Variant report

Variant	nsv1054573
Chromosome Location	chr12:85658602-86235433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3749)
CpG islands
(count:2075)
Chromatin interactive
region (count:81)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3749 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:86036581-86037005	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:85823428-85823661	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:85943398-85943797	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:85862438-85862767	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:85818707-85819018	HepG2	liver:	n/a	chr12:85818944-85818960
6	ARID3A	chr12:85871019-85871265	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:85704287-85704562	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:86215439-86216042	HepG2	liver:	n/a	n/a
9	ATF1	chr12:86104663-86104781	K562	blood:	n/a	n/a
10	ATF2	chr12:85673925-85674351	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:85818184-85818941	GM12878	blood:	n/a	n/a
12	ATF2	chr12:85818236-85818645	GM12878	blood:	n/a	n/a
13	ATF2	chr12:85674234-85674859	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr12:85817663-85818143	GM12878	blood:	n/a	n/a
15	ATF2	chr12:85920866-85921402	GM12878	blood:	n/a	n/a
16	ATF3	chr12:85673890-85674445	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:85672070-85672089	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:85862472-85862870	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:86121439-86121442	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr12:85862502-85862816	GM12878	blood:	n/a	chr12:85862676-85862687
21	BATF	chr12:85929686-85929979	GM12878	blood:	n/a	n/a
22	BATF	chr12:85862496-85862812	GM12878	blood:	n/a	chr12:85862676-85862687
23	BATF	chr12:86198461-86198632	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:85818268-85818600	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:85903612-85903886	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:86169235-86169489	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL3	chr12:86159050-86159743	A549	lung:	n/a	chr12:86159156-86159165
28	BCL3	chr12:86215330-86216088	A549	lung:	n/a	chr12:86215353-86215362
29	BHLHE40	chr12:85862437-85862686	HepG2	liver:	n/a	n/a
30	BHLHE40	chr12:85674086-85674392	HepG2	liver:	n/a	chr12:85674286-85674302
31	BHLHE40	chr12:86215633-86215635	HepG2	liver:	n/a	n/a
32	BHLHE40	chr12:85817742-85818105	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:85674051-85674416	A549	lung:	n/a	chr12:85674286-85674302
34	BHLHE40	chr12:85925172-85925543	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:85694864-85695174	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:85903677-85903924	GM12878	blood:	n/a	n/a
37	BRCA1	chr12:85725088-85725176	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr12:86229275-86230390	Hela-S3	cervix:	n/a	chr12:86229554-86229561
39	BRCA1	chr12:86227791-86228570	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr12:86215072-86216259	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr12:86217593-86217944	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:85763290-85763939	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr12:85673932-85674153	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr12:85673812-85674196	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr12:86159061-86159912	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr12:85862456-85862677	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr12:86019903-86020631	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:85674532-85675298	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr12:86176556-86176959	HCT-116	colon:	n/a	n/a
50	CBX3	chr12:86020121-86020665	HCT-116	colon:	n/a	n/a

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86230367-86230417	PrEC	prostate:	n/a
2	chr12:86230367-86230417	PrEC	prostate:	n/a
3	chr12:85673918-85673968	NT2-D1	testis:	n/a
4	chr12:85672623-85672673	HRE	kidney:	n/a
5	chr12:85671976-85672026	T-47D	breast:	n/a
6	chr12:86040467-86040517	GM12892	blood:	n/a
7	chr12:85674458-85674508	BJ	skin:	n/a
8	chr12:85673915-85673965	HRPEpiC	eye:	n/a
9	chr12:85674022-85674072	SK-N-SH	brain:	n/a
10	chr12:85673221-85673271	T-47D	breast:	n/a
11	chr12:85673915-85673965	HNPCEpiC	eye:	n/a
12	chr12:85673200-85673250	HCT-116	colon:	n/a
13	chr12:85673915-85673965	SK-N-MC	brain:	n/a
14	chr12:85671811-85671861	HAEpiC	amniotic membrane:	n/a
15	chr12:85672623-85672673	SAEC	small airway:	n/a
16	chr12:85674531-85674581	GM06990	blood:	n/a
17	chr12:85672285-85672335	HIPEpiC	eye:	n/a
18	chr12:85672285-85672335	Hela-S3	cervix:	n/a
19	chr12:85671811-85671861	HRE	kidney:	n/a
20	chr12:85674140-85674190	AoSMC	blood vessel:	n/a
21	chr12:85673915-85673965	ProgFib	skin:	n/a
22	chr12:85673347-85673397	AG04450	lung:	fetal
23	chr12:85674296-85674346	HepG2	liver:	n/a
24	chr12:85674458-85674508	HUVEC	blood vessel:	n/a
25	chr12:85673347-85673397	HCM	heart:	n/a
26	chr12:85673200-85673250	HRCEpiC	kidney:	n/a
27	chr12:85673918-85673968	HCM	heart:	n/a
28	chr12:85667353-85667403	Caco-2	colon:	n/a
29	chr12:86230176-86230226	ovcar-3	ovarian:	n/a
30	chr12:85667616-85667666	HAEpiC	amniotic membrane:	n/a
31	chr12:85671892-85671942	NB4	blood:	n/a
32	chr12:86230557-86230607	HepG2	liver:	n/a
33	chr12:85672623-85672673	HL-60	blood:	n/a
34	chr12:85673221-85673271	HCT-116	colon:	n/a
35	chr12:85674296-85674346	Jurkat	blood:	n/a
36	chr12:86230367-86230417	HRCEpiC	kidney:	n/a
37	chr12:85945089-85945139	GM19239	blood:	n/a
38	chr12:85945089-85945139	HRPEpiC	eye:	n/a
39	chr12:85667353-85667403	AG10803	skin:	n/a
40	chr12:86230367-86230417	SK-N-SH	brain:	n/a
41	chr12:85672623-85672673	NHBE	bronchial:	n/a
42	chr12:86230957-86231007	GM12891	blood:	n/a
43	chr12:85673347-85673397	HCF	heart:	n/a
44	chr12:85673879-85673929	A549	lung:	n/a
45	chr12:85667616-85667666	HCF	heart:	n/a
46	chr12:86230367-86230417	HL-60	blood:	n/a
47	chr12:86230825-86230875	HCT-116	colon:	n/a
48	chr12:86230557-86230607	Jurkat	blood:	n/a
49	chr12:85677430-85677480	NB4	blood:	n/a
50	chr12:85672623-85672673	BE2_C	brain:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:85470092..85470900-chr12:85818409..85819385,3	MCF-7	breast:
2	chr1:11968120..11968947-chr12:85674873..85675678,2	Hela-S3	cervix:
3	chr12:85745803..85747917-chr12:85750722..85752952,2	MCF-7	breast:
4	chr12:85846574..85849271-chr12:85855607..85858014,2	MCF-7	breast:
5	chr12:85861848..85863045-chr12:86266253..86266913,4	MCF-7	breast:
6	chr12:86031568..86033990-chr12:86035290..86037133,2	K562	blood:
7	chr12:86210558..86212149-chr21:9825340..9827489,2	MCF-7	breast:
8	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
9	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
10	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
11	chr12:85745803..85747917-chr12:85750722..85752952,2	MCF-7	breast:
12	chr12:85889329..85890032-chr12:85900621..85901187,2	MCF-7	breast:
13	chr12:85713980..85716222-chr12:85718443..85721765,3	MCF-7	breast:
14	chr12:85735992..85737956-chr12:85742669..85744404,2	MCF-7	breast:
15	chr12:85905968..85908916-chr17:58676509..58679332,2	MCF-7	breast:
16	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
17	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
18	chr12:86166852..86169171-chr12:86172826..86175025,3	K562	blood:
19	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
20	chr12:85549387..85549978-chr12:85835659..85836204,2	MCF-7	breast:
21	chr12:85808148..85809670-chr12:85817328..85819364,2	MCF-7	breast:
22	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
23	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
24	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
25	chr12:85735992..85737956-chr12:85742669..85744404,2	MCF-7	breast:
26	chr12:85688551..85691285-chr12:85694636..85697474,2	MCF-7	breast:
27	chr12:86166924..86169171-chr12:86172853..86175025,2	K562	blood:
28	chr12:85767120..85767969-chr12:85795392..85796211,2	MCF-7	breast:
29	chr12:85870710..85871639-chr12:86266180..86266857,2	MCF-7	breast:
30	chr12:86166924..86169171-chr12:86172853..86175025,2	K562	blood:
31	chr12:85818820..85819361-chr12:86313812..86314794,3	MCF-7	breast:
32	chr12:85808148..85809670-chr12:85817328..85819364,2	MCF-7	breast:
33	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
34	chr12:86166852..86169171-chr12:86172826..86175025,3	K562	blood:
35	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
36	chr12:85713980..85716222-chr12:85718443..85721765,3	MCF-7	breast:
37	chr12:85704116..85704872-chr12:85842034..85842872,2	MCF-7	breast:
38	chr12:85869160..85871446-chr12:85872180..85874528,2	K562	blood:
39	chr12:86212969..86215091-chr12:86229770..86232108,2	K562	blood:
40	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
41	chr12:85869160..85871446-chr12:85872180..85874528,2	K562	blood:
42	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
43	chr12:85693571..85695610-chr12:85696379..85699321,2	MCF-7	breast:
44	chr12:85712831..85715377-chr12:85729265..85730997,2	MCF-7	breast:
45	chr12:86036224..86038282-chr12:86040678..86042966,2	MCF-7	breast:
46	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
47	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
48	chr12:85889329..85890032-chr12:85900621..85901187,2	MCF-7	breast:
49	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
50	chr12:85862041..85863123-chr12:86313866..86314895,4	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALX1-1	chr12:85736216-85736970	NONHSAT029749
2	lnc-ALX1-1	chr12:85736250-85736690	ENSG00000258815
3	lnc-ALX1-2	chr12:85988245-85988373	NONHSAT029750
4	lnc-ALX1-1	chr12:85711838-85711893	ENSG00000258815
5	lnc-RASSF9-1	chr12:86175670-86176222	NONHSAT029756
6	lnc-ALX1-2	chr12:85759621-85759721	NONHSAT029750
7	lnc-ALX1-1	chr12:85712736-85712757	ENSG00000258815
8	lnc-ALX1-2	chr12:85817847-85818671	NONHSAT029751
9	lnc-ALX1-2	chr12:85793271-85793388	NONHSAT029750
10	lnc-ALX1-2	chr12:85817896-85817982	NONHSAT029750
11	lnc-ALX1-1	chr12:85712733-85712757	NONHSAT029749
12	lnc-ALX1-2	chr12:85763589-85763622	XLOC_009820
13	lnc-ALX1-2	chr12:85763588-85763622	NONHSAT029751
14	lnc-ALX1-2	chr12:85817896-85817982	XLOC_009820
15	lnc-ALX1-2	chr12:85793271-85793388	XLOC_009820
16	lnc-ALX1-2	chr12:85818315-85818671	XLOC_009820
17	lnc-ALX1-2	chr12:85793175-85793388	NONHSAT029751
18	lnc-ALX1-1	chr12:85733174-85733276	NONHSAT029749

No data

Variant related genes	Relation type
ALX1	TF binding region
RASSF9	TF binding region
ENSG00000258206	TF binding region
ENSG00000257855	TF binding region
ENSG00000258815	TF binding region
ENSG00000263449	TF binding region
ALX1	CpG island
RASSF9	CpG island
ENSG00000258206	CpG island
ENSG00000257855	CpG island
ENSG00000258815	CpG island
ENSG00000263449	CpG island
ENSG00000199347	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000263449	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000198774	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000157483	chromatin interactions
ENSG00000157470	chromatin interactions
CDC23	miRNA target sites
ID4	miRNA target sites
KCNK1	miRNA target sites

Extended variants
information (count: 13904 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:13904 , 50 per page) page: 1 2 3 4 5 6 7 ... 279

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550130758	chr12:85659748-85659749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115733129	chr12:85659770-85659771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7485353	chr12:85659774-85659775	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs192554150	chr12:85659775-85659776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538459891	chr12:85659831-85659832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556561785	chr12:85659832-85659833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7488217	chr12:85659857-85659858	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs545067957	chr12:85659860-85659861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560491143	chr12:85659872-85659873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552248007	chr12:85659885-85659886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372574397	chr12:85659886-85659887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374093418	chr12:85659888-85659889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572531113	chr12:85659937-85659938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184272107	chr12:85659957-85659958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189131677	chr12:85659966-85659967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546353990	chr12:85660000-85660001	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559383696	chr12:85660029-85660030	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs564759719	chr12:85660038-85660039	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs374293026	chr12:85660068-85660069	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs549990274	chr12:85660093-85660094	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs541611446	chr12:85660128-85660129	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs75630641	chr12:85660217-85660218	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs112440933	chr12:85660228-85660229	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs147158594	chr12:85660290-85660291	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs377607258	chr12:85660323-85660324	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs547041149	chr12:85660326-85660327	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs73365747	chr12:85660372-85660373	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs117411800	chr12:85660379-85660380	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs181176031	chr12:85660394-85660395	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs184594587	chr12:85660406-85660407	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs569444645	chr12:85660446-85660447	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs56166460	chr12:85660447-85660448	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs556760612	chr12:85660509-85660510	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs367694843	chr12:85660553-85660554	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs140519610	chr12:85660556-85660557	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs144369877	chr12:85660592-85660593	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs34136303	chr12:85660656-85660657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554173060	chr12:85660680-85660681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572494106	chr12:85660729-85660730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189864062	chr12:85660778-85660779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147851639	chr12:85660853-85660854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562206118	chr12:85660879-85660880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529273342	chr12:85660907-85660908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555091795	chr12:85660927-85660928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576528073	chr12:85660951-85660952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374576119	chr12:85660995-85660996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372932523	chr12:85666022-85666023	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs560402892	chr12:85666077-85666078	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs377122965	chr12:85666078-85666079	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs527552356	chr12:85666089-85666090	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2365 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85659600-85660000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:85659800-85660000	Enhancers	Adipose Nuclei	Adipose
3	chr12:85659800-85660800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:85660000-85660400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr12:85660000-85660600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:85660200-85660400	Enhancers	HUVEC	blood vessel
7	chr12:85660400-85660600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr12:85660400-85660600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr12:85660400-85660800	Enhancers	Primary hematopoietic stem cells	blood
10	chr12:85660600-85661000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:85666000-85666200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:85666600-85666800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr12:85666600-85666800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:85666800-85667000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
15	chr12:85666800-85667000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
16	chr12:85666800-85667200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
17	chr12:85666800-85667800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr12:85666800-85667800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:85666800-85668000	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
20	chr12:85666800-85668200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
21	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
22	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
23	chr12:85667000-85667200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:85667000-85667200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:85667000-85667200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
29	chr12:85667000-85667400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
30	chr12:85667000-85667400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
31	chr12:85667000-85667400	Bivalent Enhancer	Liver	Liver
32	chr12:85667000-85667400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
33	chr12:85667000-85667400	Bivalent Enhancer	Fetal Heart	heart
34	chr12:85667000-85667400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
35	chr12:85667000-85667400	Bivalent/Poised TSS	NH-A	brain
36	chr12:85667000-85667800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr12:85667000-85667800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
38	chr12:85667000-85667800	Bivalent/Poised TSS	NHDF-Ad	bronchial
39	chr12:85667000-85668000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr12:85667000-85668000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:85667000-85668200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
42	chr12:85667000-85668200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr12:85667200-85667400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr12:85667200-85667400	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:85667200-85667400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr12:85667200-85667400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:85667200-85667400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
48	chr12:85667200-85667400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr12:85667200-85667400	Bivalent Enhancer	Fetal Thymus	thymus
50	chr12:85667200-85667400	Bivalent Enhancer	Right Atrium	heart

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