Variant report

Variant	esv3406515
Chromosome Location	chr12:118572594-118575442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:606)
CpG islands
(count:976)
Chromatin interactive
region (count:15)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:118572943-118572954	K562	blood:	n/a	n/a
2	ARID3A	chr12:118572774-118573040	HepG2	liver:	n/a	n/a
3	ATF2	chr12:118574314-118574830	GM12878	blood:	n/a	n/a
4	ATF2	chr12:118573489-118573861	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:118573599-118574108	GM12878	blood:	n/a	n/a
6	ATF3	chr12:118573540-118574194	A549	lung:	n/a	n/a
7	BACH1	chr12:118573645-118574195	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:118573835-118573990	K562	blood:	n/a	n/a
9	BCL3	chr12:118573312-118574247	A549	lung:	n/a	chr12:118574184-118574193
10	BCLAF1	chr12:118574416-118574899	GM12878	blood:	n/a	chr12:118574718-118574731
11	BCLAF1	chr12:118573518-118574189	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:118573428-118574104	HepG2	liver:	n/a	chr12:118573980-118573996
13	BHLHE40	chr12:118573579-118574185	GM12878	blood:	n/a	chr12:118573980-118573996
14	BHLHE40	chr12:118572825-118573025	K562	blood:	n/a	n/a
15	BHLHE40	chr12:118574544-118574868	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:118572668-118572990	HepG2	liver:	n/a	chr12:118572823-118572836
17	BHLHE40	chr12:118573697-118574199	K562	blood:	n/a	chr12:118573980-118573996
18	BRCA1	chr12:118574550-118574566	HepG2	liver:	n/a	n/a
19	BRCA1	chr12:118574438-118574747	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr12:118573697-118574078	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr12:118573519-118574131	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr12:118573683-118574147	GM12878	blood:	n/a	n/a
23	BRCA1	chr12:118574634-118574826	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:118573689-118574085	HepG2	liver:	n/a	n/a
25	CBX3	chr12:118573143-118574171	K562	blood:	n/a	n/a
26	CBX3	chr12:118573409-118574225	HCT-116	colon:	n/a	n/a
27	CCNT2	chr12:118573672-118574794	K562	blood:	n/a	n/a
28	CEBPB	chr12:118574434-118574751	K562	blood:	n/a	n/a
29	CEBPB	chr12:118573627-118573931	K562	blood:	n/a	n/a
30	CEBPB	chr12:118574384-118574771	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:118573525-118574152	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:118574643-118574736	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:118573708-118574088	HepG2	liver:	n/a	n/a
34	CEBPD	chr12:118573640-118573972	HepG2	liver:	n/a	n/a
35	CEBPD	chr12:118573657-118574099	HepG2	liver:	n/a	n/a
36	CHD1	chr12:118573432-118573782	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr12:118573637-118575009	GM12878	blood:	n/a	n/a
38	CHD2	chr12:118573524-118574731	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr12:118573557-118574164	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr12:118573600-118575036	GM12878	blood:	n/a	n/a
41	CHD2	chr12:118573556-118574198	HepG2	liver:	n/a	n/a
42	CHD2	chr12:118573607-118574233	K562	blood:	n/a	n/a
43	CREB1	chr12:118573612-118573982	A549	lung:	n/a	n/a
44	CREB1	chr12:118573538-118574818	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr12:118573483-118574882	HepG2	liver:	n/a	n/a
46	CREB1	chr12:118573526-118574874	GM12878	blood:	n/a	n/a
47	CREB1	chr12:118573548-118574263	A549	lung:	n/a	n/a
48	CREB1	chr12:118573563-118574169	K562	blood:	n/a	n/a
49	CREB1	chr12:118573647-118574143	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:118573909-118574031	NHEK	skin:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118573533-118573583	CMK	blood:	n/a
2	chr12:118574268-118574318	K562	blood:	n/a
3	chr12:118573533-118573583	HRCEpiC	kidney:	n/a
4	chr12:118573888-118573938	Jurkat	blood:	n/a
5	chr12:118573845-118573895	HRCEpiC	kidney:	n/a
6	chr12:118573845-118573895	SK-N-MC	brain:	n/a
7	chr12:118573736-118573786	SKMC	muscle:	n/a
8	chr12:118574516-118574566	HEEpiC	esophagus:	n/a
9	chr12:118574730-118574780	U87	brain:	n/a
10	chr12:118573845-118573895	AG04450	lung:	fetal
11	chr12:118574730-118574780	SK-N-SH_RA	brain:	n/a
12	chr12:118573731-118573781	HCT-116	colon:	n/a
13	chr12:118574516-118574566	GM12891	blood:	n/a
14	chr12:118573845-118573895	HCM	heart:	n/a
15	chr12:118573736-118573786	RPTEC	kidney:	n/a
16	chr12:118573531-118573581	HEEpiC	esophagus:	n/a
17	chr12:118574757-118574807	HCF	heart:	n/a
18	chr12:118573533-118573583	GM12878	blood:	n/a
19	chr12:118573857-118573907	ProgFib	skin:	n/a
20	chr12:118573850-118573900	BJ	skin:	n/a
21	chr12:118573857-118573907	SK-N-MC	brain:	n/a
22	chr12:118573531-118573581	MCF10A-Er-Src	breast:	n/a
23	chr12:118574268-118574318	HL-60	blood:	n/a
24	chr12:118573745-118573795	NHBE	bronchial:	n/a
25	chr12:118574516-118574566	HRE	kidney:	n/a
26	chr12:118573850-118573900	T-47D	breast:	n/a
27	chr12:118573857-118573907	Jurkat	blood:	n/a
28	chr12:118573736-118573786	LNCaP	prostate:	n/a
29	chr12:118574516-118574566	SK-N-MC	brain:	n/a
30	chr12:118573888-118573938	MCF-7	breast:	n/a
31	chr12:118573736-118573786	NB4	blood:	n/a
32	chr12:118574268-118574318	NHDF-neo	bronchial:	n/a
33	chr12:118575033-118575083	NH-A	brain:	n/a
34	chr12:118574268-118574318	LNCaP	prostate:	n/a
35	chr12:118573845-118573895	NB4	blood:	n/a
36	chr12:118573531-118573581	U87	brain:	n/a
37	chr12:118573531-118573581	SKMC	muscle:	n/a
38	chr12:118573731-118573781	AG09319	gingival:	n/a
39	chr12:118573736-118573786	GM12891	blood:	n/a
40	chr12:118574730-118574780	LNCaP	prostate:	n/a
41	chr12:118573531-118573581	Caco-2	colon:	n/a
42	chr12:118573886-118573936	AoSMC	blood vessel:	n/a
43	chr12:118573888-118573938	AoSMC	blood vessel:	n/a
44	chr12:118573845-118573895	BJ	skin:	n/a
45	chr12:118573857-118573907	HL-60	blood:	n/a
46	chr12:118574268-118574318	BE2_C	brain:	n/a
47	chr12:118573857-118573907	U87	brain:	n/a
48	chr12:118574730-118574780	H1-hESC	embryonic stem cell:	embryo
49	chr12:118573888-118573938	NHBE	bronchial:	n/a
50	chr12:118573850-118573900	SK-N-MC	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:118496436..118502396-chr12:118572063..118576805,10	MCF-7	breast:
2	chr12:118557596..118560350-chr12:118572704..118574934,3	MCF-7	breast:
3	chr12:118573812..118576177-chr12:118596570..118599987,3	K562	blood:
4	chr12:118572856..118575962-chr12:118597469..118600285,3	K562	blood:
5	chr12:118572886..118574851-chr17:57922727..57925338,2	MCF-7	breast:
6	chr12:118499217..118500774-chr12:118572851..118574591,2	MCF-7	breast:
7	chr12:118540506..118543698-chr12:118572832..118575450,7	MCF-7	breast:
8	chr12:118558694..118561471-chr12:118568462..118574858,6	MCF-7	breast:
9	chr12:118570937..118572904-chr12:118576719..118579256,2	K562	blood:
10	chr12:118573153..118575288-chr12:118813964..118815499,2	K562	blood:
11	chr12:118572169..118574578-chr12:118813281..118815774,2	MCF-7	breast:
12	chr12:118540025..118541851-chr12:118573172..118576109,2	MCF-7	breast:
13	chr12:118573102..118576254-chr12:118808901..118815960,7	MCF-7	breast:
14	chr12:118498119..118500024-chr12:118572981..118575568,2	K562	blood:
15	chr12:118556622..118559418-chr12:118574681..118576805,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAOK3-1	chr12:118573662-118573733	XLOC_010212
2	lnc-TAOK3-1	chr12:118573662-118573735	XLOC_010212
3	lnc-TAOK3-1	chr12:118573662-118573718	NONHSAT031027
4	lnc-TAOK3-1	chr12:118573444-118573547	NONHSAT031026
5	lnc-TAOK3-1	chr12:118573662-118573711	NONHSAT031026
6	lnc-TAOK3-1	chr12:118573662-118573755	XLOC_010212
7	lnc-TAOK3-1	chr12:118573662-118573733	XLOC_010212

No data

Variant related genes	Relation type
PEBP1	TF binding region
VSIG10	TF binding region
PEBP1	CpG island
VSIG10	CpG island
ENSG00000111707	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000176834	chromatin interactions
ENSG00000089220	chromatin interactions
ENSG00000135090	chromatin interactions
ENSG00000176871	chromatin interactions
ENSG00000270482	chromatin interactions
PDIK1L	miRNA target sites

Extended variants
information (count: 111 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529248283	chr12:118572619-118572620	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs549107711	chr12:118572620-118572621	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs193276450	chr12:118572833-118572834	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs562241917	chr12:118572885-118572886	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs12312445	chr12:118572898-118572899	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs3221617	chr12:118572904-118572905	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs369060790	chr12:118572905-118572906	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs72432960	chr12:118572913-118572914	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs71069416	chr12:118572944-118572945	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs559801251	chr12:118572996-118572997	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs571864839	chr12:118572998-118572999	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs534455905	chr12:118573003-118573004	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs146883660	chr12:118573013-118573014	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs567308753	chr12:118573041-118573042	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs140736910	chr12:118573123-118573124	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs556010873	chr12:118573162-118573163	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs576057686	chr12:118573164-118573165	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs544891335	chr12:118573225-118573226	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs184361684	chr12:118573229-118573230	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs572727122	chr12:118573231-118573232	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs386766830	chr12:118573262-118573263	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs7976200	chr12:118573263-118573264	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371080384	chr12:118573303-118573304	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs533179015	chr12:118573307-118573308	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs141461063	chr12:118573404-118573405	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs529283763	chr12:118573405-118573406	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs115410200	chr12:118573431-118573432	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs35629568	chr12:118573498-118573499	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs562863528	chr12:118573534-118573535	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
30	rs531798889	chr12:118573585-118573586	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs551694981	chr12:118573613-118573614	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs571766777	chr12:118573621-118573622	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs527887741	chr12:118573625-118573626	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs17512051	chr12:118573667-118573668	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs567936509	chr12:118573750-118573751	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs536272454	chr12:118573766-118573767	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs556089666	chr12:118573773-118573774	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs569661063	chr12:118573780-118573781	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs17525587	chr12:118573790-118573791	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs114340939	chr12:118573802-118573803	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs558365531	chr12:118573858-118573859	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs571951604	chr12:118573877-118573878	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs540813644	chr12:118573907-118573908	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs11554098	chr12:118573945-118573946	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs1050547	chr12:118573955-118573956	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs149153511	chr12:118573966-118573967	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs34122664	chr12:118574010-118574011	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs542673479	chr12:118574011-118574012	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs11554097	chr12:118574034-118574035	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs11554103	chr12:118574047-118574048	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118542600-118572800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr12:118542600-118573400	Weak transcription	Primary T cells from cord blood	blood
3	chr12:118552800-118572800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:118552800-118573400	Weak transcription	Aorta	Aorta
5	chr12:118553000-118573000	Weak transcription	Fetal Brain Female	brain
6	chr12:118558800-118572800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr12:118559200-118572600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:118559200-118572600	Weak transcription	NHEK	skin
9	chr12:118559200-118572800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:118559200-118573000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:118559200-118573000	Weak transcription	Fetal Kidney	kidney
12	chr12:118559200-118573400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr12:118559200-118573400	Weak transcription	Fetal Intestine Small	intestine
14	chr12:118559400-118572600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:118559400-118572800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:118560800-118572800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr12:118561600-118572800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:118561600-118573000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr12:118563200-118573400	Weak transcription	Lung	lung
20	chr12:118564200-118572800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:118564400-118573200	Weak transcription	Fetal Stomach	stomach
22	chr12:118565000-118572800	Weak transcription	Gastric	stomach
23	chr12:118565200-118572800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:118566800-118573200	Weak transcription	Right Atrium	heart
25	chr12:118567400-118573200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:118569400-118572600	Enhancers	Liver	Liver
27	chr12:118569800-118572600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr12:118569800-118572800	Weak transcription	Placenta	Placenta
29	chr12:118569800-118573400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr12:118569800-118573600	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr12:118570000-118572600	Weak transcription	Hela-S3	cervix
32	chr12:118570000-118573000	Weak transcription	Fetal Muscle Trunk	muscle
33	chr12:118570200-118572600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:118570200-118572600	Weak transcription	Brain Hippocampus Middle	brain
35	chr12:118570200-118572600	Weak transcription	Brain Substantia Nigra	brain
36	chr12:118570200-118572600	Weak transcription	A549	lung
37	chr12:118570200-118572800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr12:118570200-118572800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr12:118570200-118572800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr12:118570200-118572800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr12:118570200-118572800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:118570200-118572800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr12:118570200-118572800	Weak transcription	Fetal Muscle Leg	muscle
44	chr12:118570200-118572800	Weak transcription	Ovary	ovary
45	chr12:118570200-118572800	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr12:118570200-118572800	Weak transcription	NHDF-Ad	bronchial
47	chr12:118570200-118573000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:118570200-118573000	Weak transcription	Brain Germinal Matrix	brain
49	chr12:118570200-118573000	Weak transcription	Psoas Muscle	Psoas
50	chr12:118570200-118573400	Weak transcription	Colonic Mucosa	Colon

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