Variant report

Variant	nsv899565
Chromosome Location	chr12:121641509-121698785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2214)
CpG islands
(count:2074)
Chromatin interactive
region (count:106)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2214 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121647750-121648099	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:121652851-121653164	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121648290-121648307	K562	blood:	n/a	n/a
4	ARID3A	chr12:121668171-121668418	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121647887-121647905	K562	blood:	n/a	n/a
6	ATF1	chr12:121647676-121648237	K562	blood:	n/a	chr12:121648086-121648100
7	ATF1	chr12:121652834-121653125	K562	blood:	n/a	n/a
8	ATF2	chr12:121647710-121648229	H1-hESC	embryonic stem cell:	n/a	chr12:121648086-121648100
9	ATF2	chr12:121695443-121695867	GM12878	blood:	n/a	n/a
10	ATF2	chr12:121665091-121665449	GM12878	blood:	n/a	n/a
11	ATF2	chr12:121695530-121695816	GM12878	blood:	n/a	n/a
12	ATF2	chr12:121647637-121648309	GM12878	blood:	n/a	chr12:121648086-121648100
13	ATF3	chr12:121690579-121690811	K562	blood:	n/a	n/a
14	BACH1	chr12:121647997-121648245	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr12:121668171-121668466	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr12:121648005-121648095	K562	blood:	n/a	n/a
17	BATF	chr12:121665014-121665421	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:121697017-121697244	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:121647701-121648284	GM12878	blood:	n/a	n/a
20	BCLAF1	chr12:121665096-121665464	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:121695445-121695888	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:121686384-121686778	GM12878	blood:	n/a	n/a
23	BCLAF1	chr12:121647703-121648385	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:121661666-121661989	K562	blood:	n/a	n/a
25	BHLHE40	chr12:121695489-121696026	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:121686365-121686733	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:121668157-121668379	K562	blood:	n/a	n/a
28	BHLHE40	chr12:121647724-121648214	HepG2	liver:	n/a	n/a
29	BHLHE40	chr12:121665104-121665375	GM12878	blood:	n/a	chr12:121665216-121665232
30	BHLHE40	chr12:121647633-121648407	K562	blood:	n/a	n/a
31	BHLHE40	chr12:121661226-121661679	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:121648744-121648827	K562	blood:	n/a	n/a
33	BHLHE40	chr12:121647625-121648261	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:121696926-121697304	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:121660712-121660918	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:121678421-121678447	K562	blood:	n/a	n/a
37	BRCA1	chr12:121665350-121665456	GM12878	blood:	n/a	n/a
38	BRCA1	chr12:121668326-121668330	HepG2	liver:	n/a	n/a
39	BRCA1	chr12:121647781-121647842	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr12:121668071-121668420	K562	blood:	n/a	n/a
41	CBX3	chr12:121643269-121643625	K562	blood:	n/a	n/a
42	CBX3	chr12:121647381-121648621	K562	blood:	n/a	n/a
43	CBX3	chr12:121652738-121653581	HCT-116	colon:	n/a	n/a
44	CCNT2	chr12:121647421-121648519	K562	blood:	n/a	n/a
45	CEBPB	chr12:121648069-121648554	MCF-7	breast:	n/a	n/a
46	CEBPB	chr12:121693515-121693578	K562	blood:	n/a	chr12:121693549-121693560
47	CEBPB	chr12:121648021-121648479	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:121664307-121664458	Hela-S3	cervix:	n/a	chr12:121664392-121664403
49	CEBPB	chr12:121664268-121664657	MCF-7	breast:	n/a	chr12:121664392-121664403
50	CEBPB	chr12:121652036-121653420	HCT-116	colon:	n/a	n/a

(count:2074 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121678720-121678770	GM12878	blood:	n/a
2	chr12:121647217-121647267	NT2-D1	testis:	n/a
3	chr12:121686604-121686654	ovcar-3	ovarian:	n/a
4	chr12:121687619-121687669	GM06990	blood:	n/a
5	chr12:121678558-121678608	GM12891	blood:	n/a
6	chr12:121647954-121648004	Hepatocyte	liver:	n/a
7	chr12:121643760-121643810	HCT-116	colon:	n/a
8	chr12:121662577-121662627	SAEC	small airway:	n/a
9	chr12:121666855-121666905	BE2_C	brain:	n/a
10	chr12:121687822-121687872	NHBE	bronchial:	n/a
11	chr12:121686502-121686552	HCM	heart:	n/a
12	chr12:121659907-121659957	HUVEC	blood vessel:	n/a
13	chr12:121678474-121678524	A549	lung:	n/a
14	chr12:121671600-121671650	AoSMC	blood vessel:	n/a
15	chr12:121648093-121648143	HCPEpiC	choroid plexus:	n/a
16	chr12:121647654-121647704	Caco-2	colon:	n/a
17	chr12:121659907-121659957	SKMC	muscle:	n/a
18	chr12:121688459-121688509	IMR90	lung:	fetal
19	chr12:121677269-121677319	MCF10A-Er-Src	breast:	n/a
20	chr12:121681590-121681640	AG09309	skin:	n/a
21	chr12:121687747-121687797	AG04449	skin:	fetal
22	chr12:121647936-121647986	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:121647217-121647267	ECC-1	luminal epithelium:	n/a
24	chr12:121666879-121666929	GM06990	blood:	n/a
25	chr12:121647954-121648004	HCPEpiC	choroid plexus:	n/a
26	chr12:121678558-121678608	NHBE	bronchial:	n/a
27	chr12:121647654-121647704	HCF	heart:	n/a
28	chr12:121666925-121666975	AG10803	skin:	n/a
29	chr12:121666879-121666929	Hela-S3	cervix:	n/a
30	chr12:121687619-121687669	PFSK-1	brain:	n/a
31	chr12:121678474-121678524	GM12891	blood:	n/a
32	chr12:121659907-121659957	HNPCEpiC	eye:	n/a
33	chr12:121666879-121666929	GM19239	blood:	n/a
34	chr12:121671600-121671650	AG09309	skin:	n/a
35	chr12:121686604-121686654	PFSK-1	brain:	n/a
36	chr12:121647205-121647255	PFSK-1	brain:	n/a
37	chr12:121678474-121678524	MCF10A-Er-Src	breast:	n/a
38	chr12:121671600-121671650	HCM	heart:	n/a
39	chr12:121648450-121648500	HUVEC	blood vessel:	n/a
40	chr12:121678474-121678524	LNCaP	prostate:	n/a
41	chr12:121647128-121647178	IMR90	lung:	fetal
42	chr12:121688317-121688367	NHBE	bronchial:	n/a
43	chr12:121647177-121647227	PFSK-1	brain:	n/a
44	chr12:121688317-121688367	RPTEC	kidney:	n/a
45	chr12:121687747-121687797	NHBE	bronchial:	n/a
46	chr12:121643760-121643810	GM06990	blood:	n/a
47	chr12:121647654-121647704	LNCaP	prostate:	n/a
48	chr12:121686604-121686654	NB4	blood:	n/a
49	chr12:121661762-121661812	AoSMC	blood vessel:	n/a
50	chr12:121659614-121659664	AG09309	skin:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:121604725..121607272-chr12:121663466..121665293,2	MCF-7	breast:
2	chr12:121648201..121650106-chr12:121683652..121685529,2	K562	blood:
3	chr12:121653275..121655297-chr12:121661373..121663256,2	MCF-7	breast:
4	chr12:121646468..121649464-chr12:121663700..121666381,2	K562	blood:
5	chr12:121673925..121677209-chr12:121686132..121689078,3	MCF-7	breast:
6	chr12:121521823..121524170-chr12:121665223..121666931,2	MCF-7	breast:
7	chr12:121646473..121649457-chr12:121658577..121662737,5	MCF-7	breast:
8	chr12:121565146..121566829-chr12:121666395..121668307,2	MCF-7	breast:
9	chr12:121660136..121663309-chr12:121663557..121666409,5	MCF-7	breast:
10	chr12:121643831..121646083-chr12:121646427..121647950,2	MCF-7	breast:
11	chr12:121613534..121614299-chr12:121664938..121665536,2	MCF-7	breast:
12	chr12:121638580..121643612-chr12:121646421..121651534,9	MCF-7	breast:
13	chr12:121646834..121652613-chr12:121661734..121667006,9	MCF-7	breast:
14	chr12:121638895..121643738-chr12:121644037..121648634,7	K562	blood:
15	chr12:121673925..121677209-chr12:121686132..121689078,3	MCF-7	breast:
16	chr12:121683810..121686610-chr12:121699891..121701425,2	K562	blood:
17	chr12:121685040..121687317-chr12:121689126..121690781,3	K562	blood:
18	chr12:121547509..121549908-chr12:121645627..121647537,2	MCF-7	breast:
19	chr12:121666865..121669227-chr12:121676180..121679076,2	MCF-7	breast:
20	chr12:121698437..121700965-chr12:121702669..121704736,2	K562	blood:
21	chr12:121660136..121663309-chr12:121663557..121666409,5	MCF-7	breast:
22	chr12:121521510..121523846-chr12:121648119..121649813,2	MCF-7	breast:
23	chr12:121651456..121655222-chr12:121658060..121661321,3	MCF-7	breast:
24	chr12:121653697..121655351-chr12:121657528..121659193,2	K562	blood:
25	chr12:120965472..120968197-chr12:121646463..121648820,2	K562	blood:
26	chr12:121648201..121650106-chr12:121683652..121685529,2	K562	blood:
27	chr12:121533631..121534218-chr12:121667773..121668734,2	K562	blood:
28	chr12:121552789..121554818-chr12:121661360..121664343,2	MCF-7	breast:
29	chr12:121647374..121649635-chr12:121733730..121735639,2	K562	blood:
30	chr12:121670055..121672601-chr12:121677371..121679007,2	K562	blood:
31	chr12:121664342..121666780-chr12:121734216..121737104,3	MCF-7	breast:
32	chr12:121676166..121678548-chr12:121679208..121682170,2	K562	blood:
33	chr12:121666090..121669827-chr12:121670263..121674205,6	K562	blood:
34	chr12:121552705..121555604-chr12:121668224..121669822,2	MCF-7	breast:
35	chr12:121685040..121687317-chr12:121689126..121690781,3	K562	blood:
36	chr12:121647374..121649276-chr12:121733272..121735230,2	K562	blood:
37	chr12:121634221..121637382-chr12:121639150..121642465,4	K562	blood:
38	chr12:121555909..121558170-chr12:121651475..121654023,2	K562	blood:
39	chr12:121661400..121663391-chr12:121663416..121665222,3	MCF-7	breast:
40	chr12:121661400..121663391-chr12:121663416..121665222,3	MCF-7	breast:
41	chr12:121664133..121666878-chr12:121668504..121670264,2	K562	blood:
42	chr12:121668796..121670934-chr12:121675457..121678613,3	MCF-7	breast:
43	chr12:121646670..121649250-chr12:121789949..121791934,2	K562	blood:
44	chr12:121657033..121659452-chr12:121666561..121668360,2	K562	blood:
45	chr12:121670055..121672601-chr12:121677371..121679007,2	K562	blood:
46	chr12:121659123..121660673-chr12:121663523..121665966,2	K562	blood:
47	chr12:121653275..121655297-chr12:121661373..121663256,2	MCF-7	breast:
48	chr12:121681997..121683544-chr12:121683866..121685441,2	K562	blood:
49	chr12:121666090..121669827-chr12:121670263..121674205,6	K562	blood:
50	chr12:121668796..121670934-chr12:121675457..121678613,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAMKK2-6	chr12:121646389-121646438	NONHSAT031413

No data

Variant related genes	Relation type
CAMKK2	TF binding region
P2RX4	TF binding region
CAMKK2	CpG island
P2RX4	CpG island
ENSG00000129993	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000157895	chromatin interactions
ENSG00000089041	chromatin interactions
ENSG00000089094	chromatin interactions
ENSG00000148943	chromatin interactions
ENSG00000245573	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000110931	chromatin interactions
ENSG00000135124	chromatin interactions

Extended variants
information (count: 2758 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2758 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1169721	chr12:121641509-121641510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185664851	chr12:121641535-121641536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572689810	chr12:121641587-121641588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1169722	chr12:121641625-121641626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs527353838	chr12:121641639-121641640	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs190062999	chr12:121641646-121641647	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376130071	chr12:121641651-121641652	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564243675	chr12:121641666-121641667	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs3850518	chr12:121641668-121641669	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs550034536	chr12:121641691-121641692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568240801	chr12:121641692-121641693	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532907036	chr12:121641699-121641700	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535787709	chr12:121641703-121641704	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547465743	chr12:121641719-121641720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549545425	chr12:121641725-121641726	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374110953	chr12:121641755-121641756	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539501509	chr12:121641808-121641809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146930842	chr12:121641809-121641810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372119923	chr12:121641850-121641851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377621267	chr12:121641869-121641870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576197299	chr12:121641872-121641873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537234653	chr12:121641888-121641889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs77461340	chr12:121641956-121641957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
24	rs182388736	chr12:121641990-121641991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541753392	chr12:121642010-121642011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559844650	chr12:121642015-121642016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139393537	chr12:121642089-121642090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545878700	chr12:121642106-121642107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542338927	chr12:121642159-121642160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529942379	chr12:121642167-121642168	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548054052	chr12:121642184-121642185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1169723	chr12:121642199-121642200	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs531461886	chr12:121642209-121642210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138331311	chr12:121642295-121642296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs144790580	chr12:121642298-121642299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548756738	chr12:121642314-121642315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372557795	chr12:121642316-121642317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143302364	chr12:121642341-121642342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186657600	chr12:121642371-121642372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs190658041	chr12:121642388-121642389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147528587	chr12:121642395-121642396	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs36041158	chr12:121642401-121642402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184110019	chr12:121642404-121642405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569566740	chr12:121642423-121642424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539464650	chr12:121642431-121642432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551397712	chr12:121642477-121642478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188711801	chr12:121642489-121642490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537198310	chr12:121642521-121642522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2567993	chr12:121642543-121642544	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs193181781	chr12:121642548-121642549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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

Chromatin state (count:2541 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121624200-121647200	Weak transcription	Brain Anterior Caudate	brain
2	chr12:121625600-121647200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:121628000-121647200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:121630400-121647200	Weak transcription	Brain Hippocampus Middle	brain
5	chr12:121637200-121642800	Weak transcription	HUVEC	blood vessel
6	chr12:121639600-121641600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:121640400-121641600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:121640400-121641600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr12:121641000-121641600	Enhancers	K562	blood
10	chr12:121641000-121647000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr12:121641400-121642600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:121641400-121642600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:121641400-121642600	Weak transcription	Fetal Heart	heart
14	chr12:121641400-121644600	Weak transcription	Placenta	Placenta
15	chr12:121641400-121646800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:121641400-121647800	Weak transcription	Gastric	stomach
17	chr12:121641600-121641800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:121641600-121643000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr12:121641600-121646800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:121641600-121646800	Weak transcription	K562	blood
21	chr12:121641600-121647200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:121641800-121647400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:121642600-121643000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr12:121642600-121643000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:121642600-121643000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:121642600-121643400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr12:121642600-121643600	Enhancers	Fetal Heart	heart
28	chr12:121642800-121643000	Enhancers	Adipose Nuclei	Adipose
29	chr12:121642800-121643800	Enhancers	HUVEC	blood vessel
30	chr12:121643000-121643600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr12:121643000-121647000	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr12:121643000-121647000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:121643000-121647200	Weak transcription	Adipose Nuclei	Adipose
34	chr12:121643000-121647600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr12:121643400-121647000	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr12:121643600-121647200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr12:121643600-121648000	Weak transcription	Fetal Heart	heart
38	chr12:121643800-121647200	Weak transcription	HUVEC	blood vessel
39	chr12:121644600-121645400	Enhancers	Placenta	Placenta
40	chr12:121645200-121647200	Weak transcription	Brain Angular Gyrus	brain
41	chr12:121645400-121647000	Weak transcription	Placenta	Placenta
42	chr12:121646800-121647000	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr12:121646800-121647000	Enhancers	Dnd41	blood
44	chr12:121646800-121647000	Enhancers	K562	blood
45	chr12:121646800-121647200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:121646800-121647200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:121646800-121647200	Weak transcription	Spleen	Spleen
48	chr12:121646800-121647600	Enhancers	Primary hematopoietic stem cells	blood
49	chr12:121646800-121647600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr12:121647000-121647200	Enhancers	Primary T cells fromperipheralblood	blood

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