Variant report

Variant	nsv560454
Chromosome Location	chr12:121457073-121745742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7013)
CpG islands
(count:5677)
Chromatin interactive
region (count:359)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:7013 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121566791-121567654	K562	blood:	n/a	n/a
2	ARID3A	chr12:121566854-121567036	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121611622-121611771	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:121647887-121647905	K562	blood:	n/a	n/a
5	ARID3A	chr12:121640397-121640895	K562	blood:	n/a	n/a
6	ARID3A	chr12:121647750-121648099	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:121648290-121648307	K562	blood:	n/a	n/a
8	ARID3A	chr12:121548072-121548453	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:121614022-121614252	K562	blood:	n/a	n/a
10	ARID3A	chr12:121562061-121562665	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:121602774-121602971	K562	blood:	n/a	n/a
12	ARID3A	chr12:121652851-121653164	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:121463440-121464449	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:121497991-121498204	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:121668171-121668418	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:121554555-121555038	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:121523699-121523880	HepG2	liver:	n/a	n/a
18	ATF1	chr12:121613883-121614325	K562	blood:	n/a	n/a
19	ATF1	chr12:121548142-121548488	K562	blood:	n/a	n/a
20	ATF1	chr12:121566717-121567709	K562	blood:	n/a	n/a
21	ATF1	chr12:121554252-121554339	K562	blood:	n/a	n/a
22	ATF1	chr12:121634776-121635095	K562	blood:	n/a	n/a
23	ATF1	chr12:121562281-121562579	K562	blood:	n/a	n/a
24	ATF1	chr12:121529137-121529138	K562	blood:	n/a	n/a
25	ATF1	chr12:121582305-121582486	K562	blood:	n/a	n/a
26	ATF1	chr12:121603228-121603427	K562	blood:	n/a	n/a
27	ATF1	chr12:121558234-121558481	K562	blood:	n/a	n/a
28	ATF1	chr12:121569831-121570036	K562	blood:	n/a	n/a
29	ATF1	chr12:121581689-121582010	K562	blood:	n/a	n/a
30	ATF1	chr12:121652834-121653125	K562	blood:	n/a	n/a
31	ATF1	chr12:121613293-121613524	K562	blood:	n/a	n/a
32	ATF1	chr12:121628353-121628648	K562	blood:	n/a	n/a
33	ATF1	chr12:121647676-121648237	K562	blood:	n/a	chr12:121648086-121648100
34	ATF1	chr12:121640398-121641107	K562	blood:	n/a	n/a
35	ATF1	chr12:121551788-121552180	K562	blood:	n/a	n/a
36	ATF1	chr12:121480947-121481240	K562	blood:	n/a	n/a
37	ATF1	chr12:121630917-121631066	K562	blood:	n/a	n/a
38	ATF1	chr12:121570380-121570704	K562	blood:	n/a	n/a
39	ATF1	chr12:121704105-121704314	K562	blood:	n/a	n/a
40	ATF2	chr12:121566798-121567437	GM12878	blood:	n/a	n/a
41	ATF2	chr12:121547862-121548404	GM12878	blood:	n/a	n/a
42	ATF2	chr12:121548101-121548552	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr12:121566714-121567459	GM12878	blood:	n/a	n/a
44	ATF2	chr12:121476753-121477249	GM12878	blood:	n/a	n/a
45	ATF2	chr12:121714720-121715269	GM12878	blood:	n/a	n/a
46	ATF2	chr12:121533611-121534068	GM12878	blood:	n/a	n/a
47	ATF2	chr12:121647637-121648309	GM12878	blood:	n/a	chr12:121648086-121648100
48	ATF2	chr12:121647710-121648229	H1-hESC	embryonic stem cell:	n/a	chr12:121648086-121648100
49	ATF2	chr12:121695530-121695816	GM12878	blood:	n/a	n/a
50	ATF2	chr12:121695443-121695867	GM12878	blood:	n/a	n/a

(count:5677 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121678474-121678524	HEK293	kidney:	embryo
2	chr12:121686604-121686654	K562	blood:	n/a
3	chr12:121661762-121661812	H1-hESC	embryonic stem cell:	embryo
4	chr12:121533668-121533718	ECC-1	luminal epithelium:	n/a
5	chr12:121678474-121678524	HEK293	kidney:	embryo
6	chr12:121686604-121686654	K562	blood:	n/a
7	chr12:121661762-121661812	H1-hESC	embryonic stem cell:	embryo
8	chr12:121533668-121533718	ECC-1	luminal epithelium:	n/a
9	chr12:121666879-121666929	PANC-1	pancreas:	n/a
10	chr12:121738449-121738499	MCF-7	breast:	n/a
11	chr12:121718499-121718549	Caco-2	colon:	n/a
12	chr12:121476792-121476842	AoSMC	blood vessel:	n/a
13	chr12:121718440-121718490	A549	lung:	n/a
14	chr12:121533475-121533525	PrEC	prostate:	n/a
15	chr12:121570677-121570727	ProgFib	skin:	n/a
16	chr12:121718556-121718606	PrEC	prostate:	n/a
17	chr12:121687822-121687872	K562	blood:	n/a
18	chr12:121714889-121714939	GM12878	blood:	n/a
19	chr12:121710771-121710821	AG04450	lung:	fetal
20	chr12:121726240-121726290	HCF	heart:	n/a
21	chr12:121513978-121514028	ovcar-3	ovarian:	n/a
22	chr12:121726240-121726290	GM12878	blood:	n/a
23	chr12:121688441-121688491	AG04449	skin:	fetal
24	chr12:121712245-121712295	CMK	blood:	n/a
25	chr12:121677269-121677319	GM06990	blood:	n/a
26	chr12:121688317-121688367	SK-N-SH_RA	brain:	n/a
27	chr12:121533668-121533718	Hepatocyte	liver:	n/a
28	chr12:121615078-121615128	ECC-1	luminal epithelium:	n/a
29	chr12:121647954-121648004	HMEC	breast:	n/a
30	chr12:121647954-121648004	PrEC	prostate:	n/a
31	chr12:121717737-121717787	HCPEpiC	choroid plexus:	n/a
32	chr12:121647936-121647986	SK-N-SH	brain:	n/a
33	chr12:121708654-121708704	HCPEpiC	choroid plexus:	n/a
34	chr12:121711847-121711897	HCF	heart:	n/a
35	chr12:121666879-121666929	AG10803	skin:	n/a
36	chr12:121666879-121666929	Jurkat	blood:	n/a
37	chr12:121533833-121533883	SKMC	muscle:	n/a
38	chr12:121688416-121688466	NHDF-neo	bronchial:	n/a
39	chr12:121678558-121678608	SKMC	muscle:	n/a
40	chr12:121731226-121731276	NHBE	bronchial:	n/a
41	chr12:121643760-121643810	HEEpiC	esophagus:	n/a
42	chr12:121477854-121477904	SKMC	muscle:	n/a
43	chr12:121712101-121712151	T-47D	breast:	n/a
44	chr12:121659907-121659957	HRE	kidney:	n/a
45	chr12:121533475-121533525	SAEC	small airway:	n/a
46	chr12:121736579-121736629	SAEC	small airway:	n/a
47	chr12:121622315-121622365	HEEpiC	esophagus:	n/a
48	chr12:121513978-121514028	Jurkat	blood:	n/a
49	chr12:121569969-121570019	MCF10A-Er-Src	breast:	n/a
50	chr12:121477854-121477904	SK-N-SH_RA	brain:	n/a

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr12:121664973..121666491-chr12:121668545..121670113,2	K562	blood:
2	chr12:121600298..121602055-chr12:121628900..121630578,2	MCF-7	breast:
3	chr12:121547911..121548611-chr12:121647690..121648251,2	MCF-7	breast:
4	chr12:121442844..121443785-chr12:121547734..121548804,3	K562	blood:
5	chr12:121548947..121551862-chr12:121555011..121556681,2	MCF-7	breast:
6	chr12:121723906..121727301-chr12:121738225..121741362,3	K562	blood:
7	chr12:121737101..121740224-chr12:121740653..121743951,4	K562	blood:
8	chr12:121733797..121736643-chr12:121740237..121742397,2	K562	blood:
9	chr12:121664973..121666491-chr12:121668545..121670113,2	K562	blood:
10	chr12:121574197..121575819-chr12:121598623..121600574,2	MCF-7	breast:
11	chr12:121569572..121570160-chr12:121640475..121641223,2	MCF-7	breast:
12	chr12:121498529..121500527-chr12:121500624..121502278,2	K562	blood:
13	chr12:121454608..121456254-chr12:121460515..121463475,3	K562	blood:
14	chr12:121702788..121704693-chr12:121708345..121710619,2	MCF-7	breast:
15	chr12:121613752..121616874-chr12:121617390..121620030,3	K562	blood:
16	chr12:121628427..121630345-chr12:121646286..121648238,2	K562	blood:
17	chr12:121666865..121669227-chr12:121676180..121679076,2	MCF-7	breast:
18	chr12:121660136..121663309-chr12:121663557..121666409,5	MCF-7	breast:
19	chr12:121629482..121631190-chr12:121637001..121639152,2	K562	blood:
20	chr12:121565146..121566829-chr12:121666395..121668307,2	MCF-7	breast:
21	chr12:121578629..121580685-chr12:121583466..121586479,3	K562	blood:
22	chr12:121676166..121678548-chr12:121679208..121682170,2	K562	blood:
23	chr12:121654852..121658533-chr12:121664523..121668061,3	K562	blood:
24	chr12:121634791..121636567-chr12:121644392..121646560,2	K562	blood:
25	chr12:121734916..121736998-chr12:121837533..121840449,2	MCF-7	breast:
26	chr12:121565146..121566829-chr12:121666395..121668307,2	MCF-7	breast:
27	chr12:121651456..121655222-chr12:121658060..121661321,3	MCF-7	breast:
28	chr12:121523299..121524824-chr12:121646920..121648679,2	MCF-7	breast:
29	chr12:121552705..121555604-chr12:121668224..121669822,2	MCF-7	breast:
30	chr12:121745242..121747818-chr12:121788534..121790623,2	MCF-7	breast:
31	chr12:121673593..121675098-chr12:121676910..121678687,2	K562	blood:
32	chr12:121613447..121614367-chr12:121622707..121623538,6	MCF-7	breast:
33	chr12:121723906..121727301-chr12:121738225..121741362,3	K562	blood:
34	chr12:121499402..121500015-chr12:121931705..121932231,2	MCF-7	breast:
35	chr12:121452592..121454438-chr12:121647839..121649379,2	MCF-7	breast:
36	chr12:121730283..121732631-chr12:121741118..121743378,2	MCF-7	breast:
37	chr12:121730096..121733083-chr12:121733229..121736419,3	K562	blood:
38	chr12:121490675..121493658-chr12:121495456..121497011,2	K562	blood:
39	chr12:121612772..121615002-chr12:121621675..121623747,2	K562	blood:
40	chr12:121552705..121555604-chr12:121668224..121669822,2	MCF-7	breast:
41	chr12:121613752..121616874-chr12:121617390..121620030,3	K562	blood:
42	chr12:121593895..121595665-chr12:121598530..121600220,2	K562	blood:
43	chr12:121647374..121649635-chr12:121733730..121735639,2	K562	blood:
44	chr12:121647374..121649276-chr12:121733272..121735230,2	K562	blood:
45	chr12:121684993..121686828-chr12:121732453..121734188,2	K562	blood:
46	chr12:121639319..121642998-chr12:121646427..121652052,9	MCF-7	breast:
47	chr12:121604306..121607108-chr12:121620261..121622933,3	MCF-7	breast:
48	chr12:121540942..121542575-chr12:121550109..121552835,2	K562	blood:
49	chr12:121698437..121700965-chr12:121702669..121704736,2	K562	blood:
50	chr12:121713150..121717520-chr12:121730584..121734759,5	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-P2RX7-1	chr12:121625345-121625355	NONHSAT031415
2	lnc-P2RX7-2	chr12:121555321-121555362	XLOC_009912
3	lnc-P2RX7-1	chr12:121625359-121625835	ENSG00000261827.1
4	lnc-CAMKK2-6	chr12:121641301-121641403	NONHSAT031413
5	lnc-P2RX7-1	chr12:121625363-121625835	NONHSAT031415
6	lnc-P2RX7-2	chr12:121557252-121558609	XLOC_009912
7	lnc-P2RX7-1	chr12:121626864-121627249	ENSG00000248728
8	lnc-P2RX7-1	chr12:121625339-121626541	ENSG00000248728
9	lnc-CAMKK2-6	chr12:121646389-121646438	NONHSAT031413
10	lnc-CAMKK2-1	chr12:121633051-121633249	ENSG00000214271
11	lnc-P2RX7-6	chr12:121517645-121517927	NONHSAT031263
12	lnc-CAMKK2-6	chr12:121600009-121600220	NONHSAT031413
13	lnc-P2RX7-2	chr12:121556258-121556287	XLOC_009912
14	lnc-P2RX7-2	chr12:121557252-121557692	XLOC_009912

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	P2RX7	hsa-miR-186-5p	chr12:121623370-121623376
2	P2RX7	hsa-miR-150-5p	chr12:121623601-121623622
3	P2RX7	hsa-miR-186-5p	chr12:121623351-121623377

Variant related genes	Relation type
ENSG00000261827	TF binding region
P2RX4	TF binding region
ENSG00000201945	TF binding region
P2RX7	TF binding region
C12orf43	TF binding region
ENSG00000257053	TF binding region
OASL	TF binding region
CAMKK2	TF binding region
ENSG00000223538	TF binding region
ENSG00000256963	TF binding region
ENSG00000261827	CpG island
P2RX4	CpG island
ENSG00000201945	CpG island
P2RX7	CpG island
C12orf43	CpG island
ENSG00000257053	CpG island
OASL	CpG island
CAMKK2	CpG island
ENSG00000223538	CpG island
ENSG00000256963	CpG island
ENSG00000135114	chromatin interactions
ENSG00000148943	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000257053	chromatin interactions
ENSG00000256963	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000114480	chromatin interactions
ENSG00000135124	chromatin interactions
ENSG00000261827	chromatin interactions
ENSG00000245573	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000110931	chromatin interactions
ENSG00000129993	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000089094	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000157895	chromatin interactions
ENSG00000167740	chromatin interactions
ENSG00000089041	chromatin interactions
ENSG00000100519	chromatin interactions
HIVEP2	miRNA target sites
SSH2	miRNA target sites
C9orf167	miRNA target sites
CCNE2	miRNA target sites

Extended variants
information (count: 12428 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:12428 , 50 per page) page: 1 2 3 4 5 6 7 ... 249

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7134141	chr12:121457073-121457074	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573474754	chr12:121457108-121457109	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539282183	chr12:121457154-121457155	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559280376	chr12:121457190-121457191	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575053544	chr12:121457238-121457239	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544072619	chr12:121457241-121457242	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs557304874	chr12:121457242-121457243	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs548805986	chr12:121457261-121457262	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs577357827	chr12:121457276-121457277	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs545685388	chr12:121457305-121457306	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs191141611	chr12:121457318-121457319	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs199615884	chr12:121457329-121457330	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs183029010	chr12:121457381-121457382	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs570149764	chr12:121457432-121457433	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs138910138	chr12:121457477-121457478	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs542256360	chr12:121457495-121457496	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs575977896	chr12:121457533-121457534	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs149398177	chr12:121457543-121457544	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs147080786	chr12:121457550-121457551	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550844386	chr12:121457574-121457575	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs570604348	chr12:121457606-121457607	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs74736552	chr12:121457618-121457619	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138405886	chr12:121457625-121457626	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544901848	chr12:121457765-121457766	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546351496	chr12:121457767-121457768	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs143891609	chr12:121457831-121457832	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2259690	chr12:121457914-121457915	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs554974522	chr12:121457923-121457924	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs568820269	chr12:121457949-121457950	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147246033	chr12:121457961-121457962	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs140707306	chr12:121457982-121457983	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2259693	chr12:121457995-121457996	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186708609	chr12:121458019-121458020	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs28969491	chr12:121458107-121458108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397844229	chr12:121458113-121458114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192627171	chr12:121458126-121458127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2259697	chr12:121458138-121458139	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs183448537	chr12:121458189-121458190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561983472	chr12:121458190-121458191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187784966	chr12:121458213-121458214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532160264	chr12:121458224-121458225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193160729	chr12:121458261-121458262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564418214	chr12:121458320-121458321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545621113	chr12:121458364-121458365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112982500	chr12:121458375-121458376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546410877	chr12:121458377-121458378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199842502	chr12:121458396-121458397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12819210	chr12:121458400-121458401	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs143558393	chr12:121458406-121458407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141382451	chr12:121458411-121458412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Breast cancer	22522925	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:7776 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121454400-121458000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:121454400-121458200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr12:121454400-121458200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:121454400-121458400	Weak transcription	Spleen	Spleen
5	chr12:121454400-121461600	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:121454400-121461800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:121454400-121462600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr12:121454400-121463200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr12:121454400-121463200	Weak transcription	Small Intestine	intestine
10	chr12:121454400-121463600	Weak transcription	Lung	lung
11	chr12:121454400-121464800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:121454400-121471600	Weak transcription	GM12878-XiMat	blood
13	chr12:121454400-121472200	Weak transcription	Primary T cells from cord blood	blood
14	chr12:121454400-121475800	Weak transcription	Adipose Nuclei	Adipose
15	chr12:121454400-121476000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr12:121454400-121476400	Weak transcription	Right Atrium	heart
17	chr12:121454600-121457600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr12:121454600-121457600	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr12:121454600-121457600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:121454600-121457800	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr12:121454600-121458800	Weak transcription	Liver	Liver
22	chr12:121454600-121461400	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr12:121454600-121462400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr12:121454600-121463400	Weak transcription	Hela-S3	cervix
25	chr12:121454600-121463800	Weak transcription	Colonic Mucosa	Colon
26	chr12:121454600-121470200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr12:121454600-121471000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr12:121454600-121471000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:121454600-121471200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr12:121454600-121471600	Weak transcription	Fetal Thymus	thymus
31	chr12:121454600-121476200	Weak transcription	Brain Hippocampus Middle	brain
32	chr12:121454600-121476200	Weak transcription	Gastric	stomach
33	chr12:121454800-121458800	Weak transcription	Stomach Mucosa	stomach
34	chr12:121454800-121461600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr12:121454800-121470400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr12:121454800-121471000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr12:121456400-121458600	Weak transcription	K562	blood
38	chr12:121456800-121459400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr12:121457000-121457200	Enhancers	HepG2	liver
40	chr12:121457600-121459200	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr12:121457600-121461600	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr12:121457600-121466000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr12:121457800-121459200	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr12:121458000-121459200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:121458200-121458800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:121458200-121458800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr12:121458400-121459000	Strong transcription	Spleen	Spleen
48	chr12:121458600-121459000	Enhancers	K562	blood
49	chr12:121458800-121460800	Enhancers	Stomach Mucosa	stomach
50	chr12:121458800-121462000	Weak transcription	Monocytes-CD14+_RO01746	blood

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