Variant report

Variant	nsv899153
Chromosome Location	chr12:62716330-62817736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:485)
CpG islands
(count:61)
Chromatin interactive
region (count:80)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:62746746-62746792	K562	blood:	n/a	n/a
2	ARID3A	chr12:62807642-62807755	K562	blood:	n/a	n/a
3	ATF1	chr12:62787812-62787902	K562	blood:	n/a	n/a
4	ATF1	chr12:62765570-62765612	K562	blood:	n/a	n/a
5	ATF1	chr12:62763062-62763076	K562	blood:	n/a	n/a
6	BACH1	chr12:62792830-62792831	K562	blood:	n/a	n/a
7	BCL3	chr12:62809633-62810295	K562	blood:	n/a	n/a
8	BCL3	chr12:62807639-62808318	K562	blood:	n/a	n/a
9	BCL3	chr12:62811352-62811976	K562	blood:	n/a	n/a
10	BHLHE40	chr12:62719187-62719197	K562	blood:	n/a	n/a
11	BRCA1	chr12:62730451-62730470	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr12:62739376-62739820	K562	blood:	n/a	n/a
13	CCNT2	chr12:62804946-62805509	K562	blood:	n/a	n/a
14	CCNT2	chr12:62804111-62804311	K562	blood:	n/a	n/a
15	CEBPB	chr12:62762294-62762528	HepG2	liver:	n/a	chr12:62762397-62762408
16	CEBPB	chr12:62762172-62762682	A549	lung:	n/a	chr12:62762397-62762408
17	CEBPB	chr12:62804676-62804876	K562	blood:	n/a	n/a
18	CEBPB	chr12:62726442-62726817	IMR90	lung:	n/a	n/a
19	CEBPB	chr12:62762215-62762594	IMR90	lung:	n/a	chr12:62762397-62762408
20	CEBPB	chr12:62786904-62787103	K562	blood:	n/a	n/a
21	CEBPB	chr12:62762217-62762573	Hela-S3	cervix:	n/a	chr12:62762397-62762408
22	CEBPB	chr12:62762212-62762586	A549	lung:	n/a	chr12:62762397-62762408
23	CEBPB	chr12:62787751-62787797	K562	blood:	n/a	n/a
24	CEBPB	chr12:62762215-62762589	HepG2	liver:	n/a	chr12:62762397-62762408
25	CEBPB	chr12:62762246-62762566	H1-hESC	embryonic stem cell:	n/a	chr12:62762397-62762408
26	CEBPB	chr12:62787756-62787763	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr12:62762287-62762557	MCF-7	breast:	n/a	chr12:62762397-62762408
28	CEBPB	chr12:62802886-62803160	HepG2	liver:	n/a	chr12:62803005-62803016 chr12:62803004-62803017
29	CEBPB	chr12:62762287-62762561	ECC-1	luminal epithelium:	n/a	chr12:62762397-62762408
30	CEBPB	chr12:62793797-62794038	HepG2	liver:	n/a	chr12:62793908-62793919 chr12:62793909-62793918
31	CEBPB	chr12:62744937-62744992	K562	blood:	n/a	n/a
32	CEBPB	chr12:62762192-62762564	MCF-7	breast:	n/a	chr12:62762397-62762408
33	CEBPB	chr12:62762171-62762541	K562	blood:	n/a	chr12:62762397-62762408
34	CEBPB	chr12:62762283-62762487	K562	blood:	n/a	chr12:62762397-62762408
35	CEBPB	chr12:62762212-62762604	K562	blood:	n/a	chr12:62762397-62762408
36	CEBPB	chr12:62802890-62803137	K562	blood:	n/a	chr12:62803005-62803016 chr12:62803004-62803017
37	CEBPB	chr12:62762255-62762614	A549	lung:	n/a	chr12:62762397-62762408
38	CHD2	chr12:62808955-62809001	K562	blood:	n/a	n/a
39	CTCF	chr12:62763767-62763833	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr12:62754800-62754950	HPF	lung:	n/a	n/a
41	CTCF	chr12:62806687-62806714	GM20000	blood:	n/a	n/a
42	CTCF	chr12:62744588-62744692	GM13976	blood:	n/a	n/a
43	CTCF	chr12:62741878-62741958	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:62801515-62801607	GM13977	blood:	n/a	n/a
45	CTCF	chr12:62807300-62807450	GM12875	blood:	n/a	n/a
46	CTCF	chr12:62729721-62729834	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:62729766-62729849	A549	lung:	n/a	n/a
48	CTCF	chr12:62736479-62736521	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:62729720-62729812	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:62760699-62760762	GM13976	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:62798679-62798729	HRCEpiC	kidney:	n/a
2	chr12:62798679-62798729	MCF-7	breast:	n/a
3	chr12:62798679-62798729	PrEC	prostate:	n/a
4	chr12:62798679-62798729	HEK293	kidney:	embryo
5	chr12:62798679-62798729	AG09309	skin:	n/a
6	chr12:62798679-62798729	A549	lung:	n/a
7	chr12:62798679-62798729	HIPEpiC	eye:	n/a
8	chr12:62798679-62798729	H1-hESC	embryonic stem cell:	embryo
9	chr12:62798679-62798729	SK-N-SH	brain:	n/a
10	chr12:62798679-62798729	T-47D	breast:	n/a
11	chr12:62798679-62798729	K562	blood:	n/a
12	chr12:62798679-62798729	HCPEpiC	choroid plexus:	n/a
13	chr12:62798679-62798729	SAEC	small airway:	n/a
14	chr12:62798679-62798729	HUVEC	blood vessel:	n/a
15	chr12:62798679-62798729	U87	brain:	n/a
16	chr12:62798679-62798729	GM12878	blood:	n/a
17	chr12:62798679-62798729	SK-N-MC	brain:	n/a
18	chr12:62798679-62798729	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:62798679-62798729	HRE	kidney:	n/a
20	chr12:62798679-62798729	PANC-1	pancreas:	n/a
21	chr12:62798679-62798729	SKMC	muscle:	n/a
22	chr12:62798679-62798729	BJ	skin:	n/a
23	chr12:62798679-62798729	MCF10A-Er-Src	breast:	n/a
24	chr12:62798679-62798729	Caco-2	colon:	n/a
25	chr12:62798679-62798729	SK-N-SH_RA	brain:	n/a
26	chr12:62798679-62798729	HCM	heart:	n/a
27	chr12:62798679-62798729	PFSK-1	brain:	n/a
28	chr12:62798679-62798729	HAEpiC	amniotic membrane:	n/a
29	chr12:62798679-62798729	HEEpiC	esophagus:	n/a
30	chr12:62798679-62798729	BE2_C	brain:	n/a
31	chr12:62798679-62798729	Hela-S3	cervix:	n/a
32	chr12:62798679-62798729	AG10803	skin:	n/a
33	chr12:62798679-62798729	NT2-D1	testis:	n/a
34	chr12:62798679-62798729	NB4	blood:	n/a
35	chr12:62798679-62798729	RPTEC	kidney:	n/a
36	chr12:62798679-62798729	CMK	blood:	n/a
37	chr12:62798679-62798729	ECC-1	luminal epithelium:	n/a
38	chr12:62798679-62798729	Jurkat	blood:	n/a
39	chr12:62798679-62798729	ProgFib	skin:	n/a
40	chr12:62798679-62798729	AG04450	lung:	fetal
41	chr12:62798679-62798729	HCF	heart:	n/a
42	chr12:62798679-62798729	GM12892	blood:	n/a
43	chr12:62798679-62798729	NH-A	brain:	n/a
44	chr12:62798679-62798729	HRPEpiC	eye:	n/a
45	chr12:62798679-62798729	HL-60	blood:	n/a
46	chr12:62798679-62798729	Hepatocyte	liver:	n/a
47	chr12:62798679-62798729	AG09319	gingival:	n/a
48	chr12:62798679-62798729	HMEC	breast:	n/a
49	chr12:62798679-62798729	HepG2	liver:	n/a
50	chr12:62798679-62798729	NHBE	bronchial:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:62742796..62744490-chr12:62747117..62749304,2	K562	blood:
2	chr12:62767512..62770487-chr12:62776323..62779154,2	K562	blood:
3	chr12:62713762..62717130-chr12:62718527..62722595,6	K562	blood:
4	chr12:62744561..62747048-chr12:62754909..62756695,2	K562	blood:
5	chr12:62755969..62758641-chr12:62761637..62764028,2	MCF-7	breast:
6	chr12:62724789..62726795-chr12:62726808..62728651,2	K562	blood:
7	chr12:62784643..62787168-chr12:62795359..62797740,2	K562	blood:
8	chr12:62720361..62722698-chr12:62723343..62725405,2	MCF-7	breast:
9	chr12:62726090..62727805-chr12:62730442..62732806,2	K562	blood:
10	chr12:62773931..62780624-chr12:62782302..62787459,6	K562	blood:
11	chr12:62653426..62656098-chr12:62745783..62748052,2	K562	blood:
12	chr12:62781223..62783552-chr12:62783907..62785428,2	MCF-7	breast:
13	chr12:62652051..62655781-chr12:62739746..62743844,4	K562	blood:
14	chr12:62809064..62811353-chr12:62812515..62814478,2	K562	blood:
15	chr12:62802154..62805925-chr12:62805959..62810469,4	K562	blood:
16	chr12:62772356..62774718-chr12:62776973..62779988,4	K562	blood:
17	chr12:62764382..62767308-chr12:62771022..62773743,2	MCF-7	breast:
18	chr12:62753776..62756311-chr12:62756816..62758534,2	MCF-7	breast:
19	chr12:62752334..62754944-chr12:62756490..62758806,2	K562	blood:
20	chr12:62783680..62786866-chr12:62789094..62791660,3	K562	blood:
21	chr12:62745934..62748051-chr12:62750275..62752783,2	K562	blood:
22	chr12:62776192..62779108-chr12:62781541..62783338,2	K562	blood:
23	chr12:62788984..62792175-chr12:62792277..62796551,3	K562	blood:
24	chr12:62653050..62656025-chr12:62764970..62768543,3	K562	blood:
25	chr12:62718154..62720534-chr12:62859482..62862399,2	MCF-7	breast:
26	chr12:62788984..62792175-chr12:62792277..62796551,3	K562	blood:
27	chr12:62742990..62745783-chr12:62746371..62748692,4	K562	blood:
28	chr12:62768643..62771307-chr12:62782206..62783812,2	MCF-7	breast:
29	chr12:62744670..62747434-chr12:62749938..62751775,3	K562	blood:
30	chr12:62747479..62749492-chr12:62788174..62790462,2	K562	blood:
31	chr12:62752334..62754944-chr12:62756490..62758806,2	K562	blood:
32	chr12:62724788..62726773-chr12:62756335..62758286,2	MCF-7	breast:
33	chr12:62726090..62727805-chr12:62730442..62732806,2	K562	blood:
34	chr12:62742990..62745783-chr12:62746371..62748692,4	K562	blood:
35	chr12:62772356..62774718-chr12:62776973..62779988,4	K562	blood:
36	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
37	chr12:62717168..62719794-chr12:62722542..62725055,3	K562	blood:
38	chr12:62792054..62795051-chr12:62803056..62804839,2	K562	blood:
39	chr12:62802154..62805925-chr12:62805959..62810469,4	K562	blood:
40	chr12:62802223..62804398-chr12:62996125..62998801,2	K562	blood:
41	chr12:62764382..62767308-chr12:62771022..62773743,2	MCF-7	breast:
42	chr12:62782304..62784105-chr12:62785748..62788359,3	K562	blood:
43	chr12:62645529..62647531-chr12:62741957..62744563,2	K562	blood:
44	chr12:62724788..62726773-chr12:62756335..62758286,2	MCF-7	breast:
45	chr12:62747479..62749492-chr12:62788174..62790462,2	K562	blood:
46	chr12:62696269..62698660-chr12:62715380..62717526,2	K562	blood:
47	chr12:62755969..62758641-chr12:62761637..62764028,2	MCF-7	breast:
48	chr12:62768949..62769464-chr12:125737941..125738665,2	MCF-7	breast:
49	chr12:62753776..62756311-chr12:62756816..62758534,2	MCF-7	breast:
50	chr12:62710181..62712790-chr12:62740670..62743497,2	K562	blood:

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP15	hsa-miR-16-5p	chr12:62798406-62798429
2	USP15	hsa-miR-16-5p	chr12:62799351-62799372
3	USP15	hsa-let-7b-5p	chr12:62799457-62799477
4	USP15	hsa-miR-16-5p	chr12:62799365-62799371
5	USP15	hsa-miR-103a-3p	chr12:62799349-62799371
6	USP15	hsa-miR-103a-3p	chr12:62798406-62798428
7	USP15	hsa-miR-16-5p	chr12:62798422-62798428

Variant related genes	Relation type
USP15	TF binding region
RNU6-595P	TF binding region
USP15	CpG island
RNU6-595P	CpG island
ENSG00000135655	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000198673	chromatin interactions
ENSG00000200814	chromatin interactions
ENSG00000061987	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000199179	chromatin interactions

Extended variants
information (count: 3240 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3240 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7305206	chr12:62716330-62716331	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189071586	chr12:62716357-62716358	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544922452	chr12:62716392-62716393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564688694	chr12:62716414-62716415	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572156398	chr12:62716430-62716431	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142294037	chr12:62716544-62716545	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs151249263	chr12:62716546-62716547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17660079	chr12:62716547-62716548	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs182163380	chr12:62716637-62716638	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140483996	chr12:62716673-62716674	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75598551	chr12:62716751-62716752	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147066491	chr12:62716765-62716766	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184648541	chr12:62716772-62716773	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117836328	chr12:62716774-62716775	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566225905	chr12:62716798-62716799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200304825	chr12:62716814-62716815	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189920405	chr12:62716846-62716847	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34251904	chr12:62716878-62716879	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs180731592	chr12:62716921-62716922	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536464404	chr12:62716931-62716932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570513113	chr12:62716960-62716961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538504168	chr12:62716972-62716973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558619504	chr12:62717014-62717015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138465743	chr12:62717019-62717020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553563994	chr12:62717042-62717043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543084276	chr12:62717055-62717056	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375002044	chr12:62717084-62717085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566928329	chr12:62717097-62717098	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534294718	chr12:62717162-62717163	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554634342	chr12:62717213-62717214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574416954	chr12:62717362-62717363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367928942	chr12:62717396-62717397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554527927	chr12:62717445-62717446	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574383896	chr12:62717499-62717500	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543564535	chr12:62717522-62717523	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142569333	chr12:62717527-62717528	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11612349	chr12:62717558-62717559	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs546513328	chr12:62717603-62717604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559843094	chr12:62717664-62717665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528666017	chr12:62717666-62717667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548456500	chr12:62717671-62717672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568657822	chr12:62717769-62717770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556686312	chr12:62717772-62717773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530863587	chr12:62717778-62717779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139681009	chr12:62717784-62717785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550667370	chr12:62717882-62717883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570502787	chr12:62717887-62717888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11174424	chr12:62717976-62717977	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577227593	chr12:62717983-62717984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371233843	chr12:62717989-62717990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:1719 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62686200-62720200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:62686400-62736400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:62687200-62718200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:62687400-62720600	Weak transcription	Right Ventricle	heart
5	chr12:62689600-62717400	Weak transcription	Brain Angular Gyrus	brain
6	chr12:62691200-62716400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr12:62691200-62736400	Weak transcription	Esophagus	oesophagus
8	chr12:62691200-62736600	Weak transcription	Lung	lung
9	chr12:62698400-62717600	Weak transcription	Brain Germinal Matrix	brain
10	chr12:62698400-62741800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr12:62698600-62716400	Weak transcription	HepG2	liver
12	chr12:62698600-62720800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr12:62698600-62725800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr12:62698600-62745800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr12:62698800-62728600	Weak transcription	Fetal Heart	heart
16	chr12:62699800-62736400	Weak transcription	Aorta	Aorta
17	chr12:62700000-62719000	Weak transcription	Fetal Brain Female	brain
18	chr12:62700000-62726600	Weak transcription	HSMMtube	muscle
19	chr12:62700000-62736400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr12:62700000-62736400	Weak transcription	Fetal Stomach	stomach
21	chr12:62700000-62737000	Weak transcription	NHLF	lung
22	chr12:62700000-62757000	Weak transcription	HUVEC	blood vessel
23	chr12:62700200-62716400	Weak transcription	Brain Substantia Nigra	brain
24	chr12:62700200-62717800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr12:62701600-62717200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr12:62701600-62730800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr12:62701600-62738600	Weak transcription	Fetal Brain Male	brain
28	chr12:62701600-62742000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr12:62701600-62769200	Weak transcription	NHEK	skin
30	chr12:62701800-62717200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr12:62707400-62717800	Strong transcription	Dnd41	blood
32	chr12:62707600-62717800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr12:62710000-62744400	Weak transcription	Pancreas	Pancrea
34	chr12:62711000-62718000	Strong transcription	Fetal Thymus	thymus
35	chr12:62711000-62720400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:62711200-62717400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr12:62711200-62717600	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr12:62711800-62717200	Strong transcription	Liver	Liver
39	chr12:62711800-62717600	Strong transcription	Primary T cells from cord blood	blood
40	chr12:62711800-62717600	Strong transcription	Fetal Intestine Large	intestine
41	chr12:62712200-62755400	Weak transcription	Small Intestine	intestine
42	chr12:62712600-62716400	Weak transcription	Hela-S3	cervix
43	chr12:62713000-62732400	Weak transcription	Fetal Muscle Leg	muscle
44	chr12:62713200-62717400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:62713200-62717600	Strong transcription	Primary hematopoietic stem cells	blood
46	chr12:62713200-62721400	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr12:62713200-62722800	Weak transcription	Fetal Intestine Small	intestine
48	chr12:62713200-62736400	Weak transcription	Gastric	stomach
49	chr12:62713600-62717400	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr12:62714200-62717800	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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