Variant report

Variant	nsv588884
Chromosome Location	chr22:30494371-30590026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:633)
CpG islands
(count:122)
Chromatin interactive
region (count:69)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30504656-30504959	K562	blood:	n/a	n/a
2	ARID3A	chr22:30515156-30515405	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:30584963-30585176	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:30543067-30543100	K562	blood:	n/a	n/a
5	ARID3A	chr22:30587301-30587845	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:30504610-30505004	HepG2	liver:	n/a	n/a
7	ATF1	chr22:30557094-30557371	K562	blood:	n/a	n/a
8	ATF1	chr22:30579886-30580213	K562	blood:	n/a	n/a
9	BACH1	chr22:30585301-30585323	K562	blood:	n/a	n/a
10	BCL3	chr22:30575574-30575845	GM12878	blood:	n/a	n/a
11	BHLHE40	chr22:30518089-30518420	GM12878	blood:	n/a	n/a
12	CBX3	chr22:30545465-30545819	HCT-116	colon:	n/a	n/a
13	CCNT2	chr22:30579872-30580232	K562	blood:	n/a	chr22:30580021-30580041
14	CEBPB	chr22:30555510-30555835	HepG2	liver:	n/a	n/a
15	CEBPB	chr22:30523720-30523980	Hela-S3	cervix:	n/a	chr22:30523804-30523815
16	CEBPB	chr22:30555549-30555804	K562	blood:	n/a	n/a
17	CEBPB	chr22:30555396-30556000	A549	lung:	n/a	n/a
18	CEBPB	chr22:30512386-30513005	IMR90	lung:	n/a	n/a
19	CEBPB	chr22:30512529-30513022	HepG2	liver:	n/a	n/a
20	CEBPB	chr22:30555493-30555865	A549	lung:	n/a	n/a
21	CEBPB	chr22:30582586-30582879	HepG2	liver:	n/a	chr22:30582630-30582641
22	CEBPB	chr22:30555444-30555936	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr22:30555486-30555950	IMR90	lung:	n/a	n/a
24	CEBPB	chr22:30523624-30524152	IMR90	lung:	n/a	chr22:30523804-30523815
25	CEBPB	chr22:30555483-30555854	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr22:30559746-30559964	HepG2	liver:	n/a	chr22:30559853-30559864
27	CEBPB	chr22:30504743-30504943	K562	blood:	n/a	n/a
28	CEBPB	chr22:30512438-30513023	A549	lung:	n/a	n/a
29	CEBPB	chr22:30523669-30523894	K562	blood:	n/a	chr22:30523804-30523815
30	CEBPB	chr22:30523671-30523861	K562	blood:	n/a	chr22:30523804-30523815
31	CEBPB	chr22:30510156-30510493	IMR90	lung:	n/a	n/a
32	CEBPB	chr22:30555587-30555846	MCF-7	breast:	n/a	n/a
33	CEBPB	chr22:30523698-30523998	HepG2	liver:	n/a	chr22:30523804-30523815
34	CEBPB	chr22:30540308-30540629	K562	blood:	n/a	n/a
35	CEBPB	chr22:30523691-30524076	A549	lung:	n/a	chr22:30523804-30523815
36	CEBPB	chr22:30582551-30582820	A549	lung:	n/a	chr22:30582630-30582641
37	CEBPB	chr22:30577752-30577952	K562	blood:	n/a	n/a
38	CEBPB	chr22:30555464-30555935	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr22:30559764-30559939	K562	blood:	n/a	chr22:30559853-30559864
40	CEBPB	chr22:30523685-30524093	A549	lung:	n/a	chr22:30523804-30523815
41	CEBPB	chr22:30541131-30541314	HepG2	liver:	n/a	n/a
42	CEBPB	chr22:30510166-30510366	A549	lung:	n/a	n/a
43	CEBPB	chr22:30523626-30523991	K562	blood:	n/a	chr22:30523804-30523815
44	CEBPB	chr22:30559792-30559967	IMR90	lung:	n/a	chr22:30559853-30559864
45	CEBPB	chr22:30521118-30521167	IMR90	lung:	n/a	n/a
46	CEBPB	chr22:30555460-30555839	A549	lung:	n/a	n/a
47	CEBPB	chr22:30512433-30512980	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr22:30575605-30575768	HepG2	liver:	n/a	n/a
49	CEBPD	chr22:30579781-30580260	K562	blood:	n/a	n/a
50	CEBPD	chr22:30579940-30580234	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30572326-30572376	LNCaP	prostate:	n/a
2	chr22:30552801-30552851	T-47D	breast:	n/a
3	chr22:30572326-30572376	U87	brain:	n/a
4	chr22:30552801-30552851	AG09319	gingival:	n/a
5	chr22:30572326-30572376	HAEpiC	amniotic membrane:	n/a
6	chr22:30552801-30552851	GM19239	blood:	n/a
7	chr22:30572326-30572376	SAEC	small airway:	n/a
8	chr22:30572326-30572376	GM06990	blood:	n/a
9	chr22:30552801-30552851	SK-N-SH_RA	brain:	n/a
10	chr22:30572326-30572376	HRE	kidney:	n/a
11	chr22:30552801-30552851	AG04450	lung:	fetal
12	chr22:30552801-30552851	AG04449	skin:	fetal
13	chr22:30572326-30572376	GM12891	blood:	n/a
14	chr22:30572326-30572376	SK-N-MC	brain:	n/a
15	chr22:30572326-30572376	GM12892	blood:	n/a
16	chr22:30552801-30552851	AoSMC	blood vessel:	n/a
17	chr22:30572326-30572376	RPTEC	kidney:	n/a
18	chr22:30552801-30552851	H1-hESC	embryonic stem cell:	embryo
19	chr22:30572326-30572376	BJ	skin:	n/a
20	chr22:30552801-30552851	U87	brain:	n/a
21	chr22:30552801-30552851	NHBE	bronchial:	n/a
22	chr22:30572326-30572376	SK-N-SH_RA	brain:	n/a
23	chr22:30572326-30572376	HEEpiC	esophagus:	n/a
24	chr22:30552801-30552851	HCF	heart:	n/a
25	chr22:30572326-30572376	Hepatocyte	liver:	n/a
26	chr22:30572326-30572376	AoSMC	blood vessel:	n/a
27	chr22:30552801-30552851	SKMC	muscle:	n/a
28	chr22:30552801-30552851	HRPEpiC	eye:	n/a
29	chr22:30572326-30572376	ProgFib	skin:	n/a
30	chr22:30572326-30572376	PrEC	prostate:	n/a
31	chr22:30552801-30552851	HepG2	liver:	n/a
32	chr22:30552801-30552851	HUVEC	blood vessel:	n/a
33	chr22:30552801-30552851	HCPEpiC	choroid plexus:	n/a
34	chr22:30572326-30572376	K562	blood:	n/a
35	chr22:30572326-30572376	HPAEpiC	pulmonary alveolar:	n/a
36	chr22:30552801-30552851	HEK293	kidney:	embryo
37	chr22:30552801-30552851	Hela-S3	cervix:	n/a
38	chr22:30552801-30552851	NHDF-neo	bronchial:	n/a
39	chr22:30572326-30572376	SK-N-SH	brain:	n/a
40	chr22:30552801-30552851	HEEpiC	esophagus:	n/a
41	chr22:30572326-30572376	NHBE	bronchial:	n/a
42	chr22:30552801-30552851	PrEC	prostate:	n/a
43	chr22:30572326-30572376	AG04450	lung:	fetal
44	chr22:30572326-30572376	HUVEC	blood vessel:	n/a
45	chr22:30572326-30572376	AG04449	skin:	fetal
46	chr22:30572326-30572376	GM12878	blood:	n/a
47	chr22:30552801-30552851	PANC-1	pancreas:	n/a
48	chr22:30552801-30552851	HNPCEpiC	eye:	n/a
49	chr22:30552801-30552851	Hepatocyte	liver:	n/a
50	chr22:30572326-30572376	PANC-1	pancreas:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:30580792..30583176-chr22:30587270..30589662,2	K562	blood:
2	chr22:30584790..30588358-chr22:30588911..30595947,7	MCF-7	breast:
3	chr22:30505986..30512409-chr22:30645938..30650817,6	MCF-7	breast:
4	chr22:30539344..30542315-chr22:30542673..30545492,2	K562	blood:
5	chr22:30504306..30505754-chr22:30651396..30652476,12	MCF-7	breast:
6	chr22:30572974..30575088-chr22:30642286..30645373,3	MCF-7	breast:
7	chr22:30502959..30506188-chr22:30648757..30654246,8	MCF-7	breast:
8	chr22:30580247..30582662-chr22:30589957..30592306,3	K562	blood:
9	chr22:30578823..30581368-chr22:30643689..30645542,2	MCF-7	breast:
10	chr22:30562125..30563712-chr22:30568524..30571379,2	MCF-7	breast:
11	chr22:30523289..30525993-chr22:30557345..30559122,2	K562	blood:
12	chr22:30552521..30555409-chr22:30604715..30606658,2	K562	blood:
13	chr22:30578196..30581092-chr22:30585737..30587811,3	MCF-7	breast:
14	chr22:30502612..30504825-chr22:30819472..30821124,2	MCF-7	breast:
15	chr22:30584790..30588358-chr22:30588911..30595947,7	MCF-7	breast:
16	chr22:30504373..30506765-chr22:30681335..30683680,2	MCF-7	breast:
17	chr22:30504280..30505360-chr22:30651538..30652426,8	K562	blood:
18	chr22:30566597..30569534-chr22:30572509..30574733,2	K562	blood:
19	chr22:30584661..30587555-chr22:30606550..30610248,3	MCF-7	breast:
20	chr22:30515123..30517427-chr22:30522395..30523982,2	MCF-7	breast:
21	chr22:30515123..30517427-chr22:30522395..30523982,2	MCF-7	breast:
22	chr22:30495376..30497069-chr22:30499975..30502698,2	MCF-7	breast:
23	chr22:30507793..30510712-chr22:30511298..30514202,2	K562	blood:
24	chr22:30502809..30506298-chr22:30639806..30643736,4	MCF-7	breast:
25	chr22:30568484..30570714-chr22:30648672..30650612,2	K562	blood:
26	chr14:62978999..62979695-chr22:30519406..30520379,2	MCF-7	breast:
27	chr22:30508949..30512192-chr22:30606244..30608279,3	MCF-7	breast:
28	chr22:30570903..30573377-chr22:30579968..30581667,2	MCF-7	breast:
29	chr22:30583372..30585537-chr22:30587327..30589279,2	K562	blood:
30	chr22:30514761..30517245-chr22:30642693..30646544,3	MCF-7	breast:
31	chr22:30580247..30582662-chr22:30589957..30592306,3	K562	blood:
32	chr22:30510247..30512648-chr22:30515643..30517309,2	K562	blood:
33	chr22:30539344..30542315-chr22:30542673..30545492,2	K562	blood:
34	chr22:30510772..30513351-chr22:30653868..30656059,2	MCF-7	breast:
35	chr22:30504126..30504835-chr22:30682136..30683020,2	K562	blood:
36	chr22:30584542..30586960-chr22:30641320..30643701,2	MCF-7	breast:
37	chr22:30494721..30496539-chr22:30641768..30644444,2	MCF-7	breast:
38	chr22:30523289..30525993-chr22:30557345..30559122,2	K562	blood:
39	chr22:30503068..30507568-chr22:30652252..30654579,5	MCF-7	breast:
40	chr22:30583139..30584831-chr22:30588932..30591308,2	K562	blood:
41	chr22:30582053..30584653-chr22:30584995..30587052,2	MCF-7	breast:
42	chr22:30578652..30582637-chr22:30590732..30593754,4	K562	blood:
43	chr22:30587225..30588741-chr22:30589978..30592265,2	K562	blood:
44	chr22:30506495..30508207-chr22:30648737..30651492,2	MCF-7	breast:
45	chr22:30500122..30506829-chr22:30640771..30648697,14	MCF-7	breast:
46	chr22:30589990..30596479-chr22:30639909..30648381,15	MCF-7	breast:
47	chr22:30588262..30589901-chr22:30592924..30594635,2	MCF-7	breast:
48	chr22:30574627..30577107-chr22:30609828..30612772,2	MCF-7	breast:
49	chr22:30562803..30564528-chr22:30605474..30607789,2	MCF-7	breast:
50	chr22:30587225..30588741-chr22:30589978..30592265,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC157-4	chr22:30500390-30500566	NONHSAT084757
2	lnc-CCDC157-4	chr22:30499426-30499489	NONHSAT084757
3	lnc-LIF-1	chr22:30588122-30588219	ENSG00000225676.1
4	lnc-ASCC2-1	chr22:30498120-30498134	ENSG00000249836
5	lnc-CCDC157-4	chr22:30494841-30494982	NONHSAT084757
6	lnc-LIF-1	chr22:30580633-30580770	ENSG00000225676.1
7	lnc-LIF-3	chr22:30501083-30501397	NONHSAT084758

No data

Variant related genes	Relation type
ENSG00000226573	TF binding region
ENSG00000225971	TF binding region
ENSG00000226573	CpG island
ENSG00000225971	CpG island
ENSG00000239282	chromatin interactions
ENSG00000128342	chromatin interactions
ENSG00000226573	chromatin interactions
ENSG00000225676	chromatin interactions
ENSG00000268812	chromatin interactions
MNX1	miRNA target sites

Extended variants
information (count: 2752 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2752 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2412971	chr22:30494371-30494372	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs531992731	chr22:30494395-30494396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181255836	chr22:30494405-30494406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371987116	chr22:30494418-30494419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5997570	chr22:30494473-30494474	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs528016925	chr22:30494492-30494493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111712915	chr22:30494495-30494496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141597584	chr22:30494533-30494534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531912978	chr22:30494547-30494548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183492380	chr22:30494564-30494565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571728840	chr22:30494620-30494621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539123206	chr22:30494637-30494638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9614143	chr22:30494642-30494643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs141834419	chr22:30494656-30494657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369133019	chr22:30494703-30494704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554541314	chr22:30494740-30494741	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs35941976	chr22:30494785-30494786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs202004062	chr22:30494827-30494828	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549841049	chr22:30494831-30494832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376899418	chr22:30494841-30494842	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs371346180	chr22:30494842-30494843	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs34305723	chr22:30494847-30494848	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs367816409	chr22:30494868-30494869	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs370632699	chr22:30494883-30494884	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs373835705	chr22:30494907-30494908	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs188160152	chr22:30494910-30494911	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs145681756	chr22:30494958-30494959	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs12157501	chr22:30495015-30495016	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375287933	chr22:30495031-30495032	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372766311	chr22:30495055-30495056	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182376975	chr22:30495080-30495081	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187376156	chr22:30495183-30495184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574316350	chr22:30495184-30495185	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs543326404	chr22:30495197-30495198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561376174	chr22:30495213-30495214	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546067605	chr22:30495218-30495219	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs117568053	chr22:30495250-30495251	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550434473	chr22:30495251-30495252	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565472263	chr22:30495278-30495279	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191763954	chr22:30495331-30495332	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs6006352	chr22:30495374-30495375	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112455038	chr22:30495375-30495376	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs566088723	chr22:30495453-30495454	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs200206440	chr22:30495463-30495464	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs373453053	chr22:30495600-30495601	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs536207035	chr22:30495642-30495643	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs548475030	chr22:30495669-30495670	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs181841900	chr22:30495673-30495674	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs376063489	chr22:30495683-30495684	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs536947176	chr22:30495694-30495695	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Melanoma	17363583	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD

Chromatin state (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30493200-30500200	Enhancers	Dnd41	blood
2	chr22:30493800-30494400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr22:30494200-30496400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr22:30494400-30497400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr22:30495200-30498000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr22:30495600-30496000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr22:30495800-30496600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr22:30495800-30496600	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr22:30495800-30496600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr22:30496000-30496400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr22:30496400-30496600	Enhancers	Primary T cells fromperipheralblood	blood
12	chr22:30496400-30496600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr22:30496400-30496600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr22:30496400-30496800	Enhancers	Fetal Thymus	thymus
15	chr22:30496400-30497000	Enhancers	Primary T cells from cord blood	blood
16	chr22:30496400-30497600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr22:30496400-30498000	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr22:30496400-30498200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr22:30496600-30497200	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr22:30496600-30497400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr22:30496600-30497400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr22:30496600-30497400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr22:30496600-30500200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr22:30496600-30500600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr22:30496800-30497200	Weak transcription	Fetal Thymus	thymus
26	chr22:30497000-30500000	Weak transcription	Primary T cells from cord blood	blood
27	chr22:30497200-30497400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr22:30497200-30498000	Enhancers	Primary T cells fromperipheralblood	blood
29	chr22:30497200-30498000	Enhancers	Thymus	Thymus
30	chr22:30497200-30498200	Enhancers	Fetal Thymus	thymus
31	chr22:30497400-30498000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr22:30497400-30498000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr22:30497400-30498000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr22:30497400-30498000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr22:30497400-30498200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr22:30497400-30500200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr22:30497600-30499800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr22:30497800-30498600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr22:30498000-30499400	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr22:30498000-30499400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr22:30498000-30499800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr22:30498000-30499800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr22:30498000-30499800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr22:30498000-30500000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr22:30498000-30501000	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr22:30498000-30501000	Weak transcription	Thymus	Thymus
47	chr22:30498200-30499800	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr22:30498200-30499800	Weak transcription	Fetal Thymus	thymus
49	chr22:30498200-30500200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr22:30498600-30499000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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