Variant report

Variant	esv1831149
Chromosome Location	chr1:155233501-155252122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1444)
CpG islands
(count:2321)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1444 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155248228-155248377	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:155242526-155242891	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:155246963-155247163	K562	blood:	n/a	chr1:155247001-155247009
4	ATF2	chr1:155248006-155248430	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:155243128-155243632	GM12878	blood:	n/a	n/a
6	ATF3	chr1:155243255-155243500	K562	blood:	n/a	n/a
7	ATF3	chr1:155242887-155243147	K562	blood:	n/a	chr1:155242939-155242948
8	BACH1	chr1:155248247-155248681	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr1:155242569-155243628	GM12878	blood:	n/a	chr1:155242936-155242949 chr1:155243259-155243268 chr1:155243265-155243274 chr1:155243262-155243275 chr1:155243334-155243343 chr1:155243262-155243271 chr1:155243263-155243276
10	BHLHE40	chr1:155247027-155247464	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:155242918-155243541	HepG2	liver:	n/a	chr1:155243262-155243278 chr1:155243207-155243223
12	BHLHE40	chr1:155242737-155243763	K562	blood:	n/a	chr1:155243262-155243278 chr1:155243207-155243223
13	BHLHE40	chr1:155246846-155247175	K562	blood:	n/a	n/a
14	BHLHE40	chr1:155248153-155248447	K562	blood:	n/a	n/a
15	BHLHE40	chr1:155242894-155243562	GM12878	blood:	n/a	chr1:155243262-155243278 chr1:155243207-155243223
16	BRCA1	chr1:155243217-155243527	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:155246928-155247180	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr1:155242480-155242625	GM12878	blood:	n/a	n/a
19	CBX3	chr1:155247942-155248454	K562	blood:	n/a	n/a
20	CBX3	chr1:155246748-155247730	K562	blood:	n/a	n/a
21	CBX3	chr1:155243121-155243851	K562	blood:	n/a	n/a
22	CCNT2	chr1:155242956-155243530	K562	blood:	n/a	chr1:155243173-155243182
23	CCNT2	chr1:155246983-155247444	K562	blood:	n/a	n/a
24	CEBPB	chr1:155245771-155245971	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:155243663-155243895	K562	blood:	n/a	n/a
26	CEBPB	chr1:155246999-155247401	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:155244695-155244882	K562	blood:	n/a	n/a
28	CEBPD	chr1:155247078-155247391	HepG2	liver:	n/a	n/a
29	CEBPD	chr1:155242957-155243549	HepG2	liver:	n/a	n/a
30	CHD2	chr1:155248082-155248498	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr1:155242712-155243083	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr1:155242910-155242912	HepG2	liver:	n/a	n/a
33	CHD2	chr1:155242915-155243544	Hela-S3	cervix:	n/a	chr1:155243431-155243441
34	CHD2	chr1:155248093-155248501	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr1:155243327-155243578	H1-hESC	embryonic stem cell:	n/a	chr1:155243431-155243441
36	CHD2	chr1:155248299-155248491	K562	blood:	n/a	n/a
37	CHD2	chr1:155242943-155243686	GM12878	blood:	n/a	chr1:155243431-155243441
38	CHD2	chr1:155246902-155247231	GM12878	blood:	n/a	n/a
39	CHD2	chr1:155248178-155248378	HepG2	liver:	n/a	n/a
40	CHD2	chr1:155248172-155248483	GM12878	blood:	n/a	n/a
41	CHD2	chr1:155246899-155247350	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr1:155243335-155243422	HepG2	liver:	n/a	n/a
43	CHD2	chr1:155243315-155243572	K562	blood:	n/a	chr1:155243431-155243441
44	CREB1	chr1:155242633-155243572	A549	lung:	n/a	n/a
45	CREB1	chr1:155246925-155247414	A549	lung:	n/a	n/a
46	CREB1	chr1:155242914-155243539	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr1:155242615-155243920	HepG2	liver:	n/a	n/a
48	CREB1	chr1:155242683-155243832	K562	blood:	n/a	n/a
49	CREB1	chr1:155242690-155243670	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr1:155242627-155243735	GM12878	blood:	n/a	n/a

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155243076-155243126	Jurkat	blood:	n/a
2	chr1:155247196-155247246	HepG2	liver:	n/a
3	chr1:155248588-155248638	GM12892	blood:	n/a
4	chr1:155243076-155243126	Jurkat	blood:	n/a
5	chr1:155247196-155247246	HepG2	liver:	n/a
6	chr1:155248588-155248638	GM12892	blood:	n/a
7	chr1:155243310-155243360	SAEC	small airway:	n/a
8	chr1:155243310-155243360	HMEC	breast:	n/a
9	chr1:155243476-155243526	NH-A	brain:	n/a
10	chr1:155243486-155243536	Jurkat	blood:	n/a
11	chr1:155239493-155239543	AG09319	gingival:	n/a
12	chr1:155247785-155247835	MCF-7	breast:	n/a
13	chr1:155243295-155243345	PrEC	prostate:	n/a
14	chr1:155239421-155239471	HepG2	liver:	n/a
15	chr1:155240608-155240658	NB4	blood:	n/a
16	chr1:155250207-155250257	Hela-S3	cervix:	n/a
17	chr1:155247548-155247598	GM12892	blood:	n/a
18	chr1:155247361-155247411	HCT-116	colon:	n/a
19	chr1:155236380-155236430	GM12892	blood:	n/a
20	chr1:155243476-155243526	HUVEC	blood vessel:	n/a
21	chr1:155247476-155247526	IMR90	lung:	fetal
22	chr1:155243295-155243345	Jurkat	blood:	n/a
23	chr1:155234528-155234578	ECC-1	luminal epithelium:	n/a
24	chr1:155243310-155243360	T-47D	breast:	n/a
25	chr1:155243300-155243350	HUVEC	blood vessel:	n/a
26	chr1:155236380-155236430	NB4	blood:	n/a
27	chr1:155243435-155243485	H1-hESC	embryonic stem cell:	embryo
28	chr1:155246828-155246878	ProgFib	skin:	n/a
29	chr1:155247476-155247526	HepG2	liver:	n/a
30	chr1:155247357-155247407	HUVEC	blood vessel:	n/a
31	chr1:155247476-155247526	SK-N-SH	brain:	n/a
32	chr1:155247610-155247660	NT2-D1	testis:	n/a
33	chr1:155247785-155247835	SKMC	muscle:	n/a
34	chr1:155247785-155247835	HCT-116	colon:	n/a
35	chr1:155240680-155240730	HL-60	blood:	n/a
36	chr1:155247785-155247835	HCPEpiC	choroid plexus:	n/a
37	chr1:155246593-155246643	H1-hESC	embryonic stem cell:	embryo
38	chr1:155243354-155243404	HCT-116	colon:	n/a
39	chr1:155242321-155242371	HCF	heart:	n/a
40	chr1:155246593-155246643	HRCEpiC	kidney:	n/a
41	chr1:155239301-155239351	CMK	blood:	n/a
42	chr1:155247610-155247660	PFSK-1	brain:	n/a
43	chr1:155243476-155243526	BE2_C	brain:	n/a
44	chr1:155243354-155243404	AG04450	lung:	fetal
45	chr1:155247117-155247167	NB4	blood:	n/a
46	chr1:155250207-155250257	SAEC	small airway:	n/a
47	chr1:155238752-155238802	MCF-7	breast:	n/a
48	chr1:155242826-155242876	HL-60	blood:	n/a
49	chr1:155243300-155243350	HL-60	blood:	n/a
50	chr1:155239493-155239543	GM12891	blood:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:155236269..155241954-chr1:155291931..155295779,5	K562	blood:
2	chr1:155232261..155234786-chr1:155281674..155283762,2	K562	blood:
3	chr1:155175880..155178580-chr1:155245010..155247529,2	K562	blood:
4	chr1:155174569..155177437-chr1:155233735..155235626,3	K562	blood:
5	chr1:155055823..155058786-chr1:155242892..155244549,2	MCF-7	breast:
6	chr1:155232307..155234764-chr1:155294401..155296535,2	K562	blood:
7	chr1:155242761..155243283-chr15:65596719..65597701,2	Hela-S3	cervix:
8	chr1:155214449..155216184-chr1:155237561..155239532,2	MCF-7	breast:
9	chr1:155234973..155237775-chr1:155290971..155293651,2	MCF-7	breast:
10	chr1:155238212..155240823-chr1:155276858..155278738,2	K562	blood:
11	chr1:155242795..155243310-chr12:7053421..7053934,2	Hela-S3	cervix:
12	chr1:155231157..155233872-chr1:155289047..155290722,2	K562	blood:
13	chr1:155230732..155234142-chr1:155291994..155295451,6	MCF-7	breast:
14	chr1:155245096..155252304-chr1:155290044..155297941,20	MCF-7	breast:
15	chr1:155241469..155243385-chr1:155277012..155279531,3	MCF-7	breast:
16	chr1:155213177..155216583-chr1:155242889..155246560,4	K562	blood:
17	chr1:155242783..155243451-chr6:26021212..26022099,2	Hela-S3	cervix:
18	chr1:155194530..155197215-chr1:155242223..155244850,3	K562	blood:
19	chr1:155246042..155249168-chr1:155274467..155279979,9	MCF-7	breast:
20	chr1:155239314..155245036-chr1:155288379..155297041,21	MCF-7	breast:
21	chr1:155246581..155249773-chr1:155532192..155535114,5	MCF-7	breast:
22	chr1:155229082..155234937-chr1:155291248..155296864,8	K562	blood:
23	chr1:155245586..155250751-chr1:155275814..155280484,11	K562	blood:
24	chr1:155211690..155216212-chr1:155231766..155235735,5	MCF-7	breast:
25	chr1:155242207..155244752-chr1:155251974..155255810,3	MCF-7	breast:
26	chr1:155240682..155244991-chr1:155289682..155296120,12	MCF-7	breast:
27	chr1:155193962..155197318-chr1:155243350..155246355,3	K562	blood:
28	chr1:155239466..155241223-chr1:155241628..155244752,3	MCF-7	breast:
29	chr1:155246252..155247659-chr1:155292568..155294638,9	K562	blood:
30	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
31	chr1:155245586..155248343-chr1:155278550..155280734,4	K562	blood:
32	chr1:155245319..155249606-chr1:155290397..155296026,10	K562	blood:
33	chr1:155242859..155243580-chr5:77589831..77590542,2	Hela-S3	cervix:
34	chr1:155241815..155243331-chr1:155532425..155534000,2	K562	blood:
35	chr1:155242211..155244809-chr1:155291827..155295187,4	K562	blood:
36	chr1:155247579..155249594-chr1:155291407..155294403,2	K562	blood:
37	chr1:155241810..155244486-chr1:155276710..155279928,5	K562	blood:
38	chr1:155237070..155244636-chr1:155291827..155295779,11	K562	blood:
39	chr1:155235972..155238803-chr1:155277477..155279791,2	MCF-7	breast:
40	chr1:155212931..155218657-chr1:155240962..155244485,5	MCF-7	breast:
41	chr1:155242577..155243301-chr7:27224203..27225069,2	Hela-S3	cervix:
42	chr1:155230699..155233655-chr6:27804645..27806252,2	MCF-7	breast:
43	chr1:155165434..155167473-chr1:155242958..155244687,2	MCF-7	breast:
44	chr1:155242307..155246012-chr1:155257653..155260333,3	MCF-7	breast:
45	chr1:155177501..155180439-chr1:155241902..155244852,3	MCF-7	breast:
46	chr1:155228693..155233633-chr1:155276892..155283389,6	K562	blood:
47	chr1:155176808..155180528-chr1:155231411..155234045,4	K562	blood:
48	chr1:155209377..155211075-chr1:155231660..155233982,2	MCF-7	breast:
49	chr1:155251831..155255812-chr1:155268570..155273078,4	K562	blood:
50	chr1:155231407..155233869-chr1:155287247..155288770,2	MCF-7	breast:

No data

Variant related genes	Relation type
SCAMP3	TF binding region
CLK2	TF binding region
HCN3	TF binding region
SCAMP3	CpG island
CLK2	CpG island
HCN3	CpG island
ENSG00000200156	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000005073	chromatin interactions
ENSG00000240990	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000132842	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000143627	chromatin interactions

Extended variants
information (count: 658 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368132695	chr1:155233553-155233554	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs2990239	chr1:155233570-155233571	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs114539447	chr1:155233630-155233631	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs181385977	chr1:155233661-155233662	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs370713416	chr1:155233708-155233709	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs375098802	chr1:155233709-155233710	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs377448536	chr1:155233727-155233728	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs370320319	chr1:155233747-155233748	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs138254335	chr1:155233763-155233764	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs374761483	chr1:155233775-155233776	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs368819963	chr1:155233812-155233813	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs372186769	chr1:155233822-155233823	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs139015683	chr1:155233823-155233824	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs201785372	chr1:155233840-155233841	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs374297704	chr1:155233843-155233844	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs200371126	chr1:155233848-155233849	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs190033484	chr1:155233914-155233915	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs141988996	chr1:155233921-155233922	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs182102889	chr1:155233947-155233948	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs368267463	chr1:155233968-155233969	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs371676013	chr1:155233990-155233991	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs567209479	chr1:155233991-155233992	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs142395925	chr1:155234014-155234015	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs534718482	chr1:155234021-155234022	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs148639197	chr1:155234022-155234023	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs374917896	chr1:155234067-155234068	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs369124429	chr1:155234113-155234114	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs371767797	chr1:155234119-155234120	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs375245438	chr1:155234120-155234121	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs187229785	chr1:155234135-155234136	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs146326736	chr1:155234217-155234218	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs538876543	chr1:155234233-155234234	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs545434812	chr1:155234243-155234244	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs557205500	chr1:155234247-155234248	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs56127810	chr1:155234253-155234254	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs367831473	chr1:155234255-155234256	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs199568173	chr1:155234256-155234257	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs34045048	chr1:155234287-155234288	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs374795363	chr1:155234368-155234369	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs370101901	chr1:155234372-155234373	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs374353302	chr1:155234449-155234450	Strong transcription Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs139698018	chr1:155234532-155234533	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs559089129	chr1:155234575-155234576	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs192160292	chr1:155234589-155234590	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs554549747	chr1:155234591-155234592	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs377657872	chr1:155234601-155234602	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs144312459	chr1:155234617-155234618	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs540715476	chr1:155234649-155234650	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs565267723	chr1:155234650-155234651	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs577744099	chr1:155234669-155234670	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
Non-syndromic sensorineural hearing loss	15273396	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
Ewing''s sarcoma	21437220	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
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
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
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
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1541 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155232000-155242400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:155232200-155236400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:155232200-155242200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:155232400-155234000	Weak transcription	HSMM	muscle
5	chr1:155232400-155241000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:155232400-155241600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:155232600-155233800	Weak transcription	Aorta	Aorta
8	chr1:155232600-155234000	Weak transcription	Ovary	ovary
9	chr1:155232600-155234400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr1:155232600-155235000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:155232600-155236200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr1:155232600-155240600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:155232600-155240600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:155232600-155240800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:155232600-155240800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr1:155232600-155240800	Strong transcription	Gastric	stomach
17	chr1:155232600-155241000	Strong transcription	HMEC	breast
18	chr1:155232600-155241200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:155232600-155241400	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr1:155232600-155241400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:155232600-155241400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:155232600-155241600	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr1:155232600-155241600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr1:155232600-155241600	Strong transcription	Fetal Thymus	thymus
25	chr1:155232600-155241600	Strong transcription	Osteobl	bone
26	chr1:155232600-155241800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
27	chr1:155232600-155241800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:155232600-155241800	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr1:155232600-155241800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:155232600-155241800	Strong transcription	Fetal Muscle Trunk	muscle
31	chr1:155232600-155242000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:155232600-155242000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr1:155232600-155242200	Weak transcription	Right Atrium	heart
34	chr1:155232800-155233600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr1:155232800-155233600	Weak transcription	Brain Substantia Nigra	brain
36	chr1:155232800-155233600	Weak transcription	Small Intestine	intestine
37	chr1:155232800-155233800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:155232800-155236200	Weak transcription	Fetal Heart	heart
39	chr1:155232800-155236600	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr1:155232800-155237800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:155232800-155237800	Weak transcription	Stomach Mucosa	stomach
42	chr1:155232800-155240000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
43	chr1:155232800-155240400	Strong transcription	GM12878-XiMat	blood
44	chr1:155232800-155240600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:155232800-155240600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:155232800-155240600	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr1:155232800-155240600	Strong transcription	Brain Germinal Matrix	brain
48	chr1:155232800-155240800	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr1:155232800-155240800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:155232800-155240800	Strong transcription	Fetal Intestine Large	intestine

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