Variant report

Variant	nsv882366
Chromosome Location	chr5:89826726-89894564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:678)
CpG islands
(count:1100)
Chromatin interactive
region (count:120)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:89854333-89854593	K562	blood:	n/a	n/a
2	ARID3A	chr5:89843923-89844296	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:89843934-89844540	K562	blood:	n/a	n/a
4	ARID3A	chr5:89864841-89864889	K562	blood:	n/a	n/a
5	ARID3A	chr5:89862763-89862814	K562	blood:	n/a	n/a
6	ATF1	chr5:89885999-89886356	K562	blood:	n/a	n/a
7	ATF2	chr5:89854192-89854712	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:89854034-89854674	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr5:89843039-89843302	K562	blood:	n/a	n/a
10	BACH1	chr5:89843920-89844216	K562	blood:	n/a	n/a
11	BACH1	chr5:89854709-89854798	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:89843933-89844336	GM12878	blood:	n/a	chr5:89844107-89844118 chr5:89844108-89844118
13	BATF	chr5:89843933-89844292	GM12878	blood:	n/a	chr5:89844107-89844118 chr5:89844108-89844118
14	BATF	chr5:89881470-89881854	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:89864741-89864845	K562	blood:	n/a	n/a
16	BHLHE40	chr5:89829652-89829947	K562	blood:	n/a	n/a
17	BHLHE40	chr5:89858006-89858376	K562	blood:	n/a	n/a
18	BHLHE40	chr5:89854240-89854657	HepG2	liver:	n/a	chr5:89854432-89854448
19	BHLHE40	chr5:89884270-89884707	K562	blood:	n/a	n/a
20	BHLHE40	chr5:89854342-89854543	A549	lung:	n/a	chr5:89854432-89854448
21	BHLHE40	chr5:89854240-89854753	K562	blood:	n/a	chr5:89854432-89854448 chr5:89854692-89854708
22	BHLHE40	chr5:89844002-89844331	K562	blood:	n/a	n/a
23	BRCA1	chr5:89854184-89855151	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr5:89854155-89854809	K562	blood:	n/a	n/a
25	CCNT2	chr5:89845704-89845820	K562	blood:	n/a	n/a
26	CCNT2	chr5:89856463-89856500	K562	blood:	n/a	n/a
27	CCNT2	chr5:89854278-89854974	K562	blood:	n/a	n/a
28	CEBPB	chr5:89857993-89858212	A549	lung:	n/a	n/a
29	CEBPB	chr5:89830769-89831136	H1-hESC	embryonic stem cell:	n/a	chr5:89830944-89830955 chr5:89830946-89830955 chr5:89830946-89830955 chr5:89830946-89830955
30	CEBPB	chr5:89849178-89849464	K562	blood:	n/a	chr5:89849312-89849323
31	CEBPB	chr5:89871628-89871975	K562	blood:	n/a	chr5:89871800-89871811
32	CEBPB	chr5:89871707-89871943	A549	lung:	n/a	chr5:89871800-89871811
33	CEBPB	chr5:89846823-89847161	HepG2	liver:	n/a	chr5:89846982-89846995 chr5:89846984-89846995 chr5:89846982-89846993 chr5:89846984-89846993
34	CEBPB	chr5:89836428-89836753	K562	blood:	n/a	chr5:89836591-89836602
35	CEBPB	chr5:89846850-89847152	IMR90	lung:	n/a	chr5:89846982-89846995 chr5:89846984-89846995 chr5:89846982-89846993 chr5:89846984-89846993
36	CEBPB	chr5:89842753-89843045	K562	blood:	n/a	chr5:89842938-89842949 chr5:89842936-89842949 chr5:89842936-89842947
37	CEBPB	chr5:89846822-89847124	A549	lung:	n/a	chr5:89846982-89846995 chr5:89846984-89846995 chr5:89846982-89846993 chr5:89846984-89846993
38	CEBPB	chr5:89836495-89836695	HepG2	liver:	n/a	chr5:89836591-89836602
39	CEBPB	chr5:89843815-89844318	MCF-7	breast:	n/a	chr5:89843926-89843937 chr5:89843926-89843939
40	CEBPB	chr5:89830718-89831168	MCF-7	breast:	n/a	chr5:89830944-89830955 chr5:89830946-89830955 chr5:89830946-89830955 chr5:89830946-89830955
41	CEBPB	chr5:89842823-89843044	K562	blood:	n/a	chr5:89842938-89842949 chr5:89842936-89842949 chr5:89842936-89842947
42	CEBPB	chr5:89882317-89882675	K562	blood:	n/a	chr5:89882495-89882506
43	CEBPB	chr5:89830762-89831440	A549	lung:	n/a	chr5:89830944-89830955 chr5:89830946-89830955 chr5:89830946-89830955 chr5:89830946-89830955
44	CEBPB	chr5:89836473-89836719	IMR90	lung:	n/a	chr5:89836591-89836602
45	CEBPB	chr5:89871674-89871939	MCF-7	breast:	n/a	chr5:89871800-89871811
46	CEBPB	chr5:89860947-89861155	K562	blood:	n/a	chr5:89861063-89861074
47	CEBPB	chr5:89830736-89831230	Hela-S3	cervix:	n/a	chr5:89830944-89830955 chr5:89830946-89830955 chr5:89830946-89830955 chr5:89830946-89830955
48	CEBPB	chr5:89830804-89831156	A549	lung:	n/a	chr5:89830944-89830955 chr5:89830946-89830955 chr5:89830946-89830955 chr5:89830946-89830955
49	CEBPB	chr5:89830755-89831123	ECC-1	luminal epithelium:	n/a	chr5:89830944-89830955 chr5:89830946-89830955 chr5:89830946-89830955 chr5:89830946-89830955
50	CEBPB	chr5:89871689-89871949	MCF-7	breast:	n/a	chr5:89871800-89871811

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89853284-89853334	HEEpiC	esophagus:	n/a
2	chr5:89853284-89853334	HCF	heart:	n/a
3	chr5:89853284-89853334	HEEpiC	esophagus:	n/a
4	chr5:89853284-89853334	HCF	heart:	n/a
5	chr5:89858378-89858428	PANC-1	pancreas:	n/a
6	chr5:89854414-89854464	SAEC	small airway:	n/a
7	chr5:89828771-89828821	IMR90	lung:	fetal
8	chr5:89858378-89858428	NHDF-neo	bronchial:	n/a
9	chr5:89854821-89854871	SAEC	small airway:	n/a
10	chr5:89854425-89854475	HEK293	kidney:	embryo
11	chr5:89854334-89854384	HRPEpiC	eye:	n/a
12	chr5:89842121-89842171	AG04449	skin:	fetal
13	chr5:89881642-89881692	BE2_C	brain:	n/a
14	chr5:89854539-89854589	PANC-1	pancreas:	n/a
15	chr5:89853284-89853334	GM19239	blood:	n/a
16	chr5:89854632-89854682	GM12891	blood:	n/a
17	chr5:89850684-89850734	RPTEC	kidney:	n/a
18	chr5:89854651-89854701	LNCaP	prostate:	n/a
19	chr5:89853771-89853821	ECC-1	luminal epithelium:	n/a
20	chr5:89853771-89853821	Hela-S3	cervix:	n/a
21	chr5:89854821-89854871	RPTEC	kidney:	n/a
22	chr5:89854539-89854589	HRE	kidney:	n/a
23	chr5:89854830-89854880	ovcar-3	ovarian:	n/a
24	chr5:89854334-89854384	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:89854364-89854414	K562	blood:	n/a
26	chr5:89854830-89854880	HEEpiC	esophagus:	n/a
27	chr5:89854979-89855029	GM19239	blood:	n/a
28	chr5:89854539-89854589	AG09319	gingival:	n/a
29	chr5:89881642-89881692	K562	blood:	n/a
30	chr5:89854364-89854414	NHDF-neo	bronchial:	n/a
31	chr5:89881642-89881692	MCF-7	breast:	n/a
32	chr5:89854979-89855029	HAEpiC	amniotic membrane:	n/a
33	chr5:89854539-89854589	MCF10A-Er-Src	breast:	n/a
34	chr5:89854651-89854701	SAEC	small airway:	n/a
35	chr5:89854425-89854475	HAEpiC	amniotic membrane:	n/a
36	chr5:89854830-89854880	HCT-116	colon:	n/a
37	chr5:89854334-89854384	AoSMC	blood vessel:	n/a
38	chr5:89854425-89854475	AG09309	skin:	n/a
39	chr5:89854293-89854343	HCF	heart:	n/a
40	chr5:89854293-89854343	Caco-2	colon:	n/a
41	chr5:89881642-89881692	NHDF-neo	bronchial:	n/a
42	chr5:89854539-89854589	HAEpiC	amniotic membrane:	n/a
43	chr5:89854414-89854464	SKMC	muscle:	n/a
44	chr5:89854293-89854343	AG09309	skin:	n/a
45	chr5:89854364-89854414	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:89850684-89850734	HepG2	liver:	n/a
47	chr5:89854539-89854589	GM12891	blood:	n/a
48	chr5:89854979-89855029	MCF-7	breast:	n/a
49	chr5:89854425-89854475	HEEpiC	esophagus:	n/a
50	chr5:89828771-89828821	BJ	skin:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:89824654..89827598-chr5:89828369..89833726,5	K562	blood:
2	chr5:89878566..89881617-chr5:89882501..89884794,5	K562	blood:
3	chr5:89705126..89706810-chr5:89842410..89844887,2	MCF-7	breast:
4	chr5:89822535..89824744-chr5:89842428..89844021,2	K562	blood:
5	chr5:89843795..89845765-chr5:89848333..89850090,2	MCF-7	breast:
6	chr5:89823946..89826713-chr5:89827951..89830249,2	MCF-7	breast:
7	chr5:89828973..89830525-chr5:89839413..89841033,2	MCF-7	breast:
8	chr5:89768870..89770487-chr5:89842476..89844601,2	MCF-7	breast:
9	chr5:89826199..89831045-chr5:89834037..89838315,7	K562	blood:
10	chr5:89826971..89828828-chr5:89846994..89849813,2	MCF-7	breast:
11	chr5:89703769..89706239-chr5:89858612..89861256,3	MCF-7	breast:
12	chr5:89767485..89770428-chr5:89849718..89851629,2	MCF-7	breast:
13	chr5:89824246..89828197-chr5:89842395..89845815,3	K562	blood:
14	chr5:89852793..89854346-chr5:89883740..89885331,2	MCF-7	breast:
15	chr5:89893486..89895205-chr5:89895612..89897548,2	K562	blood:
16	chr5:89843795..89845765-chr5:89848333..89850090,2	MCF-7	breast:
17	chr5:89769294..89771048-chr5:89829508..89832155,2	MCF-7	breast:
18	chr5:89708413..89711602-chr5:89825612..89828655,3	K562	blood:
19	chr5:89831265..89835125-chr5:89838183..89842442,4	K562	blood:
20	chr5:89705231..89707575-chr5:89854422..89857316,5	K562	blood:
21	chr5:89833046..89834867-chr5:89838183..89840243,2	K562	blood:
22	chr5:89824636..89834797-chr5:89838005..89846568,18	MCF-7	breast:
23	chr5:89825541..89827508-chr5:89852797..89855537,2	MCF-7	breast:
24	chr5:89705290..89707109-chr5:89824364..89826854,3	MCF-7	breast:
25	chr5:89705209..89706757-chr5:89853526..89855162,2	MCF-7	breast:
26	chr5:89768019..89770611-chr5:89858003..89859643,2	MCF-7	breast:
27	chr5:89825930..89827528-chr5:89867274..89868949,2	MCF-7	breast:
28	chr5:89823936..89826632-chr5:89839276..89841798,3	K562	blood:
29	chr5:89881685..89883243-chr5:89883707..89886332,2	K562	blood:
30	chr5:89857832..89860192-chr5:90676540..90678768,2	K562	blood:
31	chr5:89843926..89847301-chr5:89847464..89849372,3	K562	blood:
32	chr5:89704382..89708328-chr5:89852696..89856618,6	MCF-7	breast:
33	chr5:89766469..89774126-chr5:89823341..89829105,11	K562	blood:
34	chr5:89829601..89833585-chr5:89854929..89859978,5	MCF-7	breast:
35	chr5:89721701..89723836-chr5:89852631..89854336,2	K562	blood:
36	chr5:89768855..89773751-chr5:89822671..89829297,12	K562	blood:
37	chr5:89826684..89828882-chr5:89853247..89854802,2	K562	blood:
38	chr5:89825598..89829055-chr5:89851441..89854747,4	K562	blood:
39	chr5:89703071..89706811-chr5:89843444..89846319,3	K562	blood:
40	chr5:89828973..89830525-chr5:89839413..89841033,2	MCF-7	breast:
41	chr5:89826971..89828828-chr5:89846994..89849813,2	MCF-7	breast:
42	chr5:89862796..89864795-chr5:89866978..89869006,2	K562	blood:
43	chr5:89881685..89883243-chr5:89883707..89886332,2	K562	blood:
44	chr5:89855529..89859468-chr5:89877001..89881365,3	MCF-7	breast:
45	chr5:89703976..89707575-chr5:89854064..89857316,4	K562	blood:
46	chr5:89768878..89771391-chr5:89831167..89833333,2	MCF-7	breast:
47	chr5:89752607..89755470-chr5:89857714..89859860,2	MCF-7	breast:
48	chr5:89864609..89867407-chr5:89868607..89870565,2	K562	blood:
49	chr5:89883022..89885296-chr5:89901095..89903175,2	K562	blood:
50	chr5:89705110..89707886-chr5:89867244..89868885,2	MCF-7	breast:

No data

Variant related genes	Relation type
LYSMD3	TF binding region
GPR98	TF binding region
LYSMD3	CpG island
GPR98	CpG island
ENSG00000164199	chromatin interactions
ENSG00000176018	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000255647	chromatin interactions

Extended variants
information (count: 2268 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2268 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs499148	chr5:89826726-89826727	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547686291	chr5:89826769-89826770	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs530364605	chr5:89826837-89826838	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs567421368	chr5:89826858-89826859	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs536478615	chr5:89826893-89826894	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs547239735	chr5:89826897-89826898	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs540066183	chr5:89826939-89826940	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs369263754	chr5:89827000-89827001	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs147404947	chr5:89827005-89827006	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs139710475	chr5:89827021-89827022	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs558733607	chr5:89827022-89827023	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs538802129	chr5:89827101-89827102	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs534673147	chr5:89827169-89827170	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs114591912	chr5:89827232-89827233	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs574766876	chr5:89827243-89827244	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs543652318	chr5:89827296-89827297	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs377241607	chr5:89827328-89827329	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs557132034	chr5:89827363-89827364	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs73173989	chr5:89827380-89827381	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186375577	chr5:89827457-89827458	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs77815246	chr5:89827477-89827478	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs537943889	chr5:89827505-89827506	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs527304961	chr5:89827514-89827515	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs372989052	chr5:89827531-89827532	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs556352478	chr5:89827568-89827569	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs191577797	chr5:89827593-89827594	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs370810170	chr5:89827634-89827635	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs373852749	chr5:89827636-89827637	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs530006689	chr5:89827651-89827652	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs180841278	chr5:89827737-89827738	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs578051987	chr5:89827800-89827801	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs371245577	chr5:89827811-89827812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs532166128	chr5:89827820-89827821	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs139610498	chr5:89827821-89827822	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs566009734	chr5:89827872-89827873	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs535043527	chr5:89827887-89827888	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs149777717	chr5:89827907-89827908	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs568464789	chr5:89827953-89827954	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs139840248	chr5:89828016-89828017	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs67292166	chr5:89828017-89828018	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs199867865	chr5:89828022-89828023	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs60982946	chr5:89828023-89828024	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs376862876	chr5:89828024-89828025	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs534722326	chr5:89828178-89828179	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs537354136	chr5:89828182-89828183	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs552657279	chr5:89828218-89828219	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs557193298	chr5:89828224-89828225	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs648430	chr5:89828258-89828259	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs185181442	chr5:89828259-89828260	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs370925146	chr5:89828283-89828284	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89824400-89826800	Active TSS	Thymus	Thymus
2	chr5:89826000-89826800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:89826000-89826800	Enhancers	Small Intestine	intestine
4	chr5:89826200-89826800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr5:89826200-89826800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:89826200-89826800	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr5:89826200-89826800	Flanking Active TSS	Brain Angular Gyrus	brain
8	chr5:89826200-89826800	Flanking Active TSS	Brain Anterior Caudate	brain
9	chr5:89826200-89826800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
10	chr5:89826200-89826800	Flanking Active TSS	Colon Smooth Muscle	Colon
11	chr5:89826200-89826800	Flanking Active TSS	Rectal Smooth Muscle	rectum
12	chr5:89826200-89826800	Flanking Active TSS	Stomach Smooth Muscle	stomach
13	chr5:89826200-89827000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:89826200-89827000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:89826200-89827000	Flanking Active TSS	Liver	Liver
16	chr5:89826200-89827000	Flanking Active TSS	Brain Cingulate Gyrus	brain
17	chr5:89826200-89827200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr5:89826200-89827200	Flanking Active TSS	K562	blood
19	chr5:89826200-89827400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:89826200-89842800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:89826400-89826800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:89826400-89826800	Enhancers	Primary B cells from cord blood	blood
23	chr5:89826400-89826800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr5:89826400-89826800	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr5:89826400-89826800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr5:89826400-89826800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr5:89826400-89826800	Flanking Active TSS	Brain Hippocampus Middle	brain
28	chr5:89826400-89826800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr5:89826400-89826800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr5:89826400-89826800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:89826400-89826800	Flanking Active TSS	Fetal Brain Female	brain
32	chr5:89826400-89826800	Enhancers	A549	lung
33	chr5:89826400-89826800	Enhancers	GM12878-XiMat	blood
34	chr5:89826400-89827000	Flanking Active TSS	Brain Germinal Matrix	brain
35	chr5:89826400-89827200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr5:89826400-89827400	Enhancers	Brain Substantia Nigra	brain
37	chr5:89826600-89826800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:89826600-89826800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:89826600-89826800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:89826600-89826800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:89826600-89826800	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr5:89826600-89826800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:89826600-89826800	Enhancers	Aorta	Aorta
44	chr5:89826600-89826800	Enhancers	Fetal Intestine Large	intestine
45	chr5:89826600-89826800	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr5:89826600-89826800	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr5:89826600-89826800	Enhancers	Dnd41	blood
48	chr5:89826600-89826800	Enhancers	HMEC	breast
49	chr5:89826600-89826800	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr5:89826600-89826800	Enhancers	NHLF	lung

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