Variant report

Variant	nsv557461
Chromosome Location	chr12:10568637-10598784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:393)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:393 , 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	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
4	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:10598783-10598965	GM12878	blood:	n/a	n/a
6	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
7	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
12	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
13	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
14	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
18	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
19	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
21	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
24	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:10574917-10574984	GM19239	blood:	n/a	n/a
27	CTCF	chr12:10582123-10582221	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:10582110-10582224	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:10593080-10593174	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:10591453-10591491	A549	lung:	n/a	n/a
31	CTCF	chr12:10593138-10593151	NHEK	skin:	n/a	n/a
32	CTCF	chr12:10569981-10570054	GM13976	blood:	n/a	n/a
33	CTCF	chr12:10569402-10569452	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr12:10592724-10592809	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:10582117-10582206	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:10583540-10583606	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr12:10577736-10577759	LNCaP	prostate:	n/a	n/a
38	CTCF	chr12:10593095-10593127	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:10585469-10585543	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr12:10569608-10569679	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr12:10582121-10582214	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:10593058-10593183	A549	lung:	n/a	n/a
43	CTCF	chr12:10577638-10577785	Fibrobl	skin:	n/a	n/a
44	CTCF	chr12:10597587-10597650	Fibrobl	skin:	n/a	n/a
45	CTCF	chr12:10569292-10569341	GM10248	blood:	n/a	n/a
46	CTCF	chr12:10577670-10577781	GM19239	blood:	n/a	n/a
47	CTCF	chr12:10577683-10577798	HepG2	liver:	n/a	n/a
48	CTCF	chr12:10577713-10577786	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr12:10569977-10570074	GM10266	blood:	n/a	n/a
50	CTCF	chr12:10577725-10577792	GM19240	blood:	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	chr12:10583355-10583405	GM12891	blood:	n/a
2	chr12:10583355-10583405	GM12891	blood:	n/a
3	chr12:10586130-10586180	HEK293	kidney:	embryo
4	chr12:10583355-10583405	AG04449	skin:	fetal
5	chr12:10570179-10570229	HRCEpiC	kidney:	n/a
6	chr12:10588483-10588533	PFSK-1	brain:	n/a
7	chr12:10570179-10570229	NHBE	bronchial:	n/a
8	chr12:10586130-10586180	HMEC	breast:	n/a
9	chr12:10588483-10588533	HL-60	blood:	n/a
10	chr12:10586130-10586180	PrEC	prostate:	n/a
11	chr12:10583355-10583405	AG09309	skin:	n/a
12	chr12:10588483-10588533	HRE	kidney:	n/a
13	chr12:10586130-10586180	MCF-7	breast:	n/a
14	chr12:10586130-10586180	HCF	heart:	n/a
15	chr12:10588483-10588533	HCT-116	colon:	n/a
16	chr12:10586130-10586180	HRE	kidney:	n/a
17	chr12:10570179-10570229	AG04449	skin:	fetal
18	chr12:10588483-10588533	ovcar-3	ovarian:	n/a
19	chr12:10583355-10583405	H1-hESC	embryonic stem cell:	embryo
20	chr12:10588483-10588533	BJ	skin:	n/a
21	chr12:10570179-10570229	T-47D	breast:	n/a
22	chr12:10586130-10586180	GM12892	blood:	n/a
23	chr12:10588483-10588533	AG09319	gingival:	n/a
24	chr12:10588483-10588533	GM12892	blood:	n/a
25	chr12:10570179-10570229	HEK293	kidney:	embryo
26	chr12:10570179-10570229	HNPCEpiC	eye:	n/a
27	chr12:10583355-10583405	A549	lung:	n/a
28	chr12:10588483-10588533	GM12891	blood:	n/a
29	chr12:10570179-10570229	HRPEpiC	eye:	n/a
30	chr12:10583355-10583405	U87	brain:	n/a
31	chr12:10570179-10570229	PANC-1	pancreas:	n/a
32	chr12:10586130-10586180	Hela-S3	cervix:	n/a
33	chr12:10570179-10570229	ProgFib	skin:	n/a
34	chr12:10586130-10586180	AG04450	lung:	fetal
35	chr12:10570179-10570229	HCPEpiC	choroid plexus:	n/a
36	chr12:10586130-10586180	HUVEC	blood vessel:	n/a
37	chr12:10583355-10583405	NB4	blood:	n/a
38	chr12:10583355-10583405	AG09319	gingival:	n/a
39	chr12:10583355-10583405	HRE	kidney:	n/a
40	chr12:10570179-10570229	NH-A	brain:	n/a
41	chr12:10586130-10586180	AG09309	skin:	n/a
42	chr12:10588483-10588533	SAEC	small airway:	n/a
43	chr12:10586130-10586180	MCF10A-Er-Src	breast:	n/a
44	chr12:10586130-10586180	LNCaP	prostate:	n/a
45	chr12:10586130-10586180	HL-60	blood:	n/a
46	chr12:10583355-10583405	K562	blood:	n/a
47	chr12:10583355-10583405	HCF	heart:	n/a
48	chr12:10583355-10583405	T-47D	breast:	n/a
49	chr12:10570179-10570229	AG09309	skin:	n/a
50	chr12:10586130-10586180	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
2	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell

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
ENSG00000255641	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000205810	chromatin interactions

Extended variants
information (count: 1310 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1310 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2682498	chr12:10568637-10568638	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531790242	chr12:10568667-10568668	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139665295	chr12:10568685-10568686	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564734932	chr12:10568689-10568690	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149746652	chr12:10568694-10568695	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550123713	chr12:10568740-10568741	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547272910	chr12:10568748-10568749	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78117909	chr12:10568768-10568769	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569930941	chr12:10568778-10568779	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185113422	chr12:10568813-10568814	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144581732	chr12:10568821-10568822	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370273190	chr12:10568875-10568876	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2682497	chr12:10568911-10568912	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs535879990	chr12:10568971-10568972	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74404701	chr12:10568972-10568973	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs202074957	chr12:10568986-10568987	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386760277	chr12:10569007-10569008	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79448438	chr12:10569045-10569046	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534358287	chr12:10569051-10569052	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146133073	chr12:10569064-10569065	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148038375	chr12:10569069-10569070	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199875974	chr12:10569076-10569077	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554191665	chr12:10569077-10569078	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574229198	chr12:10569079-10569080	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142603074	chr12:10569097-10569098	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112425254	chr12:10569100-10569101	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147701735	chr12:10569126-10569127	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576507041	chr12:10569135-10569136	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142422663	chr12:10569140-10569141	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2682496	chr12:10569178-10569179	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs2460735	chr12:10569181-10569182	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs547159214	chr12:10569182-10569183	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2927556	chr12:10569195-10569196	Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561027241	chr12:10569230-10569231	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370891948	chr12:10569247-10569248	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549561329	chr12:10569250-10569251	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73258205	chr12:10569251-10569252	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538775907	chr12:10569253-10569254	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368236369	chr12:10569258-10569259	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78128895	chr12:10569265-10569266	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2447703	chr12:10569267-10569268	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148120835	chr12:10569269-10569270	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369489446	chr12:10569298-10569299	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534396424	chr12:10569303-10569304	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138941727	chr12:10569321-10569322	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554303151	chr12:10569346-10569347	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150203203	chr12:10569353-10569354	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536948017	chr12:10569382-10569383	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556309419	chr12:10569410-10569411	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113145778	chr12:10569454-10569455	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:72 , 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	chr12:10567400-10569200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:10567800-10569200	Genic enhancers	Hela-S3	cervix
5	chr12:10569200-10570200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
6	chr12:10569200-10570200	Weak transcription	Hela-S3	cervix
7	chr12:10570200-10570400	Flanking Active TSS	Hela-S3	cervix
8	chr12:10570200-10570600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr12:10570200-10571600	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:10570400-10571400	Active TSS	Hela-S3	cervix
11	chr12:10570600-10572600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr12:10571400-10572600	Weak transcription	Hela-S3	cervix
13	chr12:10571600-10573800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:10572600-10573000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
15	chr12:10572600-10573200	Active TSS	Hela-S3	cervix
16	chr12:10572600-10573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:10572800-10573000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr12:10572800-10573600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr12:10572800-10573600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr12:10572800-10573600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr12:10572800-10573600	Enhancers	A549	lung
22	chr12:10572800-10573600	Enhancers	Osteobl	bone
23	chr12:10572800-10573800	Enhancers	HUVEC	blood vessel
24	chr12:10573200-10573600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr12:10573200-10573600	Enhancers	Hela-S3	cervix
26	chr12:10573600-10575200	Weak transcription	Hela-S3	cervix
27	chr12:10573600-10578200	Weak transcription	A549	lung
28	chr12:10573800-10585600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:10575200-10575800	Enhancers	Hela-S3	cervix
30	chr12:10575800-10584400	Weak transcription	Hela-S3	cervix
31	chr12:10578000-10578800	Active TSS	Brain Hippocampus Middle	brain
32	chr12:10578000-10579000	Active TSS	Brain Anterior Caudate	brain
33	chr12:10578000-10579000	Active TSS	Brain Cingulate Gyrus	brain
34	chr12:10578000-10579000	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr12:10578000-10579000	Active TSS	Brain Substantia Nigra	brain
36	chr12:10578200-10578400	Enhancers	A549	lung
37	chr12:10578200-10578800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr12:10578200-10579000	Active TSS	Brain Angular Gyrus	brain
39	chr12:10582600-10584200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr12:10584200-10588000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:10584400-10584600	Strong transcription	Hela-S3	cervix
42	chr12:10584600-10585400	Weak transcription	Hela-S3	cervix
43	chr12:10585400-10585600	Genic enhancers	Hela-S3	cervix
44	chr12:10585600-10585800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr12:10585600-10586200	Transcr. at gene 5' and 3'	Hela-S3	cervix
46	chr12:10585800-10589000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr12:10586200-10587000	Active TSS	Hela-S3	cervix
48	chr12:10587000-10588000	Weak transcription	Hela-S3	cervix
49	chr12:10588000-10588400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr12:10588000-10588600	Active TSS	Fetal Thymus	thymus

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