Variant report

Variant	esv1809952
Chromosome Location	chr22:29595349-29661434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1996)
CpG islands
(count:977)
Chromatin interactive
region (count:77)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29641599-29641849	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:29642230-29642427	HepG2	liver:	n/a	n/a
3	ATF2	chr22:29598302-29599397	GM12878	blood:	n/a	n/a
4	ATF2	chr22:29655589-29655896	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr22:29598245-29599384	GM12878	blood:	n/a	n/a
6	BACH1	chr22:29602255-29602337	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr22:29598729-29599005	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr22:29598215-29598576	GM12878	blood:	n/a	n/a
9	BATF	chr22:29598610-29599251	GM12878	blood:	n/a	n/a
10	BATF	chr22:29611792-29612062	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:29604981-29605256	GM12878	blood:	n/a	chr22:29605192-29605205
12	BCL11A	chr22:29598759-29599229	GM12878	blood:	n/a	chr22:29599010-29599023
13	BCL11A	chr22:29598685-29599342	GM12878	blood:	n/a	chr22:29599010-29599023
14	BCL3	chr22:29607384-29607821	GM12878	blood:	n/a	n/a
15	BCL3	chr22:29627387-29627732	GM12878	blood:	n/a	n/a
16	BCL3	chr22:29656671-29656925	GM12878	blood:	n/a	n/a
17	BCL3	chr22:29607350-29607787	GM12878	blood:	n/a	n/a
18	BCL3	chr22:29598254-29599363	GM12878	blood:	n/a	chr22:29599010-29599023
19	BCL3	chr22:29627837-29628113	GM12878	blood:	n/a	n/a
20	BCL3	chr22:29656070-29656302	GM12878	blood:	n/a	n/a
21	BCL3	chr22:29628218-29628633	GM12878	blood:	n/a	n/a
22	BCL3	chr22:29598723-29599254	GM12878	blood:	n/a	chr22:29599010-29599023
23	BCL3	chr22:29655745-29655985	GM12878	blood:	n/a	n/a
24	BCLAF1	chr22:29598192-29599296	GM12878	blood:	n/a	chr22:29599010-29599023
25	BCLAF1	chr22:29598254-29599470	GM12878	blood:	n/a	chr22:29599010-29599023
26	BHLHE40	chr22:29616972-29617209	K562	blood:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
27	BHLHE40	chr22:29598272-29599266	GM12878	blood:	n/a	n/a
28	BHLHE40	chr22:29600224-29600481	GM12878	blood:	n/a	n/a
29	BHLHE40	chr22:29617036-29617131	HepG2	liver:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
30	BHLHE40	chr22:29621739-29621873	K562	blood:	n/a	chr22:29621804-29621820
31	BHLHE40	chr22:29641602-29641804	K562	blood:	n/a	n/a
32	BHLHE40	chr22:29601418-29601614	K562	blood:	n/a	n/a
33	BHLHE40	chr22:29602067-29602341	K562	blood:	n/a	n/a
34	BHLHE40	chr22:29601604-29602148	GM12878	blood:	n/a	chr22:29601941-29601957 chr22:29601938-29601954
35	BHLHE40	chr22:29641541-29641844	GM12878	blood:	n/a	n/a
36	BHLHE40	chr22:29597979-29598898	K562	blood:	n/a	n/a
37	BHLHE40	chr22:29616987-29617222	GM12878	blood:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
38	BHLHE40	chr22:29654529-29654532	K562	blood:	n/a	n/a
39	BRCA1	chr22:29598487-29599112	GM12878	blood:	n/a	n/a
40	CBX3	chr22:29601251-29601604	K562	blood:	n/a	n/a
41	CCNT2	chr22:29654324-29654461	K562	blood:	n/a	n/a
42	CCNT2	chr22:29598114-29598585	K562	blood:	n/a	n/a
43	CCNT2	chr22:29601582-29602429	K562	blood:	n/a	chr22:29601689-29601698 chr22:29601818-29601827
44	CCNT2	chr22:29656659-29656837	K562	blood:	n/a	n/a
45	CCNT2	chr22:29598854-29599111	K562	blood:	n/a	n/a
46	CEBPB	chr22:29613270-29613658	IMR90	lung:	n/a	chr22:29613465-29613476
47	CEBPB	chr22:29613294-29613677	HepG2	liver:	n/a	chr22:29613465-29613476
48	CEBPB	chr22:29613333-29613598	A549	lung:	n/a	chr22:29613465-29613476
49	CEBPB	chr22:29613260-29613670	HepG2	liver:	n/a	chr22:29613465-29613476
50	CEBPB	chr22:29598894-29599202	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29601862-29601912	HPAEpiC	pulmonary alveolar:	n/a
2	chr22:29601862-29601912	HPAEpiC	pulmonary alveolar:	n/a
3	chr22:29601862-29601912	AoSMC	blood vessel:	n/a
4	chr22:29601559-29601609	NH-A	brain:	n/a
5	chr22:29601862-29601912	T-47D	breast:	n/a
6	chr22:29601559-29601609	SKMC	muscle:	n/a
7	chr22:29602183-29602233	T-47D	breast:	n/a
8	chr22:29601559-29601609	HL-60	blood:	n/a
9	chr22:29602183-29602233	HCT-116	colon:	n/a
10	chr22:29601763-29601813	MCF-7	breast:	n/a
11	chr22:29601619-29601669	U87	brain:	n/a
12	chr22:29605147-29605197	Hela-S3	cervix:	n/a
13	chr22:29602183-29602233	BJ	skin:	n/a
14	chr22:29602004-29602054	GM19239	blood:	n/a
15	chr22:29598916-29598966	PFSK-1	brain:	n/a
16	chr22:29601772-29601822	IMR90	lung:	fetal
17	chr22:29601619-29601669	NHBE	bronchial:	n/a
18	chr22:29603194-29603244	SKMC	muscle:	n/a
19	chr22:29655981-29656031	HCPEpiC	choroid plexus:	n/a
20	chr22:29600657-29600707	GM12878	blood:	n/a
21	chr22:29605147-29605197	PrEC	prostate:	n/a
22	chr22:29602004-29602054	HL-60	blood:	n/a
23	chr22:29601559-29601609	HRCEpiC	kidney:	n/a
24	chr22:29603194-29603244	T-47D	breast:	n/a
25	chr22:29603194-29603244	HIPEpiC	eye:	n/a
26	chr22:29603194-29603244	H1-hESC	embryonic stem cell:	embryo
27	chr22:29598916-29598966	SKMC	muscle:	n/a
28	chr22:29602183-29602233	AoSMC	blood vessel:	n/a
29	chr22:29601559-29601609	LNCaP	prostate:	n/a
30	chr22:29602183-29602233	HUVEC	blood vessel:	n/a
31	chr22:29598916-29598966	GM12892	blood:	n/a
32	chr22:29603194-29603244	PANC-1	pancreas:	n/a
33	chr22:29600139-29600189	GM06990	blood:	n/a
34	chr22:29598916-29598966	AG09309	skin:	n/a
35	chr22:29655981-29656031	ovcar-3	ovarian:	n/a
36	chr22:29600657-29600707	SAEC	small airway:	n/a
37	chr22:29603194-29603244	SK-N-MC	brain:	n/a
38	chr22:29601860-29601910	HCM	heart:	n/a
39	chr22:29600657-29600707	Hepatocyte	liver:	n/a
40	chr22:29598916-29598966	AG09319	gingival:	n/a
41	chr22:29601860-29601910	HEEpiC	esophagus:	n/a
42	chr22:29601862-29601912	ovcar-3	ovarian:	n/a
43	chr22:29600139-29600189	Jurkat	blood:	n/a
44	chr22:29602183-29602233	AG09309	skin:	n/a
45	chr22:29660173-29660223	CMK	blood:	n/a
46	chr22:29602004-29602054	HEK293	kidney:	embryo
47	chr22:29601860-29601910	AG10803	skin:	n/a
48	chr22:29600139-29600189	NB4	blood:	n/a
49	chr22:29601559-29601609	T-47D	breast:	n/a
50	chr22:29603194-29603244	MCF-7	breast:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:29598263..29599277-chr22:29640793..29642655,17	MCF-7	breast:
2	chr22:29618425..29620618-chr22:29628418..29631413,2	K562	blood:
3	chr22:29601873..29603950-chr22:29609240..29612185,2	MCF-7	breast:
4	chr22:29612019..29613931-chr22:29615202..29617842,2	MCF-7	breast:
5	chr22:29619234..29621532-chr22:29627625..29630372,2	MCF-7	breast:
6	chr22:29289372..29291896-chr22:29597783..29600686,2	MCF-7	breast:
7	chr22:29598698..29599406-chr22:29641204..29641781,2	K562	blood:
8	chr22:29616773..29618442-chr22:29619234..29622066,2	MCF-7	breast:
9	chr22:29552265..29553268-chr22:29641211..29642160,5	MCF-7	breast:
10	chr22:29609413..29611410-chr22:29651943..29654586,2	MCF-7	breast:
11	chr22:29622067..29623775-chr22:29624148..29626498,2	K562	blood:
12	chr22:29598605..29599258-chr22:29640938..29642145,5	MCF-7	breast:
13	chr22:29617283..29619466-chr22:29651521..29653548,2	K562	blood:
14	chr22:29612167..29614111-chr22:29627917..29629464,2	K562	blood:
15	chr22:29598167..29600634-chr22:29663372..29666044,2	K562	blood:
16	chr22:29602636..29604550-chr22:29611942..29613555,2	K562	blood:
17	chr22:29640909..29643283-chr22:29659870..29662528,2	K562	blood:
18	chr22:29621556..29624508-chr22:29627726..29630197,3	K562	blood:
19	chr22:29601210..29603979-chr22:29627327..29629637,2	K562	blood:
20	chr22:29598605..29599258-chr22:29640938..29642145,5	MCF-7	breast:
21	chr22:29619482..29621531-chr22:29625031..29626896,2	K562	blood:
22	chr22:29601873..29603950-chr22:29609240..29612185,2	MCF-7	breast:
23	chr22:29612019..29613931-chr22:29615202..29617842,2	MCF-7	breast:
24	chr22:29600704..29601509-chr22:29641190..29641939,2	MCF-7	breast:
25	chr22:29646882..29648653-chr22:29651065..29652774,3	K562	blood:
26	chr13:60970151..60970804-chr22:29601495..29602051,2	HCT-116	colon:
27	chr22:29648630..29652956-chr22:29654339..29658530,6	K562	blood:
28	chr22:29605515..29607665-chr22:29648338..29651149,2	K562	blood:
29	chr22:29602636..29604550-chr22:29611942..29613555,2	K562	blood:
30	chr22:29654217..29657445-chr22:29658284..29661902,3	MCF-7	breast:
31	chr22:29640165..29643423-chr22:29644673..29648917,5	K562	blood:
32	chr22:29251341..29252226-chr22:29641199..29642209,3	K562	blood:
33	chr22:29599772..29601516-chr22:29662820..29665325,2	K562	blood:
34	chr22:29616331..29618039-chr22:29656036..29658500,2	MCF-7	breast:
35	chr22:29436679..29437351-chr22:29641273..29642121,2	K562	blood:
36	chr22:29549443..29550329-chr22:29641671..29642180,2	MCF-7	breast:
37	chr22:29550189..29551060-chr22:29641253..29641991,3	MCF-7	breast:
38	chr22:29601902..29603639-chr22:29605724..29608269,2	K562	blood:
39	chr22:29598263..29599277-chr22:29640793..29642655,17	MCF-7	breast:
40	chr10:95619300..95619800-chr22:29657270..29657935,2	NB4	blood:
41	chr22:29601808..29604222-chr22:29612669..29614934,2	MCF-7	breast:
42	chr22:29609378..29611506-chr22:29620734..29622343,2	MCF-7	breast:
43	chr22:29601210..29603979-chr22:29627327..29629637,2	K562	blood:
44	chr22:29622067..29623775-chr22:29624148..29626498,2	K562	blood:
45	chr22:29473166..29474828-chr22:29640994..29643456,2	K562	blood:
46	chr22:29600453..29603035-chr22:29615819..29618230,2	K562	blood:
47	chr22:29617687..29619581-chr22:29621568..29623250,2	K562	blood:
48	chr22:29616106..29618160-chr22:29628448..29630302,2	K562	blood:
49	chr22:29609378..29611506-chr22:29620734..29622343,2	MCF-7	breast:
50	chr22:29600704..29601509-chr22:29641190..29641939,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASL10A-3	chr22:29656488-29656602	NONHSAT084684
2	lnc-RHBDD3-1	chr22:29637344-29637418	l_2269_chr22:29637343-29652496_76bGuttman_hLF
3	lnc-RHBDD3-1	chr22:29652357-29652496	l_2269_chr22:29637343-29652496_76bGuttman_hLF
4	lnc-EMID1-1	chr22:29656878-29657068	ENSG00000237015.1
5	lnc-RHBDD3-1	chr22:29651128-29652355	l_2269_chr22:29637343-29652496_76bGuttman_hLF
6	lnc-RASL10A-3	chr22:29659824-29660390	NONHSAT084684
7	lnc-EWSR1-4	chr22:29627671-29629457	NONHSAT084681
8	lnc-EMID1-1	chr22:29657833-29658026	ENSG00000237015.1
9	lnc-EWSR1-4	chr22:29629603-29629851	NONHSAT084681
10	lnc-EWSR1-3	chr22:29620225-29620479	expReg_chr22_2008_+
11	lnc-RASL10A-3	chr22:29656691-29656857	NONHSAT084684

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EMID1	hsa-miR-125a-5p	chr22:29655034-29655040
2	EMID1	hsa-miR-125a-5p	chr22:29655017-29655041

Variant related genes	Relation type
EWSR1	TF binding region
ENSG00000237015	TF binding region
EMID1	TF binding region
RHBDD3	TF binding region
EWSR1	CpG island
ENSG00000237015	CpG island
EMID1	CpG island
RHBDD3	CpG island
ENSG00000083544	chromatin interactions
ENSG00000186998	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000237015	chromatin interactions
ENSG00000185340	chromatin interactions

Extended variants
information (count: 2736 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2736 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375012492	chr22:29595358-29595359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368356865	chr22:29595376-29595377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs132354	chr22:29595436-29595437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs5997453	chr22:29595442-29595443	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529440229	chr22:29595478-29595479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373146900	chr22:29595495-29595496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550894257	chr22:29595496-29595497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183058136	chr22:29595497-29595498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539841326	chr22:29595517-29595518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186928621	chr22:29595544-29595545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578134734	chr22:29595548-29595549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566965093	chr22:29595563-29595564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs5763044	chr22:29595570-29595571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555893869	chr22:29595590-29595591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191562810	chr22:29595642-29595643	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538016638	chr22:29595672-29595673	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543609076	chr22:29595676-29595677	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577827398	chr22:29595689-29595690	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143359111	chr22:29595720-29595721	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145547184	chr22:29595828-29595829	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574379019	chr22:29595852-29595853	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73399034	chr22:29595863-29595864	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs60239599	chr22:29595874-29595875	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560632220	chr22:29595893-29595894	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs132355	chr22:29595911-29595912	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550865116	chr22:29595947-29595948	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371533249	chr22:29596016-29596017	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150933004	chr22:29596024-29596025	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1012458	chr22:29596033-29596034	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551754302	chr22:29596034-29596035	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550895671	chr22:29596120-29596121	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564788910	chr22:29596145-29596146	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534174490	chr22:29596154-29596155	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369752997	chr22:29596158-29596159	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141948861	chr22:29596190-29596191	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567734492	chr22:29596212-29596213	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530737593	chr22:29596233-29596234	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538055246	chr22:29596253-29596254	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556045717	chr22:29596266-29596267	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187967231	chr22:29596312-29596313	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538605199	chr22:29596387-29596388	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146917760	chr22:29596405-29596406	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554027278	chr22:29596413-29596414	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12628053	chr22:29596440-29596441	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376820276	chr22:29596450-29596451	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58306818	chr22:29596488-29596489	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs386820569	chr22:29596502-29596503	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12627935	chr22:29596503-29596504	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs562892823	chr22:29596514-29596515	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139329050	chr22:29596558-29596559	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD

Chromatin state (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29581600-29598400	Weak transcription	Fetal Brain Female	brain
2	chr22:29588000-29598200	Weak transcription	Fetal Brain Male	brain
3	chr22:29589600-29597800	Weak transcription	Fetal Intestine Large	intestine
4	chr22:29591600-29595800	Weak transcription	Fetal Intestine Small	intestine
5	chr22:29592000-29597800	Weak transcription	Fetal Lung	lung
6	chr22:29592200-29595600	Weak transcription	Dnd41	blood
7	chr22:29592200-29596400	Weak transcription	Spleen	Spleen
8	chr22:29592200-29597000	Weak transcription	Fetal Thymus	thymus
9	chr22:29592200-29598000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr22:29592400-29597000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr22:29592400-29598000	Weak transcription	Left Ventricle	heart
12	chr22:29592400-29598200	Weak transcription	Lung	lung
13	chr22:29592600-29595600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr22:29592600-29597600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr22:29592800-29595600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr22:29593200-29595800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr22:29593400-29597800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr22:29593600-29597200	Weak transcription	K562	blood
19	chr22:29594000-29598000	Weak transcription	Small Intestine	intestine
20	chr22:29594800-29600800	Weak transcription	Pancreas	Pancrea
21	chr22:29595400-29597600	Enhancers	GM12878-XiMat	blood
22	chr22:29595600-29596200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr22:29595600-29597200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr22:29595600-29597600	Genic enhancers	Dnd41	blood
25	chr22:29595800-29596600	Strong transcription	Fetal Intestine Small	intestine
26	chr22:29595800-29597200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr22:29596200-29597200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr22:29596400-29601600	Enhancers	Spleen	Spleen
29	chr22:29596600-29597200	Weak transcription	Fetal Intestine Small	intestine
30	chr22:29597000-29598800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr22:29597000-29601000	Enhancers	Primary hematopoietic stem cells	blood
32	chr22:29597000-29601400	Enhancers	Fetal Thymus	thymus
33	chr22:29597200-29597400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr22:29597200-29598000	Enhancers	K562	blood
35	chr22:29597200-29598800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr22:29597200-29599200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr22:29597200-29599600	Enhancers	Fetal Intestine Small	intestine
38	chr22:29597400-29597800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr22:29597400-29597800	Bivalent Enhancer	HepG2	liver
40	chr22:29597600-29597800	Enhancers	Fetal Kidney	kidney
41	chr22:29597600-29597800	Enhancers	Dnd41	blood
42	chr22:29597600-29598000	Flanking Active TSS	GM12878-XiMat	blood
43	chr22:29597600-29598400	Enhancers	Duodenum Mucosa	Duodenum
44	chr22:29597600-29598600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr22:29597600-29599200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr22:29597600-29599200	Enhancers	Fetal Stomach	stomach
47	chr22:29597600-29599400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr22:29597600-29599400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr22:29597600-29599400	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr22:29597800-29598000	Bivalent Enhancer	Placenta	Placenta

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