	K562	blood:
5	chr1:247041147..247045524-chr1:247051435..247055344,4	K562	blood:
6	chr1:247028600..247030122-chr1:247031520..247034371,2	K562	blood:
7	chr1:247041147..247045524-chr1:247051435..247055344,4	K562	blood:
8	chr1:247059859..247061462-chr1:247063287..247066281,2	K562	blood:
9	chr1:247063867..247065621-chr1:247067210..247070638,3	K562	blood:
10	chr1:247069382..247071569-chr1:247094825..247096414,2	MCF-7	breast:
11	chr1:247030122..247032370-chr1:247032584..247035559,2	K562	blood:
12	chr1:247053838..247055850-chr1:247057759..247060432,2	K562	blood:
13	chr1:247015867..247018151-chr1:247054871..247056907,2	K562	blood:
14	chr1:247070542..247073488-chr1:247087102..247088901,2	K562	blood:
15	chr1:247017312..247021045-chr1:247051011..247055284,3	K562	blood:
16	chr1:247030642..247032624-chr1:247035866..247038095,2	K562	blood:
17	chr1:247051414..247053728-chr1:247080520..247082221,2	K562	blood:
18	chr1:247071509..247075202-chr1:247075216..247082853,9	K562	blood:
19	chr1:247064912..247069833-chr1:247070224..247074924,6	K562	blood:
20	chr1:247029799..247031525-chr1:247058523..247060785,2	MCF-7	breast:
21	chr1:247068134..247071071-chr1:247078852..247080355,2	K562	blood:
22	chr1:247063867..247065837-chr1:247067222..247069989,3	K562	blood:
23	chr1:247063867..247065621-chr1:247067210..247070638,3	K562	blood:
24	chr1:247066090..247069070-chr1:247069556..247072507,2	K562	blood:
25	chr1:247070489..247071341-chr1:247240399..247241137,2	MCF-7	breast:
26	chr1:247019583..247021599-chr1:247036719..247038806,2	K562	blood:
27	chr1:247058694..247061566-chr1:247068507..247070182,2	K562	blood:
28	chr1:247067231..247071071-chr1:247078833..247080355,3	K562	blood:
29	chr1:247039071..247040788-chr1:247042685..247044930,2	K562	blood:
30	chr1:247070543..247071317-chr1:247241686..247242650,5	MCF-7	breast:
31	chr1:247049317..247052263-chr1:247093673..247095503,2	K562	blood:
32	chr1:247000376..247002302-chr1:247040440..247042162,2	K562	blood:
33	chr1:247056860..247058918-chr1:247092602..247094534,2	MCF-7	breast:
34	chr1:247046300..247048217-chr1:247091357..247094558,3	K562	blood:
35	chr1:247065795..247068424-chr1:247094512..247096873,2	K562	blood:
36	chr1:247071871..247078090-chr1:247092538..247097120,9	K562	blood:
37	chr1:247028600..247030122-chr1:247031520..247034371,2	K562	blood:
38	chr1:247071846..247074365-chr1:247086927..247089836,2	MCF-7	breast:
39	chr1:247030642..247032624-chr1:247035866..247038095,2	K562	blood:
40	chr1:247063867..247065837-chr1:247067222..247069989,3	K562	blood:
41	chr1:247066090..247069070-chr1:247069556..247072507,2	K562	blood:
42	chr1:247026865..247028618-chr1:247028960..247030926,2	MCF-7	breast:
43	chr1:247053838..247055850-chr1:247057759..247060432,2	K562	blood:
44	chr1:247030122..247032370-chr1:247032584..247035559,2	K562	blood:
45	chr1:247067465..247069148-chr1:247371022..247373324,2	MCF-7	breast:
46	chr1:247069645..247071245-chr17:8075406..8078289,2	MCF-7	breast:
47	chr1:247033154..247036008-chr1:247106994..247108758,2	MCF-7	breast:
48	chr1:247069586..247071786-chr1:247495195..247496702,2	K562	blood:
49	chr1:247017685..247021797-chr1:247033247..247038806,7	K562	blood:
50	chr1:247058694..247061566-chr1:247068507..247070182,2	K562	blood:

No data

Variant related genes	Relation type
AHCTF1	TF binding region
AHCTF1	CpG island
ENSG00000188486	chromatin interactions
ENSG00000227671	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000135747	chromatin interactions

Extended variants
information (count: 1927 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1927 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571395363	chr1:247028411-247028412	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs75100583	chr1:247028465-247028466	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557124294	chr1:247028475-247028476	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs573754104	chr1:247028492-247028493	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542651331	chr1:247028497-247028498	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192209774	chr1:247028556-247028557	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11801219	chr1:247028561-247028562	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528294028	chr1:247028601-247028602	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541399332	chr1:247028624-247028625	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10924861	chr1:247028789-247028790	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs73142251	chr1:247028873-247028874	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs543581333	chr1:247028889-247028890	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563457069	chr1:247029002-247029003	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529307691	chr1:247029053-247029054	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141575447	chr1:247029062-247029063	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs34945773	chr1:247029063-247029064	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs66787763	chr1:247029064-247029065	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548968818	chr1:247029065-247029066	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112802786	chr1:247029068-247029069	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565784723	chr1:247029097-247029098	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565177797	chr1:247029138-247029139	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs528478549	chr1:247029145-247029146	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12121733	chr1:247029212-247029213	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs571498743	chr1:247029218-247029219	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536873977	chr1:247029223-247029224	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs557150704	chr1:247029230-247029231	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575992273	chr1:247029238-247029239	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550141534	chr1:247029258-247029259	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536396387	chr1:247029330-247029331	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150290650	chr1:247029363-247029364	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs572783870	chr1:247029373-247029374	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35779626	chr1:247029409-247029410	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183915973	chr1:247029569-247029570	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558189602	chr1:247029573-247029574	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138811688	chr1:247029625-247029626	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369090958	chr1:247029638-247029639	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145124901	chr1:247029658-247029659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543619435	chr1:247029672-247029673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563494825	chr1:247029673-247029674	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529444043	chr1:247029720-247029721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542754130	chr1:247029759-247029760	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs111704204	chr1:247029798-247029799	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs10558940	chr1:247029801-247029802	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559784944	chr1:247029827-247029828	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188403784	chr1:247029887-247029888	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551727525	chr1:247029889-247029890	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565051406	chr1:247029895-247029896	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556997629	chr1:247029944-247029945	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373981950	chr1:247029946-247029947	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530783547	chr1:247030091-247030092	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1296 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247002000-247038200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:247002200-247031400	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr1:247002200-247033800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:247002200-247034200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:247002200-247082400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr1:247002400-247081000	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr1:247002800-247032600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:247002800-247043200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr1:247003200-247029200	Strong transcription	Fetal Thymus	thymus
10	chr1:247003200-247042200	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:247003200-247042800	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:247003400-247043000	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:247003400-247044600	Strong transcription	Dnd41	blood
14	chr1:247004000-247040800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:247004000-247041200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr1:247004000-247042800	Strong transcription	Primary T cells from cord blood	blood
17	chr1:247004000-247053600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:247004200-247042400	Strong transcription	Primary B cells from peripheral blood	blood
19	chr1:247004200-247042800	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:247004200-247043000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:247004200-247044400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:247004200-247044400	Strong transcription	Liver	Liver
23	chr1:247004200-247083400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:247004400-247043000	Strong transcription	Adipose Nuclei	Adipose
25	chr1:247004400-247044600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr1:247005200-247079800	Weak transcription	Stomach Mucosa	stomach
27	chr1:247006000-247029000	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr1:247006600-247071600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:247009600-247031000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr1:247010000-247041200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr1:247010600-247029000	Strong transcription	Osteobl	bone
32	chr1:247013000-247032800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:247014000-247030800	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr1:247014800-247030400	Strong transcription	Hela-S3	cervix
35	chr1:247015000-247029000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:247015400-247032600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:247018400-247056400	Weak transcription	Fetal Heart	heart
38	chr1:247018600-247033000	Weak transcription	Psoas Muscle	Psoas
39	chr1:247020000-247029000	Strong transcription	HepG2	liver
40	chr1:247020400-247072800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr1:247020800-247034400	Weak transcription	Aorta	Aorta
42	chr1:247022000-247043000	Strong transcription	A549	lung
43	chr1:247022400-247042800	Weak transcription	Gastric	stomach
44	chr1:247022800-247028400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:247023000-247032800	Weak transcription	Fetal Brain Male	brain
46	chr1:247023400-247028400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr1:247023400-247032400	Weak transcription	Esophagus	oesophagus
48	chr1:247023400-247040800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:247023600-247031200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:247023600-247032400	Weak transcription	Spleen	Spleen

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