Variant report

Variant	nsv559155
Chromosome Location	chr12:62751242-62802643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:223)
CpG islands
(count:61)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:223 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:62763062-62763076	K562	blood:	n/a	n/a
2	ATF1	chr12:62787812-62787902	K562	blood:	n/a	n/a
3	ATF1	chr12:62765570-62765612	K562	blood:	n/a	n/a
4	BACH1	chr12:62792830-62792831	K562	blood:	n/a	n/a
5	CEBPB	chr12:62762287-62762561	ECC-1	luminal epithelium:	n/a	chr12:62762397-62762408
6	CEBPB	chr12:62762212-62762604	K562	blood:	n/a	chr12:62762397-62762408
7	CEBPB	chr12:62762215-62762594	IMR90	lung:	n/a	chr12:62762397-62762408
8	CEBPB	chr12:62787751-62787797	K562	blood:	n/a	n/a
9	CEBPB	chr12:62762246-62762566	H1-hESC	embryonic stem cell:	n/a	chr12:62762397-62762408
10	CEBPB	chr12:62762217-62762573	Hela-S3	cervix:	n/a	chr12:62762397-62762408
11	CEBPB	chr12:62787756-62787763	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:62762192-62762564	MCF-7	breast:	n/a	chr12:62762397-62762408
13	CEBPB	chr12:62762171-62762541	K562	blood:	n/a	chr12:62762397-62762408
14	CEBPB	chr12:62793797-62794038	HepG2	liver:	n/a	chr12:62793908-62793919 chr12:62793909-62793918
15	CEBPB	chr12:62762172-62762682	A549	lung:	n/a	chr12:62762397-62762408
16	CEBPB	chr12:62762287-62762557	MCF-7	breast:	n/a	chr12:62762397-62762408
17	CEBPB	chr12:62762294-62762528	HepG2	liver:	n/a	chr12:62762397-62762408
18	CEBPB	chr12:62786904-62787103	K562	blood:	n/a	n/a
19	CEBPB	chr12:62762215-62762589	HepG2	liver:	n/a	chr12:62762397-62762408
20	CEBPB	chr12:62762212-62762586	A549	lung:	n/a	chr12:62762397-62762408
21	CEBPB	chr12:62762255-62762614	A549	lung:	n/a	chr12:62762397-62762408
22	CEBPB	chr12:62762283-62762487	K562	blood:	n/a	chr12:62762397-62762408
23	CTCF	chr12:62760699-62760762	GM13976	blood:	n/a	n/a
24	CTCF	chr12:62801515-62801607	GM13977	blood:	n/a	n/a
25	CTCF	chr12:62754800-62754950	HPF	lung:	n/a	n/a
26	CTCF	chr12:62763767-62763833	Kidney_OC	kidney:	n/a	n/a
27	CUX1	chr12:62766029-62766131	K562	blood:	n/a	n/a
28	CUX1	chr12:62788774-62789113	K562	blood:	n/a	n/a
29	E2F4	chr12:62783941-62784244	MCF10A-Er-Src	breast:	n/a	chr12:62784211-62784220
30	E2F4	chr12:62783305-62783489	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr12:62762530-62762534	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr12:62799105-62799269	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr12:62786874-62787068	MCF10A-Er-Src	breast:	n/a	n/a
34	EP300	chr12:62769524-62769657	GM12878	blood:	n/a	n/a
35	EP300	chr12:62790468-62790834	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr12:62753845-62753869	K562	blood:	n/a	n/a
37	EP300	chr12:62772806-62773148	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr12:62784539-62784739	K562	blood:	n/a	n/a
39	EP300	chr12:62766034-62766156	K562	blood:	n/a	n/a
40	EP300	chr12:62766994-62767028	GM12878	blood:	n/a	n/a
41	EP300	chr12:62769434-62769841	SK-N-SH_RA	brain:	n/a	n/a
42	FOS	chr12:62796882-62797160	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr12:62752198-62752239	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr12:62796873-62797073	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr12:62787292-62787393	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr12:62752206-62752229	MCF10A-Er-Src	breast:	n/a	n/a
47	FOXA1	chr12:62801387-62801718	HepG2	liver:	n/a	n/a
48	FOXA2	chr12:62762300-62762500	HepG2	liver:	n/a	n/a
49	GATA1	chr12:62770242-62770518	PBDEFetal	blood:	n/a	n/a
50	GATA1	chr12:62776512-62776852	PBDEFetal	blood:	n/a	chr12:62776521-62776532

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:62798679-62798729	MCF10A-Er-Src	breast:	n/a
2	chr12:62798679-62798729	PFSK-1	brain:	n/a
3	chr12:62798679-62798729	ECC-1	luminal epithelium:	n/a
4	chr12:62798679-62798729	SK-N-SH_RA	brain:	n/a
5	chr12:62798679-62798729	HepG2	liver:	n/a
6	chr12:62798679-62798729	H1-hESC	embryonic stem cell:	embryo
7	chr12:62798679-62798729	IMR90	lung:	fetal
8	chr12:62798679-62798729	HUVEC	blood vessel:	n/a
9	chr12:62798679-62798729	LNCaP	prostate:	n/a
10	chr12:62798679-62798729	GM12878	blood:	n/a
11	chr12:62798679-62798729	HEK293	kidney:	embryo
12	chr12:62798679-62798729	NHDF-neo	bronchial:	n/a
13	chr12:62798679-62798729	HCM	heart:	n/a
14	chr12:62798679-62798729	PANC-1	pancreas:	n/a
15	chr12:62798679-62798729	MCF-7	breast:	n/a
16	chr12:62798679-62798729	HRE	kidney:	n/a
17	chr12:62798679-62798729	NH-A	brain:	n/a
18	chr12:62798679-62798729	Hepatocyte	liver:	n/a
19	chr12:62798679-62798729	Jurkat	blood:	n/a
20	chr12:62798679-62798729	AG10803	skin:	n/a
21	chr12:62798679-62798729	CMK	blood:	n/a
22	chr12:62798679-62798729	HCPEpiC	choroid plexus:	n/a
23	chr12:62798679-62798729	ProgFib	skin:	n/a
24	chr12:62798679-62798729	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:62798679-62798729	HIPEpiC	eye:	n/a
26	chr12:62798679-62798729	SAEC	small airway:	n/a
27	chr12:62798679-62798729	AoSMC	blood vessel:	n/a
28	chr12:62798679-62798729	NB4	blood:	n/a
29	chr12:62798679-62798729	Caco-2	colon:	n/a
30	chr12:62798679-62798729	GM06990	blood:	n/a
31	chr12:62798679-62798729	K562	blood:	n/a
32	chr12:62798679-62798729	SK-N-SH	brain:	n/a
33	chr12:62798679-62798729	HCT-116	colon:	n/a
34	chr12:62798679-62798729	BE2_C	brain:	n/a
35	chr12:62798679-62798729	T-47D	breast:	n/a
36	chr12:62798679-62798729	HMEC	breast:	n/a
37	chr12:62798679-62798729	HRCEpiC	kidney:	n/a
38	chr12:62798679-62798729	U87	brain:	n/a
39	chr12:62798679-62798729	A549	lung:	n/a
40	chr12:62798679-62798729	HAEpiC	amniotic membrane:	n/a
41	chr12:62798679-62798729	GM12892	blood:	n/a
42	chr12:62798679-62798729	HNPCEpiC	eye:	n/a
43	chr12:62798679-62798729	NHBE	bronchial:	n/a
44	chr12:62798679-62798729	AG09309	skin:	n/a
45	chr12:62798679-62798729	HEEpiC	esophagus:	n/a
46	chr12:62798679-62798729	PrEC	prostate:	n/a
47	chr12:62798679-62798729	GM19239	blood:	n/a
48	chr12:62798679-62798729	HL-60	blood:	n/a
49	chr12:62798679-62798729	SK-N-MC	brain:	n/a
50	chr12:62798679-62798729	AG04449	skin:	fetal

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:62753776..62756311-chr12:62756816..62758534,2	MCF-7	breast:
2	chr12:62779701..62781218-chr12:62785878..62788849,2	MCF-7	breast:
3	chr12:62802223..62804398-chr12:62996125..62998801,2	K562	blood:
4	chr12:62773931..62780624-chr12:62782302..62787459,6	K562	blood:
5	chr12:62768949..62769464-chr12:125737941..125738665,2	MCF-7	breast:
6	chr12:62753776..62756311-chr12:62756816..62758534,2	MCF-7	breast:
7	chr12:62783680..62786866-chr12:62789094..62791660,3	K562	blood:
8	chr12:62761857..62764303-chr12:62773893..62776706,2	MCF-7	breast:
9	chr12:62800166..62802965-chr12:62803094..62805711,2	K562	blood:
10	chr12:62782304..62784105-chr12:62785748..62788359,3	K562	blood:
11	chr12:62653384..62656063-chr12:62775423..62777839,2	K562	blood:
12	chr12:62788984..62792175-chr12:62792277..62796551,3	K562	blood:
13	chr12:62784643..62787168-chr12:62795359..62797740,2	K562	blood:
14	chr12:62755969..62758641-chr12:62761637..62764028,2	MCF-7	breast:
15	chr12:62761857..62764303-chr12:62773893..62776706,2	MCF-7	breast:
16	chr12:62752334..62754944-chr12:62756490..62758806,2	K562	blood:
17	chr12:62790233..62792343-chr12:62793733..62795768,2	MCF-7	breast:
18	chr12:62776192..62779108-chr12:62781541..62783338,2	K562	blood:
19	chr12:62772356..62774718-chr12:62776973..62779988,4	K562	blood:
20	chr12:62781223..62783552-chr12:62783907..62785428,2	MCF-7	breast:
21	chr12:62776192..62779108-chr12:62781541..62783338,2	K562	blood:
22	chr12:62744561..62747048-chr12:62754909..62756695,2	K562	blood:
23	chr12:62772356..62774718-chr12:62776973..62779988,4	K562	blood:
24	chr12:62783680..62786866-chr12:62789094..62791660,3	K562	blood:
25	chr12:62768643..62771307-chr12:62782206..62783812,2	MCF-7	breast:
26	chr12:62802231..62804396-chr12:62807395..62808972,2	K562	blood:
27	chr12:62764382..62767308-chr12:62771022..62773743,2	MCF-7	breast:
28	chr12:62781223..62783552-chr12:62783907..62785428,2	MCF-7	breast:
29	chr12:62793306..62795703-chr12:62795951..62798733,2	MCF-7	breast:
30	chr12:62768643..62771307-chr12:62782206..62783812,2	MCF-7	breast:
31	chr12:62653050..62656025-chr12:62764970..62768543,3	K562	blood:
32	chr12:62653268..62654795-chr12:62769057..62770700,2	MCF-7	breast:
33	chr12:62755969..62758641-chr12:62761637..62764028,2	MCF-7	breast:
34	chr12:62745934..62748051-chr12:62750275..62752783,2	K562	blood:
35	chr12:62764382..62767308-chr12:62771022..62773743,2	MCF-7	breast:
36	chr12:62724788..62726773-chr12:62756335..62758286,2	MCF-7	breast:
37	chr12:62761577..62764023-chr12:62770574..62773104,2	K562	blood:
38	chr12:62802154..62805925-chr12:62805959..62810469,4	K562	blood:
39	chr12:62748743..62751580-chr12:62752325..62755740,5	K562	blood:
40	chr12:62753967..62754837-chr12:62829198..62830040,2	MCF-7	breast:
41	chr12:62788984..62792175-chr12:62792277..62796551,3	K562	blood:
42	chr12:62752334..62754944-chr12:62756490..62758806,2	K562	blood:
43	chr12:62747479..62749492-chr12:62788174..62790462,2	K562	blood:
44	chr12:62767512..62770487-chr12:62776323..62779154,2	K562	blood:
45	chr12:62767512..62770487-chr12:62776323..62779154,2	K562	blood:
46	chr12:62761577..62764023-chr12:62770574..62773104,2	K562	blood:
47	chr12:62744670..62747434-chr12:62749938..62751775,3	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	chr12:62799365-62799371
2	USP15	hsa-miR-103a-3p	chr12:62798406-62798428
3	USP15	hsa-miR-103a-3p	chr12:62799349-62799371
4	USP15	hsa-miR-16-5p	chr12:62799351-62799372
5	USP15	hsa-miR-16-5p	chr12:62798406-62798429
6	USP15	hsa-let-7b-5p	chr12:62799457-62799477
7	USP15	hsa-miR-16-5p	chr12:62798422-62798428

Variant related genes	Relation type
USP15	TF binding region
USP15	CpG island
ENSG00000257354	chromatin interactions
ENSG00000135655	chromatin interactions
ENSG00000199179	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000198673	chromatin interactions

Extended variants
information (count: 1836 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1836 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12811821	chr12:62751242-62751243	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555389695	chr12:62751254-62751255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12317035	chr12:62751255-62751256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543931984	chr12:62751267-62751268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563923831	chr12:62751302-62751303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577610638	chr12:62751305-62751306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539859002	chr12:62751322-62751323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560793949	chr12:62751363-62751364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17660575	chr12:62751388-62751389	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs549562096	chr12:62751406-62751407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563106989	chr12:62751427-62751428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149166857	chr12:62751490-62751491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551895778	chr12:62751498-62751499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571540296	chr12:62751510-62751511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368415053	chr12:62751536-62751537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143316276	chr12:62751545-62751546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547478017	chr12:62751584-62751585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566731452	chr12:62751602-62751603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116610589	chr12:62751640-62751641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11174440	chr12:62751641-62751642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555120865	chr12:62751645-62751646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532850307	chr12:62751767-62751768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568759836	chr12:62751845-62751846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546681814	chr12:62751866-62751867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114126173	chr12:62751882-62751883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557796570	chr12:62751913-62751914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139264232	chr12:62751922-62751923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567069036	chr12:62751934-62751935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199913464	chr12:62751941-62751942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577671055	chr12:62751943-62751944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550716807	chr12:62751950-62751951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182713313	chr12:62751961-62751962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371802234	chr12:62751981-62751982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143280157	chr12:62752045-62752046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371222866	chr12:62752054-62752055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187347086	chr12:62752073-62752074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190694603	chr12:62752075-62752076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545280413	chr12:62752097-62752098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565333937	chr12:62752199-62752200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527804137	chr12:62752234-62752235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547755121	chr12:62752238-62752239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567351306	chr12:62752249-62752250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs36113274	chr12:62752251-62752252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182461285	chr12:62752262-62752263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113712326	chr12:62752266-62752267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568823106	chr12:62752277-62752278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137905230	chr12:62752312-62752313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549684576	chr12:62752349-62752350	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557692673	chr12:62752358-62752359	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571289324	chr12:62752363-62752364	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
abnormal development	18461090	CNVD

Chromatin state (count:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62700000-62757000	Weak transcription	HUVEC	blood vessel
2	chr12:62701600-62769200	Weak transcription	NHEK	skin
3	chr12:62712200-62755400	Weak transcription	Small Intestine	intestine
4	chr12:62717000-62769200	Weak transcription	Fetal Kidney	kidney
5	chr12:62717000-62777000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr12:62717000-62783200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:62717000-62784600	Weak transcription	Colon Smooth Muscle	Colon
8	chr12:62717200-62752600	Weak transcription	HepG2	liver
9	chr12:62717200-62756800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:62717200-62778400	Weak transcription	Hela-S3	cervix
11	chr12:62727200-62753000	Weak transcription	HSMMtube	muscle
12	chr12:62729200-62753000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr12:62729800-62776800	Weak transcription	HSMM	muscle
14	chr12:62730000-62763800	Weak transcription	Psoas Muscle	Psoas
15	chr12:62735600-62758600	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr12:62737600-62757000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr12:62737600-62784600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:62737600-62786600	Weak transcription	NHLF	lung
19	chr12:62737800-62780200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:62738000-62754800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr12:62738200-62777000	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr12:62738200-62787400	Weak transcription	Spleen	Spleen
23	chr12:62738200-62790600	Weak transcription	Esophagus	oesophagus
24	chr12:62738400-62757400	Weak transcription	Duodenum Mucosa	Duodenum
25	chr12:62738600-62752600	Weak transcription	Right Ventricle	heart
26	chr12:62738600-62755000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr12:62738600-62759600	Weak transcription	Fetal Lung	lung
28	chr12:62738600-62763800	Weak transcription	Left Ventricle	heart
29	chr12:62738600-62783400	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr12:62738800-62752400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr12:62738800-62752600	Weak transcription	Fetal Intestine Large	intestine
32	chr12:62738800-62756600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:62738800-62766000	Weak transcription	Aorta	Aorta
34	chr12:62738800-62769000	Weak transcription	Placenta	Placenta
35	chr12:62738800-62784000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr12:62738800-62789600	Weak transcription	Ovary	ovary
37	chr12:62738800-62792800	Weak transcription	Lung	lung
38	chr12:62739000-62752800	Weak transcription	Brain Germinal Matrix	brain
39	chr12:62739000-62761000	Weak transcription	Fetal Stomach	stomach
40	chr12:62739000-62775400	Weak transcription	Adipose Nuclei	Adipose
41	chr12:62739600-62754800	Weak transcription	Osteobl	bone
42	chr12:62739600-62782000	Weak transcription	Thymus	Thymus
43	chr12:62739800-62782600	Weak transcription	Fetal Intestine Small	intestine
44	chr12:62740000-62757400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr12:62741000-62756600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr12:62741800-62783600	Weak transcription	NHDF-Ad	bronchial
47	chr12:62742000-62752800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr12:62742000-62786800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:62742400-62757800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr12:62742600-62775200	Weak transcription	NH-A	brain

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