Variant report

Variant	nsv877558
Chromosome Location	chr3:142123841-142331360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2809)
CpG islands
(count:2385)
Chromatin interactive
region (count:180)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2809 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142166757-142167391	K562	blood:	n/a	n/a
2	ARID3A	chr3:142297425-142297909	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:142305620-142305987	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:142164559-142164562	K562	blood:	n/a	n/a
5	ARID3A	chr3:142314945-142315362	K562	blood:	n/a	n/a
6	ARID3A	chr3:142314492-142315669	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:142164561-142164907	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:142208918-142209055	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:142166751-142167232	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:142297606-142297816	K562	blood:	n/a	n/a
11	ARID3A	chr3:142155824-142156085	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:142158404-142158601	K562	blood:	n/a	n/a
13	ATF1	chr3:142166651-142167117	K562	blood:	n/a	n/a
14	ATF1	chr3:142261070-142261144	K562	blood:	n/a	n/a
15	ATF1	chr3:142158348-142158491	K562	blood:	n/a	n/a
16	ATF2	chr3:142314955-142315367	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr3:142164617-142165188	GM12878	blood:	n/a	n/a
18	ATF2	chr3:142166586-142167263	GM12878	blood:	n/a	n/a
19	ATF2	chr3:142296665-142297253	GM12878	blood:	n/a	n/a
20	ATF2	chr3:142297249-142297908	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr3:142297296-142297906	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr3:142297369-142298083	GM12878	blood:	n/a	n/a
23	ATF2	chr3:142166627-142167059	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr3:142305623-142306010	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr3:142166292-142167285	GM12878	blood:	n/a	n/a
26	ATF2	chr3:142314899-142315326	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr3:142166613-142167076	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr3:142314925-142315425	GM12878	blood:	n/a	n/a
29	ATF2	chr3:142297242-142298410	GM12878	blood:	n/a	n/a
30	ATF3	chr3:142153428-142153647	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr3:142166732-142167135	K562	blood:	n/a	n/a
32	ATF3	chr3:142166666-142167015	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr3:142314665-142315432	A549	lung:	n/a	n/a
34	ATF3	chr3:142166731-142166953	GM12878	blood:	n/a	n/a
35	ATF3	chr3:142297371-142298043	A549	lung:	n/a	chr3:142297742-142297751
36	ATF3	chr3:142153408-142153662	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF3	chr3:142166710-142167023	K562	blood:	n/a	n/a
38	ATF3	chr3:142166680-142167092	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF3	chr3:142166739-142166998	HepG2	liver:	n/a	n/a
40	ATF3	chr3:142314771-142315450	A549	lung:	n/a	chr3:142315426-142315435
41	ATF3	chr3:142297353-142297927	A549	lung:	n/a	chr3:142297742-142297751
42	ATF3	chr3:142153366-142153651	K562	blood:	n/a	n/a
43	BACH1	chr3:142297319-142297884	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr3:142314989-142315328	K562	blood:	n/a	n/a
45	BACH1	chr3:142166917-142167234	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr3:142296525-142296543	K562	blood:	n/a	n/a
47	BACH1	chr3:142314729-142315608	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr3:142239093-142239336	GM12878	blood:	n/a	chr3:142239207-142239218
49	BATF	chr3:142297399-142297972	GM12878	blood:	n/a	n/a
50	BATF	chr3:142164703-142164947	GM12878	blood:	n/a	n/a

(count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:142298018-142298068	U87	brain:	n/a
2	chr3:142297737-142297787	HEEpiC	esophagus:	n/a
3	chr3:142297295-142297345	GM19239	blood:	n/a
4	chr3:142297824-142297874	HepG2	liver:	n/a
5	chr3:142315207-142315257	HNPCEpiC	eye:	n/a
6	chr3:142166789-142166839	HL-60	blood:	n/a
7	chr3:142298018-142298068	U87	brain:	n/a
8	chr3:142297737-142297787	HEEpiC	esophagus:	n/a
9	chr3:142297295-142297345	GM19239	blood:	n/a
10	chr3:142297824-142297874	HepG2	liver:	n/a
11	chr3:142315207-142315257	HNPCEpiC	eye:	n/a
12	chr3:142166789-142166839	HL-60	blood:	n/a
13	chr3:142298018-142298068	HNPCEpiC	eye:	n/a
14	chr3:142315566-142315616	AoSMC	blood vessel:	n/a
15	chr3:142315213-142315263	PANC-1	pancreas:	n/a
16	chr3:142316082-142316132	SK-N-MC	brain:	n/a
17	chr3:142315220-142315270	HCF	heart:	n/a
18	chr3:142166789-142166839	SK-N-SH_RA	brain:	n/a
19	chr3:142294184-142294234	HRE	kidney:	n/a
20	chr3:142166203-142166253	ovcar-3	ovarian:	n/a
21	chr3:142297224-142297274	AG10803	skin:	n/a
22	chr3:142315326-142315376	Hela-S3	cervix:	n/a
23	chr3:142297747-142297797	PFSK-1	brain:	n/a
24	chr3:142164840-142164890	RPTEC	kidney:	n/a
25	chr3:142169703-142169753	SKMC	muscle:	n/a
26	chr3:142297224-142297274	BJ	skin:	n/a
27	chr3:142315207-142315257	PrEC	prostate:	n/a
28	chr3:142316082-142316132	MCF-7	breast:	n/a
29	chr3:142165032-142165082	HNPCEpiC	eye:	n/a
30	chr3:142166203-142166253	LNCaP	prostate:	n/a
31	chr3:142297900-142297950	ECC-1	luminal epithelium:	n/a
32	chr3:142297635-142297685	H1-hESC	embryonic stem cell:	embryo
33	chr3:142314968-142315018	SK-N-MC	brain:	n/a
34	chr3:142169703-142169753	GM12892	blood:	n/a
35	chr3:142297900-142297950	NB4	blood:	n/a
36	chr3:142166789-142166839	HCT-116	colon:	n/a
37	chr3:142167057-142167107	GM12892	blood:	n/a
38	chr3:142297295-142297345	A549	lung:	n/a
39	chr3:142166203-142166253	HNPCEpiC	eye:	n/a
40	chr3:142297641-142297691	HAEpiC	amniotic membrane:	n/a
41	chr3:142298018-142298068	NHBE	bronchial:	n/a
42	chr3:142296843-142296893	AG04449	skin:	fetal
43	chr3:142318115-142318165	MCF-7	breast:	n/a
44	chr3:142165032-142165082	PrEC	prostate:	n/a
45	chr3:142298018-142298068	MCF-7	breast:	n/a
46	chr3:142315064-142315114	PFSK-1	brain:	n/a
47	chr3:142297824-142297874	HEK293	kidney:	embryo
48	chr3:142297635-142297685	AG09309	skin:	n/a
49	chr3:142167057-142167107	HRCEpiC	kidney:	n/a
50	chr3:142165032-142165082	AG09319	gingival:	n/a

(count:180 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:142313378..142316741-chr3:142442748..142446550,8	K562	blood:
2	chr3:142327437..142329233-chr3:142329424..142330960,2	K562	blood:
3	chr3:142313218..142314887-chr3:142348977..142351077,2	K562	blood:
4	chr3:142164147..142165687-chr3:142176096..142178245,2	K562	blood:
5	chr3:142294568..142300006-chr3:142310942..142319455,13	MCF-7	breast:
6	chr3:142152079..142156407-chr3:142164108..142168187,4	MCF-7	breast:
7	chr3:106647215..106647782-chr3:142305386..142306279,2	MCF-7	breast:
8	chr3:142205435..142207089-chr3:142209696..142212453,2	K562	blood:
9	chr3:142297403..142299294-chr3:142720282..142722143,3	MCF-7	breast:
10	chr3:142317992..142321770-chr3:142321788..142324487,4	K562	blood:
11	chr3:142280626..142282527-chr3:142296623..142299039,2	K562	blood:
12	chr3:142255246..142257071-chr3:142259760..142261943,2	K562	blood:
13	chr3:142165266..142167494-chr3:142176108..142178776,2	K562	blood:
14	chr3:142154895..142157522-chr3:142161051..142162570,2	K562	blood:
15	chr3:142327574..142330140-chr3:142335677..142337995,2	MCF-7	breast:
16	chr3:142121474..142124130-chr3:142126023..142128529,2	MCF-7	breast:
17	chr3:142304087..142306838-chr3:142309222..142312026,2	K562	blood:
18	chr3:142296149..142300233-chr3:142313670..142315817,6	K562	blood:
19	chr3:142294568..142300006-chr3:142310942..142319455,13	MCF-7	breast:
20	chr3:133292322..133293201-chr3:142314859..142315610,2	HCT-116	colon:
21	chr3:142131465..142133801-chr3:142135541..142137461,2	K562	blood:
22	chr3:142164012..142167326-chr3:142183262..142187265,3	K562	blood:
23	chr3:142318139..142320851-chr3:142442948..142445184,2	K562	blood:
24	chr3:142297949..142299634-chr3:142710792..142712643,2	MCF-7	breast:
25	chr3:142297196..142298101-chr5:71615499..71616255,2	Hela-S3	cervix:
26	chr3:142221679..142224091-chr3:142224480..142227084,2	K562	blood:
27	chr3:142284471..142287739-chr3:142296498..142299510,3	MCF-7	breast:
28	chr3:142221745..142223373-chr3:142285789..142288084,2	K562	blood:
29	chr3:142305688..142306265-chr3:142712595..142713344,2	MCF-7	breast:
30	chr3:142305390..142308830-chr3:142313114..142316758,5	MCF-7	breast:
31	chr3:142319541..142323718-chr3:142324179..142327610,6	MCF-7	breast:
32	chr3:142241940..142244885-chr3:142296326..142298965,2	MCF-7	breast:
33	chr3:142294183..142301262-chr3:142311308..142318922,13	MCF-7	breast:
34	chr3:142293878..142296347-chr3:142313547..142315332,2	K562	blood:
35	chr3:142165499..142167998-chr3:142184965..142186898,2	MCF-7	breast:
36	chr3:142295996..142297624-chr3:142440935..142443594,2	K562	blood:
37	chr3:142267438..142270247-chr3:142280572..142282585,2	MCF-7	breast:
38	chr3:142295918..142298932-chr3:142719049..142722504,4	MCF-7	breast:
39	chr3:142167068..142168704-chr3:142178358..142179911,2	K562	blood:
40	chr3:142232153..142234194-chr3:142243013..142245479,2	MCF-7	breast:
41	chr3:142294824..142296664-chr3:142335818..142337448,2	K562	blood:
42	chr3:141746397..141747918-chr3:142295641..142297892,2	K562	blood:
43	chr3:142273455..142275768-chr3:142281419..142283017,2	K562	blood:
44	chr3:142305364..142306466-chr3:142399184..142400223,7	MCF-7	breast:
45	chr3:142226820..142229052-chr3:142234427..142237247,3	K562	blood:
46	chr3:142316986..142319598-chr3:142354070..142355822,2	MCF-7	breast:
47	chr13:98628143..98628846-chr3:142297511..142298310,2	NB4	blood:
48	chr3:142295888..142299099-chr3:142720440..142723490,3	K562	blood:
49	chr3:142164765..142166960-chr3:142189962..142191863,2	K562	blood:
50	chr3:142255246..142257071-chr3:142259760..142261943,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLS1-5	chr3:142168990-142169199	expReg_chr3_9540_+
2	lnc-PLS1-4	chr3:142169997-142170968	expReg_chr3_9541_+
3	lnc-XRN1-1	chr3:142190912-142191179	ENSG00000244327.1
4	lnc-PLS1-1	chr3:142301137-142301241	NONHSAT092476
5	lnc-PLS1-1	chr3:142300147-142300816	NONHSAT092476
6	lnc-PLS1-1	chr3:142299752-142299835	NONHSAT092476
7	lnc-XRN1-1	chr3:142184157-142184653	ENSG00000244327.1
8	lnc-PLS1-3	chr3:142171318-142171592	expReg_chr3_9542_+

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	XRN1	hsa-let-7b-5p	chr3:142136689-142136711

Variant related genes	Relation type
ENSG00000244327	TF binding region
RPL6P9	TF binding region
RNA5SP143	TF binding region
ATR	TF binding region
ENSG00000242479	TF binding region
XRN1	TF binding region
ENSG00000255637	TF binding region
RNU6-1294P	TF binding region
PLS1	TF binding region
RNU1-100P	TF binding region
ENSG00000244327	CpG island
RPL6P9	CpG island
RNA5SP143	CpG island
ATR	CpG island
ENSG00000242479	CpG island
XRN1	CpG island
ENSG00000255637	CpG island
RNU6-1294P	CpG island
PLS1	CpG island
RNU1-100P	CpG island
ENSG00000244024	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000121774	chromatin interactions
ENSG00000241570	chromatin interactions
ENSG00000213654	chromatin interactions
ENSG00000176845	chromatin interactions
ENSG00000113048	chromatin interactions
ENSG00000141985	chromatin interactions
ENSG00000268129	chromatin interactions
ENSG00000120756	chromatin interactions
ENSG00000117298	chromatin interactions
ENSG00000251804	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000103275	chromatin interactions
ENSG00000244327	chromatin interactions
ENSG00000163714	chromatin interactions
ENSG00000198242	chromatin interactions
ENSG00000153395	chromatin interactions
ENSG00000182768	chromatin interactions
ENSG00000242479	chromatin interactions
ENSG00000175040	chromatin interactions
ENSG00000065150	chromatin interactions
ENSG00000242390	chromatin interactions
ENSG00000252745	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000175387	chromatin interactions
ENSG00000156599	chromatin interactions
ENSG00000144935	chromatin interactions
ENSG00000188582	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000049883	chromatin interactions
ENSG00000091527	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000041880	chromatin interactions

Extended variants
information (count: 7582 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:7582 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2306700	chr3:142123841-142123842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191278933	chr3:142123914-142123915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547261121	chr3:142123944-142123945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558962785	chr3:142124019-142124020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200019581	chr3:142124032-142124033	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs151004426	chr3:142124122-142124123	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7349528	chr3:142124169-142124170	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs563220106	chr3:142124172-142124173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530594136	chr3:142124194-142124195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6440083	chr3:142124287-142124288	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs561486620	chr3:142124294-142124295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528792552	chr3:142124295-142124296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557447753	chr3:142124334-142124335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572774700	chr3:142124366-142124367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571717676	chr3:142124367-142124368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532530838	chr3:142124469-142124470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576010896	chr3:142124496-142124497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551132010	chr3:142124540-142124541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374604693	chr3:142124554-142124555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569271181	chr3:142124578-142124579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536701666	chr3:142124654-142124655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555278740	chr3:142124666-142124667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536713709	chr3:142124750-142124751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201104281	chr3:142124756-142124757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567444302	chr3:142124759-142124760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139608565	chr3:142124765-142124766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577252001	chr3:142124829-142124830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs57445815	chr3:142124856-142124857	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs149749789	chr3:142124858-142124859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575248664	chr3:142124877-142124878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375453024	chr3:142124909-142124910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113215937	chr3:142124932-142124933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561364356	chr3:142124957-142124958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528694041	chr3:142124979-142124980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573457720	chr3:142124989-142124990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565564522	chr3:142125022-142125023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532823309	chr3:142125029-142125030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9808996	chr3:142125087-142125088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs75719155	chr3:142125095-142125096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377365220	chr3:142125098-142125099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530172893	chr3:142125161-142125162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192988953	chr3:142125170-142125171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377114676	chr3:142125239-142125240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540146301	chr3:142125247-142125248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370465007	chr3:142125261-142125262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146774223	chr3:142125386-142125387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35227772	chr3:142125395-142125396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12485352	chr3:142125415-142125416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1905813	chr3:142125459-142125460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111944071	chr3:142125510-142125511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5893 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142076000-142136400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr3:142076800-142138200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:142083600-142158600	Weak transcription	NHEK	skin
4	chr3:142105000-142151800	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr3:142105800-142136600	Strong transcription	Fetal Intestine Large	intestine
6	chr3:142106800-142150800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:142109200-142141800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:142112200-142133200	Strong transcription	Duodenum Mucosa	Duodenum
9	chr3:142112200-142145000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:142112200-142145400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:142112200-142151600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr3:142112200-142152000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr3:142112200-142152200	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr3:142112200-142154600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr3:142112400-142142400	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr3:142112400-142146600	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr3:142112600-142141600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:142112600-142150600	Strong transcription	Placenta	Placenta
19	chr3:142112800-142142800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:142113000-142152200	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr3:142113400-142151800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr3:142113400-142151800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:142114600-142126600	Weak transcription	Fetal Heart	heart
24	chr3:142114800-142151800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:142115200-142126600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr3:142115200-142129400	Weak transcription	Small Intestine	intestine
27	chr3:142115800-142125200	Weak transcription	Psoas Muscle	Psoas
28	chr3:142115800-142125400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr3:142115800-142125400	Weak transcription	Aorta	Aorta
30	chr3:142115800-142125400	Weak transcription	Lung	lung
31	chr3:142115800-142125400	Weak transcription	Spleen	Spleen
32	chr3:142115800-142126600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr3:142115800-142126600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr3:142115800-142126800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr3:142115800-142126800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr3:142115800-142127000	Weak transcription	Gastric	stomach
37	chr3:142115800-142128200	Weak transcription	Hela-S3	cervix
38	chr3:142115800-142134800	Weak transcription	Right Ventricle	heart
39	chr3:142115800-142136400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr3:142115800-142138000	Weak transcription	Esophagus	oesophagus
41	chr3:142116000-142126800	Weak transcription	A549	lung
42	chr3:142116000-142127000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:142116200-142125400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr3:142116200-142126400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr3:142116200-142129400	Weak transcription	NHLF	lung
46	chr3:142116400-142125400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr3:142116400-142125400	Weak transcription	Brain Cingulate Gyrus	brain
48	chr3:142116400-142141800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr3:142117200-142126400	Weak transcription	Colonic Mucosa	Colon
50	chr3:142117600-142128000	Weak transcription	HSMMtube	muscle

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