Variant report

Variant	nsv455729
Chromosome Location	chr12:121525591-121761800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5829)
CpG islands
(count:5135)
Chromatin interactive
region (count:322)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:5829 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121566854-121567036	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:121640397-121640895	K562	blood:	n/a	n/a
3	ARID3A	chr12:121554555-121555038	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:121562061-121562665	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121647750-121648099	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:121648290-121648307	K562	blood:	n/a	n/a
7	ARID3A	chr12:121602774-121602971	K562	blood:	n/a	n/a
8	ARID3A	chr12:121614022-121614252	K562	blood:	n/a	n/a
9	ARID3A	chr12:121611622-121611771	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:121652851-121653164	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:121566791-121567654	K562	blood:	n/a	n/a
12	ARID3A	chr12:121647887-121647905	K562	blood:	n/a	n/a
13	ARID3A	chr12:121548072-121548453	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:121668171-121668418	HepG2	liver:	n/a	n/a
15	ATF1	chr12:121529137-121529138	K562	blood:	n/a	n/a
16	ATF1	chr12:121569831-121570036	K562	blood:	n/a	n/a
17	ATF1	chr12:121630917-121631066	K562	blood:	n/a	n/a
18	ATF1	chr12:121570380-121570704	K562	blood:	n/a	n/a
19	ATF1	chr12:121647676-121648237	K562	blood:	n/a	chr12:121648086-121648100
20	ATF1	chr12:121628353-121628648	K562	blood:	n/a	n/a
21	ATF1	chr12:121640398-121641107	K562	blood:	n/a	n/a
22	ATF1	chr12:121613293-121613524	K562	blood:	n/a	n/a
23	ATF1	chr12:121554252-121554339	K562	blood:	n/a	n/a
24	ATF1	chr12:121634776-121635095	K562	blood:	n/a	n/a
25	ATF1	chr12:121562281-121562579	K562	blood:	n/a	n/a
26	ATF1	chr12:121558234-121558481	K562	blood:	n/a	n/a
27	ATF1	chr12:121603228-121603427	K562	blood:	n/a	n/a
28	ATF1	chr12:121548142-121548488	K562	blood:	n/a	n/a
29	ATF1	chr12:121613883-121614325	K562	blood:	n/a	n/a
30	ATF1	chr12:121652834-121653125	K562	blood:	n/a	n/a
31	ATF1	chr12:121704105-121704314	K562	blood:	n/a	n/a
32	ATF1	chr12:121582305-121582486	K562	blood:	n/a	n/a
33	ATF1	chr12:121581689-121582010	K562	blood:	n/a	n/a
34	ATF1	chr12:121566717-121567709	K562	blood:	n/a	n/a
35	ATF1	chr12:121551788-121552180	K562	blood:	n/a	n/a
36	ATF2	chr12:121547862-121548404	GM12878	blood:	n/a	n/a
37	ATF2	chr12:121714720-121715269	GM12878	blood:	n/a	n/a
38	ATF2	chr12:121647710-121648229	H1-hESC	embryonic stem cell:	n/a	chr12:121648086-121648100
39	ATF2	chr12:121597229-121597614	GM12878	blood:	n/a	n/a
40	ATF2	chr12:121581584-121582101	GM12878	blood:	n/a	n/a
41	ATF2	chr12:121533611-121534068	GM12878	blood:	n/a	n/a
42	ATF2	chr12:121566714-121567459	GM12878	blood:	n/a	n/a
43	ATF2	chr12:121695530-121695816	GM12878	blood:	n/a	n/a
44	ATF2	chr12:121695443-121695867	GM12878	blood:	n/a	n/a
45	ATF2	chr12:121665091-121665449	GM12878	blood:	n/a	n/a
46	ATF2	chr12:121566798-121567437	GM12878	blood:	n/a	n/a
47	ATF2	chr12:121647637-121648309	GM12878	blood:	n/a	chr12:121648086-121648100
48	ATF2	chr12:121548101-121548552	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF3	chr12:121562226-121562539	K562	blood:	n/a	n/a
50	ATF3	chr12:121581608-121581979	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	chr12:121622315-121622365	NHBE	bronchial:	n/a
2	chr12:121718499-121718549	HRE	kidney:	n/a
3	chr12:121712245-121712295	H1-hESC	embryonic stem cell:	embryo
4	chr12:121735396-121735446	NT2-D1	testis:	n/a
5	chr12:121718556-121718606	HRE	kidney:	n/a
6	chr12:121533801-121533851	SKMC	muscle:	n/a
7	chr12:121735139-121735189	HRE	kidney:	n/a
8	chr12:121666925-121666975	MCF-7	breast:	n/a
9	chr12:121708654-121708704	ProgFib	skin:	n/a
10	chr12:121735363-121735413	IMR90	lung:	fetal
11	chr12:121686502-121686552	HepG2	liver:	n/a
12	chr12:121622315-121622365	NHBE	bronchial:	n/a
13	chr12:121718499-121718549	HRE	kidney:	n/a
14	chr12:121712245-121712295	H1-hESC	embryonic stem cell:	embryo
15	chr12:121735396-121735446	NT2-D1	testis:	n/a
16	chr12:121718556-121718606	HRE	kidney:	n/a
17	chr12:121533801-121533851	SKMC	muscle:	n/a
18	chr12:121735139-121735189	HRE	kidney:	n/a
19	chr12:121666925-121666975	MCF-7	breast:	n/a
20	chr12:121708654-121708704	ProgFib	skin:	n/a
21	chr12:121735363-121735413	IMR90	lung:	fetal
22	chr12:121686502-121686552	HepG2	liver:	n/a
23	chr12:121662577-121662627	GM12891	blood:	n/a
24	chr12:121688416-121688466	H1-hESC	embryonic stem cell:	embryo
25	chr12:121718440-121718490	NB4	blood:	n/a
26	chr12:121688441-121688491	H1-hESC	embryonic stem cell:	embryo
27	chr12:121615201-121615251	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:121647936-121647986	Hepatocyte	liver:	n/a
29	chr12:121714889-121714939	HEK293	kidney:	embryo
30	chr12:121647654-121647704	ovcar-3	ovarian:	n/a
31	chr12:121671600-121671650	NB4	blood:	n/a
32	chr12:121534028-121534078	HAEpiC	amniotic membrane:	n/a
33	chr12:121717886-121717936	HRE	kidney:	n/a
34	chr12:121711996-121712046	H1-hESC	embryonic stem cell:	embryo
35	chr12:121647183-121647233	IMR90	lung:	fetal
36	chr12:121662577-121662627	HIPEpiC	eye:	n/a
37	chr12:121569924-121569974	NH-A	brain:	n/a
38	chr12:121711996-121712046	AoSMC	blood vessel:	n/a
39	chr12:121666855-121666905	U87	brain:	n/a
40	chr12:121711996-121712046	ECC-1	luminal epithelium:	n/a
41	chr12:121647183-121647233	SK-N-SH_RA	brain:	n/a
42	chr12:121530737-121530787	AoSMC	blood vessel:	n/a
43	chr12:121711996-121712046	SK-N-MC	brain:	n/a
44	chr12:121735631-121735681	SAEC	small airway:	n/a
45	chr12:121718440-121718490	RPTEC	kidney:	n/a
46	chr12:121686502-121686552	BJ	skin:	n/a
47	chr12:121678720-121678770	NHBE	bronchial:	n/a
48	chr12:121569924-121569974	HepG2	liver:	n/a
49	chr12:121678720-121678770	HRCEpiC	kidney:	n/a
50	chr12:121734283-121734333	NH-A	brain:	n/a

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr12:121555909..121558170-chr12:121651475..121654023,2	K562	blood:
2	chr12:121685040..121687317-chr12:121689126..121690781,3	K562	blood:
3	chr12:121673925..121677209-chr12:121686132..121689078,3	MCF-7	breast:
4	chr12:121634221..121637382-chr12:121639150..121642465,4	K562	blood:
5	chr12:121661635..121663978-chr12:121665688..121668181,3	MCF-7	breast:
6	chr12:121629482..121631829-chr12:121636997..121639152,2	K562	blood:
7	chr12:121528483..121531655-chr12:121531657..121534218,3	MCF-7	breast:
8	chr12:121578629..121580685-chr12:121583466..121586479,3	K562	blood:
9	chr12:121736650..121739500-chr12:121740653..121743814,3	K562	blood:
10	chr12:121613491..121614418-chr12:121640538..121641644,9	MCF-7	breast:
11	chr12:121668796..121670934-chr12:121675457..121678613,3	MCF-7	breast:
12	chr12:121654296..121656580-chr12:121660522..121663384,2	K562	blood:
13	chr12:121548947..121551862-chr12:121555011..121556681,2	MCF-7	breast:
14	chr12:121568948..121571142-chr12:121574770..121577289,2	MCF-7	breast:
15	chr12:121666081..121668034-chr12:121878369..121881222,2	MCF-7	breast:
16	chr12:121531941..121534103-chr12:121555507..121557731,2	K562	blood:
17	chr12:121593680..121596400-chr12:121646406..121649307,2	K562	blood:
18	chr12:121612772..121615002-chr12:121621675..121623747,2	K562	blood:
19	chr12:121742230..121744210-chr12:121746039..121747596,2	K562	blood:
20	chr12:121562465..121564050-chr12:121566966..121568974,2	MCF-7	breast:
21	chr12:121550087..121552294-chr12:121646919..121649909,2	MCF-7	breast:
22	chr12:121660136..121663309-chr12:121663557..121666409,5	MCF-7	breast:
23	chr12:121666865..121669227-chr12:121676180..121679076,2	MCF-7	breast:
24	chr12:121629482..121631190-chr12:121637001..121639152,2	K562	blood:
25	chr12:121608796..121609410-chr12:121640363..121641099,2	MCF-7	breast:
26	chr12:121602385..121605208-chr12:121610974..121613689,2	MCF-7	breast:
27	chr12:121569656..121570427-chr12:121608922..121609716,2	MCF-7	breast:
28	chr12:121600298..121602055-chr12:121628900..121630578,2	MCF-7	breast:
29	chr12:121604306..121607108-chr12:121620261..121622933,3	MCF-7	breast:
30	chr12:121602385..121605208-chr12:121610974..121613689,2	MCF-7	breast:
31	chr12:121592630..121595667-chr12:121601270..121604261,3	K562	blood:
32	chr12:121631393..121634582-chr12:121643500..121647311,3	K562	blood:
33	chr12:121603770..121605309-chr12:121647342..121649708,2	MCF-7	breast:
34	chr12:121521510..121523846-chr12:121648119..121649813,2	MCF-7	breast:
35	chr12:121708573..121710146-chr12:121731716..121734639,2	MCF-7	breast:
36	chr12:121684993..121686828-chr12:121732453..121734188,2	K562	blood:
37	chr12:121647374..121649635-chr12:121733730..121735639,2	K562	blood:
38	chr12:121528483..121531655-chr12:121531657..121534218,3	MCF-7	breast:
39	chr12:121613752..121616874-chr12:121617390..121620030,3	K562	blood:
40	chr12:121609945..121611555-chr12:121644993..121647388,2	MCF-7	breast:
41	chr12:121561837..121563360-chr12:121583686..121585355,2	K562	blood:
42	chr12:121559257..121561994-chr12:121565943..121568175,2	K562	blood:
43	chr12:121559081..121561979-chr12:121605012..121606674,2	MCF-7	breast:
44	chr12:121733327..121735828-chr12:121789056..121791412,2	MCF-7	breast:
45	chr12:121634791..121636567-chr12:121644392..121646560,2	K562	blood:
46	chr12:121612772..121615002-chr12:121621675..121623747,2	K562	blood:
47	chr12:121596042..121597903-chr12:121602917..121605232,2	MCF-7	breast:
48	chr12:121629482..121631190-chr12:121637001..121639152,2	K562	blood:
49	chr12:121447305..121448170-chr12:121547918..121548565,2	MCF-7	breast:
50	chr12:121698437..121700965-chr12:121702669..121704736,2	K562	blood:

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

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

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-186-5p	chr12:121623351-121623377
3	P2RX7	hsa-miR-186-5p	chr12:121623370-121623376
4	P2RX7	hsa-miR-150-5p	chr12:121623601-121623622

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
ENSG00000114480	chromatin interactions
ENSG00000157895	chromatin interactions
ENSG00000110931	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000100519	chromatin interactions
ENSG00000148943	chromatin interactions
ENSG00000245573	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000129993	chromatin interactions
ENSG00000167740	chromatin interactions
ENSG00000089094	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000135124	chromatin interactions
ENSG00000089041	chromatin interactions
ENSG00000257053	chromatin interactions
ENSG00000256963	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000261827	chromatin interactions
SSH2	miRNA target sites
CCNE2	miRNA target sites
C9orf167	miRNA target sites
HIVEP2	miRNA target sites

Extended variants
information (count: 10367 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10367 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12819930	chr12:121525591-121525592	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371696605	chr12:121525646-121525647	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142975253	chr12:121525657-121525658	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs10492051	chr12:121525666-121525667	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs550150585	chr12:121525682-121525683	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559985276	chr12:121525705-121525706	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568460338	chr12:121525710-121525711	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567934361	chr12:121525768-121525769	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs368019121	chr12:121525779-121525780	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs372045815	chr12:121525874-121525875	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187813968	chr12:121525881-121525882	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2708092	chr12:121525886-121525887	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
13	rs146109065	chr12:121525891-121525892	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558340137	chr12:121525895-121525896	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs140078336	chr12:121525899-121525900	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs78789864	chr12:121525932-121525933	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs191436165	chr12:121525965-121525966	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs574081651	chr12:121525991-121525992	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs572788125	chr12:121525996-121525997	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112693489	chr12:121526174-121526175	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs183609962	chr12:121526189-121526190	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11065427	chr12:121526197-121526198	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538720802	chr12:121526221-121526222	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs74581461	chr12:121526249-121526250	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575079448	chr12:121526259-121526260	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545636977	chr12:121526304-121526305	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs543968500	chr12:121526329-121526330	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564274279	chr12:121526334-121526335	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531581134	chr12:121526368-121526369	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550089704	chr12:121526371-121526372	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149375532	chr12:121526391-121526392	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529249043	chr12:121526422-121526423	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547791484	chr12:121526501-121526502	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189432142	chr12:121526503-121526504	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs539926128	chr12:121526542-121526543	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551631428	chr12:121526587-121526588	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79865213	chr12:121526588-121526589	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144699258	chr12:121526598-121526599	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs555620917	chr12:121526644-121526645	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs76515243	chr12:121526668-121526669	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs574018170	chr12:121526678-121526679	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs535074314	chr12:121526680-121526681	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148503788	chr12:121526695-121526696	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181829677	chr12:121526707-121526708	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs553926896	chr12:121526719-121526720	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs185421868	chr12:121526756-121526757	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199925981	chr12:121526836-121526837	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142720298	chr12:121526862-121526863	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs561935051	chr12:121526879-121526880	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs77867358	chr12:121526885-121526886	Enhancers Weak transcription	Chromatin interactive region	2 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:7382 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121522800-121527000	Weak transcription	K562	blood
2	chr12:121524800-121526400	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr12:121524800-121527600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:121524800-121529200	Enhancers	Fetal Muscle Leg	muscle
5	chr12:121525000-121525800	Enhancers	HSMMtube	muscle
6	chr12:121525000-121526400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:121525000-121526600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:121525200-121525600	Enhancers	Primary hematopoietic stem cells	blood
9	chr12:121525200-121525600	Enhancers	Fetal Muscle Trunk	muscle
10	chr12:121525200-121526000	Enhancers	Dnd41	blood
11	chr12:121525200-121526200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr12:121525200-121526200	Enhancers	Spleen	Spleen
13	chr12:121525200-121527400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr12:121525400-121525600	Enhancers	Adipose Nuclei	Adipose
15	chr12:121525400-121525600	Enhancers	Right Atrium	heart
16	chr12:121525400-121525800	Weak transcription	Right Ventricle	heart
17	chr12:121525400-121526000	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr12:121525400-121526000	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr12:121525400-121526000	Enhancers	Fetal Thymus	thymus
20	chr12:121525400-121526000	Enhancers	Lung	lung
21	chr12:121525400-121526200	Enhancers	Primary T cells fromperipheralblood	blood
22	chr12:121525400-121526200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:121525400-121526200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr12:121525400-121526200	Enhancers	GM12878-XiMat	blood
25	chr12:121525400-121529200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr12:121525600-121526000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr12:121525600-121526000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:121525600-121526400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr12:121525600-121526800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr12:121525600-121529400	Weak transcription	Primary hematopoietic stem cells	blood
31	chr12:121525800-121526000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr12:121525800-121526000	Enhancers	Right Ventricle	heart
33	chr12:121525800-121527000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr12:121525800-121527000	Weak transcription	Adipose Nuclei	Adipose
35	chr12:121526000-121526200	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr12:121526000-121526200	Enhancers	Stomach Mucosa	stomach
37	chr12:121526000-121527000	Weak transcription	Lung	lung
38	chr12:121526000-121527800	Weak transcription	Right Atrium	heart
39	chr12:121526000-121528600	Weak transcription	Fetal Thymus	thymus
40	chr12:121526000-121528800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr12:121526000-121529600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr12:121526000-121529600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr12:121526000-121530000	Weak transcription	Dnd41	blood
44	chr12:121526000-121533400	Weak transcription	Right Ventricle	heart
45	chr12:121526200-121527200	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr12:121526200-121527400	Weak transcription	Spleen	Spleen
47	chr12:121526200-121529200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:121526200-121529600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr12:121526200-121529600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr12:121526200-121530200	Weak transcription	GM12878-XiMat	blood

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