Variant report

Variant	esv1811070
Chromosome Location	chr1:151403570-151433317
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1168)
CpG islands
(count:795)
Chromatin interactive
region (count:99)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151421861-151421865	K562	blood:	n/a	n/a
2	ARID3A	chr1:151431846-151432139	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:151429859-151429993	K562	blood:	n/a	n/a
4	ARID3A	chr1:151431901-151432274	K562	blood:	n/a	n/a
5	ARID3A	chr1:151430637-151431016	K562	blood:	n/a	n/a
6	ARID3A	chr1:151430502-151431007	HepG2	liver:	n/a	n/a
7	ATF1	chr1:151416368-151416661	K562	blood:	n/a	n/a
8	ATF1	chr1:151429548-151429740	K562	blood:	n/a	n/a
9	ATF1	chr1:151431794-151432338	K562	blood:	n/a	n/a
10	ATF2	chr1:151431858-151432211	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:151431923-151432608	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr1:151431720-151432333	A549	lung:	n/a	chr1:151431844-151431853
13	ATF3	chr1:151430456-151431089	A549	lung:	n/a	n/a
14	BACH1	chr1:151405549-151405676	K562	blood:	n/a	n/a
15	BACH1	chr1:151431236-151431276	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:151416354-151416659	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:151432451-151432677	K562	blood:	n/a	n/a
18	BACH1	chr1:151405126-151405250	K562	blood:	n/a	n/a
19	BATF	chr1:151430473-151430777	GM12878	blood:	n/a	n/a
20	BCL3	chr1:151430380-151431058	A549	lung:	n/a	n/a
21	BCL3	chr1:151431769-151432576	A549	lung:	n/a	chr1:151431978-151431987 chr1:151431845-151431854 chr1:151431843-151431856
22	BCL3	chr1:151430370-151431053	A549	lung:	n/a	n/a
23	BCLAF1	chr1:151431740-151432240	GM12878	blood:	n/a	chr1:151431978-151431987 chr1:151431845-151431854 chr1:151431843-151431856
24	BCLAF1	chr1:151430413-151431064	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:151430392-151431035	GM12878	blood:	n/a	n/a
26	BCLAF1	chr1:151416273-151416728	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:151431517-151431614	K562	blood:	n/a	n/a
28	BHLHE40	chr1:151416380-151416643	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:151432313-151432584	K562	blood:	n/a	n/a
30	BHLHE40	chr1:151431889-151432100	K562	blood:	n/a	n/a
31	BHLHE40	chr1:151431886-151432240	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:151430474-151430920	GM12878	blood:	n/a	chr1:151430779-151430795
33	BRCA1	chr1:151431881-151432057	GM12878	blood:	n/a	n/a
34	BRCA1	chr1:151430586-151430976	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr1:151431837-151432542	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr1:151431813-151432550	HCT-116	colon:	n/a	n/a
37	CBX3	chr1:151431758-151432558	K562	blood:	n/a	n/a
38	CCNT2	chr1:151431231-151432097	K562	blood:	n/a	chr1:151431844-151431853 chr1:151431591-151431600 chr1:151431721-151431730 chr1:151431868-151431877
39	CEBPB	chr1:151430712-151431073	A549	lung:	n/a	chr1:151430946-151430959
40	CEBPB	chr1:151430771-151431075	ECC-1	luminal epithelium:	n/a	chr1:151430946-151430959
41	CEBPB	chr1:151428590-151428633	A549	lung:	n/a	n/a
42	CEBPB	chr1:151421555-151421689	HepG2	liver:	n/a	chr1:151421601-151421614 chr1:151421601-151421612
43	CEBPB	chr1:151430742-151431074	K562	blood:	n/a	chr1:151430946-151430959
44	CEBPB	chr1:151431883-151432084	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:151407815-151407820	K562	blood:	n/a	n/a
46	CEBPB	chr1:151430810-151431066	K562	blood:	n/a	chr1:151430946-151430959
47	CEBPB	chr1:151407654-151407997	IMR90	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
48	CEBPB	chr1:151430604-151431097	A549	lung:	n/a	chr1:151430946-151430959
49	CEBPB	chr1:151427430-151427659	K562	blood:	n/a	chr1:151427533-151427544
50	CEBPB	chr1:151416360-151416663	Hela-S3	cervix:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151430878-151430928	AG10803	skin:	n/a
2	chr1:151431931-151431981	ovcar-3	ovarian:	n/a
3	chr1:151430878-151430928	AG10803	skin:	n/a
4	chr1:151431931-151431981	ovcar-3	ovarian:	n/a
5	chr1:151430492-151430542	GM12878	blood:	n/a
6	chr1:151416412-151416462	AG10803	skin:	n/a
7	chr1:151431477-151431527	K562	blood:	n/a
8	chr1:151432024-151432074	PrEC	prostate:	n/a
9	chr1:151430492-151430542	HEEpiC	esophagus:	n/a
10	chr1:151428287-151428337	PFSK-1	brain:	n/a
11	chr1:151416412-151416462	NB4	blood:	n/a
12	chr1:151431477-151431527	Hepatocyte	liver:	n/a
13	chr1:151430492-151430542	HRE	kidney:	n/a
14	chr1:151432386-151432436	ProgFib	skin:	n/a
15	chr1:151416412-151416462	Hela-S3	cervix:	n/a
16	chr1:151431931-151431981	U87	brain:	n/a
17	chr1:151433222-151433272	SAEC	small airway:	n/a
18	chr1:151430492-151430542	NB4	blood:	n/a
19	chr1:151430492-151430542	PrEC	prostate:	n/a
20	chr1:151431750-151431800	NT2-D1	testis:	n/a
21	chr1:151433222-151433272	U87	brain:	n/a
22	chr1:151433222-151433272	HAEpiC	amniotic membrane:	n/a
23	chr1:151432024-151432074	HCT-116	colon:	n/a
24	chr1:151431750-151431800	PANC-1	pancreas:	n/a
25	chr1:151431849-151431899	GM06990	blood:	n/a
26	chr1:151430492-151430542	AG04449	skin:	fetal
27	chr1:151430878-151430928	GM12891	blood:	n/a
28	chr1:151430878-151430928	HCPEpiC	choroid plexus:	n/a
29	chr1:151431931-151431981	Hela-S3	cervix:	n/a
30	chr1:151428287-151428337	LNCaP	prostate:	n/a
31	chr1:151428287-151428337	IMR90	lung:	fetal
32	chr1:151431849-151431899	HCPEpiC	choroid plexus:	n/a
33	chr1:151431750-151431800	Hepatocyte	liver:	n/a
34	chr1:151431477-151431527	AG09319	gingival:	n/a
35	chr1:151416412-151416462	NHDF-neo	bronchial:	n/a
36	chr1:151428287-151428337	HCT-116	colon:	n/a
37	chr1:151432386-151432436	AG09309	skin:	n/a
38	chr1:151431849-151431899	RPTEC	kidney:	n/a
39	chr1:151432001-151432051	HRPEpiC	eye:	n/a
40	chr1:151433222-151433272	A549	lung:	n/a
41	chr1:151433222-151433272	NB4	blood:	n/a
42	chr1:151431931-151431981	NHDF-neo	bronchial:	n/a
43	chr1:151431849-151431899	AG04449	skin:	fetal
44	chr1:151432001-151432051	H1-hESC	embryonic stem cell:	embryo
45	chr1:151432024-151432074	HEK293	kidney:	embryo
46	chr1:151430492-151430542	LNCaP	prostate:	n/a
47	chr1:151431931-151431981	HRE	kidney:	n/a
48	chr1:151431477-151431527	Jurkat	blood:	n/a
49	chr1:151431931-151431981	HL-60	blood:	n/a
50	chr1:151430492-151430542	SK-N-SH_RA	brain:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:151411812..151418574-chr1:151428106..151433466,11	MCF-7	breast:
2	chr1:151429106..151432636-chr1:151510898..151514410,7	MCF-7	breast:
3	1:151402394-151411623..1:151618750-151636526	GM12878	blood:
4	chr1:151402377..151405267-chr1:151416084..151418421,2	MCF-7	breast:
5	chr1:151253485..151255699-chr1:151429417..151432153,4	K562	blood:
6	chr1:151415870..151416770-chr13:91751809..91752606,2	MCF-7	breast:
7	chr1:151421812..151434588-chr1:151506621..151515599,30	MCF-7	breast:
8	chr1:151431826..151434593-chr1:151511133..151514053,3	K562	blood:
9	chr1:151417086..151418869-chr1:151427238..151429980,2	K562	blood:
10	1:151180715-151199990..1:151402394-151411623	GM12878	blood:
11	chr1:151414283..151420812-chr1:151481565..151487481,13	MCF-7	breast:
12	chr1:151413939..151417832-chr1:151429782..151433498,5	K562	blood:
13	chr1:151427202..151436068-chr1:151477865..151490153,60	MCF-7	breast:
14	chr1:151410628..151413374-chr1:151426124..151427883,2	MCF-7	breast:
15	chr1:151416766..151418637-chr1:151510989..151514187,4	MCF-7	breast:
16	chr1:151412036..151414559-chr1:151416954..151420193,3	MCF-7	breast:
17	chr1:151428567..151432402-chr1:151505978..151509700,4	MCF-7	breast:
18	chr1:151410006..151411683-chr1:151482922..151485531,2	MCF-7	breast:
19	1:151402394-151411623..1:151516085-151535167	GM12878	blood:
20	chr1:151416054..151416703-chr1:151492454..151493195,2	K562	blood:
21	chr1:151409926..151411809-chr1:151413476..151415968,2	MCF-7	breast:
22	chr1:151403440..151406242-chr1:151583210..151585470,2	MCF-7	breast:
23	chr1:151414651..151422317-chr1:151482271..151486624,12	MCF-7	breast:
24	chr1:151429853..151431454-chr1:151735705..151737586,2	K562	blood:
25	chr1:151416059..151416938-chr1:151506910..151507900,5	MCF-7	breast:
26	chr1:151423878..151427557-chr1:151430240..151433379,4	K562	blood:
27	chr1:151431169..151432846-chr1:151517361..151519624,3	MCF-7	breast:
28	chr1:151416337..151418551-chr1:151419407..151421895,2	K562	blood:
29	chr1:151429381..151432201-chr14:21736244..21738881,2	MCF-7	breast:
30	chr1:151411841..151424302-chr1:151427210..151433048,24	MCF-7	breast:
31	chr1:151402390..151403923-chr1:151409370..151412245,2	MCF-7	breast:
32	chr1:151428938..151433041-chr1:151480813..151490135,53	MCF-7	breast:
33	chr1:151415530..151418373-chr1:151510570..151514579,6	MCF-7	breast:
34	chr1:151410072..151413256-chr1:151417263..151420004,3	K562	blood:
35	chr1:151371183..151372890-chr1:151431011..151433472,2	MCF-7	breast:
36	chr1:151428600..151431654-chr1:151540611..151542217,3	MCF-7	breast:
37	chr1:151298919..151301179-chr1:151402872..151405310,2	MCF-7	breast:
38	1:151203965-151215310..1:151402394-151411623	GM12878	blood:
39	chr1:151393425..151395913-chr1:151415036..151417250,2	MCF-7	breast:
40	chr1:151371526..151374105-chr1:151428160..151432357,4	K562	blood:
41	1:151402394-151411623..1:151496437-151509688	K562	blood:
42	chr1:151406315..151409257-chr1:151430992..151432763,2	MCF-7	breast:
43	chr1:151371427..151373843-chr1:151402656..151405068,2	MCF-7	breast:
44	chr1:151429965..151433300-chr1:151491808..151494354,4	MCF-7	breast:
45	chr1:151410628..151413374-chr1:151426124..151427883,2	MCF-7	breast:
46	chr1:151401923..151403617-chr1:151404854..151407788,2	MCF-7	breast:
47	chr1:151418228..151420627-chr1:151423254..151425635,2	MCF-7	breast:
48	chr1:151418710..151423161-chr1:151426419..151432381,10	MCF-7	breast:
49	chr1:151428333..151430220-chr1:151430244..151432504,3	K562	blood:
50	chr1:151430443..151432675-chr1:151490998..151493520,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSMB4-2	chr1:151429179-151430776	NONHSAT006396
2	lnc-PSMB4-2	chr1:151415213-151415740	NONHSAT006396
3	lnc-PSMB4-2	chr1:151413618-151413745	NONHSAT006396

No data

Variant related genes	Relation type
POGZ	TF binding region
RNY4P25	TF binding region
POGZ	CpG island
RNY4P25	CpG island
ENSG00000143442	chromatin interactions
ENSG00000213930	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000143376	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000143436	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000118960	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000143450	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000250734	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000178796	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000258728	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000143367	chromatin interactions

Extended variants
information (count: 1131 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535425267	chr1:151403710-151403711	Weak transcription Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
2	rs139813688	chr1:151403713-151403714	Weak transcription Strong transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs377459305	chr1:151403791-151403792	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
4	rs544216675	chr1:151403807-151403808	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
5	rs35519129	chr1:151403895-151403896	Weak transcription Strong transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs4246526	chr1:151403916-151403917	Weak transcription Strong transcription	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs183346155	chr1:151403944-151403945	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
8	rs4246527	chr1:151403948-151403949	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs576879948	chr1:151403953-151403954	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs188043509	chr1:151404001-151404002	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs553132008	chr1:151404014-151404015	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs192086880	chr1:151404054-151404055	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs56926422	chr1:151404113-151404114	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546017238	chr1:151404164-151404165	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs377647103	chr1:151404195-151404196	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs562378942	chr1:151404197-151404198	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs183774700	chr1:151404279-151404280	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs575926413	chr1:151404298-151404299	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs544778690	chr1:151404312-151404313	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs564176970	chr1:151404317-151404318	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs187878327	chr1:151404467-151404468	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs78666020	chr1:151404472-151404473	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs559685284	chr1:151404481-151404482	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
24	rs192947956	chr1:151404514-151404515	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs147616949	chr1:151404515-151404516	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs564498215	chr1:151404520-151404521	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs184157326	chr1:151404527-151404528	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs188180831	chr1:151404564-151404565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs12074714	chr1:151404606-151404607	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs537652380	chr1:151404608-151404609	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs551207695	chr1:151404624-151404625	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs200348474	chr1:151404635-151404636	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs539582563	chr1:151404640-151404641	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs376645401	chr1:151404657-151404658	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs573180308	chr1:151404713-151404714	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs6674191	chr1:151404720-151404721	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555794922	chr1:151404832-151404833	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs528622710	chr1:151404845-151404846	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs4246528	chr1:151404848-151404849	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs375245460	chr1:151404853-151404854	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs6697902	chr1:151404882-151404883	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs16833237	chr1:151404898-151404899	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7528822	chr1:151404926-151404927	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs12752416	chr1:151404930-151404931	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs145890704	chr1:151404974-151404975	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs545078539	chr1:151404982-151404983	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs184671571	chr1:151404991-151404992	Weak transcription Strong transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs542559914	chr1:151405023-151405024	Weak transcription Strong transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs562140021	chr1:151405024-151405025	Weak transcription Strong transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs138761166	chr1:151405025-151405026	Weak transcription Strong transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:1547 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151373400-151403600	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:151373400-151403600	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr1:151373400-151403800	Strong transcription	HUES6 Cell Line	embryonic stem cell
4	chr1:151373400-151416400	Weak transcription	Stomach Mucosa	stomach
5	chr1:151373600-151403800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr1:151373600-151403800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:151373800-151403600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:151373800-151403800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:151373800-151407000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:151374000-151405400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:151374000-151406800	Strong transcription	Fetal Muscle Trunk	muscle
12	chr1:151374200-151403800	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:151374200-151403800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:151374200-151403800	Strong transcription	Fetal Thymus	thymus
15	chr1:151374600-151403800	Strong transcription	Dnd41	blood
16	chr1:151375800-151403800	Strong transcription	Fetal Intestine Large	intestine
17	chr1:151378000-151403600	Strong transcription	GM12878-XiMat	blood
18	chr1:151384600-151406200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr1:151390800-151403600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:151391800-151403800	Strong transcription	Colon Smooth Muscle	Colon
21	chr1:151392600-151403800	Strong transcription	NH-A	brain
22	chr1:151393000-151413400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:151394400-151403800	Strong transcription	HMEC	breast
24	chr1:151396000-151403800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:151398400-151429600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:151398600-151417400	Weak transcription	Fetal Heart	heart
27	chr1:151400800-151406400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:151400800-151409600	Weak transcription	Psoas Muscle	Psoas
29	chr1:151400800-151417400	Weak transcription	Aorta	Aorta
30	chr1:151401000-151404400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:151401000-151410000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr1:151401000-151412200	Weak transcription	Brain Germinal Matrix	brain
33	chr1:151401000-151416200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:151401000-151430000	Weak transcription	Esophagus	oesophagus
35	chr1:151401200-151410000	Weak transcription	Gastric	stomach
36	chr1:151401400-151407400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:151401400-151407400	Weak transcription	Lung	lung
38	chr1:151401400-151409200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr1:151401400-151409400	Weak transcription	Right Ventricle	heart
40	chr1:151401400-151413000	Weak transcription	K562	blood
41	chr1:151401400-151413200	Weak transcription	Small Intestine	intestine
42	chr1:151401400-151417400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:151401600-151407400	Weak transcription	NHLF	lung
44	chr1:151401600-151411400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr1:151401600-151429200	Weak transcription	Spleen	Spleen
46	chr1:151402200-151413200	Weak transcription	Fetal Brain Male	brain
47	chr1:151402200-151416200	Weak transcription	Colonic Mucosa	Colon
48	chr1:151402400-151407400	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr1:151402400-151409000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr1:151402800-151406800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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