Variant report

Variant	esv1824284
Chromosome Location	chr1:186358588-186441585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:562)
CpG islands
(count:427)
Chromatin interactive
region (count:62)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:186373705-186373946	K562	blood:	n/a	n/a
2	ATF1	chr1:186426101-186426191	K562	blood:	n/a	n/a
3	BACH1	chr1:186409766-186409870	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:186412778-186413091	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:186411613-186412384	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:186436124-186436278	A549	lung:	n/a	chr1:186436215-186436228 chr1:186436215-186436228 chr1:186436217-186436228
7	CEBPB	chr1:186398181-186398484	H1-hESC	embryonic stem cell:	n/a	chr1:186398334-186398345
8	CEBPB	chr1:186398163-186398493	HepG2	liver:	n/a	chr1:186398334-186398345
9	CEBPB	chr1:186398201-186398438	Hela-S3	cervix:	n/a	chr1:186398334-186398345
10	CEBPB	chr1:186427408-186427658	K562	blood:	n/a	chr1:186427565-186427574 chr1:186427563-186427574 chr1:186427564-186427575 chr1:186427563-186427576 chr1:186427563-186427576
11	CEBPB	chr1:186427556-186427623	A549	lung:	n/a	chr1:186427565-186427574 chr1:186427563-186427574 chr1:186427564-186427575 chr1:186427563-186427576 chr1:186427563-186427576
12	CEBPB	chr1:186398182-186398439	A549	lung:	n/a	chr1:186398334-186398345
13	CEBPB	chr1:186411878-186412245	A549	lung:	n/a	n/a
14	CEBPB	chr1:186404483-186404835	IMR90	lung:	n/a	chr1:186404637-186404648
15	CEBPB	chr1:186411888-186412244	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:186411844-186412268	A549	lung:	n/a	n/a
17	CEBPB	chr1:186366894-186367220	IMR90	lung:	n/a	chr1:186367067-186367076 chr1:186367067-186367078 chr1:186367065-186367078
18	CEBPB	chr1:186398168-186398513	IMR90	lung:	n/a	chr1:186398334-186398345
19	CEBPB	chr1:186418816-186419089	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:186398250-186398376	HepG2	liver:	n/a	chr1:186398334-186398345
21	CEBPB	chr1:186398276-186398383	K562	blood:	n/a	chr1:186398334-186398345
22	CEBPB	chr1:186411770-186412395	A549	lung:	n/a	n/a
23	CEBPB	chr1:186362272-186362564	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:186404612-186404838	A549	lung:	n/a	chr1:186404637-186404648
25	CEBPB	chr1:186411640-186412406	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr1:186427546-186427741	HepG2	liver:	n/a	chr1:186427565-186427574 chr1:186427563-186427574 chr1:186427564-186427575 chr1:186427563-186427576 chr1:186427563-186427576
27	CEBPB	chr1:186404527-186404792	Hela-S3	cervix:	n/a	chr1:186404637-186404648
28	CEBPB	chr1:186404573-186404805	HepG2	liver:	n/a	chr1:186404637-186404648
29	CEBPB	chr1:186398137-186398462	MCF-7	breast:	n/a	chr1:186398334-186398345
30	CHD2	chr1:186411684-186412307	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr1:186430499-186430520	GM12878	blood:	n/a	n/a
32	CREB1	chr1:186373552-186374117	K562	blood:	n/a	n/a
33	CTCF	chr1:186373700-186373850	AG09309	skin:	n/a	n/a
34	CTCF	chr1:186373557-186373977	GM12878	blood:	n/a	n/a
35	CTCF	chr1:186373720-186373870	HRE	kidney:	n/a	n/a
36	CTCF	chr1:186373700-186373850	HVMF	connective:	n/a	n/a
37	CTCF	chr1:186373648-186373872	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr1:186373700-186373850	HCT-116	colon:	n/a	n/a
39	CTCF	chr1:186373740-186373890	GM12873	blood:	n/a	n/a
40	CTCF	chr1:186373700-186373850	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr1:186373700-186373850	GM12872	blood:	n/a	n/a
42	CTCF	chr1:186371766-186371860	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:186373700-186373850	AG09319	gingival:	n/a	n/a
44	CTCF	chr1:186373640-186373901	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr1:186373700-186373850	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:186373660-186373810	GM12869	blood:	n/a	n/a
47	CTCF	chr1:186373680-186373830	K562	blood:	n/a	n/a
48	CTCF	chr1:186373740-186373890	NHEK	skin:	n/a	n/a
49	CTCF	chr1:186371790-186371861	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:186373660-186373810	Caco-2	colon:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:186369020-186369070	HMEC	breast:	n/a
2	chr1:186389413-186389463	HL-60	blood:	n/a
3	chr1:186426136-186426186	GM06990	blood:	n/a
4	chr1:186426136-186426186	HRPEpiC	eye:	n/a
5	chr1:186370528-186370578	Hela-S3	cervix:	n/a
6	chr1:186389413-186389463	HRPEpiC	eye:	n/a
7	chr1:186429967-186430017	HCT-116	colon:	n/a
8	chr1:186370528-186370578	AG04449	skin:	fetal
9	chr1:186416357-186416407	PANC-1	pancreas:	n/a
10	chr1:186370528-186370578	PFSK-1	brain:	n/a
11	chr1:186389413-186389463	NB4	blood:	n/a
12	chr1:186370528-186370578	GM12892	blood:	n/a
13	chr1:186389413-186389463	AG09309	skin:	n/a
14	chr1:186389413-186389463	Hepatocyte	liver:	n/a
15	chr1:186413580-186413630	ProgFib	skin:	n/a
16	chr1:186389413-186389463	ovcar-3	ovarian:	n/a
17	chr1:186370528-186370578	Caco-2	colon:	n/a
18	chr1:186369020-186369070	HIPEpiC	eye:	n/a
19	chr1:186429967-186430017	AoSMC	blood vessel:	n/a
20	chr1:186370528-186370578	HRCEpiC	kidney:	n/a
21	chr1:186369020-186369070	SK-N-MC	brain:	n/a
22	chr1:186389413-186389463	BJ	skin:	n/a
23	chr1:186429967-186430017	NHDF-neo	bronchial:	n/a
24	chr1:186389413-186389463	H1-hESC	embryonic stem cell:	embryo
25	chr1:186426136-186426186	AG04450	lung:	fetal
26	chr1:186370528-186370578	AG09319	gingival:	n/a
27	chr1:186369020-186369070	MCF10A-Er-Src	breast:	n/a
28	chr1:186429967-186430017	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:186389413-186389463	Hela-S3	cervix:	n/a
30	chr1:186370528-186370578	NH-A	brain:	n/a
31	chr1:186426136-186426186	A549	lung:	n/a
32	chr1:186370528-186370578	HCT-116	colon:	n/a
33	chr1:186413580-186413630	SK-N-MC	brain:	n/a
34	chr1:186426136-186426186	AG09319	gingival:	n/a
35	chr1:186416357-186416407	GM19239	blood:	n/a
36	chr1:186370528-186370578	AG09309	skin:	n/a
37	chr1:186426136-186426186	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:186413580-186413630	HRE	kidney:	n/a
39	chr1:186429967-186430017	HEEpiC	esophagus:	n/a
40	chr1:186389413-186389463	HNPCEpiC	eye:	n/a
41	chr1:186416357-186416407	MCF10A-Er-Src	breast:	n/a
42	chr1:186413580-186413630	SK-N-SH	brain:	n/a
43	chr1:186370528-186370578	MCF10A-Er-Src	breast:	n/a
44	chr1:186429967-186430017	K562	blood:	n/a
45	chr1:186389413-186389463	SK-N-SH	brain:	n/a
46	chr1:186389413-186389463	HMEC	breast:	n/a
47	chr1:186426136-186426186	AG04449	skin:	fetal
48	chr1:186369020-186369070	SK-N-SH	brain:	n/a
49	chr1:186426136-186426186	HEK293	kidney:	embryo
50	chr1:186429967-186430017	AG04450	lung:	fetal

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:186373972..186376157-chr1:186379499..186382713,3	MCF-7	breast:
2	chr1:186378179..186381084-chr1:186382062..186384910,2	K562	blood:
3	chr1:186386796..186388944-chr1:186399604..186401949,3	MCF-7	breast:
4	chr1:186359040..186360832-chr1:186378064..186380778,2	K562	blood:
5	chr1:186406204..186407888-chr1:186423532..186426225,2	K562	blood:
6	chr1:186386796..186388944-chr1:186399604..186401949,3	MCF-7	breast:
7	chr1:186361659..186366010-chr1:186371455..186375319,4	K562	blood:
8	chr1:186351786..186353546-chr1:186357204..186358890,2	K562	blood:
9	chr1:186405476..186407528-chr1:186408625..186410578,2	MCF-7	breast:
10	chr1:186378179..186381084-chr1:186382062..186384973,3	K562	blood:
11	chr1:186421096..186422603-chr1:186424178..186426031,2	K562	blood:
12	chr1:186375983..186377916-chr1:186380424..186382428,2	K562	blood:
13	chr1:186405476..186407528-chr1:186408625..186410578,2	MCF-7	breast:
14	chr1:186372550..186374489-chr1:186441138..186443259,2	MCF-7	breast:
15	chr1:186410546..186412201-chr1:186413904..186416292,2	K562	blood:
16	chr1:186359040..186360832-chr1:186378064..186380778,2	K562	blood:
17	chr1:186344089..186347008-chr1:186357824..186359860,2	K562	blood:
18	chr1:186376260..186377916-chr1:186380372..186382428,2	K562	blood:
19	chr1:186421096..186422603-chr1:186424178..186426031,2	K562	blood:
20	chr1:186373573..186374238-chr1:186954748..186955705,3	K562	blood:
21	chr1:186385586..186388507-chr1:186403237..186404810,2	K562	blood:
22	chr1:186348112..186349621-chr1:186383105..186385568,2	K562	blood:
23	chr1:186352524..186355241-chr1:186393663..186395812,2	K562	blood:
24	chr1:186374114..186376141-chr1:186408577..186410656,2	MCF-7	breast:
25	chr1:186370487..186373941-chr1:186374883..186377860,4	K562	blood:
26	chr1:186369970..186371779-chr1:186378105..186380779,2	K562	blood:
27	chr1:186416480..186419218-chr1:186423723..186425519,2	K562	blood:
28	chr1:186369970..186371779-chr1:186378105..186380779,2	K562	blood:
29	chr1:186362143..186364108-chr1:186368124..186371835,3	K562	blood:
30	chr1:186410632..186413152-chr1:186416805..186419247,2	K562	blood:
31	chr1:186420922..186422805-chr1:186448393..186449900,2	K562	blood:
32	chr1:186343907..186345654-chr1:186382510..186384256,2	MCF-7	breast:
33	chr1:186373731..186374559-chr1:186954735..186955602,2	MCF-7	breast:
34	chr1:186384905..186386985-chr1:186417327..186419013,2	K562	blood:
35	chr1:186416480..186420579-chr1:186423723..186426671,3	K562	blood:
36	chr1:186381482..186384419-chr1:186389970..186392449,3	K562	blood:
37	chr1:186357371..186360885-chr1:186362480..186365023,4	K562	blood:
38	chr1:186373326..186373968-chr1:186954948..186955674,2	MCF-7	breast:
39	chr1:186420929..186422603-chr1:186424178..186426683,3	K562	blood:
40	chr1:186378179..186381084-chr1:186382062..186384910,2	K562	blood:
41	chr1:186373386..186374034-chr1:186451869..186452455,2	MCF-7	breast:
42	chr1:186373972..186376157-chr1:186379499..186382713,3	MCF-7	breast:
43	chr1:186431573..186434062-chr1:186434612..186436808,2	MCF-7	breast:
44	chr1:186343109..186345591-chr1:186373069..186376266,4	K562	blood:
45	chr1:186406204..186407888-chr1:186423532..186426225,2	K562	blood:
46	chr1:186378179..186381084-chr1:186382062..186384973,3	K562	blood:
47	chr1:186420929..186422603-chr1:186424178..186426683,3	K562	blood:
48	chr1:186357371..186360885-chr1:186362480..186365023,4	K562	blood:
49	chr1:186374114..186376141-chr1:186408577..186410656,2	MCF-7	breast:
50	chr1:186370487..186373941-chr1:186374883..186377860,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRG4-2	chr1:186388141-186388365	NONHSAT008448
2	lnc-PRG4-2	chr1:186386509-186386786	NONHSAT008448
3	lnc-C1orf27-1	chr1:186420213-186420406	ENSG00000229739.1
4	lnc-C1orf27-1	chr1:186420762-186420881	ENSG00000229739.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C1orf27	hsa-miR-1	chr1:186389494-186389515

Variant related genes	Relation type
ENSG00000268662	TF binding region
C1orf27	TF binding region
ENSG00000229739	TF binding region
PDC	TF binding region
OCLM	TF binding region
ENSG00000268662	CpG island
C1orf27	CpG island
ENSG00000229739	CpG island
PDC	CpG island
OCLM	CpG island
ENSG00000047410	chromatin interactions
ENSG00000157181	chromatin interactions
ENSG00000268662	chromatin interactions
ENSG00000262180	chromatin interactions
ENSG00000116703	chromatin interactions
ENSG00000229739	chromatin interactions

Extended variants
information (count: 2956 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2956 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1003127	chr1:186358588-186358589	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552143956	chr1:186358602-186358603	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563968125	chr1:186358605-186358606	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141310146	chr1:186358620-186358621	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs146996047	chr1:186358676-186358677	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370380390	chr1:186358679-186358680	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs567677167	chr1:186358688-186358689	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535147512	chr1:186358730-186358731	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546765307	chr1:186358733-186358734	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs571151763	chr1:186358768-186358769	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568690895	chr1:186358786-186358787	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs193063732	chr1:186358788-186358789	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs374960484	chr1:186358797-186358798	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138195518	chr1:186358828-186358829	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs143737879	chr1:186358882-186358883	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs376583820	chr1:186358929-186358930	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs535881731	chr1:186358938-186358939	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375708786	chr1:186358975-186358976	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554519836	chr1:186358984-186358985	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs572726721	chr1:186359008-186359009	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs143847382	chr1:186359018-186359019	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564820012	chr1:186359029-186359030	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs148199841	chr1:186359064-186359065	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs539506469	chr1:186359079-186359080	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs35147149	chr1:186359181-186359182	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs74842753	chr1:186359191-186359192	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs563988410	chr1:186359214-186359215	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs531203861	chr1:186359228-186359229	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs549390615	chr1:186359240-186359241	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs376058338	chr1:186359245-186359246	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs551525562	chr1:186359263-186359264	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs141185485	chr1:186359280-186359281	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs528469403	chr1:186359343-186359344	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs150741647	chr1:186359391-186359392	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs16825282	chr1:186359392-186359393	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs534129514	chr1:186359409-186359410	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs532182695	chr1:186359474-186359475	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs185482644	chr1:186359603-186359604	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs568831431	chr1:186359606-186359607	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs77126871	chr1:186359632-186359633	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs557173093	chr1:186359675-186359676	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs560523977	chr1:186359710-186359711	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs555970257	chr1:186359725-186359726	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs3115752	chr1:186359750-186359751	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs12736676	chr1:186359763-186359764	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs533549512	chr1:186359815-186359816	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs367658772	chr1:186359826-186359827	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs139232938	chr1:186359868-186359869	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371831284	chr1:186359870-186359871	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376120716	chr1:186359890-186359891	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1228 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186345400-186358600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:186345400-186359000	Weak transcription	Lung	lung
3	chr1:186345400-186371600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:186345400-186371600	Weak transcription	Esophagus	oesophagus
5	chr1:186345400-186371600	Weak transcription	Gastric	stomach
6	chr1:186345400-186390600	Weak transcription	Small Intestine	intestine
7	chr1:186345400-186398200	Weak transcription	Spleen	Spleen
8	chr1:186345800-186361200	Weak transcription	Aorta	Aorta
9	chr1:186345800-186377400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:186346000-186366800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:186346200-186359000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr1:186346200-186359000	Weak transcription	Ovary	ovary
13	chr1:186346200-186359000	Weak transcription	Thymus	Thymus
14	chr1:186346200-186360600	Weak transcription	Brain Substantia Nigra	brain
15	chr1:186346200-186361200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr1:186346200-186361200	Weak transcription	Pancreas	Pancrea
17	chr1:186346200-186361400	Weak transcription	Right Ventricle	heart
18	chr1:186346200-186365200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr1:186346200-186365200	Weak transcription	Psoas Muscle	Psoas
20	chr1:186346200-186380400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:186346200-186388400	Weak transcription	Colonic Mucosa	Colon
22	chr1:186346400-186359400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr1:186346400-186359400	Weak transcription	Colon Smooth Muscle	Colon
24	chr1:186346400-186361000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr1:186346400-186361200	Weak transcription	Brain Angular Gyrus	brain
26	chr1:186346400-186376000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr1:186346400-186388000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:186346400-186390000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:186346600-186359400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr1:186347200-186370800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:186347400-186368000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr1:186347400-186370400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr1:186347400-186370400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:186347600-186370800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:186348000-186359400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr1:186348000-186382000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:186348600-186370200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:186348600-186370600	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr1:186348600-186372000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:186348600-186372200	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr1:186348600-186373400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:186348600-186390200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:186348800-186363600	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr1:186348800-186370200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:186348800-186370200	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr1:186348800-186370200	Strong transcription	Dnd41	blood
47	chr1:186348800-186371000	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:186348800-186372000	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr1:186348800-186372200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:186349200-186368600	Strong transcription	Primary T helper cells PMA-I stimulated	--

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