Variant report

Variant	esv1818097
Chromosome Location	chr12:124465667-124488972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124468487-124468879	K562	blood:	n/a	n/a
2	ARID3A	chr12:124468469-124468621	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:124482365-124483916	K562	blood:	n/a	n/a
4	ATF1	chr12:124482494-124483845	K562	blood:	n/a	n/a
5	ATF1	chr12:124482020-124482272	K562	blood:	n/a	n/a
6	ATF1	chr12:124476031-124476477	K562	blood:	n/a	n/a
7	BHLHE40	chr12:124483021-124483708	K562	blood:	n/a	n/a
8	BHLHE40	chr12:124468457-124468600	K562	blood:	n/a	n/a
9	BRCA1	chr12:124475696-124476289	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr12:124482888-124483133	K562	blood:	n/a	chr12:124482963-124482983
11	CEBPB	chr12:124475153-124475394	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:124475843-124476359	HCT-116	colon:	n/a	n/a
13	CEBPB	chr12:124475913-124476165	A549	lung:	n/a	n/a
14	CEBPB	chr12:124475662-124476299	HCT-116	colon:	n/a	n/a
15	CEBPB	chr12:124474571-124474908	HepG2	liver:	n/a	chr12:124474747-124474758
16	CEBPB	chr12:124483490-124483869	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:124475808-124476416	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:124483380-124483844	K562	blood:	n/a	n/a
19	CEBPB	chr12:124475857-124476113	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:124475853-124476151	IMR90	lung:	n/a	n/a
21	CEBPB	chr12:124468415-124468654	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:124474649-124474804	A549	lung:	n/a	chr12:124474747-124474758
23	CEBPB	chr12:124475823-124476152	K562	blood:	n/a	n/a
24	CEBPB	chr12:124479557-124479982	IMR90	lung:	n/a	n/a
25	CEBPB	chr12:124475139-124475451	IMR90	lung:	n/a	n/a
26	CHD2	chr12:124468486-124468652	HepG2	liver:	n/a	n/a
27	CHD2	chr12:124482869-124482880	K562	blood:	n/a	n/a
28	CTCF	chr12:124468470-124468703	GM13976	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
29	CTCF	chr12:124468477-124468720	GM10266	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
30	CTCF	chr12:124468520-124468670	HBMEC	blood vessel:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
31	CTCF	chr12:124468500-124468650	WERI-Rb-1	eye:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468583-124468599
32	CTCF	chr12:124468540-124468690	AG09309	skin:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
33	CTCF	chr12:124487780-124487930	AG09319	gingival:	n/a	n/a
34	CTCF	chr12:124487800-124487950	NHEK	skin:	n/a	n/a
35	CTCF	chr12:124487780-124487930	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr12:124487740-124487890	GM12873	blood:	n/a	n/a
37	CTCF	chr12:124468499-124468696	Kidney_OC	kidney:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
38	CTCF	chr12:124468560-124468710	HA-sp	spinal cord:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
39	CTCF	chr12:124470980-124471130	HPF	lung:	n/a	n/a
40	CTCF	chr12:124468460-124468610	GM12868	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468583-124468599
41	CTCF	chr12:124468500-124468650	GM12875	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468583-124468599
42	CTCF	chr12:124469400-124469550	GM12870	blood:	n/a	n/a
43	CTCF	chr12:124468377-124468714	K562	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
44	CTCF	chr12:124468520-124468670	GM12873	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
45	CTCF	chr12:124468520-124468670	GM12878	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599
46	CTCF	chr12:124487791-124487922	Gliobla	brain:	n/a	n/a
47	CTCF	chr12:124468500-124468650	AG04449	skin:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468583-124468599
48	CTCF	chr12:124468500-124468650	GM12872	blood:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468583-124468599
49	CTCF	chr12:124468453-124468661	ECC-1	luminal epithelium:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468583-124468599
50	CTCF	chr12:124468440-124468750	MCF-7	breast:	n/a	chr12:124468584-124468597 chr12:124468577-124468598 chr12:124468582-124468600 chr12:124468659-124468669 chr12:124468583-124468599

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124481981-124482031	Hepatocyte	liver:	n/a
2	chr12:124481981-124482031	ECC-1	luminal epithelium:	n/a
3	chr12:124481981-124482031	IMR90	lung:	fetal
4	chr12:124481981-124482031	NH-A	brain:	n/a
5	chr12:124481981-124482031	LNCaP	prostate:	n/a
6	chr12:124481981-124482031	Caco-2	colon:	n/a
7	chr12:124481981-124482031	MCF-7	breast:	n/a
8	chr12:124481981-124482031	HCPEpiC	choroid plexus:	n/a
9	chr12:124481981-124482031	GM06990	blood:	n/a
10	chr12:124481981-124482031	AG04450	lung:	fetal
11	chr12:124481981-124482031	HIPEpiC	eye:	n/a
12	chr12:124481981-124482031	AG09309	skin:	n/a
13	chr12:124481981-124482031	HCT-116	colon:	n/a
14	chr12:124481981-124482031	HEK293	kidney:	embryo
15	chr12:124481981-124482031	AG10803	skin:	n/a
16	chr12:124481981-124482031	Hela-S3	cervix:	n/a
17	chr12:124481981-124482031	HL-60	blood:	n/a
18	chr12:124481981-124482031	PANC-1	pancreas:	n/a
19	chr12:124481981-124482031	HepG2	liver:	n/a
20	chr12:124481981-124482031	T-47D	breast:	n/a
21	chr12:124481981-124482031	GM12878	blood:	n/a
22	chr12:124481981-124482031	ProgFib	skin:	n/a
23	chr12:124481981-124482031	H1-hESC	embryonic stem cell:	embryo
24	chr12:124481981-124482031	HNPCEpiC	eye:	n/a
25	chr12:124481981-124482031	NHBE	bronchial:	n/a
26	chr12:124481981-124482031	BE2_C	brain:	n/a
27	chr12:124481981-124482031	SK-N-SH_RA	brain:	n/a
28	chr12:124481981-124482031	HEEpiC	esophagus:	n/a
29	chr12:124481981-124482031	AG09319	gingival:	n/a
30	chr12:124481981-124482031	HRE	kidney:	n/a
31	chr12:124481981-124482031	HMEC	breast:	n/a
32	chr12:124481981-124482031	SK-N-MC	brain:	n/a
33	chr12:124481981-124482031	SKMC	muscle:	n/a
34	chr12:124481981-124482031	SK-N-SH	brain:	n/a
35	chr12:124481981-124482031	AG04449	skin:	fetal
36	chr12:124481981-124482031	U87	brain:	n/a
37	chr12:124481981-124482031	HAEpiC	amniotic membrane:	n/a
38	chr12:124481981-124482031	HRPEpiC	eye:	n/a
39	chr12:124481981-124482031	BJ	skin:	n/a
40	chr12:124481981-124482031	GM12892	blood:	n/a
41	chr12:124481981-124482031	HCF	heart:	n/a
42	chr12:124481981-124482031	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:124481981-124482031	CMK	blood:	n/a
44	chr12:124481981-124482031	NT2-D1	testis:	n/a
45	chr12:124481981-124482031	K562	blood:	n/a
46	chr12:124481981-124482031	A549	lung:	n/a
47	chr12:124481981-124482031	Jurkat	blood:	n/a
48	chr12:124481981-124482031	HRCEpiC	kidney:	n/a
49	chr12:124481981-124482031	MCF10A-Er-Src	breast:	n/a
50	chr12:124481981-124482031	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:124479273..124483695-chr12:124485266..124489724,5	K562	blood:
2	chr12:124284685..124287409-chr12:124473083..124475024,2	MCF-7	breast:
3	chr12:124462440..124465412-chr12:124468868..124471701,4	K562	blood:
4	chr12:124468378..124471325-chr12:124481728..124484579,2	K562	blood:
5	chr12:124433267..124435422-chr12:124476091..124477918,2	K562	blood:
6	chr12:124469541..124471956-chr12:124474758..124478951,5	K562	blood:
7	chr12:124349873..124352616-chr12:124471983..124473527,2	MCF-7	breast:
8	chr12:124461323..124463164-chr12:124465157..124466786,2	K562	blood:
9	chr12:124467883..124469775-chr12:124477187..124479710,2	MCF-7	breast:
10	chr12:124455649..124457478-chr12:124476003..124477748,2	K562	blood:
11	chr12:124467883..124469775-chr12:124477187..124479710,2	MCF-7	breast:
12	chr12:124461201..124463907-chr12:124466692..124470119,3	MCF-7	breast:
13	chr12:124449321..124452195-chr12:124463375..124466375,3	MCF-7	breast:
14	chr12:124466117..124470076-chr12:124471050..124474861,6	MCF-7	breast:
15	chr12:124292496..124294102-chr12:124468172..124469036,5	MCF-7	breast:
16	chr12:124476601..124479063-chr12:124485956..124487625,2	K562	blood:
17	chr12:124455666..124458954-chr12:124482967..124486459,4	MCF-7	breast:
18	chr12:124466117..124470076-chr12:124471050..124474861,6	MCF-7	breast:
19	chr12:124464712..124466327-chr12:124492500..124494762,2	K562	blood:
20	chr12:124285046..124286656-chr12:124466634..124468650,2	MCF-7	breast:
21	chr12:124485640..124488869-chr12:124491698..124495418,5	K562	blood:
22	chr12:124476672..124479275-chr12:124482107..124484649,2	MCF-7	breast:
23	chr12:124471751..124473354-chr12:124481862..124484429,2	K562	blood:
24	chr12:124478987..124480536-chr12:124482316..124484096,2	K562	blood:
25	chr12:124484342..124486800-chr12:124487577..124490631,4	K562	blood:
26	chr12:124457604..124459142-chr12:124475055..124476708,2	MCF-7	breast:
27	chr12:124474945..124477651-chr12:124481965..124484404,2	K562	blood:
28	chr12:124457163..124461079-chr12:124477207..124479204,3	MCF-7	breast:
29	chr12:124466662..124469603-chr12:124471217..124474094,3	K562	blood:
30	chr12:124469825..124474593-chr12:124481346..124484429,4	K562	blood:
31	chr12:124476601..124479063-chr12:124485956..124487625,2	K562	blood:
32	chr12:124479682..124481544-chr16:49621973..49623955,2	MCF-7	breast:
33	chr12:124455809..124459350-chr12:124472892..124476015,3	MCF-7	breast:
34	chr12:124469541..124471956-chr12:124474758..124478951,5	K562	blood:
35	chr12:124484342..124486800-chr12:124487577..124490631,4	K562	blood:
36	chr12:124466662..124469603-chr12:124471217..124474094,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM101A-2	chr12:124482325-124482392	NONHSAT031635
2	lnc-FAM101A-2	chr12:124482944-124483300	NONHSAT031635

Variant related genes	Relation type
ZNF664	TF binding region
ZNF664	CpG island
ENSG00000269997	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000179195	chromatin interactions

Extended variants
information (count: 794 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151271150	chr12:124465784-124465785	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs564481607	chr12:124465924-124465925	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs193246284	chr12:124465934-124465935	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4765541	chr12:124465995-124465996	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs529355042	chr12:124466044-124466045	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547799588	chr12:124466048-124466049	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565908726	chr12:124466053-124466054	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs527599349	chr12:124466056-124466057	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552461716	chr12:124466060-124466061	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367591825	chr12:124466076-124466077	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544084614	chr12:124466098-124466099	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs77968302	chr12:124466102-124466103	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571611017	chr12:124466146-124466147	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538086256	chr12:124466235-124466236	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185408004	chr12:124466243-124466244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568179843	chr12:124466258-124466259	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189078333	chr12:124466297-124466298	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553749488	chr12:124466298-124466299	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546815798	chr12:124466311-124466312	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs114342860	chr12:124466322-124466323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529398633	chr12:124466355-124466356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546096645	chr12:124466365-124466366	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191318978	chr12:124466370-124466371	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2046806	chr12:124466395-124466396	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537555649	chr12:124466511-124466512	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561926075	chr12:124466527-124466528	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549181560	chr12:124466547-124466548	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574101427	chr12:124466653-124466654	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183853989	chr12:124466692-124466693	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75989601	chr12:124466723-124466724	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs76283024	chr12:124466779-124466780	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs188621533	chr12:124466784-124466785	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556076035	chr12:124466809-124466810	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs825469	chr12:124466901-124466902	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs140523011	chr12:124466903-124466904	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544553409	chr12:124466946-124466947	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550026616	chr12:124466948-124466949	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375302584	chr12:124466999-124467000	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568132197	chr12:124467025-124467026	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181370856	chr12:124467042-124467043	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547137116	chr12:124467118-124467119	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565672884	chr12:124467164-124467165	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185268727	chr12:124467175-124467176	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190146079	chr12:124467183-124467184	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182008237	chr12:124467187-124467188	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576357952	chr12:124467203-124467204	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35099862	chr12:124467204-124467205	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs555943888	chr12:124467215-124467216	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371094649	chr12:124467270-124467271	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574111962	chr12:124467285-124467286	Weak transcription Strong transcription Enhancers	n/a	n/a	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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1375 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124458800-124466600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:124458800-124466600	Weak transcription	Spleen	Spleen
3	chr12:124459000-124465800	Weak transcription	Left Ventricle	heart
4	chr12:124459000-124466000	Weak transcription	Right Ventricle	heart
5	chr12:124459000-124468400	Weak transcription	Ovary	ovary
6	chr12:124459000-124470800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr12:124459000-124470800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr12:124459000-124472200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr12:124459000-124472600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr12:124459000-124472800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr12:124459000-124473400	Weak transcription	Esophagus	oesophagus
12	chr12:124459200-124473200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:124459200-124473400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr12:124459200-124477000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr12:124459200-124477200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr12:124459400-124466400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr12:124459400-124466600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr12:124459400-124466600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:124459400-124466800	Weak transcription	Right Atrium	heart
20	chr12:124459400-124467000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr12:124459400-124468400	Weak transcription	Adipose Nuclei	Adipose
22	chr12:124459400-124470800	Weak transcription	Primary T cells from cord blood	blood
23	chr12:124459400-124470800	Weak transcription	HSMMtube	muscle
24	chr12:124459400-124471000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr12:124459400-124472000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr12:124459400-124472600	Weak transcription	Thymus	Thymus
27	chr12:124459400-124474800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr12:124459400-124474800	Weak transcription	Colonic Mucosa	Colon
29	chr12:124459600-124466400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr12:124459600-124466600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:124459600-124468200	Weak transcription	Brain Substantia Nigra	brain
32	chr12:124459600-124468600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr12:124459600-124470200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr12:124459600-124471800	Weak transcription	NH-A	brain
35	chr12:124459600-124472600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr12:124459600-124473200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:124459600-124473400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr12:124459600-124474600	Weak transcription	Stomach Mucosa	stomach
39	chr12:124459800-124471600	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr12:124459800-124473200	Weak transcription	Colon Smooth Muscle	Colon
41	chr12:124460000-124472000	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr12:124460200-124466400	Weak transcription	Brain Anterior Caudate	brain
43	chr12:124460200-124466400	Weak transcription	Gastric	stomach
44	chr12:124460200-124467400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:124460200-124474000	Weak transcription	Small Intestine	intestine
46	chr12:124460400-124466200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr12:124460400-124468800	Weak transcription	Fetal Brain Male	brain
48	chr12:124460400-124479800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr12:124460800-124473200	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr12:124460800-124475000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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