Variant report

Variant	nsv973196
Chromosome Location	chr12:10559010-10573933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:200)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:200 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
2	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
3	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
4	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:10559427-10559772	K562	blood:	n/a	n/a
6	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
7	BRCA1	chr12:10562044-10562186	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:10562055-10562317	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:10563736-10564412	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:10563725-10564405	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:10563800-10564310	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr12:10562076-10562277	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr12:10572135-10572203	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr12:10562065-10562123	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:10564040-10564190	GM12878	blood:	n/a	n/a
17	CTCF	chr12:10569608-10569679	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr12:10563940-10564020	GM19238	blood:	n/a	n/a
19	CTCF	chr12:10563860-10564010	GM12873	blood:	n/a	n/a
20	CTCF	chr12:10563840-10563990	HepG2	liver:	n/a	n/a
21	CTCF	chr12:10563840-10563990	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr12:10563903-10564028	GM10266	blood:	n/a	n/a
23	CTCF	chr12:10563840-10563990	GM12875	blood:	n/a	n/a
24	CTCF	chr12:10563841-10564129	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:10563840-10563990	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr12:10563898-10564014	GM10248	blood:	n/a	n/a
27	CTCF	chr12:10563904-10564034	GM13977	blood:	n/a	n/a
28	CTCF	chr12:10563792-10564114	K562	blood:	n/a	n/a
29	CTCF	chr12:10563752-10564135	GM12878	blood:	n/a	n/a
30	CTCF	chr12:10563860-10564010	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:10563820-10563970	GM12869	blood:	n/a	n/a
32	CTCF	chr12:10563920-10564070	Caco-2	colon:	n/a	n/a
33	CTCF	chr12:10563860-10564010	HEK293	kidney:	n/a	n/a
34	CTCF	chr12:10563890-10564034	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:10563820-10563970	GM12872	blood:	n/a	n/a
36	CTCF	chr12:10563840-10563990	GM12874	blood:	n/a	n/a
37	CTCF	chr12:10563860-10564010	SAEC	small airway:	n/a	n/a
38	CTCF	chr12:10563883-10564035	HepG2	liver:	n/a	n/a
39	CTCF	chr12:10563760-10563910	HVMF	connective:	n/a	n/a
40	CTCF	chr12:10563860-10564010	HMEC	breast:	n/a	n/a
41	CTCF	chr12:10563858-10564046	GM12878	blood:	n/a	n/a
42	CTCF	chr12:10563840-10563990	GM12864	blood:	n/a	n/a
43	CTCF	chr12:10563860-10564010	GM12872	blood:	n/a	n/a
44	CTCF	chr12:10563900-10564050	GM12868	blood:	n/a	n/a
45	CTCF	chr12:10569292-10569341	GM10248	blood:	n/a	n/a
46	CTCF	chr12:10563860-10564010	GM12867	blood:	n/a	n/a
47	CTCF	chr12:10563920-10564070	HEK293	kidney:	n/a	n/a
48	CTCF	chr12:10563840-10563990	SAEC	small airway:	n/a	n/a
49	CTCF	chr12:10563860-10564010	GM12878	blood:	n/a	n/a
50	CTCF	chr12:10563840-10563990	Caco-2	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10560602-10560652	HRE	kidney:	n/a
2	chr12:10570179-10570229	LNCaP	prostate:	n/a
3	chr12:10560602-10560652	SK-N-SH_RA	brain:	n/a
4	chr12:10560602-10560652	NH-A	brain:	n/a
5	chr12:10560602-10560652	HEEpiC	esophagus:	n/a
6	chr12:10560602-10560652	HepG2	liver:	n/a
7	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:10570179-10570229	GM12878	blood:	n/a
9	chr12:10560602-10560652	SK-N-MC	brain:	n/a
10	chr12:10560602-10560652	HIPEpiC	eye:	n/a
11	chr12:10560602-10560652	HNPCEpiC	eye:	n/a
12	chr12:10560602-10560652	ovcar-3	ovarian:	n/a
13	chr12:10560602-10560652	PFSK-1	brain:	n/a
14	chr12:10570179-10570229	GM06990	blood:	n/a
15	chr12:10560602-10560652	K562	blood:	n/a
16	chr12:10560602-10560652	NT2-D1	testis:	n/a
17	chr12:10570179-10570229	U87	brain:	n/a
18	chr12:10570179-10570229	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:10570179-10570229	IMR90	lung:	fetal
20	chr12:10560602-10560652	SKMC	muscle:	n/a
21	chr12:10570179-10570229	NHDF-neo	bronchial:	n/a
22	chr12:10570179-10570229	Hela-S3	cervix:	n/a
23	chr12:10560602-10560652	HL-60	blood:	n/a
24	chr12:10560602-10560652	HUVEC	blood vessel:	n/a
25	chr12:10570179-10570229	NB4	blood:	n/a
26	chr12:10560602-10560652	Caco-2	colon:	n/a
27	chr12:10570179-10570229	AG09309	skin:	n/a
28	chr12:10570179-10570229	CMK	blood:	n/a
29	chr12:10570179-10570229	HRPEpiC	eye:	n/a
30	chr12:10570179-10570229	Caco-2	colon:	n/a
31	chr12:10560602-10560652	RPTEC	kidney:	n/a
32	chr12:10560602-10560652	IMR90	lung:	fetal
33	chr12:10570179-10570229	HepG2	liver:	n/a
34	chr12:10560602-10560652	AG10803	skin:	n/a
35	chr12:10560602-10560652	SAEC	small airway:	n/a
36	chr12:10560602-10560652	NB4	blood:	n/a
37	chr12:10570179-10570229	RPTEC	kidney:	n/a
38	chr12:10570179-10570229	HRCEpiC	kidney:	n/a
39	chr12:10570179-10570229	SK-N-SH_RA	brain:	n/a
40	chr12:10570179-10570229	Jurkat	blood:	n/a
41	chr12:10570179-10570229	Hepatocyte	liver:	n/a
42	chr12:10570179-10570229	HEK293	kidney:	embryo
43	chr12:10570179-10570229	AG04449	skin:	fetal
44	chr12:10560602-10560652	HCPEpiC	choroid plexus:	n/a
45	chr12:10570179-10570229	H1-hESC	embryonic stem cell:	embryo
46	chr12:10560602-10560652	AG09319	gingival:	n/a
47	chr12:10570179-10570229	NT2-D1	testis:	n/a
48	chr12:10560602-10560652	HCT-116	colon:	n/a
49	chr12:10560602-10560652	GM12878	blood:	n/a
50	chr12:10560602-10560652	AG04450	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
2	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
3	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
4	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
5	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
6	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:

No data

Variant related genes	Relation type
KLRC3	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
KLRC3	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000255641	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000167900	chromatin interactions

Extended variants
information (count: 677 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554217731	chr12:10559051-10559052	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs116286070	chr12:10559053-10559054	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs148633800	chr12:10559111-10559112	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs528680715	chr12:10559148-10559149	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs180873424	chr12:10559164-10559165	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs74643554	chr12:10559185-10559186	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs2617167	chr12:10559231-10559232	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs151141996	chr12:10559244-10559245	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs576351036	chr12:10559301-10559302	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs79936651	chr12:10559304-10559305	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs12427017	chr12:10559310-10559311	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs575377521	chr12:10559348-10559349	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553412710	chr12:10559360-10559361	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs139046330	chr12:10559381-10559382	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs542064591	chr12:10559408-10559409	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371690361	chr12:10559423-10559424	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144155723	chr12:10559435-10559436	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114994843	chr12:10559447-10559448	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1154832	chr12:10559481-10559482	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1154831	chr12:10559492-10559493	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563958416	chr12:10559504-10559505	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142131702	chr12:10559548-10559549	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186419031	chr12:10559549-10559550	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544115947	chr12:10559550-10559551	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539817889	chr12:10559558-10559559	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559830898	chr12:10559621-10559622	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs528913811	chr12:10559624-10559625	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs548376708	chr12:10559693-10559694	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs568312373	chr12:10559718-10559719	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs531150999	chr12:10559797-10559798	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs36057288	chr12:10559851-10559852	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs551241650	chr12:10559857-10559858	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs11053787	chr12:10559914-10559915	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs35103745	chr12:10559928-10559929	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs74404007	chr12:10559931-10559932	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs539845246	chr12:10560020-10560021	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553060292	chr12:10560022-10560023	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs35219249	chr12:10560023-10560024	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs80131636	chr12:10560062-10560063	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535907114	chr12:10560146-10560147	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555638676	chr12:10560186-10560187	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2617168	chr12:10560188-10560189	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575492284	chr12:10560206-10560207	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs17514000	chr12:10560228-10560229	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542905075	chr12:10560284-10560285	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146324289	chr12:10560296-10560297	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138156966	chr12:10560298-10560299	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146507468	chr12:10560323-10560324	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12308865	chr12:10560367-10560368	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201205058	chr12:10560377-10560378	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10547800-10559400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:10548600-10564000	Weak transcription	Brain Angular Gyrus	brain
3	chr12:10549200-10559400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:10550600-10562000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:10550800-10564000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:10557200-10560000	Active TSS	Primary T killer memory cells from peripheral blood	blood
7	chr12:10557800-10559400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
8	chr12:10558200-10562200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:10558200-10562200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:10558400-10559400	Weak transcription	Hela-S3	cervix
11	chr12:10558800-10559600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:10558800-10560000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr12:10558800-10562400	Active TSS	Primary T cells fromperipheralblood	blood
14	chr12:10559000-10559200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
15	chr12:10559000-10559200	Enhancers	Adipose Nuclei	Adipose
16	chr12:10559000-10559400	Active TSS	Primary T cells from cord blood	blood
17	chr12:10559000-10559600	Enhancers	Primary hematopoietic stem cells	blood
18	chr12:10559000-10559800	Enhancers	Primary B cells from cord blood	blood
19	chr12:10559000-10559800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:10559000-10559800	Enhancers	NHEK	skin
21	chr12:10559000-10560000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr12:10559000-10560000	Enhancers	Primary B cells from peripheral blood	blood
23	chr12:10559000-10560000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
24	chr12:10559000-10560200	Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr12:10559200-10559600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr12:10559200-10559600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:10559200-10559600	Enhancers	Fetal Thymus	thymus
28	chr12:10559200-10559600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr12:10559200-10559800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
30	chr12:10559400-10559600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:10559400-10559600	Enhancers	Esophagus	oesophagus
32	chr12:10559400-10559600	Enhancers	K562	blood
33	chr12:10559400-10559800	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr12:10559400-10559800	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
35	chr12:10559400-10559800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:10559400-10559800	Genic enhancers	Hela-S3	cervix
37	chr12:10559600-10561400	Weak transcription	K562	blood
38	chr12:10559600-10561600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr12:10559600-10561600	Weak transcription	Fetal Thymus	thymus
40	chr12:10559600-10562200	Weak transcription	Primary hematopoietic stem cells	blood
41	chr12:10559800-10561800	Weak transcription	Hela-S3	cervix
42	chr12:10559800-10562200	Active TSS	Primary T cells from cord blood	blood
43	chr12:10559800-10562400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr12:10559800-10562400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:10559800-10563800	Weak transcription	Primary B cells from cord blood	blood
46	chr12:10559800-10564000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr12:10560000-10561400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr12:10560000-10561400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr12:10560200-10561400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr12:10561400-10561600	Active TSS	Primary hematopoietic stem cells short term culture	blood

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