Variant report

Variant	nsv1037542
Chromosome Location	chr12:12506839-12542868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1250)
CpG islands
(count:1162)
Chromatin interactive
region (count:74)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1250 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:12537535-12538151	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:12510182-12510546	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:12506748-12507137	K562	blood:	n/a	n/a
4	ARID3A	chr12:12534087-12534699	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:12529578-12529897	K562	blood:	n/a	n/a
6	ARID3A	chr12:12529544-12529933	HepG2	liver:	n/a	n/a
7	ATF1	chr12:12506808-12507158	K562	blood:	n/a	n/a
8	ATF1	chr12:12509825-12510182	K562	blood:	n/a	n/a
9	ATF2	chr12:12509546-12510232	GM12878	blood:	n/a	n/a
10	ATF2	chr12:12509500-12510468	GM12878	blood:	n/a	n/a
11	ATF3	chr12:12509815-12510156	K562	blood:	n/a	n/a
12	BACH1	chr12:12509802-12510264	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr12:12509293-12509509	GM12878	blood:	n/a	n/a
14	BATF	chr12:12509963-12510302	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:12509986-12510369	GM12878	blood:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
16	BCL11A	chr12:12509979-12510322	GM12878	blood:	n/a	chr12:12510259-12510272
17	BCL3	chr12:12509580-12510800	A549	lung:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
18	BCLAF1	chr12:12529473-12530001	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:12509815-12510972	GM12878	blood:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
20	BCLAF1	chr12:12509548-12510871	GM12878	blood:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
21	BHLHE40	chr12:12510670-12510801	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:12537880-12538299	HepG2	liver:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
23	BHLHE40	chr12:12506759-12507279	K562	blood:	n/a	n/a
24	BHLHE40	chr12:12509671-12510294	K562	blood:	n/a	n/a
25	BHLHE40	chr12:12540555-12540803	K562	blood:	n/a	n/a
26	BHLHE40	chr12:12537973-12538300	GM12878	blood:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
27	BHLHE40	chr12:12537916-12538205	HepG2	liver:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
28	BHLHE40	chr12:12532622-12533229	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:12509578-12510342	GM12878	blood:	n/a	chr12:12510323-12510339
30	BHLHE40	chr12:12537940-12538255	K562	blood:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
31	BRCA1	chr12:12510011-12510309	HepG2	liver:	n/a	n/a
32	BRCA1	chr12:12533035-12533038	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr12:12509658-12510699	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr12:12540708-12540758	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr12:12509792-12510212	GM12878	blood:	n/a	n/a
36	BRCA1	chr12:12529604-12529918	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr12:12506807-12507195	K562	blood:	n/a	n/a
38	CBX3	chr12:12509644-12509955	K562	blood:	n/a	n/a
39	CBX3	chr12:12540482-12540872	HCT-116	colon:	n/a	n/a
40	CBX3	chr12:12509519-12510283	K562	blood:	n/a	n/a
41	CCNT2	chr12:12509824-12510471	K562	blood:	n/a	n/a
42	CCNT2	chr12:12506817-12507046	K562	blood:	n/a	n/a
43	CEBPB	chr12:12526280-12526626	HepG2	liver:	n/a	chr12:12526452-12526465 chr12:12526452-12526465 chr12:12526452-12526463
44	CEBPB	chr12:12526293-12526610	IMR90	lung:	n/a	chr12:12526452-12526465 chr12:12526452-12526465 chr12:12526452-12526463
45	CEBPB	chr12:12526386-12526600	H1-hESC	embryonic stem cell:	n/a	chr12:12526452-12526465 chr12:12526452-12526465 chr12:12526452-12526463
46	CEBPB	chr12:12509695-12510153	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr12:12527754-12527951	H1-hESC	embryonic stem cell:	n/a	chr12:12527840-12527851
48	CEBPB	chr12:12509344-12510412	GM12878	blood:	n/a	n/a
49	CEBPB	chr12:12519053-12519362	A549	lung:	n/a	chr12:12519199-12519210
50	CEBPB	chr12:12509818-12510443	HepG2	liver:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12510074-12510124	T-47D	breast:	n/a
2	chr12:12510064-12510114	HMEC	breast:	n/a
3	chr12:12510155-12510205	MCF-7	breast:	n/a
4	chr12:12510074-12510124	T-47D	breast:	n/a
5	chr12:12510064-12510114	HMEC	breast:	n/a
6	chr12:12510155-12510205	MCF-7	breast:	n/a
7	chr12:12509922-12509972	HCF	heart:	n/a
8	chr12:12510001-12510051	MCF10A-Er-Src	breast:	n/a
9	chr12:12509922-12509972	HRCEpiC	kidney:	n/a
10	chr12:12510074-12510124	NHDF-neo	bronchial:	n/a
11	chr12:12509940-12509990	Hela-S3	cervix:	n/a
12	chr12:12509725-12509775	HEEpiC	esophagus:	n/a
13	chr12:12514228-12514278	SK-N-SH_RA	brain:	n/a
14	chr12:12509940-12509990	Hepatocyte	liver:	n/a
15	chr12:12509922-12509972	HAEpiC	amniotic membrane:	n/a
16	chr12:12509963-12510013	HCM	heart:	n/a
17	chr12:12509940-12509990	HCF	heart:	n/a
18	chr12:12510067-12510117	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:12510067-12510117	HCT-116	colon:	n/a
20	chr12:12509705-12509755	HCF	heart:	n/a
21	chr12:12518875-12518925	PANC-1	pancreas:	n/a
22	chr12:12510241-12510291	GM12878	blood:	n/a
23	chr12:12514228-12514278	HUVEC	blood vessel:	n/a
24	chr12:12510070-12510120	GM12891	blood:	n/a
25	chr12:12514228-12514278	AoSMC	blood vessel:	n/a
26	chr12:12510074-12510124	NH-A	brain:	n/a
27	chr12:12518875-12518925	BE2_C	brain:	n/a
28	chr12:12510007-12510057	HepG2	liver:	n/a
29	chr12:12510074-12510124	HRPEpiC	eye:	n/a
30	chr12:12511223-12511273	AG04450	lung:	fetal
31	chr12:12509922-12509972	Jurkat	blood:	n/a
32	chr12:12510074-12510124	MCF-7	breast:	n/a
33	chr12:12514228-12514278	RPTEC	kidney:	n/a
34	chr12:12507213-12507263	NHBE	bronchial:	n/a
35	chr12:12509725-12509775	ProgFib	skin:	n/a
36	chr12:12509963-12510013	NB4	blood:	n/a
37	chr12:12507213-12507263	A549	lung:	n/a
38	chr12:12510155-12510205	T-47D	breast:	n/a
39	chr12:12509940-12509990	HCPEpiC	choroid plexus:	n/a
40	chr12:12510412-12510462	Hela-S3	cervix:	n/a
41	chr12:12510001-12510051	GM12892	blood:	n/a
42	chr12:12509963-12510013	NH-A	brain:	n/a
43	chr12:12514228-12514278	HEK293	kidney:	embryo
44	chr12:12509940-12509990	HL-60	blood:	n/a
45	chr12:12509725-12509775	PANC-1	pancreas:	n/a
46	chr12:12507213-12507263	CMK	blood:	n/a
47	chr12:12510064-12510114	IMR90	lung:	fetal
48	chr12:12509922-12509972	GM19239	blood:	n/a
49	chr12:12509963-12510013	GM12892	blood:	n/a
50	chr12:12507213-12507263	H1-hESC	embryonic stem cell:	embryo

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:12532395..12535127-chr12:12868296..12871166,2	MCF-7	breast:
2	chr12:12510113..12510632-chr3:101405456..101406387,2	Hela-S3	cervix:
3	chr12:12510200..12513346-chr12:12523638..12526361,3	K562	blood:
4	chr12:12510121..12510777-chr12:12876546..12877095,2	MCF-7	breast:
5	chr12:12515022..12517464-chr12:12520422..12522586,3	MCF-7	breast:
6	chr12:12509983..12510584-chr7:150020762..150021311,2	Hela-S3	cervix:
7	chr12:12510495..12512125-chr12:12760276..12763273,2	MCF-7	breast:
8	chr12:12501083..12504981-chr12:12508403..12511914,10	MCF-7	breast:
9	chr12:12529698..12531231-chr12:12536062..12538015,2	K562	blood:
10	chr12:12524724..12527440-chr12:12848940..12850671,2	MCF-7	breast:
11	chr12:12509354..12513359-chr12:12517458..12522131,6	K562	blood:
12	chr12:12509843..12512441-chr12:12520561..12523436,3	MCF-7	breast:
13	chr12:12509841..12511521-chr12:12518131..12519993,2	MCF-7	breast:
14	chr12:12508497..12510863-chr12:12526548..12530591,3	MCF-7	breast:
15	chr12:12531751..12533905-chr12:12536172..12537730,2	K562	blood:
16	chr12:12509503..12512182-chr12:12513037..12516438,6	MCF-7	breast:
17	chr12:12508799..12512106-chr12:12876417..12880418,4	MCF-7	breast:
18	chr12:12509167..12512867-chr12:12713185..12715471,5	MCF-7	breast:
19	chr12:12522631..12525556-chr12:12525783..12528472,2	MCF-7	breast:
20	chr12:12529636..12530613-chr12:12656069..12656681,3	MCF-7	breast:
21	chr12:12538899..12542001-chr12:12714080..12716309,3	MCF-7	breast:
22	chr12:12517934..12520693-chr12:12524024..12526072,2	MCF-7	breast:
23	chr12:12534486..12536460-chr12:12761134..12763160,2	MCF-7	breast:
24	chr12:12526769..12529809-chr12:12714703..12717328,3	K562	blood:
25	chr12:12515022..12517464-chr12:12520422..12522586,3	MCF-7	breast:
26	chr12:12502870..12504833-chr12:12508269..12511200,3	K562	blood:
27	chr12:12529340..12531603-chr12:12711147..12714466,3	MCF-7	breast:
28	chr12:12529157..12530332-chr12:12857224..12858201,8	MCF-7	breast:
29	chr12:12529613..12530179-chr12:12808665..12809480,2	MCF-7	breast:
30	chr12:12509330..12511597-chr12:12874960..12877485,2	K562	blood:
31	chr12:12529698..12531231-chr12:12536062..12538015,2	K562	blood:
32	chr12:12517934..12520693-chr12:12524024..12526072,2	MCF-7	breast:
33	chr12:12522631..12525556-chr12:12525783..12528472,2	MCF-7	breast:
34	chr12:12529065..12530274-chr12:12856801..12858158,7	K562	blood:
35	chr12:12500672..12504766-chr12:12505204..12507584,5	K562	blood:
36	chr12:12531751..12533905-chr12:12536172..12537730,2	K562	blood:
37	chr12:12508560..12511489-chr12:12514245..12515884,2	MCF-7	breast:
38	chr12:12419370..12422118-chr12:12510348..12512093,2	MCF-7	breast:
39	chr12:12507773..12511633-chr12:12848137..12852132,5	K562	blood:
40	chr12:12502870..12505613-chr12:12507814..12511200,4	K562	blood:
41	chr12:12510176..12510943-chr19:3500464..3501174,2	Hela-S3	cervix:
42	chr12:12505451..12508886-chr12:12510975..12514166,3	K562	blood:
43	chr12:12510093..12511651-chr12:12512844..12515772,2	K562	blood:
44	chr12:12505451..12508886-chr12:12510975..12514166,3	K562	blood:
45	chr12:12539967..12541683-chr12:12547549..12549266,2	MCF-7	breast:
46	chr12:12419774..12421330-chr12:12508637..12511348,2	MCF-7	breast:
47	chr12:12518944..12521734-chr12:12847277..12849075,2	MCF-7	breast:
48	chr12:12505582..12507087-chr12:12510779..12513309,2	MCF-7	breast:
49	chr12:12507988..12510235-chr12:12714031..12716523,2	MCF-7	breast:
50	chr12:12525607..12527513-chrX:39488072..39490988,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007621.1-1	chr12:12508344-12509739	XLOC_010020
2	lnc-AC007621.1-1	chr12:12509862-12510001	XLOC_010020
3	lnc-AC007621.1-1	chr12:12509862-12510001	NR_024061
4	lnc-AC007621.1-1	chr12:12508342-12509739	NR_024061

No data

Variant related genes	Relation type
MANSC1	TF binding region
LOH12CR1	TF binding region
LOH12CR2	TF binding region
MANSC1	CpG island
LOH12CR1	CpG island
LOH12CR2	CpG island
ENSG00000114391	chromatin interactions
ENSG00000205791	chromatin interactions
ENSG00000183150	chromatin interactions
ENSG00000106526	chromatin interactions
ENSG00000214078	chromatin interactions
ENSG00000111266	chromatin interactions
ENSG00000111276	chromatin interactions
ENSG00000111261	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000070018	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000244462	chromatin interactions
ENSG00000105483	chromatin interactions
ENSG00000129932	chromatin interactions
ENSG00000256658	chromatin interactions
ENSG00000178878	chromatin interactions

Extended variants
information (count: 1501 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1501 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148925668	chr12:12506881-12506882	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs181461297	chr12:12506911-12506912	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs543119293	chr12:12506912-12506913	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs376860965	chr12:12506936-12506937	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs112276668	chr12:12506939-12506940	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs560755793	chr12:12506985-12506986	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372086309	chr12:12507001-12507002	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs528024200	chr12:12507026-12507027	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs186883745	chr12:12507030-12507031	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs144233655	chr12:12507049-12507050	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs531947727	chr12:12507054-12507055	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs146573632	chr12:12507070-12507071	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs563085282	chr12:12507084-12507085	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs190126677	chr12:12507120-12507121	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs535841430	chr12:12507121-12507122	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs11054839	chr12:12507135-12507136	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372975544	chr12:12507213-12507214	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs369507423	chr12:12507214-12507215	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs75011408	chr12:12507237-12507238	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs141275965	chr12:12507261-12507262	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs558837571	chr12:12507297-12507298	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73279312	chr12:12507343-12507344	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs544407597	chr12:12507421-12507422	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556376805	chr12:12507448-12507449	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs181821536	chr12:12507462-12507463	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186504548	chr12:12507481-12507482	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572008305	chr12:12507488-12507489	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs71457148	chr12:12507552-12507553	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527707121	chr12:12507554-12507555	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs546484586	chr12:12507574-12507575	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564810398	chr12:12507598-12507599	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531765212	chr12:12507599-12507600	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189663724	chr12:12507604-12507605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182328747	chr12:12507678-12507679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs71457149	chr12:12507683-12507684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558280294	chr12:12507685-12507686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145055462	chr12:12507698-12507699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186106798	chr12:12507739-12507740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369039928	chr12:12507771-12507772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552150549	chr12:12507778-12507779	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs191402720	chr12:12507783-12507784	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376896240	chr12:12507803-12507804	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148026289	chr12:12507817-12507818	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556355821	chr12:12507828-12507829	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs574963197	chr12:12507875-12507876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183106496	chr12:12507878-12507879	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554322042	chr12:12507883-12507884	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs60756645	chr12:12507885-12507886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs398044272	chr12:12507898-12507899	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs150162674	chr12:12507903-12507904	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	21088497	CNVD

Chromatin state (count:1506 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12503600-12509200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr12:12503600-12509400	Weak transcription	Fetal Lung	lung
3	chr12:12503800-12509200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:12503800-12509200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr12:12503800-12509200	Weak transcription	Fetal Brain Female	brain
6	chr12:12503800-12509400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:12503800-12509400	Weak transcription	Adipose Nuclei	Adipose
8	chr12:12503800-12509400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr12:12503800-12509400	Weak transcription	Osteobl	bone
10	chr12:12503800-12509600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr12:12503800-12509600	Weak transcription	Fetal Stomach	stomach
12	chr12:12503800-12509600	Weak transcription	HUVEC	blood vessel
13	chr12:12503800-12510000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr12:12504000-12509200	Weak transcription	GM12878-XiMat	blood
15	chr12:12504200-12507000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr12:12504200-12508400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:12504200-12509200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr12:12504200-12509200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr12:12504200-12509200	Weak transcription	Brain Anterior Caudate	brain
20	chr12:12504200-12509200	Weak transcription	Hela-S3	cervix
21	chr12:12504200-12509200	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr12:12504200-12509400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr12:12504200-12509400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr12:12504200-12509400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr12:12504200-12509400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr12:12504200-12509400	Weak transcription	Brain Substantia Nigra	brain
27	chr12:12504200-12509400	Weak transcription	Pancreas	Pancrea
28	chr12:12504200-12509400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr12:12504200-12509600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr12:12504400-12507000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:12504400-12508600	Weak transcription	Primary hematopoietic stem cells	blood
32	chr12:12504400-12509400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:12504400-12509400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr12:12504400-12509400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:12504400-12509400	Weak transcription	Liver	Liver
36	chr12:12504400-12509400	Weak transcription	Brain Angular Gyrus	brain
37	chr12:12504400-12509400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr12:12504400-12509400	Weak transcription	Brain Hippocampus Middle	brain
39	chr12:12504400-12509400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr12:12504400-12509400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr12:12504400-12509400	Weak transcription	Fetal Kidney	kidney
42	chr12:12504400-12509400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr12:12504400-12509400	Weak transcription	Thymus	Thymus
44	chr12:12504400-12510000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:12504600-12509200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr12:12504600-12509200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr12:12504600-12509200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:12504600-12509200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr12:12504600-12509400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:12504600-12509400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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