Variant report

Variant	nsv899154
Chromosome Location	chr12:62764909-62811328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:61)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:62807642-62807755	K562	blood:	n/a	n/a
2	ATF1	chr12:62765570-62765612	K562	blood:	n/a	n/a
3	ATF1	chr12:62787812-62787902	K562	blood:	n/a	n/a
4	BACH1	chr12:62792830-62792831	K562	blood:	n/a	n/a
5	BCL3	chr12:62807639-62808318	K562	blood:	n/a	n/a
6	BCL3	chr12:62809633-62810295	K562	blood:	n/a	n/a
7	CCNT2	chr12:62804946-62805509	K562	blood:	n/a	n/a
8	CCNT2	chr12:62804111-62804311	K562	blood:	n/a	n/a
9	CEBPB	chr12:62786904-62787103	K562	blood:	n/a	n/a
10	CEBPB	chr12:62793797-62794038	HepG2	liver:	n/a	chr12:62793908-62793919 chr12:62793909-62793918
11	CEBPB	chr12:62787751-62787797	K562	blood:	n/a	n/a
12	CEBPB	chr12:62787756-62787763	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:62804676-62804876	K562	blood:	n/a	n/a
14	CEBPB	chr12:62802886-62803160	HepG2	liver:	n/a	chr12:62803005-62803016 chr12:62803004-62803017
15	CEBPB	chr12:62802890-62803137	K562	blood:	n/a	chr12:62803005-62803016 chr12:62803004-62803017
16	CHD2	chr12:62808955-62809001	K562	blood:	n/a	n/a
17	CTCF	chr12:62807300-62807450	GM12875	blood:	n/a	n/a
18	CTCF	chr12:62806687-62806714	GM20000	blood:	n/a	n/a
19	CTCF	chr12:62801515-62801607	GM13977	blood:	n/a	n/a
20	CUX1	chr12:62788774-62789113	K562	blood:	n/a	n/a
21	CUX1	chr12:62803095-62803141	K562	blood:	n/a	n/a
22	CUX1	chr12:62766029-62766131	K562	blood:	n/a	n/a
23	E2F4	chr12:62783941-62784244	MCF10A-Er-Src	breast:	n/a	chr12:62784211-62784220
24	E2F4	chr12:62799105-62799269	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr12:62783305-62783489	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr12:62786874-62787068	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr12:62772806-62773148	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr12:62790468-62790834	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr12:62766034-62766156	K562	blood:	n/a	n/a
30	EP300	chr12:62769434-62769841	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr12:62766994-62767028	GM12878	blood:	n/a	n/a
32	EP300	chr12:62769524-62769657	GM12878	blood:	n/a	n/a
33	EP300	chr12:62784539-62784739	K562	blood:	n/a	n/a
34	FOS	chr12:62796873-62797073	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr12:62796882-62797160	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:62787292-62787393	MCF10A-Er-Src	breast:	n/a	n/a
37	FOXA1	chr12:62801387-62801718	HepG2	liver:	n/a	n/a
38	GATA1	chr12:62776512-62776852	PBDEFetal	blood:	n/a	chr12:62776521-62776532
39	GATA1	chr12:62765594-62766283	PBDE	blood:	n/a	chr12:62766076-62766083
40	GATA1	chr12:62770242-62770518	PBDEFetal	blood:	n/a	n/a
41	GATA1	chr12:62763994-62765177	PBDE	blood:	n/a	chr12:62764172-62764182 chr12:62764935-62764944 chr12:62764175-62764182 chr12:62764174-62764184
42	GATA2	chr12:62765998-62766213	SH-SY5Y	brain:	n/a	chr12:62766076-62766083
43	GATA2	chr12:62790378-62790904	SH-SY5Y	brain:	n/a	n/a
44	GATA2	chr12:62765989-62766231	HUVEC	blood vessel:	n/a	chr12:62766076-62766083
45	GATA3	chr12:62798164-62798362	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr12:62790527-62790857	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr12:62794653-62794850	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr12:62765920-62766217	T-47D	breast:	n/a	chr12:62766076-62766083
49	GATA3	chr12:62765994-62766312	MCF-7	breast:	n/a	chr12:62766076-62766083
50	GATA3	chr12:62765922-62766263	MCF-7	breast:	n/a	chr12:62766076-62766083

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:62798679-62798729	A549	lung:	n/a
2	chr12:62798679-62798729	AG09319	gingival:	n/a
3	chr12:62798679-62798729	Hepatocyte	liver:	n/a
4	chr12:62798679-62798729	GM12891	blood:	n/a
5	chr12:62798679-62798729	PANC-1	pancreas:	n/a
6	chr12:62798679-62798729	Caco-2	colon:	n/a
7	chr12:62798679-62798729	HNPCEpiC	eye:	n/a
8	chr12:62798679-62798729	H1-hESC	embryonic stem cell:	embryo
9	chr12:62798679-62798729	HUVEC	blood vessel:	n/a
10	chr12:62798679-62798729	SK-N-SH_RA	brain:	n/a
11	chr12:62798679-62798729	U87	brain:	n/a
12	chr12:62798679-62798729	ovcar-3	ovarian:	n/a
13	chr12:62798679-62798729	Hela-S3	cervix:	n/a
14	chr12:62798679-62798729	BJ	skin:	n/a
15	chr12:62798679-62798729	LNCaP	prostate:	n/a
16	chr12:62798679-62798729	SK-N-SH	brain:	n/a
17	chr12:62798679-62798729	HCF	heart:	n/a
18	chr12:62798679-62798729	HRPEpiC	eye:	n/a
19	chr12:62798679-62798729	HMEC	breast:	n/a
20	chr12:62798679-62798729	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:62798679-62798729	HEK293	kidney:	embryo
22	chr12:62798679-62798729	HEEpiC	esophagus:	n/a
23	chr12:62798679-62798729	PFSK-1	brain:	n/a
24	chr12:62798679-62798729	AoSMC	blood vessel:	n/a
25	chr12:62798679-62798729	MCF10A-Er-Src	breast:	n/a
26	chr12:62798679-62798729	HRE	kidney:	n/a
27	chr12:62798679-62798729	NHBE	bronchial:	n/a
28	chr12:62798679-62798729	HAEpiC	amniotic membrane:	n/a
29	chr12:62798679-62798729	HRCEpiC	kidney:	n/a
30	chr12:62798679-62798729	PrEC	prostate:	n/a
31	chr12:62798679-62798729	BE2_C	brain:	n/a
32	chr12:62798679-62798729	K562	blood:	n/a
33	chr12:62798679-62798729	GM19239	blood:	n/a
34	chr12:62798679-62798729	HL-60	blood:	n/a
35	chr12:62798679-62798729	GM12878	blood:	n/a
36	chr12:62798679-62798729	HepG2	liver:	n/a
37	chr12:62798679-62798729	NB4	blood:	n/a
38	chr12:62798679-62798729	HCM	heart:	n/a
39	chr12:62798679-62798729	AG04449	skin:	fetal
40	chr12:62798679-62798729	AG10803	skin:	n/a
41	chr12:62798679-62798729	IMR90	lung:	fetal
42	chr12:62798679-62798729	CMK	blood:	n/a
43	chr12:62798679-62798729	NH-A	brain:	n/a
44	chr12:62798679-62798729	T-47D	breast:	n/a
45	chr12:62798679-62798729	ECC-1	luminal epithelium:	n/a
46	chr12:62798679-62798729	GM06990	blood:	n/a
47	chr12:62798679-62798729	AG04450	lung:	fetal
48	chr12:62798679-62798729	SK-N-MC	brain:	n/a
49	chr12:62798679-62798729	NHDF-neo	bronchial:	n/a
50	chr12:62798679-62798729	SKMC	muscle:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:62767512..62770487-chr12:62776323..62779154,2	K562	blood:
2	chr12:62653384..62656063-chr12:62775423..62777839,2	K562	blood:
3	chr12:62653268..62654795-chr12:62769057..62770700,2	MCF-7	breast:
4	chr12:62767512..62770487-chr12:62776323..62779154,2	K562	blood:
5	chr12:62783680..62786866-chr12:62789094..62791660,3	K562	blood:
6	chr12:62776192..62779108-chr12:62781541..62783338,2	K562	blood:
7	chr12:62802154..62805925-chr12:62805959..62810469,4	K562	blood:
8	chr12:62773931..62780624-chr12:62782302..62787459,6	K562	blood:
9	chr12:62802223..62804398-chr12:62996125..62998801,2	K562	blood:
10	chr12:62788984..62792175-chr12:62792277..62796551,3	K562	blood:
11	chr12:62802231..62804396-chr12:62807395..62808972,2	K562	blood:
12	chr12:62761857..62764303-chr12:62773893..62776706,2	MCF-7	breast:
13	chr12:62779701..62781218-chr12:62785878..62788849,2	MCF-7	breast:
14	chr12:62772356..62774718-chr12:62776973..62779988,4	K562	blood:
15	chr12:62792054..62795051-chr12:62803056..62804839,2	K562	blood:
16	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
17	chr12:62764382..62767308-chr12:62771022..62773743,2	MCF-7	breast:
18	chr12:62747479..62749492-chr12:62788174..62790462,2	K562	blood:
19	chr12:62768643..62771307-chr12:62782206..62783812,2	MCF-7	breast:
20	chr12:62800166..62802965-chr12:62803094..62805711,2	K562	blood:
21	chr12:62764382..62767308-chr12:62771022..62773743,2	MCF-7	breast:
22	chr12:62802231..62804396-chr12:62807395..62808972,2	K562	blood:
23	chr12:62781223..62783552-chr12:62783907..62785428,2	MCF-7	breast:
24	chr12:62793306..62795703-chr12:62795951..62798733,2	MCF-7	breast:
25	chr12:62809064..62811353-chr12:62812515..62814478,2	K562	blood:
26	chr12:62768949..62769464-chr12:125737941..125738665,2	MCF-7	breast:
27	chr12:62782304..62784105-chr12:62785748..62788359,3	K562	blood:
28	chr12:62800166..62802965-chr12:62803094..62805711,2	K562	blood:
29	chr12:62772356..62774718-chr12:62776973..62779988,4	K562	blood:
30	chr12:62790233..62792343-chr12:62793733..62795768,2	MCF-7	breast:
31	chr12:62776192..62779108-chr12:62781541..62783338,2	K562	blood:
32	chr12:62788984..62792175-chr12:62792277..62796551,3	K562	blood:
33	chr12:62784643..62787168-chr12:62795359..62797740,2	K562	blood:
34	chr12:62781223..62783552-chr12:62783907..62785428,2	MCF-7	breast:
35	chr12:62783680..62786866-chr12:62789094..62791660,3	K562	blood:
36	chr12:62802154..62805925-chr12:62805959..62810469,4	K562	blood:
37	chr12:62761577..62764023-chr12:62770574..62773104,2	K562	blood:
38	chr12:62768643..62771307-chr12:62782206..62783812,2	MCF-7	breast:
39	chr12:62653050..62656025-chr12:62764970..62768543,3	K562	blood:

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP15	hsa-miR-16-5p	chr12:62798422-62798428
2	USP15	hsa-miR-16-5p	chr12:62798406-62798429
3	USP15	hsa-let-7b-5p	chr12:62799457-62799477
4	USP15	hsa-miR-103a-3p	chr12:62798406-62798428
5	USP15	hsa-miR-16-5p	chr12:62799351-62799372
6	USP15	hsa-miR-103a-3p	chr12:62799349-62799371
7	USP15	hsa-miR-16-5p	chr12:62799365-62799371

Variant related genes	Relation type
USP15	TF binding region
USP15	CpG island
ENSG00000199179	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000198673	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000135655	chromatin interactions

Extended variants
information (count: 1563 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1563 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11174446	chr12:62764909-62764910	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542797741	chr12:62764944-62764945	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572292218	chr12:62765010-62765011	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563011441	chr12:62765031-62765032	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs116279081	chr12:62765043-62765044	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs114680299	chr12:62765057-62765058	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368331367	chr12:62765142-62765143	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs188923408	chr12:62765164-62765165	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs191705293	chr12:62765187-62765188	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554766681	chr12:62765216-62765217	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546369702	chr12:62765251-62765252	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs566598189	chr12:62765258-62765259	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376861541	chr12:62765289-62765290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535647463	chr12:62765363-62765364	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182966659	chr12:62765381-62765382	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs574758447	chr12:62765391-62765392	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs11174447	chr12:62765442-62765443	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs73136864	chr12:62765443-62765444	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs557818322	chr12:62765550-62765551	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs17717265	chr12:62765577-62765578	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs534544088	chr12:62765631-62765632	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs554395599	chr12:62765634-62765635	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550862426	chr12:62765635-62765636	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs543211310	chr12:62765700-62765701	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs556358157	chr12:62765746-62765747	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576499431	chr12:62765747-62765748	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143393091	chr12:62765813-62765814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs1496859	chr12:62765830-62765831	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186841902	chr12:62765837-62765838	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372885576	chr12:62765862-62765863	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs151337289	chr12:62766026-62766027	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560397945	chr12:62766042-62766043	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570918998	chr12:62766043-62766044	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372859972	chr12:62766052-62766053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549176124	chr12:62766053-62766054	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs11174448	chr12:62766056-62766057	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs140607961	chr12:62766075-62766076	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs34350513	chr12:62766120-62766121	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs117936650	chr12:62766175-62766176	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533782211	chr12:62766179-62766180	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs145190149	chr12:62766228-62766229	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567973115	chr12:62766275-62766276	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567503669	chr12:62766307-62766308	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556752129	chr12:62766334-62766335	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs137893729	chr12:62766336-62766337	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs527460598	chr12:62766373-62766374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547583557	chr12:62766375-62766376	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs558519489	chr12:62766419-62766420	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572060047	chr12:62766437-62766438	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs36123016	chr12:62766511-62766512	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62701600-62769200	Weak transcription	NHEK	skin
2	chr12:62717000-62769200	Weak transcription	Fetal Kidney	kidney
3	chr12:62717000-62777000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr12:62717000-62783200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:62717000-62784600	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:62717200-62778400	Weak transcription	Hela-S3	cervix
7	chr12:62729800-62776800	Weak transcription	HSMM	muscle
8	chr12:62737600-62784600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:62737600-62786600	Weak transcription	NHLF	lung
10	chr12:62737800-62780200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:62738200-62777000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr12:62738200-62787400	Weak transcription	Spleen	Spleen
13	chr12:62738200-62790600	Weak transcription	Esophagus	oesophagus
14	chr12:62738600-62783400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr12:62738800-62766000	Weak transcription	Aorta	Aorta
16	chr12:62738800-62769000	Weak transcription	Placenta	Placenta
17	chr12:62738800-62784000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr12:62738800-62789600	Weak transcription	Ovary	ovary
19	chr12:62738800-62792800	Weak transcription	Lung	lung
20	chr12:62739000-62775400	Weak transcription	Adipose Nuclei	Adipose
21	chr12:62739600-62782000	Weak transcription	Thymus	Thymus
22	chr12:62739800-62782600	Weak transcription	Fetal Intestine Small	intestine
23	chr12:62741800-62783600	Weak transcription	NHDF-Ad	bronchial
24	chr12:62742000-62786800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:62742600-62775200	Weak transcription	NH-A	brain
26	chr12:62745600-62769000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr12:62747600-62769200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr12:62747800-62777200	Weak transcription	A549	lung
29	chr12:62749600-62772600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr12:62751200-62768000	Weak transcription	HMEC	breast
31	chr12:62751200-62782800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr12:62753400-62770200	Weak transcription	Liver	Liver
33	chr12:62753600-62779800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:62753800-62767800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr12:62755000-62766600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:62755200-62778800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr12:62757200-62782000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr12:62757600-62778400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr12:62757800-62765400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr12:62758200-62766800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr12:62758200-62787400	Weak transcription	Fetal Muscle Leg	muscle
42	chr12:62758600-62769200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:62758800-62765000	Weak transcription	Fetal Thymus	thymus
44	chr12:62758800-62767800	Weak transcription	Primary B cells from cord blood	blood
45	chr12:62758800-62774200	Weak transcription	Dnd41	blood
46	chr12:62758800-62775200	Weak transcription	Duodenum Mucosa	Duodenum
47	chr12:62759000-62766600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:62759000-62775400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:62760000-62782200	Weak transcription	Fetal Lung	lung
50	chr12:62762400-62796600	Weak transcription	Fetal Brain Male	brain

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