Variant report

Variant	nsv899560
Chromosome Location	chr12:121371233-121560581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5058)
CpG islands
(count:3360)
Chromatin interactive
region (count:177)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:5058 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121418090-121418322	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:121415630-121415655	K562	blood:	n/a	n/a
3	ARID3A	chr12:121399918-121400154	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:121548072-121548453	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121497991-121498204	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:121523699-121523880	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:121410742-121410940	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:121379851-121379968	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:121463440-121464449	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:121554555-121555038	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:121443216-121443451	K562	blood:	n/a	n/a
12	ARID3A	chr12:121432640-121432909	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:121454126-121454492	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:121416006-121416515	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:121397714-121398030	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:121443210-121443412	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:121455416-121455815	HepG2	liver:	n/a	n/a
18	ATF1	chr12:121480947-121481240	K562	blood:	n/a	n/a
19	ATF1	chr12:121456015-121456311	K562	blood:	n/a	n/a
20	ATF1	chr12:121548142-121548488	K562	blood:	n/a	n/a
21	ATF1	chr12:121554252-121554339	K562	blood:	n/a	n/a
22	ATF1	chr12:121454106-121454550	K562	blood:	n/a	n/a
23	ATF1	chr12:121558234-121558481	K562	blood:	n/a	n/a
24	ATF1	chr12:121529137-121529138	K562	blood:	n/a	n/a
25	ATF1	chr12:121409535-121409969	K562	blood:	n/a	n/a
26	ATF1	chr12:121551788-121552180	K562	blood:	n/a	n/a
27	ATF2	chr12:121454059-121454576	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr12:121547862-121548404	GM12878	blood:	n/a	n/a
29	ATF2	chr12:121397536-121398098	GM12878	blood:	n/a	n/a
30	ATF2	chr12:121476753-121477249	GM12878	blood:	n/a	n/a
31	ATF2	chr12:121454087-121454511	GM12878	blood:	n/a	n/a
32	ATF2	chr12:121548101-121548552	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr12:121397652-121398080	GM12878	blood:	n/a	n/a
34	ATF2	chr12:121533611-121534068	GM12878	blood:	n/a	n/a
35	ATF2	chr12:121454054-121454531	GM12878	blood:	n/a	n/a
36	ATF3	chr12:121454171-121454453	K562	blood:	n/a	chr12:121454331-121454339 chr12:121454330-121454343 chr12:121454330-121454341 chr12:121454332-121454339 chr12:121454329-121454339 chr12:121454336-121454345 chr12:121454332-121454342 chr12:121454330-121454341 chr12:121454328-121454343 chr12:121454332-121454340
37	ATF3	chr12:121548098-121548416	K562	blood:	n/a	n/a
38	ATF3	chr12:121378630-121378970	K562	blood:	n/a	n/a
39	ATF3	chr12:121454074-121454461	H1-hESC	embryonic stem cell:	n/a	chr12:121454331-121454339 chr12:121454330-121454343 chr12:121454330-121454341 chr12:121454332-121454339 chr12:121454329-121454339 chr12:121454336-121454345 chr12:121454332-121454342 chr12:121454330-121454341 chr12:121454328-121454343 chr12:121454332-121454340
40	ATF3	chr12:121419340-121419824	A549	lung:	n/a	n/a
41	ATF3	chr12:121397614-121398071	K562	blood:	n/a	n/a
42	ATF3	chr12:121488586-121488835	GM12878	blood:	n/a	n/a
43	ATF3	chr12:121484435-121484678	K562	blood:	n/a	n/a
44	ATF3	chr12:121382379-121382738	K562	blood:	n/a	n/a
45	ATF3	chr12:121523628-121523846	HepG2	liver:	n/a	n/a
46	BACH1	chr12:121533719-121533919	K562	blood:	n/a	n/a
47	BACH1	chr12:121533616-121534030	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr12:121537496-121537848	GM12878	blood:	n/a	n/a
49	BATF	chr12:121397586-121398075	GM12878	blood:	n/a	n/a
50	BATF	chr12:121382360-121382707	GM12878	blood:	n/a	n/a

(count:3360 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121415499-121415549	SK-N-SH_RA	brain:	n/a
2	chr12:121416315-121416365	Caco-2	colon:	n/a
3	chr12:121476720-121476770	AG04449	skin:	fetal
4	chr12:121454269-121454319	H1-hESC	embryonic stem cell:	embryo
5	chr12:121416510-121416560	HMEC	breast:	n/a
6	chr12:121415499-121415549	SK-N-SH_RA	brain:	n/a
7	chr12:121416315-121416365	Caco-2	colon:	n/a
8	chr12:121476720-121476770	AG04449	skin:	fetal
9	chr12:121454269-121454319	H1-hESC	embryonic stem cell:	embryo
10	chr12:121416510-121416560	HMEC	breast:	n/a
11	chr12:121454272-121454322	HCM	heart:	n/a
12	chr12:121388227-121388277	CMK	blood:	n/a
13	chr12:121443309-121443359	GM06990	blood:	n/a
14	chr12:121420721-121420771	HCT-116	colon:	n/a
15	chr12:121416612-121416662	PFSK-1	brain:	n/a
16	chr12:121416612-121416662	HNPCEpiC	eye:	n/a
17	chr12:121476792-121476842	SK-N-SH	brain:	n/a
18	chr12:121533475-121533525	AG10803	skin:	n/a
19	chr12:121535941-121535991	BJ	skin:	n/a
20	chr12:121441714-121441764	AoSMC	blood vessel:	n/a
21	chr12:121404850-121404900	HRE	kidney:	n/a
22	chr12:121450381-121450431	ProgFib	skin:	n/a
23	chr12:121416315-121416365	NB4	blood:	n/a
24	chr12:121498343-121498393	GM12891	blood:	n/a
25	chr12:121427010-121427060	NH-A	brain:	n/a
26	chr12:121416512-121416562	SK-N-MC	brain:	n/a
27	chr12:121533833-121533883	K562	blood:	n/a
28	chr12:121410855-121410905	NH-A	brain:	n/a
29	chr12:121411269-121411319	Hela-S3	cervix:	n/a
30	chr12:121454162-121454212	SKMC	muscle:	n/a
31	chr12:121410996-121411046	NB4	blood:	n/a
32	chr12:121415506-121415556	AG09319	gingival:	n/a
33	chr12:121513978-121514028	HMEC	breast:	n/a
34	chr12:121477061-121477111	AoSMC	blood vessel:	n/a
35	chr12:121534028-121534078	ProgFib	skin:	n/a
36	chr12:121535941-121535991	HRPEpiC	eye:	n/a
37	chr12:121416512-121416562	Jurkat	blood:	n/a
38	chr12:121498343-121498393	Hepatocyte	liver:	n/a
39	chr12:121454837-121454887	GM12891	blood:	n/a
40	chr12:121454162-121454212	ECC-1	luminal epithelium:	n/a
41	chr12:121454133-121454183	HL-60	blood:	n/a
42	chr12:121450381-121450431	GM06990	blood:	n/a
43	chr12:121416796-121416846	HUVEC	blood vessel:	n/a
44	chr12:121454162-121454212	BE2_C	brain:	n/a
45	chr12:121477061-121477111	AG04450	lung:	fetal
46	chr12:121416612-121416662	HEEpiC	esophagus:	n/a
47	chr12:121454451-121454501	PrEC	prostate:	n/a
48	chr12:121533475-121533525	HCPEpiC	choroid plexus:	n/a
49	chr12:121533833-121533883	MCF-7	breast:	n/a
50	chr12:121454272-121454322	IMR90	lung:	fetal

(count:177 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr12:121454608..121456254-chr12:121460515..121463475,3	K562	blood:
2	chr12:121444400..121446365-chr12:121447661..121449624,2	K562	blood:
3	chr12:121521823..121524170-chr12:121665223..121666931,2	MCF-7	breast:
4	chr12:121533631..121534218-chr12:121667773..121668734,2	K562	blood:
5	chr12:121175837..121176393-chr12:121409274..121410074,2	MCF-7	breast:
6	chr12:121388948..121393139-chr12:121395354..121400145,4	K562	blood:
7	chr12:121388985..121390758-chr12:121403541..121406125,2	K562	blood:
8	chr12:121442812..121445650-chr12:121451524..121454471,3	K562	blood:
9	chr12:121384723..121388163-chr12:121389149..121391910,3	K562	blood:
10	chr12:121548947..121551862-chr12:121555011..121556681,2	MCF-7	breast:
11	chr12:121018462..121021089-chr12:121462711..121464261,2	MCF-7	breast:
12	chr12:121452643..121457408-chr12:121461392..121466070,6	MCF-7	breast:
13	chr12:121427353..121429838-chr12:121441548..121443367,3	K562	blood:
14	chr12:121442771..121443720-chr12:121533793..121534340,2	K562	blood:
15	chr12:121401463..121403474-chr12:121406949..121408762,2	K562	blood:
16	chr12:121447247..121448275-chr12:121533293..121534356,3	MCF-7	breast:
17	chr12:121384723..121388163-chr12:121389149..121391910,3	K562	blood:
18	chr12:121499365..121500300-chr12:121547555..121548757,7	MCF-7	breast:
19	chr12:121421859..121423940-chr12:121426161..121428350,2	K562	blood:
20	chr12:121443251..121443780-chr12:121667749..121668757,4	K562	blood:
21	chr12:121488415..121490899-chr12:121492548..121494191,2	K562	blood:
22	chr12:121427353..121429838-chr12:121441548..121443367,3	K562	blood:
23	chr12:121446939..121449086-chr12:121451348..121453290,2	MCF-7	breast:
24	chr12:121445828..121451054-chr12:121451445..121454709,11	K562	blood:
25	chr12:121498418..121499035-chr12:121547998..121548758,2	K562	blood:
26	chr12:121552705..121555604-chr12:121668224..121669822,2	MCF-7	breast:
27	chr12:121509410..121511926-chr12:121521670..121523636,2	K562	blood:
28	chr12:121409514..121410021-chr12:121548070..121548945,2	K562	blood:
29	chr12:121547509..121549908-chr12:121645627..121647537,2	MCF-7	breast:
30	chr12:121442839..121443768-chr12:121497604..121498594,3	MCF-7	breast:
31	chr12:121443137..121444963-chr12:121449625..121451218,2	K562	blood:
32	chr12:121403725..121406245-chr12:121406756..121408586,2	MCF-7	breast:
33	chr12:121391443..121393286-chr12:121397886..121399951,2	K562	blood:
34	chr12:121499402..121500015-chr12:121931705..121932231,2	MCF-7	breast:
35	chr12:121416581..121418752-chr12:121419164..121421756,2	K562	blood:
36	chr12:121443137..121445900-chr12:121447661..121451218,5	K562	blood:
37	chr12:121555909..121558170-chr12:121651475..121654023,2	K562	blood:
38	chr12:121410040..121412493-chr12:121417620..121420402,3	MCF-7	breast:
39	chr12:121382478..121383151-chr12:121441198..121441773,2	MCF-7	breast:
40	chr12:121447247..121448275-chr12:121533293..121534356,3	MCF-7	breast:
41	chr12:121463705..121464632-chr12:121497652..121498532,2	MCF-7	breast:
42	chr12:121498058..121498974-chr12:121533466..121534380,2	K562	blood:
43	chr12:121398625..121400416-chr12:121405425..121406992,2	K562	blood:
44	chr12:121174261..121175937-chr12:121403993..121406712,2	MCF-7	breast:
45	chr12:121412159..121414001-chr12:121420552..121422609,2	MCF-7	breast:
46	chr12:121426408..121429065-chr12:121429959..121431966,2	MCF-7	breast:
47	chr12:121463340..121465773-chr12:121472717..121474961,3	MCF-7	breast:
48	chr12:121401463..121403474-chr12:121406949..121408762,2	K562	blood:
49	chr12:121547911..121548611-chr12:121647690..121648251,2	MCF-7	breast:
50	chr12:121498251..121499029-chr12:121533532..121534500,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf43-1	chr12:121418447-121418709	ENSG00000241388.2
2	lnc-C12orf43-1	chr12:121405937-121406811	NONHSAT031257
3	lnc-P2RX7-6	chr12:121517645-121517927	NONHSAT031263
4	lnc-P2RX7-2	chr12:121557252-121558609	XLOC_009912
5	lnc-C12orf43-1	chr12:121407641-121410095	ENSG00000241388.2
6	lnc-C12orf43-1	chr12:121407933-121408173	ENSG00000241388.2
7	lnc-C12orf43-1	chr12:121418447-121418768	ENSG00000241388.2
8	lnc-C12orf43-1	chr12:121410457-121412502	NONHSAT031257
9	lnc-C12orf43-1	chr12:121414602-121414724	ENSG00000241388.2
10	lnc-C12orf43-1	chr12:121408046-121410443	NONHSAT031257
11	lnc-C12orf43-1	chr12:121406416-121406811	ENSG00000241388.2
12	lnc-C12orf43-1	chr12:121412288-121412401	ENSG00000241388.2
13	lnc-C12orf43-1	chr12:121417417-121417550	ENSG00000241388.2
14	lnc-C12orf43-3	chr12:121438289-121439071	ENSG00000271769.1
15	lnc-P2RX7-2	chr12:121557252-121557692	XLOC_009912
16	lnc-P2RX7-2	chr12:121556258-121556287	XLOC_009912
17	lnc-C12orf43-1	chr12:121412188-121412401	ENSG00000241388.2
18	lnc-P2RX7-2	chr12:121555321-121555362	XLOC_009912

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HNF1A	hsa-miR-320a	chr12:121439680-121439702

Variant related genes	Relation type
ENSG00000271769	TF binding region
HNF1A-AS1	TF binding region
ENSG00000223538	TF binding region
ENSG00000272214	TF binding region
HNF1A	TF binding region
ENSG00000201945	TF binding region
ENSG00000256963	TF binding region
C12orf43	TF binding region
OASL	TF binding region
ENSG00000271769	CpG island
HNF1A-AS1	CpG island
ENSG00000223538	CpG island
ENSG00000272214	CpG island
HNF1A	CpG island
ENSG00000201945	CpG island
ENSG00000256963	CpG island
C12orf43	CpG island
OASL	CpG island
ENSG00000256963	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000135100	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000135097	chromatin interactions
ENSG00000157782	chromatin interactions
ENSG00000157837	chromatin interactions
ENSG00000272214	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000157895	chromatin interactions
ENSG00000256569	chromatin interactions
ENSG00000110917	chromatin interactions
ENSG00000241388	chromatin interactions
ENSG00000256008	chromatin interactions
ENSG00000135114	chromatin interactions
ENSG00000271769	chromatin interactions
ENSG00000265455	chromatin interactions
ENSG00000175970	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000135124	chromatin interactions
HIVEP2	miRNA target sites

Extended variants
information (count: 7745 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:7745 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs868795	chr12:121371233-121371234	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567580023	chr12:121371265-121371266	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs536633866	chr12:121371319-121371320	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs115968213	chr12:121371393-121371394	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs373726261	chr12:121371414-121371415	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs564822841	chr12:121371425-121371426	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs113308477	chr12:121371435-121371436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs11065342	chr12:121371436-121371437	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545283805	chr12:121371449-121371450	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs558628471	chr12:121371479-121371480	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs189333223	chr12:121371505-121371506	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs369174744	chr12:121371519-121371520	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs2701191	chr12:121371577-121371578	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs3999400	chr12:121371610-121371611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs3999399	chr12:121371636-121371637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3999398	chr12:121371650-121371651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3999397	chr12:121371710-121371711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200192042	chr12:121371722-121371723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537965709	chr12:121371730-121371731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73224341	chr12:121371731-121371732	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs370823044	chr12:121371736-121371737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561024756	chr12:121371754-121371755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571205191	chr12:121371777-121371778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139740795	chr12:121371778-121371779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113931348	chr12:121371784-121371785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77620531	chr12:121371791-121371792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377269656	chr12:121371793-121371794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370015876	chr12:121371795-121371796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574417352	chr12:121371798-121371799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113532121	chr12:121371809-121371810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11065343	chr12:121371866-121371867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77350597	chr12:121371899-121371900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2004955	chr12:121371941-121371942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2004954	chr12:121371946-121371947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543429262	chr12:121371959-121371960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144852941	chr12:121371963-121371964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73224342	chr12:121372005-121372006	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1106108	chr12:121372033-121372034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181670007	chr12:121372067-121372068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148593490	chr12:121372081-121372082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35883953	chr12:121372113-121372114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs5801410	chr12:121372114-121372115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576773578	chr12:121372115-121372116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533398891	chr12:121372122-121372123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567763961	chr12:121372156-121372157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536302700	chr12:121372257-121372258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550158607	chr12:121372292-121372293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544992209	chr12:121372306-121372307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564972649	chr12:121372323-121372324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185934914	chr12:121372335-121372336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Intracranial arachnoid cysts	20187927	CNVD

Chromatin state (count:3115 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121364400-121374000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:121367000-121374800	Weak transcription	Fetal Intestine Small	intestine
3	chr12:121367400-121394400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:121367600-121374800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:121370800-121371400	Enhancers	Duodenum Mucosa	Duodenum
6	chr12:121370800-121371400	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr12:121370800-121371800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr12:121370800-121373200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr12:121371000-121371400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:121371000-121371600	Enhancers	Placenta	Placenta
11	chr12:121371200-121371400	Weak transcription	Spleen	Spleen
12	chr12:121371200-121371600	Bivalent Enhancer	HepG2	liver
13	chr12:121371200-121375000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:121371200-121380200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr12:121371400-121373400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr12:121371600-121374200	Weak transcription	Placenta	Placenta
17	chr12:121372400-121375600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr12:121373200-121375200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr12:121373400-121373600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr12:121373600-121373800	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr12:121373800-121374000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr12:121373800-121374200	Enhancers	Primary B cells from cord blood	blood
23	chr12:121373800-121374400	Enhancers	GM12878-XiMat	blood
24	chr12:121374000-121374200	Enhancers	Primary B cells from peripheral blood	blood
25	chr12:121374000-121374200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr12:121374000-121374200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr12:121374000-121375600	Enhancers	Placenta Amnion	Placenta Amnion
28	chr12:121374000-121379000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:121374200-121375000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr12:121374200-121375800	Enhancers	Placenta	Placenta
31	chr12:121374800-121375000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr12:121374800-121375200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:121374800-121375200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:121374800-121375600	Enhancers	Fetal Intestine Large	intestine
35	chr12:121374800-121375600	Enhancers	Fetal Intestine Small	intestine
36	chr12:121374800-121375800	Enhancers	HepG2	liver
37	chr12:121375000-121375200	Enhancers	Adipose Nuclei	Adipose
38	chr12:121375000-121375200	Enhancers	Duodenum Mucosa	Duodenum
39	chr12:121375000-121375400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:121375000-121375800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr12:121375200-121377600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr12:121375400-121377600	Weak transcription	Adipose Nuclei	Adipose
43	chr12:121375600-121376000	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr12:121375600-121376800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr12:121375600-121382600	Weak transcription	Fetal Intestine Small	intestine
46	chr12:121375800-121376600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr12:121375800-121377400	Weak transcription	HepG2	liver
48	chr12:121376000-121376800	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:121376200-121378000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:121376600-121377800	Enhancers	Primary hematopoietic stem cells	blood

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