Variant report

Variant	esv1796748
Chromosome Location	chr12:10567764-10594710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:245)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
2	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
3	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
4	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
5	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
7	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
8	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
15	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
18	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
19	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
22	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr12:10569608-10569679	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr12:10593080-10593174	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:10582110-10582224	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:10593047-10593172	Fibrobl	skin:	n/a	n/a
28	CTCF	chr12:10570075-10570189	ProgFib	skin:	n/a	n/a
29	CTCF	chr12:10577685-10577811	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:10593932-10594014	A549	lung:	n/a	n/a
31	CTCF	chr12:10569402-10569452	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr12:10577638-10577785	Fibrobl	skin:	n/a	n/a
33	CTCF	chr12:10577678-10577792	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr12:10591453-10591491	A549	lung:	n/a	n/a
35	CTCF	chr12:10593058-10593183	A549	lung:	n/a	n/a
36	CTCF	chr12:10592724-10592809	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr12:10577664-10577750	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:10593076-10593192	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:10577736-10577759	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:10574917-10574984	GM19239	blood:	n/a	n/a
41	CTCF	chr12:10582123-10582221	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:10577670-10577781	GM19239	blood:	n/a	n/a
43	CTCF	chr12:10593084-10593189	Gliobla	brain:	n/a	n/a
44	CTCF	chr12:10585469-10585543	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr12:10582121-10582214	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:10577654-10577777	A549	lung:	n/a	n/a
47	CTCF	chr12:10593082-10593151	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:10569977-10570074	GM10266	blood:	n/a	n/a
49	CTCF	chr12:10577683-10577798	HepG2	liver:	n/a	n/a
50	CTCF	chr12:10593138-10593151	NHEK	skin:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10570179-10570229	GM19239	blood:	n/a
2	chr12:10570179-10570229	GM19239	blood:	n/a
3	chr12:10570179-10570229	Caco-2	colon:	n/a
4	chr12:10586130-10586180	HCF	heart:	n/a
5	chr12:10588483-10588533	H1-hESC	embryonic stem cell:	embryo
6	chr12:10583355-10583405	AG04449	skin:	fetal
7	chr12:10570179-10570229	HRCEpiC	kidney:	n/a
8	chr12:10583355-10583405	MCF10A-Er-Src	breast:	n/a
9	chr12:10588483-10588533	HRCEpiC	kidney:	n/a
10	chr12:10583355-10583405	GM19239	blood:	n/a
11	chr12:10570179-10570229	HCF	heart:	n/a
12	chr12:10586130-10586180	T-47D	breast:	n/a
13	chr12:10586130-10586180	AG09309	skin:	n/a
14	chr12:10570179-10570229	Jurkat	blood:	n/a
15	chr12:10570179-10570229	Hepatocyte	liver:	n/a
16	chr12:10586130-10586180	NB4	blood:	n/a
17	chr12:10583355-10583405	HL-60	blood:	n/a
18	chr12:10586130-10586180	HIPEpiC	eye:	n/a
19	chr12:10586130-10586180	MCF10A-Er-Src	breast:	n/a
20	chr12:10583355-10583405	CMK	blood:	n/a
21	chr12:10583355-10583405	LNCaP	prostate:	n/a
22	chr12:10586130-10586180	HUVEC	blood vessel:	n/a
23	chr12:10570179-10570229	HUVEC	blood vessel:	n/a
24	chr12:10570179-10570229	NHDF-neo	bronchial:	n/a
25	chr12:10588483-10588533	GM12892	blood:	n/a
26	chr12:10583355-10583405	RPTEC	kidney:	n/a
27	chr12:10588483-10588533	SK-N-SH	brain:	n/a
28	chr12:10570179-10570229	T-47D	breast:	n/a
29	chr12:10570179-10570229	HRPEpiC	eye:	n/a
30	chr12:10588483-10588533	HEK293	kidney:	embryo
31	chr12:10583355-10583405	HCPEpiC	choroid plexus:	n/a
32	chr12:10583355-10583405	Hela-S3	cervix:	n/a
33	chr12:10588483-10588533	NH-A	brain:	n/a
34	chr12:10588483-10588533	HIPEpiC	eye:	n/a
35	chr12:10583355-10583405	PFSK-1	brain:	n/a
36	chr12:10586130-10586180	HCPEpiC	choroid plexus:	n/a
37	chr12:10586130-10586180	Hepatocyte	liver:	n/a
38	chr12:10586130-10586180	NHDF-neo	bronchial:	n/a
39	chr12:10570179-10570229	U87	brain:	n/a
40	chr12:10588483-10588533	PrEC	prostate:	n/a
41	chr12:10570179-10570229	AG09319	gingival:	n/a
42	chr12:10583355-10583405	HCM	heart:	n/a
43	chr12:10570179-10570229	NH-A	brain:	n/a
44	chr12:10570179-10570229	PrEC	prostate:	n/a
45	chr12:10570179-10570229	AG04450	lung:	fetal
46	chr12:10588483-10588533	LNCaP	prostate:	n/a
47	chr12:10586130-10586180	AG04449	skin:	fetal
48	chr12:10588483-10588533	PFSK-1	brain:	n/a
49	chr12:10588483-10588533	BE2_C	brain:	n/a
50	chr12:10570179-10570229	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
2	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
3	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:

No data

Variant related genes	Relation type
KLRC3	TF binding region
ENSG00000255641	TF binding region
KLRC2	TF binding region
KLRC3	CpG island
ENSG00000255641	CpG island
KLRC2	CpG island
ENSG00000205809	chromatin interactions
ENSG00000205810	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000255641	chromatin interactions

Extended variants
information (count: 1213 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533377290	chr12:10567792-10567793	Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs2741888	chr12:10567793-10567794	Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs566982998	chr12:10567798-10567799	Transcr. at gene 5' and 3' Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186683141	chr12:10567803-10567804	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs549208939	chr12:10567814-10567815	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2741887	chr12:10567827-10567828	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143792466	chr12:10567834-10567835	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557647183	chr12:10567836-10567837	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2741886	chr12:10567851-10567852	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2682501	chr12:10567857-10567858	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146220476	chr12:10567898-10567899	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs114425229	chr12:10567991-10567992	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs113126391	chr12:10568025-10568026	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs137925127	chr12:10568031-10568032	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2682500	chr12:10568047-10568048	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs555954357	chr12:10568079-10568080	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561798932	chr12:10568080-10568081	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533445682	chr12:10568106-10568107	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575731375	chr12:10568137-10568138	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544756387	chr12:10568169-10568170	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564789302	chr12:10568181-10568182	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368930437	chr12:10568242-10568243	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149679250	chr12:10568250-10568251	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145456037	chr12:10568251-10568252	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115905385	chr12:10568253-10568254	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200631653	chr12:10568259-10568260	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200006578	chr12:10568277-10568278	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199503280	chr12:10568284-10568285	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145137620	chr12:10568342-10568343	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569300623	chr12:10568344-10568345	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531430108	chr12:10568347-10568348	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370281229	chr12:10568349-10568350	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138974556	chr12:10568354-10568355	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370768044	chr12:10568367-10568368	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201997887	chr12:10568381-10568382	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542624954	chr12:10568387-10568388	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140645842	chr12:10568395-10568396	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185060408	chr12:10568402-10568403	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376950129	chr12:10568417-10568418	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79481984	chr12:10568445-10568446	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567128229	chr12:10568448-10568449	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536380262	chr12:10568514-10568515	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555998726	chr12:10568517-10568518	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77926410	chr12:10568525-10568526	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564720033	chr12:10568543-10568544	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2682499	chr12:10568555-10568556	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs2741885	chr12:10568557-10568558	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs578262810	chr12:10568592-10568593	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139567617	chr12:10568608-10568609	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189031325	chr12:10568612-10568613	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10562200-10572800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:10564400-10570200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr12:10566600-10567800	Strong transcription	Hela-S3	cervix
4	chr12:10567400-10569200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:10567800-10569200	Genic enhancers	Hela-S3	cervix
6	chr12:10569200-10570200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:10569200-10570200	Weak transcription	Hela-S3	cervix
8	chr12:10570200-10570400	Flanking Active TSS	Hela-S3	cervix
9	chr12:10570200-10570600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
10	chr12:10570200-10571600	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:10570400-10571400	Active TSS	Hela-S3	cervix
12	chr12:10570600-10572600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr12:10571400-10572600	Weak transcription	Hela-S3	cervix
14	chr12:10571600-10573800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:10572600-10573000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
16	chr12:10572600-10573200	Active TSS	Hela-S3	cervix
17	chr12:10572600-10573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:10572800-10573000	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr12:10572800-10573600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr12:10572800-10573600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:10572800-10573600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr12:10572800-10573600	Enhancers	A549	lung
23	chr12:10572800-10573600	Enhancers	Osteobl	bone
24	chr12:10572800-10573800	Enhancers	HUVEC	blood vessel
25	chr12:10573200-10573600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr12:10573200-10573600	Enhancers	Hela-S3	cervix
27	chr12:10573600-10575200	Weak transcription	Hela-S3	cervix
28	chr12:10573600-10578200	Weak transcription	A549	lung
29	chr12:10573800-10585600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:10575200-10575800	Enhancers	Hela-S3	cervix
31	chr12:10575800-10584400	Weak transcription	Hela-S3	cervix
32	chr12:10578000-10578800	Active TSS	Brain Hippocampus Middle	brain
33	chr12:10578000-10579000	Active TSS	Brain Anterior Caudate	brain
34	chr12:10578000-10579000	Active TSS	Brain Cingulate Gyrus	brain
35	chr12:10578000-10579000	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr12:10578000-10579000	Active TSS	Brain Substantia Nigra	brain
37	chr12:10578200-10578400	Enhancers	A549	lung
38	chr12:10578200-10578800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:10578200-10579000	Active TSS	Brain Angular Gyrus	brain
40	chr12:10582600-10584200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:10584200-10588000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:10584400-10584600	Strong transcription	Hela-S3	cervix
43	chr12:10584600-10585400	Weak transcription	Hela-S3	cervix
44	chr12:10585400-10585600	Genic enhancers	Hela-S3	cervix
45	chr12:10585600-10585800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:10585600-10586200	Transcr. at gene 5' and 3'	Hela-S3	cervix
47	chr12:10585800-10589000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:10586200-10587000	Active TSS	Hela-S3	cervix
49	chr12:10587000-10588000	Weak transcription	Hela-S3	cervix
50	chr12:10588000-10588400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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