Variant report

Variant	nsv1054878
Chromosome Location	chr12:121519880-121761800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5859)
CpG islands
(count:5135)
Chromatin interactive
region (count:328)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:5859 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121647887-121647905	K562	blood:	n/a	n/a
2	ARID3A	chr12:121611622-121611771	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121566791-121567654	K562	blood:	n/a	n/a
4	ARID3A	chr12:121554555-121555038	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121548072-121548453	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:121523699-121523880	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:121602774-121602971	K562	blood:	n/a	n/a
8	ARID3A	chr12:121562061-121562665	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:121652851-121653164	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:121614022-121614252	K562	blood:	n/a	n/a
11	ARID3A	chr12:121647750-121648099	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:121648290-121648307	K562	blood:	n/a	n/a
13	ARID3A	chr12:121566854-121567036	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:121640397-121640895	K562	blood:	n/a	n/a
15	ARID3A	chr12:121668171-121668418	HepG2	liver:	n/a	n/a
16	ATF1	chr12:121582305-121582486	K562	blood:	n/a	n/a
17	ATF1	chr12:121554252-121554339	K562	blood:	n/a	n/a
18	ATF1	chr12:121630917-121631066	K562	blood:	n/a	n/a
19	ATF1	chr12:121613883-121614325	K562	blood:	n/a	n/a
20	ATF1	chr12:121634776-121635095	K562	blood:	n/a	n/a
21	ATF1	chr12:121558234-121558481	K562	blood:	n/a	n/a
22	ATF1	chr12:121613293-121613524	K562	blood:	n/a	n/a
23	ATF1	chr12:121570380-121570704	K562	blood:	n/a	n/a
24	ATF1	chr12:121529137-121529138	K562	blood:	n/a	n/a
25	ATF1	chr12:121704105-121704314	K562	blood:	n/a	n/a
26	ATF1	chr12:121652834-121653125	K562	blood:	n/a	n/a
27	ATF1	chr12:121628353-121628648	K562	blood:	n/a	n/a
28	ATF1	chr12:121551788-121552180	K562	blood:	n/a	n/a
29	ATF1	chr12:121569831-121570036	K562	blood:	n/a	n/a
30	ATF1	chr12:121603228-121603427	K562	blood:	n/a	n/a
31	ATF1	chr12:121640398-121641107	K562	blood:	n/a	n/a
32	ATF1	chr12:121548142-121548488	K562	blood:	n/a	n/a
33	ATF1	chr12:121647676-121648237	K562	blood:	n/a	chr12:121648086-121648100
34	ATF1	chr12:121581689-121582010	K562	blood:	n/a	n/a
35	ATF1	chr12:121562281-121562579	K562	blood:	n/a	n/a
36	ATF1	chr12:121566717-121567709	K562	blood:	n/a	n/a
37	ATF2	chr12:121597229-121597614	GM12878	blood:	n/a	n/a
38	ATF2	chr12:121547862-121548404	GM12878	blood:	n/a	n/a
39	ATF2	chr12:121533611-121534068	GM12878	blood:	n/a	n/a
40	ATF2	chr12:121548101-121548552	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr12:121665091-121665449	GM12878	blood:	n/a	n/a
42	ATF2	chr12:121566714-121567459	GM12878	blood:	n/a	n/a
43	ATF2	chr12:121647710-121648229	H1-hESC	embryonic stem cell:	n/a	chr12:121648086-121648100
44	ATF2	chr12:121714720-121715269	GM12878	blood:	n/a	n/a
45	ATF2	chr12:121695530-121695816	GM12878	blood:	n/a	n/a
46	ATF2	chr12:121581584-121582101	GM12878	blood:	n/a	n/a
47	ATF2	chr12:121647637-121648309	GM12878	blood:	n/a	chr12:121648086-121648100
48	ATF2	chr12:121695443-121695867	GM12878	blood:	n/a	n/a
49	ATF2	chr12:121566798-121567437	GM12878	blood:	n/a	n/a
50	ATF3	chr12:121562226-121562539	K562	blood:	n/a	n/a

(count:5135 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121733425-121733475	AG04450	lung:	fetal
2	chr12:121647128-121647178	U87	brain:	n/a
3	chr12:121735450-121735500	AG10803	skin:	n/a
4	chr12:121570752-121570802	HCF	heart:	n/a
5	chr12:121662577-121662627	NB4	blood:	n/a
6	chr12:121570081-121570131	BE2_C	brain:	n/a
7	chr12:121717737-121717787	AG04450	lung:	fetal
8	chr12:121708654-121708704	HRCEpiC	kidney:	n/a
9	chr12:121570081-121570131	A549	lung:	n/a
10	chr12:121662577-121662627	HEEpiC	esophagus:	n/a
11	chr12:121533475-121533525	AG04449	skin:	fetal
12	chr12:121733425-121733475	AG04450	lung:	fetal
13	chr12:121647128-121647178	U87	brain:	n/a
14	chr12:121735450-121735500	AG10803	skin:	n/a
15	chr12:121570752-121570802	HCF	heart:	n/a
16	chr12:121662577-121662627	NB4	blood:	n/a
17	chr12:121570081-121570131	BE2_C	brain:	n/a
18	chr12:121717737-121717787	AG04450	lung:	fetal
19	chr12:121708654-121708704	HRCEpiC	kidney:	n/a
20	chr12:121570081-121570131	A549	lung:	n/a
21	chr12:121662577-121662627	HEEpiC	esophagus:	n/a
22	chr12:121533475-121533525	AG04449	skin:	fetal
23	chr12:121687747-121687797	HCT-116	colon:	n/a
24	chr12:121726240-121726290	NHDF-neo	bronchial:	n/a
25	chr12:121735631-121735681	PANC-1	pancreas:	n/a
26	chr12:121570081-121570131	SAEC	small airway:	n/a
27	chr12:121735111-121735161	CMK	blood:	n/a
28	chr12:121530737-121530787	GM19239	blood:	n/a
29	chr12:121615078-121615128	A549	lung:	n/a
30	chr12:121647128-121647178	AG09309	skin:	n/a
31	chr12:121688317-121688367	MCF-7	breast:	n/a
32	chr12:121681590-121681640	SK-N-MC	brain:	n/a
33	chr12:121718499-121718549	ProgFib	skin:	n/a
34	chr12:121615201-121615251	Jurkat	blood:	n/a
35	chr12:121570081-121570131	Hepatocyte	liver:	n/a
36	chr12:121659907-121659957	HRCEpiC	kidney:	n/a
37	chr12:121735111-121735161	SAEC	small airway:	n/a
38	chr12:121734283-121734333	IMR90	lung:	fetal
39	chr12:121711996-121712046	HepG2	liver:	n/a
40	chr12:121615201-121615251	ProgFib	skin:	n/a
41	chr12:121678558-121678608	HL-60	blood:	n/a
42	chr12:121718440-121718490	HCM	heart:	n/a
43	chr12:121717886-121717936	SAEC	small airway:	n/a
44	chr12:121647654-121647704	Caco-2	colon:	n/a
45	chr12:121662577-121662627	ovcar-3	ovarian:	n/a
46	chr12:121569924-121569974	GM06990	blood:	n/a
47	chr12:121533668-121533718	SAEC	small airway:	n/a
48	chr12:121570081-121570131	PrEC	prostate:	n/a
49	chr12:121647217-121647267	HCM	heart:	n/a
50	chr12:121711847-121711897	AG04450	lung:	fetal

(count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr12:121533067..121535799-chr12:121628437..121630049,2	K562	blood:
2	chr12:121021041..121021897-chr12:121661173..121662030,2	MCF-7	breast:
3	chr12:119608953..119609635-chr12:121613462..121614267,2	MCF-7	breast:
4	chr12:121629482..121631829-chr12:121636997..121639152,2	K562	blood:
5	chr12:121684993..121686828-chr12:121732453..121734188,2	K562	blood:
6	chr12:121654852..121658533-chr12:121664523..121668061,3	K562	blood:
7	chr12:121590684..121593729-chr12:121595219..121598462,4	K562	blood:
8	chr12:121499365..121500300-chr12:121547555..121548757,7	MCF-7	breast:
9	chr12:121569636..121570366-chr12:121640682..121641273,2	MCF-7	breast:
10	chr12:121521823..121524170-chr12:121665223..121666931,2	MCF-7	breast:
11	chr12:121447247..121448275-chr12:121533293..121534356,3	MCF-7	breast:
12	chr12:121600298..121602055-chr12:121628900..121630578,2	MCF-7	breast:
13	chr12:121570400..121573469-chr12:121573505..121577665,4	K562	blood:
14	chr12:121638895..121643738-chr12:121644037..121648634,7	K562	blood:
15	chr12:121706801..121708995-chr12:121713234..121716382,3	MCF-7	breast:
16	chr12:121547911..121548611-chr12:121647690..121648251,2	MCF-7	breast:
17	chr12:121613752..121616874-chr12:121617390..121620030,3	K562	blood:
18	chr12:121634221..121637382-chr12:121639150..121642465,4	K562	blood:
19	chr12:121719593..121722706-chr12:121731899..121734872,4	K562	blood:
20	chr12:121676166..121678548-chr12:121679208..121682170,2	K562	blood:
21	chr12:121647374..121649276-chr12:121733272..121735230,2	K562	blood:
22	chr12:121666865..121669227-chr12:121676180..121679076,2	MCF-7	breast:
23	chr12:121613447..121614367-chr12:121622707..121623538,6	MCF-7	breast:
24	chr12:121622459..121624219-chr12:121638414..121640723,2	MCF-7	breast:
25	chr12:121612772..121615002-chr12:121621675..121623747,2	K562	blood:
26	chr12:121522589..121524911-chr12:121528205..121530297,3	K562	blood:
27	chr12:121683810..121686610-chr12:121699891..121701425,2	K562	blood:
28	chr12:121602385..121605208-chr12:121610974..121613689,2	MCF-7	breast:
29	chr12:121736650..121739500-chr12:121740653..121743814,3	K562	blood:
30	chr12:121732846..121736440-chr12:121741046..121746496,5	MCF-7	breast:
31	chr12:121713637..121715499-chr12:121719759..121721908,2	MCF-7	breast:
32	chr12:121676166..121678548-chr12:121679208..121682170,2	K562	blood:
33	chr12:121685040..121687317-chr12:121689126..121690781,3	K562	blood:
34	chr12:121533067..121535799-chr12:121628437..121630049,2	K562	blood:
35	chr12:121731583..121733176-chr12:121734919..121737416,2	K562	blood:
36	chr12:121604306..121607108-chr12:121620261..121622933,3	MCF-7	breast:
37	chr12:121550087..121552294-chr12:121646919..121649909,2	MCF-7	breast:
38	chr12:121640765..121641418-chr12:121664955..121665790,2	MCF-7	breast:
39	chr12:121498251..121499029-chr12:121533532..121534500,2	MCF-7	breast:
40	chr12:121606603..121608744-chr12:121610968..121612550,2	K562	blood:
41	chr12:121574197..121575819-chr12:121598623..121600574,2	MCF-7	breast:
42	chr12:121499386..121500506-chr12:121533456..121534392,4	K562	blood:
43	chr12:121559257..121561994-chr12:121565943..121568175,2	K562	blood:
44	chr12:121629482..121631190-chr12:121637001..121639152,2	K562	blood:
45	chr12:121596042..121597903-chr12:121602917..121605232,2	MCF-7	breast:
46	chr12:121525079..121528154-chr12:121532572..121535295,3	MCF-7	breast:
47	chr12:121521510..121523846-chr12:121648119..121649813,2	MCF-7	breast:
48	chr12:121706801..121708995-chr12:121713234..121716382,3	MCF-7	breast:
49	chr12:121731746..121735132-chr12:121837281..121839785,4	K562	blood:
50	chr12:121664133..121666878-chr12:121668504..121670264,2	K562	blood:

(count:13 , 50 per page) page: 1

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

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ANAPC5	hsa-miR-93-5p	chr12:121755888-121755913
2	P2RX7	hsa-miR-150-5p	chr12:121623601-121623622
3	P2RX7	hsa-miR-186-5p	chr12:121623370-121623376
4	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
ANAPC5	TF binding region
ENSG00000257053	TF binding region
CAMKK2	TF binding region
ENSG00000223538	TF binding region
ENSG00000261827	CpG island
P2RX4	CpG island
ENSG00000201945	CpG island
P2RX7	CpG island
ANAPC5	CpG island
ENSG00000257053	CpG island
CAMKK2	CpG island
ENSG00000223538	CpG island
ENSG00000256963	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000261827	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000245573	chromatin interactions
ENSG00000114480	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000148943	chromatin interactions
ENSG00000167740	chromatin interactions
ENSG00000100519	chromatin interactions
ENSG00000089094	chromatin interactions
ENSG00000135124	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000157895	chromatin interactions
ENSG00000110931	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000129993	chromatin interactions
ENSG00000089041	chromatin interactions
ENSG00000257053	chromatin interactions
SSH2	miRNA target sites
C9orf167	miRNA target sites
HIVEP2	miRNA target sites
CCNE2	miRNA target sites

Extended variants
information (count: 10569 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10569 , 50 per page) page: 1 2 3 4 5 6 7 ... 212

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73216105	chr12:121519921-121519922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113165092	chr12:121519941-121519942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542339341	chr12:121519969-121519970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369651723	chr12:121520011-121520012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139680887	chr12:121520034-121520035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533152716	chr12:121520074-121520075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368123192	chr12:121520153-121520154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2464844	chr12:121520157-121520158	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs376034791	chr12:121520168-121520169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537159515	chr12:121520205-121520206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545158307	chr12:121520221-121520222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189793027	chr12:121520231-121520232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541172230	chr12:121520275-121520276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117344076	chr12:121520277-121520278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192876943	chr12:121520283-121520284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144327181	chr12:121520325-121520326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112882707	chr12:121520338-121520339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115858714	chr12:121520352-121520353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140057307	chr12:121520385-121520386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576013291	chr12:121520398-121520399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371890355	chr12:121520400-121520401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111636788	chr12:121520412-121520413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561806848	chr12:121520423-121520424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376745919	chr12:121520440-121520441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369751570	chr12:121520452-121520453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60572958	chr12:121520461-121520462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs550499614	chr12:121520465-121520466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78879677	chr12:121520509-121520510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61688404	chr12:121520510-121520511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34853586	chr12:121520534-121520535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs398070197	chr12:121520536-121520537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184600761	chr12:121520581-121520582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77500317	chr12:121520587-121520588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189536442	chr12:121520609-121520610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551447637	chr12:121520633-121520634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563706272	chr12:121520666-121520667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530863393	chr12:121520676-121520677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549054447	chr12:121520677-121520678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180675531	chr12:121520684-121520685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534866051	chr12:121520757-121520758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200828216	chr12:121520780-121520781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73216108	chr12:121520918-121520919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs186287438	chr12:121520924-121520925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544131000	chr12:121520978-121520979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375561464	chr12:121520986-121520987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539326691	chr12:121521015-121521016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557421358	chr12:121521046-121521047	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575985532	chr12:121521050-121521051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537078006	chr12:121521086-121521087	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555480061	chr12:121521120-121521121	Weak transcription	Chromatin interactive region	1 gene(s)	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
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	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:7396 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121518000-121525200	Weak transcription	Spleen	Spleen
2	chr12:121522000-121522800	Enhancers	K562	blood
3	chr12:121522400-121523200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:121522400-121523400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:121522600-121522800	Bivalent Enhancer	HepG2	liver
6	chr12:121522800-121527000	Weak transcription	K562	blood
7	chr12:121523200-121523600	Bivalent Enhancer	HepG2	liver
8	chr12:121523600-121524200	Flanking Bivalent TSS/Enh	HepG2	liver
9	chr12:121523600-121524400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:121524000-121524200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr12:121524000-121524400	Enhancers	Fetal Muscle Leg	muscle
12	chr12:121524200-121524600	Bivalent Enhancer	HepG2	liver
13	chr12:121524400-121524800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:121524400-121524800	Weak transcription	Fetal Muscle Leg	muscle
15	chr12:121524800-121526400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr12:121524800-121527600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:121524800-121529200	Enhancers	Fetal Muscle Leg	muscle
18	chr12:121525000-121525400	Enhancers	Right Ventricle	heart
19	chr12:121525000-121525800	Enhancers	HSMMtube	muscle
20	chr12:121525000-121526400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:121525000-121526600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:121525200-121525600	Enhancers	Primary hematopoietic stem cells	blood
23	chr12:121525200-121525600	Enhancers	Fetal Muscle Trunk	muscle
24	chr12:121525200-121526000	Enhancers	Dnd41	blood
25	chr12:121525200-121526200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr12:121525200-121526200	Enhancers	Spleen	Spleen
27	chr12:121525200-121527400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr12:121525400-121525600	Enhancers	Adipose Nuclei	Adipose
29	chr12:121525400-121525600	Enhancers	Right Atrium	heart
30	chr12:121525400-121525800	Weak transcription	Right Ventricle	heart
31	chr12:121525400-121526000	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr12:121525400-121526000	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr12:121525400-121526000	Enhancers	Fetal Thymus	thymus
34	chr12:121525400-121526000	Enhancers	Lung	lung
35	chr12:121525400-121526200	Enhancers	Primary T cells fromperipheralblood	blood
36	chr12:121525400-121526200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr12:121525400-121526200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr12:121525400-121526200	Enhancers	GM12878-XiMat	blood
39	chr12:121525400-121529200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr12:121525600-121526000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr12:121525600-121526000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr12:121525600-121526400	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr12:121525600-121526800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr12:121525600-121529400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr12:121525800-121526000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:121525800-121526000	Enhancers	Right Ventricle	heart
47	chr12:121525800-121527000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr12:121525800-121527000	Weak transcription	Adipose Nuclei	Adipose
49	chr12:121526000-121526200	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr12:121526000-121526200	Enhancers	Stomach Mucosa	stomach

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